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阿仑膦酸钠从复合微粒中的反馈控制释放。

Feedback-Controlled Release of Alendronate from Composite Microparticles.

作者信息

Matrali Sofia S H, Ghag Anita K

机构信息

School of Chemical Engineering, University of Birmingham, Birmingham B15 2TT, UK.

出版信息

J Funct Biomater. 2020 Jul 1;11(3):46. doi: 10.3390/jfb11030046.

DOI:10.3390/jfb11030046
PMID:32630317
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7564771/
Abstract

Extended bone fractures or fractures coexisting with bone disorders can lead to non-unions where surgical intervention is required. Composite drug delivery systems are being used increasingly more in order to treat such defects locally. Alendronate (ALD), a bisphosphonate extensively used in clinical practice to treat conditions, such as osteoporosis, has been shown to assist bone fracture healing through its antiresorptive capacity. This study reports the development of a polymeric composite system for the in situ delivery of ALD, which possesses enhanced encapsulation efficiency (EE%) and demonstrates controlled release over a 70-day period. ALD and calcium phosphate (CaP) were incorporated within poly (lactic-co-glycolic acid) (PLGA) microspheres, giving rise to a 70% increase in EE% compared to a control system. Finally, a preliminary toxicological evaluation demonstrated a positive effect of the system on pre-osteoblastic cells over 72 h.

摘要

长骨骨折或与骨疾病并存的骨折可导致骨不连,此时需要进行手术干预。为了局部治疗此类缺损,复合药物递送系统的应用越来越广泛。阿仑膦酸盐(ALD)是一种在临床实践中广泛用于治疗骨质疏松症等病症的双膦酸盐,已显示出通过其抗吸收能力促进骨折愈合。本研究报道了一种用于原位递送ALD的聚合物复合系统的开发,该系统具有更高的包封效率(EE%),并在70天内实现控释。将ALD和磷酸钙(CaP)掺入聚(乳酸-乙醇酸)(PLGA)微球中,与对照系统相比,EE%提高了70%。最后,初步毒理学评估表明该系统在72小时内对前成骨细胞有积极作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/684f/7564771/85f07be756c5/jfb-11-00046-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/684f/7564771/ada879fc6335/jfb-11-00046-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/684f/7564771/77f2016a99a8/jfb-11-00046-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/684f/7564771/fd02d33ca1ff/jfb-11-00046-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/684f/7564771/e34c997f4734/jfb-11-00046-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/684f/7564771/3c11e94da5bb/jfb-11-00046-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/684f/7564771/d27876b85679/jfb-11-00046-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/684f/7564771/85f07be756c5/jfb-11-00046-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/684f/7564771/ada879fc6335/jfb-11-00046-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/684f/7564771/77f2016a99a8/jfb-11-00046-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/684f/7564771/fd02d33ca1ff/jfb-11-00046-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/684f/7564771/e34c997f4734/jfb-11-00046-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/684f/7564771/3c11e94da5bb/jfb-11-00046-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/684f/7564771/d27876b85679/jfb-11-00046-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/684f/7564771/85f07be756c5/jfb-11-00046-g007.jpg

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