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Simultaneous determination of imidazolinone herbicides from soil and natural waters using soil column extraction and off-line solid-phase extraction followed by liquid chromatography with UV detection or liquid chromatography/electrospray mass spectroscopy.
Anal Chem. 1998 Jan 01; 70(1):121-30.AC

Abstract

This paper describes the simultaneous quantification of the imidazolinone herbicides (IMIs) imazapyr, m-imazamethabenz, p-imazamethabenz, m,p-imazamethabenz-methyl, imazethapyr, and imazaquin in two types of samples. (a) Groundwater, lake water, and river water samples were enriched by off-line solid-phase extraction with a Carbograph-1 cartridge and analyzed by reversed-phase liquid chromatography using a UV detector (lambda = 240 nm). The overall recoveries of IMIs extracted from 1 L of groundwater (fortified with 500-100 ng/L), 0.5 L of lake water (fortified with 500-100 ng/L), and 0.5 L of river water (fortified with 1000-200 ng/L) samples were not lower than 89%. The mean relative standard deviation (RSD) was 5.1% (ranging from 4.1% to 6.8%) in natural water. The detection limits were 30-39 ng/L in groundwater, 43-51 ng/L in lake water, and 55-67 ng/L in river water. The method involves confirmatory analysis by LC/ES-MS in full-scan mode. The dependence of the ion signal intensities on proton concentration in the mobile phase was investigated with a view to optimizing the sensitivity of the ES-MS detector. When LC/ES-MS was used, the limit of detection, calculated from extracted-ion current profiles (EICPs), was 4-7 ng/L for ground-water and 9-13 ng/L for river water. (b) Soil sample analysis utilized combined soil column extraction (SCE) and off-line solid phase extraction (SPE) for sample preparation, analyzing with LC/ES-MS under selected ion monitoring (SIM). Several different extractants were evaluated for the purpose of SCE optimization. The system that best optimizes the extractability IMIs from the soil was found to be the mixture CH3OH/(NH4)2CO3 (0.1 M, 50:50 v/v). The effect of IMI concentration in the matrix on recovery was evaluated. The total recovery of each IMI from soil at each of the two levels investigated ranged from 87% to 95%. Under three ion SIM conditions, the limit of detection (S/N = 3) was 0.1-0.05 ng/g in soil samples.

Authors+Show Affiliations

Department of Chemistry, La Sapienza University, Roma, Italy.No affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

9435470

Citation

Laganà, A, et al. "Simultaneous Determination of Imidazolinone Herbicides From Soil and Natural Waters Using Soil Column Extraction and Off-line Solid-phase Extraction Followed By Liquid Chromatography With UV Detection or Liquid Chromatography/electrospray Mass Spectroscopy." Analytical Chemistry, vol. 70, no. 1, 1998, pp. 121-30.
Laganà A, Fago G, Marino A. Simultaneous determination of imidazolinone herbicides from soil and natural waters using soil column extraction and off-line solid-phase extraction followed by liquid chromatography with UV detection or liquid chromatography/electrospray mass spectroscopy. Anal Chem. 1998;70(1):121-30.
Laganà, A., Fago, G., & Marino, A. (1998). Simultaneous determination of imidazolinone herbicides from soil and natural waters using soil column extraction and off-line solid-phase extraction followed by liquid chromatography with UV detection or liquid chromatography/electrospray mass spectroscopy. Analytical Chemistry, 70(1), 121-30.
Laganà A, Fago G, Marino A. Simultaneous Determination of Imidazolinone Herbicides From Soil and Natural Waters Using Soil Column Extraction and Off-line Solid-phase Extraction Followed By Liquid Chromatography With UV Detection or Liquid Chromatography/electrospray Mass Spectroscopy. Anal Chem. 1998 Jan 1;70(1):121-30. PubMed PMID: 9435470.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Simultaneous determination of imidazolinone herbicides from soil and natural waters using soil column extraction and off-line solid-phase extraction followed by liquid chromatography with UV detection or liquid chromatography/electrospray mass spectroscopy. AU - Laganà,A, AU - Fago,G, AU - Marino,A, PY - 1998/1/22/pubmed PY - 1998/1/22/medline PY - 1998/1/22/entrez SP - 121 EP - 30 JF - Analytical chemistry JO - Anal Chem VL - 70 IS - 1 N2 - This paper describes the simultaneous quantification of the imidazolinone herbicides (IMIs) imazapyr, m-imazamethabenz, p-imazamethabenz, m,p-imazamethabenz-methyl, imazethapyr, and imazaquin in two types of samples. (a) Groundwater, lake water, and river water samples were enriched by off-line solid-phase extraction with a Carbograph-1 cartridge and analyzed by reversed-phase liquid chromatography using a UV detector (lambda = 240 nm). The overall recoveries of IMIs extracted from 1 L of groundwater (fortified with 500-100 ng/L), 0.5 L of lake water (fortified with 500-100 ng/L), and 0.5 L of river water (fortified with 1000-200 ng/L) samples were not lower than 89%. The mean relative standard deviation (RSD) was 5.1% (ranging from 4.1% to 6.8%) in natural water. The detection limits were 30-39 ng/L in groundwater, 43-51 ng/L in lake water, and 55-67 ng/L in river water. The method involves confirmatory analysis by LC/ES-MS in full-scan mode. The dependence of the ion signal intensities on proton concentration in the mobile phase was investigated with a view to optimizing the sensitivity of the ES-MS detector. When LC/ES-MS was used, the limit of detection, calculated from extracted-ion current profiles (EICPs), was 4-7 ng/L for ground-water and 9-13 ng/L for river water. (b) Soil sample analysis utilized combined soil column extraction (SCE) and off-line solid phase extraction (SPE) for sample preparation, analyzing with LC/ES-MS under selected ion monitoring (SIM). Several different extractants were evaluated for the purpose of SCE optimization. The system that best optimizes the extractability IMIs from the soil was found to be the mixture CH3OH/(NH4)2CO3 (0.1 M, 50:50 v/v). The effect of IMI concentration in the matrix on recovery was evaluated. The total recovery of each IMI from soil at each of the two levels investigated ranged from 87% to 95%. Under three ion SIM conditions, the limit of detection (S/N = 3) was 0.1-0.05 ng/g in soil samples. SN - 0003-2700 UR - https://www.unboundmedicine.com/medline/citation/9435470/Simultaneous_determination_of_imidazolinone_herbicides_from_soil_and_natural_waters_using_soil_column_extraction_and_off_line_solid_phase_extraction_followed_by_liquid_chromatography_with_UV_detection_or_liquid_chromatography/electrospray_mass_spectroscopy_ L2 - https://doi.org/10.1021/ac9707491 DB - PRIME DP - Unbound Medicine ER -