Biocompatible nanoparticles containing hydrophobic nickel-bis(dithiolene) complexes for NIR-mediated doxorubicin release and photothermal therapy

被引:20
作者
Ciancone, Mathieu [1 ]
Mebrouk, Kenny [1 ]
Bellec, Nathalie [1 ]
Le Goff-Gaillard, Catherine [2 ]
Arlot-Bonnemains, Yannick [2 ]
Benvegnu, Thierry [1 ]
Fourmigue, Marc [1 ]
Camerel, Franck [1 ]
Cammas-Marion, Sandrine [1 ]
机构
[1] Univ Rennes, ENSCR, CNRS, UMR 6226,ISCR, F-35000 Rennes, France
[2] Univ Rennes, CNRS, UMR 6290, IGDR,BIOSIT,UMS 3480, Rennes, France
关键词
DRUG-DELIVERY SYSTEMS; CANCER-THERAPY; INDOCYANINE GREEN; IN-VITRO; MICELLES; NANOMEDICINE; NANOCARRIERS; ACID; DESIGN; ESTERS;
D O I
10.1039/c7tb03289g
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Biocompatible nanoparticles (NPs) constituted by amphiphilic poly(ethylene glycol)-block-poly(benzyl malate), PEG-b-PMLABe, have been designed for site-specific PhotoThermal Controlled Release (PTCR) of drugs thanks to the presence of a near infra-red (NIR) photothermally active nickel-bis(dithiolene) complex in the inner core of the NPs, together with doxorubicin (Dox). A nanoprecipitation technique was used to prepare well-defined nickel-bis(dithiolene) and nickel-bis(dithiolene)/Dox loaded NPs, which were characterized by dynamic light scattering (DLS), zeta-potential measurements and Transmission Electron Microscopy (TEM). We have shown that the Dox release was effectively controlled by NIR irradiation (long or pulsed NIR laser irradiation). Cytotoxicity experiments on HeLa and MDA-MB-231 cells have shown that the incorporation of more than 10 w% of nickel-bis(dithiolene) complexes does not increase the intrinsic toxicity of the polymer nanoparticles. Finally, the viability of MDA-MB-231 cells was assessed after their incubation, for 24 hours, with empty NPs, Ni4C(12) loaded NPs, Dox loaded NPs or Ni4C(12)/Dox loaded NPs, without or with NIR irradiation. Above all, the results have highlighted that the Ni4C(12) loaded NPs after 5 min NIR laser irradiation can induce strong cell death up to 80% at 50 g mL(-1). These results demonstrate that these NPs are good candidates for photothermal therapy.
引用
收藏
页码:1744 / 1753
页数:10
相关论文
共 54 条
[1]   Stimulus-Responsive Degradable Polylactide-Based Block Copolymer Nanoassemblies for Controlled/Enhanced Drug Delivery [J].
Bawa, Kamaljeet K. ;
Oh, Jung Kwon .
MOLECULAR PHARMACEUTICS, 2017, 14 (08) :2460-2474
[2]   Polymeric mixed micelles as nanomedicines: Achievements and perspectives [J].
Cagel, Maximiliano ;
Tesan, Fiorella C. ;
Bernabeu, Ezequiel ;
Salgueiro, Maria J. ;
Zubillaga, Marcela B. ;
Moretton, Marcela A. ;
Chiappetta, Diego A. .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2017, 113 :211-228
[3]   Poly(beta-malic acid): Obtaining high molecular weights by improvement of the synthesis route [J].
Cammas, S ;
Renard, I ;
Langlois, V ;
Guerin, P .
POLYMER, 1996, 37 (18) :4215-4220
[4]  
Cammas-Marion S, 2000, MACROMOL CHEM PHYSIC, V201, P355, DOI 10.1002/(SICI)1521-3935(20000201)201:3<355::AID-MACP355>3.0.CO
[5]  
2-9
[6]  
Cammas-Marion S, 2000, MACROMOL SYMP, V153, P167, DOI 10.1002/1521-3900(200003)153:1<167::AID-MASY167>3.0.CO
[7]  
2-Q
[8]   Nanochemistry and Nanomedicine for Nanoparticle-based Diagnostics and Therapy [J].
Chen, Guanying ;
Roy, Indrajit ;
Yang, Chunhui ;
Prasad, Paras N. .
CHEMICAL REVIEWS, 2016, 116 (05) :2826-2885
[9]   Neuroendocrine Tumor-Targeted Upconversion Nanoparticle-Based Micelles for Simultaneous NIR-Controlled Combination Chemotherapy and Photodynamic Therapy, and Fluorescence Imaging [J].
Chen, Guojun ;
Jaskula-Sztul, Renata ;
Esquibel, Corinne R. ;
Lou, Irene ;
Zheng, Qifeng ;
Dammalapati, Ajitha ;
Harrison, April ;
Eliceiri, Kevin W. ;
Tang, Weiping ;
Chen, Herbert ;
Gong, Shaoqin .
ADVANCED FUNCTIONAL MATERIALS, 2017, 27 (08)
[10]   Targeting tumors with cyclic RGD-conjugated lipid nanoparticles loaded with an IR780 NIR dye: In vitro and in vivo evaluation [J].
Choi, Jungyoon ;
Rustique, Emilie ;
Henry, Maxime ;
Guidetti, Melanie ;
Josserand, VRonique ;
Sancey, Lucie ;
Boutet, Jerome ;
Coll, Jean-Luc .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2017, 532 (02) :677-685