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载有妥布霉素和克拉霉素的新型组合前体脂质体对抗铜绿假单胞菌生物膜有效。

Novel combination proliposomes containing tobramycin and clarithromycin effective against Pseudomonas aeruginosa biofilms.

机构信息

Department of Pharmaceutics, School of Pharmacy, Shenyang Pharmaceutical University, 103 Wen hua Road, Shenyang 110016, China.

Advanced Drug Delivery Group, School of Pharmacy, University of Sydney, Sydney, New South Wales, Australia.

出版信息

Int J Pharm. 2018 Dec 1;552(1-2):130-138. doi: 10.1016/j.ijpharm.2018.09.061. Epub 2018 Sep 26.

Abstract

Tobramycin (TOB) and clarithromycin (CLA) can potentially be used synergistically for the treatment of respiratory infections caused by Pseudomonas aeruginosa (P. aeruginosa) in cystic fibrosis (CF) patients. This study aimed to develop a novel combination proliposome formulation (TOB/CLA-CPROLips) containing both hydrophilic TOB and hydrophobic CLA via a core-carrier approach. The combination proliposomes were produced by spray drying a suspension comprising spray-driedmannitol (SD-MAN, 0.45%) and spray-dried tobramycin (SD-TOB, 0.05%) particles suspended in an ethanolic lipid solution of CLA (0.05%). The lipid layer coated on the surface of the dry proliposome particles conferred moisture protection and sustained drug release properties in comparison to the pure drugs. The optimized TOB/CLA-CPROLips formulation was stable after 3 months of storage at 60% relative humidity (RH) and 25 °C. The combination drug proliposomes showed a synergistic antimicrobial activity against planktonic cells and biofilm cultures of P. aeruginosa. In conclusion, the core-carrier method coupled with spray-drying provided a novel approach for the preparation of combination antibiotics proliposomes.

摘要

妥布霉素(TOB)和克拉霉素(CLA)联合应用可能对囊性纤维化(CF)患者铜绿假单胞菌(P. aeruginosa)引起的呼吸道感染具有协同作用。本研究旨在通过核心载体法开发一种新型亲水妥布霉素和疏水性克拉霉素的组合前体脂质体(TOB/CLA-CPROLips)制剂。采用喷雾干燥法,以喷雾干燥甘露醇(SD-MAN,0.45%)和悬浮于含克拉霉素(0.05%)的乙醇脂质溶液中的喷雾干燥妥布霉素(SD-TOB,0.05%)颗粒的混悬液为原料制备组合前体脂质体。与纯药物相比,包被在干燥前体脂质体颗粒表面的脂质层提供了水分保护并具有持续释放药物的性能。在相对湿度(RH)为 60%和 25°C 下储存 3 个月后,优化的 TOB/CLA-CPROLips 制剂仍稳定。联合药物前体脂质体对铜绿假单胞菌浮游细胞和生物膜培养物显示出协同抗菌活性。总之,核心载体法与喷雾干燥相结合为制备联合抗生素前体脂质体提供了一种新方法。

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