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用于间质化疗的三周缓释卡氮芥亲水聚乳酸-羟基乙酸共聚物微球:对人胶质母细胞瘤细胞的研发及活性

Three weeks release BCNU loaded hydrophilic-PLGA microspheres for interstitial chemotherapy: Development and activity against human glioblastoma cells.

作者信息

Esther Gil-Alegre María, González-Alvarez Isabel, Gutiérrez-Paúls Laura, Torres-Suárez Ana Isabel

机构信息

Department of Pharmacy and Pharmaceutical Technology, Complutense University of Madrid, Spain.

出版信息

J Microencapsul. 2008 Dec;25(8):561-8. doi: 10.1080/02652040802075799.

Abstract

The aim of this study is the development of microspheres of BCNU for intracranial administration, as an alternative to marketed novel Gliadel Implant in the treatment of brain tumours. H poly-lactide-co-glycolide biodegradable microspheres of BCNU with a mean size of 33.5 + or - 1.8 microm were obtained by an oil-in-water emulsion solvent evaporation method. Their small size would allow their intracranial administration through a needle by cerebral stereotaxia if tumour recurrence occurs, without a surgical intervention, as Gliadel needs. BCNU was released from these microspheres during 21 days, mainly by a mechanism of diffusion from the polymer matrix (K = 2.91 mg days(-(1/2))). The cytotoxic effects of these microspheres on human glioblastoma cells were demonstrated all through 21 days and the value of percentage of viable cells was less than 40%. These microspheres should be commercialized as a freeze-dried product to keep at -20 degrees C. Three hundred and twenty milligrams of microspheres contain 61.6 mg of BCNU, the same amount of BCNU contained in 1600 mg or eight wafers of Gliadel usually implanted after the tumour resection.

摘要

本研究的目的是开发用于颅内给药的卡莫司汀微球,作为市售新型格利雅得植入剂治疗脑肿瘤的替代方案。通过水包油乳液溶剂蒸发法获得了平均粒径为33.5±1.8微米的卡莫司汀聚丙交酯-乙交酯可生物降解微球。如果肿瘤复发,其小尺寸将允许通过脑立体定向术经针进行颅内给药,而无需像格利雅得那样进行手术干预。卡莫司汀在21天内从这些微球中释放,主要通过从聚合物基质扩散的机制(K = 2.91毫克·天^(-1/2))。这些微球对人胶质母细胞瘤细胞的细胞毒性作用在21天内均得到证实,活细胞百分比值小于40%。这些微球应以冻干产品形式商业化,保存在-20℃。320毫克微球含有61.6毫克卡莫司汀,与肿瘤切除后通常植入的1600毫克或八片格利雅得中所含的卡莫司汀量相同。

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