Tenofovir disoproxil
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Pronunciation | /ˌtəˈnoʊfəvɪər ˌdɪsəˈprɑːksəl/ |
Trade names | Viread, others |
Other names | Bis(POC)PMPA |
AHFS/Drugs.com | Monograph |
MedlinePlus | a602018 |
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Routes of administration | By mouth (tablets) |
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Pharmacokinetic data | |
Bioavailability | 25% |
Metabolism | Ester hydrolysis |
Metabolites | Tenofovir |
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Clinical data | |
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Other names | 9-(2-Phosphonyl-methoxypropyly)adenine (PMPA) |
MedlinePlus | a602018 |
ATC code |
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Pharmacokinetic data | |
Protein binding | < 1% |
Metabolism | Phosphorylation |
Metabolites | Tenofovir diphosphate (active metabolite) |
Elimination half-life | 17 hours |
Excretion | Kidney |
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Tenofovir disoproxil, sold under the trade name Viread among others, is a medication used to treat chronic hepatitis B and to prevent and treat HIV/AIDS.[3] It is generally recommended for use with other antiretrovirals.[3] It may be used for prevention of HIV/AIDS among those at high risk before exposure, and after a needlestick injury or other potential exposure.[3] It is sold both by itself and together in combinations such as emtricitabine/tenofovir, efavirenz/emtricitabine/tenofovir,[3] and elvitegravir/cobicistat/emtricitabine/tenofovir.[4] It does not cure HIV/AIDS or hepatitis B.[3][5] It is available by mouth as a tablet or powder.[3]
Common side effects include nausea, rash, diarrhea, headache, pain, depression, and weakness.[3] Severe side effects include high blood lactate and an enlarged liver.[3] There are no absolute contraindications.[3] It is often recommended during pregnancy and appears to be safe.[3] It is a nucleotide reverse transcriptase inhibitor and works by decreasing the ability of the viruses to replicate.[3]
Tenofovir was patented in 1996 and approved for use in the United States in 2001.
Medical uses
Tenofovir disoproxil is used for HIV-1 infection and chronic hepatitis B treatment. For HIV-1 infection, tenofovir is indicated in combination with other antiretroviral agents for people 2 years of age and older. For chronic hepatitis B patients, tenofovir is indicated for patients 12 years of age and older.[9]
HIV risk reduction
Tenofovir can be used for HIV prevention in people who are at high risk for infection through sexual transmission or injecting drug use. A
Adverse effects
Tenofovir disoproxil is generally well tolerated with low discontinuation rates among the HIV and chronic hepatitis B population.[12] There are no contraindications for use of this drug.[9] The most commonly reported side effects due to use of tenofovir disoproxil were dizziness, nausea, and diarrhea.[12] Other adverse effects include depression, sleep disturbances, headache, itching, rash, and fever. The US boxed warning cautions potential onset of lactic acidosis or liver damage due to use of tenofovir disoproxil.[13]
Long term use of tenofovir disoproxil is associated with nephrotoxicity and bone loss. Presentation of nephrotoxicity can appear as Fanconi syndrome, acute kidney injury, or decline of glomerular filtration rate (GFR).[14] Discontinuation of tenofovir disoproxil can potentially lead to reversal of renal impairment. Nephrotoxicity may be due to proximal tubules accumulation of Tenofovir disoproxil leading to elevated serum concentrations.[12]
Interactions
Tenofovir interacts with didanosine and HIV-1 protease inhibitors. Tenofovir increases didanosine concentrations and can result in adverse effects such as pancreatitis and neuropathy. Tenofovir also interacts with HIV-1 protease inhibitors such as atazanavir, by decreasing atazanavir concentrations while increasing tenofovir concentrations.[9] In addition, since tenofovir is excreted by the kidney, medications that impair renal function can also cause problems.[15]
Pharmacology
Mechanism of action
Tenofovir disoproxil is a nucleotide analog reverse-transcriptase inhibitor (NtRTI).[16] It selectively inhibits viral reverse transcriptase, a crucial enzyme in retroviruses such as human immunodeficiency virus (HIV), while showing limited inhibition of human enzymes, such as DNA polymerases α, β, and mitochondrial DNA polymerase γ.[9][16] In vivo tenofovir disoproxil fumarate is converted to tenofovir, an acyclic analog of deoxyadenosine 5'-monophosphate (dAMP). Tenofovir lacks a hydroxyl group in the position corresponding to the 3' carbon of the dAMP, preventing the formation of the 5′ to 3′ phosphodiester linkage essential for DNA chain elongation.[16] Once incorporated into a growing DNA strand, tenofovir causes premature termination of DNA transcription, preventing viral replication.[16]
Pharmacokinetics
Tenofovir disoproxil is a
In fasting persons, bioavailability is 25%, and highest blood plasma concentrations are reached after one hour.[16] When taken with fatty food, highest plasma concentrations are reached after two hours, and the area under the curve is increased by 40%.[16] It is an inhibitor of cytochrome P450 1A2.[17]
Tenofovir is mainly excreted via the kidneys, both by
Detection in body fluids
Tenofovir may be measured in plasma by liquid chromatography. Such testing is useful for monitoring therapy and to prevent drug accumulation and toxicity in people with kidney or liver problems.[18][19][20]
Chemistry
Tenofovir is a derivative of adenine and this was the chemical starting point for its first published synthesis[21] which was included in patents to the compound.[22] During drug development, attention switched to the phosphonate ester derivative, tenofovir disoproxil, which was the subject of extensive process chemistry to provide a viable manufacturing route.
Adenine is first reacted with a
History
Tenofovir was initially synthesized by
In 1985, De Clercq and Holý described the activity of PMPA against HIV in cell culture.[26] Shortly thereafter, a collaboration with the biotechnology company Gilead Sciences led to the investigation of PMPA's potential as a treatment for HIV infected patients. In 1997 researchers from Gilead and the University of California, San Francisco demonstrated that tenofovir exhibits anti-HIV effects in humans when dosed by subcutaneous injection.[27]
The initial form of tenofovir used in these studies had limited potential for widespread use because it poorly penetrated cells and was not absorbed when given by mouth. Gilead developed a pro-drug version of tenofovir, tenofovir disoproxil. This version of tenofovir is often referred to simply as "tenofovir". In this version of the drug, the two negative charges of the tenofovir phosphonic acid group are masked, thus enhancing oral absorption.
Tenofovir disoproxil was approved in the U.S. in 2001, for the treatment of HIV, and in 2008, for the treatment of
Drug forms
Tenofovir disoproxil can be taken
Tenofovir disoproxil is also available in pills which combine a number of antiviral drugs into a single dose. Well-known combinations include
Gilead has created a second pro-drug form of the active drug, tenofovir diphosphate, called
References
- ^ FDA. Retrieved 22 Oct 2023.
- ^ "Prescription medicines: registration of new generic medicines and biosimilar medicines, 2017". Therapeutic Goods Administration (TGA). 21 June 2022. Retrieved 30 March 2024.
- ^ a b c d e f g h i j k "Tenofovir Disoproxil Fumarate". The American Society of Health-System Pharmacists. Archived from the original on 30 November 2016. Retrieved 29 November 2016.
- ^ "Stribild". PubChem. U.S. National Library of Medicine. Retrieved 6 February 2022.
- PMID 26188135.
- ISBN 9783527607495. Archivedfrom the original on 2017-09-08.
- hdl:10665/325771. WHO/MVP/EMP/IAU/2019.06. License: CC BY-NC-SA 3.0 IGO.
- ^ "Teva Announces Exclusive Launch of a Generic version of Viread in the United States". www.tevapharm.com. Archived from the original on 2018-11-06. Retrieved 2018-11-06.
- ^ a b c d e "Tenofovirdisoproxil Prescribing Information" (PDF). Gilead Sciences, Inc. November 2012. Archived from the original (PDF) on 7 February 2013.
- PMID 22786505.
- ^ Bourke E (14 June 2013). "Preventive drug could reduce HIV transmission among injecting drug users". The Conversation Australia. The Conversation Media Group. Archived from the original on 1 November 2013. Retrieved 17 June 2013.
- ^ PMID 26032649.
- ^ "Tenofovir: MedlinePlus Drug Information". MedlineP. U.S. National Library of Medicine. Archived from the original on 2016-11-10. Retrieved 2016-11-09.
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- ^ a b c Haberfeld, H, ed. (2015). Austria-Codex (in German). Vienna: Österreichischer Apothekerverlag.
- ^ a b c d e f g "Tenofovir". DrugBank. Archived from the original on 8 September 2015.
- ^ "Tenofovir disoproxil". Pubchem. U.S. National Library of Medicine. Retrieved 2018-04-17.
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- ^ Baselt R (2008). Disposition of Toxic Drugs and Chemicals in Man (8th ed.). Foster City, California: Biomedical Publications. pp. 1490–1492.
- .
- ^ a b US patent 4808716, Holy A, Rosenberg I, "9-(phosponylmethoxyalkyl) adenines, the method of preparation and utilization thereof", published 1989-02-28, assigned to Czech Academy of Sciences
- ^ .
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- ^ US 4724233, De Clercq E, Holy A, Rosenberg I, "Therapeutical application of phosphonylmethoxyalkyl adenines"
- PMID 9736567.
- ^ Shwiff K. "FDA letter of approval (regarding treatment of hepatitis B)" (PDF). Food and Drug Administration. Archived from the original (PDF) on 25 February 2009.
- ^ Shwiff, Kathy (11 August 2008). "FDA Clears Viread for Hepatitis B". The Wall Street Journal. Dow Jones & Company, Inc. Archived from the original on 8 September 2017.
- ^ a b "Drugs@FDA: FDA Approved Drug Products". www.accessdata.fda.gov. Archived from the original on 2016-11-10. Retrieved 2016-11-09.
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