Kim Da Hun, Lee Sa-Won, Lee Jun Hak, Park Jin Woo, Park Sung Mo, Maeng Han-Joo, Koo Tae-Sung, Cho Kwan Hyung
College of Pharmacy and Inje Institute of Pharmaceutical Sciences and Research, Inje University, 197 Inje-ro, Gimhae 50834, Republic of Korea.
Department of Pharmaceutical Engineering, Inje University, 197 Inje-ro, Gimhae 50834, Republic of Korea.
Pharmaceutics. 2024 Sep 24;16(10):1242. doi: 10.3390/pharmaceutics16101242.
The aim of this work was to prepare and characterize gastroretentive floating combination tablets (GRCTs) containing 500 mg of amoxicillin trihydrate (AMX) and 125 mg of levofloxacin (LVX) that provide sustained drug release and stability at gastric pH levels for the eradication of resistant . GRCTs were prepared with low-density excipients and hydrophilic swellable polymers, including hydroxypropyl methylcellulose (HPMC) of various viscosities, polyethylene oxide (PEO), and carboxymethylcellulose (CMC), by the direct compression method. The prepared GRCTs were investigated and optimized in terms of pH stability, tablet hardness, floating lag time and total floating time, drug release rate, gel strength. AMX and LVX in GRCT were stable at the HP eradication target pH above 4.0. The effervescent GRCT composition (AMX/LVX/HPMC [4000 cP]/CMC/microcrystalline cellulose/citric acid/sodium bicarbonate/calcium silicate/silicon dioxide/magnesium stearate = 500/125/50/50/125/40/60/30/10/10, /) yielded acceptable hardness (>6 kp), reduced floating lag time (<5 s), a long floating duration (>12 h), and sustained release rates of AMX and LVX (>90% until 12 h). This optimized GRCT had a gel strength of 107.33 ± 10.69 g and pH > 4.0, which maintained the tablets' shape and AMX stability for 12 h. Collectively, the formulated effervescent GRCTs combining AMX and LVX represented a promising candidate dosage form for eradicating resistant .
本研究的目的是制备并表征胃滞留漂浮复方片剂(GRCTs),其含有500mg三水合阿莫西林(AMX)和125mg左氧氟沙星(LVX),能在胃内pH水平下实现药物的持续释放和稳定,以根除耐药菌。采用直接压片法,用低密度辅料和亲水性可溶胀聚合物制备GRCTs,这些聚合物包括不同粘度的羟丙基甲基纤维素(HPMC)、聚环氧乙烷(PEO)和羧甲基纤维素(CMC)。对制备的GRCTs进行了pH稳定性、片剂硬度、漂浮滞后时间和总漂浮时间、药物释放速率、凝胶强度等方面的研究和优化。GRCTs中的AMX和LVX在根除幽门螺杆菌的目标pH高于4.0时是稳定的。泡腾GRCT组合物(AMX/LVX/HPMC[4000 cP]/CMC/微晶纤维素/柠檬酸/碳酸氢钠/硅酸钙/二氧化硅/硬脂酸镁=500/125/50/50/125/40/60/30/10/10,/)产生了可接受的硬度(>6 kp),缩短了漂浮滞后时间(<5 s),延长了漂浮持续时间(>12 h),以及AMX和LVX的持续释放率(至12 h时>90%)。这种优化后的GRCT凝胶强度为107.33±10.69 g,pH > 4.0,能使片剂形状和AMX稳定性保持12 h。总体而言,所制备的将AMX和LVX结合的泡腾GRCTs是一种有前景的根除耐药菌的候选剂型。