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July 11, 2023Pharmaceutics51 citationsOpen Access

Reduction of Doxorubicin-Induced Cardiotoxicity by Co-Administration of Smart Liposomal Doxorubicin and Free Quercetin: In Vitro and In Vivo Studies

HDHamidreza DorostkarBHBibi Fatemeh HaghiralsadatMHMahdie Hemati

Key Points

  • This study aims to evaluate the effectiveness of liposomal doxorubicin and free quercetin in reducing doxorubicin-induced cardiotoxicity.
  • Designed and synthesized liposomal doxorubicin via thin-film method with physicochemical characterization.

Structured PICO

Does co-administration of liposomal doxorubicin and free quercetin reduce doxorubicin-induced cardiotoxicity in rat models and H9c2 cells?

P
Population
Rat models and H9c2 cells
I
Intervention
Co-administration of liposomal doxorubicin and free quercetin
C
Comparator
Free doxorubicin, empty liposomes, and carrier
O
Outcome
Cardiotoxicity measured by cardiac enzymes (CK-MB, LDH), oxidative stress markers (MDA), antioxidant markers, and histopathologysurrogate

Co-administration of liposomal doxorubicin and free quercetin shows promise in mitigating doxorubicin-induced cardiotoxicity by reducing oxidative stress and apoptosis in preclinical models.

Abstract

Doxorubicin is one of the most effective chemotherapeutic agents; however, it has various side effects, such as cardiotoxicity. Therefore, novel methods are needed to reduce its adverse effects. Quercetin is a natural flavonoid with many biological activities. Liposomes are lipid-based carriers widely used in medicine for drug delivery. In this study, liposomal doxorubicin with favorable characteristics was designed and synthesized by the thin-film method, and its physicochemical properties were investigated by different laboratory techniques. Then, the impact of the carrier, empty liposomes, free doxorubicin, liposomal doxorubicin, and quercetin were analyzed in animal models. To evaluate the interventions, measurements of cardiac enzymes, oxidative stress and antioxidant markers, and protein expression were performed, as well as histopathological studies. Additionally, cytotoxicity assay and cellular uptake were carried out on H9c2 cells. The mean size of the designed liposomes was 98.8 nm, and the encapsulation efficiency (EE%) was about 85%. The designed liposomes were anionic and pH-sensitive and had a controlled release pattern with excellent stability. Co-administration of liposomal doxorubicin with free quercetin to rats led to decreased weight loss, creatine kinase (CK-MB), lactate dehydrogenase (LDH), and malondialdehyde (MDA), while it increased the activity of glutathione peroxidase, catalase, and superoxide dismutase enzymes in their left ventricles. Additionally, it changed the expression of NOX1, Rac1, Rac1-GTP, SIRT3, and Bcl-2 proteins, and caused tissue injury and cell cytotoxicity. Our data showed that interventions can increase antioxidant capacity, reduce oxidative stress and apoptosis in heart tissue, and lead to fewer complications. Overall, the use of liposomal doxorubicin alone or the co-administration of free doxorubicin with free quercetin showed promising results.

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Cite This Study

Dorostkar et al. (2023) studied this question.

synapsesocial.com/papers/69d7ccd161e2ce1627d18111https://doi.org/10.3390/pharmaceutics15071920
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