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首页> 外文期刊>Biomaterials >Design of an injectable system based on bioerodible polyanhydride microspheres for sustained drug delivery.
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Design of an injectable system based on bioerodible polyanhydride microspheres for sustained drug delivery.

机译:基于生物蚀解性聚酸酐微球的可注射系统设计,用于持续药物输送。

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The fabrication, morphological characterization, and drug release kinetics from microspheres of three bioerodible polyanhydrides, poly[1,6-bis(p-carboxyphenoxy)hexane] (poly(CPH)), poly(sebacic anhydride) (poly(SA)), and the copolymer poly(CPH-co-SA) 50:50 (CPH:SA 50:50) is reported. The fabrication technique yields microspheres with different morphologies for each of the three polymers studied, ranging from very smooth exterior surfaces for poly(CPH) to coarse surface roughness with large pores for poly(SA). Release profiles for the model drug, p-nitroaniline are also different for each polymer. The release profile from poly(CPH) has a large initial burst and shows little additional release after 2 days. The release from poly(SA) is nearly zero-order and lasts for about 8 days. The release profile from CPH:SA 50:50 shows a relatively small burst and then exhibits zero-order release for about I month. The different release profiles are attributed to both polymer erosion rates and drug distribution characteristics of the microspheres. Tailored release profiles of a burst followed by zero-order release are obtained by appropriately combining the microspheres. This technique enables independent modulation of both the burst and the zero-order release rate by varying the number of poly(CPH) and poly(SA) microspheres respectively. Additionally, the zero-order release can be extended from about a week to a month by including CPH:SA 50:50 microspheres.
机译:三种生物蚀解性聚酸酐,聚[1,6-双(对羧基苯氧基)己烷](poly(CPH)),聚癸二酸酐(poly(SA)),微球的制备,形态表征和药物释放动力学并且报道了共聚物聚(CPH-co-SA)50:50(CPH:SA 50:50)。对于所研究的三种聚合物中的每一种,该制造技术都能产生具有不同形态的微球,其范围从用于聚(CPH)的非常光滑的外表面到聚(SA)的具有大孔的粗糙表面粗糙度。每种聚合物的模型药物对硝基苯胺的释放曲线也不同。聚(CPH)的释放曲线具有较大的初始爆发,并且在2天后几乎没有其他释放。 poly(SA)的释放几乎为零级,持续约8天。 CPH:SA 50:50的释放曲线显示相对较小的爆发,然后在大约1个月的时间内呈现零级释放。不同的释放曲线归因于聚合物的腐蚀速率和微球的药物分布特征。通过适当地组合微球获得突发的量身定制的释放曲线,然后是零级释放。通过分别改变poly(CPH)和poly(SA)微球的数量,该技术可以独立调制爆发和零级释放速率。此外,通过包含CPH:SA 50:50微球,零级释放可以从大约一周延长至一个月。

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