Synergy of photoacoustic and fluorescence flow cytometry of circulating cells with negative and positive contrasts

被引:50
作者
Nedosekin, Dmitry A. [1 ]
Sarimollaoglu, Mustafa [1 ]
Galanzha, Ekaterina I. [1 ]
Sawant, Rupa [2 ]
Torchilin, Vladimir P. [2 ]
Verkhusha, Vladislav V. [3 ,4 ]
Ma, Jie [5 ]
Frank, Markus H. [5 ]
Biris, Alexandru S. [6 ,7 ]
Zharov, Vladimir P. [1 ]
机构
[1] Univ Arkansas Med Sci, Arkansas Nanomed Ctr, Phillips Class Laser & Nanomed Labs, Little Rock, AR 72205 USA
[2] Northeastern Univ, Bouve Coll Hlth Sci, Ctr Pharmaceut Biotechnol & Nanomed, Boston, MA 02115 USA
[3] Albert Einstein Coll Med, Dept Anat & Struct Biol, Bronx, NY 10461 USA
[4] Albert Einstein Coll Med, Gruss Lipper Biophoton Ctr, Bronx, NY 10461 USA
[5] Harvard Univ, Sch Med, Childrens Hosp Boston, Transplantat Res Ctr, Boston, MA USA
[6] Univ Arkansas, Dept Appl Sci, Little Rock, AR 72205 USA
[7] Univ Arkansas, Nanotechnol Ctr, Little Rock, AR 72205 USA
基金
美国国家科学基金会;
关键词
in vivo cytometry; photoacoustics; fluorescence detection; negative contrast; circulating tumor cells; liposomes; nanoparticles; in vitro flow cytometry; MELANOMA-CELLS; BLOOD; ENRICHMENT; TRACKING; LYMPH;
D O I
10.1002/jbio.201200047
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In vivo photoacoustic (PA) and fluorescence flow cytometry were previously applied separately using pulsed and continuous wave lasers respectively, and positive contrast detection mode only. This paper introduces a real-time integration of both techniques with positive and negative contrast modes using only pulsed lasers. Various applications of this new tool are summarized, including detection of liposomes loaded with Alexa-660 dye, red blood cells labeled with Indocyanine Green, B16F10 melanoma cells co-expressing melanin and green fluorescent protein (GFP), C8161-GFP melanoma cells targeted by magnetic nanoparticles, MTLn3 adenocarcinoma cells expressing novel near-infrared iRFP protein, and quantum dot-carbon nanotube conjugates. Negative contrast flow cytometry provided label-free detection of low absorbing or weakly fluorescent cells in blood absorption and autofluorescence background, respectively. The use of pulsed laser for time-resolved discrimination of objects with long fluorescence lifetime (e.g., quantum dots) from shorter autofluorescence background (e.g., blood plasma) is also highlighted in this paper. The supplementary nature of PA and fluorescence detection increased the versatility of the integrated method for simultaneous detection of probes and cells having various absorbing and fluorescent properties, and provided verification of PA data using a more established fluorescence based technique. ((c) 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim)
引用
收藏
页码:425 / 434
页数:10
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