| Literature DB >> 19603795 |
Yin Fun Poon1, Ye Cao, Yabin Zhu, Zaher M A Judeh, Mary B Chan-Park.
Abstract
Poly(malic acid) is water-soluble, functionalizable, and biodegradable, making it attractive as a precursor of hydrogels for biomedical applications. However, homopoly(malic acid), with pK(1/2) of 4.3, is too acidic for biocompatibility. To overcome the acidity, we have synthesized beta-malic acid-containing poly(ethylene glycol) dimethacrylate (PEGMAc) with pK(a) of 5.02. Solutions of methacrylated O-carboxymethylchitosan (OCMCS), PEGMAc, and poly(ethylene glycol) diacrylate (PEGDA; 7:7:86 and 6:20:74 (w/w/w)) in water (80%) have near neutral pHs (6.8-6.9). These solutions form firm hydrogels when photopolymerized. These are referred to as O7-PEGMAc7-B86 and O6-PEGMAc20-B74 (where the numerals refer to the weight content of each component, O is OCMCS and B is PEGDA added to make blend). The carboxyl groups in PEGMAc permit the surface grafting of hydrogels with Arg-Gly-Asp (RGD). The cytocompatibilities of smooth muscle cells (SMCs) on RGD-grafted hydrogels were studied. From the tetrazolium salt reduction assay, O6-PEGMAc20-B74 was found to have significantly better 10th day cytocompatibility compared to hydrogels containing lower or no PEGMAc. These gels degrade upon hydrolysis releasing malic acid, PEG and OCMCS. The increased cell compatibility of O6-PEGMAc20-B74 is possibly due to increased surface RGD content and near neutral pH even during biodegradation. Our novel PEGMAc-modified blends are a promising functionalizable biodegradable hydrogel precursor providing improved cell proliferation.Entities:
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Year: 2009 PMID: 19603795 DOI: 10.1021/bm801367n
Source DB: PubMed Journal: Biomacromolecules ISSN: 1525-7797 Impact factor: 6.988