Direct detection of malaria infected red blood cells by surface enhanced Raman spectroscopy

被引:51
作者
Chen, Funing [1 ,2 ]
Flaherty, Briana R. [3 ,4 ]
Cohen, Charli E. [3 ]
Peterson, David S. [3 ,4 ]
Zhao, Yiping [1 ,2 ]
机构
[1] Univ Georgia, Dept Phys & Astron, Athens, GA 30602 USA
[2] Univ Georgia, Nanoscale Sci & Engn Ctr, Athens, GA 30602 USA
[3] Univ Georgia, Dept Infect Dis, Athens, GA 30602 USA
[4] Univ Georgia, Ctr Trop & Emerging Global Dis, Athens, GA 30602 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
SERS; Malaria; Diagnostics; Cell membrane; Red blood cell; Biosensors; FOODBORNE PATHOGENIC BACTERIA; SILVER NANOROD ARRAYS; PLASMODIUM-FALCIPARUM; DIAGNOSIS; PARASITE; SERS; MICROSCOPY; IDENTIFICATION; ERYTHROCYTES; SUBSTRATE;
D O I
10.1016/j.nano.2016.03.001
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Surface enhanced Raman spectra (SERS) of normal red blood cells (RBCs) and Plasmodium falciparum infected RBCs (iRBCs) at different post invasion time were obtained based on silver nanorod array substrates. Distinct spectral differences were observed due to the cell membrane modification of RBCs during malaria infection. The SERS spectra of ring stage iRBCs had a characteristic Raman peak Delta nu = 1599 cm(-1) as compared to those of normal RBCs, while the trophozoite and schizoid stages had identical SERS spectra with a characteristic peak Delta nu = 723 cm(-1), which is significantly different from ring stage iRBCs, consistent with ongoing modification of the iRBC membrane. Since ring stage iRBCs of P. falciparum are found circulating in blood, such a difference provides a new strategy for rapid malaria detection. The limit of detection as well as the ability to detect a mixed iRBC and RBC solution was also investigated. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:1445 / 1451
页数:7
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