Eflornithine
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| Image:Eflornithine-2D-skeletal.png | |
| Image:Eflornithine-3D-vdW.png | |
| Eflornithine
| |
| Systematic (IUPAC) name | |
| 2,5-diamino-2-(difluoromethyl)pentanoic acid | |
| Identifiers | |
| CAS number | |
| ATC code | D11 P01CX03 |
| PubChem | |
| Chemical data | |
| Formula | C6H12F2N2O2 |
| Mol. mass | 182.2 g/mol |
| Pharmacokinetic data | |
| Bioavailability | 100% (Intravenous) 13% (Dermal) |
| Metabolism | Not metabolised |
| Half life | 8 hours |
| Excretion | Renal |
| Therapeutic considerations | |
| Licence data |
|
| Pregnancy cat. |
Category C for dermal cream |
| Legal status |
℞ Prescription only |
| Routes | Intravenous (discontinued) Dermal |
Eflornithine (α-difluoromethylornithine or DFMO) is a drug manufactured by Sanofi-Aventis which has various uses. It was initially developed for cancer treatment, but while having little use in treating malignancies, it was found to be highly effective in African trypanosomiasis (sleeping sickness), especially the West African form (Trypanosoma brucei gambiense).[1] In the United States it is known by the brand name Ornidyl®.[1]
Sleeping sickness treatment
Function
Eflornithine appears to kill trypanosomes by acting as a suicide inhibitor of the enzyme ornithine decarboxylase (EC 4.1.1.17), this enzyme regulates cell division by catalysing the first step in polyamine biosynthesis.
Eflornithine's effects against Trypanosoma brucei gambiense were discovered by chance and because of its ability to bring patients back from coma, it became known as "Resurrection Drug".
It is hoped that eflornithine will replace the relatively toxic melarsoprol.
Production
Supplies of eflornithine are limited as its manufacturer does not consider it cost effective.
Its production was halted by its manufacturer, Aventis, in 1995 because the company did not consider it a profitable drug. The disease mainly affects poor people unable to pay for any sort of treatment.
In 2001, after lobbying at the WHO World Health Organization by Médecins Sans Frontières ("Doctors Without Borders"), the manufacturer resumed production of eflornithine, melarsoprol and pentamidine in sufficient amounts to cover existing needs. This 5-year agreement with the WHO also envisaged MSF working on the distribution of the drugs. The yearly value of the drugs donated by Aventis under this agreement is US$5 million. In addition, under the agreement, Bristol-Myers Squibb, the manufacturer of Vaniqa, will pay for part of the eflornithine. The 5-year agreement expired in 2006.[1] The trade name of eflornithine as manufactured for the treatment of sleeping sickness is Ornidyl®.
Once the five years period is over, Sanofi-Aventis (its new name after merging with another drugs company, Sanofi-Synthélabo) would start transferring technology and giving technical assistance to any possible manufacturer willing to continue production on their own.[1]
As of September 2005, the World Health Organization reports that the India Institute of Chemical Technology in Hyderabad, India and ILEX Oncology in Texas, United States are both working on new ways of making eflornithine more cheaply. The WHO goes on to say that ILEX is experimenting with an oral formulation of the drug as a treatment for cancer and that trials of the new oral formulation for efficacy against sleeping sickness are underway.
Dosing
When used for sleeping sickness, eflornithine is given intravenously, 50 mg/kg every six hours for 14 days.[1]
Hair growth inhibitor cream
Eflornithine is also an effective hair growth inhibiting agent. As a topical application, the drug has been shown to be an effective hair growth retardant in some patients, and is sold under the brand name Vaniqa® (eflornithine hydrochloride 13.9%). Efficacy data submitted to Food and Drug Administration (FDA) observed about 58% of women using it on facial hair had improvement.[1] This study suggested it may be particularly effective in postmenopausal women. One large published study on safety found the product rarely caused significant side effects such as acne, follicle irritation, itching or dryness.[1] This corroborates unpublished data submitted to FDA showing about 2% of subjects discontinued use due to adverse reactions.
It is partly the development of the hair removal market that encouraged Aventis to re-start the manufacture of eflornithine, and which allowed it to once again become available for use in sleeping sickness.
References
External links
Other dermatological preparations (D11) | |
|---|---|
| Medicated shampoos | Cetrimide - Cadmium compounds - Selenium compounds - Povidone-iodine - Sulfur compounds - Xenysalate |
| Other dermatologicals | seborrhoeic dermatitis/dandruff (Lithium succinate, Pyrithione zinc) - skin whitening/depigmenting (Hydroquinone, Mequinol, Monobenzone) - anti-inflammatory/Immunomodulators (Oxaceprol, Gamolenic acid), Pimecrolimus, Tacrolimus) - baldness treatments (Finasteride, Minoxidil) - hair growth inhibiting agent (Eflornithine) - other (Calcium gluconate, Magnesium sulfate, Tiratricol) |
Antiprotozoals: Agents against leishmaniasis and trypanosomiasis (P01C) | |
|---|---|
| Nitroimidazole derivatives | Benznidazole |
| Antimony compounds | Pentavalent antimonials (Meglumine antimoniate, Sodium stibogluconate) |
| Nitrofuran derivatives | Nifurtimox |
| Arsenic compounds | Melarsoprol |
| Other agents | Pentamidine · Suramin · Eflornithine · Miltefosine |
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .
