Host-guest kinetic interactions between HP-beta-cyclodextrin and drugs for prediction of bitter taste masking
文献类型:期刊论文
作者 | Guo, Zhen1,3; Wu, Fei2; Singh, Vikramjeet1; Guo, Tao1; Ren, Xiaohong1; Yin, Xianzhen1,3; Shao, Qun3; York, Peter3; Patterson, Laurence H.3; Zhang, Jiwen1![]() |
刊名 | JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS
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出版日期 | 2017-06-05 |
卷号 | 140页码:232-238 |
关键词 | Cyclodextrin Kinetic parameters Taste masking Surface plasmon resonance imaging Modeling Prediction |
ISSN号 | 0731-7085 |
DOI | 10.1016/j.jpba.2017.03.042 |
文献子类 | Article |
英文摘要 | Cyclodextrins (CD) are widely used bitter taste masking agents, for which the binding equilibrium constant (K) for the drug-CD complex is a conventional parameter for quantitating the taste masking effects. However, some exceptions have been reported to the expected relationship between K and bitterness reduction and the relationship between kinetic parameters of a drug-CD interaction, including association rate constant (K-a) and disassociation rate constant (K-d), and taste masking remains unexplored. In this study, based upon a database of kinetic parameters of drugs-HP-beta-CD generated by Surface Plasmon Resonance Imaging for 485 drugs, the host-guest kinetic interactions between drugs and HP-beta-CD for prediction of taste masking effects have been investigated. The taste masking effects of HP-beta-CD for 13 bitter drugs were quantitatively determined using an electronic gustatory system (alpha-Astree e-Tongue). Statistical software was used to establish a model based on Euclidean distance measurements, K-a and K-d of the bitter drugs/HP-beta-CD-complexes (R-2 = 0.96 and P < 0.05). Optimized parameters, K-a(3), K-d, K-a, k(d) K-d(3), K-a(2) and K-a/K-d with notable influence, were obtained by stepwise regression from 12 parameters derived from K-a, K-d and K (K-a/K-d). 10-fold cross-validation was used to verify the reliability of the model (correlation coefficient of 0.84, P < 0.05). The established model indicated a relationship between K-a, K-d, K and taste masking by HP-beta-CD and was successful in predicting the extent of taste masking by HP-beta-CD of 44 bitter drugs, which was in accordance with the literature reported. In conclusion, the relationship between kinetics of drug-CD interactions and taste masking was established and providing a new strategy for predicting the cyclodextrin mediated bitter taste masking. (C) 2017 Elsevier B.V. All rights reserved. |
WOS关键词 | FLUORESCENCE CORRELATION SPECTROSCOPY ; BIOLOGICAL-MEMBRANES ; ELECTRONIC TONGUE ; FORMULATION ; COMPLEXES ; MECHANISMS ; DYNAMICS ; CHILDREN ; BROMIDE ; FOODS |
资助项目 | National Natural Science Foundation of China[81430087] ; National Natural Science Foundation of China[81573392] ; National Science and Technology Major Project[2013ZX09402103] |
WOS研究方向 | Chemistry ; Pharmacology & Pharmacy |
语种 | 英语 |
WOS记录号 | WOS:000402850500028 |
出版者 | ELSEVIER SCIENCE BV |
源URL | [http://119.78.100.183/handle/2S10ELR8/272619] ![]() |
专题 | 药物制剂研究中心 |
通讯作者 | Patterson, Laurence H.; Zhang, Jiwen |
作者单位 | 1.Chinese Acad Sci, Shanghai Inst Mat Med, Ctr Drug Delivery Syst, 501 Haike Rd, Shanghai 201203, Peoples R China; 2.Shanghai Univ Tradit Chinese Med, Engn Res Ctr Modern Preparat Technol Tradit Chine, Minist Educ, Shanghai 201203, Peoples R China 3.Univ Bradford, Sch Med Sci, Bradford BD7 1DP, W Yorkshire, England; |
推荐引用方式 GB/T 7714 | Guo, Zhen,Wu, Fei,Singh, Vikramjeet,et al. Host-guest kinetic interactions between HP-beta-cyclodextrin and drugs for prediction of bitter taste masking[J]. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS,2017,140:232-238. |
APA | Guo, Zhen.,Wu, Fei.,Singh, Vikramjeet.,Guo, Tao.,Ren, Xiaohong.,...&Zhang, Jiwen.(2017).Host-guest kinetic interactions between HP-beta-cyclodextrin and drugs for prediction of bitter taste masking.JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS,140,232-238. |
MLA | Guo, Zhen,et al."Host-guest kinetic interactions between HP-beta-cyclodextrin and drugs for prediction of bitter taste masking".JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS 140(2017):232-238. |
入库方式: OAI收割
来源:上海药物研究所
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