MIcrospher-iiUM, a novel, controlled-released drug/gene delivery system

Multiple-emulsion, solvent-evaporation method is employed to synthesise MICROSPHERiiUM. A biodegradable co-polymer, poly(L-lactic-co-glycolic acid) (PLGA), is used as the matrix to form the microspheres. Briefly, an appropriate amount of PLGA is dissolved in dichloromethane to form the primary emul...

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Main Authors: Mohamed, Farahidah, Doolanea, Abd Almonem, Harun Ismail, Ahmad Fahmi
Format: Book Chapter
Language:English
Published: IIUM Press 2011
Subjects:
Online Access:http://irep.iium.edu.my/5939/
http://irep.iium.edu.my/5939/1/Content_Page_IIUM_Research.pdf
id iium-5939
recordtype eprints
spelling iium-59392019-09-05T03:01:48Z http://irep.iium.edu.my/5939/ MIcrospher-iiUM, a novel, controlled-released drug/gene delivery system Mohamed, Farahidah Doolanea, Abd Almonem Harun Ismail, Ahmad Fahmi RS Pharmacy and materia medica Multiple-emulsion, solvent-evaporation method is employed to synthesise MICROSPHERiiUM. A biodegradable co-polymer, poly(L-lactic-co-glycolic acid) (PLGA), is used as the matrix to form the microspheres. Briefly, an appropriate amount of PLGA is dissolved in dichloromethane to form the primary emulsion. This phase is then homogenised with on aqueous phase, containing surfactant and a model drug (e.g. plasmid DNA or small molecules drug) for a certain duration and at an appropriate speed. The resultant waterin- oil-in-water (w/o/w) emulsion is then dispersed in a bigger volume of aqueous stabiliser. Then the mixture is transferred to a continuously stirred hardening tank containing the same stabiliser. Stirring is continued for a certain duration to allow complete evaporation of the solvent. The hardened MICROSPHER-iiUM isharvested by means of centrifugation and washing with distilled before it was freeze-dried. Characterisation of the MICROSPHERiiUM is conducted to investigate its surface morphology, size distribution, encapsulation efficiency and in-vitro release profile. Different protocols are adopted depending on the types of the madel drug to analyse the model drug. This MICROSPHER-iium has demonstrated robustness in encapsulating different types of agents with substantial encapsulation efficiency. The controlled-release profile is also achievable due to the inherent degradation rate of the co-polymers, PLGA, of which the rate and duration are dependent on its molecular weight. The colloidal size of this delivery system and the release of drug that can be controlled are envisaged to enhance the quality of therapy in chronic diseases as it can improve patient compliance towards drug regiment owing to reduction in frequency of dosing and reduction in side effects. IIUM Press 2011 Book Chapter PeerReviewed application/pdf en http://irep.iium.edu.my/5939/1/Content_Page_IIUM_Research.pdf Mohamed, Farahidah and Doolanea, Abd Almonem and Harun Ismail, Ahmad Fahmi (2011) MIcrospher-iiUM, a novel, controlled-released drug/gene delivery system. In: IIUM Research, Invention & Innovation Exhibition 2011. IIUM Press, Kuala Lumpur, p. 183. ISBN 978-983-3124-14-9
repository_type Digital Repository
institution_category Local University
institution International Islamic University Malaysia
building IIUM Repository
collection Online Access
language English
topic RS Pharmacy and materia medica
spellingShingle RS Pharmacy and materia medica
Mohamed, Farahidah
Doolanea, Abd Almonem
Harun Ismail, Ahmad Fahmi
MIcrospher-iiUM, a novel, controlled-released drug/gene delivery system
description Multiple-emulsion, solvent-evaporation method is employed to synthesise MICROSPHERiiUM. A biodegradable co-polymer, poly(L-lactic-co-glycolic acid) (PLGA), is used as the matrix to form the microspheres. Briefly, an appropriate amount of PLGA is dissolved in dichloromethane to form the primary emulsion. This phase is then homogenised with on aqueous phase, containing surfactant and a model drug (e.g. plasmid DNA or small molecules drug) for a certain duration and at an appropriate speed. The resultant waterin- oil-in-water (w/o/w) emulsion is then dispersed in a bigger volume of aqueous stabiliser. Then the mixture is transferred to a continuously stirred hardening tank containing the same stabiliser. Stirring is continued for a certain duration to allow complete evaporation of the solvent. The hardened MICROSPHER-iiUM isharvested by means of centrifugation and washing with distilled before it was freeze-dried. Characterisation of the MICROSPHERiiUM is conducted to investigate its surface morphology, size distribution, encapsulation efficiency and in-vitro release profile. Different protocols are adopted depending on the types of the madel drug to analyse the model drug. This MICROSPHER-iium has demonstrated robustness in encapsulating different types of agents with substantial encapsulation efficiency. The controlled-release profile is also achievable due to the inherent degradation rate of the co-polymers, PLGA, of which the rate and duration are dependent on its molecular weight. The colloidal size of this delivery system and the release of drug that can be controlled are envisaged to enhance the quality of therapy in chronic diseases as it can improve patient compliance towards drug regiment owing to reduction in frequency of dosing and reduction in side effects.
format Book Chapter
author Mohamed, Farahidah
Doolanea, Abd Almonem
Harun Ismail, Ahmad Fahmi
author_facet Mohamed, Farahidah
Doolanea, Abd Almonem
Harun Ismail, Ahmad Fahmi
author_sort Mohamed, Farahidah
title MIcrospher-iiUM, a novel, controlled-released drug/gene delivery system
title_short MIcrospher-iiUM, a novel, controlled-released drug/gene delivery system
title_full MIcrospher-iiUM, a novel, controlled-released drug/gene delivery system
title_fullStr MIcrospher-iiUM, a novel, controlled-released drug/gene delivery system
title_full_unstemmed MIcrospher-iiUM, a novel, controlled-released drug/gene delivery system
title_sort microspher-iium, a novel, controlled-released drug/gene delivery system
publisher IIUM Press
publishDate 2011
url http://irep.iium.edu.my/5939/
http://irep.iium.edu.my/5939/1/Content_Page_IIUM_Research.pdf
first_indexed 2023-09-18T20:14:45Z
last_indexed 2023-09-18T20:14:45Z
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