Literature DB >> 18774278

Preparation and properties of PLGA microspheres containing hydrophilic drugs by the SPG (shirasu porous glass) membrane emulsification technique.

Fuminori Ito1, Hiroyuki Honnami, Hiroyoshi Kawakami, Kiyoshi Kanamura, Kimiko Makino.   

Abstract

In the present paper, monodisperse poly (lactide-co-glycolide) (PLGA) microspheres containing the hydrophilic model drug, blue dextran (BLD), were manufactured by the solvent evaporation method and the shirasu porous glass (SPG) membrane emulsification technique. In order to prepare PLGA microspheres with a higher drug loading efficiency by the membrane emulsification technique, the test of stability and productivity of the primary emulsion (w(1)/o emulsion) was preliminary examined by change species or concentration of the oil-soluble surfactant and the ratio of water and organic solvent. The primary emulsion (w(1)/o) composed of the BLD aqueous solution and dichloromethane (DCM) dissolved PLGA was prepared with the micro homogenizer. The secondary emulsion (w(1)/o/w(2)) was prepared by the SPG membrane emulsification technique. BLD/PLGA microspheres of various micro level sizes of 2.0-10 microm prepared by variation of pore size of the using SPG membrane. The highly monodisperse BLD/PLGA microspheres were also manufactured by added polyethylene glycol (PEG) into the water phase, as reported in a previous paper. The initial release rate of the drug from such microspheres controlled than the sample manufactured without an additive.

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Year:  2008        PMID: 18774278     DOI: 10.1016/j.colsurfb.2008.07.008

Source DB:  PubMed          Journal:  Colloids Surf B Biointerfaces        ISSN: 0927-7765            Impact factor:   5.268


  6 in total

1.  Building membrane emulsification into pulmonary drug delivery and targeting.

Authors:  Decai Bao; Yanjun Zhao
Journal:  Pharm Res       Date:  2010-08-12       Impact factor: 4.200

2.  Control of drug loading efficiency and drug release behavior in preparation of hydrophilic-drug-containing monodisperse PLGA microspheres.

Authors:  Fuminori Ito; Hiroyuki Fujimori; Hiroyuki Honnami; Hiroyoshi Kawakami; Kiyoshi Kanamura; Kimiko Makino
Journal:  J Mater Sci Mater Med       Date:  2010-02-03       Impact factor: 3.896

3.  Long-term sustained release Poly(lactic-co-glycolic acid) microspheres of asenapine maleate with improved bioavailability for chronic neuropsychiatric diseases.

Authors:  Junqiu Zhai; Yu-E Wang; Xiangping Zhou; Yan Ma; Shixia Guan
Journal:  Drug Deliv       Date:  2020-12       Impact factor: 6.419

Review 4.  Poly(lactic Acid): A Versatile Biobased Polymer for the Future with Multifunctional Properties-From Monomer Synthesis, Polymerization Techniques and Molecular Weight Increase to PLA Applications.

Authors:  Evangelia Balla; Vasileios Daniilidis; Georgia Karlioti; Theocharis Kalamas; Myrika Stefanidou; Nikolaos D Bikiaris; Antonios Vlachopoulos; Ioanna Koumentakou; Dimitrios N Bikiaris
Journal:  Polymers (Basel)       Date:  2021-05-31       Impact factor: 4.329

5.  A biodegradable polymeric system for peptide-protein delivery assembled with porous microspheres and nanoparticles, using an adsorption/infiltration process.

Authors:  Sergio Alcalá-Alcalá; Zaida Urbán-Morlán; Irene Aguilar-Rosas; David Quintanar-Guerrero
Journal:  Int J Nanomedicine       Date:  2013-06-10

6.  Control of Alginate Core Size in Alginate-Poly (Lactic-Co-Glycolic) Acid Microparticles.

Authors:  Daniel Lio; David Yeo; Chenjie Xu
Journal:  Nanoscale Res Lett       Date:  2016-01-08       Impact factor: 4.703

  6 in total

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