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角叉菜胶和 ι-卡拉胶的季铵化——两性多糖的特性和性质。

Cationization of kappa- and iota-carrageenan--Characterization and properties of amphoteric polysaccharides.

机构信息

Departamento de Química Orgánica - CIHIDECAR (CONICET-UBA), Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Pabellón 2, 1428EGA Buenos Aires, Argentina.

PINMATE - Departamento de Industrias, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, 1428EGA Buenos Aires, Argentina; Cátedra de Tecnología Farmacéutica II, Departamento de Tecnología Farmacéutica, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Junín 956, 1113AAD Buenos Aires, Argentina.

出版信息

Carbohydr Polym. 2015 Aug 1;126:70-7. doi: 10.1016/j.carbpol.2015.02.053. Epub 2015 Mar 5.

Abstract

Commercial kappa- and iota carrageenans were cationized with 3-chloro-2-hydroxypropyltrimethylammonium chloride in aqueous sodium hydroxide solution. For kappa-carrageenan three derivatives with different degrees of substitution were obtained. Native and amphoteric kappa-carrageenans were characterized by NMR and infrared spectroscopy, scanning electron and atomic force microscopy; methanolysis products were studied by electrospray ionization mass spectrometry. Young moduli and the strain at break of films, differential scanning calorimetry, rheological and flocculation behavior were also evaluated; the native and the amphoteric derivatives showed different and interesting properties. Cationization of iota-carrageenan was more difficult, indicating as it was previously observed for agarose, that substitution starts preferentially on the 2-position of 3,6-anhydrogalactose residues; in iota-carrageenan this latter unit is sulfated.

摘要

商业用κ-和 ι-卡拉胶在氢氧化钠水溶液中用 3-氯-2-羟丙基三甲基氯化铵进行季铵化。对于 κ-卡拉胶,得到了三种不同取代度的衍生物。天然和两性 κ-卡拉胶通过 NMR 和红外光谱、扫描电子显微镜和原子力显微镜进行了表征;甲醇解产物通过电喷雾电离质谱进行了研究。还评估了薄膜的杨氏模量和断裂伸长率、差示扫描量热法、流变和絮凝行为;天然和两性衍生物表现出不同的有趣性质。ι-卡拉胶的季铵化更为困难,这表明正如以前在琼脂糖中观察到的那样,取代首先在 3,6-脱水半乳糖残基的 2-位开始;在 ι-卡拉胶中,后一种单元是硫酸化的。

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