4.7 Article

Electrochemical flow injection approach for routine screening of lipase activity in pancreatic preparations

Journal

TALANTA
Volume 260, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.talanta.2023.124588

Keywords

Cobalt (II) phthalocyanine; Electrochemical detection; Fat digestive power; Flow injection analysis; Lipase activity

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A state-of-the-art strategy for lipase activity determination in pancreatic preparations using FIA-ED was described. The optimized method showed good correlation with the titrimetric method and manufacturer's declaration. The procedure allowed for the determination of lipase activity in a range of 0.8 to 18 U L-1 with LOD and LOQ values of 0.3 U L-1 and 1 U L-1, respectively.
A state-of-the-art strategy for the determination of lipase activity in pancreatic preparations using flow injection analysis (FIA) with electrochemical detection (FIA-ED) is described. The procedure is based on the enzymatic reaction of a specific substrate (1,3-dilinoleoyl-glycerol) with lipase from porcine pancreas and determination of enzymatically formed linoleic acid (LA) at +0.4 V by applying a cobalt (II) phthalocyanine-multiwalled carbon-nanotubes modified carbon paste electrode (Co(II)PC/MWCNT/CPE). In order to get a high-performance analytical method, sample preparation, flow system, and electrochemical conditions were optimized. Under optimized conditions the lipase activity of porcine pancreatic lipase was calculated to be 0.47 units per mg lipase protein based on the definition that 1 unit hydrolyses 1 microequivalent linoleic acid from 1,3-dilinoleoyl-glyc-erol per 1 min at pH 9 and 20 degrees C (kinetic measurement: 0-25 min). Moreover, the developed procedure was shown to be easily adaptable for the fixed-time assay (incubation time 25 min) as well. In this case, linear correlation between flow signal and lipase activity was found in the range from 0.8 to 18 U L-1. LOD and LOQ were determined to be 0.3 U L-1 and 1 U L-1, respectively. The kinetic assay was further preferred for the determination of lipase activity in commercially available pancreatic preparations. The lipase activities of all preparations obtained by the present method were found to be in good correlation with those obtained by the titrimetric method and declared by manufacturers.

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