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用于临床应用的GMP级载钬聚(L-乳酸)微球的生产。

Production of GMP-grade radioactive holmium loaded poly(L-lactic acid) microspheres for clinical application.

作者信息

Zielhuis S W, Nijsen J F W, de Roos R, Krijger G C, van Rijk P P, Hennink W E, van het Schip A D

机构信息

Department of Nuclear Medicine, University Medical Center, Utrecht, The Netherlands.

出版信息

Int J Pharm. 2006 Mar 27;311(1-2):69-74. doi: 10.1016/j.ijpharm.2005.12.034. Epub 2006 Jan 24.

DOI:10.1016/j.ijpharm.2005.12.034
PMID:16439073
Abstract

Radioactive holmium-166 loaded poly(L-lactic acid) microspheres are promising systems for the treatment of liver malignancies. The microspheres are loaded with holmium acetylacetonate (HoAcAc) and prepared by a solvent evaporation method. After preparation, the microspheres (Ho-PLLA-MS) are activated by neutron irradiation in a nuclear reactor. In this paper, the aspects of the production of a (relatively) large-scale GMP batch (4 g, suitable for treatment of 5-10 patients) of Ho-PLLA-MS are described. The critical steps of the Ho-PLLA-MS production process (sieving procedure, temperature control during evaporation and raw materials) were considered and the pharmaceutical quality of the microspheres was evaluated. The pharmaceutical characteristics (residual solvents, possible bacterial contaminations and endotoxins) of the produced Ho-PLLA-MS batches were in compliance with the requirements of the European Pharmacopoeia. Moreover, neutron irradiated Ho-PLLA-MS retained their morphological integrity and the holmium remained stably associated with the microspheres; it was observed that after 270h (10 times the half-life of Ho-166) only 0.3+/-0.1% of the loading was released from the microspheres in an aqueous solution. In conclusion, Ho-PLLA-MS which are produced as described in this paper, can be clinically applied, with respect to their pharmaceutical quality.

摘要

负载放射性钬 - 166的聚(L - 乳酸)微球是治疗肝脏恶性肿瘤的有前景的体系。这些微球负载乙酰丙酮钬(HoAcAc),并通过溶剂蒸发法制备。制备后,微球(Ho - PLLA - MS)在核反应堆中通过中子辐照进行活化。本文描述了生产一批(相对)大规模的符合药品生产质量管理规范(GMP)的Ho - PLLA - MS(4 g,适用于治疗5 - 10名患者)的各个方面。考虑了Ho - PLLA - MS生产过程的关键步骤(筛分程序、蒸发过程中的温度控制和原材料),并对微球的药物质量进行了评估。所生产的Ho - PLLA - MS批次的药物特性(残留溶剂、可能的细菌污染和内毒素)符合欧洲药典的要求。此外,经中子辐照的Ho - PLLA - MS保持其形态完整性,钬与微球保持稳定结合;观察到在270小时(Ho - 166半衰期的10倍)后,微球在水溶液中仅释放0.3±0.1%的负载量。总之,本文所述方法生产的Ho - PLLA - MS,就其药物质量而言,可用于临床应用。

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