This article is about essential oil isolated form the leaves of the tea tree, Melaleuca alternifolia. For the sweet seasoning oil pressed from Camellia seeds, C. sinensis or C. oleifera, see tea seed oil.
Origin of this essential oil, the tea tree,
Melaleuca alternifolia.
Tea tree oil composition,
as per ISO 4730 (2004)[1]
| Component |
Concentration |
| terpinen-4-ol |
30–48% |
| γ-terpinene |
10–28% |
| α-terpinene |
5–13% |
| 1,8-Cineole |
0–15% |
| α-terpinolene |
1.5–5% |
| α-terpineol |
1.5–8% |
| α-pinene |
1–6% |
| p-Cymene |
0.5–8% |
Tea tree plantation, Coraki.
Tea tree oil (TTO), or melaleuca oil, is an essential oil with a fresh camphoraceous odor and a color that ranges from pale yellow to nearly colorless and clear.[2] It is taken from the leaves of the Melaleuca alternifolia, which is native to Southeast Queensland and the Northeast coast of New South Wales, Australia.
Tea tree oil is toxic when taken by mouth,[3][4] but is widely used in low concentrations in cosmetics and skin washes.[1] Tea tree oil has been claimed to be useful for treating a wide variety of medical conditions. It shows some promise as an antimicrobial. Tea tree oil may be effective in a variety of dermatologic conditions including dandruff, acne, lice, herpes, and other skin infections.[5]
Contents
- 1 History and extraction
- 2 Composition and characteristics
- 3 Medical use
- 4 Safety
- 5 See also
- 6 References
- 7 External links
History and extraction
The name tea tree is used for several plants, mostly from Australia and New Zealand, from the family Myrtaceae, related to the myrtle. The use of the name probably originated from Captain Cook's description of one of these shrubs, that he used to make an infusion, to drink in place of tea.
The commercial tea tree oil industry originated in the 1920s when Arthur Penfold, an Australian, investigated the business potential of a number of native extracted oils; he reported that tea tree oil had promise as it exhibited powerful antiseptic properties.[6]
Tea tree oil is extracted from Melaleuca alternifolia commercially.
Composition and characteristics
Tea tree oil is defined by the International Standard ISO 4730 ("Oil of Melaleuca, Terpinen-4-ol type"), which specifies levels of 15 components which are needed to define the oil as "tea tree oil." The oil has been described as having a fresh, camphor-like smell.[7]
Tea tree oils have six types, oils with different chemical compositions. These include a terpinen-4-ol type, a terpinolene type, and four 1,8-cineole types. These various oil types contain over 98 compounds, with terpinen-4-ol the major component responsible for antimicrobial and anti-inflammatory properties.[8] A second component 1,8-cineole, is likely responsible for most allergies in TTO products. Adverse reactions to TTO diminish with minimization of 1,8-cineole content. In commercial production, TTO is prepared as a terpinen-4-ol type.[5]
Medical use
In vitro studies have shown that tea tree oil kills methicillin-resistant Staphylococcus aureus (MRSA),[9] in nasal or extra-nasal (topical) colonisation studies possibly comparable to treatment with mupirocin,[10] but as of 2005 there appeared to be insufficient evidence to recommend it for clinical use.[9] A 2008 article from the American Cancer Society says that studies have found some promise of a possible role for the topical application of tea tree oil as an antiseptic,[3] but that "despite years of use, available clinical evidence does not support the effectiveness of tea tree oil for treating skin problems and infections in humans".[3] A 2012 review by the NIH rates Tea tree oil as "possibly effective" for three applications, saying that "a 5% tea tree oil gel appears to be as effective as 5% benzoyl peroxide" for treating mild to moderate acne, that "topical application of 100% tea tree oil solution, twice daily for six months, can cure fungal toenail infection in about 18% of people who try it," and that "a 10% tea tree oil cream works about as well as tolnaftate 1% cream" in treating symptoms of athlete's foot, although being less effective than clotrimazole or terbinafine.[11]
A 2006 review of the toxicity of tea tree oil concludes that it may be used externally in its diluted form by the majority of individuals without adverse effect (provided oxidization is avoided).[12] Tea Tree oil is poisonous when taken internally.[3] Tea tree oil may be effective in a variety of dermatologic conditions including dandruff, acne, lice, herpes, and other skin infections.[5] A 2012 review of head lice treatment recommended against the use of tea tree oil on children because it could cause skin irritation or allergic reactions, because of contraindications, and because of a lack of knowledge about the oil's safety and effectiveness.[13]
Safety
Tea tree oil is a commercially refined composition of several naturally occurring chemical compounds and is hazardous if misused. Available literature suggests that tea tree oil can be used topically in diluted form by the majority of individuals without adverse effects. Topical application of tea tree oil can cause adverse reactions at high concentration. Adverse effects including skin irritation, allergic contact dermatitis, systemic contact dermatitis, linear immunoglobulin A disease, erythema multiforme like reactions, and systemic hypersensitivity reactions.[5][14]
Tea tree oil is toxic when swallowed.[14] According to the American Cancer Society, ingesting tea tree oil has been reported to cause drowsiness, confusion, hallucinations, coma, unsteadiness, weakness, vomiting, diarrhea, stomach upset, blood cell abnormalities, and severe rashes. It should be kept away from pets and children.[3] Tea tree oil should not be used in or around the mouth.[4] There is at least one case of poisoning reported in medical literature.[15]
Exposure of tea tree oil to air and light results in oxidation of some of its components. Oxidized tea tree oil should not be used.[16] Some people experience allergic contact dermatitis as a reaction to dermal contact with tea tree oil. Allergic reactions may be due to the various oxidation products that are formed by exposure of the oil to light and/or air.[14][17]
In vitro testing of tea tree oil shows that it contains chemicals which are weakly estrogenic, causing particular concern for use with children. However in tests, the chemicals which show this effect failed to show absorption into the skin, and evidence of a hormonal effect is therefore considered implausible by an EU scientific committee.[1]
In dogs and cats, death[18][19] or transient signs of toxicity (lasting 2 to 3 days), such as depression, weakness, incoordination and muscle tremors, have been reported after external application at high doses.[20] In rats the LD50 is 1.9–2.4 ml/kg.[21]
Undiluted tea tree oil can cause some hearing loss when used in the ears of non-human animals; however, a 2% concentration has not been shown to have any lasting effect. It is not known whether the same is true for humans.[22]
See also
- Cajuput oil – derived from Melaleuca leucadendra
References
- ^ a b c [1] SCCP/1155/08 Scientific Committee on Consumer Products SCCP OPINION ON Tea tree oil- European Union Commission Health and Consumer Union protection director general- adopted 18th plenary of 16 December 2008
- ^ [unreliable source?]"Directory of Essential Oils for Aromatherapy: Tea-Tree Oil (Melaleuca alternifolia)". Holistics Online.
- ^ a b c d e "Tea Tree Oil". American Cancer Society. November 2008. Retrieved September 2013.
- ^ a b "Tea Tree Oil". National Capital Poison Center. Retrieved 4 December 2013.
- ^ a b c d Pazyar, N; Yaghoobi, R; Bagherani, N; Kazerouni, A (Jul 2013). "A review of applications of tea tree oil in dermatology.". International Journal of Dermatology 52 (7): 784–90. doi:10.1111/j.1365-4632.2012.05654.x. PMID 22998411.
- ^ Carson, C. F.; Hammer, K. A.; Riley, T. V. (2006). "Melaleuca alternifolia (Tea Tree) Oil: A Review of Antimicrobial and Other Medicinal Properties". Clinical Microbiology Reviews 19 (1): 50–62. doi:10.1128/CMR.19.1.50-62.2006. PMC 1360273. PMID 16418522.
- ^ Billee Sharp (18 September 2013). Lemons and Lavender: The Eco Guide to Better Homekeeping. Cleis Press. pp. 43–. ISBN 978-1-936740-11-6.
- ^ Hart, P.H.; Brand, C.; Carson, C.F.; Riley, T.V.; Prager, R.H.; Finlay-Jones, J.J. (2000). "Terpinen-4-ol, the main component of the essential oil of Melaleuca alternifolia (tea tree oil), suppresses inflammatory mediator production by activated human monocytes.". Inflammation Research 49 (11): 619–26. doi:10.1007/s000110050639. PMID 11131302.
- ^ a b Flaxman, D.; Griffiths, P. (2005). "Is tea tree oil effective at eradicating MRSA colonization? A review". Br. J. Community Nurs. 10 (3, March): 123–126. PMID 15824699.
- ^ Bradley, Suzanne F (January 2011). "MRSA colonisation (eradicating colonisation in people without active/invasive infection)". Clinical Evidence 2011. PMID 21477403.
- ^ "Tea tree oil". U.S. National Library of Medicine. Retrieved 15 December 2014.
- ^ Hammer, KA; Carson, CF; Riley, TV; Nielsen, JB (May 2006). "A review of the toxicity of Melaleuca alternifolia (tea tree) oil.". Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association 44 (5): 616–25. doi:10.1016/j.fct.2005.09.001. PMID 16243420.
- ^ Eisenhower, Christine; Farrington, Elizabeth Anne (2012). "Advancements in the Treatment of Head Lice in Pediatrics". Journal of Pediatric Health Care 26 (6): 451–61; quiz 462–4. doi:10.1016/j.pedhc.2012.05.004. PMID 23099312.
- ^ a b c Hammer, K; Carson, C; Riley, T; Nielsen, J (2006). "A review of the toxicity of Melaleuca alternifolia (tea tree) oil". Food and Chemical Toxicology 44 (5): 616–25. doi:10.1016/j.fct.2005.09.001. PMID 16243420.
- ^ "Ingestion of tea tree oil (Melaleucaoil) by a 4‐year‐old boy".
- ^ "THE EFFECTIVENESS AND SAFETY OF AUSTRALIAN TEA TREE OIL". Australian Government - Rural Industries and Development Corporation. Retrieved 26 February 2014.
- ^ Aberer, W (January 2008). "Contact allergy and medicinal herbs". Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG 6 (1): 15–24. doi:10.1111/j.1610-0387.2007.06425.x. PMID 17919303.
- ^ "Tea Tree Oil and Dogs, Tea Tree Oil and Cats". Petpoisonhelpline.com. Retrieved December 13, 2012.
- ^ "Tea Tree Oil Toxicity". Veterinarywatch. Retrieved December 13, 2012.
- ^ Villar, D; Knight, MJ; Hansen, SR; Buck, WB (April 1994). "Toxicity of melaleuca oil and related essential oils applied topically on dogs and cats". Veterinary and human toxicology 36 (2): 139–42. PMID 8197716.
- ^ [2] Clinical Microbiological Reviews: Melaleuca alternifolia (Tea Tree) Oil: a Review of Antimicrobial and Other Medicinal Properties-C. F. Carson,1 K. A. Hammer,1 and T. V. Riley
- ^ "Tea tree oil". Medline Plus, a service of the U.S. National Library of Medicine from the National Institutes of Health. 27 July 2012.
External links
- "The Marshall Centre: Tea Tree Oil". , research group at the University of Western Australia
- "Tea Tree Oil". at the American Cancer Society
- "Australian Tea Tree Oil database". , a searchable abstract database containing 1200+ journal articles on Tea Tree Oil.
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Acne-treating agents (D10)
|
|
| Antibacterial |
- Azelaic acid
- Benzoyl peroxide#
- 8-Hydroxyquinoline
- Blue light therapy
- Tea tree oil
|
|
| Keratolytic |
- Glycolic acid
- Salicylic acid#
- Sulfur
- Benzoyl peroxide#
|
|
| Anti-inflammatory |
- Nicotinamide
- Ibuprofen #
- Aspirin #
- Red light therapy
|
|
| Antibiotics |
- Clindamycin
- Dapsone
- Erythromycin
- Sulfacetamide
- Tetracyclines (Lymecycline
- Minocycline
- Doxycycline)
|
|
| Hormonal |
- Antiandrogens
- Contraceptives
|
|
| Retinoids |
- Adapalene
- Isotretinoin
- Motretinide
- Tazarotene
- Tretinoin
|
|
| Other |
- Benzamycin
- Epristeride
- Mesulfen
- Pelretin
- Stridex
- Tioxolone
|
|
| Combinations |
- Adapalene/benzoyl peroxide
- Benzoyl peroxide/clindamycin
- Clindamycin/tretinoin
- Erythromycin/isotretinoin
- Sulfacetamide/sulfur
|
|
-
- #WHO-EM
- ‡Withdrawn from market
- Clinical trials:
- †Phase III
- §Never to phase III
|
|
|
Index of skin appendages
|
|
| Description |
- Anatomy
- Physiology
- Development
|
|
| Disease |
- Congenital
- Neoplasms and cancer
- Other
- Symptoms and signs
|
|
| Treatment |
|
|
|
|
Antifungals (D01 and J02)
|
|
Wall/
membrane |
Ergosterol
inhibitors |
Azoles
(lanosterol 14
alpha-demethylase inhibitors) |
| Imidazoles |
- Topical: bifonazole
- butoconazole
- chlormidazole
- clotrimazole#
- croconazole
- econazole
- fenticonazole
- ketoconazole
- isoconazole
- miconazole#
- neticonazole
- omoconazole
- oxiconazole
- sertaconazole
- sulconazole
- tioconazole
|
|
| Triazoles |
- Topical: (fluconazole#, fosfluconazole
- terconazole)
- Systemic: (fluconazole
- hexaconazole
- isavuconazole
- itraconazole
- posaconazole
- voriconazole)
|
|
| Thiazoles |
|
|
|
Polyene antimycotics
(ergosterol binding) |
- Topical: (hamycin
- natamycin
- nystatin#)
Systemic: (amphotericin B#, hamycin)
|
|
Allylamines
(squalene monooxygenase
inhibitors) |
- Topical: (amorolfine
- butenafine
- naftifine
- terbinafine)
Systemic: terbinafine
|
|
|
β-glucan synthase
inhibitors |
- echinocandins (anidulafungin
- caspofungin
- micafungin)
|
|
|
| Intracellular |
Pyrimidine analogues/
thymidylate synthase inhibitors |
|
|
| Mitotic inhibitors |
|
|
| Aminoacyl tRNA synthetase inhibitors |
|
|
|
| Others |
- bromochlorosalicylanilide
- methylrosaniline
- tribromometacresol
- undecylenic acid
- polynoxylin
- chlorophetanol
- chlorphenesin
- ticlatone
- sulbentine
- ethylparaben
- haloprogin
- salicylic acid
- selenium disulfide#
- ciclopirox
- amorolfine
- dimazole
- tolnaftate
- tolciclate
- sodium thiosulfate#
- Whitfield's ointment#
- potassium iodide#
- taurolidine
- tea tree oil
- citronella oil
- lemon grass
- orange oil
- patchouli
- lemon myrtle
- PCP: pentamidine
- dapsone
- atovaquone
|
|
- #WHO-EM
- ‡Withdrawn from market
- Clinical trials:
- †Phase III
- §Never to phase III
|
Index of fungal disease
|
|
| Description |
|
|
| Disease |
|
|
| Treatment |
|
|
|