Add to ORKGABSTRACT: The aim of the work was to analyse the influence of storage conditions such as time and temperature on the stability of fluoxetine in biological material. De-termination of fluoxetine in blood, urine and liver samples was carried out using the HPLC method. Analysis revealed that fluoxetine showed consistent stability in sam-ples which were stored at –200C. Fluoxetine was stable in biological material stored at +40C and +250C for a period of only one month
Background : Therapeutic nonadherence is a major health problem, particularly when therapeutic regim...
BACKGROUND: It has long been recognized that ensuring analyte stability is of crucial importance in ...
The chemical stability of flutamide (FLT) was investigated using a new validated stability-indicatin...
To ensure a drug exhibits maximum efficacy and does not compromise patient acceptability or safety, ...
Stability testing of an active substance or fi nished product provides information of the variation ...
Charles University in Prague Faculty of Pharmacy in Hradec Králové Department of Pharmaceutical Chem...
International audienceIn order to perform a human and ecological risk assessment of pharmaceutical p...
It is well established that bacteria are capable of degrading selected drugs during decomposition. T...
Abstract STUDY OBJECTIVE: The aim of this study is to determine the content of 5 important emergenc...
A standardization of the analytical procedures for monitoring of fluoxetine and norfluoxetine enanti...
Sampling and drug stability in oral fluid (OF) are crucial factors when interpreting forensic toxico...
The delay that occurs between specimen acquisition and analysis in clinical and forensic toxicology ...
WOS: 000321748400016This study was aimed to evaluate the state of utilization of florfenicol, along ...
The analysis of designer drugs, including those in the synthetic cathinone and piperazine classes, m...
Chemical degradation of drugs may result in altered therapeutic efficacy and even toxic effects. The...
Background : Therapeutic nonadherence is a major health problem, particularly when therapeutic regim...
BACKGROUND: It has long been recognized that ensuring analyte stability is of crucial importance in ...
The chemical stability of flutamide (FLT) was investigated using a new validated stability-indicatin...
To ensure a drug exhibits maximum efficacy and does not compromise patient acceptability or safety, ...
Stability testing of an active substance or fi nished product provides information of the variation ...
Charles University in Prague Faculty of Pharmacy in Hradec Králové Department of Pharmaceutical Chem...
International audienceIn order to perform a human and ecological risk assessment of pharmaceutical p...
It is well established that bacteria are capable of degrading selected drugs during decomposition. T...
Abstract STUDY OBJECTIVE: The aim of this study is to determine the content of 5 important emergenc...
A standardization of the analytical procedures for monitoring of fluoxetine and norfluoxetine enanti...
Sampling and drug stability in oral fluid (OF) are crucial factors when interpreting forensic toxico...
The delay that occurs between specimen acquisition and analysis in clinical and forensic toxicology ...
WOS: 000321748400016This study was aimed to evaluate the state of utilization of florfenicol, along ...
The analysis of designer drugs, including those in the synthetic cathinone and piperazine classes, m...
Chemical degradation of drugs may result in altered therapeutic efficacy and even toxic effects. The...
Background : Therapeutic nonadherence is a major health problem, particularly when therapeutic regim...
BACKGROUND: It has long been recognized that ensuring analyte stability is of crucial importance in ...
The chemical stability of flutamide (FLT) was investigated using a new validated stability-indicatin...