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• W1522382340 endingPage "3882" @default.
• W1522382340 startingPage "3872" @default.
• W1522382340 abstract "Tissue engineering strategies can be applied to enhancing osseous integration of soft tissue grafts during ligament reconstruction. Ligament rupture results in a hemarthrosis, an acute intra-articular bleed rich in osteogenic human mesenchymal stem cells (hMSCs). With the aim of identifying an appropriate biomaterial with which to combine hemarthrosis fluid-derived hMSCs (HF-hMSCs) for therapeutic application, this work has investigated the biocompatibility of microparticles manufactured from two forms of poly(D,L-lactic-co-glycolic acid) (PLGA), one synthesized with equal monomeric ratios of lactic acid to glycolic acid (PLGA 50:50) and the other with a higher proportion of lactic acid (PLGA 85:15) which confers a longer biodegradation time. The surfaces of both types of microparticles were functionalized by plasma polymerization with allylamine to increase hydrophilicity and promote cell attachment. HF-hMSCs attached to and spread along the surface of both forms of PLGA microparticle. The osteogenic response of HF-hMSCs was enhanced when cultured with PLGA compared with control cultures differentiated on tissue culture plastic and this was independent of the type of polymer used. We have demonstrated that surface engineered PLGA microparticles are an appropriate biomaterial for combining with HF-hMSCs and the selection of PLGA is relevant only when considering the biodegradation time for each biomedical application." @default.
• W1522382340 created "2016-06-24" @default.
• W1522382340 creator A5007355607 @default.
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• W1522382340 creator A5023518920 @default.
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• W1522382340 date "2013-12-20" @default.
• W1522382340 modified "2023-10-15" @default.
• W1522382340 title "Biocompatibility and enhanced osteogenic differentiation of human mesenchymal stem cells in response to surface engineered poly(d,l-lactic-co-glycolic acid) microparticles" @default.
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• W1522382340 doi "https://doi.org/10.1002/jbm.a.35063" @default.
• W1522382340 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24339408" @default.
• W1522382340 hasPublicationYear "2013" @default.
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