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用于提高α-淀粉酶稳定性的壳聚糖-海藻酸盐反相聚电解质复合物:优化及理化特性表征

Reversed chitosan-alginate polyelectrolyte complex for stability improvement of alpha-amylase: optimization and physicochemical characterization.

作者信息

Sankalia Mayur G, Mashru Rajashree C, Sankalia Jolly M, Sutariya Vijay B

机构信息

Center of Relevance and Excellence in Novel Drug Delivery Systems, Pharmacy Department, The M. S. University of Baroda, Vadodara 390-002, India.

出版信息

Eur J Pharm Biopharm. 2007 Feb;65(2):215-32. doi: 10.1016/j.ejpb.2006.07.014. Epub 2006 Aug 12.

Abstract

The present work explores, using response surface methodology, the main and interaction effects of some process variables on the preparation of a reversed chitosan-alginate polyelectrolyte complex (PEC) with entrapped alpha-amylase for stability improvement. A 3(3) full factorial design was used to investigate the effect of the chitosan and alginate concentrations and hardening time on the percent entrapment, time required for 50% (T(50)) and 90% (T(90)) enzyme release, and particle size. The beads were prepared by dropping chitosan containing alpha-amylase into a sodium alginate solution without any salt. The in vitro enzyme release profile of the beads was fitted to various release kinetics models to study the release mechanism. A topographical characterization was carried out using scanning electron microscopy (SEM), and the entrapment was confirmed using Fourier transform infrared (FTIR) spectroscopy and differential scanning calorimetry (DSC). Stability testing was carried out according to the International Conference on Harmonization (ICH) guidelines for zones III and IV. Beads prepared using 2.5%w/v chitosan and 3%w/v sodium alginate with a hardening time of 60 min had more than 90% entrapment and a T(90) value greater than 48 min. Moreover, the shelf-life of the enzyme-loaded beads was found to increase to 3.68 years, compared with 0.99 years for the conventional formulation. It can be inferred that the proposed methodology can be used to prepare a reversed PEC of chitosan and alginate with good mechanical strength, provided both the reactants are in a completely ionized form at the time of the reaction. Proper selection of the reaction pH, polymer concentration and hence charge density, and hardening time is important and determines the characteristics of the PEC.

摘要

本研究采用响应面法,探究了一些工艺变量对制备包埋α-淀粉酶的壳聚糖-海藻酸钠反向聚电解质复合物(PEC)以提高稳定性的主要和交互作用。采用3(3)全因子设计,研究壳聚糖和海藻酸钠浓度以及硬化时间对包封率、50%(T(50))和90%(T(90))酶释放所需时间以及粒径的影响。通过将含有α-淀粉酶的壳聚糖滴入无盐的海藻酸钠溶液中来制备微球。将微球的体外酶释放曲线拟合到各种释放动力学模型,以研究释放机制。使用扫描电子显微镜(SEM)进行形貌表征,并使用傅里叶变换红外光谱(FTIR)和差示扫描量热法(DSC)确认包封情况。根据国际协调会议(ICH)针对III区和IV区的指南进行稳定性测试。使用2.5%w/v壳聚糖和3%w/v海藻酸钠且硬化时间为60分钟制备的微球包封率超过90%,T(90)值大于48分钟。此外,发现载酶微球的保质期增加到3.68年,而传统制剂为0.99年。可以推断,所提出的方法可用于制备具有良好机械强度的壳聚糖和海藻酸钠反向PEC,前提是两种反应物在反应时均处于完全电离形式。正确选择反应pH、聚合物浓度以及电荷密度和硬化时间很重要,并且决定了PEC的特性。

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