专题：Analytical Methods in Pharmaceuticals

This cluster of papers focuses on the development and validation of green analytical chemistry methods for pharmaceutical analysis. It includes topics such as the validation of HPLC methods, stability indicating assays, forced degradation studies, impurity profiling, and the use of spectrophotometric methods. The cluster emphasizes the importance of environmentally friendly analytical procedures in pharmaceutical analysis.
最新文献
Inhalable formulations in pharmacy: from basic research to clinical applications

article Full Text OpenAlex

Identification of Novel Drug-Drug Interactions as Out-of-Distribution Samples

article Full Text OpenAlex

Development of stability indicating RP-HPLC method for simultaneous estimation of sacubitril and valsartan in pure and pharmaceutical dosage form

book-chapter Full Text OpenAlex

Author response for "Bicyclic anionic receptors for carboxylates in water"

peer-review Full Text OpenAlex

Novel Stability‐Indicating Reversed‐Phase High‐Performance Liquid Chromatography Method Development and Validation for Quantification of Celecoxib in Marketed Formulations and Transfersomes: Quality by Design‐Driven Optimization

article Full Text OpenAlex

Design and Performance Evaluation of Tamsulosin Prolonged Release Matrix Tablets Using Different Polymers

article Full Text OpenAlex

Analytical Method Validation: A Comprehensive Review of Current Practices

review Full Text OpenAlex

VALIDATION OF METHODS FOR DETERMINING THE COMPOSITION OF FATTY ACIDS IN PHARMACY

article Full Text OpenAlex

A comprehensive stability indicating method for clonidine hydrochloride impurities profiling and degradation analysis in tablet formulations: green metric study

article Full Text OpenAlex

Unique Quality by Design Approach for Developing High‐Performance Liquid Chromatography and Estimation of Rifaximin and Its Degradants by Mass Spectrometry

article Full Text OpenAlex

近5年高被引文献
Management of validation of HPLC method for determination of acetylsalicylic acid impurities in a new pharmaceutical product

article Full Text OpenAlex 1819 FWCI227.853

Blue applicability grade index (BAGI) and software: a new tool for the evaluation of method practicality

article Full Text OpenAlex 620 FWCI125.33

Stability Testing of Pharmaceutical Products

article Full Text OpenAlex 241 FWCI8.904

Stability Testing of Pharmaceutical Products

article Full Text OpenAlex 228 FWCI12.536

Advances in PHARMACOLOGY

book-chapter Full Text OpenAlex 224 FWCI123.315

Drug Stability: ICH versus Accelerated Predictive Stability Studies

review Full Text OpenAlex 120 FWCI4.218

Voltammetric analysis of antihistamine drug cetirizine and paracetamol at poly(L-Leucine) layered carbon nanotube paste electrode

article Full Text OpenAlex 106 FWCI11.021

Green metric tools for analytical methods assessment critical review, case studies and crucify

article Full Text OpenAlex 102 FWCI22.848

Development of the general chapters of the Chinese Pharmacopoeia 2020 edition: A review

review Full Text OpenAlex 89 FWCI2.081

Green analytical chemistry as an integral part of sustainable education development

article Full Text OpenAlex 87 FWCI9.887