Gold nanoparticle-based rapid detection and isolation of cells using ligand-receptor chemistry

被引:20
作者
Rauta, Pradipta Ranjan [1 ]
Hallur, Pavan M. [1 ]
Chaubey, Aditya [1 ]
机构
[1] Mazumdar Shaw Ctr Translat Res, Anticanc Technol Program, Bangalore 560099, Karnataka, India
关键词
CIRCULATING TUMOR-CELLS; EFFICIENT CAPTURE; CANCER-CELLS; IN-VITRO; CD44; SIZE; NANOSPHERES; HYALURONAN; RELEASE; FILMS;
D O I
10.1038/s41598-018-21068-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Identification and isolation of low-frequency cells of interest from a heterogeneous cell mixture is an important aspect of many diagnostic applications (including enumeration of circulating tumor cells) and is integral to various assays in (cancer) biology. Current techniques typically require expensive instrumentation and are not amenable to high throughput. Here, we demonstrate a simple and effective platform for cell detection and isolation using gold nanoparticles (Au NPs) conjugated with hyaluronic acid (HA) i.e. Au-PEG-HA NPs. The proposed platform exploits ligand-receptor chemistry to detect/isolate cells with high specificity and efficiency. When the Au-PEG-HA NPs come in contact with cells that express CD44 (the receptor for HA), a clear colorimetric change occurs (along with an accompanying SPR peak shift from 521 nm to 559 nm) in the solution due to NPs-cell interaction. This clearly discernible, colorimetric change can be leveraged by point-of-care devices employed in diagnostic applications. Finally, we show that we can successfully isolate viable cells from a heterogeneous cell population (including from human blood samples) with high specificity, which can be used in further downstream applications. The developed NPs-based platform can be a convenient and cost-efficient alternative for diagnostic applications and for cell isolation or sorting in research laboratories.
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页数:13
相关论文
共 59 条
[1]   Tumor cells circulate in the peripheral blood of all major carcinomas but not in healthy subjects or patients with nonmalignant diseases [J].
Allard, WJ ;
Matera, J ;
Miller, MC ;
Repollet, M ;
Connelly, MC ;
Rao, C ;
Tibbe, AGJ ;
Uhr, JW ;
Terstappen, LWMM .
CLINICAL CANCER RESEARCH, 2004, 10 (20) :6897-6904
[2]  
Bhana S, 2015, NANOMEDICINE-UK, V10, P1973, DOI [10.2217/NNM.15.32, 10.2217/nnm.15.32]
[3]   A nanostructured SAW chip-based biosensor detecting cancer cells [J].
Broeker, Patrick ;
Luecke, Klaus ;
Perpeet, Markus ;
Gronewold, Thomas M. A. .
SENSORS AND ACTUATORS B-CHEMICAL, 2012, 165 (01) :1-6
[4]  
Chamorro-Garcia Alejandro, 2016, Nanobiomedicine (Rij), V3, p1849543516663574, DOI 10.1177/1849543516663574
[5]   Single-cell analysis at the threshold [J].
Chen, Xi ;
Love, J. Christopher ;
Navin, Nicholas E. ;
Pachter, Lior ;
Stubbington, Michael J. T. ;
Svensson, Valentine ;
Sweedler, Jonathan V. ;
Teichmann, Sarah A. .
NATURE BIOTECHNOLOGY, 2016, 34 (11) :1111-1118
[6]   CD44 and its ligand hyaluronan as potential biomarkers in malignant pleural mesothelioma: evidence and perspectives [J].
Cortes-Dericks, Lourdes ;
Schmid, Ralph Alexander .
RESPIRATORY RESEARCH, 2017, 18
[7]   Methods in cell separations [J].
Dainiak, Maria B. ;
Kumar, Ashok ;
Galaev, Igor Yu. ;
Mattiasson, Bo .
CELL SEPARATION: FUNDAMENTALS, ANALYTICAL AND PREPARATIVE METHODS, 2007, 106 :1-18
[8]   Cell Isolation and Recovery Using Hollow Glass Microspheres Coated with Nanolayered Films for Applications in Resource-Limited Settings [J].
Dong, Ziye ;
Ahrens, Caroline C. ;
Yu, Dan ;
Ding, Zhenya ;
Lim, HyunTaek ;
Li, Wei .
ACS APPLIED MATERIALS & INTERFACES, 2017, 9 (18) :15265-15273
[9]   A protein assay based on colloidal gold conjugates with trypsin [J].
Dykman, LA ;
Bogatyrev, VA ;
Khlebtsov, BN ;
Khlebtsov, NG .
ANALYTICAL BIOCHEMISTRY, 2005, 341 (01) :16-21
[10]   Multifunctional, inexpensive, and reusable nanoparticle-printed biochip for cell manipulation and diagnosis [J].
Esfandyarpour, Rahim ;
DiDonato, Matthew J. ;
Yang, Yuxin ;
Durmus, Naside Gozde ;
Harris, James S. ;
Davis, Ronald W. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2017, 114 (08) :E1306-E1315