[Article]
Get our E-Alerts
Articles ▼ All Issues About Us ▼ Submit Manuscript Get our E-Alerts
Review Article
06 Aug 2025
Essential Oils in Dermatology
Thineesha Gnaneswaran, MSc, Audrey Fotouhi, MD, Kathryn Lynam, MD, Sarah Utz, MD, Steven Daveluy, MD
Review Article
28 Apr 2025
Essential Oils in Dermatology
Thineesha Gnaneswaran, MSc, Audrey Fotouhi, MD, Kathryn Lynam, MD, Sarah Utz, MD, Steven Daveluy, MD
DOI:
10.64550/joid.nt5zgk07
Reviewed by:
Peter Lio, MD, Sarah Sung, MD
Abstract

The global essential oils market was valued at 24.75 billion USD in 2024, driven by increasing consumer interest in natural healthcare alternatives. With a significant portion of the population seeking health-related information online, essential oils have gained popularity for various purposes, including skincare and alternative medicines. However, healthcare providers often lack formal training in this area, necessitating the need for evidence-based information to effectively counsel patients. This narrative review aims to fill the existing knowledge gap associated with the use of essential oils in dermatology. By summarizing available evidence, our objective is to provide healthcare professionals with a reliable resource detailing the studied uses, benefits, potential risks, and reported adverse effects of commonly used essential oils. Our narrative review combines data from extensive searches on PubMed and Science Direct. In a world where essential oils are viewed as accessible, natural remedies, it is vital for healthcare providers to have comprehensive knowledge of their dermatological implications. This concise narrative review serves as a valuable resource for clinicians, offering a balanced and accurate understanding of the use of essential oils in dermatology to facilitate informed discussions with patients.

[Article - Top - Sidebar]
Introduction

In 2024, the global revenue of the essential oils market was valued at 24.75 billion USD.1 As consumer awareness surrounding the importance of health-conscious decisions continues to increase, the demand for alternative medicine and products with natural or organic origins is also increasing.2 In the United States, it is estimated that six million individuals use the internet to retrieve information related to their health on a daily basis, with approximately 40% of these users looking to gain more information about alternative medicines.3 The use of essential oils, especially in their pure form, is increasing rapidly.4 A general population survey found that essential oils were used in a variety of ways including while experimenting with alternative medicine, following previous treatment failures or because it was believed that essential oils were safer than conventional treatment options.5

Essential oils are widely used for their aromatic and therapeutic properties however some consumers are unaware of how they differ from other products in the market such as plant extracts and cold-pressed oils. What differentiates these products are the methods of extraction used and applications of the product. Essential oils are conventionally obtained through steam distillation, producing highly concentrated, impurity-free, volatile aromatic compounds used in aromatherapy and alternative medicine. Other extraction techniques used include solvent extraction, water distillation and cold pressing. Mechanical extraction via cold pressing is also used for citrus fruit peels including oranges and lemons, maintaining heat-sensitive compounds and antioxidants.6 In contrast, extracts are made by soaking plant material in various solvents such as water or alcohol, and producing compounds for flavoring, supplements, and herbal remedies.7,8 Finally, cold-pressed oils can be made from plant materials including fruits, nuts, and seeds. Cold-pressed oils are mechanically pressed without heat, preserving vitamins, and antioxidants, making them suitable for culinary and skincare applications.9 By understanding these differences, patients and providers can better assess the benefits and use cases of essential oils.

Many healthcare providers are uncomfortable with discussing the use of complementary medicine, including essentials oils, with patients as there is a lack of formal education and training on these topics. However, as patients increasingly turn to the internet for medical advice, the use of essential oils continues to grow amongst patients who view these products as easily accessible, natural, and safer than traditional medications. To effectively counsel patients, healthcare providers need to become familiar with evidence-based information on the subject.10

Currently, there is a gap in the literature regarding the benefits and risks of using essential oils and its impact on health.11 This article will serve as a resource for clinicians regarding several commonly used essential oils. We emphasize their studied uses and benefits as well as their potential risks and reported adverse effects to aid providers in offering balanced and accurate information to their patients who may be using these home remedies.

For this narrative review, a list of the most used essential oils was determined via PubMed and Google searches for “Essential Oils,” “Dermatology,” and “Skin.” Upon finalizing a list of essential oils, databases including PubMed and Science Direct were used to identify the potential benefits, risks, and reported adverse effects of these essential oils.

Lavender Oil

Lavender essential oil (LEO), extracted from Lavandula angustifolia, is one of the most popular and commonly used essential oils.4 The current body of literature proposes that lavender essential oil exhibits antimicrobial activity against microbes such as Streptococcus pyogenes (S. pyogenes), Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli) which may be useful against surface infections. LEO also lends itself to multiple dermatologic uses including the treatment of atopic dermatitis, psoriasis, and acne given its antibacterial and antifungal properties.12–15 In treatment-resistant acne, LEO has been shown to be effective against certain antibiotic-resistant bacteria.12 Another reported therapeutic benefit of LEO is its ability to shorten wound healing time. Data has shown that LEO can decrease wound size and shorten time to healing by supporting collagen production.16,17 Marked concentration-dependent increases in the production of IL-6, IL-8, and VEGF, key signaling molecules important for wound healing, were observed in a human keratinocyte cell line.18 In addition, LEO has been shown to reduce inflammation by decreasing proinflammatory cytokine production and assisting in chronic wound healing via the inhibition of macrophage pyroptosis.19

One study also discussed the benefits of LEO on hair growth. Of 86 study patients with alopecia areata, approximately half of the study population showed an improvement in hair growth after 7 weeks of treatment with essential oils containing lavender.20 Small animal studies have also shown increased hair growth with LEO as compared to placebo.21

One of the most widely acclaimed properties of LEO is its ability to induce relaxation.22 After cutaneous application or inhalation of LEO or its main constituent, linalool, three studies reported a decrease in autonomic stimulation as evidenced by decreased heart rate, blood pressure, or skin temperature; indicating that lavender oil does affect the parasympathetic nervous system.22–25

While LEO is known for its therapeutic benefits, recent studies have expressed concerns regarding its potential endocrine disrupting effects.26,27 Within the literature, LEO has been linked to premature thelarche and prepubertal gynecomastia due to its estrogenic and antiandrogenic properties.28 Case reports show that continuous exposure to lavender-containing fragrance products were associated with breast growth in children, which dissipated in all patients upon discontinuation/removal of the products.28,29 In vitro studies also confirmed that components of LEO exhibit endocrine-disrupting activities, suggesting it may be a potential source of idiopathic prepubertal breast development.26

Despite being derived from natural sources, LEO’s use has been reported to cause adverse effects including contact dermatitis and photoallergic reactions, which have become more recognizable with the increased popularity of essential oils for aromatherapy.4,30–36 Lavender oil in its pure form has been demonstrated to be a weak sensitizer; however, its oxidized counterpart was identified to be a moderate allergen causing one of the highest positive patch test rates when tested among other compounds such as oxidized linalyl acetate and linool, major components found in other essential oils.37,38

When advising patients on the utilization of lavender essential oil (LEO), the most robust evidence supports its efficacy in promoting relaxation.22 Due to the potential risk of contact dermatitis associated with topical application, it is recommended to employ LEO as an aromatherapy agent via inhalation.37,38 Additionally, a small study indicates potential benefits of LEO in the management of alopecia areata.20 For patients inclined towards “natural” remedies, topical application to the scalp could be considered as an adjunct to standard treatments for alopecia areata, provided that the patient does not exhibit contact dermatitis upon application.

Frankincense Oil

Frankincense essential oil (FREO), derived from the oleogum resins of the Boswellia species, has been used for multiple centuries for both its aromatic and medicinal benefits.39,40 Due to a push towards natural remedies, studies exploring the anti-inflammatory, antimicrobial, and anti-tumoral properties of FREO and its therapeutic uses have increased.40

FREO as a microemulsion (oil content of 7.8%) displayed higher anti-inflammatory effects when compared to the common synthetic anti-inflammatory medication piroxicam in non-steroidal anti-inflammatory drug (NSAID) gel upon transdermal application. This was evidenced by the FREO microemulsion having an increased percentage of inhibition of inflammation within an in vivo mouse model.41 Studies completed on human cell lines showed that treatment with FREO decreased proliferation of fibroblasts and the production of tissue remodeling molecules, such as collagen III, in vitro, elucidating potential benefits in wound healing and the prevention of scar formation.42,43

FREO has also been shown to have antimicrobial properties, demonstrating activity against common skin pathogens including Propionibacterium acnes (P. acnes), Malassezia spp. and Candida albicans (C. albicans), with maximum antimicrobial activity against Trichophyton* spp. When used alongside azoles in the treatment of skin and nail infections, it has been shown to have synergistic anti-fungal effects.44,45

Regarding its anti-tumoral properties, high concentrations of boswellic acid, FREO’s active molecule, have shown in-vitro cytotoxic and cytostatic effects on certain malignant cell lines, including melanoma.46,47 It has also demonstrated antitumoral activity in mouse models.48 However, there are limited in vivo studies assessing FREO’s effect on cutaneous malignancies.3

Additional reported properties of FREO include its potential to increase the transdermal uptake of drugs via increased skin perfusion and permeability and decrease erythema in patients with atopic dermatitis and psoriasis.49–51

Adverse reactions to FREO are limited and therefore may allow for daily use, however there are reports of FREO causing harm due to online misinformation.3,52 One paper reported a blistering reaction to topical FREO when a patient attempted to use it for mole removal. The “mole” was eventually biopsied and found to be a nodular basal cell carcinoma.3 This once again emphasizes the importance of educating patients on best practices for the use of alternative medications and when medical care should be sought.

Currently there are multiple in vitro benefits reported for FREO.42–47,49 With regards to its use in a clinical setting, FREO may be used in cases of atopic dermatitis and psoriasis to decrease erythema.51

Geranium Oil

Geranium essential oil (GEO), extracted from the leaves of Pelargonium graveolens and belonging to the Geraniaceae family, is popularly used for its fragrant properties within the cosmetics industries as well as medicinally.53

GEO has demonstrated dose-dependent anti-inflammatory properties in rodent models by reducing edema and peritoneal inflammation.54,55 In one study, GEO was found to have significant antiproliferative activity against human dermal fibroblasts which may play a role in wound healing.42

Research shows that GEO may also have anti-aging and photo-protective effects.56,57 GEO demonstrates an ability to reduce and prevent oxidative stress. When introduced into a skincare routine, GEO can leverage its antioxidant properties to aid in slowing down the process of skin aging. When combined with calendula essential oil, the antioxidant and SPF properties of both oils can provide increased photoprotective effects and may enhance cosmeceutical formulations.57

GEO also has antimicrobial and antiparasitic properties, and can be a useful adjunct to antibiotics in treatment-resistant infections.58,59 Out of 14 essential oils, GEO was amongst the top five most active against test fungi including Microsporum gypseum (M. gypseum), Microsporum canis (M. canis), and Trichophyton mentagrophytes (T. mentagrophytes).60

GEO has been shown to promote hair growth in vitro and in vivo through regulation of the involved cellular response.61 It also serves as an effective component of bug repellent mixtures; however, all the essential oil mixtures tested were significantly shorter acting than DEET 19%.62–64

Current data on the adverse effects of GEO is limited, requiring further research to clearly define its usage risks. Given the lack of data on adverse effects, there is insufficient evidence to recommend GEO’s use in a clinical setting.

Myrrh Oil

Myrrh essential oil (MEO) is derived from the resins of the Commiphora myrrh plant.65 It is widely used as a natural remedy in Asia and Africa and traditionally revered for its medicinal properties.66

Although MEO has not been extensively studied, there are animal studies that support MEO as an effective agent in wound healing.67,68 Mice treated with myrrh had higher leukocyte counts both prior to and after skin injury.67 Additionally, mice with skin wounds treated topically with myrrh had an increased rate of wound contraction, shorter re-epithelialization times and increased wound tensile strength. MEO was also found to inhibit elastase, a biomarker of inflammation produced by neutrophils.68

In addition to this, MEO also demonstrated significant activity against a wide variety of pathogens thus showcasing its antimicrobial properties. Its antimicrobial effects measured by zone of inhibition were shown to be similar to that of the broad-spectrum antibiotic ciprofloxacin. Gram negative bacteria including E. coli, Vibrio cholerae (V. cholerae) and Salmonella typhi Ty2 (S. typhi) were the most inhibited by MEO. Similarly, MEO was shown to be ~78.9% as active as the antifungal medication griseofulvin against test fungi which included C. albicans, Aspergillus niger (A. niger), Penicillium funiculosum (P. funiculosum), and Penicillium notatum (P. notatum).68

MEO has been described as non-irritating when administered in low concentrations (ointment 4%).68 However there are multiple case reports in the literature of MEO-induced allergic contact dermatitis with subsequent positive patch tests to myrrh.69–71 Similar contact reactions to those induced by MEO have been seen after topically applying traditional Chinese medicine pain relievers.71

At this time, there is insufficient evidence to recommend MEO’s use in a clinical setting.

Neroli Oil

Neroli essential oil (NEO), extracted from Citrus aurantium flowers, is known for its widespread use in floral perfumery. In addition to its use in fragrances, it is also thought to possess antimicrobial, antifungal, and antioxidant properties.72

NEO’s antimicrobial activity is most pronounced against gram negative bacteria, with increased activity seen against Pseudomonas aeruginosa (P. aeruginosa). NEO also demonstrated strong anti-fungal activity against Saccharomyces cerevisiae (S. cerevisiae) and C. albicans, evidenced by inhibition zones comparable to the antifungal medication nystatin which was used as a positive reference. The antioxidant properties of NEO are dependent on its chemical composition. Despite γ-terpine, a minor component of NEO, being shown to have high antioxidant activity, limonene, a major component of NEO, was shown to have low antioxidant properties as evidenced by low free radical scavenging activity.72 Regarding its anti-inflammatory properties, NEO has been shown to block signaling pathways activated during the acute and chronic inflammatory response, including the mitogen-activated protein kinase pathway.72,73

Adverse effects of NEO have been documented in the literature. Exposure to neroli oil in the context of perfume factory workers resulted in multiple cases of contact dermatitis.74,75 There are reports of Belgian patients using ketoprofen, a topical NSAID cream, combined with fragrance components from NEO who subsequently developed photoallergic dermatitis.75

Given numerous reported adverse effects, currently we do not recommend use of NEO in a clinical setting.

Patchouli Oil

Patchouli essential oil (PEO), an essential oil derived from the Pogostemon cablin plant, rich in sesquiterpenes, has widespread use in both Indian and Chinese traditional medicine.76,77 PEO has been used in the treatment of various dermatologic conditions including in the treatment of acne and eczema.78 PEO has also demonstrated pharmacological benefits including antioxidant, antimicrobial, and sedative properties.79–81

There is some preliminary evidence to support PEO’s use in anti-aging, specifically protection against photo-aging. Animal studies showed that application of an isolated component of PEO, pogostone, prior to UV sun exposure resulted in decreased wrinkles, improved maintenance of skin elasticity, and decreased epidermal thickening on histology in mouse models. The proposed mechanism of protection against photoaging is via antioxidant free radical scavenging and subsequent decreased inflammation.82,83

PEO has also shown benefit in wound healing and prevention of scarring. PEO demonstrated significant antiproliferative effects against dermal fibroblasts in vitro, and inhibitory effects towards a tissue remodeling biomarker (PAI-1).42

PEO may also be used against two of the main organisms implicated in acne, P. acnes and Staphylococcus epidermidis (S. epidermidis).80 Although no synergistic effects amongst combinations of PEO with 69 other essential oils were observed, additive effects were noted.80 Finally, PEO has insecticidal properties. Among 38 different oils, PEO ranked within the top four repellants against three different species of mosquito.84

Current data on the adverse effects of PEO is limited, requiring further research to clearly define its usage risks. At this time, there is insufficient evidence to recommend PEO’s use in a clinical setting.

Rose Oil

Rose essential oil (REO) is derived from the petals of the Rosa species. REO is most commonly extracted from the Rosa x damascena Mill. due to the superior quality of oil that can be procured from it.85 It is popularly used for its fragrance in both the cosmetic and food industries.86 REO is known to be expensive due to the low oil content in the plant itself and the lack of available synthetic substitutes.87

There is some evidence emerging in the literature that rose oil may have anti-aging benefits. REO was found to be hydrating to dry skin, with one study finding that it improved skin barrier function when used in combination with tea tree extract within a topical gel formulation, thereby demonstrating its potential uses in cosmetic anti-aging formulations.88,89 Rose oil was also found to have additive antioxidant properties when mixed with clove oil.90

REO may be used as an adjunct to wound healing. An animal study showed that the topical application of REO accelerated the recovery of the barrier function in mouse skin.91 In one study, REO extracted from the Rosa rugosa ‘Plena’ flower, significantly reduced both oxidative and inflammatory biomarkers such as nitric oxide, superoxide dismutase, and monodialdehyde.92 Additionally, REO has been shown to have antibacterial activity against bacteria including P. aeruginosa, E. coli, Chromobacterium violaceum (C. violaceum), and S. aureus.93,94 REO has also been shown to have antifungal properties against P. notatum, A. niger, and C. albicans.95

The relaxation properties of REO have also been studied. Human studies demonstrated that inhaling rose essential oil inhibited the typical effects of chronic stress, including increased salivary cortisol levels and transepidermal water loss, as observed during and after students completed a scheduled academic exam. Whether this effect is clinically significant remains to be seen.96 Another study demonstrated a decrease in several autonomic parameters in those who massaged REO topically on the skin for five minutes.97 Additionally, a study demonstrated that REO was an agonist of transient receptor potential vanillioid subtype 1 (TRPV1), receptors activated by capsaicin, with activity equivalent to 45% that of capsaicin; identifying rose oil as a potential agent in treating pain. In addition to being involved in peripheral nociception, TRPV1 has also been shown to be expressed in the keratinocytes of the human epidermis and hair follicles. One study showed that TRPV1 activation was involved in inhibiting hair matrix keratinocyte proliferation and the induction of apoptosis, thereby elucidating a role for REO in skin disorders.98 However further research is needed to understand REO’s therapeutic potential in the latter context.

A study on the pharmacokinetics of phenylethyl alcohol, one of the main constituents of rose oil, indicated that it is safe for use. Both human and rat studies determined that REO is safe up to 2600 mg/kg applied topically and is likely safe in pregnancy as well.99 However, there may be some variations in this maximum level of REO that should be incorporated in formulations as rose oil has been shown to be absorbed very differently depending on which area of the body it is applied to.100 There are several case reports highlighting allergic contact dermatitis to rose oil found in cosmetic products or applied to skin in its pure form.101–103 A study investigating the effects of rose oil on workers in a perfume factory also demonstrated the effects of sensitization and indicates that more cases of allergy to rose oil and other essential oils may occur as the use of essential oils increases.104

The relaxation properties of REO have been well-documented.96,97,99 Currently, REO could be considered for use as a relaxation agent for aromatherapy, administered via inhalation.

Tea Tree Oil

Tea tree oil (TTO) is a monoterpene-rich essential oil derived from the Melaleuca alternifolia plant.105 TTO has been cited in the literature for its antimicrobial and anti-inflammatory properties which provides the foundation for its use in treating acne.106

As TTO treatments are available without a prescription, it has been difficult to gauge its use and feedback. However, among online patients it was identified as the second most used topical product for treating acne secondary to benzoyl peroxide (2.5%).107 Tea tree oil gels are effective for acne treatment due to their sustained release, enhanced penetration, and anti-inflammatory properties, allowing prolonged contact with the skin while minimizing irritation. They are non-greasy, easily absorbed, and demonstrate a low incidence of adverse events across studies, making them ideal for topical use in acne-prone and sensitive skin.108 A double-blind RCT reported that the use of TTO 5% gel for 45 days resulted in a significant decrease in total lesion count, acne severity index, comedones, papules, and pustules among patients with mild-moderate acne vulgaris.109 An uncontrolled open-label multicentric phase III RCT reported that the use of TTO 5% gel for 4 weeks resulted in a significant decrease in blackheads, papules, and pustules among patients with mild-moderate acne vulgaris.110 A comparative investigator-blind study reported that in comparison to a 2% erythromycin gel, a 5% topical TTO gel was found to be more effective in reducing acne lesion count and acne severity index.111 Despite its proven benefits, tea tree oil (5% water based gel) was found to be less effective than benzoyl peroxide (5% water based lotion) in reducing inflammatory lesions and skin oiliness. However, benzoyl peroxide was found to have more adverse effects such as skin irritation, erythema, and itching.112 Many previous studies investigated products with up to 5% TTO in the treatment of acne; however, these products are not readily commercially available. A dual center-open label phase II pilot study was thus undertaken and reported that the use of tea tree medicated gel (200 mg/g) resulted in a significant decrease in total lesion count, investigator global assessment mean, and facial oiliness among patients with mild-moderate acne vulgaris. This efficacy was hypothesized to be due to the antibacterial activity of TTO against P. acnes and supports its potential as a treatment option for mild to moderate acne. However, the effectiveness of TTO in treating acne depends on the concentration, treatment frequency, and formulation.113

TTO’s demonstrated fungicidal properties have resulted in its use as a treatment of onychomyosis.114 A double blind, single-arm clinical trial showed that the use of 100% tea tree oil twice daily for 6 months resulted in 89% of patients achieving mycological cure and 27% patients being clinically cured.115 A double-blind RCT showed that the use of 100% tea tree oil twice daily for 6 months resulted in 82% of the patients achieving a mycological cure.116 An in- vitro study demonstrated that TTO (at concentrations < 0.5%) inhibited the growth of Trichophyton schoenleinii, Trichophyton tonsurans, and Trichophyton rubrum, three common causative agents of nail infections, suggesting TTO’s potential as an alternative treatment for onychomycosis.117

Over the last few decades, TTO has become an increasingly popular essential oil which continues to be incorporated into skin care and alternative medicine formulations.118 This may explain why TTO has the most documented allergic reactions when compared to all other essential oils within the published literature; with most reactions induced by the pure form of the essential oil.119 Adverse reactions to TTO (5%) include burning, erythema, and pruritus. However, significantly fewer adverse events were recorded in patients given TTO when directly compared with patients given 5% benzoyl peroxide.112

While TTO is widely praised for its antimicrobial and anti-inflammatory properties, similar to LEO, recent studies have expressed concerns regarding TTO’s potential endocrine disrupting effects.26,27 Case reports show that repeated topical application of products containing TTO were associated with prepubertal gynecomastia with symptoms resolving after discontinuation.26 In-vitro studies also indicated that components of TTO exhibits estrogenic and antiandrogenic activity, potentially disrupting the hormonal balance necessary for normal puberty.26

Although tea tree oil (TTO) has the highest incidence of documented allergic reactions among essential oils, it also possesses the most robust evidence for treating acne.106,111,113,119 Currently, TTO gel formulations could be considered for use as an adjunct to conventional acne treatments in appropriate candidates and 100% TTO could be considered for use in cases of onychomycosis.

Ylang-Ylang Oil

Ylang-ylang essential oil (YEO) is procured from the flower of the Cananga odorata plant and is widely used for its fragrant properties within the cosmetics, culinary, and aromatherapy industries.120 YEO is also reported to have medicinal properties demonstrating antimicrobial, antioxidant, wound healing, anti-aging, and mood regulating effects.42,80,120–124

YEO shows strong synergistic activity against two of the main bacteria implicated in the development of acne, P. acnes, and S. epidermidis when used alongside myrrh and petit grain oil.80 At high doses, YEO also showed activity against scabies mites due to its main chemical constituent isoeugenol.121

Additionally, in vitro YEO was shown to decrease proliferation of human fibroblasts and inhibit tissue remodeling biomarkers, with potential to be useful in wound healing and scar prevention.42

During transdermal application on human subjects, YEO was found to decrease blood pressure, increase skin temperature, and increase subjective calmness and relaxation.122 Similar effects were observed when inhaled, but attentiveness and alertness were also increased.123

YEO was found to be safe when consumed as a food additive and posed virtually no risk to human health when consumed at levels of 0.0001 mg/kg/day.125 The National Toxicology program found that isoeugenol, the main component of YEO, was non-mutagenic in two bacterial assays (Salmonella typhimurium and E. coli). However, in male rats there was evidence of a significant increase in carcinogenic activity when isoeugenol was ingested at large doses (75, 150, 300 mg/kg). Specifically, these mice developed hepatocellular adenoma and or carcinoma.126 There are multiple cases of YEO induced contact dermatitis and resultant hyperpigmentation.127–129 Sensitivity to YEO determined via patch testing was also shown to be the highest in comparison to all other essential oils tested.130–137 The Scientific Community on Consumer Safety found ylang-ylang oil to be a contact allergen with an “alarming” prevalence of sensitization defined by 100-1000 reported cases.138 When applied to the skin, ylang-ylang oil also has the potential to alter the absorption of other substances.138 YEO has also been shown to cause heat sensitization reactions in both humans and animals.124

Given numerous reported adverse effects when used topically, YEO could be considered for use for relaxation via inhalation aromatherapy.

Lemongrass Oil

Lemongrass essential oil (LGEO) comes from the tropical plant Cymbopogon citratus and is cultivated in Asia, Africa, and South America where it is widely used.139 In addition to its aromatic properties, published literature supports its medicinal value attributed to its antifungal, antitumoral, antioxidant, anti-aging properties.140–142

Both in silico and in vitro studies among fungi, parasites, and humans provide evidence of its specific inhibitory action against ATP catalyzing enzymes thus highlighting its usability as an antifungal and antitumoral drugs. With regards to its antitumoral properties in specific, the effect is maximally seen when LGEO is combined with Geraniol and Citral oil.141 LGEO also demonstrated its capacity to serve as an antifungal agent against all Candida tropicalis (C. tropicalis) strains by significantly reducing growth and biofilm formation when applied to silicone rubber prostheses and medical devices. This was in comparison to lemon and cumin essential oil which showed limited antifungal effects.143

LGEO has been shown to reduce the expression of inflammatory cytokines, oxidative stress, and hydrocarbon induced DNA damage in human cell lines.144 Additionally, LGEO has also demonstrated high antioxidant activity indicating its potential use in anti-aging spa and cosmetic formulations.145

Current data on the adverse effects of LGEO is limited, requiring further research to clearly define its usage risks. At this time, there is insufficient evidence to recommend LGEO’s use in a clinical setting.

Sandalwood Oil

The use of sandalwood essential oil (SEO) derived from the Santalum album tree can be traced back multiple centuries in both Ayurvedic and Chinese medicine. It continues to be used to date for its anti-inflammatory, antimicrobial, and anti-proliferative properties.146

Studies have shown that SEO interacts with transcription factors and decreases pro-inflammatory enzymes.147 SEO has thus been used in the treatment of skin conditions including atopic dermatitis and psoriasis because of its anti-inflammatory properties.147

SEO demonstrates antimicrobial properties that have been leveraged against antibiotic-resistant bacteria such as methicillin resistant S. aureus (MRSA) and vancomycin resistant S. aureus (VRSA), with its mechanism of action hypothesized to be via the disruption of the cell membrane.146 SEO has also shown activity against herpes simplex virus, human papillomavirus, and molluscum contagiosum virus. When used transdermally on warts, 80% of patients experienced a resolution of warts upon 12 weeks of daily treatment with no associated irritation, pain, or discomfort.148

The anti-proliferative effects of SEO have been studied in mice and human cancer cell lines.146,149–153 In relation to skin cancer, sandalwood oil has been seen to induce autophagy and cell cycle death in actively proliferating keratinocytes, showing evidence for possible integration into the treatment of skin cancer.149 In addition to possessing chemo-preventive benefits and inducing apoptosis in cancer cells as seen within all 60 of the tumor cell lines within the National Cancer Institute’s NCI-60 panel, this cytotoxicity is not observed in non-cancerous cells.146

With regards to its safety, like YEO, the Scientific Community on Consumer Safety found SEO to be a contact allergen with an “alarming” prevalence of sensitization defined by 100-1000 reported cases.138 Despite this, sandalwood oil is reported to have low oral and dermal toxicity in laboratory animals and is also demonstrated to be non-mutagenic.146,154

Clinically, SEO could be utilized in patients seeking alternative treatments for warts, particularly given that the primary objective of wart treatment is to induce an irritant reaction.148

Carrot Seed Oil

Carrot seed essential oil (CSEO) is derived from the seeds of the Daucus carota plant.155 Of all the essential oils reviewed, CSEO is the least studied. It has been proposed CSEO possesses anti-inflammatory properties by minimizing the production of nitric oxide and strong antimicrobial activity against gram positive bacteria including Bacillus subtilis (B. subtilis), S. aureus, Cryptococcus neoformans (C. neoformans), and dermatophytes.156 CSEO also has the potential to be a skin rejuvenating agent based on several properties including its stability and free radical scavenging ability. Animal studies demonstrated that the application of CSEO prior to UV radiation decreased collagen bundle disorganization to a higher degree than the current commercially available anti-aging formulations.157 Furthermore, all CSEO emulsions studied produced no more than slight irritation when applied to rat skin, with many of the mixtures producing none.158

Although CSEO is one of the most recommended oils for sun protection, a study found the SPF of CSEO to be 2.5. Thus, claims of its ability to protect humans from UVB radiation can thus be misleading and dangerous.159 In addition to this, in terms of safety, a primary constituent of CSEO, carotol, exhibited moderate non-selective cytotoxic effects on a human pharyngeal squamous cell carcinoma cell line and on green monkey kidney.158

At this time, there is insufficient evidence to recommend CSEO’s use in a clinical setting.

Conclusion

Essential oils in dermatology have a variety of benefits. Yet, supporting scientific evidence is currently limited and continues to grow as the use of these products increases. This narrative review is primarily rooted in basic science data with extrapolation into clinical utility. While there are documented advantages, it is crucial to acknowledge the associated risks of using these products. Contact dermatitis and photoallergic dermatitis were cited as two of the most common concerns with the use of popular essential oils. Clinicians are recommended to exercise caution and ensure patients are well-informed about the potential risks involved when incorporating essential oils into their healthcare regimens. It is imperative to address misleading claims made about essential oils on the internet that may lead to a delay or lack of proper treatment. Thus, a balanced and informed approach to the use of essential oils is needed to maximize the potential benefits and reduce any risks associated with its use. The use of many of these oils in insecticidal and cosmeceutical formulations represents a promising area for future research.

278397 Reported Benefits and Risks of Common Essential Oils in Dermatology

Essential Oil Reported In-Vitro Benefits Reported In-Vivo Benefits Risks
Lavender Essential Oil (LEO) - Antibacterial against surface infections by S. pyogenes, S. Aureus and E. coli15- Increased concentration-dependent production of key signaling molecules involved in wound healing18 - Promotes hair growth in patients with alopecia areata20- Reduces inflammation by decreasing cytokine production and assists in chronic wound healing by inhibiting macrophage pyroptosis19- Induces relaxation via decreases in autonomic stimulation22–25- May be effective in treatment-resistant acne12,15 - Endocrine disrupting effects including premature thelarche and prepubertal gynecomastia26–29- Contact dermatitis30–35- Photoallergic reactions31
Frankincense Essential Oil (FREO) - Anti-inflammatory via production of tissue remodeling molecules and decreased proliferation of fibroblasts42,43- Antimicrobial against P. acnes, Malassezia spp. C. albicans, Trichophyton spp.44,45- Anti-tumoral properties via cytotoxic and cytostatic effects46,47- Enhances skin permeability of other transdermal drugs49 - FREO microemulsion (oil content 7.8%) displayed higher anti-inflammatory effects when compared to piroxicam in NSAID gel upon transdermal application41- Decreases erythema in skin conditions such as atopic dermatitis and psoriasis51- Enhances skin perfusion50 - Blistering reactions when misused ex. for mole removal3
Geranium Essential Oil (GEO) - Anti-inflammatory via antiproliferative activity against dermal fibroblasts42- Reduces and prevents oxidative stress57- Antimicrobial and antiparasitic effects, with antifungal effects against M. gypseum, M. canis, and T. mentagrophytes58–60- Photoprotective effects when combined with calendula essential oil57 - Dose-dependent anti-inflammatory properties in rodent models54,55- Promotes hair growth through regulation of growth factors and the involved cellular response61- Can be effective when used as a component of bug repellant62–64 Limited data on adverse effects, further research needed
Myrrh Essential Oil (MEO) - Antibacterial against E. coli, V. cholerae, and S. typhi Ty268- Antifungal against C. albicans, A. niger, P. funiculosum, and P. notatum68 - Promotes wound healing via increased wound contraction, shorter re-epithelialization times and increased wound tensile strength68 - Allergic contact dermatitis69–71
Neroli Essential Oil (NEO) - Antibacterial against P. aeruginosa72- Antifungal against S. cerevisiae and C. albicans72- Anti-inflammatory by blocking mitogen-activated protein kinase pathway72,73 - Contact dermatitis74,75- Photoallergic reactions75
Patchouli Essential Oil (PEO) - Antibacterial against P. acnes and S. epidermidis80- Promotes wound healing42 - Sedative properties when inhaled81- Anti-aging via antioxidant free radical scavenging82,83- Anti-insecticidal properties against mosquitos84 Limited data on adverse effects, further research needed
Rose Essential Oil (REO) - Antibacterial activity against P. aeruginosa, E. coli, C. violaceum, and S. Aureus93,94- Antifungal against P. notatum, A. niger, and C. albicans95- Antioxidant properties when mixed with clove oil90- Promotes wound healing by reducing both oxidative and inflammatory biomarkers92- Pain relief via TRPV1receptor activation98 - Hydrating and improved skin barrier function when coupled with tea tree essential oil88- Induces relaxation96,97 - Allergic contact dermatitis101–103- Potential sensitization in cosmetic workers104
Tea Tree Essential Oil (TTEO) - Antibacterial against P. acnes113- Anti-inflammatory properties106 - Effective in treatment of mild to moderate acne by reducing acne lesion count and acne severity index108–110,113- Effective in the treatment of onychomycosis114–117 - Endocrine disrupting effects including prepubertal gynecomastia26,27- Documented allergic reactions106,111,113,119- Potential irritation, burning, erythema112
Ylang-Ylang Essential Oil (YEO) - Synergistic antibacterial activity P. acnes and S. epidermidis when combined with myrrh and petit grain oil80- Antioxidant properties124- Promotes wound healing and scar prevention by decreasing proliferation of human fibroblasts and inhibiting tissue remodeling biomarkers42 - Induces relaxation and mood regulation by increasing parasympathetic activity122,123 - Contact dermatitis and resultant hyperpigmentation127–129- High sensitization potential138
Lemongrass Essential Oil (LMEO) - Antifungal activity against C. tropicalis strains143- Antioxidant by reducing expression of inflammatory cytokines, oxidative stress, and hydrocarbon induced DNA damage144- Anti-aging via high antioxidant activity145- Antitumoral effects when combined with Geraniol and Citral oil141 Limited data on adverse effects, further research needed
Sandalwood Essential Oil (SEO) - Antibacterial activity against antibiotic resistant bacteria such as MRSA and VRSA146- Anti-inflammatory by decreasing pro-inflammatory enzymes147- Anti-proliferative properties including inducing autophagy and cell cycle death in actively proliferating keratinocytes148,149 - Antiviral properties against herpes simplex virus, human papillomavirus, and molluscum contagiosum virus148 - Contact allergen with high sensitization prevalence138
Carrot Seed Essential Oil (CSEO) - Antimicrobial properties156- Antioxidant properties156- Anti-inflammatory properties- Skin rejuvenation based on its stability and free radical scavenging ability157- Protection against UV radiation by decreasing collagen bundle disorganization157 - Moderate cytotoxic effects on certain cell lines158- SPF claims may be misleading159

Conflicts of Interest

None declared.

Funding

None

References
2. Haque A., Anwar N., Yasmin F., Kumar Tarofder A., Maziz N. M. H.. "Purchase Intention towards Alternative Medicine: A Study from Consumers’ Perspective in Malaysia." Iran J Public Health, vol. 49, 2020, p. 193. DOI: 10.18502/ijph.v49i1.3071.
Google Scholar
3. Kornreich D., Saedi N.. "Home Treatment of Presumed Melanocytic Nevus With Frankincense." Cutis, vol. 107, 2021, p. E56. DOI: 10.12788/cutis.0259.
Google Scholar
4. Sindle A., Martin K.. "Art of Prevention: Essential Oils - Natural Products Not Necessarily Safe." Int J Womens Dermatol, vol. 7, 2021, p. 304. DOI: 10.1016/j.ijwd.2020.10.013.
Google Scholar
5. Goodier M. C., Zhang A. J., Nikle A. B., Hylwa S. A., Goldfarb N. I., Warshaw E. M.. "Use of essential oils: A general population survey." Contact Dermatitis, vol. 80, 2019, p. 391. DOI: 10.1111/cod.13198.
Google Scholar
6. Pandey V. K., Tripathi A., Srivastava S... "Exploiting the bioactive properties of essential oils and their potential applications in food industry." Food Sci Biotechnol, vol. 32, 2023, p. 885. DOI: 10.1007/s10068-023-01287-0.
Google Scholar
7. Monagas M., Brendler T., Brinckmann J... "Understanding plant to extract ratios in botanical extracts." Front Pharmacol, vol. 13, 2022, p. . DOI: 10.3389/fphar.2022.981978.
Google Scholar
8. Ullah H., De Filippis A., Baldi A... "Beneficial Effects of Plant Extracts and Bioactive Food Components in Childhood Supplementation." Nutrients, vol. 13, 2021, p. 3157. DOI: 10.3390/nu13093157.
Google Scholar
9. Sookwong P., Yuenyong J., Bennett C.. "Bioactive Constituents in Cold-Pressed Plant Oils: Their Structure, Bioactivity and Chromatographic Analysis." J Oleo Sci, vol. 73, 2024, p. ess23164. DOI: 10.5650/jos.ess23164.
Google Scholar
10. Boesl R., Saarinen H.. "Essential Oil Education for Health Care Providers." Integr Med (Encinitas), vol. 15, 2016, p. 38. DOI: .
11. Pezantes-Orellana C., German Bermúdez F., Matías De la Cruz C., Montalvo J. L., Orellana-Manzano A.. "Essential oils: a systematic review on revolutionizing health, nutrition, and omics for optimal well-being." Front Med (Lausanne), vol. 11, 2024, p. . DOI: 10.3389/fmed.2024.1337785.
Google Scholar
12. Nurzyńska-Wierdak R., Pietrasik D., Walasek-Janusz M.. "Essential Oils in the Treatment of Various Types of Acne-A Review." Plants (Basel), vol. 12, 2022, p. . DOI: 10.3390/plants12010090.
Google Scholar
13. Ben Djemaa F. G., Bellassoued K., Zouari S., El Feki A., Ammar E.. "Antioxidant and wound healing activity of Lavandula aspic L. ointment." J Tissue Viability, vol. 25, 2016, p. 193. DOI: 10.1016/j.jtv.2016.10.002.
Google Scholar
14. Mori H. M., Kawanami H., Kawahata H., Aoki M.. "Wound healing potential of lavender oil by acceleration of granulation and wound contraction through induction of TGF-β in a rat model." BMC Complement Altern Med, vol. 16, 2016, p. 144. DOI: 10.1186/s12906-016-1128-7.
Google Scholar
15. Cavanagh H. M. A., Wilkinson J. M.. "Biological activities of Lavender essential oil." Phytotherapy Research, vol. 16, 2002, p. 301. DOI: 10.1002/ptr.1103.
Google Scholar
16. Ben Djemaa F. G., Bellassoued K., Zouari S., El Feki A., Ammar E.. "Antioxidant and wound healing activity of Lavandula aspic L. ointment." J Tissue Viability, vol. 25, 2016, p. 193. DOI: 10.1016/j.jtv.2016.10.002.
Google Scholar
17. Mori H. M., Kawanami H., Kawahata H., Aoki M.. "Wound healing potential of lavender oil by acceleration of granulation and wound contraction through induction of TGF-β in a rat model." BMC Complement Altern Med, vol. 16, 2016, p. 144. DOI: 10.1186/s12906-016-1128-7.
Google Scholar
18. Miastkowska M., Kantyka T., Bielecka E... "Enhanced Biological Activity of a Novel Preparation of Lavandula angustifolia Essential Oil." Molecules, vol. 26, 2021, p. 2458. DOI: 10.3390/molecules26092458.
Google Scholar
19. Ao X., Yan H., Huang M... "Lavender essential oil accelerates lipopolysaccharide-induced chronic wound healing by inhibiting caspase-11-mediated macrophage pyroptosis." Kaohsiung J Med Sci, vol. 39, 2023, p. 511. DOI: 10.1002/kjm2.12654.
Google Scholar
20. Hay I. C., Jamieson M., Ormerod A. D.. "Randomized Trial of Aromatherapy." Arch Dermatol, vol. 134, 1998, p. . DOI: 10.1001/archderm.134.11.1349.
Google Scholar
21. Lee B. H., Lee J. S., Kim Y. C.. "Hair Growth-Promoting Effects of Lavender Oil in C57BL/6 Mice." Toxicol Res, vol. 32, 2016, p. 103. DOI: 10.5487/TR.2016.32.2.103.
Google Scholar
22. Heuberger E., Redhammer S., Buchbauer G.. "Transdermal Absorption of (−)-Linalool Induces Autonomic Deactivation but has No Impact on Ratings of Well-Being in Humans." Neuropsychopharmacology, vol. 29, 2004, p. 1925. DOI: 10.1038/sj.npp.1300521.
Google Scholar
23. Sayorwan W., Siripornpanich V., Piriyapunyaporn T., Hongratanaworakit T., Kotchabhakdi N., Ruangrungsi N.. "The effects of lavender oil inhalation on emotional states, autonomic nervous system, and brain electrical activity." J Med Assoc Thai, vol. 95, 2012, p. 598. DOI: .
24. Hongratanaworakit T.. "Aroma-therapeutic effects of massage blended essential oils on humans." Nat Prod Commun, vol. 6, 2011, p. 1199. DOI: 10.1177/1934578X1100600838.
Google Scholar
25. Grunebaum L. D., Murdock J., Castanedo-Tardan M. P., Baumann L. S.. "Effects of lavender olfactory input on cosmetic procedures." J Cosmet Dermatol, vol. 10, 2011, p. 89. DOI: 10.1111/j.1473-2165.2011.00554.x.
Google Scholar
26. Henley D. V., Lipson N., Korach K. S., Bloch C. A.. "Prepubertal Gynecomastia Linked to Lavender and Tea Tree Oils." New England Journal of Medicine, vol. 356, 2007, p. 479. DOI: 10.1056/NEJMoa064725.
Google Scholar
27. Hawkins J., Hires C., Dunne E., Baker C.. "The relationship between lavender and tea tree essential oils and pediatric endocrine disorders: A systematic review of the literature." Complement Ther Med, vol. 49, 2020, p. 102288. DOI: 10.1016/j.ctim.2019.102288.
Google Scholar
28. Ramsey J. T., Li Y., Arao Y... "Lavender Products Associated With Premature Thelarche and Prepubertal Gynecomastia: Case Reports and Endocrine-Disrupting Chemical Activities." J Clin Endocrinol Metab, vol. 104, 2019, p. 5393. DOI: 10.1210/jc.2018-01880.
Google Scholar
29. Diaz A., Luque L., Badar Z., Kornic S., Danon M.. "Prepubertal gynecomastia and chronic lavender exposure: report of three cases." Journal of Pediatric Endocrinology and Metabolism, vol. 29, 2016, p. . DOI: 10.1515/jpem-2015-0248.
Google Scholar
30. Coulson I. H., Khan A. S.. "Facial “pillow” dermatitis due to lavender oil allergy." Contact Dermatitis, vol. 41, 1999, p. 111. DOI: 10.1111/j.1600-0536.1999.tb06244.x.
Google Scholar
31. Goiriz R., Delgado-Jiménez Y., Sánchez-Pérez J., García-Diez A.. "Photoallergic contact dermatitis from lavender oil in topical ketoprofen." Contact Dermatitis, vol. 57, 2007, p. 381. DOI: 10.1111/j.1600-0536.2007.01102.x.
Google Scholar
32. Sugiura M., Hayakawa R., Kato Y., Sugiura K., Hashimoto R.. "Results of patch testing with lavender oil in Japan." Contact Dermatitis, vol. 43, 2000, p. 157. DOI: 10.1034/j.1600-0536.2000.043003157.x.
Google Scholar
33. Hagvall L., Sköld M., Bråred-Christensson J., Börje A., Karlberg A.T.. "Lavender oil lacks natural protection against autoxidation, forming strong contact allergens on air exposure." Contact Dermatitis, vol. 59, 2008, p. 143. DOI: 10.1111/j.1600-0536.2008.01402.x.
Google Scholar
34. Sköld M., Hagvall L., Karlberg A.T.. "Autoxidation of linalyl acetate, the main component of lavender oil, creates potent contact allergens." Contact Dermatitis, vol. 58, 2007, p. 9. DOI: 10.1111/j.1600-0536.2007.01262.x.
Google Scholar
35. Prashar A., Locke I. C., Evans C. S.. "Cytotoxicity of lavender oil and its major components to human skin cells." Cell Prolif, vol. 37, 2004, p. 221. DOI: 10.1111/j.1365-2184.2004.00307.x.
Google Scholar
36. Evandri M. G., Battinelli L., Daniele C., Mastrangelo S., Bolle P., Mazzanti G.. "The antimutagenic activity of Lavandula angustifolia (lavender) essential oil in the bacterial reverse mutation assay." Food and Chemical Toxicology, vol. 43, 2005, p. 1381. DOI: 10.1016/j.fct.2005.03.013.
Google Scholar
37. Corazza M., Amendolagine G., Borghi A., Toni G., Lauriola M. M.. "Aromatherapy and occupational allergic contact dermatitis: Two further cases caused by lavender oil and other essential oils." Contact Dermatitis, vol. 81, 2019, p. 378. DOI: 10.1111/cod.13328.
Google Scholar
38. Hagvall L., Christensson J.. "Patch Testing with Main Sensitizers Does Not Detect All Cases of Contact Allergy to Oxidized Lavender Oil." Acta Dermato Venereologica, vol. 96, 2016, p. 679. DOI: 10.2340/00015555-2319.
Google Scholar
39. Du Z., Liu Z., Ning Z... "Prospects of boswellic acids as potential pharmaceutics." Planta Med, vol. 81, 2015, p. 259. DOI: 10.1055/s-0034-1396313.
Google Scholar
40. Almeida-da-Silva C. L. C., Sivakumar N., Asadi H... "Effects of Frankincense Compounds on Infection, Inflammation, and Oral Health." Molecules, vol. 27, 2022, p. . DOI: 10.3390/molecules27134174.
Google Scholar
41. Mostafa D. M., Ammar N. M., Basha M., Hussein R. A., El Awdan S., Awad G.. "Transdermal microemulsions of Boswellia carterii Bird: formulation, characterization and in vivo evaluation of anti-inflammatory activity." Drug Deliv, vol. 22, 2015, p. 748. DOI: 10.3109/10717544.2014.898347.
Google Scholar
42. Han X., Beaumont C., Stevens N.. "Chemical composition analysis and in vitro biological activities of ten essential oils in human skin cells." Biochim Open, vol. 5, 2017, p. 1. DOI: 10.1016/j.biopen.2017.04.001.
Google Scholar
43. Han X., Rodriguez D., Parker T.L.. "Biological activities of frankincense essential oil in human dermal fibroblasts." Biochim Open, vol. 4, 2017, p. 31. DOI: 10.1016/j.biopen.2017.01.003.
Google Scholar
44. Sadhasivam S., Palanivel S., Ghosh S.. "Synergistic antimicrobial activity of Boswellia serrata Roxb. ex Colebr. (Burseraceae) essential oil with various azoles against pathogens associated with skin, scalp and nail infections." Lett Appl Microbiol, vol. 63, 2016, p. 495. DOI: 10.1111/lam.12683.
Google Scholar
45. Ljaljević Grbić M., Unković N., Dimkić I... "Frankincense and myrrh essential oils and burn incense fume against micro-inhabitants of sacral ambients. Wisdom of the ancients?." J Ethnopharmacol, vol. 219, 2018, p. 1. DOI: 10.1016/j.jep.2018.03.003.
Google Scholar
46. Eichhorn T., Greten H. J., Efferth T.. "Molecular Determinants of the Response of Tumor Cells to Boswellic Acids." Pharmaceuticals, vol. 4, 2011, p. 1171. DOI: 10.3390/ph4081171.
Google Scholar
47. Zhao W., Entschladen F., Liu H... "Boswellic acid acetate induces differentiation and apoptosis in highly metastatic melanoma and fibrosarcoma cells." Cancer Detect Prev, vol. 27, 2003, p. 67. DOI: 10.1016/s0361-090x(02)00170-8.
Google Scholar
48. Huang M. T., Badmaev V., Ding Y., Liu Y., Xie J. G., Ho C. T.. "Anti-tumor and anti-carcinogenic activities of triterpenoid, beta-boswellic acid." Biofactors, vol. 13, 2000, p. 225. DOI: 10.1002/biof.5520130135.
Google Scholar
49. Guan Y. M., Tao L., Zhu X. F., Zang Z. Z., Jin C., Chen L. H.. "[Effects of Frankincense and Myrrh essential oil on transdermal absorption of ferulic acid in Chuanxiong]." Zhongguo Zhong Yao Za Zhi, vol. 42, 2017, p. 3350. DOI: 10.19540/j.cnki.cjcmm.20170719.001.
Google Scholar
50. Zhu X. F., Luo J., Guan Y. M... "[Effects of Frankincense and Myrrh essential oil on transdermal absorption in vitro of Chuanxiong and penetration mechanism of skin blood flow]." Zhongguo Zhong Yao Za Zhi, vol. 42, 2017, p. 680. DOI: 10.19540/j.cnki.cjcmm.20170103.025.
Google Scholar
51. Togni S., Maramaldi G., Di Pierro F., Biondi M.. "A cosmeceutical formulation based on boswellic acids for the treatment of erythematous eczema and psoriasis." Clin Cosmet Investig Dermatol, vol. 7, 2014, p. 321. DOI: 10.2147/CCID.S69240.
Google Scholar
52. Khosravi Samani M., Mahmoodian H., Moghadamnia A., Poorsattar Bejeh Mir A., Chitsazan M.. "The effect of Frankincense in the treatment of moderate plaque-induced gingivitis: a double blinded randomized clinical trial." Daru, vol. 19, 2011, p. 288. DOI: .
53. Senthil Kumar K. J., Gokila Vani M., Wang C. S... "Geranium and Lemon Essential Oils and Their Active Compounds Downregulate Angiotensin-Converting Enzyme 2 (ACE2), a SARS-CoV-2 Spike Receptor-Binding Domain, in Epithelial Cells." Plants, vol. 9, 2020, p. 770. DOI: 10.3390/plants9060770.
Google Scholar
54. Nadjib Boukhatem M., Kameli A., Amine Ferhat M., Saidi F., Mekarnia M.. "Rose geranium essential oil as a source of new and safe anti-inflammatory drugs." Libyan Journal of Medicine, vol. 8, 2013, p. 22520. DOI: 10.3402/ljm.v8i0.22520.
Google Scholar
55. Maruyama N., Sekimoto Y., Ishibashi H... "Suppression of neutrophil accumulation in mice by cutaneous application of geranium essential oil." J Inflamm (Lond), vol. 2, 2005, p. 1. DOI: 10.1186/1476-9255-2-1.
Google Scholar
56. Lohani A., Verma A., Hema G., Pathak K.. "Topical Delivery of Geranium/Calendula Essential Oil-Entrapped Ethanolic Lipid Vesicular Cream to Combat Skin Aging." Biomed Res Int, vol. 2021, 2021, p. 1. DOI: 10.1155/2021/4593759.
Google Scholar
57. Lohani A., Mishra A.K., Verma A.. "Cosmeceutical potential of geranium and calendula essential oil: Determination of antioxidant activity and in vitro sun protection factor." J Cosmet Dermatol, vol. 18, 2019, p. 550. DOI: 10.1111/jocd.12789.
Google Scholar
58. Sienkiewicz M., Poznańska-Kurowska K., Kaszuba A., Kowalczyk E.. "The antibacterial activity of geranium oil against Gram-negative bacteria isolated from difficult-to-heal wounds." Burns, vol. 40, 2014, p. 1046. DOI: 10.1016/j.burns.2013.11.002.
Google Scholar
59. Fang F., Candy K., Melloul E... "In vitro activity of ten essential oils against Sarcoptes scabiei." Parasit Vectors, vol. 9, 2016, p. 594. DOI: 10.1186/s13071-016-1889-3.
Google Scholar
60. Michalczyk A., Ostrowska P.. "Essential oils and their components in combating fungal pathogens of animal and human skin." Journal of Medical Mycology, vol. 31, 2021, p. 101118. DOI: 10.1016/j.mycmed.2021.101118.
Google Scholar
61. Boisvert W. A., Yu M., Choi Y... "Hair growth-promoting effect of Geranium sibiricum extract in human dermal papilla cells and C57BL/6 mice." BMC Complement Altern Med, vol. 17, 2017, p. 109. DOI: 10.1186/s12906-017-1624-4.
Google Scholar
62. Barnard D. R.. "Repellency of essential oils to mosquitoes (Diptera: Culicidae)." J Med Entomol, vol. 36, 1999, p. 625. DOI: 10.1093/jmedent/36.5.625.
Google Scholar
63. Chang K. S., Tak J. H., Kim S. I., Lee W. J., Ahn Y. J.. "Repellency of Cinnamomum cassia bark compounds and cream containing cassia oil toAedes aegypti (Diptera: Culicidae) under laboratory and indoor conditions." Pest Manag Sci, vol. 62, 2006, p. 1032. DOI: 10.1002/ps.1268.
Google Scholar
64. Kim S. I., Chang K. S., Yang Y. C., Kim B. S., Ahn Y. J.. "Repellency of aerosol and cream products containing fennel oil to mosquitoes under laboratory and field conditions." Pest Manag Sci, vol. 60, 2004, p. 1125. DOI: 10.1002/ps.921.
Google Scholar
65. Lamichhane R., Lee K. H., Pandeya P. R... "Subcutaneous Injection of Myrrh Essential Oil in Mice: Acute and Subacute Toxicity Study." Evidence-Based Complementary and Alternative Medicine, vol. 2019, 2019, p. 1. DOI: 10.1155/2019/8497980.
Google Scholar
66. Younis N. S., Mohamed M. E.. "Protective effects of myrrh essential oil on isoproterenol-induced myocardial infarction in rats through antioxidant, anti-inflammatory, Nrf2/HO-1 and apoptotic pathways." J Ethnopharmacol, vol. 270, 2021, p. 113793. DOI: 10.1016/j.jep.2021.113793.
Google Scholar
67. Haffor A. S. A.. "Effect of myrrh ( Commiphora molmol ) on leukocyte levels before and during healing from gastric ulcer or skin injury." J Immunotoxicol, vol. 7, 2010, p. 68. DOI: 10.3109/15476910903409835.
Google Scholar
68. Gebrehiwot M., Asres K., Bisrat D., Mazumder A., Lindemann P., Bucar F.. "Evaluation of the wound healing property of Commiphora guidottii Chiov. ex. Guid.." BMC Complement Altern Med, vol. 15, 2015, p. 282. DOI: 10.1186/s12906-015-0813-2.
Google Scholar
69. Gallo R., Rivara G., Cattarini G., Cozzani E., Guarrera M.. "Allergic contact dermatitis from myrrh." Contact Dermatitis, vol. 41, 1999, p. 230. DOI: 10.1111/j.1600-0536.1999.tb06143.x.
Google Scholar
70. Al-Suwaidan S. N., Gad el Rab M. O., Al-Fakhiry S., Al Hoqail I. A., Al-Maziad A., Sherif A. B.. "Allergic contact dermatitis from myrrh, a topical herbal medicine used to promote healing." Contact Dermatitis, vol. 39, 1998, p. 137. DOI: 10.1111/j.1600-0536.1998.tb05867.x.
Google Scholar
71. Xu Y. Y., Li L., Xuan L., Guan K.. "Patch test diagnosis of non-immediate cutaneous reaction to myrrh following oral intake of a traditional Chinese medicine decoction." Contact Dermatitis, vol. 80, 2019, p. 135. DOI: 10.1111/cod.13144.
Google Scholar
72. Ammar A. H., Bouajila J., Lebrihi A., Mathieu F., Romdhane M., Zagrouba F.. "Chemical composition and in vitro antimicrobial and antioxidant activities of Citrus aurantium l. flowers essential oil (Neroli oil)." Pak J Biol Sci, vol. 15, 2012, p. 1034. DOI: 10.3923/pjbs.2012.1034.1040.
Google Scholar
73. Shen C. Y., Jiang J. G., Zhu W., Ou-Yang Q.. "Anti-inflammatory Effect of Essential Oil from Citrus aurantium L. var. amara Engl.." J Agric Food Chem, vol. 65, 2017, p. 8586. DOI: 10.1021/acs.jafc.7b02586.
Google Scholar
74. Schubert H. J.. "Skin diseases in workers at a perfume factory." Contact Dermatitis, vol. 55, 2006, p. 81. DOI: 10.1111/j.0105-1873.2006.00881.x.
Google Scholar
75. Matthieu L., Meuleman L., Van Hecke E... "Contact and photocontact allergy to ketoprofen. The Belgian experience." Contact Dermatitis, vol. 50, 2004, p. 238. DOI: 10.1111/j.0105-1873.2004.00323.x.
Google Scholar
76. Singh M., Sharma S., Ramesh S.. "Herbage, oil yield and oil quality of patchouli (Blanco) Benth. influenced by irrigation, organic mulch and nitrogen application in semi-arid tropical climate." Ind Crops Prod, vol. 16, 2002, p. 101. DOI: 10.1016/S0926-6690(02)00013-4.
Google Scholar
77. Croteau R., Munck S. L., Akoh C. C., Fisk H. J., Satterwhite D. M.. "Biosynthesis of the sesquiterpene patchoulol from farnesyl pyrophosphate in leaf extracts of Pogostemon cablin (patchouli): Mechanistic considerations." Arch Biochem Biophys, vol. 256, 1987, p. 56. DOI: 10.1016/0003-9861(87)90425-5.
Google Scholar
78. Deguerry F., Pastore L., Wu S., Clark A., Chappell J., Schalk M.. "The diverse sesquiterpene profile of patchouli, Pogostemon cablin, is correlated with a limited number of sesquiterpene synthases." Arch Biochem Biophys, vol. 454, 2006, p. 123. DOI: 10.1016/j.abb.2006.08.006.
Google Scholar
79. Wei A., Shibamoto T.. "Antioxidant Activities and Volatile Constituents of Various Essential Oils." J Agric Food Chem, vol. 55, 2007, p. 1737. DOI: 10.1021/jf062959x.
Google Scholar
80. Orchard A., van Vuuren S. F., Viljoen A. M., Kamatou G.. "The in vitro antimicrobial evaluation of commercial essential oils and their combinations against acne." Int J Cosmet Sci, vol. 40, 2018, p. 226. DOI: 10.1111/ics.12456.
Google Scholar
81. Ito K., Ito M.. "Sedative effects of vapor inhalation of the essential oil of Microtoena patchoulii and its related compounds." J Nat Med, vol. 65, 2011, p. 336. DOI: 10.1007/s11418-010-0502-x.
Google Scholar
82. Wang X. F., Huang Y. F., Wang L... "Photo-protective activity of pogostone against UV-induced skin premature aging in mice." Exp Gerontol, vol. 77, 2016, p. 76. DOI: 10.1016/j.exger.2016.02.017.
Google Scholar
83. Lin R. F., Feng X. X., Li C. W... "Prevention of UV radiation-induced cutaneous photoaging in mice by topical administration of patchouli oil." J Ethnopharmacol, vol. 154, 2014, p. 408. DOI: 10.1016/j.jep.2014.04.020.
Google Scholar
84. Trongtokit Y., Rongsriyam Y., Komalamisra N., Apiwathnasorn C.. "Comparative repellency of 38 essential oils against mosquito bites." Phytotherapy Research, vol. 19, 2005, p. 303. DOI: 10.1002/ptr.1637.
Google Scholar
85. Dobreva A., Nedeltcheva-Antonova D.. "Comparative Chemical Profiling and Citronellol Enantiomers Distribution of Industrial-Type Rose Oils Produced in China." Molecules, vol. 28, 2023, p. 1281. DOI: 10.3390/molecules28031281.
Google Scholar
86. Mileva M., Ilieva Y., Jovtchev G... "Rose Flowers—A Delicate Perfume or a Natural Healer?." Biomolecules, vol. 11, 2021, p. 127. DOI: 10.3390/biom11010127.
Google Scholar
87. Boskabady M. H., Shafei M. N., Saberi Z., Amini S.. "Pharmacological effects of rosa damascena." Iran J Basic Med Sci, vol. 14, 2011, p. 295. DOI: .
88. Yapar E. A., Ýnal Ö., Erdal M. S.. "Design and in vivo evaluation of emulgel formulations including green tea extract and rose oil." Acta Pharmaceutica, vol. 63, 2013, p. 531. DOI: 10.2478/acph-2013-0037.
Google Scholar
89. Casetti F., Wölfle U., Gehring W., Schempp C. M.. "Dermocosmetics for Dry Skin: A New Role for Botanical Extracts." Skin Pharmacol Physiol, vol. 24, 2011, p. 289. DOI: 10.1159/000329214.
Google Scholar
90. Wei A., Shibamoto T.. "Antioxidant Activities of Essential Oil Mixtures toward Skin Lipid Squalene Oxidized by UV Irradiation." Cutan Ocul Toxicol, vol. 26, 2007, p. 227. DOI: 10.1080/15569520701224501.
Google Scholar
91. Kim J. H., Choi D. K., Lee S. S... "Enhancement of Keratinocyte Differentiation by Rose Absolute Oil." Ann Dermatol, vol. 22, 2010, p. 255. DOI: 10.5021/ad.2010.22.3.255.
Google Scholar
92. Raka R. N., Zhiqian D., Yue Y... "Pingyin rose essential oil alleviates LPS-Induced inflammation in RAW 264.7 cells via the NF-κB pathway: an integrated in vitro and network pharmacology analysis." BMC Complement Med Ther, vol. 22, 2022, p. 272. DOI: 10.1186/s12906-022-03748-1.
Google Scholar
93. Ulusoy S., Boşgelmez-Tınaz G., Seçilmiş-Canbay H.. "Tocopherol, Carotene, Phenolic Contents and Antibacterial Properties of Rose Essential Oil, Hydrosol and Absolute." Curr Microbiol, vol. 59, 2009, p. 554. DOI: 10.1007/s00284-009-9475-y.
Google Scholar
94. Andoğan B. C., Baydar H., Kaya S., Demirci M., Özbaşar D., Mumcu E.. "Antimicrobial activity and chemical composition of some essential oils." Arch Pharm Res, vol. 25, 2002, p. 860. DOI: 10.1007/BF02977005.
Google Scholar
95. Shohayeb M., Abdel-Hameed E. S. S., Bazaid S. A., Maghrabi I.. "Antibacterial and Antifungal Activity of Rosa damascena MILL. Essential Oil, Different Extracts of Rose Petals." Global Journal of Pharmacology, vol. 8, 2014, p. 01. DOI: .
96. Fukada M., Kano E., Miyoshi M., Komaki R., Watanabe T.. "Effect of “Rose Essential Oil” Inhalation on Stress-Induced Skin-Barrier Disruption in Rats and Humans." Chem Senses, vol. 37, 2012, p. 347. DOI: 10.1093/chemse/bjr108.
Google Scholar
97. Hongratanaworakit T.. "Relaxing effect of rose oil on humans." Nat Prod Commun, vol. 4, 2009, p. 291. DOI: 10.1177/1934578X0900400226.
Google Scholar
98. Ohkawara S., Tanaka-Kagawa T., Furukawa Y., Nishimura T., Jinno H.. "Activation of the human transient receptor potential vanilloid subtype 1 by essential oils." Biol Pharm Bull, vol. 33, 2010, p. 1434. DOI: 10.1248/bpb.33.1434.
Google Scholar
99. Politano V. T., Diener R. M., Christian M. S., Hawkins D. R., Ritacco G., Api A. M.. "The Pharmacokinetics of Phenylethyl Alcohol (PEA)." Int J Toxicol, vol. 32, 2013, p. 39. DOI: 10.1177/1091581812471688.
Google Scholar
100. Schmitt S., Schäfer U. F., Döbler L., Reichling J.. "Variation of in vitro Human Skin Permeation of Rose Oil between Different Application Sites." Forschende Komplementärmedizin / Research in Complementary Medicine, vol. 17, 2010, p. 2. DOI: 10.1159/000315043.
Google Scholar
101. Ochando-Ibernón G., Schneller-Pavelescu L., Silvestre-Salvador J. F.. "Allergic contact dermatitis caused by “Rosa mosqueta” oil." Contact Dermatitis, vol. 79, 2018, p. 259. DOI: 10.1111/cod.13083.
Google Scholar
102. Scheinman P. L.. "Is it really fragrance-free?." Am J Contact Dermat, vol. 8, 1997, p. 239. DOI: .
103. Vilaplana J., Romaguera C., Grimalt F.. "Contact dermatitis from geraniol in Bulgarian rose oil." Contact Dermatitis, vol. 24, 1991, p. 301. DOI: 10.1111/j.1600-0536.1991.tb01726.x.
Google Scholar
104. Akkaya A., Ornek Z., Kaleli S.. "Occupational asthma, eosinophil and skin prick tests and serum total IgE values of the workers in a plant manufacturing rose oil." Asian Pac J Allergy Immunol, vol. 22, , p. 103. DOI: .
105. Padovan A., Keszei A., Hassan Y... "Four terpene synthases contribute to the generation of chemotypes in tea tree ()." BMC Plant Biol, vol. 17, 2017, p. 160. DOI: 10.1186/s12870-017-1107-2.
Google Scholar
106. Mondello F., De Bernardis F., Girolamo A., Cassone A., Salvatore G.. "In vivo activity of terpinen-4-ol, the main bioactive component of Melaleuca alternifolia Cheel (tea tree) oil against azole-susceptible and -resistant human pathogenic Candida species." BMC Infect Dis, vol. 6, 2006, p. 158. DOI: 10.1186/1471-2334-6-158.
Google Scholar
107. Armstrong A. W., Cheeney S., Wu J., Harskamp C. T., Schupp C. W.. "Harnessing the power of crowds: crowdsourcing as a novel research method for evaluation of acne treatments." Am J Clin Dermatol, vol. 13, 2012, p. 405. DOI: 10.2165/11634040-000000000-00000.
Google Scholar
108. Nascimento T., Gomes D., Simões R., da Graça Miguel M.. "Tea Tree Oil: Properties and the Therapeutic Approach to Acne—A Review." Antioxidants, vol. 12, 2023, p. 1264. DOI: 10.3390/antiox12061264.
Google Scholar
109. Enshaieh S., Jooya A., Siadat A.E.S., Iraji F.. "The efficacy of 5% topical tea tree oil gel in mild to moderate acne vulgaris: A randomized, double-blind placebo-controlled study." Indian J Dermatol Venereol Leprol, vol. 73, 2007, p. 22. DOI: 10.4103/0378-6323.30646.
Google Scholar
110. Yadav N., Singh A., Chatterjee A., Belemkar S.. "Evaluation of Efficacy and Safety of Perfact Face Gel and Perfact Face Tablets in Management of Acne." Journal of Clinical & Experimental Dermatology, vol. 02, 2011, p. . DOI: 10.4172/2155-9554.1000118.
Google Scholar
111. Darabi R., Hafezi M. A., Akbarloo N.. "A comparative, investigator-blind study of topical tea tree oil versus erythromycin gel in the treatment of acne." 15th European Congress of Clinical Microbiology and Infectious Diseases, vol. , 2005, p. . DOI: .
112. Bassett I. B., Barnetson R. S. C., Pannowitz D. L.. "A comparative study of tea-tree oil versus benzoylperoxide in the treatment of acne." Medical Journal of Australia, vol. 153, 1990, p. 455. DOI: 10.5694/j.1326-5377.1990.tb126150.x.
Google Scholar
113. Malhi H. K., Tu J., Riley T. V., Kumarasinghe S. P., Hammer K. A.. "Tea tree oil gel for mild to moderate acne; a 12 week uncontrolled, open-label phase II pilot study." Australasian Journal of Dermatology, vol. 58, 2017, p. 205. DOI: 10.1111/ajd.12465.
Google Scholar
114. Nickles M. A., Lio P. A., Mervak J. E.. "Complementary and Alternative Therapies for Onychomycosis: A Systematic Review of the Clinical Evidence." Skin Appendage Disord, vol. 8, 2022, p. 269. DOI: 10.1159/000521703.
Google Scholar
115. AbdelHamid Dina, Gomaa Amal H. A., Mohammed Ghada F., Eyada Moustafa M. K., El_Sweify Mohamed Aly. "Evaluation of the Therapeutic Efficacy of Tea Tree Oil in Treatment of Onychomycosis." International Journal of Pharmacognosy and Phytochemical Research, vol. 9, 2017, p. 1414. DOI: .
116. Buck D. S., Nidorf D. M., Addino J. G.. "Comparison of two topical preparations for the treatment of onychomycosis: Melaleuca alternifolia (tea tree) oil and clotrimazole." J Fam Pract, vol. 38, 1994, p. 601. DOI: .
117. Mingorance Álvarez E., Villar Rodríguez J., López Ripado O., Mayordomo R.. "Antifungal Activity of Tea Tree (Melaleuca alternifolia Cheel) Essential Oils against the Main Onychomycosis-Causing Dermatophytes." Journal of Fungi, vol. 10, 2024, p. 675. DOI: 10.3390/jof10100675.
Google Scholar
118. Carson C. F., Hammer K. A., Riley T. V.. "Melaleuca alternifolia (Tea Tree) Oil: a Review of Antimicrobial and Other Medicinal Properties." Clin Microbiol Rev, vol. 19, 2006, p. 50. DOI: 10.1128/CMR.19.1.50-62.2006.
Google Scholar
119. de Groot A.C., Schmidt E.. "Tea tree oil: contact allergy and chemical composition." Contact Dermatitis, vol. 75, 2016, p. 129. DOI: 10.1111/cod.12591.
Google Scholar
120. de Freitas Junior R. A., Lossavaro P. K. de M. B., Kassuya C. A. L... "Effect of Ylang-Ylang (Cananga odorata Hook. F. & Thomson) Essential Oil on Acute Inflammatory Response In Vitro and In Vivo." Molecules, vol. 27, 2022, p. 3666. DOI: 10.3390/molecules27123666.
Google Scholar
121. Pasay C., Mounsey K., Stevenson G... "Acaricidal Activity of Eugenol Based Compounds against Scabies Mites." PLoS One, vol. 5, 2010, p. e12079. DOI: 10.1371/journal.pone.0012079.
Google Scholar
122. Hongratanaworakit T., Buchbauer G.. "Relaxing effect of ylang ylang oil on humans after transdermal absorption." Phytotherapy Research, vol. 20, 2006, p. 758. DOI: 10.1002/ptr.1950.
Google Scholar
123. Hongratanaworakit T., Buchbauer G.. "Evaluation of the Harmonizing Effect of Ylang-Ylang Oil on Humans after Inhalation." Planta Med, vol. 70, 2004, p. 632. DOI: 10.1055/s-2004-827186.
Google Scholar
125. Burdock G. A., Carabin I. G.. "Safety assessment of Ylang–Ylang (Cananga spp.) as a food ingredient." Food and Chemical Toxicology, vol. 46, 2008, p. 433. DOI: 10.1016/j.fct.2007.09.105.
Google Scholar
127. Srivastava P., Bajaj A.. "Ylang-ylang oil not an uncommon sensitizer in India." Indian J Dermatol, vol. 59, 2014, p. 200. DOI: 10.4103/0019-5154.127693.
Google Scholar
128. Kenerva L., Estlander T., Jolanki R.. "Occupational allergic contact dermatitis caused by ylang-ylang oil." Contact Dermatitis, vol. 33, 1995, p. 198. DOI: 10.1111/j.1600-0536.1995.tb00547.x.
Google Scholar
129. Imokawa G., Kawai M.. "Differential hypermelanosis induced by allergic contact dermatitis." J Invest Dermatol, vol. 89, 1987, p. 540. DOI: 10.1111/1523-1747.ep12461181.
Google Scholar
130. Warshaw E. M., Zug K. A., Belsito D. v... "Positive Patch-Test Reactions to Essential Oils in Consecutive Patients From North America and Central Europe." Dermatitis, vol. 28, 2017, p. 246. DOI: 10.1097/DER.0000000000000293.
Google Scholar
131. Kieć-Swierczyńska M., Krecisz B., Swierczyńska-Machura D.. "[Contact allergy to fragrances]." Med Pr, vol. 57, 2006, p. 431. DOI: .
132. Sabroe R. A., Holden C. R., Gawkrodger D. J.. "Contact allergy to essential oils cannot always be predicted from allergy to fragrance markers in the baseline series." Contact Dermatitis, vol. 74, 2016, p. 236. DOI: 10.1111/cod.12528.
Google Scholar
133. Frosch P. J., Duus Johansen J., Schuttelaar M. L. A... "Patch test results with fragrance markers of the baseline series - analysis of the European Surveillance System on Contact Allergies (ESSCA) network 2009-2012." Contact Dermatitis, vol. 73, 2015, p. 163. DOI: 10.1111/cod.12420.
Google Scholar
134. Uter W., Geier J., Schnuch A., Frosch P.. "Patch test results with patients’ own perfumes, deodorants and shaving lotions: results of the IVDK 1998?2002." Journal of the European Academy of Dermatology and Venereology, vol. 21, 2007, p. 374. DOI: 10.1111/j.1468-3083.2006.01973.x.
Google Scholar
135. Uter W., Schmidt E., Geier J., Lessmann H., Schnuch A., Frosch P.. "Contact allergy to essential oils: current patch test results (2000-2008) from the Information Network of Departments of Dermatology (IVDK)*." Contact Dermatitis, vol. 63, 2010, p. 277. DOI: 10.1111/j.1600-0536.2010.01768.x.
Google Scholar
136. Frosch P. J., Johansen J. D., Menné T... "Further important sensitizers in patients sensitive to fragrances." Contact Dermatitis, vol. 47, 2002, p. 279. DOI: 10.1034/j.1600-0536.2002.470204.x.
Google Scholar
137. Larsen W., Nakayama H., Lindberg M... "Fragrance contact dermatitis: a worldwide multicenter investigation (Part I)." Am J Contact Dermat, vol. 7, 1996, p. 77. DOI: .
138. Uter W.. "Contact allergy to fragrances: current clinical and regulatory trends." Allergol Select, vol. 1, 2017, p. 190. DOI: 10.5414/ALX01604E.
Google Scholar
139. Boukhatem M. N., Ferhat M. A., Kameli A., Saidi F., Kebir H. T.. "Lemon grass (Cymbopogon citratus) essential oil as a potent anti-inflammatory and antifungal drugs." Libyan Journal of Medicine, vol. 9, 2014, p. 25431. DOI: 10.3402/ljm.v9.25431.
Google Scholar
140. Han X., Parker T. L.. "Lemongrass () essential oil demonstrated anti-inflammatory effect in pre-inflamed human dermal fibroblasts." Biochim Open, vol. 4, 2017, p. 107. DOI: 10.1016/j.biopen.2017.03.004.
Google Scholar
141. Gaonkar R., Singh J., Chauhan A., Avti P.K., Hegde G.. "Geraniol and Citral as potential therapeutic agents targeting the HSP90 activity: An in silico and experimental approach." Phytochemistry, vol. 195, 2022, p. 113058. DOI: 10.1016/j.phytochem.2021.113058.
Google Scholar
142. Ishijima S. A., Ezawa K., Abe S.. "Lemongrass and Perilla Essential Oils Synergistically Increased Antimicrobial Activity." Med Mycol J, vol. 62, 2021, p. 21. DOI: 10.3314/mmj.21-00011.
Google Scholar
143. Sahal G., Woerdenbag H. J., Hinrichs W. L. J... "Antifungal and biofilm inhibitory effect of (lemongrass) essential oil on biofilm forming by isolates; an in vitro study." J Ethnopharmacol, vol. 246, 2020, p. 112188. DOI: 10.1016/j.jep.2019.112188.
Google Scholar
144. Habib S., Gupta P., Bhat S.S., Gupta J.. "In silico, in-vitro and in vivo screening of biological activities of citral." International Journal for Vitamin and Nutrition Research, vol. 91, 2021, p. 251. DOI: 10.1024/0300-9831/a000625.
Google Scholar
145. Leelapornpisid P., Wickett R. R., Chansakaow S., Wongwattananukul N.. "Potential of native Thai aromatic plant extracts in antiwrinkle body creams." J Cosmet Sci, vol. 66, , p. 219. DOI: .
146. Moy R. L., Levenson C.. "Sandalwood Album Oil as a Botanical Therapeutic in Dermatology." J Clin Aesthet Dermatol, vol. 10, 2017, p. 34. DOI: .
147. Sharma M., Levenson C., Browning J.C... "East Indian Sandalwood Oil Is a Phosphodiesterase Inhibitor: A New Therapeutic Option in the Treatment of Inflammatory Skin Disease." Front Pharmacol, vol. 9, 2018, p. . DOI: 10.3389/fphar.2018.00200.
Google Scholar
148. Rajsmita B., Keshavamurthy V.. "Re-discovering sandalwood: Beyond beauty and fragrance." Indian Dermatol Online J, vol. 10, 2019, p. 296. DOI: 10.4103/idoj.IDOJ_357_18.
Google Scholar
149. Hartman-Petrycka M., Lebiedowska A.. "The Assessment of Quality of Products Called Sandalwood Oil Based on the Information Provided by Manufacturer of the Oil on Polish, German, and English Websites." Evidence-Based Complementary and Alternative Medicine, vol. 2021, 2021, p. 1. DOI: 10.1155/2021/9934143.
Google Scholar
150. Dwivedi C., Abu-Ghazaleh A.. "Chemopreventive effects of sandalwood oil on skin papillomas in mice." European Journal of Cancer Prevention, vol. 6, 1997, p. 399. DOI: 10.1097/00008469-199708000-00013.
Google Scholar
151. Bommareddy A., Rule B., VanWert A.L., Santha S., Dwivedi C.. "α-Santalol, a derivative of sandalwood oil, induces apoptosis in human prostate cancer cells by causing caspase-3 activation." Phytomedicine, vol. 19, 2012, p. 804. DOI: 10.1016/j.phymed.2012.04.003.
Google Scholar
152. Dave K., Alsharif F. M., Islam S., Dwivedi C., Perumal O.. "Chemoprevention of Breast Cancer by Transdermal Delivery of α-Santalol through Breast Skin and Mammary Papilla (Nipple)." Pharm Res, vol. 34, 2017, p. 1897. DOI: 10.1007/s11095-017-2198-z.
Google Scholar
153. Ortiz C., Morales L., Sastre M., Haskins W. E., Matta J.. "Cytotoxicity and Genotoxicity Assessment of Sandalwood Essential Oil in Human Breast Cell Lines MCF-7 and MCF-10A." Evid Based Complement Alternat Med, vol. 2016, 2016, p. 3696232. DOI: 10.1155/2016/3696232.
Google Scholar
154. Burdock G. A., Carabin I. G.. "Safety assessment of sandalwood oil (Santalum album L.)." Food Chem Toxicol, vol. 46, 2008, p. 421. DOI: 10.1016/j.fct.2007.09.092.
Google Scholar
155. Goyal A., Sharma A., Kaur J... "Bioactive-Based Cosmeceuticals: An Update on Emerging Trends." Molecules, vol. 27, 2022, p. . DOI: 10.3390/molecules27030828.
Google Scholar
156. Alves-Silva J. M., Zuzarte M., Gonçalves M. J... "New Claims for Wild Carrot ( Daucus carota subsp. carota ) Essential Oil." Evidence-Based Complementary and Alternative Medicine, vol. 2016, 2016, p. 1. DOI: 10.1155/2016/9045196.
Google Scholar
157. Singh S., Lohani A., Mishra A.K., Verma A.. "Formulation and evaluation of carrot seed oil-based cosmetic emulsions." Journal of Cosmetic and Laser Therapy, vol. 21, 2019, p. 99. DOI: 10.1080/14764172.2018.1469769.
Google Scholar
158. Sieniawska E., Świątek Ł., Rajtar B., Kozioł E., Polz-Dacewicz M., Skalicka-Woźniak K.. "Carrot seed essential oil—Source of carotol and cytotoxicity study." Ind Crops Prod, vol. 92, 2016, p. 109. DOI: 10.1016/j.indcrop.2016.08.001.
Google Scholar
159. Ácsová A., Hojerová J., Janotková L... "The real UVB photoprotective efficacy of vegetable oils: in vitro and in vivo studies." Photochemical & Photobiological Sciences, vol. 20, 2021, p. 139. DOI: 10.1007/s43630-020-00009-3.
Google Scholar
Similar Submissions
Integrative Therapies for Warts and Molluscum Contagiosum
Thineesha Gnaneswaran, MSc, Audrey Fotouhi, MD, Kathryn Lynam, MD, Sarah Utz, MD, Steven Daveluy, MD
Patient Reported Outcome Measures in Complementary & Alternative Medicine for Atopic Dermatitis: A Systematic Review
Thineesha Gnaneswaran, MSc, Audrey Fotouhi, MD, Kathryn Lynam, MD, Sarah Utz, MD, Steven Daveluy, MD
An Integrative Algorithm for Atopic Dermatitis
Thineesha Gnaneswaran, MSc, Audrey Fotouhi, MD, Kathryn Lynam, MD, Sarah Utz, MD, Steven Daveluy, MD
Proceedings of the 4th Annual Integrative Dermatology Symposium, Sacramento, CA
Thineesha Gnaneswaran, MSc, Audrey Fotouhi, MD, Kathryn Lynam, MD, Sarah Utz, MD, Steven Daveluy, MD
Proceedings of the 6th Annual Integrative Dermatology Symposium in Reno, Nevada
Thineesha Gnaneswaran, MSc, Audrey Fotouhi, MD, Kathryn Lynam, MD, Sarah Utz, MD, Steven Daveluy, MD
A Review on the Incorporation of Sodium Lauryl Sulfate into Homemade Cleansers to Avoid Fragrances and Preservatives
Thineesha Gnaneswaran, MSc, Audrey Fotouhi, MD, Kathryn Lynam, MD, Sarah Utz, MD, Steven Daveluy, MD
Complementary and Alternative Approaches to Skin Cancer
Thineesha Gnaneswaran, MSc, Audrey Fotouhi, MD, Kathryn Lynam, MD, Sarah Utz, MD, Steven Daveluy, MD
Topical Integrative Approaches to Vitiligo: A Systematic Review
Thineesha Gnaneswaran, MSc, Audrey Fotouhi, MD, Kathryn Lynam, MD, Sarah Utz, MD, Steven Daveluy, MD
Integrative Approaches to Skin Cancer Chemoprevention and Sun Protection: Beyond Sunscreen
Thineesha Gnaneswaran, MSc, Audrey Fotouhi, MD, Kathryn Lynam, MD, Sarah Utz, MD, Steven Daveluy, MD
Increased Popularity of Goat Milk Soap: Analyzing Five Years of Google Trends
Thineesha Gnaneswaran, MSc, Audrey Fotouhi, MD, Kathryn Lynam, MD, Sarah Utz, MD, Steven Daveluy, MD

You may also start an advanced similarity search for this article.

[Article - Top - Sidebar]
211
Downloads
289
Total Views
Article impact
Share
Cite
Article Info
DOI:
10.64550/joid.nt5zgk07
Reviewed by:
Peter Lio, MD, Sarah Sung, MD
View PDF
Citation
Cite as
[1]
“Essential Oils in Dermatology: This narrative review evaluates the dermatological uses, benefits, and risks of essential oils, providing evidence-based guidance amid growing interest in natural healthcare alternatives”., JOID, vol. 1, no. 1, Apr. 2025, doi: 10.64550/joid.nt5zgk07.
Export citation
Select the format you want to export the citation of this publication.
Download Citation
Export Citation