2013
DOI: 10.1016/j.electacta.2013.09.017
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Electrochemical and spectrophotometric characterisation of protein kinase inhibitor and anticancer drug danusertib

Abstract: This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain. A c c e p t e d M a n u s c r i p t 2 AbstractThe … Show more

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Cited by 17 publications
(8 citation statements)
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“…The expected mechanism behind the generated irreversible oxidation current at the higher potential is the loss of an electron in the piperazine ring as reported for other piperazine‐containing compounds . Thus, the deprotonated piperazine functional group may be regarded as the electroactive form.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…The expected mechanism behind the generated irreversible oxidation current at the higher potential is the loss of an electron in the piperazine ring as reported for other piperazine‐containing compounds . Thus, the deprotonated piperazine functional group may be regarded as the electroactive form.…”
Section: Resultsmentioning
confidence: 99%
“…To decrease the volume of blood sampling, SPE was used for the determination of the drug in human plasma and DBS after sample pretreatment. The results obtained by the proposed method were compared with those obtained from the reported methods ,, respectively according to t‐test and F‐test (Table ).…”
Section: Resultsmentioning
confidence: 99%
“…Longer incubation times would cause the oxidation peak to reduce where intercalation of the drug with DNA will take over as the main interaction mechanism. [29][30][31] Figure 5B shows a linear regression curve obtained (r 2 = 0.99) for the detection of ciprofloxacin in acetate buffer (background measurement was subtracted from each reading) with a wide linear range of 0.1 -100 μM and a detection limit of 0.1 μM . The limit of detection in this investigation, which corresponds to the amount of ciprofloxacin that can be truly detected in a sample solution, 32 was acquired by visual evaluation.…”
Section: Analytical Performance Of Dna Based Biosensormentioning
confidence: 99%
“…6B) for SNPC using the method reported in literature. 36 The 2 nd oxidation signal of SNPC showed saturation at 0.7 mM due to the possible adsorption of the oxidation product formed around 0.3 V. Therefore, the peak at 0.3 V was used for analytical determination. constant was determined at different temperatures for the calculation of G # was then calculated.…”
Section: Resultsmentioning
confidence: 99%