Recent Strategic Developments in the Use of Superdisintegrants for Drug Delivery

被引:3
作者
Tran, Phuong H. L. [1 ]
Tran, Thao T. D. [2 ,3 ]
机构
[1] Deakin Univ, Sch Med, Geelong, Vic, Australia
[2] Ton Duc Thang Univ, Dept Management Sci & Technol Dev, Ho Chi Minh City, Vietnam
[3] Ton Duc Thang Univ, Fac Pharm, Ho Chi Minh City, Vietnam
基金
澳大利亚研究理事会;
关键词
Superdisintegrant; controlled release; drug delivery system; nanoparticle; solid dosage form; drug bioavailability; ORALLY DISINTEGRATING TABLETS; CONTROLLED-RELEASE; SOLID DISPERSIONS; DISSOLUTION RATE; ORODISPERSIBLE TABLETS; LIQUISOLID COMPACTS; SORPTION PROPERTIES; DIRECT COMPRESSION; IN-VITRO; FORMULATION;
D O I
10.2174/1381612826666200122124621
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Improving drug bioavailability in the pharmaceutical field is a challenge that has attracted substantial interest worldwide. The controlled release of a drug can be achieved with a variety of strategies and novel materials in the field. In addition to the vast development of innovative materials for improving therapeutic effects and reducing side effects, the exploration of remarkable existing materials could encourage the discovery of diverse approaches for adapted drug delivery systems. Recently, superdisintegrants have been proposed for drug delivery systems as alternative approaches to maximize the efficiency of therapy. Although superdisintegrants are well known and used in solid dosage forms, studies on strategies for the development of drug delivery systems using superdisintegrants are lacking. Therefore, this study reviews the use of superdisintegrants in controlled drug release dosage formulations. This overview of superdisintegrants covers developed strategies, types (including synthetic and natural materials), dosage forms and techniques and will help to improve drug delivery systems.
引用
收藏
页码:701 / 709
页数:9
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