2000
DOI: 10.1016/s0378-4347(00)00262-0
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Validation of high-performance liquid chromatographic assay methods for the analysis of carboplatin in plasma ultrafiltrate

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Cited by 14 publications
(8 citation statements)
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“…With regard to selective methods for the determination of free carboplatin, high performance liquid chromatography (HPLC) separation coupled to various detection techniques appears to be the method of choice. Carboplatin has been analyzed using reversed phase [9,10], hydrophilic [1], and strong cation exchange [4] chromatographic conditions. Due to its very polar property, carboplatin has minimal k values on most reversed phase columns.…”
Section: Introductionmentioning
confidence: 99%
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“…With regard to selective methods for the determination of free carboplatin, high performance liquid chromatography (HPLC) separation coupled to various detection techniques appears to be the method of choice. Carboplatin has been analyzed using reversed phase [9,10], hydrophilic [1], and strong cation exchange [4] chromatographic conditions. Due to its very polar property, carboplatin has minimal k values on most reversed phase columns.…”
Section: Introductionmentioning
confidence: 99%
“…Due to its very polar property, carboplatin has minimal k values on most reversed phase columns. Different detection techniques including UV [9,11], electrochemical [12], MS [10,13], ICP-MS [14,15], MS/MS [4] have been applied in the determination of carboplatin. UV detection of carboplatin is limited by its low sensitivity and non-specificity because of the lack of favorable UV absorption properties and the interference of either endogenous compounds or biotransformation products.…”
Section: Introductionmentioning
confidence: 99%
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“…Detection of intact carboplatin is usually required for pharmacokinetic investigations. High-performance liquid chromatography (HPLC) appears to be the method of choice for carboplatin determination in biological samples, with assays using either normal-phase [2][3][4][5] or reverse-phase liquid chromatography (LC) [6][7][8][9][10][11][12][13][14][15][16][17] with UV [2,3,[8][9][10][11]14,15], electrochemical detection [6], LC/mass spectrometry (LC/MS) [12,16] or LC-inductively coupled plasma-MS (LC-ICP-MS) [13,17]. UV detection is affected by non-specificity due to the lack of absorbance by carboplatin and the interference of either endogenous compounds or biotransformation products.…”
Section: Introductionmentioning
confidence: 99%
“…It possesses broad antineoplastic activity. Development of a method by RP-HPLC was difficult owing to its extreme hydrophilicity; it has minimal k values on most ODS columns and is hence not retained on RP-based cartridges and it does not get partitioned extensively into water immiscible solvents [6,7]. Reported methods of analysis of platinum analogs are based upon atomic absorption (flame and nonflame) [8], inductively coupled plasma atomic emission (ICP-AE) [9], electroanalytical techniques [10], neutron activation analysis [11] and gas [12] and normal phase liquid chromatography [13].…”
Section: Introductionmentioning
confidence: 99%