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新型鲑鱼降钙素反胶束在含氟烷烃推进剂中的配方与评价。

Formulation and evaluation of novel reverse microemulsions containing salmon calcitonin in hydrofluoroalkane propellants.

机构信息

School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, China; Research and Development Center of Pharmaceutical Engineering, Sun Yat-sen University, Guangzhou, China.

School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, China.

出版信息

Int J Pharm. 2014 May 15;466(1-2):390-9. doi: 10.1016/j.ijpharm.2014.03.032. Epub 2014 Mar 20.

Abstract

To develop reverse microemulsion as a potential strategy for pulmonary delivery of salmon calcitonin (sCT) in HFA134a propellant of pressurized metered dose inhalers (pMDIs), pluronic P85 (P85) was chosen as the most appropriate surfactant to form microemulsions containing sCT. Formulation parameters, including the surfactant and ethanol content, water content, and sCT loading, were optimized to obtain two desired pMDI formulations A and B with clear and transparent appearance, Tyndall effect, good physical stability and aerosolization properties. Aerosolization properties of the optimized pMDIs were assessed by next generation impactor (NGI) and twin-stage impactor (TSI), and the dose of sCT in each stage was assayed by HPLC. The fine particle fraction (FPF) of formulations A and B were both at the range of approximately 28.0-36.0%. Cytotoxicity studies indicated the cell viability determined by MTT assay only slightly dropped when the A549 cells were exposed to the pMDI formulations. Pharmacological study performed on the male Wistar rats showed the intratracheal administration of the microemulsion pMDIs containing sCT exhibited similar but prolonged hypocalcemic activity compared with the intravenous injection of sCT solution. Therefore, such reverse microemulsions are potential for pulmonary delivery of therapeutic peptides using HFA-pMDIs.

摘要

为了开发反微乳液作为一种将鲑鱼降钙素(sCT)递送至加压计量吸入器(pMDI)中的 HFA134a 推进剂中的肺部的潜在策略,选择了泊洛沙姆 P85(P85)作为最适合的表面活性剂以形成含有 sCT 的微乳液。制剂参数,包括表面活性剂和乙醇含量、水含量和 sCT 负载量,经过优化,得到了两种具有清晰透明外观、廷德尔效应、良好的物理稳定性和雾化性质的理想 pMDI 制剂 A 和 B。通过下一代撞击器(NGI)和双级撞击器(TSI)评估了优化的 pMDI 的雾化性质,并通过 HPLC 测定了每个阶段的 sCT 剂量。制剂 A 和 B 的细颗粒分数(FPF)均在约 28.0-36.0%的范围内。细胞毒性研究表明,当 A549 细胞暴露于 pMDI 制剂时,通过 MTT 测定确定的细胞活力仅略有下降。在雄性 Wistar 大鼠上进行的药理学研究表明,与 sCT 溶液的静脉内注射相比,含有 sCT 的反微乳液 pMDI 的气管内给药表现出相似但延长的降血钙活性。因此,这种反微乳液有可能使用 HFA-pMDI 来肺部递送治疗性肽。

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