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Validation of a commercial enzyme immunoassay to assess urinary oxytocin in humans

Within the last decade, oxytocin (OT) has attracted a lot of attention in the context of various human social behaviors. Besides its importance in regulating physiological processes in females related to giving birth and lactation, OT is involved in the establishment and maintenance of social relati...

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Autores principales: Schaebs, Franka S, Wirobski, Gwen, Marshall-Pescini, Sarah, Range, Friederike, Deschner, Tobias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8052582/
https://www.ncbi.nlm.nih.gov/pubmed/33617463
http://dx.doi.org/10.1530/EC-20-0583
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author Schaebs, Franka S
Wirobski, Gwen
Marshall-Pescini, Sarah
Range, Friederike
Deschner, Tobias
author_facet Schaebs, Franka S
Wirobski, Gwen
Marshall-Pescini, Sarah
Range, Friederike
Deschner, Tobias
author_sort Schaebs, Franka S
collection PubMed
description Within the last decade, oxytocin (OT) has attracted a lot of attention in the context of various human social behaviors. Besides its importance in regulating physiological processes in females related to giving birth and lactation, OT is involved in the establishment and maintenance of social relationships, trust and emotion recognition. However, results are not always consistent across studies, which may partly be due to the incomplete validation of methods used to assess OT levels. Carefully validating a method before its use is of crucial importance to ensure that it can be used to accurately, reliably and repeatedly assess OT levels. With this study we evaluated a commercially available Enzyme Immunoassay to assess OT in human urine samples by conducting a careful analytical validation. Results indicate that, with regard to parallelism and immunoreactivity, human urinary OT can be assessed reliably. However, extraction methods need further improvement to optimize measures of accuracy and extraction efficiency, especially in the lower range of the assay system. Tests on OT stability indicate that OT is affected by degradation when stored at 4°C or room temperature. Storing urine samples over longer periods revealed that OT levels are most stable when stored as ethanol extracts at −20°C compared to being stored as samples at −20°C or −80°C. Although some of the validated parameters did not reach the intended quality criteria, this study highlights the importance of such in depth validation procedures and reporting results to make them available to researchers embarking on projects utilizing such methods.
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spelling pubmed-80525822021-04-21 Validation of a commercial enzyme immunoassay to assess urinary oxytocin in humans Schaebs, Franka S Wirobski, Gwen Marshall-Pescini, Sarah Range, Friederike Deschner, Tobias Endocr Connect Research Within the last decade, oxytocin (OT) has attracted a lot of attention in the context of various human social behaviors. Besides its importance in regulating physiological processes in females related to giving birth and lactation, OT is involved in the establishment and maintenance of social relationships, trust and emotion recognition. However, results are not always consistent across studies, which may partly be due to the incomplete validation of methods used to assess OT levels. Carefully validating a method before its use is of crucial importance to ensure that it can be used to accurately, reliably and repeatedly assess OT levels. With this study we evaluated a commercially available Enzyme Immunoassay to assess OT in human urine samples by conducting a careful analytical validation. Results indicate that, with regard to parallelism and immunoreactivity, human urinary OT can be assessed reliably. However, extraction methods need further improvement to optimize measures of accuracy and extraction efficiency, especially in the lower range of the assay system. Tests on OT stability indicate that OT is affected by degradation when stored at 4°C or room temperature. Storing urine samples over longer periods revealed that OT levels are most stable when stored as ethanol extracts at −20°C compared to being stored as samples at −20°C or −80°C. Although some of the validated parameters did not reach the intended quality criteria, this study highlights the importance of such in depth validation procedures and reporting results to make them available to researchers embarking on projects utilizing such methods. Bioscientifica Ltd 2021-02-17 /pmc/articles/PMC8052582/ /pubmed/33617463 http://dx.doi.org/10.1530/EC-20-0583 Text en © 2021 The authors https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. (https://creativecommons.org/licenses/by-nc/4.0/)
spellingShingle Research
Schaebs, Franka S
Wirobski, Gwen
Marshall-Pescini, Sarah
Range, Friederike
Deschner, Tobias
Validation of a commercial enzyme immunoassay to assess urinary oxytocin in humans
title Validation of a commercial enzyme immunoassay to assess urinary oxytocin in humans
title_full Validation of a commercial enzyme immunoassay to assess urinary oxytocin in humans
title_fullStr Validation of a commercial enzyme immunoassay to assess urinary oxytocin in humans
title_full_unstemmed Validation of a commercial enzyme immunoassay to assess urinary oxytocin in humans
title_short Validation of a commercial enzyme immunoassay to assess urinary oxytocin in humans
title_sort validation of a commercial enzyme immunoassay to assess urinary oxytocin in humans
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8052582/
https://www.ncbi.nlm.nih.gov/pubmed/33617463
http://dx.doi.org/10.1530/EC-20-0583
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