可持续高效液相色谱法与二极管阵列检测相结合,用于固定剂量降压制剂中替米沙坦、氯沙坦和氨氯地平的多功能定量分析和溶出研究

IF 4.3 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY BMC Chemistry Pub Date : 2024-09-12 DOI:10.1186/s13065-024-01276-2
Mona A. Kamel, Christine K. Nessim, Adel M. Michael, Samah S. Abbas, Hoda M. Marzouk
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引用次数: 0

摘要

心血管疾病,尤其是高血压,是造成全球死亡的主要原因。高血压通常被称为 "无声杀手综合征",需要使用多种药物进行有效控制和管理。本研究介绍了一种新型环保型 HPLC-DAD 方法,用于同时分析纯品和复方药物剂型中的替米沙坦(TEL)、氯沙坦(CHT)和苯磺酸氨氯地平(AML)。色谱分离采用等度洗脱模式,使用 Inertsil C18 色谱柱(250 × 4.6 mm,5.0 µm)和乙腈与磷酸盐缓冲液(pH 3.0 ± 0.1)混合流动相(体积比为 35:65)。流速为 1.0 mL/min,10 分钟内完成分离。根据国际协调理事会(ICH)的指导方针,对所建议的方法进行了验证。TEL的线性范围为1.0-140.0 μg/mL,CHT和AML的线性范围为1.0-100.0 μg/mL,定量限分别为0.061、0.177和0.313 μg/mL。体外溶出度研究表明,固定复方片剂具有可接受的释放曲线。所研究的溶出介质为 pH 值为 7.5 的磷酸盐缓冲液、0.01 N HCl 和水,使用 USP II 型仪器,温度为 37 ± 0.5 °C,搅拌速率为 75 rpm。所提议的方法成功地应用于 Telma-ACT® 片剂的质量评估,具有良好的精确度和准确性。该方法使用了多种工具来评估绿色程度,包括绿色分析程序指数(GAPI)、样品制备分析绿色度量(AGREEprep)、分析生态尺度(AES)和分析方法绿色度评分(AMGS)。这些工具证实了拟议方法的生态友好性。此外,还专门开发了新引入的白色分析化学(WAC)和蓝色适用性等级指数(BAGI),以评估该方法的可持续性和适用性。
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A sustainable HPLC method coupled with diode array detection for versatile quantification of telmisartan, chlorthalidone and amlodipine in a fixed-dose antihypertensive formulation and dissolution studies

Cardiovascular diseases, especially hypertension, stand as prominent contributors to global mortality. Hypertension, often referred to as a silent killer syndrome, necessitates the use of multiple medications for effective control and management. A new environmentally friendly HPLC–DAD method is introduced in this study for the concurrent analysis of telmisartan (TEL), chlorthalidone (CHT) and amlodipine besylate (AML), in both pure forms and combined pharmaceutical dosage form. An isocratic elution mode was employed to achieve chromatographic separation, utilizing an Inertsil C18 column (250 × 4.6 mm, 5.0 µm) and a mobile phase mixture of acetonitrile and phosphate buffer (pH 3.0 ± 0.1) with ratio of 35:65, v/v. The separation was achieved within 10 min at a flow rate of 1.0 mL/min. The proposed method's validation was carried out following the guidelines outlined by the International Council for Harmonisation (ICH). The achieved linearity range was 1.0–140.0 μg/mL for TEL and 1.0–100.0 μg/mL for CHT and AML with quantification limits of 0.061, 0.177, and 0.313 μg/mL for TEL, CHT, and AML, respectively. The fixed combination tablet dosage form demonstrated acceptable release profile, as indicated by the in-vitro dissolution studies. The studied dissolution media were phosphate buffer pH 7.5, 0.01 N HCl, and water, utilizing a USP type II apparatus at 37 ± 0.5 °C with a stirring rate of 75 rpm. The proposed method was applied successfully for the quality assessment of Telma-ACT® Tablets with good precision and accuracy. Various tools were used for evaluating the level of greenness, including Green Analytical Procedure Index (GAPI), Analytical Greenness Metric for Sample Preparation (AGREEprep), Analytical Eco-Scale (AES), and Analytical Method Greenness Score (AMGS). These tools had confirmed the eco-friendliness of the proposed method. Additionally, the newly introduced White Analytical Chemistry (WAC), and the Blue Applicability Grade Index (BAGI) have been specifically developed to evaluate the sustainability and the applicability of the method.

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来源期刊
BMC Chemistry
BMC Chemistry Chemistry-General Chemistry
CiteScore
5.30
自引率
2.20%
发文量
92
审稿时长
27 weeks
期刊介绍: BMC Chemistry, formerly known as Chemistry Central Journal, is now part of the BMC series journals family. Chemistry Central Journal has served the chemistry community as a trusted open access resource for more than 10 years – and we are delighted to announce the next step on its journey. In January 2019 the journal has been renamed BMC Chemistry and now strengthens the BMC series footprint in the physical sciences by publishing quality articles and by pushing the boundaries of open chemistry.
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