利用微计算机断层扫描技术对甲磺酸多沙唑嗪缓释片进行基于结构的释放动力学分析

IF 10.7 1区 医学 Q1 PHARMACOLOGY & PHARMACY Asian Journal of Pharmaceutical Sciences Pub Date : 2024-09-21 DOI:10.1016/j.ajps.2024.100966
Qian Liu , Mengqing Zan , Hanhan Huang , Hai Su , Wenjing Zhang , Lingyun Ma , Guangchao Zhang , Zunjian Zhang , Jiwen Zhang , Jianzhao Niu , Mingdi Xu
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引用次数: 0

摘要

固体制剂的结构决定了其释放行为,是设计和评估固体制剂的关键属性。本文采用显微计算机断层扫描(micro-CT)技术同时评估了甲磺酸多沙唑嗪缓释片的三维结构。在常规溶出试验中,RLD与普通制剂的释放曲线无明显差异,但在酒精诱导剂量倾倒试验中,普通制剂在含有乙醇的介质中释放速度稍快。通过显微 CT 检测获得的三维结构,研究了 RLD 和普通制剂的独特释放行为,揭示了内部精细结构对释放动力学的影响。在常规溶出试验中,两种制剂的结构参数相似,而在乙醇介质中,RLD 和普通制剂的溶出由于其静态和动态结构而存在一些差异。此外,研究结果表明,乙醇的存在加速了 RLD 和普通制剂的溶解,并导致其内部结构发生变化。此外,两种制剂在 40% 乙醇中的结构参数,如外廓体积和面积、剩余固体体积和空腔体积并不相同。总之,本研究获得的结构数据为药物开发和质量控制中观察到的各种改良释放制剂的不同释放行为提供了宝贵的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Structure based release kinetics analysis of doxazosin mesylate sustained-release tablets using micro-computed tomography
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.
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来源期刊
Asian Journal of Pharmaceutical Sciences
Asian Journal of Pharmaceutical Sciences Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
18.30
自引率
2.90%
发文量
11
审稿时长
14 days
期刊介绍: The Asian Journal of Pharmaceutical Sciences (AJPS) serves as the official journal of the Asian Federation for Pharmaceutical Sciences (AFPS). Recognized by the Science Citation Index Expanded (SCIE), AJPS offers a platform for the reporting of advancements, production methodologies, technologies, initiatives, and the practical application of scientific knowledge in the field of pharmaceutics. The journal covers a wide range of topics including but not limited to controlled drug release systems, drug targeting, physical pharmacy, pharmacodynamics, pharmacokinetics, pharmacogenomics, biopharmaceutics, drug and prodrug design, pharmaceutical analysis, drug stability, quality control, pharmaceutical engineering, and material sciences.
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