Literature DB >> 15784247

Effect of viscosity and concentration of wall former, emulsifier and pore-inducer on the properties of amoxicillin microcapsules prepared by emulsion solvent evaporation.

Mingna Song1, Ning Li, Shuying Sun, Lourens R Tiedt, Wilna Liebenberg, Melgardt M de Villiers.   

Abstract

This study reports the laboratory optimization for the preparation of sustained release amoxicillin (AMX) ethylcellulose microcapsules by an emulsion solvent evaporation process by adjusting the viscosity and concentration of ethylcellulose, ratio of amoxicillin to ethylcellulose, and concentration of emulsifier and pore inducer. When ethylcellulose with a viscosity of 45 mPa.s was used, almost no material stuck to the inside wall of the beaker and uniform microcapsules were prepared. The average diameter of microcapsules increased and yield and release rate decreased as the concentration of ethylcellulose increased from 1% to 8%. The release of amoxicillin from microcapsules was influenced by the ratio of the weight of drug to that of ethylcellulose and ratios of 2:1 and 4:1 were most suited for optimum amoxicillin release. The average diameter of microcapsules decreased and the release rate increased as the concentration of the emulsifier increased from 1.5% to 6.0%, however, the size distribution became significantly wider with the increase in the concentration of sorbitan monooleate. Addition of small amounts of a water-soluble agent sucrose improved the release of active ingredient from the microcapsule matrix without influencing the morphology and particulate properties of the microcapsules.

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Year:  2005        PMID: 15784247     DOI: 10.1016/j.farmac.2004.11.009

Source DB:  PubMed          Journal:  Farmaco        ISSN: 0014-827X


  7 in total

1.  Dental mold: a novel formulation to treat common dental disorders.

Authors:  Soma Ghosh; Gopa Roy; Biswajit Mukherjee
Journal:  AAPS PharmSciTech       Date:  2009-05-23       Impact factor: 3.246

2.  In vitro and in vivo evaluation of hydroxyzine hydrochloride microsponges for topical delivery.

Authors:  Christianne Mounir Zaki Rizkalla; Randa latif Aziz; Iman Ibrahim Soliman
Journal:  AAPS PharmSciTech       Date:  2011-07-29       Impact factor: 3.246

3.  Preparation and characterization of highly porous direct compression carrier particles with improved drug loading during an interactive mixing process.

Authors:  Mingna Song; Ning Li; Louwrens R Tiedt; Michael D Degennaro; Melgardt M de Villiers
Journal:  AAPS PharmSciTech       Date:  2010-04-23       Impact factor: 3.246

4.  Ethyl cellulose microcapsules for protecting and controlled release of folic acid.

Authors:  Satit Prasertmanakit; Nalena Praphairaksit; Worawadee Chiangthong; Nongnuj Muangsin
Journal:  AAPS PharmSciTech       Date:  2009-09-10       Impact factor: 3.246

5.  A trial for the design and optimization of pH-sensitive microparticles for intestinal delivery of cinnarizine.

Authors:  Hussein O Ammar; Mahmoud Ghorab; Rabab Kamel; Alaa H Salama
Journal:  Drug Deliv Transl Res       Date:  2016-06       Impact factor: 4.617

6.  Continuous generation of ethyl cellulose drug delivery nanocarriers from microbubbles.

Authors:  Oguzhan Gunduz; Zeeshan Ahmad; Eleanor Stride; Mohan Edirisinghe
Journal:  Pharm Res       Date:  2012-09-06       Impact factor: 4.200

7.  Maximizing the encapsulation efficiency and the bioavailability of controlled-release cetirizine microspheres using Draper-Lin small composite design.

Authors:  Khalid Mohamed El-Say
Journal:  Drug Des Devel Ther       Date:  2016-02-24       Impact factor: 4.162

  7 in total

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