Suppr超能文献

对一种新型羟考酮速释制剂(RoxyBond™)通过注射途径被滥用的可能性进行体外评估。

In vitro evaluation of a novel immediate-release formulation of oxy-codone (RoxyBond™) for the potential for abuse via injection.

作者信息

Kinzler Eric R, Pantaleon Carmela, Iverson Matthew, Aigner Stefan

机构信息

Inspirion Delivery Sciences, LLC, Morristown, New Jersey.

出版信息

J Opioid Manag. 2020;16(5):383-390. doi: 10.5055/jom.2020.0593.

Abstract

OBJECTIVE

Immediate-release (IR) oxycodone formulations may be manipulated for nonoral routes of administration. Oxycodone abuse-resistant immediate-release (ARIR) is a novel abuse-deterrent formulation (ADF) of IR oxycodone. This study aimed to assess the intravenous (IV) abuse potential of oxycodone ARIR relative to commercially available IR oxycodone tablets using in vitro laboratory studies.

DESIGN

Intact or manipulated tablets were incubated in 5 or 10 mL of room temperature water for increasing amounts of time. For each timepoint, syringeability, defined as the ability to draw up water-immersed intact or manipulated tablets into a syringe, was assessed on a scale of 1 (very easy) to 10 (impossible). If the prepared sample could be drawn into a syringe, the proportion of syringeable oxycodone was measured analytically.

RESULTS

In all conditions, it was nearly impossible to draw any liquid into a syringe from samples containing manipulated oxycodone ARIR tablets (N = 5/group), and most samples released very low concentrations (<10 percent) of their total oxycodone content, regardless of sample volume. In contrast, samples containing crushed IR oxycodone (N = 5/group) in small volumes of fluid were easily drawn into a syringe through the smallest needle, and more than 90 percent of the oxycodone content was released from relatively small sample volumes (5 mL).

CONCLUSION

The difficulty required to prepare an injectable solution from oxycodone ARIR when manipulated suggests that oxycodone ARIR has abuse-deterrent properties that may deter IV abuse.

摘要

目的

速释(IR)羟考酮制剂可能会被用于非口服给药途径。抗滥用速释(ARIR)羟考酮是一种新型的IR羟考酮抗滥用剂型(ADF)。本研究旨在通过体外实验室研究评估ARIR羟考酮相对于市售IR羟考酮片剂的静脉注射(IV)滥用潜力。

设计

将完整或经过处理的片剂在5或10 mL室温水中孵育不同时间。对于每个时间点,评估可注射器性,即把水浸过的完整或经过处理的片剂吸入注射器的能力,范围为1(非常容易)至10(不可能)。如果制备的样品能够被吸入注射器,则通过分析测量可注射羟考酮的比例。

结果

在所有条件下,从含有经过处理的ARIR羟考酮片剂的样品中几乎不可能将任何液体吸入注射器(每组N = 5),并且大多数样品释放的总羟考酮含量浓度非常低(<10%),与样品体积无关。相比之下,在少量液体中含有碾碎的IR羟考酮的样品(每组N = 5)很容易通过最小的针头被吸入注射器,并且从相对少量的样品体积(5 mL)中释放出超过90%的羟考酮含量。

结论

处理后的ARIR羟考酮制备可注射溶液所需的难度表明ARIR羟考酮具有可能阻止静脉注射滥用的抗滥用特性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验