Molecular Interactions in Solid Dispersions of Poorly Water-Soluble Drugs

被引:43
作者
Tran, Thao T. D. [1 ,2 ]
Tran, Phuong H. L. [3 ]
机构
[1] Duy Tan Univ, Inst Res & Dev, Danang 550000, Vietnam
[2] Duy Tan Univ, Fac Pharm, Danang 550000, Vietnam
[3] Deakin Univ, Sch Med, Inst Innovat Phys & Mental Hlth & Clin Translat, IMPACT, Geelong, Vic, Australia
基金
澳大利亚研究理事会;
关键词
solid dispersion; molecular interaction; poorly water-soluble drug; physicochemical characterization; bonding formation; bonding force; ACID-BASE INTERACTIONS; MELT EXTRUSION; ORAL BIOAVAILABILITY; POLYMER INTERACTIONS; RAMAN-SPECTROSCOPY; CONTROLLED-RELEASE; VAPOR ABSORPTION; SALT FORMATION; INDOMETHACIN; STATE;
D O I
10.3390/pharmaceutics12080745
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Physicochemical characterization is a crucial step for the successful development of solid dispersions, including the determination of drug crystallinity and molecular interactions. Typically, the detection of molecular interactions will assist in the explanation of different drug performances (e.g., dissolution, solubility, stability) in solid dispersions. Various prominent reviews on solid dispersions have been reported recently. However, there is still no overview of recent techniques for evaluating the molecular interactions that occur within solid dispersions of poorly water-soluble drugs. In this review, we aim to overview common methods that have been used for solid dispersions to identify different bond formations and forces via the determination of interaction energy. In addition, a brief background on the important role of molecular interactions will also be described. The summary and discussion of methods used in the determination of molecular interactions will contribute to further developments in solid dispersions, especially for quick and potent drug delivery applications.
引用
收藏
页码:1 / 12
页数:12
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