Investigating surrogate cerebrospinal fluid matrix compositions for use in quantitative LC-MS analysis of therapeutic antibodies in the cerebrospinal fluid

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Investigating surrogate cerebrospinal fluid matrix compositions for use in quantitative LC-MS analysis of therapeutic antibodies in the cerebrospinal fluid. / Fogh, Jens Rose; Jacobsen, Anne-Marie; Nguyen, Tam T T N; Rand, Kasper D; Olsen, Line Rørbæk.

In: Analytical and Bioanalytical Chemistry, Vol. 412, 2020, p. 1653-1661.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Fogh, JR, Jacobsen, A-M, Nguyen, TTTN, Rand, KD & Olsen, LR 2020, 'Investigating surrogate cerebrospinal fluid matrix compositions for use in quantitative LC-MS analysis of therapeutic antibodies in the cerebrospinal fluid', Analytical and Bioanalytical Chemistry, vol. 412, pp. 1653-1661. https://doi.org/10.1007/s00216-020-02403-3

APA

Fogh, J. R., Jacobsen, A-M., Nguyen, T. T. T. N., Rand, K. D., & Olsen, L. R. (2020). Investigating surrogate cerebrospinal fluid matrix compositions for use in quantitative LC-MS analysis of therapeutic antibodies in the cerebrospinal fluid. Analytical and Bioanalytical Chemistry, 412, 1653-1661. https://doi.org/10.1007/s00216-020-02403-3

Vancouver

Fogh JR, Jacobsen A-M, Nguyen TTTN, Rand KD, Olsen LR. Investigating surrogate cerebrospinal fluid matrix compositions for use in quantitative LC-MS analysis of therapeutic antibodies in the cerebrospinal fluid. Analytical and Bioanalytical Chemistry. 2020;412:1653-1661. https://doi.org/10.1007/s00216-020-02403-3

Author

Fogh, Jens Rose ; Jacobsen, Anne-Marie ; Nguyen, Tam T T N ; Rand, Kasper D ; Olsen, Line Rørbæk. / Investigating surrogate cerebrospinal fluid matrix compositions for use in quantitative LC-MS analysis of therapeutic antibodies in the cerebrospinal fluid. In: Analytical and Bioanalytical Chemistry. 2020 ; Vol. 412. pp. 1653-1661.

Bibtex

@article{96dbcfa61cee4142a0d710ce080f2c03,
title = "Investigating surrogate cerebrospinal fluid matrix compositions for use in quantitative LC-MS analysis of therapeutic antibodies in the cerebrospinal fluid",
abstract = "As quantitative analysis of biotherapeutics in cerebrospinal fluid (CSF) with LC-MS becomes increasingly widespread, there is a need for method developments towards higher sensitivity. By using artificial CSF (aCSF) in the development phase, the consumption of costly and sparsely available CSF can be limited. The aCSF compositions tested here were made from various dilutions of bovine serum albumin (BSA) or rat plasma to mimic the total protein concentration found in CSF. Focusing on monoclonal antibodies, the aCSF was spiked with human immunoglobulin (hIgG) and prepared with the bottom-up analysis technique using LC-MS. Assuming that the composition of the aCSF would affect the digest, the response from aCSF matrices was compared with CSF from rat, monkey, and dog in terms of estimated sample concentration and matrix effects. The samples were spiked with hIgG in the range of 10 to 1000 ng/mL and volumes of 10 μL were transferred to sample preparation. The results indicate that BSA dilutions from 300 to 2000 μg/mL and rat plasma dilutions of 0.5-2% provide the most accurate concentration estimates when compared with rat CSF. 1000 μg/mL BSA did not produce significantly different concentration estimates for 500 ng/mL samples when compared with CSF from rat, monkey, and dog, and can therefore be used as aCSF for several different species.",
author = "Fogh, {Jens Rose} and Anne-Marie Jacobsen and Nguyen, {Tam T T N} and Rand, {Kasper D} and Olsen, {Line R{\o}rb{\ae}k}",
year = "2020",
doi = "10.1007/s00216-020-02403-3",
language = "English",
volume = "412",
pages = "1653--1661",
journal = "Analytical and Bioanalytical Chemistry",
issn = "1618-2642",
publisher = "Springer",

}

RIS

TY - JOUR

T1 - Investigating surrogate cerebrospinal fluid matrix compositions for use in quantitative LC-MS analysis of therapeutic antibodies in the cerebrospinal fluid

AU - Fogh, Jens Rose

AU - Jacobsen, Anne-Marie

AU - Nguyen, Tam T T N

AU - Rand, Kasper D

AU - Olsen, Line Rørbæk

PY - 2020

Y1 - 2020

N2 - As quantitative analysis of biotherapeutics in cerebrospinal fluid (CSF) with LC-MS becomes increasingly widespread, there is a need for method developments towards higher sensitivity. By using artificial CSF (aCSF) in the development phase, the consumption of costly and sparsely available CSF can be limited. The aCSF compositions tested here were made from various dilutions of bovine serum albumin (BSA) or rat plasma to mimic the total protein concentration found in CSF. Focusing on monoclonal antibodies, the aCSF was spiked with human immunoglobulin (hIgG) and prepared with the bottom-up analysis technique using LC-MS. Assuming that the composition of the aCSF would affect the digest, the response from aCSF matrices was compared with CSF from rat, monkey, and dog in terms of estimated sample concentration and matrix effects. The samples were spiked with hIgG in the range of 10 to 1000 ng/mL and volumes of 10 μL were transferred to sample preparation. The results indicate that BSA dilutions from 300 to 2000 μg/mL and rat plasma dilutions of 0.5-2% provide the most accurate concentration estimates when compared with rat CSF. 1000 μg/mL BSA did not produce significantly different concentration estimates for 500 ng/mL samples when compared with CSF from rat, monkey, and dog, and can therefore be used as aCSF for several different species.

AB - As quantitative analysis of biotherapeutics in cerebrospinal fluid (CSF) with LC-MS becomes increasingly widespread, there is a need for method developments towards higher sensitivity. By using artificial CSF (aCSF) in the development phase, the consumption of costly and sparsely available CSF can be limited. The aCSF compositions tested here were made from various dilutions of bovine serum albumin (BSA) or rat plasma to mimic the total protein concentration found in CSF. Focusing on monoclonal antibodies, the aCSF was spiked with human immunoglobulin (hIgG) and prepared with the bottom-up analysis technique using LC-MS. Assuming that the composition of the aCSF would affect the digest, the response from aCSF matrices was compared with CSF from rat, monkey, and dog in terms of estimated sample concentration and matrix effects. The samples were spiked with hIgG in the range of 10 to 1000 ng/mL and volumes of 10 μL were transferred to sample preparation. The results indicate that BSA dilutions from 300 to 2000 μg/mL and rat plasma dilutions of 0.5-2% provide the most accurate concentration estimates when compared with rat CSF. 1000 μg/mL BSA did not produce significantly different concentration estimates for 500 ng/mL samples when compared with CSF from rat, monkey, and dog, and can therefore be used as aCSF for several different species.

U2 - 10.1007/s00216-020-02403-3

DO - 10.1007/s00216-020-02403-3

M3 - Journal article

C2 - 32008082

VL - 412

SP - 1653

EP - 1661

JO - Analytical and Bioanalytical Chemistry

JF - Analytical and Bioanalytical Chemistry

SN - 1618-2642

ER -

ID: 236320181