Department of Pharmaceutical Sciences and Technology, Institute of Chemical Technology, University under Section 3 of UGC Act - 1956, Elite Status and Center of Excellence - Govt. of Maharashtra, Matunga (E), Mumbai, 400019, India.
Department of Pharmaceutics, R. C. Patel Institute of Pharmaceutical Education and Research, Shirpur, Maharashtra, 425405, India.
AAPS PharmSciTech. 2022 Sep 7;23(7):251. doi: 10.1208/s12249-022-02404-8.
Trazodone hydrochloride (TZN) is a serotonin reuptake inhibitor that treats a major depressive disorder. It exhibits a short plasma half-life of 4.1 h and shows pH-dependent solubility. Above its pKa (6.74), solubility of TZN is very low, affecting its dissolution in the lower part of GIT. Hence, the present work aimed to develop gastro-retentive floating tablet of TZN. Central composite design was employed to optimize the formulation. Formulation variables like the concentration of HPMC-K100M, Polyox WSR 303 Leo, and sodium bicarbonate were evaluated for the responses like floating lag time and drug release. X-ray imaging study was performed on rabbits to determine the in vivo gastric retention of the optimized formulation. The accelerated stability study was conducted on optimized tablets as per ICH guidelines. Floating lag time and f value of the optimized formulation were found to be 2.51±0.02 min and 62.79, respectively. X-ray imaging studies in rabbits determined the in vivo gastro retention time. After 12 h of administration, tablet remained in the gastric region, indicating better retentive power. Accelerated stability studies showed sufficient formulation stability even after 3 months of storage. All these studies depict that the floating gastro-retentive system could be used as an alternative to the innovator formulation.
盐酸曲唑酮(TZN)是一种可治疗重度抑郁症的 5-羟色胺再摄取抑制剂。它的血浆半衰期为 4.1 小时,表现出 pH 依赖性溶解度。在其 pKa(6.74)以上,TZN 的溶解度非常低,这会影响其在胃肠道下部的溶解。因此,本工作旨在开发 TZN 的胃滞留漂浮片。采用中心复合设计对制剂进行优化。评价了 HPMC-K100M、聚氧乙烯 WSR 303 Leo 和碳酸氢钠等配方变量对漂浮滞后时间和药物释放等响应的影响。对兔进行 X 射线成像研究,以确定优化配方的体内胃滞留情况。根据 ICH 指南对优化后的片剂进行了加速稳定性研究。优化配方的漂浮滞后时间和 f 值分别为 2.51±0.02 分钟和 62.79。对兔进行的 X 射线成像研究确定了体内胃滞留时间。给药 12 小时后,片剂仍保留在胃区,表明具有更好的滞留能力。加速稳定性研究表明,即使在储存 3 个月后,制剂仍具有足够的稳定性。所有这些研究表明,漂浮胃滞留系统可以替代创新制剂。