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玉米醇溶蛋白-壳聚糖复合超细纤维的制备、胃黏附性、溶胀和降解。

Fabrication, gastromucoadhesivity, swelling, and degradation of zein-chitosan composite ultrafine fibers.

机构信息

Dept. of Food Engineering, Faculty of Engineering, King Mongkut's Univ. of Technology Thonburi, 126 Pracha u-tit Rd., Tungkru, Bangkok 10140, Thailand.

出版信息

J Food Sci. 2013 Jun;78(6):N926-35. doi: 10.1111/1750-3841.12126. Epub 2013 Apr 29.

Abstract

Fabrication, via electrospinning, and characterization of an ultrafine structure architected from a blend of hydrophobic zein and hydrophilic chitosan (CS) were conducted. Poly(ethylene oxide) (PEO) and nonionic surfactant, namely, Tween 40, were employed to improve the electrospinnability of the blend, while ethanol was used as a solvent for zein. The effects of ethanol (EtOH) concentration (85% and 90%) and ratio of zein/PEO/CS (95/2.5/2.5 and 87.5/10/2.5) on the fiber morphology as well as gastromucoadhesivity against porcine stomach mucosa were then investigated; polymer-mucosa adhesion was also investigated via Fourier-transform infrared spectroscopy. Swelling and degradation of the composite ultrafine fibers were investigated under 2 simulated gastric conditions, namely, at pH 2 without pepsin and at pH 1.2 with pepsin. Using 85% EtOH as a solvent for zein resulted in a spider-web-like morphology; the maximum detachment force (MDF), which is an indirect indicator of the gastromucoadhesivity was nevertheless higher. Zein-based ultrafine fibers exhibited higher MDF than the zein-PEO-CS composite; however, the cohesiveness of the composite fibers was higher. FTIR spectroscopic results indicated molecular interactions between the composite fibers and mucin functional groups. Swelling of the composite ultrafine fibers in simulated gastric fluid (SGF) at pH 2 without pepsin was not different from that in SGF at pH 1.2 with pepsin. Nevertheless, degradation of the composite fibers in SGF at pH 2 without pepsin was much less than that in SGF at pH 1.2 with pepsin; only 20% degradation was noted in the former case.

摘要

通过静电纺丝制备和表征了由疏水性玉米醇溶蛋白和亲水性壳聚糖(CS)的混合物构成的超细结构。聚环氧乙烷(PEO)和非离子表面活性剂,即吐温 40,被用于改善混合物的可纺性,而乙醇则用作玉米醇溶蛋白的溶剂。然后研究了乙醇(EtOH)浓度(85%和 90%)和玉米醇溶蛋白/PEO/CS 比例(95/2.5/2.5 和 87.5/10/2.5)对纤维形态以及对猪胃粘膜的胃粘膜粘附性的影响;还通过傅里叶变换红外光谱研究了聚合物-粘膜的粘附性。在 2 种模拟胃条件下研究了复合超细纤维的溶胀和降解,即在没有胃蛋白酶的 pH 2 和有胃蛋白酶的 pH 1.2。使用 85%的 EtOH 作为玉米醇溶蛋白的溶剂会导致蜘蛛网状形态;然而,间接指示胃粘膜粘附性的最大分离力(MDF)更高。基于玉米醇溶蛋白的超细纤维的 MDF 高于玉米醇溶蛋白-PEO-CS 复合材料;然而,复合纤维的内聚性更高。FTIR 光谱结果表明复合纤维与粘蛋白功能基团之间存在分子相互作用。在 pH 2 无胃蛋白酶的模拟胃液(SGF)中,复合超细纤维的溶胀与在 pH 1.2 有胃蛋白酶的 SGF 中的溶胀没有区别。然而,在 pH 2 无胃蛋白酶的 SGF 中,复合纤维的降解程度远小于在 pH 1.2 有胃蛋白酶的 SGF 中的降解程度;在前者中仅观察到 20%的降解。

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