Controlled release of lysozyme from double-walled poly(Lactide-Co-Glycolide) (PLGA) microspheres

Double-walled microspheres based on poly(lactide-co-glycolide) (PLGA) are potential delivery systems for reducing a very high initial burst release of encapsulated protein and peptide drugs. In this study, double-walled microspheres made of glucose core, hydroxyl-terminated poly(lactide-co-glycol...

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Main Authors: Ansary, Rezaul H., Rahman, Mohd. Mokhlesur, Mohamad, Nasir A.N., Arrif, Tengku M, Abdul Latif, Ahmad Zubaidi, Katas, Haliza, Wan Nik, Wan Sani, Awang, Mohamed
Format: Article
Language:English
English
Published: MDPI AG 2017
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Online Access:http://irep.iium.edu.my/62789/1/62789_Controlled%20Release%20of%20Lysozyme%20from%20Double-Walled_article.pdf
http://irep.iium.edu.my/62789/2/62789_Controlled%20Release%20of%20Lysozyme%20from%20Double-Walled_scopus.pdf
http://irep.iium.edu.my/62789/
http://www.mdpi.com/2073-4360/9/10/485/htm
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Institution: Universiti Islam Antarabangsa Malaysia
Language: English
English
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Summary:Double-walled microspheres based on poly(lactide-co-glycolide) (PLGA) are potential delivery systems for reducing a very high initial burst release of encapsulated protein and peptide drugs. In this study, double-walled microspheres made of glucose core, hydroxyl-terminated poly(lactide-co-glycolide) (Glu-PLGA), and carboxyl-terminated PLGA were fabricated using a modified water-in-oil-in-oil-in-water (w1/o/o/w2) emulsion solvent evaporation technique for the controlled release of a model protein, lysozyme. Microspheres size, morphology, encapsulation efficiency, lysozyme in vitro release profiles, bioactivity, and structural integrity, were evaluated. Scanning electron microscopy (SEM) images revealed that double-walled microspheres comprising of Glu-PLGA and PLGA with a mass ratio of 1:1 have a spherical shape and smooth surfaces. A statistically significant increase in the encapsulation efficiency (82.52 ± 3.28%) was achieved when 1% (w/v) polyvinyl alcohol (PVA) and 2.5% (w/v) trehalose were incorporated in the internal and external aqueous phase, respectively, during emulsification. Double-walled microspheres prepared together with excipients (PVA and trehalose) showed a better control release of lysozyme. The released lysozyme was fully bioactive, and its structural integrity was slightly affected during microspheres fabrication and in vitro release studies. Therefore, double-walled microspheres made of Glu-PLGA and PLGA together with excipients (PVA and trehalose) provide a controlled and sustained release for lysozyme.