首页> 外文期刊>Journal of Polymer Science, Part A. Polymer Chemistry >Synthesis and characterization of novel biodegradable unsaturated poly(ester amide)/poly(ethylene glycol) diacrylate hydrogels
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Synthesis and characterization of novel biodegradable unsaturated poly(ester amide)/poly(ethylene glycol) diacrylate hydrogels

机译:新型可生物降解的不饱和聚(酯酰胺)/聚(乙二醇)二丙烯酸酯水凝胶的合成与表征

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A series of novel biodegradable hydrogels were designed and synthesized from four types of unsaturated poly(ester amide) (UPEA) and poly(ethylene glycol) diacrylate (PEG-DA) precursors by UV photocrosslinking. These newly synthesized biodegradable UPEA/PEG-DA hydrogels were characterized by their gel fraction (G(f)), equilibrium swelling ratio (Q(eq)), compressive modulus, and interior morphology. The effect of the precursor feed ratio (UPEAs to PEG-DA) on the properties of the hydrogels was also studied. The incorporation of UPEA polymers into the PEG-DA hydrogels increased their hydrophobicity, crosslinking density (denser network), and mechanical strength (higher compressive modulus) but reduced Qeq. When different types of UPEA precursors were coupled with PEG-DA at the same feed ratio (20 wt %), the resulting hydrogels had similar Q(eq) values and porous three-dimensional interior morphologies but different Gf and compressive modulus values. These differences in the hydrogel properties were correlated to the chemical structures of the UPEA precursors; that is, the different locations of the > C=C < double bonds in individual UPEA segments resulted in their different reactivities toward PEG-DA to form hydrogels. (c) 2005 Wiley Periodicals, Inc.
机译:通过紫外光交联,从四种不饱和聚(酰胺)(UPEA)和聚(乙二醇)二丙烯酸酯(PEG-DA)前体中设计并合成了一系列新型的可生物降解水凝胶。这些新合成的可生物降解的UPEA / PEG-DA水凝胶的特征在于其凝胶分数(G(f)),平衡溶胀率(Q(eq)),压缩模量和内部形态。还研究了前体进料比(UPEA与PEG-DA)对水凝胶性能的影响。将UPEA聚合物掺入PEG-DA水凝胶可提高其疏水性,交联密度(密度网络)和机械强度(较高的压缩模量),但降低了Qeq。当以相同的进料比(20 wt%)将不同类型的UPEA前体与PEG-DA偶联时,所得水凝胶具有相似的Q(eq)值和多孔三维内部形貌,但具有不同的Gf和压缩模量值。水凝胶性质的这些差异与UPEA前体的化学结构有关。也就是说,各个UPEA片段中> C = C <双键的不同位置导致它们对PEG-DA的反应性不同,从而形成水凝胶。 (c)2005年Wiley Periodicals,Inc.

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