对体药物载体的体外释放测试方法的评估:缺乏标准化的协议
Laura Gómez-Lázaro1, Cristina Martín-Sabroso1,2, Juan Aparicio-Blanco1,2
1Department of Pharmaceutics and Food Technology, Faculty of Pharmacy, Complutense University of Madrid, 28040 Madrid, Spain.
Pharmaceutics
|January 23, 2024
概括
对于合体载体缺乏标准化药物释放测试,原因是分离从封装药物释放的药物存在挑战. 本综述比较了常见的体外试验方法,强调了它们的优点,缺点和影响因素.
科学领域:
- 制药科学 制药科学
- 药物运输 药物运输 药物运输
- 材料科学 材料科学 材料科学
背景情况:
- 结合体载体已经开发了几十年,但缺乏在药库中进行标准化药物释放测试.
- 在体外药物释放评估对于开发和质量控制纳米和微载体至关重要.
- 从封装药物中分离释放的困难阻碍了标准化.
研究的目的:
- 为了比较流行的体外药物释放测试方法用于合体载体.
- 分析每个方法的优缺点.
- 在不同的测试技术中确定影响药物释放的关键参数.
主要方法:
- 对膜扩散技术的审查.
- 样本分析和单独的方法.
- 在现场检测技术的评估.
主要成果:
- 每种方法都有独特的优势和局限性.
- 从封装药物中分离释放的药物是一个常见的挑战.
- 具体的参数显著影响药物释放动力学,取决于所使用的方法.
结论:
- 对于体载体的标准化体外药物释放测试协议,有极大需要.
- 了解方法特定的参数对于准确的药物释放评估至关重要.
- 需要进一步的研究来建立普遍接受的测试方法.
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