The aim of the current research was to make force degradation study of the morpholinium 2-((4-(2-methoxyphenyl)-5-(pyridin-4-yl)-4H-1,2,4-triazol-3-yl)thio)acetate (API) for additional confirmation of the selectivity of API and impurity determination method, propose possible structures of degradation products. Agilent 1260 Infinity (degasser, binary pump, autosampler, column thermostat, diode array detector) was used. Mass selective detector was single-quadrupole LC/MS 6120 with electrospray ion source (ESI). The chromatography study was carried out by isocratic elution with a water-acetonitrile mixture (84:16) with the addition of 0.1% methanoic acid. A column Zorbax SB-C18, 30 mm x 4.6 mm, 1.8 um. A column temperature was 40oC. The flow r...
Forced degradation study on doxorubicin (DOX) was carried out under hydrolytic condition in acidic, ...
The present research work describes comprehensive stress testing of eprosartan mesylate (EM) accordi...
A selective method for separation and determination of potential related impurities (starting materi...
The aim of the current research was to make force degradation study of the morpholinium 2-((4-(2-met...
Aim. The purpose of this study is to reveal the determination of the structure of the main metabolit...
Objective: The aim of the research work to monitor impurities profiling and degradation kinetics of ...
Objective: The main objective of this study was to investigate the degradation products (DPs) of Eto...
The present study the stability of a drug product or a drug substance is a critical parameter which ...
A simple, sensitive, precise, accurate, economic and rapid visible spectroscopic method has be...
The aim of the research was to study the stability of a new pharmaceutical substance 3-[2-(4-phenyl-...
Objective: The aim of the research work is to study the degradation of Lansoprazole in stress condit...
Objective: The objective of the present study was to investigate the stability of TRZ against differ...
This study describes the investigation of degradation products of donepezil (DP) using stability ...
The present research work describes comprehensive stress testing of eprosartan mesylate (EM) accordi...
Force degradation studies of drug substance give perceptive knowledge about the intrinsic stability ...
Forced degradation study on doxorubicin (DOX) was carried out under hydrolytic condition in acidic, ...
The present research work describes comprehensive stress testing of eprosartan mesylate (EM) accordi...
A selective method for separation and determination of potential related impurities (starting materi...
The aim of the current research was to make force degradation study of the morpholinium 2-((4-(2-met...
Aim. The purpose of this study is to reveal the determination of the structure of the main metabolit...
Objective: The aim of the research work to monitor impurities profiling and degradation kinetics of ...
Objective: The main objective of this study was to investigate the degradation products (DPs) of Eto...
The present study the stability of a drug product or a drug substance is a critical parameter which ...
A simple, sensitive, precise, accurate, economic and rapid visible spectroscopic method has be...
The aim of the research was to study the stability of a new pharmaceutical substance 3-[2-(4-phenyl-...
Objective: The aim of the research work is to study the degradation of Lansoprazole in stress condit...
Objective: The objective of the present study was to investigate the stability of TRZ against differ...
This study describes the investigation of degradation products of donepezil (DP) using stability ...
The present research work describes comprehensive stress testing of eprosartan mesylate (EM) accordi...
Force degradation studies of drug substance give perceptive knowledge about the intrinsic stability ...
Forced degradation study on doxorubicin (DOX) was carried out under hydrolytic condition in acidic, ...
The present research work describes comprehensive stress testing of eprosartan mesylate (EM) accordi...
A selective method for separation and determination of potential related impurities (starting materi...