Literature DB >> 15567308

Study of the physicochemical properties and stability of solid dispersions of loperamide and PEG6000 prepared by spray drying.

Ilse Weuts1, Dieter Kempen, Geert Verreck, Annelies Decorte, Koen Heymans, Jef Peeters, Marcus Brewster, Guy Van den Mooter.   

Abstract

Solid dispersions of PEG6000 and loperamide-a poorly water-soluble agent-were prepared by spray drying. Their physicochemical properties were evaluated immediately after preparation. The dissolution was higher than that of pure crystalline loperamide. DSC- and XRD-measurements revealed that in the dispersions, loperamide is partially present in the crystalline state. A eutectic state diagram was obtained. The samples containing 20% loperamide were stored under different conditions (40 degrees C and 0% RH, 25 degrees C and 52% RH, 4 degrees C and 0% RH) to investigate their stability as a function of time. The dissolution properties deteriorate upon storage at high temperature (40 degrees C and 0% RH) and in conditions of higher relative humidity (25 degrees C and 52% RH). The DSC-curves clearly indicate an increase in the amount of crystalline compound under these conditions. From these observations it could be concluded that loperamide, which is partially crystalline and partially amorphous in the freshly prepared samples, continues to crystallize under these conditions, resulting in progressively poorer dissolution properties.

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Year:  2005        PMID: 15567308     DOI: 10.1016/j.ejpb.2004.05.011

Source DB:  PubMed          Journal:  Eur J Pharm Biopharm        ISSN: 0939-6411            Impact factor:   5.571


  7 in total

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2.  Stabilization and improved in vivo performance of amorphous etoricoxib using Gelucire 50/13.

Authors:  Shamkant L Shimpi; Bhaskar Chauhan; K R Mahadik; Anant Paradkar
Journal:  Pharm Res       Date:  2005-09-22       Impact factor: 4.200

3.  Kinetics and bixine extraction time from achiote (Bixa Orellana L.).

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Journal:  J Food Sci Technol       Date:  2021-07-20       Impact factor: 2.701

4.  Formulation of Gelucire®-Based Solid Dispersions of Atorvastatin Calcium: In Vitro Dissolution and In Vivo Bioavailability Study.

Authors:  Basmah N Aldosari; Alanood S Almurshedi; Iman M Alfagih; Bushra T AlQuadeib; Mohammad A Altamimi; Syed Sarim Imam; Afzal Hussain; Faleh Alqahtani; Ehab Elzayat; Sultan Alshehri
Journal:  AAPS PharmSciTech       Date:  2021-05-24       Impact factor: 4.026

5.  Improved dissolution and anti-inflammatory activity of ibuprofen-polyethylene glycol 8000 solid dispersion systems.

Authors:  Kenneth C Ofokansi; Franklin C Kenechukwu; Richard O Ezugwu; Anthony A Attama
Journal:  Int J Pharm Investig       Date:  2016 Jul-Sep

6.  Solubility and bioavailability enhancement of poorly aqueous soluble atorvastatin: in vitro, ex vivo, and in vivo studies.

Authors:  Madhuri S Rodde; Ganesh T Divase; Tejas B Devkar; Avinash R Tekade
Journal:  Biomed Res Int       Date:  2014-06-03       Impact factor: 3.411

Review 7.  Pharmaceutical Dispersion Techniques for Dissolution and Bioavailability Enhancement of Poorly Water-Soluble Drugs.

Authors:  Xingwang Zhang; Huijie Xing; Yue Zhao; Zhiguo Ma
Journal:  Pharmaceutics       Date:  2018-06-23       Impact factor: 6.321

  7 in total

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