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Multicommuted flow system for the determination of glucose in animal blood serum exploiting enzymatic reaction and chemiluminescence detection

An automatic flow procedure based on multicommutation dedicated for the determination of glucose in animal blood serum using glucose oxidase with chemiluminescence detection is described. The flow manifold consisted of a set of three-way solenoid valves assembled to implement multicommutation. A mic...

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Autores principales: Pires, Cherrine K., Martelli, Patrícia B., Reis, Boaventura F., Lima, José L. F. C., Saraiva, Maria Lúcia M. F. S.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2548390/
https://www.ncbi.nlm.nih.gov/pubmed/18924619
http://dx.doi.org/10.1155/S1463924603000191
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author Pires, Cherrine K.
Martelli, Patrícia B.
Reis, Boaventura F.
Lima, José L. F. C.
Saraiva, Maria Lúcia M. F. S.
author_facet Pires, Cherrine K.
Martelli, Patrícia B.
Reis, Boaventura F.
Lima, José L. F. C.
Saraiva, Maria Lúcia M. F. S.
author_sort Pires, Cherrine K.
collection PubMed
description An automatic flow procedure based on multicommutation dedicated for the determination of glucose in animal blood serum using glucose oxidase with chemiluminescence detection is described. The flow manifold consisted of a set of three-way solenoid valves assembled to implement multicommutation. A microcomputer furnished with an electronic interface and software written in Quick BASIC 4.5 controlled the manifold and performed data acquisition. Glucose oxidase was immobilized on porous silica beads (glass aminopropyl) and packed in a minicolumn (15 × 5 mm). The procedure was based on the enzymatic degradation of glucose, producing hydrogen peroxide, which oxidized luminol in the presence of hexacyanoferrate(III), causing the chemiluminescence. The system was tested by analysing a set of serum animal samples without previous treatment. Results were in agreement with those obtained with the conventional method (LABTEST Kit) at the 95% confidence level. The detection limit and variation coefficient were estimated as 12.0 mg l(−1) (99.7% confidence level) and 3.5% (n = 20), respectively. The sampling rate was about 60 determinations h(−1) with sample concentrations ranging from 50 to 600 mg l(−1) glucose. The consumptions of serum sample, hexacyanoferrate(III) and luminol were 46 μl, 10.0 mg and 0.2 mg/determination, respectively.
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spelling pubmed-25483902008-10-16 Multicommuted flow system for the determination of glucose in animal blood serum exploiting enzymatic reaction and chemiluminescence detection Pires, Cherrine K. Martelli, Patrícia B. Reis, Boaventura F. Lima, José L. F. C. Saraiva, Maria Lúcia M. F. S. J Autom Methods Manag Chem Research Article An automatic flow procedure based on multicommutation dedicated for the determination of glucose in animal blood serum using glucose oxidase with chemiluminescence detection is described. The flow manifold consisted of a set of three-way solenoid valves assembled to implement multicommutation. A microcomputer furnished with an electronic interface and software written in Quick BASIC 4.5 controlled the manifold and performed data acquisition. Glucose oxidase was immobilized on porous silica beads (glass aminopropyl) and packed in a minicolumn (15 × 5 mm). The procedure was based on the enzymatic degradation of glucose, producing hydrogen peroxide, which oxidized luminol in the presence of hexacyanoferrate(III), causing the chemiluminescence. The system was tested by analysing a set of serum animal samples without previous treatment. Results were in agreement with those obtained with the conventional method (LABTEST Kit) at the 95% confidence level. The detection limit and variation coefficient were estimated as 12.0 mg l(−1) (99.7% confidence level) and 3.5% (n = 20), respectively. The sampling rate was about 60 determinations h(−1) with sample concentrations ranging from 50 to 600 mg l(−1) glucose. The consumptions of serum sample, hexacyanoferrate(III) and luminol were 46 μl, 10.0 mg and 0.2 mg/determination, respectively. Hindawi Publishing Corporation 2003 /pmc/articles/PMC2548390/ /pubmed/18924619 http://dx.doi.org/10.1155/S1463924603000191 Text en Copyright © 2003 Hindawi Publishing Corporation. http://creativecommons.org/licenses/by/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Pires, Cherrine K.
Martelli, Patrícia B.
Reis, Boaventura F.
Lima, José L. F. C.
Saraiva, Maria Lúcia M. F. S.
Multicommuted flow system for the determination of glucose in animal blood serum exploiting enzymatic reaction and chemiluminescence detection
title Multicommuted flow system for the determination of glucose in animal blood serum exploiting enzymatic reaction and chemiluminescence detection
title_full Multicommuted flow system for the determination of glucose in animal blood serum exploiting enzymatic reaction and chemiluminescence detection
title_fullStr Multicommuted flow system for the determination of glucose in animal blood serum exploiting enzymatic reaction and chemiluminescence detection
title_full_unstemmed Multicommuted flow system for the determination of glucose in animal blood serum exploiting enzymatic reaction and chemiluminescence detection
title_short Multicommuted flow system for the determination of glucose in animal blood serum exploiting enzymatic reaction and chemiluminescence detection
title_sort multicommuted flow system for the determination of glucose in animal blood serum exploiting enzymatic reaction and chemiluminescence detection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2548390/
https://www.ncbi.nlm.nih.gov/pubmed/18924619
http://dx.doi.org/10.1155/S1463924603000191
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