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A multicommuted system using bacterial cellulose for urease immobilization and copper (II)-MOF colorimetric sensor for urea spectrophotometric determination in milk.
Rodrigues, Julyana C; Bezerra, Caio S; Lima, Lidiane M A; Neves, Danielle D; Paim, Ana Paula S; Silva, Wagner E; Lavorante, André F.
Affiliation
  • Rodrigues JC; Departamento de Química, Universidade Federal Rural de Pernambuco, Rua Dom Manuel de Medeiros, s/n, Dois Irmão, 52171-900 Recife, PE, Brazil.
  • Bezerra CS; Departamento de Ciências da Computação, Universidade Federal Rural de Pernambuco, Rua Dom Manuel de Medeiros, s/n, Dois Irmão, 52171-900 Recife, PE, Brazil. Electronic address: cbbs@cin.ufpe.br.
  • Lima LMA; Departamento de Química, Universidade Federal Rural de Pernambuco, Rua Dom Manuel de Medeiros, s/n, Dois Irmão, 52171-900 Recife, PE, Brazil.
  • Neves DD; Departamento de Química, Universidade Federal Rural de Pernambuco, Rua Dom Manuel de Medeiros, s/n, Dois Irmão, 52171-900 Recife, PE, Brazil.
  • Paim APS; Departamento de Química Fundamental, Universidade Federal de Pernambuco, Av. Jornalista Aníbal Fernandes s/n, Cidade Universitária, 50740-560 Recife, PE, Brazil. Electronic address: ana.paim@ufpe.br.
  • Silva WE; Departamento de Química, Universidade Federal Rural de Pernambuco, Rua Dom Manuel de Medeiros, s/n, Dois Irmão, 52171-900 Recife, PE, Brazil.
  • Lavorante AF; Departamento de Química, Universidade Federal Rural de Pernambuco, Rua Dom Manuel de Medeiros, s/n, Dois Irmão, 52171-900 Recife, PE, Brazil. Electronic address: andre.lavorante@ufrpe.br.
Food Chem ; 460(Pt 1): 140454, 2024 Dec 01.
Article in En | MEDLINE | ID: mdl-39033642
ABSTRACT
This work describes determining urea in milk samples using a multicommuted approach with a urease enzyme immobilized in bacterial cellulose and solid MOF as a colorimetric reagent. The Cu(2+)-MOF was characterized by FTIR spectroscopy, XRD, and SEM. The urea quantification was based on the urea hydrolysis reaction catalyzed by urease and reacted with Cu(2+)-MOF forming [Cu(NH3)4]2+, monitored at 450 nm. Linear responses were obtained from 1.0 to 50.0 mg dL-1 urea (R = 0.9959, n = 11), detection and quantitation limits of 0.082 mg dL-1 and 0.272 mg dL-1 respectively, analytical frequency of 8 determinations per hour, 0.8 mL sample solution consumption. Potential interfering studies have shown the selectivity of the proposed method. Addition and recovery tests were performed obtaining variation from 90 to 103%. Applying the F-test and t-test, the results showed no significant difference at the 95% confidence level Comparing the proposed and the reference method.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Urea / Urease / Cellulose / Colorimetry / Copper / Milk / Enzymes, Immobilized Limits: Animals Language: En Journal: Food Chem Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Urea / Urease / Cellulose / Colorimetry / Copper / Milk / Enzymes, Immobilized Limits: Animals Language: En Journal: Food Chem Year: 2024 Document type: Article