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采用三种不同乳化技术制备的可生物降解载胰岛素 PLGA 微球:用于软骨组织工程的研究。

Biodegradable insulin-loaded PLGA microspheres fabricated by three different emulsification techniques: investigation for cartilage tissue engineering.

机构信息

Berlin-Brandenburg Center for Regenerative Therapies, Department of Rheumatology and Clinical Immunology, Charité-Universitätsmedizin Berlin, Berlin, Germany.

出版信息

Acta Biomater. 2011 Apr;7(4):1485-95. doi: 10.1016/j.actbio.2010.12.014. Epub 2010 Dec 17.

Abstract

Growth, differentiation and migration factors facilitate the engineering of tissues but need to be administered with defined gradients over a prolonged period of time. In this study insulin as a growth factor for cartilage tissue engineering and a biodegradable PLGA delivery device were used. The aim was to investigate comparatively three different microencapsulation techniques, solid-in-oil-in-water (s/o/w), water-in-oil-in-water (w/o/w) and oil-in-oil-in-water (o/o/w), for the fabrication of insulin-loaded PLGA microspheres with regard to protein loading efficiency, release and degradation kinetics, biological activity of the released protein and phagocytosis of the microspheres. Insulin-loaded PLGA microspheres prepared by all three emulsification techniques had smooth and spherical surfaces with a negative zeta potential. The preparation technique did not affect particle degradation nor induce phagocytosis by human leukocytes. The delivery of structurally intact and biologically active insulin from the microspheres was shown using circular dichroism spectroscopy and a MCF7 cell-based proliferation assay. However, the insulin loading efficiency (w/o/w about 80%, s/o/w 60%, and o/o/w 25%) and the insulin release kinetics were influenced by the microencapsulation technique. The results demonstrate that the w/o/w microspheres are most appropriate, providing a high encapsulation efficiency and low initial burst release, and thus these were finally used for cartilage tissue engineering. Insulin released from w/o/w PLGA microspheres stimulated the formation of cartilage considerably in chondrocyte high density pellet cultures, as determined by increased secretion of proteoglycans and collagen type II. Our results should encourage further studies applying protein-loaded PLGA microspheres in combination with cell transplants or cell-free in situ tissue engineering implants to regenerate cartilage.

摘要

生长、分化和迁移因子有助于组织工程的构建,但需要在较长时间内以定义的梯度方式进行给药。在这项研究中,使用胰岛素作为软骨组织工程的生长因子和可生物降解的 PLGA 递送装置。目的是比较三种不同的微囊化技术,即固-油-水(s/o/w)、水-油-水(w/o/w)和油-油-水(o/o/w),用于制备载有胰岛素的 PLGA 微球,考察其蛋白载量效率、释放和降解动力学、释放蛋白的生物活性以及微球的吞噬作用。通过所有三种乳化技术制备的载有胰岛素的 PLGA 微球具有光滑的球形表面和负的 ζ 电位。制备技术不影响颗粒降解,也不会诱导人白细胞吞噬。使用圆二色性光谱和 MCF7 细胞增殖测定法证实了微球从结构完整和具有生物活性的胰岛素中释放。然而,胰岛素的载量效率(w/o/w 约 80%,s/o/w 60%,o/o/w 25%)和胰岛素释放动力学受到微囊化技术的影响。结果表明,w/o/w 微球最合适,具有较高的包封效率和较低的初始突释,因此最终用于软骨组织工程。w/o/w PLGA 微球释放的胰岛素在软骨细胞高密度微球培养中显著刺激软骨形成,这可通过增加糖胺聚糖和 II 型胶原的分泌来确定。我们的结果应该鼓励进一步研究应用载有蛋白质的 PLGA 微球与细胞移植或无细胞原位组织工程植入物相结合,以再生软骨。

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