Why the study?
Because of the myocardial toxicity and cardiotoxicity limiting doxorubicin dosing, monitoring its concentration in body fluids is important, prompting the development of a simple and quick spectrophotometric detection method in blood and plasma.
A simple spectrophotometric method was developed to detect doxorubicin concentrations in blood and plasma, which may facilitate monitoring to prevent cardiotoxicity.
May enable plasma monitoring to limit doxorubicin cardiotoxicity; leaves open clinical validation before practice adoption.
The aim of presented research is to develop a simple and quick method of spectrophotometric detection for the determination of doxorubicin hydrochloride in blood and plasma. Anthracycline antibiotics are among the most effective antineoplastic agents. However, despite their high efficacy in the treatment of various types of cancer, their administration is limited primarily because they exhibit myocardial toxicity. This may be a limiting factor in the dosage of medications; nevertheless, drugs exhibiting this mechanism of action constitute a very important group of chemotherapeutics. One of the more widely studied antibiotics from the anthracycline group is doxorubicin. It exhibits the highest antineoplastic activity from among a number of derivative compounds. Because of the adverse effects of doxorubicin, especially cardiotoxicity, it is important to maintain control of its concentration in body fluids. The method in the study consists of extraction doxorubicin from the plasma or blood and measurements of the absorbance of light in the visible light range in a DOX solution with respect to a reference sample. The research used blood and plasma samples spiked with doxorubicin to give concentrations in the range of 0.2-10 µg/mL. Obtained LODs were 1.6 µg/mL and 1.2 µg/mL, respectively.
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Sikora et al. (2022) studied this question.
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