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海藻酸钙/葡聚糖甲基丙烯酰胺互穿网络珠粒作为蛋白质递送的保护载体。

Calcium alginate/dextran methacrylate IPN beads as protecting carriers for protein delivery.

机构信息

Department of Drug Chemistry and Technologies, Sapienza University of Rome, Piazzale Aldo Moro 5, 00185, Rome, Italy.

出版信息

J Mater Sci Mater Med. 2012 Jul;23(7):1715-22. doi: 10.1007/s10856-012-4644-0. Epub 2012 Apr 24.

DOI:10.1007/s10856-012-4644-0
PMID:22528076
Abstract

In the present study, mechanical and protein delivery properties of a system based on the interpenetration of calcium-alginate (Ca-Alg) and dextran-methacrylate (Dex-MA) networks are shown. Interpenetrated hydrogels beads were prepared by means of the alginate chains crosslinking with calcium ions, followed by the exposure to UV light that allows the Dex-MA network formation. Optical microscope analysis showed an average diameter of the IPN beads (Ca-Alg/Dex-MA) of 2 mm. This dimension was smaller than that of Ca-Alg beads because of the Dex-MA presence. Moreover, the strength of the IPN beads, and of their corresponding hydrogels, was influenced by the Dex-MA concentration and the crosslinking time. Model proteins (BSA and HRP) were successfully entrapped into the beads and released at a controlled rate, modulated by changing the Dex-MA concentration. The enzymatic activity of HRP released from the beads was maintained. These novel IPN beads have great potential as protein delivery system.

摘要

在本研究中,展示了基于钙-海藻酸钠 (Ca-Alg) 和葡聚糖甲基丙烯酰胺 (Dex-MA) 网络互穿的系统的机械和蛋白质输送性能。通过用钙离子交联海藻酸盐链来制备互穿水凝胶珠,然后暴露于允许 Dex-MA 网络形成的紫外线下。光学显微镜分析显示,IPN 珠(Ca-Alg/Dex-MA)的平均直径为 2mm。由于 Dex-MA 的存在,该尺寸小于 Ca-Alg 珠的尺寸。此外,IPN 珠及其相应水凝胶的强度受 Dex-MA 浓度和交联时间的影响。模型蛋白(BSA 和 HRP)成功地包埋在珠中,并通过改变 Dex-MA 浓度以控制速率释放。从珠中释放的 HRP 的酶活性得以保持。这些新型的 IPN 珠具有作为蛋白质输送系统的巨大潜力。

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Recent developments in liposomes, microparticles and nanoparticles for protein and peptide drug delivery.脂质体、微粒和纳米粒在蛋白质和肽类药物传递中的最新进展。
Peptides. 2010 Jan;31(1):184-93. doi: 10.1016/j.peptides.2009.10.002. Epub 2009 Oct 9.
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