Chitosan-based binary dry powder inhaler carrier with nanometer roughness for improving in vitro and in vivo aerosolization performance

被引:10
作者
Huang, Ying [1 ]
Huang, Zhengwei [1 ]
Zhang, Xuejuan [1 ,2 ]
Zhao, Ziyu [1 ]
Zhang, Xuan [1 ,3 ]
Wang, Kexin [1 ]
Ma, Cheng [1 ]
Zhu, Chune [2 ]
Pan, Xin [1 ]
Wu, Chuanbin [1 ]
机构
[1] Sun Yat Sen Univ, Sch Pharmaceut Sci, Guangzhou 510006, Guangdong, Peoples R China
[2] Guangdong Univ Technol, Inst Biomed & Pharmaceut Sci, Guangzhou 510006, Guangdong, Peoples R China
[3] Northern Jiangsu Peoples Hosp, Dept Pharm, Yangzhou 225001, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Dry powder inhaler; Chitosan; Nanometer roughness; Fine particle fraction; Carrier; SURFACE-ROUGHNESS; FLUTICASONE PROPIONATE; LACTOSE; MORPHOLOGY; PARTICLES; FORMULATIONS; MODEL; MANNITOL; POLYMORPHS; DISPERSION;
D O I
10.1007/s13346-018-0564-y
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
Suitable nanometer roughness favors interactions between drugs and carriers, and it is a promising approach to enhance the aerosolization performance of carrier-based thy powder inhalers (DPIs). In this study, by altering the molecular migration rates, chitosan-based binary carriers (CBBCs) with nanometer roughness were fabricated for DPIs. Comprehensive physicochemical characterizations were conducted to elucidate the formation mechanism of the CBBCs. It was hypothesized that different constituent ratios in the formulations would result in different assembling of the particles and diverse roughness scales. The fine particle fractions (FPF, approximately 40 similar to 60%) of nanometer roughness CBBC-based DPI formulations were satisfactory, demonstrating the enhancement of the in vitro aerodynamic performance. The positive correlation (R-2 = 0.9883) between the nanometcr roughness and FPF was revealed, and the surface roughness of 20 nm might achieve the best aerosolization performance. CBBCs (optimal formulations) showed no difference in cytotoxicity on A549 and Calu-3 cells (p > 0.05). Additionally, the increased C-max and AUC(0-8h) of the formulation with the nanometer roughness (p < 0.05) were observed in pharmacokinetic studies, which resulted from the improved in vivo aerosolization performance. In summary, the CBBCs were a prospective tool to improve the in vitro and in vivo aerosolization performance of DPIs.
引用
收藏
页码:1274 / 1288
页数:15
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