• Title of article

    Formulations for modulation of protein release from large-size PLGA microparticles for tissue engineering

  • Author/Authors

    Helen C. and Qodratnama، نويسنده , , Roozbeh and Serino، نويسنده , , Lorenzo Pio and Cox، نويسنده , , Helen C. and Qutachi، نويسنده , , Omar and White، نويسنده , , Lisa J.، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2015
  • Pages
    7
  • From page
    230
  • To page
    236
  • Abstract
    In this study we present an approach to pre-program lysozyme release from large size (100–300 μm) poly(dl-lactic acid-co-glycolic acid) (PLGA) microparticles. This approach involved blending in-house synthesized triblock copolymers with a PLGA 85:15. In this work it is demonstrated that the lysozyme release rate and the total release are related to the mass of triblock copolymer present in polymer formulation. Two triblock copolymers (PLGA–PEG1500–PLGA and PLGA–PEG1000–PLGA) were synthesized and used in this study. In a like-for-like comparison, these two triblock copolymers appeared to have similar effects on the release of lysozyme. It was shown that blending resulted in the increase of the total lysozyme release and shortened the release period (70% release within 30 days). These results demonstrated that blending PLGA–PEG–PLGA triblock copolymer with PLGA 85:15 can be used as a method to pre-program protein release from microparticles. These microparticles with modulated protein release properties may be used to create microparticle-based tissue engineering constructs with pre-programmed release properties.
  • Keywords
    Triblock copolymer , Microparticle , Lysozyme , PLGA–PEG–PLGA , glass transition temperature , Controlled release
  • Journal title
    Materials Science and Engineering C
  • Serial Year
    2015
  • Journal title
    Materials Science and Engineering C
  • Record number

    2105521