Chemosensitization and mitigation of Adriamycin-induced cardiotoxicity using combinational polymeric micelles for co-delivery of quercetin/resveratrol and resveratrol/curcumin in ovarian cancer

被引:46
作者
Al Fatease, Adel [1 ,4 ]
Shah, Vidhi [1 ]
Nguyen, Duc X. [1 ]
Cote, Brianna [1 ]
LeBlanc, Nicole [2 ]
Rao, Deepa A. [3 ]
Alani, Adam W. G. [1 ,5 ]
机构
[1] Oregon State Univ, Coll Pharm, Corvallis, OR 97331 USA
[2] Oregon State Univ, Carlson Coll Vet Med, Corvallis, OR 97331 USA
[3] Pacific Univ, Sch Pharm, Forest Grove, OR USA
[4] King Khalid Univ, Coll Pharm, Abha, Saudi Arabia
[5] Oregon Hlth & Sci Univ, Dept Biomed Engn, Portland, OR 97201 USA
关键词
Adriamycin; Chemosensitization; Cardioprotection; Ovarian cancer; Micellar Polyphenols; DOXORUBICIN-INDUCED CARDIOMYOPATHY; LIPOSOMAL DOXORUBICIN; BREAST-CANCER; IN-VITRO; ANTHRACYCLINE; CARDIOPROTECTION; DEXRAZOXANE; MANAGEMENT; TOXICITY; OPINION;
D O I
10.1016/j.nano.2019.03.011
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
This work looks to improve the efficacy of Adriamycin (ADR) while mitigating its cardiotoxicity using combinations of micellar resveratrol (R): quercetin (Q) (mRQ) or R: curcumin (C) (mRC) in healthy mice and ovarian cancer xenograft models. Ovarian cancer cells, ES2-Luc, or A2780ADR are inoculated in mice (n =4/group) and sorted into eight cohorts. Mice are treated weekly for 4 weeks with ADR, ADR+mRQ, ADR+mRC, or controls (saline, empty micelles, ADR+EM, mRQ, or mRC). To evaluate the degree of cardioprotection, serum is collected to determine the cardiac Troponin I (cTnI). Cardiac tissue is collected for morphological evaluation and evaluation of creatine kinase levels. Our results indicate that mRQ+ADR is statistically significant in tumor reduction in xenograft models. In healthy mice, the left ventricular ejection fraction and fractional shortening in the ADR treated group is most compromised. Co-administration of mRQ with ADR can reduce ADR dosing through chemosensitization while being cardioprotective. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:39 / 48
页数:10
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