Covalently Combining Carbon Nanotubes with Anticancer Agent: Preparation and Antitumor Activity

被引:197
作者
Wu, Wei [1 ,2 ]
Li, Rutian [3 ,4 ]
Bian, Xiaochen [5 ]
Zhu, Zhenshu [1 ,2 ]
Ding, Dan [1 ,2 ]
Li, Xiaolin [3 ,4 ]
Jia, Zhijun [6 ]
Jiang, Xiqun [1 ,2 ]
Hu, Yiqiao [5 ]
机构
[1] Nanjing Univ, Lab Mesoscop Chem, Nanjing 210093, Peoples R China
[2] Nanjing Univ, Coll Chem & Chem Engn, Dept Polymer Sci & Engn, Nanjing 210093, Peoples R China
[3] Nanjing Univ, Sch Med, Drum Tower Hosp, Ctr Comprehens Canc, Nanjing 210008, Peoples R China
[4] Nanjing Univ, Clin Canc Inst, Nanjing 210008, Peoples R China
[5] Nanjing Univ, Coll Life Sci, Dept Biochem, Nanjing 210093, Peoples R China
[6] Nanjing Univ, Drum Tower Hosp, Dept Nucl Med, Nanjing 210008, Peoples R China
关键词
carbon nanotubes; drug delivery; 10-hydroxycamptothecin; antitumor performance; biodistribution; IN-VIVO; CANCER-CELLS; DELIVERY; FUNCTIONALIZATION; PHARMACOKINETICS; ACCUMULATION; LIPOSOMES; CARRIERS; SIRNA;
D O I
10.1021/nn9005686
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A multiwalled carbon nanotube (MWNT)-based drug delivery system was developed by covalently combining carbon nanotubes with the antitumor agent 10-hydroxycamptothecin (HCPT) using hydrophilic diaminotriethylene glycol as the spacer between nanotube and drug moieties. The surface functionalizations of the nanotube were carried out by enrichment of carboxylic groups with optimized oxidization treatment, followed by covalently linking hydrophilic diaminotriethylene glycol via amidation reaction, and then HCPT was chemically attached to carbon nanotubes through a cleavable ester linkage. It is demonstrated that the obtained MWNT-HCPT conjugates are superior in antitumor activity both in vitro and in vivo to clinical HCPT formulation. In vivo single photon emission computed tomography (SPECT) imaging and ex vivo gamma scintillation counting analyses reveal that MWNT-HCPT conjugates have relatively long blood circulation and high drug accumulation in the tumor site. These properties together with the enhanced cell uptake and multivalent presentation of HCPT on a single nanotube benefit substantially the antitumor effects and would boost significantly the applications of carbon nanotubes in the biomedicine field.
引用
收藏
页码:2740 / 2750
页数:11
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