Abstract
Solubility of a drug/drug candidate is one of the most important required physico-chemical properties in pharmaceutical area and nearly 40% of drug candidates fail to proceed to the higher trial phases of new drug development process because of their poor solubility. The commonly used method is to determine the experimental values of either thermodynamic or kinetic solubility. Numerous efforts were made to develop predictive tools for replacing the time consuming and costly experimental methods.
Subject
Pharmacology, Toxicology and Pharmaceutics (miscellaneous),Applied Microbiology and Biotechnology,Food Science
Cited by
4 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