Nanoconjugation and Encapsulation Strategies for Improving Drug Delivery and Therapeutic Efficacy of Poorly Water-Soluble Drugs

被引:53
|
作者
Thao T D Tran [1 ,2 ]
Phuong H L Tran [3 ]
机构
[1] Ton Duc Thang Univ, Dept Management Sci & Technol Dev, Ho Chi Minh City, Vietnam
[2] Ton Duc Thang Univ, Fac Pharm, Ho Chi Minh City, Vietnam
[3] Deakin Univ, Sch Med, Geelong, Vic 3216, Australia
基金
澳大利亚研究理事会;
关键词
nanoconjugate; nanotechnology; poorly water-soluble drugs; theranostic; drug delivery; biomedical applications; SELF-ASSEMBLED NANOPARTICLES; IRON-OXIDE NANOPARTICLES; OLEIC ACID CONJUGATE; SOLID DISPERSION; GLYCYRRHETINIC ACID; ORAL BIOAVAILABILITY; ANTITUMOR-ACTIVITY; HYDROXYL GROUP; CO-DELIVERY; CANCER;
D O I
10.3390/pharmaceutics11070325
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Nanoconjugations have been demonstrated to be a dominant strategy for drug delivery and biomedical applications. In this review, we intend to describe several strategies for drug formulation, especially to improve the bioavailability of poorly water-soluble molecules for future application in the therapy of numerous diseases. The context of current studies will give readers an overview of the conjugation strategies for fabricating nanoparticles, which have expanded from conjugated materials to the surface conjugation of nanovehicles. Moreover, nanoconjugates for theranostics are also discussed and highlighted. Overall, these state-of-the-art conjugation methods and these techniques and applications for nanoparticulate systems of poorly water-soluble drugs will inspire scientists to explore and discover more productive techniques and methodologies for drug development.
引用
收藏
页数:14
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