Naseem Faiza, Shah Shefaat Ullah, Rashid Sheikh Abdur, Farid Arshad, Almehmadi Mazen, Alghamdi Saad
Skin/Regenerative Medicine and Drug Delivery Research, GCPS, Faculty of Pharmacy, Gomal University, Dera Ismail Khan 29050, Pakistan.
Gomal Center of Biochemistry and Biotechnology, Gomal University, Dera Ismail Khan 29050, Pakistan.
Polymers (Basel). 2022 Jan 27;14(3):519. doi: 10.3390/polym14030519.
Metronidazole has the potential to produce local stomach specific action in order to treat induced peptic ulcer disease. The current project executes the development of osmotically controlled bioadhesive metronidazole loaded effervescent floating tablets with optimized floating and swelling behavior. Direct compression technique was used to prepare the tablets. The designed formulations exhibited physico-chemical properties within acceptable optimum limits as per pharmacopeial requirements. The results of tablet floating studies revealed that all formulations, except F1 and F5, had good buoyancy characteristics (TFT > 12 h except F2 and F8 with TFT of 6 h). Formulation F2 containing guar gum in higher concentration with carbopol and formulation F8 containing guar gum in 50% decreased concentration in combination with HPMC and carbopol had enhanced FLT appreciably, with least TFT as compared to formulations F3, F4, and F6 (ANOVA; ≤ 0.05). Formulation batches of F3, F4, and F6 exhibited appreciable FLT as well as TFT and were optimized formulations. Out of the above mentioned optimized batches, F4 and F6 formulations showed low FLT (4 and 5 s respectively). The results of the swelling study indicated a proportionate increase in the swelling index with increase in time. A significantly higher swelling ratio was found with formulation F6 and F4 compared with that of F7 and F8 (ANOVA; ≤ 0.05). Additionally, the impact of pH change, agitational intensity, as well as increasing concentration of NaCl was investigated on drug release. It was observed that agitational intensity had no effect on drug release rate while increasing concentration of NaCl produced an increased drug release from the dosage form as compared to the drug release exhibited by the formulations in the absence of NaCl. Overall, this project could have valuable contribution in the fabrication of metronidazole loaded effervescent floating tablets. Gastro-retentive systems are expected to enhance local stomach specific action of anti agents based on their buoyancy and swelling behavior.
甲硝唑有产生局部胃部特异性作用以治疗诱发性消化性溃疡疾病的潜力。当前项目开展了具有优化漂浮和溶胀行为的渗透控释生物黏附性甲硝唑泡腾漂浮片的研发。采用直接压片技术制备片剂。所设计的制剂根据药典要求在可接受的最佳限度内展现出理化性质。片剂漂浮研究结果显示,除F1和F5外,所有制剂均具有良好的漂浮特性(除F2和F8的漂浮时间为6小时外,其余制剂的漂浮时间均大于12小时)。含有较高浓度瓜尔胶与卡波姆的F2制剂以及含有50%较低浓度瓜尔胶与羟丙甲纤维素和卡波姆组合的F8制剂,其漂浮滞后时间明显延长,与F3、F4和F6制剂相比,漂浮时间最短(方差分析;P≤0.05)。F3、F4和F6制剂批次展现出可观的漂浮滞后时间以及漂浮时间,且为优化制剂。在上述优化批次中,F4和F6制剂的漂浮滞后时间较短(分别为4秒和5秒)。溶胀研究结果表明,溶胀指数随时间增加呈比例增加。与F7和F8相比,F6和F4制剂的溶胀率显著更高(方差分析;P≤0.05)。此外,还研究了pH变化、搅拌强度以及氯化钠浓度增加对药物释放的影响。观察到搅拌强度对药物释放速率无影响,而与无氯化钠时制剂的药物释放相比,氯化钠浓度增加使剂型的药物释放增加。总体而言,该项目在甲硝唑泡腾漂浮片的制备方面可能有重要贡献。胃滞留系统有望基于其漂浮和溶胀行为增强抗溃疡药物的局部胃部特异性作用。