Tuberculosis (TB) is a chronic infectious disease caused by Mycobacterium tuberculosis (Mtb) and is the leading cause of morbidity and mortality among all infectious diseases. The emergence of resistant forms of tuberculosis, strong epidemiological coexistence of HIV, poor patient compliance due ...

Recently discovery of relation between cyclooxygenase–2 (COX–2) inhibition and prevention of growth of cansar cells is a major area for research in medicinal chemistry, as it is free from side effects which are genetically shown by developed anticancer agents. In an attempt to develop potent ...

The objective of the present study was to prepare and evaluate fast-dissolving oral films of prochlorperazine maleate (PCM), in order to enhance the bioavailability of the drug and to provide rapid onset of action thereby improving patient compliance. The solubility of the drug was increased by p...

The aim of the present work was to develop and validate an accurate, precise, simple, and efficient stability indicating Reversed phase High Performance Liquid Chromatography method for determination of an abrisentan and its process impurities in bulk and pharmaceutical dosage forms. The drug sub...

A simple, sensitive and precise high performance thin layer chromatographic (HPTLC)method has been developed for the estimation of ondansetron (OND) and ranitidine (RAN) in combination. The method was employed on thin layer chromatography (TLC) and aluminium plates were precoated with silica gel ...

The main objective of the current study was to develop a simple, accurate, precise and rapid RPHPLC method and subsequent validation using ICH suggested approach for the determination of bimatoprost in bulk and pharmaceutical dosage form. The chromatographic separation of bimatoprost was achieved...

A series of 4-(4-substituted benzylideneamino)-5-phenyl-4H-1,2,4-triazole-3-thiols (IVa-e) was obtained by reaction of 4-(amino)-5-phenyl-4H-1,2,4-triazole-3-thiol with aromatic aldehyde in presence of concentrated sulphuric acid. The synthesised compounds were characterized by FT-IR, 1H-NMR and ...

Orodispersible tablets are uncoated tablets which when taken into the mouth, get easily dispersed within 3 min before swallowing. they are also known as orally disintegrating tablets, mouth-dissolving tablets, rapid dissolving tablets fast-disintegrating tablets, fast-dissolving tablets. In this ...