Jump to content

Abacavir

From Wikipedia, the free encyclopedia
(Redirected from Ziagen)

Abacavir
Chemical structure of abacavir
Clinical data
Pronunciation/əˈbækəvɪər/ ⓘ
Trade namesZiagen
Other namesAbacavir sulfate (USAN US)
AHFS/Drugs.comMonograph
MedlinePlusa699012
License data
Pregnancy
category
  • AU: B3
Routes of
administration		By mouth
ATC code
Legal status
Legal status
Pharmacokinetic data
Bioavailability83%
MetabolismLiver
Elimination half-life1.54 ± 0.63 h
ExcretionKidney (1.2% abacavir, 30% 5'-carboxylic acid metabolite, 36% 5'-glucuronide metabolite, 15% unidentified minor metabolites). Fecal (16%)
Identifiers
  • {(1S,4R)-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]cyclopent-2-en-1-yl}methanol
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
NIAID ChemDB
CompTox Dashboard (EPA)
ECHA InfoCard100.149.341 Edit this at Wikidata
Chemical and physical data
FormulaC14H18N6O
Molar mass286.339 g·mol−1
3D model (JSmol)
Melting point165 °C (329 °F)
  • n3c1c(ncn1[C@H]2/C=C\[C@@H](CO)C2)c(nc3N)NC4CC4
  • InChI=1S/C14H18N6O/c15-14-18-12(17-9-2-3-9)11-13(19-14)20(7-16-11)10-4-1-8(5-10)6-21/h1,4,7-10,21H,2-3,5-6H2,(H3,15,17,18,19)/t8-,10+/m1/s1 checkY
  • Key:MCGSCOLBFJQGHM-SCZZXKLOSA-N checkY
  (verify)

Abacavir, sold under the brand name Ziagen among others, is a medication used to treat HIV/AIDS.[3][4][5][6] Similar to other nucleoside analog reverse-transcriptase inhibitors (NRTIs), abacavir is used together with other HIV medications, and is not recommended by itself.[7] It is taken by mouth as a tablet or solution and may be used in children over the age of three months.[5][8]

Abacavir is generally well tolerated.[8] Common side effects include vomiting, insomnia (trouble sleeping), fever, and feeling tired.[5] Other common side effects include loss of appetite, headache, nausea (feeling sick), diarrhea, rash, and lethargy (lack of energy).[4] More severe side effects include hypersensitivity, liver damage, and lactic acidosis.[5] Genetic testing can indicate whether a person is at higher risk of developing hypersensitivity.[5] Symptoms of hypersensitivity include rash, vomiting, and shortness of breath.[8] Abacavir is in the NRTI class of medications, which work by blocking reverse transcriptase, an enzyme needed for HIV virus replication.[9] Within the NRTI class, abacavir is a carbocyclic nucleoside.[5]

Abacavir was patented in 1988, and approved for use in the United States in 1998.[10][11] It is on the World Health Organization's List of Essential Medicines.[12] It is available as a generic medication.[5] Abacavir is used together with other HIV medications, such as abacavir/lamivudine/zidovudine, abacavir/dolutegravir/lamivudine, and abacavir/lamivudine.[8][9] The combination abacavir/lamivudine is an essential medicine.[12]

Medical uses

[edit]

Abacavir, in combination with other antiretroviral agents, is indicated for the treatment of HIV-1 infection.[3][4] Abacavir should be used in combination with other antiretroviral agents.[3][4]

Contraindications

[edit]

Abacavir is contraindicated for people who have the HLA‑B*5701 allele or who have moderate or severe liver disease (hepatic impairment).[3][4]

Side effects

[edit]

Common adverse reactions include nausea, headache, fatigue, vomiting, diarrhea, Anorexia (symptom) (loss of appetite), and insomnia (trouble sleeping). Rare but serious side effects include hypersensitivity reaction such as rash, elevated AST and ALT, depression, anxiety, fever/chills, URI, lactic acidosis, hypertriglyceridemia, and lipodystrophy.[13]

Hypersensitivity syndrome

[edit]

Hypersensitivity to abacavir is strongly associated with a specific allele at the human leukocyte antigen B locus namely HLA-B*5701.[14][15][16] The mechanism for this hypersensitivity reaction is due to abacavir binding in the antigen-binding cleft of HLA-B*57:01, allowing alternative peptides to bind, which appear as "non-self" when presented to T cells.[17] There is an association between the prevalence of HLA-B*5701 and ancestry. The prevalence of the allele is estimated to be 3.4 to 5.8 percent on average in populations of European ancestry, 17.6 percent in Indian Americans, 3.0 percent in Hispanic Americans, and 1.2 percent in Chinese Americans.[18][19] There is significant variability in the prevalence of HLA-B*5701 among African populations. In African Americans, the prevalence is estimated to be 1.0 percent on average, 0 percent in the Yoruba from Nigeria, 3.3 percent in the Luhya from Kenya, and 13.6 percent in the Masai from Kenya, although the average values are derived from highly variable frequencies within sample groups.[20]

Common symptoms of abacavir hypersensitivity syndrome include fever, malaise, nausea, and diarrhea. Some patients may also develop a skin rash.[21] Symptoms of AHS typically manifest within six weeks of treatment using abacavir, although they may be confused with symptoms of HIV, immune reconstitution syndrome, hypersensitivity syndromes associated with other drugs, or infection.[22] The U.S. Food and Drug Administration (FDA) released an alert concerning abacavir and abacavir-containing medications on 24 July 2008,[23] and the FDA-approved drug label for abacavir recommends pre-therapy screening for the HLA-B*5701 allele and the use of alternative therapy in subjects with this allele.[3] Additionally, both the Clinical Pharmacogenetics Implementation Consortium and the Dutch Pharmacogenetics Working Group recommend use of an alternative therapy in individuals with the HLA-B*5701 allele.[24][25]

Patch test

Skin-patch testing may also be used to determine whether an individual will experience a hypersensitivity reaction to abacavir, although some patients susceptible to developing AHS may not react to the patch test.[26]

The development of suspected hypersensitivity reactions to abacavir requires immediate and permanent discontinuation of abacavir therapy in all patients, including patients who do not possess the HLA-B*5701 allele. On 1 March 2011, the FDA informed the public about an ongoing safety review of abacavir and a possible increased risk of heart attack associated with the drug.[27] A meta-analysis of 26 studies conducted by the FDA, however, did not find any association between abacavir use and heart attack[28][29]

Immunopathogenesis

[edit]

The mechanism underlying abacavir hypersensitivity syndrome is related to the change in the HLA-B*5701 protein product. Abacavir binds with high specificity to the HLA-B*5701 protein, changing the shape and chemistry of the antigen-binding cleft. This results in a change in immunological tolerance and the subsequent activation of abacavir-specific cytotoxic T cells, which produce a systemic reaction known as abacavir hypersensitivity syndrome.[17]

Interaction

[edit]

Abacavir, and in general NRTIs, do not undergo hepatic metabolism and therefore have very limited (to none) interaction with the CYP enzymes and drugs that effect these enzymes. That being said there are still few interactions that can affect the absorption or the availability of abacavir. Below are few of the common established drug and food interaction that can take place during abacavir co-administration:

  • Protease inhibitors such as tipranavir or ritonovir may decrease the serum concentration of abacavir through induction of glucuronidation. Abacavir is metabolized by both alcohol dehydrogenase and glucuronidation.[30][31]
  • Ethanol may result in increased levels of abacavir through the inhibition of alcohol dehydrogenase. Abacavir is metabolized by both alcohol dehydrogenase and glucuronidation.[30][32]
  • Methadone may diminish the therapeutic effect of Abacavir. Abacavir may decrease the serum concentration of Methadone.[33][34]
  • Orlistat may decrease the serum concentration of antiretroviral drugs. The mechanism of this interaction is not fully established but it is suspected that it is due to the decreased absorption of abacavir by orlistat.[35]
  • Cabozantinib: Drugs from the MRP2 inhibitor (Multidrug resistance-associated protein 2 inhibitors) family such as abacavir could increase the serum concentration of Cabozantinib.[36]

Mechanism of action

[edit]

Abacavir is a nucleoside reverse transcriptase inhibitor that inhibits viral replication. It is a guanosine analogue that is phosphorylated to carbovir triphosphate (CBV-TP). CBV-TP competes with the viral molecules and is incorporated into the viral DNA. Once CBV-TP is integrated into the viral DNA, transcription and HIV reverse transcriptase is inhibited.[37]

Pharmacokinetics

[edit]

Abacavir is given orally and is rapidly absorbed with a high bioavailability of 83%.[38] Solution and tablet have comparable concentrations and bioavailability. Abacavir can be taken with or without food.[39]

Abacavir can cross the blood–brain barrier. Abacavir is metabolized primarily through the enzymes alcohol dehydrogenase and glucuronyl transferase to an inactive carboxylate and glucuronide metabolites. It has a half-life of approximately 1.5-2.0 hours. If a person has liver failure, abacavir's half life is increased by 58%.[40]

Abacavir is eliminated via excretion in the urine (83%) and feces (16%).[41] It is unclear whether abacavir can be removed by hemodialysis or peritoneal dialysis.[37]

History

[edit]

Robert Vince and Susan Daluge along with Mei Hua, a visiting scientist from China, developed the medication in the '80s.[42][43][44]

Abacavir was approved by the US Food and Drug Administration (FDA) in December 1998, and is the fifteenth approved antiretroviral drug in the United States.[45]

Synthesis

[edit]
Abacavir synthesis:[46]

References

[edit]
  1. ^ "FDA-sourced list of all drugs with black box warnings (Use Download Full Results and View Query links.)". nctr-crs.fda.gov. FDA. Retrieved 22 October 2023.
  2. ^ "TGA eBS - Product and Consumer Medicine Information Licence". Archived from the original on 24 March 2022. Retrieved 23 August 2022.
  3. ^ a b c d e f "Ziagen- abacavir sulfate tablet, film coated label". DailyMed. 30 September 2015. Archived from the original on 11 January 2017. Retrieved 9 September 2019.
  4. ^ a b c d e f "Ziagen EPAR". European Medicines Agency. 17 September 2018. Archived from the original on 30 July 2022. Retrieved 22 August 2022. Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
  5. ^ a b c d e f g "Abacavir Sulfate". The American Society of Health-System Pharmacists. Archived from the original on 21 August 2017. Retrieved 31 July 2015.
  6. ^ "Drug Name Abbreviations Adult and Adolescent ARV Guidelines". AIDSinfo. Archived from the original on 9 November 2016. Retrieved 8 November 2016.
  7. ^ "What Not to Use Adult and Adolescent ARV Guidelines". AIDSinfo. Archived from the original on 9 November 2016. Retrieved 8 November 2016.
  8. ^ a b c d Yuen GJ, Weller S, Pakes GE (2008). "A review of the pharmacokinetics of abacavir". Clinical Pharmacokinetics. 47 (6): 351–371. doi:10.2165/00003088-200847060-00001. PMID 18479171. S2CID 31107341.
  9. ^ a b "Nucleoside reverse transcriptase inhibitors (NRTIs or 'nukes') - HIV/AIDS". www.hiv.va.gov. Archived from the original on 9 November 2016. Retrieved 8 November 2016.
  10. ^ Fischer J, Ganellin CR (2006). Analogue-based Drug Discovery. John Wiley & Sons. p. 505. ISBN 9783527607495. Archived from the original on 8 September 2017.
  11. ^ Kane BM (2008). HIV/AIDS Treatment Drugs. Infobase Publishing. p. 56. ISBN 9781438102078. Archived from the original on 8 September 2017.
  12. ^ a b World Health Organization (2023). The selection and use of essential medicines 2023: web annex A: World Health Organization model list of essential medicines: 23rd list (2023). Geneva: World Health Organization. hdl:10665/371090. WHO/MHP/HPS/EML/2023.02.
  13. ^ "Abacavir Adverse Reactions". Epocrates Online. Archived from the original on 23 August 2021. Retrieved 9 November 2012.
  14. ^ Mallal S, Phillips E, Carosi G, Molina JM, Workman C, Tomazic J, et al. (February 2008). "HLA-B*5701 screening for hypersensitivity to abacavir". The New England Journal of Medicine. 358 (6): 568–579. doi:10.1056/nejmoa0706135. PMID 18256392. Archived from the original on 22 January 2021. Retrieved 9 July 2019.
  15. ^ Rauch A, Nolan D, Martin A, McKinnon E, Almeida C, Mallal S (July 2006). "Prospective genetic screening decreases the incidence of abacavir hypersensitivity reactions in the Western Australian HIV cohort study". Clinical Infectious Diseases. 43 (1): 99–102. doi:10.1086/504874. PMID 16758424.
  16. ^ Dean L (2015). "Abacavir Therapy and HLA-B*57:01 Genotype". In Pratt VM, McLeod HL, Rubinstein WS, et al. (eds.). Medical Genetics Summaries. National Center for Biotechnology Information (NCBI). PMID 28520363. Bookshelf ID: NBK315783. Archived from the original on 26 October 2020. Retrieved 14 January 2019.
  17. ^ a b Illing PT, Vivian JP, Dudek NL, Kostenko L, Chen Z, Bharadwaj M, et al. (June 2012). "Immune self-reactivity triggered by drug-modified HLA-peptide repertoire". Nature. 486 (7404): 554–558. Bibcode:2012Natur.486..554I. doi:10.1038/nature11147. PMID 22722860. S2CID 4408811.
  18. ^ Hetherington S, Hughes AR, Mosteller M, Shortino D, Baker KL, Spreen W, et al. (March 2002). "Genetic variations in HLA-B region and hypersensitivity reactions to abacavir". Lancet. 359 (9312): 1121–1122. doi:10.1016/s0140-6736(02)08158-8. PMID 11943262. S2CID 9434238.
  19. ^ Mallal S, Nolan D, Witt C, Masel G, Martin AM, Moore C, et al. (March 2002). "Association between presence of HLA-B*5701, HLA-DR7, and HLA-DQ3 and hypersensitivity to HIV-1 reverse-transcriptase inhibitor abacavir". Lancet. 359 (9308): 727–732. doi:10.1016/s0140-6736(02)07873-x. PMID 11888582. S2CID 12923232.
  20. ^ Rotimi CN, Jorde LB (October 2010). "Ancestry and disease in the age of genomic medicine". The New England Journal of Medicine. 363 (16): 1551–1558. doi:10.1056/nejmra0911564. PMID 20942671.
  21. ^ Phillips E, Mallal S (2009). "Successful translation of pharmacogenetics into the clinic: the abacavir example". Molecular Diagnosis & Therapy. 13 (1): 1–9. doi:10.1007/bf03256308. PMID 19351209. S2CID 45896364.
  22. ^ Phillips E, Mallal S (August 2007). "Drug hypersensitivity in HIV". Current Opinion in Allergy and Clinical Immunology. 7 (4): 324–330. doi:10.1097/aci.0b013e32825ea68a. PMID 17620824. S2CID 37549824.
  23. ^ "Information for Healthcare Professionals: Abacavir (marketed as Ziagen) and Abacavir-Containing Medications". Food and Drug Administration (FDA). 24 July 2008. Archived from the original on 11 December 2013. Retrieved 29 November 2013.
  24. ^ Swen JJ, Nijenhuis M, de Boer A, Grandia L, Maitland-van der Zee AH, Mulder H, et al. (May 2011). "Pharmacogenetics: from bench to byte--an update of guidelines". Clinical Pharmacology and Therapeutics. 89 (5): 662–673. doi:10.1038/clpt.2011.34. PMID 21412232. S2CID 2475005.
  25. ^ Martin MA, Hoffman JM, Freimuth RR, Klein TE, Dong BJ, Pirmohamed M, et al. (May 2014). "Clinical Pharmacogenetics Implementation Consortium Guidelines for HLA-B Genotype and Abacavir Dosing: 2014 update". Clinical Pharmacology and Therapeutics. 95 (5): 499–500. doi:10.1038/clpt.2014.38. PMC 3994233. PMID 24561393.
  26. ^ Shear NH, Milpied B, Bruynzeel DP, Phillips EJ (May 2008). "A review of drug patch testing and implications for HIV clinicians". AIDS. 22 (9): 999–1007. doi:10.1097/qad.0b013e3282f7cb60. PMID 18520343. S2CID 2972984.
  27. ^ "FDA Drug Safety Communication: Safety Review update of Abacavir and possible increased risk of heart attack". Food and Drug Administration (FDA). 1 March 2011. Archived from the original on 13 December 2019. Retrieved 9 September 2019.
  28. ^ "FDA Alert: Abacavir - Ongoing Safety Review: Possible Increased Risk of Heart Attack". Drugs.com. Archived from the original on 10 December 2013. Retrieved 29 November 2013.
  29. ^ Ding X, Andraca-Carrera E, Cooper C, Miele P, Kornegay C, Soukup M, Marcus KA (December 2012). "No association of abacavir use with myocardial infarction: findings of an FDA meta-analysis". Journal of Acquired Immune Deficiency Syndromes. 61 (4): 441–447. doi:10.1097/QAI.0b013e31826f993c. PMID 22932321. S2CID 7997822.
  30. ^ a b Prescribing information. Ziagen (abacavir). Research Triangle Park, NC: GlaxoSmithKline, July 2002
  31. ^ Vourvahis M, Kashuba AD (June 2007). "Mechanisms of pharmacokinetic and pharmacodynamic drug interactions associated with ritonavir-enhanced tipranavir". Pharmacotherapy. 27 (6): 888–909. doi:10.1592/phco.27.6.888. PMID 17542771. S2CID 23591048.
  32. ^ McDowell JA, Chittick GE, Stevens CP, Edwards KD, Stein DS (June 2000). "Pharmacokinetic interaction of abacavir (1592U89) and ethanol in human immunodeficiency virus-infected adults". Antimicrobial Agents and Chemotherapy. 44 (6): 1686–1690. doi:10.1128/aac.44.6.1686-1690.2000. PMC 89933. PMID 10817729.
  33. ^ Berenguer J, Pérez-Elías MJ, Bellón JM, Knobel H, Rivas-González P, Gatell JM, et al. (February 2006). "Effectiveness and safety of abacavir, lamivudine, and zidovudine in antiretroviral therapy-naive HIV-infected patients: results from a large multicenter observational cohort". Journal of Acquired Immune Deficiency Syndromes. 41 (2): 154–159. doi:10.1097/01.qai.0000194231.08207.8a. PMID 16394846. S2CID 17609676.
  34. ^ Dolophine(methadone) [prescribing information]. Columbus, OH: Roxane Laboratories, Inc.; March 2015.
  35. ^ Gervasoni C, Cattaneo D, Di Cristo V, Castoldi S, Gervasi E, Clementi E, Riva A (June 2016). "Orlistat: weight lost at cost of HIV rebound". The Journal of Antimicrobial Chemotherapy. 71 (6): 1739–1741. doi:10.1093/jac/dkw033. PMID 26945709.
  36. ^ Cometriq (cabozantinib) [prescribing information]. South San Francisco, CA: Exelixis, Inc.; May 2016.
  37. ^ a b Product Information: ZIAGEN(R) oral tablets, oral solution, abacavir sulfate oral tablets, oral solution. ViiV Healthcare (per Manufacturer), Research Triangle Park, NC, 2015.
  38. ^ Chittick GE, Gillotin C, McDowell JA, Lou Y, Edwards KD, Prince WT, Stein DS (August 1999). "Abacavir: absolute bioavailability, bioequivalence of three oral formulations, and effect of food". Pharmacotherapy. 19 (8): 932–942. doi:10.1592/phco.19.11.932.31568. PMID 10453964. S2CID 20131476.
  39. ^ Jones A (May 2019). "Food requirements for anti-HIV medications". aidsmap.com. Archived from the original on 25 April 2021. Retrieved 21 December 2020.
  40. ^ Wyles DL, Gerber JG (March 2005). "Abacavir pharmacokinetics in hepatic dysfunction". Clinical Infectious Diseases. 40 (6): 909–910. doi:10.1086/429247. PMID 15736035.
  41. ^ Yuen GJ, Weller S, Pakes GE (2008). "A review of the pharmacokinetics of abacavir". Clinical Pharmacokinetics. 47 (6): 351–71. doi:10.2165/00003088-200847060-00001. PMID 18479171. S2CID 31107341.
  42. ^ "Dr. Robert Vince - 2010 Inductee". Minnesota Inventors Hall of Fame. Archived from the original on 15 February 2016. Retrieved 10 February 2016.
  43. ^ "Robert Vince, PhD (faculty listing)". University of Minnesota. Archived from the original on 17 February 2016.
  44. ^ Daluge SM, Good SS, Faletto MB, Miller WH, St Clair MH, Boone LR, et al. (May 1997). "1592U89, a novel carbocyclic nucleoside analog with potent, selective anti-human immunodeficiency virus activity". Antimicrobial Agents and Chemotherapy. 41 (5): 1082–1093. doi:10.1128/AAC.41.5.1082. PMC 163855. PMID 9145874.
  45. ^ Mary Annette Banach. "How HIV Clinicians Acquire Representational Fluency: A Case Study of the HIV Resistance Preceptorship Archived 23 August 2022 at the Wayback Machine", University of California, Berkeley, 2003.
  46. ^ Crimmins MT, King BW (June 1996). "An Efficient Asymmetric Approach to Carbocyclic Nucleosides: Asymmetric Synthesis of 1592U89, a Potent Inhibitor of HIV Reverse Transcriptase". The Journal of Organic Chemistry. 61 (13): 4192–4193. doi:10.1021/jo960708p. PMID 11667311.

Further reading

[edit]
[edit]
Wikimedia Commons has media related to Abacavir.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Abacavir&oldid=1260354107"