Antimicrobial, anticancer and antioxidant activities of nano-heart of Phoenix dactylifera tree extract loaded chitosan nanoparticles: In vitro and in vivo study

被引:25
作者
Sahyon, Heba A. [1 ]
Al-Harbi, Sami A. [2 ]
机构
[1] Kafrelsheikh Univ, Fac Sci, Chem Dept, Kafrelsheikh 33516, Egypt
[2] Umm Al Qura Univ, Univ Coll Al Jamoum, Chem Dept, Mecca 21955, Saudi Arabia
关键词
Anticancer; Antibacterial; Heart of P. dactylifera extract; Chitosan nanoparticles; PD-1; Apoptosis; DOXORUBICIN-INDUCED CARDIOTOXICITY; OXIDATIVE STRESS; ANTHRACYCLINE ANTIBIOTICS; ELLAGIC ACID; CELL-GROWTH; DELIVERY; CANCER; ASSAY; BIOAVAILABILITY; APOPTOSIS;
D O I
10.1016/j.ijbiomac.2020.05.224
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This study aimed to present a new heart of P. dactylifera (HP) extract loaded chitosan nanoparticles and estimate its anticancer, antimicrobial, antioxidant activity and free radical scavenger effect (in vitro). This nano-supplement may prevent doxorubicin cardiotoxicity and nephrotoxicity in rat model. The HP extract was loaded on chitosan nanoparticles producing HP-ChNPs, then characterized. The antioxidant properties of the HP-ChNPs was assessed in vitro. The antibacterial activity against three-gram positive bacteria and two gram-negative bacteria were done. The in vitro studies of cytotoxicity against MCF7, CaCo3, and Hela cell lines were also evaluated. Then, the protective effect of the HP-ChNPs (2 mg/kg, IP) was evaluated against doxorubicin induce organ toxicity in a rat model. The in vitro studies revealed the antibacterial, anticancer and antioxidant activities of the HP-ChNPs. The in vivo study demonstrates reduction of heart and kidney apoptosis with increased programmed cell death protein-1 (PD-1); as the major anticancer drug (doxorubicin) pathway is to release free radicals with decreased PD-1 levels and induction of apoptosis. In conclusion, the HP-ChNPs, in a very small dose, might be a promising supplement to avoid doxorubicin toxicity with improvment the antioxidant enzymes without affecting its anticancer activity. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:1230 / 1241
页数:12
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