Department of Pharmaceutical Science, School of Pharmacy, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang 110016, China.
Department of Biochemistry and Molecular Biology, School of Life Sciences and Biopharmaceutics, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang 110016, China.
J Control Release. 2016 Apr 10;227:13-22. doi: 10.1016/j.jconrel.2016.02.027. Epub 2016 Feb 16.
In patches, a drug must release from patches prior to its percutaneous absorption. Chemical enhancers have been used for several decades, but their roles in drug release from patches are poorly understood. In this work, the roles of chemical enhancers in bisoprolol tartrate (BSP-T) release from patches were probed in vitro and in vivo. More importantly, an innovative mechanism insight of chemical enhancers in drug release process was provided at molecular level. FT-IR spectroscopy and molecular modeling were employed to investigate the influence of chemical enhancers on drug-adhesive interaction. The results showed chemical enhancers like Span 80, which had a strong ability forming hydrogen bonds, could decrease drug-adhesive interaction leading to the release of drug from adhesive of patches. Thermal analysis was conducted to research the influence of chemical enhancers on the thermodynamic properties of patch system. It showed that chemical enhancers promoted the formation of free volume of adhesive, which facilitated drug release process. By contrast, the influence on the thermodynamic properties of BSP-T was less effective in influencing BSP-T release process. In conclusion, chemical enhancers played an important role in facilitating BSP-T release from the adhesive DURO-TAK® 87-2287 of patches by decreasing drug-adhesive interaction and promoting the formation of free volume of adhesive. This work may be an important step in understanding the important roles of chemical enhancers in drug release process.
在贴剂中,药物必须在经皮吸收之前从贴剂中释放出来。化学增塑剂已经使用了几十年,但它们在贴剂中药物释放中的作用仍未被充分理解。在这项工作中,体外和体内研究了化学增塑剂在酒石酸美托洛尔(BSP-T)从贴剂中释放的作用。更重要的是,在分子水平上提供了化学增塑剂在药物释放过程中的作用的创新机制见解。傅里叶变换红外光谱和分子建模被用来研究化学增塑剂对药物-粘合剂相互作用的影响。结果表明,具有强形成氢键能力的化学增塑剂,如司盘 80,可以降低药物-粘合剂相互作用,从而导致药物从贴剂的粘合剂中释放出来。热分析用于研究化学增塑剂对贴剂系统热力学性质的影响。结果表明,化学增塑剂促进了粘合剂自由体积的形成,从而促进了药物释放过程。相比之下,化学增塑剂对 BSP-T 热力学性质的影响对 BSP-T 释放过程的影响较小。总之,化学增塑剂通过降低药物-粘合剂相互作用和促进粘合剂自由体积的形成,在促进酒石酸美托洛尔从贴剂 DURO-TAK®87-2287 中的释放方面发挥了重要作用。这项工作可能是理解化学增塑剂在药物释放过程中的重要作用的重要一步。