Drug impurity profiling, ie identification, structure elucidation and quantitative determination
of impurities and degradation products in bulk drug materials and pharmaceutical …

In the current paper the application of multiobjective optimization (MOOP) technique, via
Derringer's desirability function, to a microemulsion liquid chromatographic (MELC) method …

The objective of this present work was to develop and validate analytical method for
quantitative determination of Perindopril Erbumine and Amlodipine Besylate in a tablet …

Two specific, sensitive, and precise stability-indicating chromatographic methods have been
developed, optimized and validated for determination of perindopril arginin (PER) and …

The absolute photoionization cross-sections of 24 nitrogenous compounds were measured
in the photon energy range from their respective ionization thresholds to 11.5 eV, including n …

Proline is a unique, endogenous amino acid, prevalent in proteins and essential for living
organisms. It is appreciated as a tecton for the rational design of new bio-active substances …

This review describes the recent trends in analytical perspectives of impurity profiling and
forced degradation of pharmaceutical drug and drug products used for the treatment of …

Robustness testing is an important part of method validation. Many ideas on robustness
testing can be found in the literature, but the most useful approach is application of …

A kinetic spectrophotometric method has been developed for the determination of
perindopril erbumine in pure and commercial dosage forms. The method is based on the …

A stability-indicating ultra-high-performance liquid chromatography (UHPLC) method with a
diode array detector was developed and validated for the determination of cis/trans isomers …