2011
DOI: 10.4314/tjpr.v10i5.16
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Development and Validation of a Bioanalytical Method for Direct Extraction of Diclofenac Potassium from Spiked Plasma

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Cited by 5 publications
(4 citation statements)
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“…Validation of the developed method was performed under the International Conference on Harmonization guidelines and Guidance for Industry: Bioanalytical Method Validation [ 21 , 22 ]. The developed method was further validated against spiked plasma samples under strict compliance as we did previously [ 23 , 24 ]. Before lysis the liposome to determine OA concentration, the free OA was separated from the OA encapsulated liposomes.…”
Section: Methodsmentioning
confidence: 99%
“…Validation of the developed method was performed under the International Conference on Harmonization guidelines and Guidance for Industry: Bioanalytical Method Validation [ 21 , 22 ]. The developed method was further validated against spiked plasma samples under strict compliance as we did previously [ 23 , 24 ]. Before lysis the liposome to determine OA concentration, the free OA was separated from the OA encapsulated liposomes.…”
Section: Methodsmentioning
confidence: 99%
“…Reported dissociation constant (pKa) is found to be 4.0 ± 0.2 at 25°C in water while the partition coefficient in n-octanol at pH 7.4 is 13.4 and at pH 5.2 is 1545. [44][45]…”
Section: Introductionmentioning
confidence: 99%
“…Reported dissociation constant (pKa) is found to be 4.0 ± 0.2 at 25°C in water while the partition coefficient in n-octanol at pH 7.4 is 13.4 and at pH 5.2 is 1545. [44][45]…”
Section: Introductionmentioning
confidence: 99%