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Application of drug–metal ion interaction principle in conductometric determination of imatinib, sorafenib, gefitinib and bosutinib
- Source :
- Open Chemistry, Vol 18, Iss 1, Pp 798-807 (2020)
- Publication Year :
- 2020
- Publisher :
- De Gruyter, 2020.
-
Abstract
- An analytical method for the quantification of anticancer agents such as imatinib, sorafenib, gefitinib and bosutinib using conductometry was developed. Each drug solution was mixed with measured concentration of metal ion (Cu2+) solution resulting in drug–metal ion complexation in the titration cell. Conductance was progressively decreased on addition of the analyte solution up to a point of maximum reduction, that is, the end point. Corrected conductance values were calculated from the observed conductance and used to plot a graph against the volume of drug solution added. No interferences were observed from blank and placebo as they gave no clear inflection in the conductivity during titration. The precision and the accuracy of the developed method was established by the analysis of quality control samples; %RSD of corrected conductance values R2 > 0.99). The drugs were successfully analyzed in their respective dosage forms prepared in-house. The method has offered easier, faster and cost-effective analysis of the selected drugs and can be used for routine determinations in the quality control laboratories. More importantly, it is an environmental friendly procedure, as no organic solvent was used throughout the analysis.
- Subjects :
- Sorafenib
Drug
0303 health sciences
conductometric analysis
Chemistry
media_common.quotation_subject
gefitinib
Imatinib
General Chemistry
bosutinib
lcsh:Chemistry
03 medical and health sciences
0302 clinical medicine
Gefitinib
imatinib
lcsh:QD1-999
030220 oncology & carcinogenesis
Materials Chemistry
medicine
Cancer research
sorafenib
Bosutinib
030304 developmental biology
medicine.drug
media_common
Subjects
Details
- Language :
- English
- ISSN :
- 23915420
- Volume :
- 18
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Open Chemistry
- Accession number :
- edsair.doi.dedup.....be01b6a917bd0ac52f9552111fca73f9