Intercellular adhesion molecule 1 antibody-mediated mesoporous drug delivery system for targeted treatment of triple-negative breast cancer

被引:31
作者
Wang, Mengru [1 ]
Liu, Wanhua [1 ]
Zhang, Yanqiu [2 ]
Dang, Meng [5 ,6 ]
Zhang, Yunlei [3 ]
Tao, Jun [5 ,6 ]
Chen, Kun [5 ,6 ]
Peng, Xin [1 ]
Teng, Zhaogang [3 ,4 ,5 ,6 ]
机构
[1] Southeast Univ, Sch Med, Jiangsu Key Lab Mol & Funct Imaging, Dept Radiol,Zhongda Hosp, Nanjing 210009, Jiangsu, Peoples R China
[2] Nanjing Univ, Med Sch, Nanjing Drum Tower Hosp, Nanjing 210002, Jiangsu, Peoples R China
[3] Nanjing Univ, Sch Med, Jinling Hosp, Dept Med Imaging, Nanjing 210002, Jiangsu, Peoples R China
[4] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Analyt Chem Life Sci, Nanjing 210093, Jiangsu, Peoples R China
[5] Nanjing Univ Posts & Telecommun, Key Lab Organ Elect & Informat Displays, Nanjing 210046, Jiangsu, Peoples R China
[6] Nanjing Univ Posts & Telecommun, IAM, Nanjing 210046, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Triple-negative breast cancer; Periodic mesoporous organosilica; Drug delivery system; Targeted therapy; ICAM-1; SILICA NANOPARTICLES; THERAPY; GENE; FRAMEWORK; PATTERNS; EFFICACY;
D O I
10.1016/j.jcis.2018.12.032
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The development of effective targeted therapies for triple negative breast cancer (TNBC) remains a challenge. This targeted drug delivery system used a near-infrared fluorescence dye cyanine 5.5 (Cy5.5) and an ICAM-1 antibody on thioether-bridged periodic mesoporous organosilica nanoparticles (PMOs). The ICAM-1 antibody and cyanine 5.5-engineered PMOs (PMO-Cy5.5-ICAM) offer excellent in vivo and in vitro biocompatibility. The PMO-Cy5.5-ICAM shows a loading capacity up to 400 mg/g of doxorubicin (DOX). The drug release profile of the DOX-loaded targeted delivery system (DOX@PMO-Cy5.5-ICAM) is pH-sensitive. Confocal microscopy showed that the PMO-Cy5.5-ICAM efficiently targets and enters TNBC cells. In in vivo experiments, the DOX@PMO-Cy5.5-ICAM accumulates more in TNBCs than in the control groups and exhibits better therapeutic effects on TNBC; thus, it is a promising treatment strategy for TNBC. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:630 / 637
页数:8
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