Division on Substance Abuse, New York State Psychiatric Institute, 1051 Riverside Drive, New York, NY 10032, USA.
Addiction. 2013 Jun;108(6):1095-106. doi: 10.1111/add.12114. Epub 2013 Mar 13.
To examine whether tamper-resistant formulations (TRFs) of tapentadol hydrochloride extended-release (ER) 50 mg (TAP50) and tapentadol hydrochloride 250 mg (TAP250) could be converted into forms amenable to intranasal (study 1) or intravenous abuse (study 2).
Randomized, repeated-measures study designs were employed. A non-TRF of OxyContin® 40 mg (OXY40) served as a positive control. No drug was taken in either study.
The studies took place in an out-patient setting in New York, NY.
Twenty-five experienced, healthy ER oxycodone abusers participated in each study.
The primary outcome for study 1 was the percentage of participants who indicated that they would snort the tampered tablets, while the primary outcome for study 2 was the percentage yield of active drug in solution. Other descriptive variables, such as time spent manipulating the tablets, were also examined to characterize tampering behaviors more clearly.
Tampered TRF tablets were less desirable than the tampered OXY40 tablets. Few individuals were willing to snort the TRF particles (TAP50: 24%, TAP250: 16%; OXY40: 100% P < 0.001). There was less drug extracted from the TAP50 tablet than from the OXY40 tablet (3.52 versus 37.02%, P = 0.008), and no samples from the TAP250 tablets contained analyzable solutions of the drug. It took participants longer to tamper with the TAPs (study 1: TAP50 versus OXY40, P < 0.01; TAP250 versus OXY40, P < 0.01; study 2: TAP250 versus OXY40, P < 0.05).
Tamper-resistant formulations of taptentadol (pain relief) tablets do not appear to be well-liked by individuals who tamper regularly with extended-release oxycodone tablets. Employing tamper-resistant technology may be a promising approach towards reducing the abuse potential of tapentadol extended-release.
研究盐酸曲马多控释(ER)50mg(TAP50)和盐酸曲马多 250mg(TAP250)的耐篡改制剂(TRF)是否可以转化为适合鼻内(研究 1)或静脉内滥用(研究 2)的形式。
采用随机、重复测量研究设计。非 TRF 的 OxyContin®40mg(OXY40)作为阳性对照。在两项研究中均未服用任何药物。
研究在纽约州纽约市的一家门诊进行。
每项研究均有 25 名经验丰富的健康 ER 羟考酮滥用者参加。
研究 1 的主要结果是表示愿意鼻吸篡改片剂的参与者百分比,而研究 2 的主要结果是溶液中活性药物的产率百分比。还检查了其他描述性变量,例如花在处理片剂上的时间,以更清楚地描述篡改行为。
耐篡改的 TRF 片剂不如耐篡改的 OXY40 片剂受欢迎。很少有人愿意鼻吸 TRF 颗粒(TAP50:24%,TAP250:16%;OXY40:100%P<0.001)。从 TAP50 片剂中提取的药物比从 OXY40 片剂中提取的药物少(3.52 与 37.02%,P=0.008),并且没有来自 TAP250 片剂的样品含有可分析的药物溶液。参与者需要更长的时间来篡改 TAPs(研究 1:TAP50 与 OXY40,P<0.01;TAP250 与 OXY40,P<0.01;研究 2:TAP250 与 OXY40,P<0.05)。
经常篡改延长释放羟考酮片剂的个体似乎不太喜欢曲马多(止痛)片剂的耐篡改制剂。采用耐篡改技术可能是减少曲马多延长释放滥用潜力的一种有前途的方法。