Pattern Recognition of Cancer Cells Using Aptamer-Conjugated Magnetic Nanoparticles

被引:151
作者
Bamrungsap, Suwussa [1 ,2 ,3 ]
Chen, Tao [1 ,2 ,3 ]
Shukoor, Mohammed Ibrahim [1 ,2 ,3 ]
Chen, Zhuo [4 ,5 ]
Sefah, Kwame [1 ,2 ,3 ]
Chen, Yan [1 ,2 ,3 ,4 ,5 ]
Tan, Weihong [1 ,2 ,3 ,4 ,5 ]
机构
[1] Univ Florida, Ctr Res Bionano Interface, Dept Chem, Gainesville, FL 32611 USA
[2] Univ Florida, Dept Physiol & Funct Genom, Shands Canc Ctr, UF Genet Inst, Gainesville, FL 32611 USA
[3] Univ Florida, McKnight Brain Inst, Gainesville, FL 32611 USA
[4] Hunan Univ, State Key Lab Chemo Biosensing & Chemometr, Coll Biol, Changsha 410082, Hunan, Peoples R China
[5] Hunan Univ, Coll Chem & Chem Engn, Changsha 410082, Hunan, Peoples R China
基金
中国国家自然科学基金; 美国国家卫生研究院;
关键词
aptamer; cancer cell recognition; complex media; magnetic nanoparticle; spin-spin relaxation time; IRON-OXIDE NANOPARTICLES; LIVE CELLS; MOLECULAR RECOGNITION; RELAXATION; SELECTION; PROBES; COLLECTION; PARTICLES; LIGANDS; MEDIA;
D O I
10.1021/nn3002328
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Biocompatible magnetic nanosensors based on reversible self-assembly of dispersed magnetic nanoparticles into stable nanoassemblies have been used as effective magnetic relaxation switches (MRSw) for the detection of molecular interactions. We report, for the first time, the design of MRSw based on aptamer-conjugated magnetic nanoparticles (ACMNPs). The ACMNPs capitalize on the ability of aptamers to specifically bind target cancer cells, as well as the large surface area of MNPs to accommodate multiple aptamer binding events. The ACMNPs can detect as few as 10 cancer cells in 250 mu L of sample. The ACMNPs' specificity and sensitivity are also demonstrated by detection In cell mixtures and complex biological media, including fetal bovine serum, human plasma, and whole blood. Furthermore, by using an array of ACMNPs, various cell types can be differentiated through pattern recognition, thus creating a cellular molecular profile that will allow clinicians to accurately identify cancer cells at the molecular and single-cell level.
引用
收藏
页码:3974 / 3981
页数:8
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