College of Pharmacy, Chongqing Medical University, Chongqing, 400042, China.
Yaopharma Co, Ltd, No. 100, Xingguang Ave, Chongqing, 401121, China.
Drug Deliv Transl Res. 2023 Nov;13(11):2819-2833. doi: 10.1007/s13346-023-01349-0. Epub 2023 May 9.
The objective of this study was to develop phospholipid-based injectable phase transition in situ gels (PTIGs) for the sustained release of Brexpiprazole (Brex). Phospholipid (Lipoid S100, S100) and stearic acid (SA) were used as the gel matrix which was dissolved in biocompatible solvent medium-chain triglyceride (MCT), N-methyl pyrrolidone (NMP), and ethanol to obtain PTIGs solution. The Brex PTIG showed a solution condition of low viscosity in vitro and was gelatinized in situ in vivo after subcutaneous injection. Both in vitro release assay and in vivo pharmacokinetics study in SD rats displayed that Brex in PTIGs could achieve a sustained release, compared with brexpiprazole solution (Brex-Sol) or brexpiprazole suspension (Brex-Sus). The Brex-PTIGs had good degradability and biocompatibility in vivo with rare inflammation at the injection site. Among the three Brex-PTIG formulations, Brex-PTIG-3 with the SA in the formulation had the greatest gelation viscosity, the lowest initial release rate, and the most stable release profile with sustained release of up to 60 days. The above results indicated that, as a novel drug delivery system, the Brex-PTIGs offered a new option for the clinical treatment of patients with schizophrenia.
本研究旨在开发基于磷脂的可注射相转变原位凝胶(PTIGs),以实现 Brexpiprazole(Brex)的持续释放。磷脂(Lipoid S100、S100)和硬脂酸(SA)用作凝胶基质,溶解在生物相容性溶剂中-中链甘油三酯(MCT)、N-甲基吡咯烷酮(NMP)和乙醇中,以获得 PTIGs 溶液。Brex PTIG 显示出体外低粘度的溶液条件,并在皮下注射后在体内原位胶凝。SD 大鼠的体外释放试验和体内药代动力学研究表明,与 Brexiprazole 溶液(Brex-Sol)或 Brexiprazole 混悬剂(Brex-Sus)相比,PTIGs 中的 Brex 能够实现持续释放。Brex-PTIGs 在体内具有良好的降解性和生物相容性,注射部位炎症罕见。在三种 Brex-PTIG 制剂中,制剂中含有 SA 的 Brex-PTIG-3 具有最大的凝胶化粘度、最低的初始释放率和最稳定的释放曲线,可持续释放长达 60 天。上述结果表明,作为一种新型药物递送系统,Brex-PTIGs 为精神分裂症患者的临床治疗提供了新的选择。