Search results for "Detection limit"
showing 10 items of 810 documents
A method for measuring low-weight carboxylic acids from biosolid compost
2006
Concentration of low-weight carboxylic acids (LWCA) is one of the important parameters that should be taken into consideration when compost is applied as soil improver for plant cultivation, because high amounts of LWCA can be toxic to plants. The present work describes a method for analysis of LWCA in compost as a useful tool for monitoring compost quality and safety. The method was tested on compost samples of two different ages: 3 (immature) and 6 (mature) months old. Acids from compost samples were extracted at high pH, filtered, and freeze-dried. The dried sodium salts were derivatized with a sulfuric acid–methanol mixture and concentrations of 11 low-weight fatty acids (C1–C10) were a…
Measurement of pollution levels of N-nitroso compounds of health concern in water using ultra-performance liquid chromatography–tandem mass spectrome…
2017
International audience; This paper reports the development of a highly sensitive analytical method combining solid-phase extraction (SPE) with ultra-high performance liquid chromatography coupled with tandem mass spectrometry (UHPLC–MS/MS), for the monitoring of ultra-trace levels of N-nitrosamines in water samples. Under optimized analytical conditions, chromatographic separation was performed in 3 min, in isocratic mode, using an Acquity UHPLC C18 column and a mobile phase consisting of acetonitrile, water, and formic acid (60:40:0.1, v/v/v) at a flow rate of 0.4 mL min−1. Electrospray ionization tandem interface was employed prior to mass spectrometric detection. Good linearity (R2 ≥ 0.9…
Immunochemical rapid determination of quinoxyfen, a priority hazardous pollutant
2018
In 2013, quinoxyfen was included in the list of priority hazard pollutants of the European Water Framework Directive due to its toxicity to aquatic organisms. However, few analytical methods for the analysis of this fungicide have been reported and no rapid immunochemical methods have been published so far. In the present study, immunoreagents for quinoxyfen analysis were generated for the first time and an enzyme-linked immunosorbent assay was developed. Two carboxylated derivatives of quinoxyfen were designed on the basis of the minimum energy conformation of the target compound. Active esters of those novel compounds were prepared using N,N′-disuccinimidyl carbonate, and purified for cov…
Immunoreagent generation and competitive assay development for cyprodinil analysis.
2012
Cyprodinil is an anilinopyrimidine fungicide applied worldwide for the prevention and treatment of highly destructive plant diseases in a large variety of crops, including cereals, fruits, and vegetables. This paper describes the development of the first reported immunoassays for cyprodinil. Two original haptens have been synthesized and conjugated to different carrier proteins, and polyclonal antibodies have been produced. Moreover, competitive enzyme-linked immunosorbent assays have been developed and characterized for the analysis of this widely used pesticide. The influence of organic solvents and buffer conditions over the assay analytical parameters was studied. The IC 50 values of th…
Gold nanoparticles/electrochemically expanded graphite composite: A bifunctional platform toward glucose sensing and SERS applications
2019
Abstract An integrated nanogold/expanded graphite based sensor was fabricated by a former electrochemical etching of the pencil lead electrode (PLE) and a later in-situ deposition of gold nanoparticles (AuNPs). The electrochemical pretreatment of PLE (EPLE) created a 3D graphene-like surface, enhanced the electrode surface area and facilitated the electron transfer ability within 5 min without any hazardous chemicals added. The obtained AuNPs/EPLE sensor had an excellent electrochemical response to glucose with a wide linear concentration range, from 0.05 to 38 mM and 38 to 60 mM, and a low detection limit of 5 μM (S/N = 3). Furthermore, the AuNPs/EPLE sensor was successfully employed to de…
Simultaneous determination of four 5-hydroxy polymethoxyflavones by reversed-phase high performance liquid chromatography with electrochemical detect…
2009
Accumulating evidence has suggested the potential health-promoting effects of 5-hydroxy polymethoxyflavones (5-OH-PMFs) naturally existing in citrus genus. However, research efforts are hampered by the lack of reliable and sensitive methods for their determination in plant materials and biological samples. Using reversed-phase high performance liquid chromatography (HPLC) equipped with electrochemical (EC) detection, we have developed a fast and highly sensitive method for quantification of four 5-OH-PMFs, namely 5-hydroxy-6,7,8,3',4'-pentamethoxyflavone, 5-hydroxy-3,6,7,8,3',4'-hexamethoxyflavone, 5-hydroxy-6,7,4'-trimethoxyflavone, and 5-hydroxy-6,7,8,4'-tetramethoxyflavone. The method wa…
Implementation of multicommutation principle with flow-through multioptosensors
2005
Abstract For the first time, the combination of multicommutation concept with flow-through multioptosensors is exploited and a biparameter multicommutated UV sensor is developed. A very easy-operated and automated sensing device is proposed here and demonstrated to be useful in the routine analysis by applying it to the determination of two widely used pharmaceuticals chosen as model analytes: salicylamide and caffeine. The particulated solid phase used performs two functions: (a) states selectivity conditions by itself in the flow cell and (b) provides appropriate separation of the analytes in the on-line precolumn, thus making possible the sequential arrival of the analytes to the detecti…
Flow injection biamperometric determination of metronidazole with on-line photodegradation
1999
Abstract The determination of metronidazole is performed in a flow injection assembly, provided with a 40 W low pressure mercury lamp and a home-made biamperometric flow-cell furnished with two platinum electrodes polarized at 100 mV. The sample solution after being irradiated is inserted into a pure water stream. It then merges with an in situ mixed solution containing potassium iodide in sulphuric acid. The calibration graph was linear over the range 0.2–8.0 mg l −1 metronidazole; the 3 σ limit of detection was 0.008 mg l −1 ; the relative standard deviation was 0.6% (for 4 mg l −1 n = 13) and the sample throughput 50 h −1 . The influence of foreign compounds is slight and the method is …
Fourier transform infrared spectrometric strategies for the determination of Buprofezin in pesticide formulations
2002
Abstract Two different strategies for Buprofezin determination, an off-line extraction and stopped-flow determination and an automated procedure, based on the on-line extraction of Buprofezin samples with chloroform and flowing action analysis–fourier transform infrared (FIA–FT-IR) spectrometric measurement of the extracts, have been developed. For the treatment of the off-line extraction mode, data a three-factor partial least squares (PLSs) calibration was developed, using the region from 1465.7 to 1342.3 cm−1 with a single point baseline defined at 2051.9 cm−1 and based on the use of chloroform solutions of Buprofezin. The method provides a R.S.D. On the other hand, the recommended FIA m…
Direct flow injection chemiluminescence determination of salicylamide
1999
Abstract A new direct flow injection chemiluminescence method is proposed for the determination of salicylamide, based upon the oxidation of the drug by potassium permanganate in dilute sulphuric acid. The calibration graph is linear over the range 20 ng ml−1 (30 limit of detection)–8 μg ml−1 salicylamide, with a relative standard deviation (n=50, 0.5 μg ml−1) of 1.7%. The average sample insertion rate is 142 h−1. The influence of relevant foreign compounds is found to be relatively slight. The method is applied to the determination of salicylamide in a pharmaceutical formulation and human urine.