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用于药物研发研究的自动化分析系统。II——一种溶出度测试系统。

Automated analytical systems for drug development studies. II--A system for dissolution testing.

作者信息

Shah K P, Chang M, Riley C M

机构信息

Department of Pharmaceutical Chemistry, University of Kansas, Lawrence 66045, USA.

出版信息

J Pharm Biomed Anal. 1994 Dec;12(12):1519-27. doi: 10.1016/0731-7085(94)00103-0.

Abstract

Microdialysis is a non-equilibrium dynamic sampling method in which the analytes diffuse across a semipermeable membrane due to a concentration gradient and are carried away by the constantly pumping perfusion medium for on-line analysis. A BAS, Inc. microinfusion pump/injector and an on-line LC system were interfaced with a dissolution apparatus to automate dissolution testing of tablets. A DL-5 microdialysis loop probe was suspended in the dissolution medium for sampling. The automated system was used reproducibly (RSD < 2%) to measure the dissolution of acetaminophen and Sulfatrim tablets. Drug recovery from the microdialysis probe was a function of the perfusion rate at constant temperature. However, microdialysis recovery was independent of drug concentration over the linear ranges of the assays for the analytes of interest. Dissolution profiles determined by microdialysis sampling were compared with manual sampling. Identical profiles were obtained for acetaminophen tablets in water at 37 degrees C and 50 rpm by both sampling methods. Dissolution of Sulfatrim tablets was determined in 0.1 M hydrochloride acid at 37 degrees C and 75 rpm. Microdialysis sampling permitted the use of a specially designed perfusion medium to buffer the acidic samples before injecting onto the LC column. Dissolution profiles of sulphamethoxazole were comparable for both sampling methods; however, microdialysis sampling indicated slightly higher release of trimethoprim from the Sulfatrim tablets, which was attributed to release of adsorbed drug from the connecting tubing.

摘要

微透析是一种非平衡动态采样方法,其中分析物由于浓度梯度而扩散穿过半透膜,并被不断泵送的灌注介质带走以进行在线分析。将BAS公司的微量输注泵/注射器和在线液相色谱系统与溶出度测定仪连接,以实现片剂溶出度测试的自动化。将DL-5微透析环路探头悬浮在溶出介质中进行采样。该自动化系统可重复使用(相对标准偏差<2%)来测量对乙酰氨基酚片和复方新诺明片的溶出度。在恒定温度下,从微透析探头回收的药物是灌注速率的函数。然而,在所关注分析物的测定线性范围内,微透析回收率与药物浓度无关。将通过微透析采样测定的溶出曲线与手动采样测定的进行比较。两种采样方法在37℃和50转/分钟的水中对乙酰氨基酚片的溶出曲线相同。在37℃和75转/分钟的0.1M盐酸中测定复方新诺明片的溶出度。微透析采样允许使用专门设计的灌注介质在注入液相色谱柱之前缓冲酸性样品。两种采样方法测定的磺胺甲恶唑溶出曲线具有可比性;然而,微透析采样表明复方新诺明片中甲氧苄啶的释放略高,这归因于连接管中吸附药物的释放。

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