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通过竞争两种酶反应实现一步法制备包封细胞的双层微胶囊。

Competing two enzymatic reactions realizing one-step preparation of cell-enclosing duplex microcapsules.

机构信息

Div. of Chemical Engineering, Dept. of Materials Engineering Science, Graduate School of Engineering Science, Osaka University, 1-3 Machikaneyama-cho, Toyonaka, Osaka, 560-8531, Japan.

出版信息

Biotechnol Prog. 2013 Nov-Dec;29(6):1528-34. doi: 10.1002/btpr.1800. Epub 2013 Sep 12.

DOI:10.1002/btpr.1800
PMID:23955874
Abstract

The usefulness of cell-enclosing microcapsules in biomedical and biopharmaceutical fields is widely recognized. In this study, we developed a method enabling the preparation of microcapsules with a liquid core in one step using two enzymatic reactions, both of which consume H2 O2 competitively. The microcapsule membrane prepared in this study is composed of the hydrogel obtained from an alginate derivative possessing phenolic hydroxyl moieties (Alg-Ph). The cell-enclosing microcapsules with a hollow core were obtained by extruding an aqueous solution of Alg-Ph containing horseradish peroxidase (HRP), catalase, and cells into a co-flowing stream of liquid paraffin containing H2 O2 . Formation of the microcapsule membrane progressed from the surface of the droplets through HRP-catalyzed cross-linking of Ph moieties by consuming H2 O2 supplied from the ambient liquid paraffin. A hollow core structure was induced by catalase-catalyzed decomposition of H2 O2 resulting in the center region being at an insufficient level of H2 O2 . The viability of HeLa cells was 93.1% immediately after encapsulation in the microcapsules with about 250 µm diameter obtained from an aqueous solution of 2.5% (w/v) Alg-Ph, 100 units mL(-1) HRP, 9.1 × 10(4) units mL(-1) catalase. The enclosed cells grew much faster than those in the microparticles with a solid core. In addition, the thickness of microcapsule membrane could be controlled by changing the concentrations of HRP and catalase in the range of 13-48 µm. The proposed method could be versatile for preparing the microcapsules from the other polymer derivatives of carboxymetylcellulose and gelatin.

摘要

包封细胞的微胶囊在生物医药和生物制药领域的用途已得到广泛认可。在本研究中,我们开发了一种使用两步酶反应一步制备具有液相核的微胶囊的方法,这两步反应均消耗 H2O2。本研究中制备的微胶囊膜由具有酚羟基的海藻酸盐衍生物(Alg-Ph)得到的水凝胶组成。通过将含有辣根过氧化物酶(HRP)、过氧化氢酶和细胞的 Alg-Ph 水溶液挤出到含有 H2O2 的液体石蜡的共流中,获得具有中空核的包封细胞的微胶囊。微胶囊膜的形成从液滴的表面开始,通过 HRP 催化 Ph 部分与从周围液体石蜡供应的 H2O2 交联进行。过氧化氢酶催化 H2O2 的分解诱导中空核结构,导致中心区域的 H2O2 水平不足。用直径约为 250 µm 的 2.5%(w/v)Alg-Ph、100 单位 mL(-1) HRP 和 9.1×10(4)单位 mL(-1)过氧化氢酶的水溶液包封的 HeLa 细胞的活力在封装后立即为 93.1%。包封的细胞比具有实心核的微颗粒中的细胞生长得更快。此外,通过改变 HRP 和过氧化氢酶在 13-48 µm 范围内的浓度,可以控制微胶囊膜的厚度。该方法可用于从羧甲基纤维素和明胶的其他聚合物衍生物制备微胶囊。

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