过饱和度
成核
机制(生物学)
药品
药物输送
晶体生长
材料科学
纳米技术
药理学
化学工程
生物物理学
化学
结晶学
医学
有机化学
工程类
物理
生物
量子力学
作者
Prachi Joshi,Abhay T. Sangamwar
标识
DOI:10.4155/tde-2018-0031
摘要
A supersaturated drug-delivery system is capable of enhancing oral bioavailability of hydrophobic drugs. Maintenance of the supersaturated system both in vitro and in vivo is one of the most challenging parts, for that it is required to keenly understand the nucleation and crystal growth behavior. Polymers are widely used to stabilize supersaturated solutions; screening of polymers is done on the basis of their interaction with drug. Nucleation and crystal growth inhibition and drug–polymer interactions can be investigated by using various spectroscopic methods. Various formulations are prepared as supersaturated systems using different drug-delivery systems utilizing different polymers, which illustrates that supersaturation is worthwhile to increase the solubility and hence oral bioavailability of poorly soluble drugs.
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