Division of Pharmaceutical Analysis, Office of Testing and Research, Center for Drug Evaluation and Research, Food and Drug Administration, St. Louis, MO 63110, USA.
Office of Research and Standards, Office of Generic Drugs, Center for Drug Evaluation and Research, Food and Drug Administration, Silver Spring, MD 20993, USA.
Int J Pharm. 2019 Apr 20;561:305-313. doi: 10.1016/j.ijpharm.2019.03.017. Epub 2019 Mar 9.
The introduction of prescription opioids with abuse-deterrent (AD) properties to the marketplace has created a need for new testing methodologies to evaluate the performance of potentially abuse-deterrent opioid products. Drug abusers may attempt to chew solid oral extended-release (ER) opioids prior to ingestion to bypass the ER mechanism of the formulation to achieve euphoria. In the present study, a chewing apparatus was utilized to develop an in vitro chewing method for Hysingla ER tablets, a prescription opioid with labeling describing abuse deterrence via the oral route when chewed. Simulated chewing of Hysingla resulted in initially faster drug release during chewing while subsequent dissolution testing demonstrated that the masticated tablets still maintained ER properties. The degree of mastication and corresponding drug release were influenced by the compression gap and the resulting chewing forces. Simulated chewing followed by dissolution testing with different strengths of Hysingla indicated similar AD performance across strengths. By contrast, an opioid product with labeling that does not describe abuse-deterrent properties showed lower resistance to chewing resulting in higher drug release. The results of the present study suggest that the chewing methodology evaluated in this work may provide a useful in vitro tool for the comparative evaluation of AD properties.
将具有滥用防御(AD)特性的处方类阿片药物引入市场,这就需要新的测试方法来评估潜在具有滥用防御能力的阿片类产品的性能。药物滥用者可能会试图在服用之前咀嚼固体口服延长释放(ER)类阿片药物,以绕过制剂的 ER 机制来获得快感。在本研究中,利用一种咀嚼装置开发了一种体外咀嚼方法,用于 Hysingla ER 片剂,这是一种具有标签描述的处方类阿片药物,通过口腔途径咀嚼时具有滥用防御作用。模拟咀嚼 Hysingla 导致在咀嚼过程中最初更快地释放药物,而随后的溶解测试表明,咀嚼后的片剂仍保持 ER 特性。咀嚼的程度和相应的药物释放受到压缩间隙和产生的咀嚼力的影响。用不同强度的 Hysingla 进行模拟咀嚼后进行溶解测试表明,不同强度的药物具有相似的 AD 性能。相比之下,具有标签描述不具有滥用防御特性的阿片类药物对咀嚼的抵抗力较低,导致药物释放更高。本研究结果表明,本研究中评估的咀嚼方法可能为比较评估 AD 特性提供有用的体外工具。