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同步辐射X射线显微计算机断层扫描揭示微球中表面活性剂的三维分布

Three dimensional distribution of surfactant in microspheres revealed by synchrotron radiation X-ray microcomputed tomography.

作者信息

Wu Li, Wang Manli, Singh Vikramjeet, Li Haiyan, Guo Zhen, Gui Shuangying, York Peter, Xiao Tiqiao, Yin Xianzhen, Zhang Jiwen

机构信息

Center for Drug Delivery Systems, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201210, China.

School of Pharmaceutical Sciences, Anhui University of Chinese Medicine, Hefei 230038, China.

出版信息

Asian J Pharm Sci. 2017 Jul;12(4):326-334. doi: 10.1016/j.ajps.2017.02.001. Epub 2017 Feb 15.

DOI:10.1016/j.ajps.2017.02.001
PMID:32104343
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7032157/
Abstract

This study investigated the formulation mechanism of microspheres via internal surfactant distribution. Eudragit L100 based microspheres loaded with bovine serum albumin were prepared by solid in oil in oil emulsion solvent evaporation method using acetone and liquid paraffin system containing sucrose stearate as a surfactant. The fabricated microspheres were evaluated for encapsulation efficiency, particle size, production yield, and release characteristics. The internal structures of microspheres were characterized using synchrotron radiation X-ray microcomputed tomography (SR-µCT). The enhanced contrast made the sucrose stearate distinguished from Eudragit to have its three dimensional (3D) distribution. Results indicated that the content and concentration determined the state of sucrose stearate and had significant influences on the release kinetics of protein. The dispersity of sucrose stearate was the primary factor that controlled the structure of the microspheres and further affected the encapsulation efficiency, effective drug loading, as well as release behavior. In conclusion, the 3D internal distribution of surfactant in microspheres and its effects on protein release behaviors have been revealed for the first time. The highly resolved 3D architecture provides new evidence for the deep understanding of the microsphere formation mechanism.

摘要

本研究通过内部表面活性剂分布研究了微球的形成机制。以含有蔗糖硬脂酸酯作为表面活性剂的丙酮和液体石蜡体系,采用油包油乳液溶剂蒸发法制备了负载牛血清白蛋白的基于Eudragit L100的微球。对制备的微球进行了包封率、粒径、产率和释放特性评估。使用同步辐射X射线微计算机断层扫描(SR-µCT)对微球的内部结构进行了表征。增强的对比度使蔗糖硬脂酸酯与Eudragit区分开来,从而得到其三维(3D)分布。结果表明,含量和浓度决定了蔗糖硬脂酸酯的状态,并对蛋白质的释放动力学有显著影响。蔗糖硬脂酸酯的分散性是控制微球结构的主要因素,进而影响包封率、有效载药量以及释放行为。总之,首次揭示了微球中表面活性剂的三维内部分布及其对蛋白质释放行为的影响。高度解析的三维结构为深入理解微球形成机制提供了新的证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2221/7032157/fdfefae9ea4b/ajps427-fig-0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2221/7032157/70bd63d04998/ajps427-ga-5001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2221/7032157/c45526e7396c/ajps427-fig-0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2221/7032157/f62d6bb397ab/ajps427-fig-0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2221/7032157/14c78b2c4883/ajps427-fig-0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2221/7032157/df650f51c9a4/ajps427-fig-0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2221/7032157/6fc0a5f9a76f/ajps427-fig-0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2221/7032157/fdfefae9ea4b/ajps427-fig-0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2221/7032157/70bd63d04998/ajps427-ga-5001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2221/7032157/c45526e7396c/ajps427-fig-0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2221/7032157/f62d6bb397ab/ajps427-fig-0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2221/7032157/14c78b2c4883/ajps427-fig-0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2221/7032157/df650f51c9a4/ajps427-fig-0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2221/7032157/6fc0a5f9a76f/ajps427-fig-0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2221/7032157/fdfefae9ea4b/ajps427-fig-0006.jpg

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