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Controlled PLGA degradation within Calcium Phosphate Cement for Bone Tissue Engineering

机译:骨组织工程磷酸钙水泥内的受控PLGA降解

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Calcium phosphate cements (CPCs) are increasingly used as bone substitute materials. Porosity and pore size of CPC scaffolds play a critical role in bone formation. CPCs present intrinsic nanoporosity that enables fluid flow inside the composite but it is too small for tissue ingrowth. Macroporosity is an important parameter to enhance tissue ingrowth and CPC degradation. PLGA (Poly (D,L-lactic-co-glycolic) acid) microspheres can be included in CPC and after degradation a porous CPC scaffold is obtained. The loss of mechanical strength due to the degradation of PLGA microspheres is ideally compensated by bone ingrowth inside the CPC scaffold. It has been described that PLGA degradation is affected, among other factors, by the molecular weight of the polymer. In this study different PLGA molecular weights and different end terminations are tested to fine tune polymer degradation in CPC. To study the polymer degradation a new High Pressure Liquid Chromatography (HPLC) method to quantify lactic and glycolic acid monomers has been developed.
机译:磷酸钙水泥(CPC)越来越多地用作骨替代材料。 CPC支架的孔隙度和孔径在骨形成中发挥着关键作用。 CPC存在内在的纳米型纳米光度,使得复合材料内的流体流动,但是对于组织成长而言,它太小。宏观度是增强组织凸起和CPC劣化的重要参数。 PLGA(聚(D,L-乳酸二乙醇酸)酸)微球可以包含在CPC中,并在降解后获得多孔CPC支架。由于PLGA微球的降解而导致的机械强度的损失理想地通过CPC支架内的骨骼注入来补偿。已经描述了通过聚合物的分子量影响PLGA降解受到其他因素的影响。在该研究中,在CPC中测试不同的PLGA分子量和不同的端终止剂以微调聚合物降解。为了研究聚合物降解,已经开发出了量化乳酸和乙醇酸单体的新型高压液相色谱(HPLC)方法。

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