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采用连续超临界乳液萃取技术制备的可注射 PLGA/氢化可的松制剂。

Injectable PLGA/hydrocortisone formulation produced by continuous supercritical emulsion extraction.

机构信息

Department of Industrial Engineering, University of Salerno, Via Ponte don Melillo 1, 84084 Fisciano (SA), Italy.

出版信息

Int J Pharm. 2013 Jan 30;441(1-2):589-97. doi: 10.1016/j.ijpharm.2012.10.039. Epub 2012 Nov 2.

DOI:10.1016/j.ijpharm.2012.10.039
PMID:23124104
Abstract

The objective of the present study was to develop an anti-inflammatory prolonged action formulation for local injection in prefilled syringes. Hydrocortisone acetate (HA) was selected as a model corticosteroid drug to be incorporated in poly(lactic-co-glycolic) (PLGA) microspheres. The formulation was obtained by supercritical emulsion extraction in continuous operation layout (SEE-C) to test the process robustness for a continuous industrial production. PLGA/HA microspheres with mean sizes between 1 μm (SD±0.20) and 5 μm (SD±1.45) were obtained when operating at 80 bar and 38 °C with a L/G ratio of 0.1 in the counter-current tower. The produced microdevices showed excellent encapsulation efficiencies between 75% and 80%, depending on the emulsion formulations tested, and different sustained release in the range of 6-15 days. In dependence of the different emulsion (single or double) processed by SEE-C, different products can be obtained according to the therapeutic requests. SEE-C confirms to be an innovative and flexible technology for biopolymer microdevices production, coupling the efficiency of continuous operation to the easy process scalability.

摘要

本研究的目的是开发一种用于预充注射器局部注射的抗炎长效制剂。醋酸氢化可的松(HA)被选为模型皮质类固醇药物,以掺入聚(乳酸-共-乙醇酸)(PLGA)微球中。该制剂是通过连续操作布局的超临界乳液萃取(SEE-C)获得的,以测试连续工业生产的过程稳健性。当在 80 巴和 38°C 下操作,逆流塔中的 L/G 比为 0.1 时,获得粒径在 1 μm(SD±0.20)和 5 μm(SD±1.45)之间的 PLGA/HA 微球。所制备的微器件的包封效率在 75%至 80%之间,这取决于所测试的乳液配方,并且在 6-15 天的范围内具有不同的持续释放。根据 SEE-C 加工的不同乳液(单乳液或双乳液),可以根据治疗要求获得不同的产品。SEE-C 被证实是一种用于生物聚合物微器件生产的创新和灵活的技术,将连续操作的效率与易于扩展的工艺相结合。

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