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用于碱性磷酸酶包封的海藻酸-羟丙基纤维素水凝胶微球。

Alginate-hydroxypropylcellulose hydrogel microbeads for alkaline phosphatase encapsulation.

机构信息

Faculty of Chemistry, Jagiellonian University , 30-060 Kraków, Ingardena 3 , Poland .

出版信息

J Microencapsul. 2014;31(1):68-76. doi: 10.3109/02652048.2013.805841. Epub 2013 Jul 8.

Abstract

There is a growing interest in using proteins as therapeutics agents. Unfortunately, they suffer from limited stability and bioavailability. We aimed to develop a new delivery system for proteins. ALP, a model protein, was successfully encapsulated in the physically cross-linked sodium alginate/hydroxypropylcellulose (ALG-HPC) hydrogel microparticles. The obtained objects had regular, spherical shape and a diameter of ∼4 µm, as confirmed by optical microscopy and SEM analysis. The properties of the obtained microbeads could be controlled by temperature and additional coating or crosslinking procedures. The slow, sustained release of ALP in its active form with no initial burst effect was observed for chitosan-coated microspheres at pH = 7.4 and 37 °C. Activity of ALP released from ALG/HPC microspheres was confirmed by the occurance of effectively induced mineralization. SEM and AFM images revealed formation of the interpenetrated three-dimensional network of mineral, originating from the microbeads' surfaces. FTIR and XRD analyses confirmed formation of hydroxyapatite.

摘要

人们越来越感兴趣地将蛋白质用作治疗剂。不幸的是,它们的稳定性和生物利用度有限。我们旨在开发一种新的蛋白质递送系统。ALP,一种模型蛋白,成功地封装在物理交联的海藻酸钠/羟丙基纤维素(ALG-HPC)水凝胶微球中。通过光学显微镜和 SEM 分析证实,所得到的物体具有规则的球形形状和约 4μm 的直径。通过温度和额外的涂层或交联过程可以控制所得微球的性质。在 pH = 7.4 和 37°C 下,壳聚糖涂层的微球观察到 ALP 以其活性形式缓慢、持续释放,没有初始突释效应。从 ALG/HPC 微球中释放的 ALP 的活性通过有效诱导矿化的发生得到证实。SEM 和 AFM 图像显示了源自微球表面的矿物质互穿三维网络的形成。FTIR 和 XRD 分析证实了羟基磷灰石的形成。

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