Development And Validation Method for Estimation for Liraglutide By RP-HPLC From Its Injectable Dosage Form

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Main Author: Akhil Bhakhar*, Khyati Bhupta, Dhirendra Kumar Tarai, Dr. Santosh Kirtane
Format: Recurso digital
Published: Zenodo 2025
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author Akhil Bhakhar*, Khyati Bhupta, Dhirendra Kumar Tarai, Dr. Santosh Kirtane
author_facet Akhil Bhakhar*, Khyati Bhupta, Dhirendra Kumar Tarai, Dr. Santosh Kirtane
contents <p><span>This study provides a comprehensive overview of Type 2 Diabetes Mellitus (T2D), focusing on its pathophysiology, symptoms, causes, genetic influences, and global epidemiology. T2D is characterized by insulin resistance and inadequate insulin production, leading to chronic hyperglycemia and associated complications. The increasing global prevalence, especially in low-to-middle-income countries, underscores the urgency of effective diagnosis and management strategies. Additionally, the role of analytical chemistry in pharmaceutical research is highlighted, with emphasis on High Performance Liquid Chromatography (HPLC) as a reliable and precise tool for drug analysis. The process of analytical method development and validation is detailed, including key parameters such as accuracy, precision, linearity, specificity, and robustness. This framework ensures that pharmaceutical products meet stringent quality standards and regulatory requirements, which is crucial for the effective monitoring and treatment of chronic diseases like T2D.</span></p>
format Recurso digital
id zenodo_https___doi_org_10_5281_zenodo_15607231
institution Zenodo
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publishDate 2025
publisher Zenodo
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spellingShingle Development And Validation Method for Estimation for Liraglutide By RP-HPLC From Its Injectable Dosage Form
Akhil Bhakhar*, Khyati Bhupta, Dhirendra Kumar Tarai, Dr. Santosh Kirtane
Type 2 Diabetes Mellitus, antidiabetic drugs, high-performance liquid chromatography (HPLC), method development, method validation, ICH guidelines, simultaneous estimation, pharmaceutical analysis, quality control, and drug formulations
<p><span>This study provides a comprehensive overview of Type 2 Diabetes Mellitus (T2D), focusing on its pathophysiology, symptoms, causes, genetic influences, and global epidemiology. T2D is characterized by insulin resistance and inadequate insulin production, leading to chronic hyperglycemia and associated complications. The increasing global prevalence, especially in low-to-middle-income countries, underscores the urgency of effective diagnosis and management strategies. Additionally, the role of analytical chemistry in pharmaceutical research is highlighted, with emphasis on High Performance Liquid Chromatography (HPLC) as a reliable and precise tool for drug analysis. The process of analytical method development and validation is detailed, including key parameters such as accuracy, precision, linearity, specificity, and robustness. This framework ensures that pharmaceutical products meet stringent quality standards and regulatory requirements, which is crucial for the effective monitoring and treatment of chronic diseases like T2D.</span></p>
title Development And Validation Method for Estimation for Liraglutide By RP-HPLC From Its Injectable Dosage Form
topic Type 2 Diabetes Mellitus, antidiabetic drugs, high-performance liquid chromatography (HPLC), method development, method validation, ICH guidelines, simultaneous estimation, pharmaceutical analysis, quality control, and drug formulations
url https://doi.org/10.5281/zenodo.15607231