Influence of chitosan coating on magnetic nanoparticles in endothelial cells and acute tissue biodistribution

被引:15
作者
Agotegaray, Mariela [1 ]
Campelo, Adrian [2 ]
Zysler, Roberto [3 ]
Gumilar, Fernanda [2 ]
Bras, Cristina [2 ]
Minetti, Alejandra [2 ]
Massheimer, Virginia [2 ]
Lassalle, Veronica [1 ]
机构
[1] Univ Nacl Sur, Dept Quim, INQUISUR, CONICET, Avda Alem 1253,B8000CPB, Bahia Blanca, Buenos Aires, Argentina
[2] Univ Nacl Sur, INBIOSUR, CONICET, DBByF, San Juan 670, RA-8000 Bahia Blanca, Buenos Aires, Argentina
[3] Consejo Nacl Invest Cient & Tecn, Div Resonancias Magnet, CNEA, Ctr Atom Bariloche, Avda Bustillo Km 9,5, RA-8400 San Carlos De Bariloche, Rio Negro, Argentina
关键词
Magnetic carriers; nanoparticles; chitosan; endothelial cells; biodistribution; IRON-OXIDE NANOPARTICLES; IN-VIVO; VITRO; BIOCOMPATIBILITY; CYTOTOXICITY; CLEARANCE; PARTICLES; MECHANISM; TOXICITY; EFFICACY;
D O I
10.1080/09205063.2016.1170417
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Chitosan coating on magnetic nanoparticles (MNPs) was studied on biological systems as a first step toward the application in the biomedical field as drug-targeted nanosystems. Composition of MNPs consists of magnetite functionalized with oleic acid and coated with the biopolymer chitosan or glutaraldehyde-cross-linked chitosan. The influence of the biopolymeric coating has been evaluated by in vitro and in vivo assays on the effects of these MNPs on rat aortic endothelial cells (ECs) viability and on the random tissue distribution in mice. Results were correlated with the physicochemical properties of the nanoparticles. Nitric oxide (NO) production by ECs was determined, considering that endothelial NO represents one of the major markers of ECs function. Cell viability was studied by MTT assay. Different doses of the MNPs (1, 10 and 100g/mL) were assayed, revealing that MNPs coated with non-cross-linked chitosan for 6 and 24 h did not affect neither NO production nor cell viability. However, a significant decrease in cell viability was observed after 36 h treatment with the highest dose of this nanocarrier. It was also revealed that the presence and dose of glutaraldehyde in the MNPs structureimpact on the cytotoxicity. The study of the acute tissue distribution was performed acutely in mice after 24 h of an intraperitoneal injection of the MNPs and sub acutely, after 28days of weekly administration. Both formulations greatly avoided the initial clearance by the reticuloendothelial system (RES) in liver. Biological properties found for N1 and N2 in the performed assays reveal that chitosan coating improves biocompatibility of MNPs turning these magnetic nanosystems as promising devices for targeted drug delivery.
引用
收藏
页码:1069 / 1085
页数:17
相关论文
共 38 条
[11]   Overcoming in vivo barriers to targeted nanodelivery [J].
Chrastina, Adrian ;
Massey, Kerri A. ;
Schnitzer, Jan E. .
WILEY INTERDISCIPLINARY REVIEWS-NANOMEDICINE AND NANOBIOTECHNOLOGY, 2011, 3 (04) :421-437
[12]   Magnetic brain tumor targeting and biodistribution of long-circulating PEG-modified, cross-linked starch-coated iron oxide nanoparticles [J].
Cole, Adam J. ;
David, Allan E. ;
Wang, Jianxin ;
Galban, Craig J. ;
Yang, Victor C. .
BIOMATERIALS, 2011, 32 (26) :6291-6301
[13]   Nanotoxicology [J].
Donaldson, K ;
Stone, V ;
Tran, CL ;
Kreyling, W ;
Borm, PJA .
OCCUPATIONAL AND ENVIRONMENTAL MEDICINE, 2004, 61 (09) :727-728
[14]   The cytotoxicity evaluation of magnetic iron oxide nanoparticles on human aortic endothelial cells [J].
Ge, Gaoyuan ;
Wu, Hengfang ;
Xiong, Fei ;
Zhang, Yu ;
Guo, Zhirui ;
Bian, Zhiping ;
Xu, Jindan ;
Gu, Chunrong ;
Gu, Ning ;
Chen, Xiangjian ;
Yang, Di .
NANOSCALE RESEARCH LETTERS, 2013, 8 :1-10
[15]   Cytotoxicity of glutaraldehyde crosslinked collagen/poly(vinyl alcohol) films is by the mechanism of apoptosis [J].
Gough, JE ;
Scotchford, CA ;
Downes, S .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 2002, 61 (01) :121-130
[16]  
Hall J. E., 2020, Guyton and Hall textbook of medical physiology
[17]   Biodistribution, clearance, and biocompatibility of iron oxide magnetic nanoparticles in rats [J].
Jain, Tapan K. ;
Reddy, Maram K. ;
Morales, Marco A. ;
Leslie-Pelecky, Diandra L. ;
Labhasetwar, Vinod .
MOLECULAR PHARMACEUTICS, 2008, 5 (02) :316-327
[18]   Cellular uptake of magnetic fluid particles and their effects on human adenocarcinoma cells exposed to AC magnetic fields in vitro [J].
Jordan, A ;
Wust, P ;
Scholz, R ;
Tesche, B ;
Fahling, H ;
Mitrovics, T ;
Vogl, T ;
CervosNavarro, J ;
Felix, R .
INTERNATIONAL JOURNAL OF HYPERTHERMIA, 1996, 12 (06) :705-722
[19]   Biodistribution of chitosan-based magnetite suspensions for targeted hyperthermia in ICR mice [J].
Kim, DH ;
Lee, SH ;
Im, KH ;
Kim, KN ;
Kim, KM ;
Kim, KD ;
Park, H ;
Shim, IB ;
Lee, YK .
IEEE TRANSACTIONS ON MAGNETICS, 2005, 41 (10) :4158-4160
[20]   Chitosan and its derivatives for tissue engineering applications [J].
Kim, In-Yong ;
Seo, Seog-Jin ;
Moon, Hyun-Seuk ;
Yoo, Mi-Kyong ;
Park, In-Young ;
Kim, Bom-Chol ;
Cho, Chong-Su .
BIOTECHNOLOGY ADVANCES, 2008, 26 (01) :1-21