Poster Presenter
In situ Forming Heparin-Conjugated PLGA-PEG-PLGA
Hydrogels for Controlled Release of Growth Factors
Eugene Lih, Yoon Ki Joung, Ki Dong Park
Republic of Korea
In situ forming hydrogels have been studied as injectable
drug delivery carrier for the controlled release of bioactive molecules,
including therapeutic peptides, proteins, and nucleic acids. Recently,
a number of studies on these hydrogel systems are focused on localized
delivery vehicle for tissue engineering which can effectively carry
cell-signaling molecules. Heparin is well known to have the binding
affinity with a number of biologically important proteins such as
growth factors and cytokines, thereby controlling cellular behaviors.
Herein, we present an in situ forming heparin conjugated
PLGA-PEG-PLGA hydrogels as bioactive scaffolds for tissue engineering
and drug delivery. Heparin-conjugated hydrogels were simply prepared
via Michael-type addition between thiolated heparin and PLGA-PEG-PLGA
diacrylate. The thiolated heparin and PLGA-PEG-PLGA diacrylate were
characterized including physico-chemical properties and biological
activities, respectively. Phase diagram of hydrogels was recorded
by vial tilting method and heparin release study from the hydrogels
was performed in vitro. Obtained results demonstrated that
in situ forming heparin-conjugated hydrogels can be suggested
as bioactive scaffolds for tissue engineering and drug delivery including
controlled release of growth factors. Acknowledgement: This work was
supported by a grant from Nano-biotechnology Project (Regenomics),
Ministry of Science & Technology, Republic of Korea (B020214).
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