Faculty of Pharmacy, Department of Pharmaceutics, University of Karachi, Karachi, Pakistan.
Department of Pharmaceutics, Institute of Pharmaceutical Sciences, Jinnah Sindh Medical University, Karachi, Pakistan.
PLoS One. 2022 May 24;17(5):e0267791. doi: 10.1371/journal.pone.0267791. eCollection 2022.
Polypharmacy may be considered as the customary practice to provide optimum care services to patients but inter resulted in augmented probability of multiple drug interaction. Keeping in view the importance of drug interaction possibility, this study was designed to evaluate the effect of ranitidine on pharmacokinetics of amoxicillin in the local population of Karachi, Pakistan. Amoxicillin and ranitidine are the most commonly prescribed drugs to treat duodenal ulcer caused by Helicobacter pylori. The current investigation was carried out as a single center, open label, two phase, single dose, randomized way in cross over manner to evaluate the potential of pharmacokinetic interaction among amoxicillin formulation and ranitidine in adult healthy male volunteers. Post dosing blood samples were collected at multiple time points that are 0.5, 1, 1.5, 2, 3, 4, 6, 8 and 10 hours after administering amoxicillin 250mg capsule with and without ranitidine. For estimation of amoxicillin concentration in plasma, an HPLC method was developed and validated. The solvent system consisted of 0.025M phosphate buffer: acetonitrile (94:6 v/v). C18 column was employed with a flow rate of 1.0 ml/minute and at 230nm. A linear pattern with a correlation coefficient of 0.999 in the concentration ranges of 25μg/mL to 0.097μg/mL for amoxicillin and 25μg/mL to 0.048μg/mL for ranitidine was observed. Amoxicillin retention time was about 8 minutes and ranitidine retention time was around 12 minutes. Amoxicillin levels were computed and the concentrations were applied to calculate the pharmacokinetic parameters. Pharmacokinetic parameters were estimated by Kinetica TM 4.4.1 (Thermo Electron Corp. USA). The analysis of variance (two way) and t test (two one sided) were applied on log transformed pharmacokinetic parameters of amoxicillin. The Tmax was determined between amoxicillin alone and amoxicillin with ranitidine by Friedman test. The 90% confidence interval values for Cmax(calc) (0.687-0.743) and Tmax(calc) (1.148-1.742) for amoxicillin with or without ranitidine were not found within the FDA acceptable limits of 0.8-1.25. Study demonstrated the significant reduction in peak plasma levels of amoxicillin in presence of ranitidine. It is advisable to administer both drugs with time interval to avoid such interactions and increases in the bactericidal efficacy of amoxicillin.
多药治疗可能被认为是为患者提供最佳护理服务的常规做法,但会增加多种药物相互作用的可能性。鉴于药物相互作用可能性的重要性,本研究旨在评估雷尼替丁对卡拉奇当地人群中阿莫西林药代动力学的影响,巴基斯坦。阿莫西林和雷尼替丁是最常用于治疗幽门螺杆菌引起的十二指肠溃疡的药物。目前的研究是作为一个单一中心、开放标签、两期、单剂量、随机交叉方式进行的,以评估阿莫西林制剂与雷尼替丁之间潜在的药代动力学相互作用在成年健康男性志愿者中。给药后,在 0.5、1、1.5、2、3、4、6、8 和 10 小时后采集多个时间点的血样,以评估阿莫西林 250mg 胶囊与雷尼替丁联合或不联合使用后的药代动力学相互作用。为了估计血浆中阿莫西林的浓度,开发并验证了一种 HPLC 方法。溶剂系统由 0.025M 磷酸盐缓冲液:乙腈(94:6v/v)组成。采用 C18 柱,流速为 1.0ml/min,检测波长为 230nm。阿莫西林浓度范围为 25μg/mL 至 0.097μg/mL,雷尼替丁浓度范围为 25μg/mL 至 0.048μg/mL,呈线性关系,相关系数为 0.999。阿莫西林的保留时间约为 8 分钟,雷尼替丁的保留时间约为 12 分钟。计算阿莫西林水平并应用浓度计算药代动力学参数。药代动力学参数由 Kinetica TM 4.4.1(美国热电公司)估算。采用方差分析(双向)和 t 检验(双侧)对阿莫西林的对数转化药代动力学参数进行分析。通过 Friedman 检验确定阿莫西林单独使用和阿莫西林与雷尼替丁联合使用时的 Tmax。阿莫西林与或不与雷尼替丁的 Cmax(计算)(0.687-0.743)和 Tmax(计算)(1.148-1.742)的 90%置信区间值不在 FDA 可接受的 0.8-1.25 范围内。研究表明,雷尼替丁存在时,阿莫西林的峰值血浆水平显著降低。建议两种药物同时使用以避免这种相互作用,并提高阿莫西林的杀菌效果。