Parenteral nanosuspensions: a brief review from solubility enhancement to more novel and specific applications

• 来源期刊: 药学学报（英文版）
• 关键词: Parenteral Nanosuspension Stabilizer In vivo fate Solidification Scalability
• 年，卷（期）: 2018,（5）
• 页码范围: 733-755
• 页数: 23页
• 语种: 英文

摘要

Advancements in in silico techniques of lead molecule selection have resulted in the failure of around 70％ of new chemical entities (NCEs).Some of these molecules are getting rejected at final developmental stage resulting in wastage of money and resources.Unfavourable physicochemical properties affect ADME profile of any efficacious and potent molecule,which may ultimately lead to killing of NCE at final stage.Numerous techniques are being explored including nanocrystals for solubility enhancement purposes.Nanocrystals are the most successful and the ones which had a shorter gap between invention and subsequent commercialization of the first marketed product.Several nanocrystal-based products are commercially available and there is a paradigm shift in using approach from simply being solubility enhancement technique to more novel and specific applications.Some other aspects in relation to parenteral nanosuspensions are concentrations of surfactant to be used,scalability and in vivo fate.At present,there exists a wide gap due to poor understanding of these critical factors,which we have tried to address in this review.This review will focus on parenteral nanosuspensions,coveting varied aspects especially stabilizers used,GRAS (Generally Recognized as Safe) status of stabilizers,scalability challenges,issues of physical and chemical stability,solidification techniques to combat stability problems and in vivo fate.