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藻酸盐-透明质酸微球作为一种有前途的细胞递送方法用于肾脏再生的体外和体内生物相容性研究。

Examination of In vitro and In vivo biocompatibility of alginate-hyaluronic acid microbeads As a promising method in cell delivery for kidney regeneration.

机构信息

Institute of Tissue Regeneration, Soonchunhyang University366-1, Ssangyong-dong, Cheonan, ChungCheongNam-Do 330-090, Republic of Korea.

Department of Regenerative Medicine, College of Medicine, Soonchunhyang University 366-1, Ssangyong-dong, Cheonan, ChungCheongNam-Do 330-090, Republic of Korea.

出版信息

Int J Biol Macromol. 2017 Dec;105(Pt 1):143-153. doi: 10.1016/j.ijbiomac.2017.07.019. Epub 2017 Jul 8.

DOI:10.1016/j.ijbiomac.2017.07.019
PMID:28698077
Abstract

In this study, alginate (ALG) and alginate-hyaluronic acid (ALG-HA) injectable microbeads, with the purpose of delivering stem cells for tissue engineering, were prepared by a spraying method into a CaCl solution that shows high porosity for the exchange of nutrition and waste. In addition, the size distribution and surface morphology was investigated using optical and scanning electron microscopy, respectively. The chemical structural properties of the ALG-HA microbeads were examined by Fourier transform infrared spectroscopy. The biocompatibility of ALG and ALG-HA microbeads was examined in vitro. Rat bone marrow stem cells were encapsulated in microbeads to investigate cell release, cell viability, proliferation, and secretion of growth factors such as VEGF and PDGF. Growth factors were released for the 21day experimental period. Cells were found to be released from the microbeads after 7days. Furthermore, the in vivo biocompatibility of ALG-HA microbeads was examined using microbeads without cell encapsulation in the kidney capsule, in order to assess the foreign body reaction and inflammatory response, for 14days. The desired in vivo response to ALG-HA microbeads hydrogel makes it an exquisite candidate for subcapsular cell and drug delivery to kidney tissue.

摘要

在这项研究中,通过喷雾法将藻酸盐(ALG)和藻酸盐-透明质酸(ALG-HA)可注射微球制备到 CaCl2 溶液中,该溶液具有高孔隙率,可用于营养物质和废物的交换。此外,分别使用光学显微镜和扫描电子显微镜研究了微球的粒径分布和表面形貌。通过傅里叶变换红外光谱法检查了 ALG-HA 微球的化学结构性质。体外研究了 ALG 和 ALG-HA 微球的生物相容性。将大鼠骨髓干细胞包封在微球中,以研究细胞释放、细胞活力、增殖以及生长因子(如 VEGF 和 PDGF)的分泌情况。在 21 天的实验期间释放生长因子。发现细胞在 7 天后从微球中释放出来。此外,为了评估异物反应和炎症反应,将未包封细胞的 ALG-HA 微球在肾包膜中进行体内生物相容性研究,为期 14 天。ALG-HA 微球水凝胶的理想体内反应使其成为肾组织细胞和药物亚细胞递送的理想候选物。

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