Liu Qian, Zan Mengqing, Huang Hanhan, Su Hai, Zhang Wenjing, Ma Lingyun, Zhang Guangchao, Zhang Zunjian, Zhang Jiwen, Niu Jianzhao, Xu Mingdi
NMPA Key Laboratory for Quality Research and Evaluation of Chemical Drugs, National Institutes for Food and Drug Control, Beijing 100050, China.
China Pharmaceutical University, Nanjing 210009, China.
Asian J Pharm Sci. 2024 Dec;19(6):100966. doi: 10.1016/j.ajps.2024.100966. Epub 2024 Sep 21.
The structures of solid dosage forms determine their release behaviors and are critical attributes for the design and evaluation of the solid dosage forms. Here, the 3D structures of doxazosin mesylate sustained-release tablets were parallelly assessed by micro-computed tomography (micro-CT). There were no significant differences observed in the release profiles between the RLD and the generic formulation in the conventional dissolution, but the generic preparation released slightly faster in media with ethanol during an alcohol-induced dose-dumping test. With their 3D structures obtained via micro-CT determination, the unique release behaviors of both RLD and the generic were investigated to reveal the effects of internal fine structure on the release kinetics. The structural parameters for both preparations were similar in conventional dissolution test, while the dissolutions in ethanol media showed some distinctions between RLD and generic preparations due to their static and dynamic structures. Furthermore, the findings revealed that the presence of ethanol accelerated dissolution and induced changes in internal structure of both RLD and generic preparations. Moreover, structure parameters like volume and area of outer contour, remaining solid volume and cavity volume were not equivalent between the two formulations in 40 % ethanol. In conclusion, the structure data obtained from this study provided valuable insights into the diverse release behaviors observed in various modified-release formulations in drug development and quality control.
固体剂型的结构决定其释放行为,是固体剂型设计和评价的关键属性。在此,采用微计算机断层扫描(micro-CT)对甲磺酸多沙唑嗪缓释片的三维结构进行了平行评估。在常规溶出度试验中,参比制剂(RLD)与仿制制剂的释放曲线未观察到显著差异,但在酒精诱导的剂量倾泻试验中,仿制制剂在含乙醇介质中的释放稍快。通过micro-CT测定获得两者的三维结构后,对RLD和仿制制剂的独特释放行为进行了研究,以揭示内部精细结构对释放动力学的影响。在常规溶出度试验中,两种制剂的结构参数相似,但在乙醇介质中的溶出度因静态和动态结构而在RLD和仿制制剂之间表现出一些差异。此外,研究结果表明,乙醇的存在加速了溶出,并引起RLD和仿制制剂内部结构的变化。而且,在40%乙醇中,两种制剂的结构参数如外轮廓体积和面积、剩余固体体积和腔体积并不相同。总之,本研究获得的结构数据为药物开发和质量控制中各种缓释制剂中观察到的不同释放行为提供了有价值的见解。