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

被引:13
作者
Ye, Tiantian [1 ]
Sun, Siping [2 ]
Sugianto, Tiffanie Daisy [2 ]
Tang, Patricia [2 ]
Parumasivam, Thaigarajan [2 ]
Chang, Yoon Kyung [2 ]
Astudillo, Ariel [2 ]
Wang, Shujun [1 ]
Chan, Hak-Kim [2 ]
机构
[1] Shenyang Pharmaceut Univ, Sch Pharm, Dept Pharmaceut, 103 Wen Hua Rd, Shenyang 110016, Liaoning, Peoples R China
[2] Univ Sydney, Sch Pharm, Adv Drug Delivery Grp, Sydney, NSW, Australia
关键词
Combination proliposome; Tobramycin; Clarithromycin; Spray dying; Synergy; Pseudomonas aeruginosa; IN-VITRO; CYSTIC-FIBROSIS; LIPOSOMAL CIPROFLOXACIN; EFFICACY; INFECTIONS; MACROLIDE; CULTURE; MODEL; VIVO;
D O I
10.1016/j.ijpharm.2018.09.061
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Tobramycin (FOB) 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 (SDTOB, 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 degrees 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.
引用
收藏
页码:130 / 138
页数:9
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