Statistical Design of Experiment (DoE) based development and optimization of DB213 in situ thermosensitive gel for intranasal delivery

被引:35
作者
Wang, Qianwen [1 ]
Wong, Chun-Ho [2 ]
Chan, H. Y. Edwin [2 ,3 ]
Lee, Wai-Yip [1 ]
Zuo, Zhong [1 ]
机构
[1] Chinese Univ Hong Kong, Sch Pharm, Shatin, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Sch Life Sci, Shatin, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, Gerald Choa Neurosci Ctr, Shatin, Hong Kong, Peoples R China
关键词
Intranasal; DoE; DB213; In situ thermosensitive gel; REPLICATION INHIBITOR DB213; PLURONIC F-127 GELS; TO-BRAIN DELIVERY; CONTROLLED-RELEASE; NASAL DELIVERY; DRUG-DELIVERY; CHITOSAN; SYSTEMS; VITRO; FORMULATIONS;
D O I
10.1016/j.ijpharm.2018.01.032
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
DB213 is an HIV-1 replication inhibitor targeting the Central Nervous System for the treatment of HIV-associated neurocognitive disorders. Current study aims to develop an in situ thermosensitive gelling system for intranasal delivery of DB213 facilitated by Statistical Design of Experiment (DoE) to conduct a more efficient experimentation by extracting the maximum amount of information from limited experiments. In our current study, information was extracted from twenty-five experimental designs from MODDE (R) Software and a mathematical model was successfully developed to predict formulations to achieve desired performance as well as to analyze relationships between the amount of Pluronic F-127, Pluronic F-68, Chitosan, DB213 and the performances of in situ thermosensitive gels. Based on DoE, in situ thermosensitive gels of 1% DB213 (F1) and 5% DB213 (F2) were developed for further in vivo bioavailability and brain uptake evaluations in Sprague-Dawley rats and C57BL/6 mice, respectively. In comparison to DB213 water solution, intranasal administrations of F1 at 1 mg/kg in rats and F2 at 25 mg/kg in mice demonstrated relative bioavailabilities of 145% and 165% with significant increase in brain uptake.
引用
收藏
页码:50 / 57
页数:8
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