Solid Dispersion as a Technical Solution to Boost the Dissolution Rate and Bioavailability of Poorly Water-Soluble Drugs

被引:11
|
作者
Attia, Mohamed Salah [1 ]
Hasan, Azza Ali [1 ]
Ghazy, Fakhr-Eldin Soliman [1 ]
Gomaa, Eman [1 ]
机构
[1] Zagazig Univ, Dept Pharmaceut, Fac Pharm, Zagazig 44519, Egypt
关键词
Solid dispersion; Solvent evaporation; Fusion; Co-milling; Kneading; Electrospinning; KinetiSol (R); HOT-MELT EXTRUSION; PHYSICOCHEMICAL CHARACTERIZATION; PHARMACEUTICAL APPLICATIONS; SOLUBILITY ENHANCEMENT; ORAL BIOAVAILABILITY; RELEASE; DELIVERY; INDOMETHACIN; FORMULATION; NANOFIBERS;
D O I
10.5530/ijper.55.2s.103
中图分类号
G40 [教育学];
学科分类号
040101 ; 120403 ;
摘要
Solid dispersion (SD) is one of the oldest and widely utilized techniques to improve the solubility of slowly dissolving drugs. A variety of pharmaceutically compatible additives using different emerging technology is used for preparing SDs. Multiple approaches were designed to prepare SDs by such as kneading, co-milling, fusion, solvent evaporation and various solvent-associated methods. The selection of appropriate preparation method and carrier is vital for producing a homogenous product affecting its stability and biological activity. Many attempts were recently carried out to improve the scalability of the applied approaches and the results were novel preparation methods such as KinetiSol, Electrospinning and Hot-melt extrusion. In the present review, drug carriers used to formulate SD were classified as small molecular weight carriers, large molecular weight named polymeric carriers and functionalized polymeric ones. Moreover, new attractive SD formulated using the newly emerged natural carriers recently joined the field of the pharmaceutical industry.
引用
收藏
页码:S327 / S339
页数:13
相关论文
共 50 条
  • [1] Pharmaceutical Dispersion Techniques for Dissolution and Bioavailability Enhancement of Poorly Water-Soluble Drugs
    Zhang, Xingwang
    Xing, Huijie
    Zhao, Yue
    Ma, Zhiguo
    PHARMACEUTICS, 2018, 10 (03)
  • [2] To enhance dissolution rate of poorly water-soluble drugs: Glucosamine hydrochloride as a potential carrier in solid dispersion formulations
    Al-Hamidi, Hiba
    Edwards, Alison A.
    Mohammad, Mohammad A.
    Nokhodchi, Ali
    COLLOIDS AND SURFACES B-BIOINTERFACES, 2010, 76 (01) : 170 - 178
  • [3] Microcrystals for dissolution rate enhancement of poorly water-soluble drugs
    Rasenack, N
    Hartenhauer, H
    Müller, BW
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2003, 254 (02) : 137 - 145
  • [4] Amorphous solid dispersion: a promising technique for improving oral bioavailability of poorly water-soluble drugs
    Ghule, Prashant
    Gilhotra, Ritu
    Jithan, Aukunuru
    Bairagi, Shripad
    Aher, Abhijeet
    SA PHARMACEUTICAL JOURNAL, 2018, 85 (01) : 50 - 56
  • [5] Eutectic mixtures as an approach to enhance solubility, dissolution rate and oral bioavailability of poorly water-soluble drugs
    Bazzo, Giovana Carolina
    Pezzini, Bianca Ramos
    Stulzer, Hellen Karine
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2020, 588
  • [6] Improving the dissolution rate of poorly water soluble drug by solid dispersion and solid solution - Pros and cons
    Chokshi, Rina J.
    Zia, Hossein
    Sandhu, Harpreet K.
    Shah, Navnit H.
    Malick, Waseem A.
    DRUG DELIVERY, 2007, 14 (01) : 33 - 45
  • [7] Dissolution rate enhancement by in situ micronization of poorly water-soluble drugs
    Rasenack, N
    Müller, BW
    PHARMACEUTICAL RESEARCH, 2002, 19 (12) : 1894 - 1900
  • [8] Dissolution Rate Enhancement by in Situ Micronization of Poorly Water-Soluble Drugs
    Norbert Rasenack
    Bernd W. Müller
    Pharmaceutical Research, 2002, 19 : 1894 - 1900
  • [9] Application of supercritical fluid technology for solid dispersion to enhance solubility and bioavailability of poorly water-soluble drugs
    Tran, Phuong
    Park, Jeong-Sook
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2021, 610
  • [10] Solid Dispersion as an Approach for Bioavailability Enhancement of Poorly Water-Soluble Drug Ritonavir
    Shilpi Sinha
    Mushir Ali
    Sanjula Baboota
    Alka Ahuja
    Anil Kumar
    Javed Ali
    AAPS PharmSciTech, 2010, 11 : 518 - 527