Flow induced dispersion analysis rapidly quantifies proteins in human plasma samples

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Standard

Flow induced dispersion analysis rapidly quantifies proteins in human plasma samples. / Poulsen, Nicklas N; Andersen, Nina Z; Østergaard, Jesper; Zhuang, Guisheng; Petersen, Nickolaj J; Jensen, Henrik.

In: The Analyst, Vol. 140, No. 13, 07.07.2015, p. 4365-69.

Research output: Contribution to journalLetterResearchpeer-review

Harvard

Poulsen, NN, Andersen, NZ, Østergaard, J, Zhuang, G, Petersen, NJ & Jensen, H 2015, 'Flow induced dispersion analysis rapidly quantifies proteins in human plasma samples', The Analyst, vol. 140, no. 13, pp. 4365-69. https://doi.org/10.1039/c5an00697j

APA

Poulsen, N. N., Andersen, N. Z., Østergaard, J., Zhuang, G., Petersen, N. J., & Jensen, H. (2015). Flow induced dispersion analysis rapidly quantifies proteins in human plasma samples. The Analyst, 140(13), 4365-69. https://doi.org/10.1039/c5an00697j

Vancouver

Poulsen NN, Andersen NZ, Østergaard J, Zhuang G, Petersen NJ, Jensen H. Flow induced dispersion analysis rapidly quantifies proteins in human plasma samples. The Analyst. 2015 Jul 7;140(13):4365-69. https://doi.org/10.1039/c5an00697j

Author

Poulsen, Nicklas N ; Andersen, Nina Z ; Østergaard, Jesper ; Zhuang, Guisheng ; Petersen, Nickolaj J ; Jensen, Henrik. / Flow induced dispersion analysis rapidly quantifies proteins in human plasma samples. In: The Analyst. 2015 ; Vol. 140, No. 13. pp. 4365-69.

Bibtex

@article{6d1847a59d3c4b5bb79ac3b143ee49bb,
title = "Flow induced dispersion analysis rapidly quantifies proteins in human plasma samples",
abstract = "Rapid and sensitive quantification of protein based biomarkers and drugs is a substantial challenge in diagnostics and biopharmaceutical drug development. Current technologies, such as ELISA, are characterized by being slow (hours), requiring relatively large amounts of sample and being subject to cumbersome and expensive assay development. In this work a new approach for quantification based on changes in diffusivity is presented. The apparent diffusivity of an indicator molecule interacting with the protein of interest is determined by Taylor Dispersion Analysis (TDA) in a hydrodynamic flow system. In the presence of the analyte the apparent diffusivity of the indicator changes due to complexation. This change in diffusivity is used to quantify the analyte. This approach, termed Flow Induced Dispersion Analysis (FIDA), is characterized by being fast (minutes), selective (quantification is possible in a blood plasma matrix), fully automated, and being subject to a simple assay development. FIDA is demonstrated for quantification of the protein Human Serum Albumin (HSA) in human plasma as well as for quantification of an antibody against HSA. The sensitivity of the FIDA assay depends on the indicator-analyte dissociation constant which in favourable cases is in the sub-nanomolar to picomolar range for antibody-antigen interactions.",
author = "Poulsen, {Nicklas N} and Andersen, {Nina Z} and Jesper {\O}stergaard and Guisheng Zhuang and Petersen, {Nickolaj J} and Henrik Jensen",
year = "2015",
month = jul,
day = "7",
doi = "10.1039/c5an00697j",
language = "English",
volume = "140",
pages = "4365--69",
journal = "The Analyst",
issn = "0003-2654",
publisher = "Royal Society of Chemistry",
number = "13",

}

RIS

TY - JOUR

T1 - Flow induced dispersion analysis rapidly quantifies proteins in human plasma samples

AU - Poulsen, Nicklas N

AU - Andersen, Nina Z

AU - Østergaard, Jesper

AU - Zhuang, Guisheng

AU - Petersen, Nickolaj J

AU - Jensen, Henrik

PY - 2015/7/7

Y1 - 2015/7/7

N2 - Rapid and sensitive quantification of protein based biomarkers and drugs is a substantial challenge in diagnostics and biopharmaceutical drug development. Current technologies, such as ELISA, are characterized by being slow (hours), requiring relatively large amounts of sample and being subject to cumbersome and expensive assay development. In this work a new approach for quantification based on changes in diffusivity is presented. The apparent diffusivity of an indicator molecule interacting with the protein of interest is determined by Taylor Dispersion Analysis (TDA) in a hydrodynamic flow system. In the presence of the analyte the apparent diffusivity of the indicator changes due to complexation. This change in diffusivity is used to quantify the analyte. This approach, termed Flow Induced Dispersion Analysis (FIDA), is characterized by being fast (minutes), selective (quantification is possible in a blood plasma matrix), fully automated, and being subject to a simple assay development. FIDA is demonstrated for quantification of the protein Human Serum Albumin (HSA) in human plasma as well as for quantification of an antibody against HSA. The sensitivity of the FIDA assay depends on the indicator-analyte dissociation constant which in favourable cases is in the sub-nanomolar to picomolar range for antibody-antigen interactions.

AB - Rapid and sensitive quantification of protein based biomarkers and drugs is a substantial challenge in diagnostics and biopharmaceutical drug development. Current technologies, such as ELISA, are characterized by being slow (hours), requiring relatively large amounts of sample and being subject to cumbersome and expensive assay development. In this work a new approach for quantification based on changes in diffusivity is presented. The apparent diffusivity of an indicator molecule interacting with the protein of interest is determined by Taylor Dispersion Analysis (TDA) in a hydrodynamic flow system. In the presence of the analyte the apparent diffusivity of the indicator changes due to complexation. This change in diffusivity is used to quantify the analyte. This approach, termed Flow Induced Dispersion Analysis (FIDA), is characterized by being fast (minutes), selective (quantification is possible in a blood plasma matrix), fully automated, and being subject to a simple assay development. FIDA is demonstrated for quantification of the protein Human Serum Albumin (HSA) in human plasma as well as for quantification of an antibody against HSA. The sensitivity of the FIDA assay depends on the indicator-analyte dissociation constant which in favourable cases is in the sub-nanomolar to picomolar range for antibody-antigen interactions.

U2 - 10.1039/c5an00697j

DO - 10.1039/c5an00697j

M3 - Letter

C2 - 26031223

VL - 140

SP - 4365

EP - 4369

JO - The Analyst

JF - The Analyst

SN - 0003-2654

IS - 13

ER -

ID: 144456869