Sclareol is a potent enhancer of doxorubicin: Evaluation of the free combination and co-loaded nanostructured lipid carriers against breast cancer

• Published in: Life sciences (1973) 2019-09, Vol.232, p.116678-116678, Article 116678
• Main Authors: Borges, Gabriel Silva Marques, Silva, Juliana de Oliveira, Fernandes, Renata Salgado, de Souza, Ângelo Malachias, Cassali, Geovanni Dantas, Yoshida, Maria Irene, Leite, Elaine Amaral, de Barros, André Luis Branco, Ferreira, Lucas Antônio Miranda
• Format: Article
• Language: English
• Subjects: Anticancer properties; Antitumor activity; Biocompatibility; Body weight; Body weight loss; Breast cancer; Calorimetry; Cancer therapies; Co-encapsulation; Cytotoxicity; Differential scanning calorimetry; Doxorubicin; Encapsulation; Hematology; In vivo methods and tests; Intravenous administration; Light microscopy; Lipids; Nanostructure; Nanostructured lipid carriers; Sclareol; Side effects; Small angle X ray scattering; Synergism; Toxicity; Tumors; Weight loss; X-ray scattering; Zeta potential
• ISSN: 0024-3205; 1879-0631
• DOI: 10.1016/j.lfs.2019.116678

In this work, it was sought to determine if there was synergism between doxorubicin (DOX), a well-known antineoplastic, and sclareol (SC), a diterpene from natural origin, in breast cancer treatment. Moreover, it was investigated if their co-loading in the same nanocarrier would result in a gain of activity and/or a toxicity diminishment. The synergism of the DOX:SC combination was evaluated in MDA-MB-231 and 4T1 cells. A nanostructured lipid carrier (NLC) co-encapsulating DOX and SC in their synergistic molar ratio was prepared and characterised, in terms of mean diameter, zeta potential, DOX encapsulation efficiency, small angle X-ray scattering, differential scanning calorimetry, and polarised light microscopy for further intravenous administration. The anticancer activity of the combination, free and encapsulated, was evaluated in 4T1-tumour bearing mice. It was determined that DOX:SC combination at the molar ratio 1:1.9 presents better synergistic anticancer activity than the molar ratio 1:7.5 in vitro. DOX:SC-loaded NLC (NLC-DOX-SC) improved in vitro cytotoxic and in vivo antitumour activity compared to free DOX. Although NLC-DOX-SC and free DOX:SC, at the synergistic molar ratio, showed similar activity in the in vivo study, the free combination provoked body weight loss, behaviour alterations and haematological toxicity in the animals, while this was not observed for NLC-DOX-SC. This work shows that SC and DOX present synergistic anticancer activity for breast cancer treatment whereas NLC-DOX-SC was a feasible alternative to attain the benefits posed by DOX:SC combination but with none to fewer side effects. Intravenous administered NLC-DOX-SC has a higher antitumour activity in 4T1 tumour-bearing mice than free DOX and is a safer option than the free combination (free DOX + free SC). Abbreviation: NLC-DOX-SC, doxorubicin and sclareol in their synergic molar ratio co-loaded nanostructured lipid carrier; 4T1; murine breast cancer cells; DOX, doxorubicin; SC, sclareol; free DOX + free SC, doxorubicin and sclareol in their synergic molar ratio. [Display omitted]