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Clinical on-site monitoring of ß-lactam antibiotics for a personalized antibiotherapy

An appropriate antibiotherapy is crucial for the safety and recovery of patients. Depending on the clinical conditions of patients, the required dose to effectively eradicate an infection may vary. An inadequate dosing not only reduces the efficacy of the antibiotic, but also promotes the emergence...

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Autores principales: Bruch, R., Chatelle, C., Kling, A., Rebmann, B., Wirth, S., Schumann, S., Weber, W., Dincer, C., Urban, G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5466632/
https://www.ncbi.nlm.nih.gov/pubmed/28600499
http://dx.doi.org/10.1038/s41598-017-03338-z
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author Bruch, R.
Chatelle, C.
Kling, A.
Rebmann, B.
Wirth, S.
Schumann, S.
Weber, W.
Dincer, C.
Urban, G.
author_facet Bruch, R.
Chatelle, C.
Kling, A.
Rebmann, B.
Wirth, S.
Schumann, S.
Weber, W.
Dincer, C.
Urban, G.
author_sort Bruch, R.
collection PubMed
description An appropriate antibiotherapy is crucial for the safety and recovery of patients. Depending on the clinical conditions of patients, the required dose to effectively eradicate an infection may vary. An inadequate dosing not only reduces the efficacy of the antibiotic, but also promotes the emergence of antimicrobial resistances. Therefore, a personalized therapy is of great interest for improved patients’ outcome and will reduce in long-term the prevalence of multidrug-resistances. In this context, on-site monitoring of the antibiotic blood concentration is fundamental to facilitate an individual adjustment of the antibiotherapy. Herein, we present a bioinspired approach for the bedside monitoring of free accessible ß-lactam antibiotics, including penicillins (piperacillin) and cephalosporins (cefuroxime and cefazolin) in untreated plasma samples. The introduced system combines a disposable microfluidic chip with a naturally occurring penicillin-binding protein, resulting in a high-performance platform, capable of gauging very low antibiotic concentrations (less than 6 ng ml(−1)) from only 1 µl of serum. The system’s applicability to a personalized antibiotherapy was successfully demonstrated by monitoring the pharmacokinetics of patients, treated with ß-lactam antibiotics, undergoing surgery.
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spelling pubmed-54666322017-06-14 Clinical on-site monitoring of ß-lactam antibiotics for a personalized antibiotherapy Bruch, R. Chatelle, C. Kling, A. Rebmann, B. Wirth, S. Schumann, S. Weber, W. Dincer, C. Urban, G. Sci Rep Article An appropriate antibiotherapy is crucial for the safety and recovery of patients. Depending on the clinical conditions of patients, the required dose to effectively eradicate an infection may vary. An inadequate dosing not only reduces the efficacy of the antibiotic, but also promotes the emergence of antimicrobial resistances. Therefore, a personalized therapy is of great interest for improved patients’ outcome and will reduce in long-term the prevalence of multidrug-resistances. In this context, on-site monitoring of the antibiotic blood concentration is fundamental to facilitate an individual adjustment of the antibiotherapy. Herein, we present a bioinspired approach for the bedside monitoring of free accessible ß-lactam antibiotics, including penicillins (piperacillin) and cephalosporins (cefuroxime and cefazolin) in untreated plasma samples. The introduced system combines a disposable microfluidic chip with a naturally occurring penicillin-binding protein, resulting in a high-performance platform, capable of gauging very low antibiotic concentrations (less than 6 ng ml(−1)) from only 1 µl of serum. The system’s applicability to a personalized antibiotherapy was successfully demonstrated by monitoring the pharmacokinetics of patients, treated with ß-lactam antibiotics, undergoing surgery. Nature Publishing Group UK 2017-06-09 /pmc/articles/PMC5466632/ /pubmed/28600499 http://dx.doi.org/10.1038/s41598-017-03338-z Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Bruch, R.
Chatelle, C.
Kling, A.
Rebmann, B.
Wirth, S.
Schumann, S.
Weber, W.
Dincer, C.
Urban, G.
Clinical on-site monitoring of ß-lactam antibiotics for a personalized antibiotherapy
title Clinical on-site monitoring of ß-lactam antibiotics for a personalized antibiotherapy
title_full Clinical on-site monitoring of ß-lactam antibiotics for a personalized antibiotherapy
title_fullStr Clinical on-site monitoring of ß-lactam antibiotics for a personalized antibiotherapy
title_full_unstemmed Clinical on-site monitoring of ß-lactam antibiotics for a personalized antibiotherapy
title_short Clinical on-site monitoring of ß-lactam antibiotics for a personalized antibiotherapy
title_sort clinical on-site monitoring of ß-lactam antibiotics for a personalized antibiotherapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5466632/
https://www.ncbi.nlm.nih.gov/pubmed/28600499
http://dx.doi.org/10.1038/s41598-017-03338-z
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