A LSER-based model to predict the solubilizing effect of drugs by inclusion with cucurbit[7]uril
Author:
Affiliation:
1. College of Chemistry and Chemical Engineering
2. Xiamen University
3. Xiamen 361005
4. China
5. Collaborative Innovation Center of Chemistry for Energy Materials
Abstract
A LSER model was built for predicting the solubility of inclusion complexes.
Funder
National Natural Science Foundation of China
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2020/RA/D0RA03394D
Reference48 articles.
1. Acyclic cucurbit[n]uril molecular containers enhance the solubility and bioactivity of poorly soluble pharmaceuticals
2. Cucurbit[7]uril encapsulated cisplatin overcomes cisplatin resistance via a pharmacokinetic effect
3. Thermodynamic parameters for the complexation of water‐insoluble betulin derivatives with (2‐hydroxypropyl)‐γ‐cyclodextrin determined by phase‐solubility technique combined with capillary zone electrophoresis
4. Sulfobutylether-β-cyclodextrin
5. The influence of hydroxypropyl-β-cyclodextrin on the solubility, dissolution, cytotoxicity, and binding of riluzole with human serum albumin
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Study on the host–guest interactions between tetramethyl cucurbit[6]uril and 2-heterocyclic-substituted benzimidazoles;RSC Advances;2024
2. Vapor-liquid equilibrium (VLE) prediction for dimethyl ether (DME) and water system in DME injection process with Peng-Robinson equation of state and composition dependent binary interaction coefficient;Journal of Petroleum Science and Engineering;2022-04
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