Paclitaxel/gelatin coated magnetic mesoporous silica nanoparticles: Preparation and antitumor efficacy in vivo

被引:43
作者
Che, Erxi [1 ]
Gao, Yikun [2 ]
Wan, Long [1 ]
Zhang, Ying [1 ]
Han, Ning [1 ]
Bai, Junling [1 ]
Li, Jia [1 ]
Sha, Zhou [1 ]
Wang, Siling [1 ]
机构
[1] Shenyang Pharmaceut Univ, Dept Pharmaceut, Shenyang 110016, Liaoning Provin, Peoples R China
[2] Shenyang Pharmaceut Univ, Sch Med Devices, Shenyang 110016, Liaoning Provin, Peoples R China
基金
中国国家自然科学基金;
关键词
Magnetic targeted drug delivery; Gelatin coating; Sustained release; Paclitaxel; In vivo anticancer therapy; SENTINEL LYMPH-NODES; DRUG-DELIVERY; ANTICANCER DRUG; RELEASE; SYSTEMS;
D O I
10.1016/j.micromeso.2014.11.013
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
We reported a magnetic targeted drug delivery system based on core/shell structural magnetic mesoporous silica nanoparticles (MMSNs) and the surface of MMSNs was coated by gelatin layer. In this system, the gelatin layer retarded the diffusion of paclitaxel (PTX, model drug) from quickly moving into the bulk solution to achieve sustained release of PTX. In addition, glutaraldehyde (GA) was used as crosslinking agent to crosslink the coating layer and the release of PTX could be regulated by adjusting the degree of crosslinking of the gelatin layer. The gelatin coated MMSNs (MMSN@GELs) had a saturated magnetization of 5.53 emu/g and could facilely response to an external magnet. To confirm our hypothesis that the carriers could be guided by an external magnetic field in vivo, the ex vivo imaging study and quantitative analysis were conducted. The results reflected that the external magnet altered the biodistribution of the magnetic carriers, so that more magnetic carriers were found to accumulate in tumors rather than to accumulate in normal tissues. Moreover, tumor reduction study reflected that the tumor growth of the group treated with PTX/MMSN@GELs in the presence of an external magnetic field were significantly delayed without an obvious body weight loss compared with PTX/MMSN@GELs in the absence of the magnet and with the commercial Taxol at the same dose. All the results suggested that MMSNs coated by gelatin would be promising drug carriers for effective delivery of chemotherapeutic agents. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:226 / 234
页数:9
相关论文
共 34 条
[1]   In vitro release dynamics of an anticancer drug from swellable gelatin nanoparticles [J].
Bajpai, A. K. ;
Choubey, Jyoti .
JOURNAL OF APPLIED POLYMER SCIENCE, 2006, 101 (04) :2320-2332
[2]   FT-IR study for hydroxyapatite/collagen nanocomposite cross-linked by glutaraldehyde [J].
Chang, MC ;
Tanaka, J .
BIOMATERIALS, 2002, 23 (24) :4811-4818
[3]   Gelatin-based nanoparticles as drug and gene delivery systems: Reviewing three decades of research [J].
Elzoghby, Ahmed O. .
JOURNAL OF CONTROLLED RELEASE, 2013, 172 (03) :1075-1091
[4]   Protein-based nanocarriers as promising drug and gene delivery systems [J].
Elzoghby, Ahmed O. ;
Samy, Wael M. ;
Elgindy, Nazik A. .
JOURNAL OF CONTROLLED RELEASE, 2012, 161 (01) :38-49
[5]   Self-assembly of ordered, robust, three-dimensional gold nanocrystal/silica arrays [J].
Fan, HY ;
Yang, K ;
Boye, DM ;
Sigmon, T ;
Malloy, KJ ;
Xu, HF ;
López, GP ;
Brinker, CJ .
SCIENCE, 2004, 304 (5670) :567-571
[6]   FTIR study of hydration phenomena in protein-sugar systems [J].
Farhat, IA ;
Orset, S ;
Moreau, P ;
Blanshard, JMV .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1998, 207 (02) :200-208
[7]   Gelatin behaviour in dilute aqueous solution: Designing a nanoparticulate formulation [J].
Farrugia, CA ;
Groves, MJ .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1999, 51 (06) :643-649
[8]   Synthesis of Biomolecule-Modified Mesoporous Silica Nanoparticles for Targeted Hydrophobic Drug Delivery to Cancer Cells [J].
Ferris, Daniel P. ;
Lu, Jie ;
Gothard, Chris ;
Yanes, Rolando ;
Thomas, Courtney R. ;
Olsen, John-Carl ;
Stoddart, J. Fraser ;
Tamanoi, Fuyuhiko ;
Zink, Jeffrey I. .
SMALL, 2011, 7 (13) :1816-1826
[9]   A magnetic, reversible pH-responsive nanogated ensemble based on Fe3O4 nanoparticles-capped mesoporous silica [J].
Gan, Qi ;
Lu, Xunyu ;
Yuan, Yuan ;
Qian, Jiangchao ;
Zhou, Huanjun ;
Lu, Xun ;
Shi, Jianlin ;
Liu, Changsheng .
BIOMATERIALS, 2011, 32 (07) :1932-1942
[10]   An anticancer drug delivery system based on surfactant-templated mesoporous silica nanoparticles [J].
He, Qianjun ;
Shi, Jianlin ;
Chen, Feng ;
Zhu, Min ;
Zhang, Lingxia .
BIOMATERIALS, 2010, 31 (12) :3335-3346