Cellular uptake, antitumor response and tumor penetration of cisplatin-loaded milk protein nanoparticles

被引:112
作者
Zhen, Xu
Wang, Xin
Xie, Chen
Wu, Wei
Jiang, Xiqun [1 ]
机构
[1] Nanjing Univ, Coll Chem & Chem Engn, Lab Mesoscop Chem, Nanjing 210093, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Casein; Protein nanoparticles; Drug delivery; Multicellular tumor spheroids; Tumor penetration; ALBUMIN-BOUND PACLITAXEL; DRUG-DELIVERY SYSTEMS; HIV-1 TAT PROTEIN; MULTICELLULAR SPHEROIDS; POLYMERIC MICELLES; CASEIN MICELLES; CREMOPHOR-FREE; SOLID TUMORS; IN-VIVO; TRANSGLUTAMINASE;
D O I
10.1016/j.biomaterials.2012.10.061
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The casein nanoparticles cross-linked by transglutaminase were prepared, and cisplatin (CDDP), as a model antitumor drug, was loaded into the casein nanoparticles. These nanoparticles were characterized by dynamic light scattering (DLS), transmission electron microscopy (TEM), and zeta potential. The uptake and penetration of nanoparticles in 2- and 3-dimensional SH-SY5Y cells were examined at 37 degrees C and 4 degrees C. The in vivo biodistribution of the nanoparticles was investigated using near-infrared fluorescence (NIRF) imaging and ion-coupled plasma mass spectrometry (ICP-MS). The antitumor effect of CDDP-loaded nanoparticles was evaluated on hepatic H22 tumor-bearing mice model via intravenous administration. It is found that the obtained nanoparticles showed spherical shape with the size of 257 nm, and drug loading content of 10%. These CDDP-loaded casein nanoparticles have the extraordinary capabilities to penetrate cell membrane barriers, target tumor and inhibit tumor growth. The tumor growth inhibition of CDDP-loaded nanoparticles is 1.5-fold higher than that of free CDDP. Further, the penetration examination of the CDDP-loaded casein nanoparticles in the tumor tissue demonstrated that the nanoparticles had the ability to penetrate the tumor and deliver CDDP to the tumor more deeply and affect the cells far from the vasculature. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1372 / 1382
页数:11
相关论文
共 34 条
[1]   The angiogenesis induced by HIV-1 Tat protein is mediated by the Flk-1/KDR receptor on vascular endothelial cells [J].
Albini, A ;
Soldi, R ;
Giunciuglio, D ;
Giraudo, E ;
Benelli, R ;
Primo, L ;
Noonan, D ;
Salio, M ;
Camussi, G ;
Rockl, W ;
Bussolino, F .
NATURE MEDICINE, 1996, 2 (12) :1371-1375
[2]   Design of a peptide-based vector, PepFect6, for efficient delivery of siRNA in cell culture and systemically in vivo [J].
Andaloussi, Samir E. L. ;
Lehto, Taavi ;
Maeger, Imre ;
Rosenthal-Aizman, Katri ;
Oprea, Iulian I. ;
Simonson, Oscar E. ;
Sork, Helena ;
Ezzat, Kariem ;
Copolovici, Dana M. ;
Kurrikoff, Kaido ;
Viola, Joana R. ;
Zaghloul, Eman M. ;
Sillard, Rannar ;
Johansson, Henrik J. ;
Hassane, Fatouma Said ;
Guterstam, Peter ;
Suhorutsenko, Julia ;
Moreno, Pedro M. D. ;
Oskolkov, Nikita ;
Haelldin, Jonas ;
Tedebark, Ulf ;
Metspalu, Andres ;
Lebleu, Bernard ;
Lehtioe, Janne ;
Smith, C. I. Edvard ;
Langel, Uelo .
NUCLEIC ACIDS RESEARCH, 2011, 39 (09) :3972-3987
[3]   Development and characterization of a novel drug nanocarrier for oral delivery, based on self-assembled β-casein micelles [J].
Bachar, Michal ;
Mandelbaum, Amitai ;
Portnaya, Irina ;
Perlstein, Hadas ;
Even-Chen, Simcha ;
Barenholz, Yechezkel ;
Danino, Dganit .
JOURNAL OF CONTROLLED RELEASE, 2012, 160 (02) :164-171
[4]   Increased antitumor activity, intratumor paclitaxel concentrations, and endothelial cell transport of Cremophor-free, albumin-bound paclitaxel, ABI-007, compared with Cremophor-based paclitaxel [J].
Desai, N ;
Trieu, V ;
Yao, ZW ;
Louie, L ;
Ci, S ;
Yang, A ;
Tao, CL ;
De, T ;
Beals, B ;
Dykes, D ;
Noker, P ;
Yao, R ;
Labao, E ;
Hawkins, M ;
Soon-Shiong, P .
CLINICAL CANCER RESEARCH, 2006, 12 (04) :1317-1324
[5]   Tumor Accumulation, Penetration, and Antitumor Response of Cisplatin-Loaded Gelatin/Poly(acrylic acid) Nanoparticles [J].
Ding, Dan ;
Wang, Jing ;
Zhu, Zhenshu ;
Li, Rutian ;
Wu, Wei ;
Liu, Baorui ;
Jiang, Xiqun .
ACS APPLIED MATERIALS & INTERFACES, 2012, 4 (03) :1838-1846
[6]   Nanospheres-Incorporated Implantable Hydrogel as a Trans-Tissue Drug Delivery System [J].
Ding, Dan ;
Zhu, Zhenshu ;
Li, Rutian ;
Li, Xiaolin ;
Wu, Wei ;
Jiang, Xiqun ;
Liu, Baorui .
ACS NANO, 2011, 5 (04) :2520-2534
[7]   Cisplatin-loaded gelatin-poly(acrylic acid) nanoparticles: Synthesis, antitumor efficiency in vivo and penetration in tumors [J].
Ding, Dan ;
Zhu, Zhenshu ;
Liu, Qin ;
Wang, Jing ;
Hu, Yong ;
Jiang, Xiqun ;
Liu, Baorui .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2011, 79 (01) :142-149
[8]   Albumin-based nanoparticles as potential controlled release drug delivery systems [J].
Elzoghby, Ahmed O. ;
Samy, Wael M. ;
Elgindy, Nazik A. .
JOURNAL OF CONTROLLED RELEASE, 2012, 157 (02) :168-182
[9]   Casein-based formulations as promising controlled release drug delivery systems [J].
Elzoghby, Ahmed O. ;
El-Fotoh, Wael S. Abo ;
Elgindy, Nazik A. .
JOURNAL OF CONTROLLED RELEASE, 2011, 153 (03) :206-216
[10]   Multicellular spheroids as an in vitro tumor model [J].
Hamilton, G .
CANCER LETTERS, 1998, 131 (01) :29-34