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Effects of buprenorphine versus buprenorphine/naloxone tablets in non- dependent opioid abusers

Producción científica: Articlerevisión exhaustiva

88 Citas (Scopus)

Resumen

Rationale: Buprenorphine is an opioid agonist-antagonist under development in the United States as a sublingual medication for treatment of opioid dependence. Buprenorphine may be abused; therefore, tablets combining buprenorphine with naloxone have been developed with the intent of reducing the abuse risk in people physically dependent upon opioids. The characteristics and abuse potential of buprenorphine and buprenorphine/naloxone tablets in non-dependent opioid abusers have not been determined. Non-parenteral abuse of opioids such as buprenorphine may be more likely in people who have less severe substance abuse disorders (e.g., are not physically dependent upon opioids). Objectives: To assess the abuse potential of sublingual buprenorphine and buprenorphine/naloxone tablets in non-dependent opioid abusers. Methods: Subjects (n=7) were tested with sublingual buprenorphine (4, 8, 16 mg), sublingual buprenorphine/naloxone (1/0.25, 2/0.5, 4/1, 8/2, 16/4 mg), as well as intramuscular hydromorphone as an opioid agonist control (2, 4 mg) and placebo in laboratory sessions conducted twice per week. Dosing was double-blind and double-dummy. Results: The higher doses of both buprenorphine and buprenorphine/naloxone produced similar opioid agonist-like effects. The onset of these effects was slowed, consistent with the sublingual route of administration, and the magnitude of effects was moderate. There was no evidence to suggest the addition of naloxone attenuated buprenorphine's opioid agonist effects in this population when buprenorphine was delivered by the sublingual route. Conclusions: These results suggest that sublingual buprenorphine and buprenorphine/naloxone may both be abused by opioid users who are not physically dependent upon opioids.

Idioma originalEnglish
Páginas (desde-hasta)374-383
Número de páginas10
PublicaciónPsychopharmacology
Volumen148
N.º4
DOI
EstadoPublished - 2000

Nota bibliográfica

Funding Information:
Acknowledgements The authors thank Richard Hernandez, Marcella Rosen, Michael Webb, Banu Ozkazanc, Tim Mudric, Linda Felch, John Yingling, and the residential nursing staff for assistance in data collection and analysis. This study was supported by US Public Health Service Research Scientist Award K05 DA00050 (G. E. B.), Scientist Development Award K02 DA00332 (E. C. S.), and R01 DA08045 from the National Institute on Drug Abuse.

Financiación

Acknowledgements The authors thank Richard Hernandez, Marcella Rosen, Michael Webb, Banu Ozkazanc, Tim Mudric, Linda Felch, John Yingling, and the residential nursing staff for assistance in data collection and analysis. This study was supported by US Public Health Service Research Scientist Award K05 DA00050 (G. E. B.), Scientist Development Award K02 DA00332 (E. C. S.), and R01 DA08045 from the National Institute on Drug Abuse.

FinanciadoresNúmero del financiador
US Public Health ServiceK02 DA00332, R01 DA08045, K05 DA00050
National Institute on Drug AbuseK02DA000332

    ODS de las Naciones Unidas

    Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

    1. Good health and well being
      Good health and well being

    ASJC Scopus subject areas

    • Pharmacology

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