Abdelgawad Mohamed A, Abdelaleem Eglal A, Gamal Mohammed, Abourehab Mohammed A S, Abdelhamid Nessreen S
Department of Pharmaceutical Chemistry, College of Pharmacy, Jouf University Aljouf 72341 Saudi Arabia
Pharmaceutical Analytical Chemistry Department, Faculty of Pharmacy, Beni-Suef University Alshaheed Shehata Ahmad Hegazy St. 62514 Beni-Suef Egypt
RSC Adv. 2022 Jun 1;12(25):16301-16309. doi: 10.1039/d2ra02395d. eCollection 2022 May 23.
One of the main aims of green analytical chemistry (GAC) is the reduction of solvents and chemicals consumed. Recycling the mobile phase in chromatographic techniques provides an efficient way to implement GAC principles. However, this is not an easy job, particularly in the case of the gradient mode. Analysis of multi-pharmaceuticals for the same manufacturer using one mobile phase system dramatically reduces consumed solvents, time, and cost for pharmaceuticals analysis in quality control laboratories. This work is an attempt to reduce time, cost and effort needed for quality control analysis of several dosage forms produced by the same manufacturer. Our novel and green RP-HPLC method is able to separate and quantify a tertiary mixture of piracetam, ketoprofen and omeprazole produced by the same manufacturers. The analyst can easily quantify the three drugs in the three dosage forms in one run using the gradient elution mode of methanol and water (from 50% methanol to 85% methanol in ten minutes) with a flow rate 1.5 mL min on a non-polar C column. Suitable dilutions were done for the working solution of the mixed pharmaceutical formulations prior to chromatographic analysis. This procedure will dramatically reduce the consumed solvents and save time and money during pharmaceutical analysis. The calibration ranges are (5-25), (5-25) and (3-20) μg mL for the three studied drugs. The International Council for Harmonization (ICH) procedures were followed in the validation process and the results were evaluated in comparison with official HPLC methods, where no noteworthy differences were found. The green profile of the method and pictograms of AGREE and Green Analytical Procedure Index (GAPI) approaches proved the eco-friendly character for the studied drugs. The simultaneous quantitative analysis for Stimulan® and Hyposec® capsules, and Ketolgin® tablets from the Amoun Pharmaceutical Company, Egypt, can be accomplished the novel method. Also, Memoral® ampoules, Topfam® tablets, and Gastroloc® capsules from Sigma Pharmaceutical Industries, Egypt, could be analyzed simultaneously. Omez® capsules and Ketogesic® tablets from the Pharaonia Pharmaceuticals, Egypt, could be determined simultaneously too. Applying this RP-HPLC method, a significant reduction of the total cost is assured as the required amount of solvent is noticeably decreased when performing multi-analyses in comparison to single component analysis.
绿色分析化学(GAC)的主要目标之一是减少溶剂和化学试剂的消耗。在色谱技术中循环使用流动相为实施GAC原则提供了一种有效途径。然而,这并非易事,尤其是在梯度模式下。使用一种流动相系统对同一制造商生产的多种药物进行分析,可显著减少质量控制实验室中药物分析所消耗的溶剂、时间和成本。这项工作旨在减少对同一制造商生产的几种剂型进行质量控制分析所需的时间、成本和精力。我们新颖的绿色反相高效液相色谱(RP-HPLC)方法能够分离并定量同一制造商生产的吡拉西坦、酮洛芬和奥美拉唑的三元混合物。分析人员可以在非极性C柱上,使用甲醇和水的梯度洗脱模式(十分钟内从50%甲醇到85%甲醇),流速为1.5 mL/min,在一次运行中轻松定量三种剂型中的三种药物。在色谱分析之前,对混合药物制剂的工作溶液进行了适当稀释。该程序将显著减少溶剂消耗,并在药物分析过程中节省时间和金钱。三种研究药物的校准范围分别为(5-25)、(5-25)和(3-20)μg/mL。在验证过程中遵循了国际协调理事会(ICH)程序,并将结果与官方HPLC方法进行比较评估,未发现显著差异。该方法的绿色概况以及AGREE和绿色分析程序指数(GAPI)方法的示意图证明了所研究药物的环保特性。使用该新方法可以同时对埃及阿蒙制药公司生产的Stimulan®和Hyposec®胶囊以及Ketolgin®片剂进行定量分析。此外,还可以同时分析埃及西格玛制药工业公司生产的Memoral®安瓿、Topfam®片剂和Gastroloc®胶囊。埃及法老制药公司生产的Omez®胶囊和Ketogesic®片剂也可以同时测定。应用这种RP-HPLC方法,与单组分分析相比,在进行多分析时所需的溶剂量显著减少,从而确保总成本大幅降低。