| Content Provider |
World Health Organization (WHO)-Global Index Medicus |
| Author |
Wang, Caifen Wang, Xiaobo Xu, Xiaonan Liu, Botao Xu, Xu Sun, Lixin Li, Haiyan Zhang, Jiwen |
| Description |
Country affiliation: China Author Affiliation: Wang C ( Center for Drug Delivery Systems, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China); Wang X ( Department of Pharmaceutical Analysis, School of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China.); Xu X ( Center for Drug Delivery Systems, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China); Liu B ( School of Chemical and Environmental Engineering, Shanghai Institute of Technology, Shanghai 201418, China.); Xu X ( School of Chemical and Environmental Engineering, Shanghai Institute of Technology, Shanghai 201418, China.); Sun L ( Department of Pharmaceutical Analysis, School of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China. Electronic address: slx04@163.com.); Li H ( Center for Drug Delivery Systems, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China. Electronic address: lihaiyan821005@163.com.); Zhang J ( Center for Drug Delivery Systems, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China) |
| Abstract |
The individual determination of the apparent dissociation rate constant (kd,app) using high performance affinity chromatography (HPAC) is a tedious process requiring numerous separate tests and massive data fitting, unable to provide the apparent association rate constant (ka) and equilibrium binding constant (Ka). In this study, a HPAC with mass spectrometry detection (HPAC-MS/MS) was employed to determine the drug-cyclodextrin (CD) interaction kinetics with low sample loading quantity (<10 ng per injection for single compound) and high-throughput yield as twenty drugs determined in one injection. The kd,app measured by HPAC-MS/MS approach were 0.89 ± 0.07, 4.34 ± 0.01, 1.48 ± 0.01 and 7.77 ± 0.04 s(-1) for ketoprofen, trimethoprim, indapamide and acetaminophen, with kd,app for acetaminophen consistent with that from the HPAC method with UV detector in our previous studies. For twenty drugs with diverse structures and chemical properties, good correlationship was found between kd,app measured by single compound analysis method and high-throughput HPAC-MS/MS approach, with the correlation coefficient of 0.987 and the significance F less than 0.001. Comprehensive quantification of ka,app, kd,app and Ka values was further performed based on the measurement of kd,app by peak profiling method and Ka by the peak fitting method. And the investigation of the drug-CD interaction kinetics under different conditions indicated that the column temperature and mobile phase composition significantly affected the determination of ka,app, kd,app and Ka while also dependent on the acidity and basicity of drugs. In summary, the high-throughput HPAC-MS/MS approach has been demonstrated high efficiency in determination of the drug-CD primary interaction kinetic parameter, especially, kd,app, being proven as a novel tool in screening the right CD for the solubilization of the right drug. |
| File Format |
HTM / HTML |
| ISSN |
00032670 |
| Volume Number |
909 |
| e-ISSN |
18734324 |
| Journal |
Analytica Chimica Acta |
| Language |
English |
| Publisher |
Elsevier |
| Publisher Date |
2016-02-25 |
| Publisher Place |
Netherlands |
| Access Restriction |
One Nation One Subscription (ONOS) |
| Subject Keyword |
Discipline Analytical Discipline Chemistry Cyclodextrins Analysis Chemistry High-throughput Screening Assays Pharmaceutical Preparations Chromatography, High Pressure Liquid Kinetics Mass Spectrometry Journal Article Research Support, Non-u.s. Gov't |
| Content Type |
Text |
| Resource Type |
Article |
| Subject |
Spectroscopy Environmental Chemistry Analytical Chemistry Biochemistry |
