Evaluation of biocompatibility and antioxidant efficiency of chitosan-alginate nanoparticles loaded with quercetin

被引:96
作者
Aluani, Denitsa [1 ]
Tzankova, Virginia [1 ]
Kondeva-Burdina, Magdalena [1 ]
Yordanov, Yordan [1 ]
Nikolova, Elena [2 ]
Odzhakov, Feodor [3 ]
Apostolov, Alexandar [3 ]
Markova, Tzvetanka [4 ]
Yoncheva, Krassimira [5 ]
机构
[1] Med Univ Sofia, Fac Pharm, Dept Pharmacol Pharmacotherapy & Toxicol, 2 Dunav St, Sofia 1000, Bulgaria
[2] Bulgarian Acad Sci, Inst Expt Morphol Pathol & Anthropol Museum, Acad G Bonchev St,Bl 25, BG-1113 Sofia, Bulgaria
[3] Med Univ Sofia, Med Fac, Dept Forens Med & Deontol, Sofia 1431, Bulgaria
[4] Med Univ Sofia, Fac Med, Dept Pharmacol & Toxicol, 2 Zdrave St, Sofia 1407, Bulgaria
[5] Med Univ Sofia, Fac Pharm, Dept Pharmaceut Technol & Biopharmaceut, 2 Dunav St, Sofia 1000, Bulgaria
关键词
Chitosan/alginate nanoparticles; Quercetin; Antioxidant activity; CORE-SHELL NANOPARTICLES; TERT-BUTYL HYDROPEROXIDE; CELL LINE HEPG2; OXIDATIVE STRESS; IN-VIVO; THERAPEUTIC-EFFICACY; ISOLATED HEPATOCYTES; DEFENSE SYSTEM; DRUG-DELIVERY; CYTOTOXICITY;
D O I
10.1016/j.ijbiomac.2017.05.062
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
The present study deals with development and evaluation of the safety profile of chitosan/alginate nanoparticles as a platform for delivery of a natural antioxidant quercetin. The nanoparticles were prepared by varying the ratios between both biopolymers giving different size and charge of the formulations. The biocompatibility was explored in vitro in cells from different origin: cultivated HepG2 cells, isolated primary rat hepatocytes, isolated murine spleen lymphocytes and macrophages. In vivo toxicological evaluation was performed after repeated 14-day oral administration to rats. The study revealed that chitosan/alginate nanoparticles did not change body weight, the relative weight of rat livers, liver histology, hematology and biochemical parameters. The protective effects of quercetin-loaded nanoparticles were investigated in the models of iron/ascorbic acid (Fe2+/AA) induced lipid peroxidation in microsomes and tert-butyl hydroperoxide oxidative stress in isolated rat hepatocytes. Interesting finding was that the empty chitosan/alginate nanoparticles possessed protective activity themselves, The antioxidant effects of quercetin loaded into the nanoparticles formulated with higher concentration of chitosan were superior compared to quercetin encapsulated in nanoparticles with higher amount of sodium alginate. In conclusion, chitosan/alginate nanoparticles can be considered appropriate carrier for quercetin, combining safety profile and improved protective activity of the encapsulated antioxidant. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:771 / 782
页数:12
相关论文
共 47 条
[1]   Influence of quercetin and rutin on growth and antioxidant defense system of a human hepatoma cell line (HepG2) [J].
Alía, M ;
Mateos, R ;
Ramos, S ;
Lecumberri, E ;
Bravo, L ;
Goya, L .
EUROPEAN JOURNAL OF NUTRITION, 2006, 45 (01) :19-28
[2]   Response of the antioxidant Defense system to tert-butyl hydroperoxide and hydrogen peroxide in a human hepatoma cell line (HepG2) [J].
Alía, M ;
Ramos, S ;
Mateos, R ;
Bravo, L ;
Goya, L .
JOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGY, 2005, 19 (02) :119-128
[3]   Polymeric colloidal particulate systems: intelligent tools for intracellular targeting of antileishmanial cargos [J].
Asthana, Shalini ;
Gupta, Pramod K. ;
Chaurasia, Mohini ;
Dube, Anuradha ;
Chourasia, Manish K. .
EXPERT OPINION ON DRUG DELIVERY, 2013, 10 (12) :1633-1651
[4]   Alginate coated chitosan core shell nanoparticles for oral delivery of enoxaparin: In vitro and in vivo assessment [J].
Bagre, Archana Pataskar ;
Jain, Keerti ;
Jain, Narendra K. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2013, 456 (01) :31-40
[5]  
Bai XP, 2007, ASIA PAC J CLIN NUTR, V16, P169
[6]   Bioavailability of Quercetin: Problems and Promises [J].
Cai, X. ;
Fang, Z. ;
Dou, J. ;
Yu, A. ;
Zhai, G. .
CURRENT MEDICINAL CHEMISTRY, 2013, 20 (20) :2572-2582
[7]   Therapeutic efficacy of quercetin enzyme-responsive nanovesicles for the treatment of experimental colitis in rats [J].
Castangia, Ines ;
Nacher, Amparo ;
Caddeo, Carla ;
Merino, Virginia ;
Diez-Sales, Octavio ;
Catalan-Latorre, Ana ;
Fernandez-Busquets, Xavier ;
Fadda, Anna Maria ;
Manconi, Maria .
ACTA BIOMATERIALIA, 2015, 13 :216-227
[8]   Elucidating the mechanism of cellular uptake and removal of protein-coated gold nanoparticles of different sizes and shapes [J].
Chithrani, B. Devika ;
Chan, Warren C. W. .
NANO LETTERS, 2007, 7 (06) :1542-1550
[9]  
Christine B. S., 2012, PHARM RES, V65, P523
[10]   Fruit and vegetable intake and mortality from ischaemic heart disease: results from the European Prospective Investigation into Cancer and Nutrition (EPIC)-Heart study [J].
Crowe, Francesca L. ;
Roddam, Andrew W. ;
Key, Timothy J. ;
Appleby, Paul N. ;
Overvad, Kim ;
Jakobsen, Marianne U. ;
Tjonneland, Anne ;
Hansen, Louise ;
Boeing, Heiner ;
Weikert, Cornelia ;
Linseisen, Jakob ;
Kaaks, Rudolf ;
Trichopoulou, Antonia ;
Misirli, Gesthimani ;
Lagiou, Pagona ;
Sacerdote, Carlotta ;
Pala, Valeria ;
Palli, Domenico ;
Tumino, Rosario ;
Panico, Salvatore ;
Bueno-de-Mesquita, H. Bas ;
Boer, Jolanda ;
van Gils, Carla H. ;
Beulens, Joline W. J. ;
Barricarte, Aurelio ;
Rodriguez, Laudina ;
Larranaga, Nerea ;
Sanchez, Maria-Jose ;
Tormo, Maria-Jose ;
Buckland, Genevieve ;
Lund, Eiliv ;
Hedblad, Bo ;
Melander, Olle ;
Jansson, Jan-Hakan ;
Wennberg, Patrik ;
Wareham, Nicholas J. ;
Slimani, Nadia ;
Romieu, Isabelle ;
Jenab, Mazda ;
Danesh, John ;
Gallo, Valentina ;
Norat, Teresa ;
Riboli, Elio .
EUROPEAN HEART JOURNAL, 2011, 32 (10) :1235-1243