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911.
Fluorescein isothiocyanate (FITC), a fluorescent probe, is coupled to amphiphilic monomethoxy poly(ethylene glycol)‐block‐poly(ε‐caprolactone) (mPEG‐PCL) copolymers. FITC‐labeled mPEG‐PCL copolymers self‐assemble into micelles through the solvent evaporation method. The cellular internalization is examined using fluorescence microscopy on incubation of NIH‐3T3 fibroblasts with micelles or free FITC solution. The effect of the hydrophilic/hydrophobic ratio on the endocytosis mechanisms is evaluated by fluorescence microscopy on culturing of human hepatoblastoma cells and human umbilical vein endothelial cells, individually, mixed with the micelles holding the same parameters including micelle size, shape, and surface charges.

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912.

?‐Caprolactone and glycolide were copolymerized in bulk at 100, 120 or 140°C. When tetra(ethylene glycol) was used as coinitiator, a preferential formation of alternating triads was observed. This tendency was surprisingly favored at the higher temperature, and thus, cannot be explained by a general equilibration (transesterification) process. In the absence of a coinitiator the tendency towards alternating sequences was less pronounced. The polymerization mechanism is discussed.  相似文献   
913.
Fully biodegradable micro/nano-composite resins were prepared by reinforcing soy protein concentrate (SPC) with micro/nano-fibrillated cellulose (MFC) and then blending with gellan. The composite resins showed excellent mechanical and physical properties under testing conditions. Due to the high aspect ratio of MFC, excellent mechanical properties of MFC and MFC/SPC interfacial properties, the SPC (100 parts) reinforced with glycerol (1.5 parts) and MFC (40 parts) showed fracture stress of 88.2 MPa and Young's modulus of about 4.1 GPa, which are higher than those of many conventional petroleum-based plastics. MFC reinforced SPC composite resins were then further modified by blending with gellan to obtain further improvement in fracture stress and Young's modulus. SPC resin containing glycerol (1.5 parts), gellan (40 parts) and MFC (40 parts) had fracture stress of over 122 MPa and Young's modulus of about 5.8 GPa. Although the moisture sensitivity of the specimens was high, they have the potential to replace petroleum-based materials in many fields, particularly for indoor applications.  相似文献   
914.
Hyperbranched polyurethanes are synthesized using TDI, PCL diol, butanediol, and pentaerythritol (1–5 wt%) as the B4 reactant with and without the monoglyceride of sunflower oil. The biodegradation, physico‐mechanical, and thermal properties are found to be tailored by varying the percentage weight of the branching unit. An MTT/hemolytic assay and subcutaneous implantation in Wistar rats followed by cytokine/ALP assay and histopathology studies confirm a better biocompatibility of HBPU with MG than without MG. HBPU supports the proliferation of dermatocytes with no toxic effect in major organs, in addition the in vitro degraded products are non‐toxic. Cell adherence and proliferation endorse the bio‐based HBPU as a prospective scaffold material in the niche of tissue engineering.

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在骨-器械界面建立和维持成熟骨是骨科植入材料长期成功的关键. 镁合金由于其生物可降解性、天然骨组织的力学相似性以及成骨潜力, 并且在体内不抑制间充质干细胞(hBMSCs)的成骨特性, 成为有前途的承重骨科植入物的候选材料. 但其高降解率和植入物相关感染的风险以及不佳的力学性能, 对其临床应用提出了巨大的挑战. 有限元分析方法能对复杂结构、形态、载荷和材料力学性能进行应力分析, 可有效地帮助临床医生了解镁合金植入器械的应力及生物力学性能.  相似文献   
920.
Glycerol polymers are attracting increased attention due to the diversity of polymer compositions and architectures available. This article provides a brief chronological review on the current status of these polymers along with representative examples of their use for biomedical applications. First, the underlying chemistry of glycerol that provides access to a range of monomers for subsequent polymerizations is described. Then, the various synthetic methodologies to prepare glycerol‐based polymers including polyethers, polycarbonates, polyesters, and so forth are reviewed. Next, several biomedical applications where glycerol polymers are being investigated including carriers for drug delivery, sealants or coatings for tissue repair, and agents possessing antibacterial activity are described. Fourth, the growing market opportunity for the use of polymers in medicine is described. Finally, the findings are concluded and summarized, as well as the potential opportunities for continued research efforts are discussed.

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