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This method has been used as an analytical method for the quantification of TCA and TeCA in red wine samples that were selected for this study, yielding good results.
The aim of this study was to develop and optimise an analytical method for the quantification of a bactericide and 13 pharmaceutical products, including 8 antibiotics (fluoroquinolones, tetracyclines, sulfonamides, macrolide), in various aqueous environmental samples: soil water and aqueous fractions of pig slurry, digested pig slurry and sewage sludge.
As indicated earlier, the analytical method for the quantification of protein S-glutathionylation is not sensitive enough to quantify microtubule S-glutathionylation.
4– 6 When combined with a laser as an intense excitation source, the concept of PAS detection has already proven an effective analytical method for the quantification of lutein in biological matrix, 7 lycopene in the tomato based products, 8, 9 and total carotenes in various margarine matrices.
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The sample size for MEOHP and MEHHP was 208 because analytical methods for the quantification of these analytes were only recently implemented in this study.
Reliable and fast analytical methods for the quantification of these plasticizers are needed.
The controversy triggered several environmental and epidemiologic studies, and it generated needs for sensitive and selective analytical methods for the quantification of atrazine, atrazine metabolites, and degradation or hydrolysis products.
Fast and low cost analytical method for the quantification and stability evaluation of the pheromone rhynchophorol; Analytical method for the adsorption and recovery of pheromone using inorganic matrices; Elaboration of an inorganic matrix/pheromone composite aimed at pest control through controlled pheromone release.
The present study was carried out to develop and validate an analytical method for the detection and quantification of lambda-cyhalothrin, a synthetic pyrethroid insecticide, in tomato using gas chromatography-electron capture detector (GC-ECD).
In the current study, a SIC system was coupled with a fluorescence (FL) detector to provide an analytical method for the separation and quantification of AML and FSM in human urine and pharmaceutical formulation.
Developing suitable analytical methods for the concurrent quantification of multiple exposure biomarkers is challenging because optimal conditions for the hydrolysis of such conjugates (e.g., O-glucuronides, N-glucuronides, sulfates) may differ depending on the biomarker.
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