Characterization and Applications of Colloidal Systems as Versatile Drug Delivery Carriers for Parenteral Formulations

被引:16
|
作者
Kolluru, Lakshmi Prasanna [1 ,2 ]
Atre, Prachi [3 ]
Rizvi, Syed A. A. [4 ]
机构
[1] Mercer Univ, Coll Pharm, Vaccine Nanotechnol Lab, 3001 Mercer Univ Dr, Atlanta, GA 30341 USA
[2] Capstone Dev Serv, Rosemont, IL 60018 USA
[3] St Johns Univ, Coll Pharm & Hlth Sci, Jamaica, NY 11439 USA
[4] Hampton Univ, Sch Pharm, Hampton, VA 23668 USA
关键词
drug delivery; natural surfactants; self-assembled systems; drug solubility;
D O I
10.3390/ph14020108
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Preparing a suitable formulation for parenteral administration is already a difficult task; this, coupled with poor water-soluble new chemical entity (NCE), complicates this situation even further. There are several methodologies available to enhance water solubility, but this alone does not entail successful formulation. Making a micro/nano emulsion with a suitable surfactant not only increases the drug solubility but also the cell membrane permeability. Thus, not only biopharmaceutic classification system (BCS)-II (low solubility compounds) but also BCS-III (low permeability) and BCS-IV drugs (low solubility and low permeability) can be further exploited. Those drug candidates otherwise will not move further in NCE evaluation or clinical trials. This succinct review article delves into various aspects of biphasic micro/nano emulsion systems for parenteral drug delivery including the structure of the biphasic colloidal systems, characterization parameters, stability issues, regulatory considerations, and applications in life sciences.
引用
收藏
页码:1 / 12
页数:12
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