Ultrabright fluorescent mesoporous silica nanoparticles for prescreening of cervical cancer

被引:38
|
作者
Palantavida, Shajesh [1 ,2 ]
Guz, Nataliia V. [1 ,2 ]
Woodworth, C. D.
Sokolov, I. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Tufts Univ, Dept Mech Engn, Medford, MA 01255 USA
[2] Tufts Univ, Dept Biomed Engn, Medford, MA 01255 USA
[3] Clarkson Univ, Dept Phys, Potsdam, NY 13699 USA
[4] Clarkson Univ, Dept Biol, Potsdam, NY 13699 USA
[5] Clarkson Univ, Nanoengn & Biotechnol Labs Ctr NABLAB, Potsdam, NY 13699 USA
基金
美国国家科学基金会;
关键词
Cervical cancer; Early cancer detection; Novel detection methods; Fluorescent silica particles; Pap smear/liquid cytology tests; FORCE MICROSCOPY; CELLS; SIZE; PARTICLES;
D O I
10.1016/j.nano.2013.04.011
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
We report on the first functional use of recently introduced ultrabright fluorescent mesoporous silica nanoparticles, which are functionalized with folic acid, to distinguish cancerous and precancerous cervical epithelial cells from normal cells. The high brightness of the particles is advantageous for fast and reliable identification of both precancerous and cancerous cells. Normal and cancer cells were isolated from three healthy women and three cancer patients. Three precancerous cell lines were derived by immortalization of primary cultures of normal cells with human papillomavirus type-16 (HPV-16) DNA. We observed substantially different particle internalization by normal and cancerous/precancerous cells after a short incubation time of 15 minutes. Compared to HPV-DNA and cell pathology tests, which are currently used for prescreening of cervical cancer, we demonstrated that the specificity of our method was similar (94-95%), whereas its sensitivity was significantly better (95-97%) than the sensitivity of those currently used tests (30-80%). From the Clinical Editor: This team of investigators reports on the development of a new screening test for cervical cancer using ultrabright fluorescent mesoporous silica nanoparticles functionalized with folic acid, enabling significantly better sensitivity (95-97% vs. 30-80%) and maintained specificity (94-95%) compared with current clinical tests. This test should find a way to clinical use in the near future. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:1255 / 1262
页数:8
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