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

LIFE SCIENCES

卷:232

Article

Marques Borges, Gabriel Silva¹  Silva, Juliana de Oliveira¹  Fernandes, Renata Salgado¹  de Souza, Angelo Malachias²  Cassali, Geovanni Dantas³  Yoshida, Maria Irene⁴  Leite, Elaine Amaral¹  Branco de Barros, Andre Luis⁵  Miranda Ferreira, Lucas Antonio¹ 

[1] Univ Fed Minas Gerais, Fac Pharm, Dept Pharmaceut, Belo Horizonte, MG, Brazil

[2] Univ Fed Minas Gerais, Exact Sci Inst, Dept Phys, Belo Horizonte, MG, Brazil

[3] Univ Fed Minas Gerais, Inst Biol Sci, Dept Gen Pathol, Belo Horizonte, MG, Brazil

[4] Univ Fed Minas Gerais, Exact Sci Inst, Dept Chem, Belo Horizonte, MG, Brazil

[5] Univ Fed Minas Gerais, Fac Pharm, Dept Clin Anal & Toxicol, Belo Horizonte, MG, Brazil

关键词: Doxorubicin;    Sclareol;    Co-encapsulation;    Synergism;    Breast cancer;    Nanostructured lipid carriers;   

DOI  :  10.1016/j.lfs.2019.116678

来源: Elsevier

【 摘 要 】

Aims: 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. Main methods: 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. Key findings: 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. Significance: 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.

【 授权许可】

Free