Essential oil

An essential oil is a concentrated hydrophobic liquid containing volatile aroma compounds from plants. Essential oils are also known as volatile oils, ethereal oils, aetherolea, or simply as the oil of the plant from which they were extracted, such as oil of clove. An oil is "essential" in the sense that it contains the "essence of" the plant's fragrance—the characteristic fragrance of the plant from which it is derived.[1] The term essential used here does not mean indispensable as with the terms essential amino acid or essential fatty acid which are so called since they are nutritionally required by a given living organism.[2]

Essential oils are generally extracted by distillation, often by using steam. Other processes include expression, solvent extraction, absolute oil extraction, resin tapping, and cold pressing. They are used in perfumes, cosmetics, soaps and other products, for flavoring food and drink, and for adding scents to incense and household cleaning products.

History

Essential oils have been used medicinally throughout history. The earliest recorded mention of the techniques and methods used to produce essential oils is believed to be that of Ibn al-Baitar (1188–1248), an Al-Andalusian (Muslim-controlled Spain) physician, pharmacist and chemist.[3]

Rather than refer to essential oils themselves, modern works typically discuss specific chemical compounds of which the essential oils are composed. For example: methyl salicylate rather than "oil of wintergreen".[4][5]

Interest in essential oils has revived in recent decades with the popularity of aromatherapy, a branch of alternative medicine that uses essential oils and other aromatic compounds. Oils are volatilized, diluted in a carrier oil and used in massage, diffused in the air by a nebulizer, heated over a candle flame, or burned as incense.

Medical applications proposed by those who sell medicinal oils range from skin treatments to remedies for cancer and often are based solely on historical accounts of use of essential oils for these purposes. Claims for the efficacy of medical treatments, and treatment of cancers in particular, are now subject to regulation in most countries.

Production

Distillation

Most common essential oils such as lavender, peppermint, tea tree oil, patchouli, and eucalyptus are distilled. Raw plant material, consisting of the flowers, leaves, wood, bark, roots, seeds, or peel, is put into an alembic (distillation apparatus) over water. As the water is heated, the steam passes through the plant material, vaporizing the volatile compounds. The vapors flow through a coil, where they condense back to liquid, which is then collected in the receiving vessel.

Most oils are distilled in a single process. One exception is ylang-ylang (Cananga odorata) which is purifed through a fractional distillation.

The recondensed water is referred to as a hydrosol, hydrolat, herbal distillate, or plant water essence, which may be sold as another fragrant product. Popular hydrosols include rose water, lavender water, lemon balm, clary sage, and orange blossom water. The use of herbal distillates in cosmetics is increasing. Some plant hydrosols have unpleasant smells and are therefore not sold.

Expression

Most citrus peel oils are expressed mechanically or cold-pressed (similar to olive oil extraction). Due to the relatively large quantities of oil in citrus peel and low cost to grow and harvest the raw materials, citrus-fruit oils are cheaper than most other essential oils. Lemon or sweet orange oils are obtained as byproducts of the citrus industry.

Before the discovery of distillation, all essential oils were extracted by pressing.[6]

Solvent extraction

Most flowers contain too little volatile oil to undergo expression, but their chemical components are too delicate and easily denatured by the high heat used in steam distillation. Instead, a solvent such as hexane or supercritical carbon dioxide is used to extract the oils [7]. Extracts from hexane and other hydrophobic solvents are called concretes, which are a mixture of essential oil, waxes, resins, and other lipophilic (oil-soluble) plant material.

Although highly fragrant, concretes contain large quantities of non-fragrant waxes and resins. Often, another solvent, such as ethyl alcohol, which is more polar in nature, is used to extract the fragrant oil from the concrete. The alcohol solution is chilled to −18 °C (0 °F) for more than 48 hours which causes the waxes and lipids to precipitate out. The precipitates are then filtered out and the ethanol is removed from the remaining solution by evaporation, vacuum purge, or both, leaving behind the absolute.

Supercritical carbon dioxide is used as a solvent in supercritical fluid extraction. This method has many benefits, including avoiding petrochemical residues in the product and the loss of some "top notes" when steam distillation is used. It does not yield an absolute directly. The supercritical carbon dioxide will extract both the waxes and the essential oils that make up the concrete. Subsequent processing with liquid carbon dioxide, achieved in the same extractor by merely lowering the extraction temperature, will separate the waxes from the essential oils. This lower temperature process prevents the decomposition and denaturing of compounds. When the extraction is complete, the pressure is reduced to ambient and the carbon dioxide reverts to a gas, leaving no residue.

Florasols extraction

Florasol is another solvent used to obtain essential oils. It was originally developed as a refrigerant to replace Freon. Although Florasol is an "ozone-friendly" product, it has a high global warming potential (GWP; 100-yr GWP = 1430).[8] The European Union has banned its use, with a phase-out process that began in 2011, to be completed in 2017.[9] One advantage of Florasol is that the extraction of essential oils occurs at or below room temperature so degradation through high temperature extremes does not occur. The essential oils are mostly pure and contain little to no foreign substances.

Production quantities

Estimates of total production of essential oils are difficult to obtain. One estimate, compiled from data in 1989, 1990, and 1994 from various sources, gives the following total production, in tonnes, of essential oils for which more than 1,000 tonnes were produced.[10]

Oil Tonnes
Sweet orange 12,000
Mentha arvensis 4,800
Peppermint 3,200
Cedarwood 2,600
Lemon 2,300
Eucalyptus globulus 2,070
Litsea cubeba 2,000
Clove (leaf) 2,000
Spearmint 1,300

Pharmacology and medical uses

Carvacrol, a terpene found in oregano oil, inhibits the growth of several bacteria strains including Escherichia coli and Bacillus cereus. In Pseudomonas aeruginosa, it causes damages to the cell membrane of these bacteria and, unlike other terpenes, inhibits their proliferation. The cause of the antimicrobial properties is believed to be disruption of the bacteria membrane. Carvacrol is a potent activator of the human ion channels transient receptor potential V3 (TRPV3) and A1 (TRPA1).

Another example of the medicinal value of essential oils is thymol, isomeric with carvacrol and found in oil of the common spice thyme. Thymol is part of a naturally occurring class of compounds known as biocides, with strong antimicrobial attributes when used alone or with other biocides such as carvacrol.[11][12][13] In addition, naturally occurring biocidal agents such as thymol can reduce bacterial resistance to common drugs such as penicillin. Numerous studies have demonstrated the antimicrobial effects of thymol, ranging from inducing antibiotic susceptibility in drug-resistant pathogens to powerful antioxidant properties. Research demonstrates that thymol and carvacrol reduce bacterial resistance to antibiotics through a synergistic effect, and thymol has been shown to be an effective fungicide, particularly against fluconazole-resistant strains. Carvacrol and thymol have been demonstrated to have a strong antimutagenic effect. In addition, there is evidence that thymol has antitumor properties. Though the exact mechanism is unknown, some evidence suggests thymol effects at least some of its biocidal properties by membrane disruption. Thymol has been shown to act as a positive allosteric modulator of GABAA in vitro.

Studies have shown that certain essential oils may have the ability to prevent the transmission of some drug-resistant strains of pathogen, specifically Staphylococcus, Streptococcus and Candida.[14]

Taken by mouth, many essential oils can be dangerous in high concentrations. Typical effects begin with a burning feeling, followed by salivation. In the stomach, the effect is carminative, relaxing the gastric sphincter and encouraging eructation (belching). Further down the gut, the effect typically is antispasmodic.[15][16] Typical ingredients for such applications include eucalyptus oils, menthol, capsaicin, anise and camphor.

Different essential oils may have drastically different pharmacology. Those that do work well for upper respiratory tract and bronchial problems act variously as mild expectorants and decongestants. Some act as locally anesthetic counterirritants and, thereby, exert an antitussive effect.[15][17]

Some essential oils, such as those of juniper and agathosma, are valued for their diuretic effects.[18] With relatively recent concerns about the overuse of antibacterial agents,[19] many essential oils have seen a resurgence in off-label use for such properties and are being examined for this use clinically.[20]

Many essential oils affect the skin and mucous membranes in ways that are valuable or harmful. Many essential oils, particularly tea tree oil, may cause contact dermatitis.[21][22][23][24] They are used in antiseptics and liniments in particular. Typically, they produce rubefacient irritation at first and then counterirritant numbness. Turpentine oil and camphor are two typical examples of oils that cause such effects. Menthol and some others produce a feeling of cold followed by a sense of burning. This is caused by its effect on heat-sensing nerve endings. Some essential oils, such as clove oil or eugenol, were popular for many hundred years in dentistry as antiseptics and local anesthetics.

Use in aromatherapy

Essential oils are used in aromatherapy as part of, for example, essential oil diffusers.

Aromatherapy is a form of alternative medicine in which healing effects are ascribed to the aromatic compounds in essential oils and other plant extracts. Aromatherapy appears to be useful to induce relaxation, especially when administered with massage.[25] Use of essential oils may cause harm including allergic reactions and skin irritation; there has been at least one case of death.[26]

Dilution

Essential oils are usually lipophilic (literally: "oil-loving") compounds that usually are not miscible with water. They can be diluted in solvents like pure ethanol and polyethylene glycol.

Raw materials

Essential oils are derived from sections of plants. Some plants, like the bitter orange, are sources of several types of essential oil.

Bark
Berries
Flowers
Leaves
Peel
Resin
Rhizome
Roots
Seeds
Woods

Balsam of Peru

Balsam of Peru, an essential oil derived from the Myroxylon, is used in food and drink for flavoring, in perfumes and toiletries for fragrance, and in medicine and pharmaceutical items for healing properties.[27] However, a number of national and international surveys have identified Balsam of Peru as being in the "top five" allergens most commonly causing patch test allergic reactions in people referred to dermatology clinics.[28][29][30]

Eucalyptus oil

Most eucalyptus oil on the market is produced from the leaves of Eucalyptus globulus. Steam-distilled eucalyptus oil is used throughout Asia, Africa, Latin America and South America as a primary cleaning/disinfecting agent added to soaped mop and countertop cleaning solutions; it also possesses insect and limited vermin control properties.[31] Note, however, there are hundreds of species of eucalyptus, and perhaps some dozens are used to various extents as sources of essential oils. Not only do the products of different species differ greatly in characteristics and effects, but also the products of the very same tree can vary grossly.[32]

Lavender essential oil

Lavender essential oil has long been used in the production of perfume.[33] However, it can be estrogenic and antiandrogenic, causing problems for prepubescent boys and pregnant women, in particular.[34] Lavender essential oil is also used as an insect repellent.[35]

Rose oil

Rose oil is produced from the petals of Rosa damascena and Rosa centifolia. Steam-distilled rose oil is known as "rose otto", while the solvent extracted product is known as "rose absolute".

Dangers

The potential danger of an essential oil is sometimes relative to its level or grade of purity, and sometimes related to the toxicity of specific chemical components of the oil. Many essential oils are designed exclusively for their aroma-therapeutic quality; these essential oils generally should not be applied directly to the skin in their undiluted or "neat" form. Some can cause severe irritation, provoke an allergic reaction and, over time, prove hepatotoxic.

Some essential oils, including many of the citrus peel oils, are photosensitizers, increasing the skin's vulnerability to sunlight.[36]

Industrial users of essential oils should consult the safety data sheets (SDS) to determine the hazards and handling requirements of particular oils. Even certain therapeutic grade oils can pose potential threats to individuals with epilepsy or pregnant women.

Flammability

The flash point of each essential oil is different. Many of the common essential oils, such as tea tree, lavender, and citrus oils, are classed as a Class 3 Flammable Liquid, as they have a flash point of 50–60 °C.

Gynecomastia

Estrogenic and antiandrogenic activity have been reported by in vitro study of tea tree oil and lavender essential oils. Case reports suggest the oils may be implicated in some cases of gynecomastia, an abnormal breast tissue growth in prepubescent boys.[37][38] However, these claims have been challenged [39] and the European Commission's Scientific Committee on Consumer Safety has dismissed the claims saying "Since the hormonal active ingredients of Tea Tree Oil were shown not to penetrate the skin, the hypothesized correlation of the finding of 3 cases of gynecomastia to the topical use of Tea Tree Oil is considered implausible." [40]

Handling

Exposure to essential oils may cause a contact dermatitis.[22][23][24] Essential oils can be aggressive toward rubbers and plastics, so care must be taken in choosing the correct handling equipment. Glass syringes are often used, but have coarse volumetric graduations. Chemistry syringes are ideal, as they resist essential oils, are long enough to enter deep vessels, and have fine graduations, facilitating quality control. Unlike traditional pipettes, which have difficulty handling viscous fluids, the chemistry syringe has a seal and piston arrangement which slides inside the pipette, wiping the essential oil off the pipette wall.

Ingestion

Essential oils are used extensively as GRAS flavoring agents in foods, beverages, and confectioneries according to strict Good Manufacturing Practice (GMP) and flavorist standards. Pharmacopoeia standards for medicinal oils should be heeded. Some oils can be toxic to some domestic animals, cats in particular.[41] The internal use of essential oils can pose hazards to pregnant women, as some can be abortifacients in dose 0.5–10 ml, and thus should not be used during pregnancy.

Pesticide residues

There is some concern about pesticide residues in essential oils, particularly those used therapeutically. For this reason, many practitioners of aromatherapy buy organically produced oils. Not only are pesticides present in trace quantities, but also the oils themselves are used in tiny quantities and usually in high dilutions. Where there is a concern about pesticide residues in food essential oils, such as mint or orange oils, the proper criterion is not solely whether the material is organically produced, but whether it meets the government standards based on actual analysis of its pesticide content.[42]

Pregnancy

The use of essential oils in pregnancy is not recommended due to inadequate published evidence to demonstrate evidence of safety.[43] Pregnant women often report an abnormal sensitivity to smells and taste,[44] and essential oils can cause irritation and nausea.

Toxicology

The following table lists the LD50 or median lethal dose for common oils; this is the dose required to kill half the members of a tested animal population. LD50 is intended as a guideline only, and reported values can vary widely due to differences in tested species and testing conditions.[45]

Common Name Oral LD50 Dermal LD50 Notes
Neem 14 g/kg >2 g/kg
Lemon myrtle 2.43 g/kg 2.25 g/kg
Frankincense >5 g/kg >5 g/kg Boswellia carterii
Frankincense >2 g/kg >2 g/kg Boswellia sacra
Indian frankincense >2 g/kg >2 g/kg Boswellia serrata
Ylang-ylang >5 g/kg >5 g/kg
Cedarwood >5 g/kg >5 g/kg
Roman chamomile >5 g/kg >5 g/kg
White camphor >5 g/kg >5 g/kg Cinnamomum camphora, extracted from leaves
Yellow camphor 3.73 g/kg >5 g/kg Cinnamomum camphora, extracted from bark
Hot oil 3.80 g/kg >5 g/kg Cinnamomum camphora, oil extracted from leaves
Cassia 2.80 g/kg 0.32 g/kg

Standardization of its derived products

In 2002, ISO published ISO 4720 in which the botanical names of the relevant plants are standardized.[46] The rest of the standards with regards to this topic can be found in the section of ICS 71.100.60 [47]

See also

References

  1. "essential oil". Oxford English Dictionary (online, American English ed.). Retrieved 2014-07-21.
  2. Reeds, P. J. (2000). "Dispensable and indispensable amino acids for humans". The Journal of nutrition. 130 (7): 1835S–40S. PMID 10867060.
  3. Houtsma, M.Th. (1993). E. J. Brill's First Encyclopaedia of Islam, 1913–1936. 4. Brill. pp. 1011–. ISBN 978-90-04-09790-2.
  4. Gilman, A. G.; Rall, T. W.; Nies, Alan S.; Taylor, Palmer, eds. (1990). Goodman & Gilman's The Pharmacological Basis of Therapeutics (8th ed.). New York: Pergamon. ISBN 0-08-040296-8.
  5. Klaassen, Curtis D.; Amdur, Mary O.; Casarett, Louis J.; Doull, John (1991). Casarett and Doull's Toxicology: The Basic Science of Poisons. New York: McGraw-Hill. ISBN 0071052399.
  6. Ryman, Daniele (1984). The Aromatherapy Handbook: The Secret Healing Power Of Essential Oils. Century Publishing CO. Ltd. pp. Chapter 3. ISBN 9780852072158.
  7. Aizpurua-Olaizola, Oier; Ormazabal, Markel; Vallejo, Asier; Olivares, Maitane; Navarro, Patricia; Etxebarria, Nestor; Usobiaga, Aresatz (2015-01-01). "Optimization of supercritical fluid consecutive extractions of fatty acids and polyphenols from Vitis vinifera grape wastes". Journal of Food Science. 80 (1): E101–107. ISSN 1750-3841. PMID 25471637. doi:10.1111/1750-3841.12715.
  8. Forster, P; et al. (2007). "Changes in Atmospheric Constituents and in Radiative Forcing" (PDF). In Solomon, S; et al. Climate Change 2007: The Physical Science Basis. Contribution of Working Group I to the Fourth Assessment Report of the Intergovernmental Panel on Climate Change. Cambridge University Press.
  9. Refrigerant 1234YF's Potential Impact in Automotive Applications
  10. "ISO TC 54 Business Plan – Essential oils" (PDF). Retrieved 2006-09-14. It is unclear from the source what period of time the quoted figures include.
  11. "Carvacrol data sheet from Sigma-Aldrich".
  12. Soares, I.H.; Loreto, É.S.; Rossato, L.; Mario, D.N.; Venturini, T.P.; Baldissera, F.; Santurio, J.M.; Alves, S.H. (2015). "In vitro activity of essential oils extracted from condiments against fluconazole-resistant and -sensitive Candida glabrata". Journal de Mycologie Médicale / Journal of Medical Mycology. 25 (3): 213–7. PMID 26281965. doi:10.1016/j.mycmed.2015.06.003.
  13. Mandras, Narcisa; Nostro, Antonia; Roana, Janira; Scalas, Daniela; Banche, Giuliana; Ghisetti, Valeria; Del Re, Simonetta; Fucale, Giacomo; Cuffini, Anna Maria; Tullio, Vivian (2016). "Liquid and vapour-phase antifungal activities of essential oils against Candida albicans and non-albicans Candida". BMC Complementary and Alternative Medicine. 16 (1): 330. PMC 5006570Freely accessible. PMID 27576581. doi:10.1186/s12906-016-1316-5.
  14. Warnke, Patrick H.; Becker, Stephan T.; Podschun, Rainer; Sivananthan, Sureshan; Springer, Ingo N.; Russo, Paul A.J.; Wiltfang, Joerg; Fickenscher, Helmut; Sherry, Eugene (2009). "The battle against multi-resistant strains: Renaissance of antimicrobial essential oils as a promising force to fight hospital-acquired infections". Journal of Cranio-Maxillofacial Surgery. 37 (7): 392–7. PMID 19473851. doi:10.1016/j.jcms.2009.03.017.
  15. 1 2 Sapeika, Norman (1963). Actions and Uses of Drugs. A.A. Balkema.
  16. Braun, Leslie (2005). Herbs & Natural Supplements. Australia: Elsevier. pp. 42–43. ISBN 978-0-7295-3910-4.
  17. Haneke, Karen E (February 2002), Turpentine (Turpentine Oil, Wood Turpentine, Sulfate Turpentine, Sulfite Turpentine) [8006-64-2]: Review of Toxicological Literature (PDF) (Contract No. N01–ES–65402), National Institute of Environmental Health Sciences
  18. Watt, John Mitchell; Breyer-Brandwijk, Maria Gerdina (1962). The Medicinal and Poisonous Plants of Southern and Eastern Africa (2nd ed.). Edinburgh: E & S Livingstone.
  19. Levy, Stuart B. (2001). "Antibacterial Household Products: Cause for Concern". Emerging Infectious Diseases. 7 (7): 512–5. PMC 2631814Freely accessible. PMID 11485643. doi:10.3201/eid0707.017705.
  20. Singh, G.; Kapoor, I. P. S.; Pandey, S. K.; Singh, U. K.; Singh, R. K. (2002). "Studies on essential oils: Part 10; Antibacterial activity of volatile oils of some spices". Phytotherapy Research. 16 (7): 680–2. PMID 12410554. doi:10.1002/ptr.951.
  21. Larson, David; Jacob, Sharon E. (2012). "Tea Tree Oil". Dermatitis. 23 (1): 48–9. PMID 22653070. doi:10.1097/DER.0b013e31823e202d.
  22. 1 2 Trattner, Akiva; David, Michael; Lazarov, Aneta (2008). "Occupational contact dermatitis due to essential oils". Contact Dermatitis. 58 (5): 282–4. PMID 18416758. doi:10.1111/j.1600-0536.2007.01275.x.
  23. 1 2 Bleasel, Narelle; Tate, Bruce; Rademaker, Marius (2002). "Allergic contact dermatitis following exposure to essential oils". Australasian Journal of Dermatology. 43 (3): 211–3. PMID 12121401. doi:10.1046/j.1440-0960.2002.00598.x.
  24. 1 2 Isaksson, M; Brandão, F. M.; Bruze, M; Goossens, A (2000). "Short Communications". Contact Dermatitis. 43 (1): 41–2. PMID 10902588. doi:10.1034/j.1600-0536.2000.043001041.x.
  25. Lee, Myeong Soo; Choi, Jiae; Posadzki, Paul; Ernst, Edzard (2012). "Aromatherapy for health care: An overview of systematic reviews". Maturitas. 71 (3): 257–60. PMID 22285469. doi:10.1016/j.maturitas.2011.12.018.
  26. Posadzki, P; Alotaibi, A; Ernst, E (2012). "Adverse effects of aromatherapy: A systematic review of case reports and case series". The International journal of risk & safety in medicine. 24 (3): 147–61. PMID 22936057. doi:10.3233/JRS-2012-0568 (inactive 2017-04-02).
  27. "Balsam, Peru". www.hippylife.co.uk. Hippylife. Retrieved 2006-08-17.
  28. Arenholt-Bindslev, D; Jolanki, R; Kanerva, L (2008). "Diagnosis of Side Effects of Dental Materials, with Special Emphasis on Delayed and Immediate Allergic Reactions". In Schmalz, Gottfried; Arenholt-Bindslev, Dorthe. Biocompatibility of Dental Materials. Springer. p. 352. ISBN 9783540777823. doi:10.1007/978-3-540-77782-3_14. Retrieved March 5, 2014.
  29. Habif, Thomas P. (2009). Clinical Dermatology. Elsevier Health Sciences. ISBN 9780323080378. Retrieved March 6, 2014.
  30. Yiannias, JA (2013). "Contact Dermatitis". In Bope, Edward T.; Kellerman, Rick D. Conn's Current Therapy 2014: Expert Consult. Elsevier Health Sciences. ISBN 9780323225724. Retrieved March 6, 2014.
  31. . doi:10.1016/j.foreco.2008.08.008. Missing or empty |title= (help)
  32. Thorpe's Dictionary of Applied Chemistry. 8 (4th ed.). Longmans Green. 1947.
  33. N. Groom. New Perfume Handbook. Springer Science & Business Media, 1997 ISBN 9780751404036, pp. 184-186
  34. . doi:10.1056/NEJMoa064725. Missing or empty |title= (help)
  35. Debboun, Mustapha; Frances, Stephen P.; Strickman, Daniel, eds. (2014). Insect Repellents Handbook (2nd ed.). CRC Press. p. 362. ISBN 1466553553.
  36. Kaddu, Steven; Kerl, Helmut; Wolf, Peter (2001). "Accidental bullous phototoxic reactions to bergamot aromatherapy oil". Journal of the American Academy of Dermatology. 45 (3): 458–61. PMID 11511848. doi:10.1067/mjd.2001.116226.
  37. Henley, Derek V.; Lipson, Natasha; Korach, Kenneth S.; Bloch, Clifford A. (2007). "Prepubertal Gynecomastia Linked to Lavender and Tea Tree Oils". New England Journal of Medicine. 356 (5): 479–85. PMID 17267908. doi:10.1056/NEJMoa064725.
  38. "Oils make male breasts develop". BBC News. February 1, 2007. Retrieved September 9, 2007.
  39. Carson, Christine F.; Tisserand, Robert; Larkman, Tony (2014). "Lack of evidence that essential oils affect puberty". Reproductive Toxicology. 44: 50–1. PMID 24556344. doi:10.1016/j.reprotox.2013.09.010.
  40. Scientific Committee on Consumer Products (December 16, 2008), Opinion on tea tree oil (PDF) (Report No. SCCP/1155/08), Directorate-General for Health and Consumers: European Commission: European Union
  41. Bischoff, K.; Guale, Fessesswork (1998). "Australian Tea Tree (Melaleuca Alternifolia) Oil Poisoning in Three Purebred Cats". Journal of Veterinary Diagnostic Investigation. 10 (2): 208–10. PMID 9576358. doi:10.1177/104063879801000223.
  42. Menary, RC (2008). Minimising pesticide residues in essential oils. Rural Industries Research and Development Corporation. ISBN 9781741517095.
  43. Bone, Kerry (2000). Principles and Practice of Phytotherapy: Modern Herbal Medicine. Elsevier. p. 453. ISBN 978-0-443-06992-5.
  44. Nordin, S.; Broman, D. A.; Olofsson, J. K.; Wulff, M (2004). "A Longitudinal Descriptive Study of Self-reported Abnormal Smell and Taste Perception in Pregnant Women". Chemical Senses. 29 (5): 391–402. PMID 15201206. doi:10.1093/chemse/bjh040.
  45. Dweck, AC (September 2009). "Toxicology of essential oils reviewed" (PDF). Personal Care.
  46. International Organization for Standardization. "ISO 4720:2002 Essential oils – Nomenclature". Retrieved April 23, 2009.
  47. International Organization for Standardization. "71.100.60: Essential oils". Retrieved June 14, 2009.

Further reading

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.