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A sustainable HPLC method coupled with diode array detection for versatile quantification of telmisartan,
Mona A Kamel1, Christine K Nessim1, Adel M Michael1
1Pharmaceutical Chemistry Department, Faculty of Pharmacy, Ahram Canadian University, 6th of October City, Cairo, 12566, Egypt.
Insights
A new eco-friendly HPLC-DAD method accurately analyzes telmisartan, chlorthalidone, and amlodipine in hypertension medications. This validated method ensures quality control for pharmaceutical formulations and confirms the drug
Area of Science:
- Analytical Chemistry
- Pharmaceutical Analysis
- Green Chemistry
Background:
- Cardiovascular diseases, particularly hypertension, are leading causes of global mortality.
- Effective hypertension management often requires combination therapy with multiple drugs.
- Accurate and efficient analytical methods are crucial for quality control of these pharmaceuticals.
Purpose of the Study:
- To develop and validate an environmentally friendly High-Performance Liquid Chromatography with Diode Array Detection (HPLC-DAD) method.
- To enable the simultaneous quantification of telmisartan (TEL), chlorthalidone (CHT), and amlodipine besylate (AML).
- To assess the quality and in-vitro dissolution profile of a fixed-combination pharmaceutical product.
Main Methods:
- Utilized an isocratic elution mode with an Inertsil C18 column and a mobile phase of acetonitrile and phosphate buffer (pH 3.0).
- Validated the method according to International Council for Harmonisation (ICH) guidelines, determining linearity, quantification limits, and precision.
- Performed in-vitro dissolution studies using USP type II apparatus in various media (pH 7.5 phosphate buffer, 0.01 N HCl, water).
Main Results:
- Achieved excellent linearity for TEL (1.0-140.0 μg/mL) and CHT/AML (1.0-100.0 μg/mL) with low quantification limits.
- The method demonstrated good precision and accuracy for the analysis of Telma-ACT® Tablets.
- In-vitro dissolution studies indicated an acceptable release profile for the fixed-combination tablet.
Conclusions:
- The developed HPLC-DAD method is accurate, precise, and suitable for the quality assessment of telmisartan, chlorthalidone, and amlodipine.
- The method's eco-friendly nature was confirmed through various greenness evaluation tools (GAPI, AGREEprep, AES, AMGS, WAC, BAGI).
- This validated, green analytical approach supports the quality control of essential hypertension medications.
Abstract:
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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