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在较高pH值下用阳离子聚合物对β-乳球蛋白原纤维进行静电稳定化处理。

Electrostatic stabilization of β-lactoglobulin fibrils at increased pH with cationic polymers.

作者信息

Gilbert Jay, Campanella Osvaldo, Jones Owen G

机构信息

Purdue University , Department of Food Science, 745 Agriculture Mall Drive, West Lafayette, Indiana 47907, United States ;

出版信息

Biomacromolecules. 2014 Aug 11;15(8):3119-27. doi: 10.1021/bm500762u. Epub 2014 Jul 22.

Abstract

In order to improve the stability of β-lactoglobulin fibrils formed in acidic conditions to increased pH values (pH 3-7), formation of electrostatic complexes between fibrils and cationic polymers chitosan (CH), amine-terminated poly(ethylene glycol) (APEG), low molecular weight poly(ethylenimine) (LPEI), and high molecular weight poly(ethylenimine) (HPEI) was investigated by electrophoretic mobility, turbidimetry, and atomic force microscopy. Except for suspensions with APEG, addition of polycations increased ζ-potential values of the fibrils at pH 5, 6, and 7, verifying their interactions with fibrils. Maximal increase in ζ-potential at pH 7, indicating optimal electrostatic interactivity, occurred at concentrations (w/w) of 0.05, 0.01, and 0.01% (corresponding to 6.9, 50, and 4 μmol·kg(-1)) for CH, LPEI, and HPEI, respectively. Turbidity of fibril solutions at pH 5, indicating isoelectric instability, was decreased significantly with increasing concentration of CH, LPEI, and BPEI, but not with added APEG. Turbidity was increased at pH 7 with added polycation, except for suspensions containing ≥0.02% HPEI. Fibril length and resistance to aggregation, as observed by atomic force microscopy, were increased at pH 5 with increasing concentration of CH and LPEI, yet only HPEI was capable of maintaining the morphology of fibrils at pH 7. Calculated persistence lengths of the fibrils, as compared to pure fibrils at pH 3 (∼4 μm), were only slightly reduced at pH 5 with CH and at pH 7 with HPEI, but increased at pH 5 with LPEI and HPEI. Improvement in the stability of β-lactoglobulin fibrils at higher pH conditions with the addition of polycations will contribute to their potential utilization in packaging, food, and pharmaceutical applications.

摘要

为了提高在酸性条件下形成的β-乳球蛋白原纤维在pH值升高(pH 3 - 7)时的稳定性,通过电泳迁移率、比浊法和原子力显微镜研究了原纤维与阳离子聚合物壳聚糖(CH)、胺基封端的聚乙二醇(APEG)、低分子量聚乙烯亚胺(LPEI)和高分子量聚乙烯亚胺(HPEI)之间静电复合物的形成。除了含有APEG的悬浮液外,在pH 5、6和7时添加聚阳离子会增加原纤维的ζ电位值,证实了它们与原纤维的相互作用。在pH 7时ζ电位的最大增加表明静电相互作用最佳,CH、LPEI和HPEI的浓度(w/w)分别为0.05%、0.01%和0.01%(分别对应6.9、50和4 μmol·kg⁻¹)。在pH 5时原纤维溶液的浊度表明等电点不稳定,随着CH、LPEI和BPEI浓度的增加显著降低,但添加APEG时没有降低。在pH 7时添加聚阳离子会增加浊度,但含有≥0.02% HPEI的悬浮液除外。通过原子力显微镜观察,在pH 5时,随着CH和LPEI浓度的增加,原纤维长度和抗聚集性增加,但只有HPEI能够在pH 7时保持原纤维的形态。与pH 3时的纯原纤维(约4 μm)相比,计算得到的原纤维持久长度在pH 5时与CH、在pH 7时与HPEI作用下仅略有降低,但在pH 5时与LPEI和HPEI作用下增加。添加聚阳离子提高了β-乳球蛋白原纤维在较高pH条件下的稳定性,这将有助于其在包装、食品和制药应用中的潜在利用。

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