2003
DOI: 10.1016/s0731-7085(02)00593-9
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The determination of a potential impurity in Thalidomide drug substance and product by HPLC with indirect UV detection

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Cited by 10 publications
(3 citation statements)
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“…Samples need to be promptly cooled, acidified and stored at −20 • in order to avoid hydrolytic degradation of thalidomide [5][6][7][8][9][10][11][12][13][14]. The method developed was simple, with good precision and accuracy.…”
Section: Overviewmentioning
confidence: 99%
See 1 more Smart Citation
“…Samples need to be promptly cooled, acidified and stored at −20 • in order to avoid hydrolytic degradation of thalidomide [5][6][7][8][9][10][11][12][13][14]. The method developed was simple, with good precision and accuracy.…”
Section: Overviewmentioning
confidence: 99%
“…Many methods have been developed to quantify thalidomide and its metabolites from a variety of biological matrices [7][8][9][10][11][12][13][14][15][16][17]. Most of these methods are achiral, being based on HPLC using reverse phase separation with UV, MS (mass spectrometry) or tandem MS detection.…”
Section: Introductionmentioning
confidence: 99%
“…Also, thalidomide is a synthetic derivative of glutamine and at physiologic pH can undergo hydrolysis to form this compound again. Li et al have been developed a HPLC method with indirect UV detection, for study the purity of thalidomide and determine glutamine in thalidomide drug substances and products [20].…”
Section: Introductionmentioning
confidence: 99%