Blend microspheres of poly (glycolide-co-ε-caprolactone) and ethyl cellulose for the controlled release of 5-fluorouracil

Q3 Engineering
Asma Ziane, Hichem Bakouri, Oum Khoukhi, Kaddour Guemra
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引用次数: 0

Abstract

In this present study, a series of copolymers with diverse compositions were produced using bulk ring-opening polymerization of glycolide and ?-caprolactone, using stannous(II) octoate as initiator. 1H, 13C NMR, and FTIR spectroscopy were used to characterize the resultant copolymers. After-wards, the oil/water emulsion evaporation technique was used to create blend microspheres of poly (glycolide-co-?-caprolactone) and ethylcellulose in order to investigate the controlled release of 5-fluorouracil, an anticancer drug. The size distribution of the microspheres was studied by optical microscope, which confirmed their spherical nature with sizes ranging from 112 to 186?m, FTIR and X-ray diffraction were used to confirm the polymer blend compatibility and to confirm the absence of drug-polymer interactions. Moreover, in vitro release experiments were performed at 37?C in simulated buffer medium of the stomach (pH=1.2) for 2h, and simulated intestinal medium (pH=7.4). It was found that the release of 5-fluorouracil from blend microspheres followed pH-independent release as compared to that of plain poly(?-caprolactone) and ethylcellulose microspheres for more than 10h. Furthermore, to better understand the nature of the drug release profiles, release data was fitted to empirical models.
将聚乙二醇-co-ε-己内酯微球与乙基纤维素混合控释5-氟尿嘧啶
本研究以八酸亚锡为引发剂,采用乙醇酸酯和-己内酯的开环聚合法制备了一系列不同组成的共聚物。用1H, 13C NMR和FTIR光谱对所得共聚物进行了表征。随后,采用油水乳化蒸发技术制备聚乙二醇-己内酯与乙基纤维素混合微球,研究抗癌药物5-氟尿嘧啶的控释作用。用光学显微镜研究了微球的粒径分布,证实了微球的球形性质,粒径范围为112 ~ 186?利用红外光谱(FTIR)、x射线衍射(X-ray)证实了聚合物的共混相容性,并证实了不存在药物-聚合物相互作用。体外释放实验在37?C分别在模拟胃缓冲介质(pH=1.2)和模拟肠介质(pH=7.4)中放置2h。结果表明,与普通聚己内酯微球和乙基纤维素微球相比,混合微球对5-氟尿嘧啶的释放具有不依赖ph的特性,且释放时间超过10h。此外,为了更好地了解药物释放谱的性质,释放数据拟合到经验模型中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Acta Periodica Technologica
Acta Periodica Technologica Engineering-Engineering (all)
CiteScore
0.60
自引率
0.00%
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0
审稿时长
8 weeks
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