| Literature DB >> 29366939 |
Qianwen Wang1, Chun-Ho Wong2, H Y Edwin Chan3, Wai-Yip Lee1, Zhong Zuo4.
Abstract
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® 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.Entities:
Keywords: DB213; DoE; In situ thermosensitive gel; Intranasal
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Year: 2018 PMID: 29366939 DOI: 10.1016/j.ijpharm.2018.01.032
Source DB: PubMed Journal: Int J Pharm ISSN: 0378-5173 Impact factor: 5.875