Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 6 de 6
Filter
Add more filters










Database
Language
Publication year range
1.
J Agric Food Chem ; 63(21): 5107-19, 2015 Jun 03.
Article in English | MEDLINE | ID: mdl-25702899

ABSTRACT

A new, automated, high-throughput, mini-column solid-phase extraction (c-SPE) cleanup method for QuEChERS extracts was developed, using a robotic X-Y-Z instrument autosampler, for analysis of pesticide residues in fruits and vegetables by LC-MS/MS. Removal of avocado matrix and recoveries of 263 pesticides and metabolites were studied, using various stationary phase mixtures, including zirconia-based sorbents, and elution with acetonitrile. These experiments allowed selection of a sorbent mixture consisting of zirconia, C18, and carbon-coated silica, that effectively retained avocado matrix but also retained 53 pesticides with <70% recoveries. Addition of MeOH to the elution solvent improved pesticide recoveries from zirconia, as did citrate ions in CEN QuEChERS extracts. Finally, formate buffer in acetonitrile/MeOH (1:1) was required to give >70% recoveries of all 263 pesticides. Analysis of avocado extracts by LC-Q-Orbitrap-MS showed that the method developed was removing >90% of di- and triacylglycerols. The method was validated for 269 pesticides (including homologues and metabolites) in avocado and citrus. Spike recoveries were within 70-120% and 20% RSD for 243 of these analytes in avocado and 254 in citrus, when calibrated against solvent-only standards, indicating effective matrix removal and minimal electrospray ionization suppression.


Subject(s)
Citrus/chemistry , Food Contamination/analysis , Persea/chemistry , Pesticide Residues/isolation & purification , Solid Phase Extraction/methods , Adsorption , Chromatography, High Pressure Liquid , Fruit/chemistry , Pesticide Residues/chemistry , Solid Phase Extraction/instrumentation , Tandem Mass Spectrometry , Zirconium/chemistry
2.
J Chem Ecol ; 35(1): 50-7, 2009 Jan.
Article in English | MEDLINE | ID: mdl-19093152

ABSTRACT

The banded sunflower moth (BSFM), Cochylis hospes Walshingham (Lepidoptera: Cochylidae) is a specialist insect, the larvae of which feed on sunflowers, Helianthus spp., and a few other species of Compositae. It is one of the most important pests of sunflower in the USA. Previous work on H. annuus, the cultivated sunflower, revealed two diterpenoids that function as oviposition stimulants for female BSFM, and that other, more polar compounds also stimulated oviposition. Using a bioassay-guided approach, we isolated three additional diterpenoids, grandifloric acid (1), 15beta-hydroxy-ent-trachyloban-19-oic acid (2), and 17-hydroxy-16alpha-ent-kauran-19-oic acid (3), from polar fractions of pre-bloom sunflower head extracts. In laboratory bioassays, purified natural samples of each of these compounds stimulated oviposition by female BSFM. Structure-activity relationships of the five diterpenoids known to stimulate oviposition by female BSFM are discussed.


Subject(s)
Diterpenes/isolation & purification , Diterpenes/metabolism , Helianthus/chemistry , Helianthus/parasitology , Moths/physiology , Animals , Biological Assay , Diterpenes/chemistry , Diterpenes, Kaurane/isolation & purification , Diterpenes, Kaurane/metabolism , Female , Oviposition , Structure-Activity Relationship
3.
J Chem Ecol ; 31(1): 89-102, 2005 Jan.
Article in English | MEDLINE | ID: mdl-15839482

ABSTRACT

Two diterpenoid alcohols, ent-kauran-16alpha-ol (1) and ent-atisan-16alpha-ol (2), were isolated from pre bloom (R3-R4 stage) sunflower heads as oviposition stimulants for the banded sunflower moth, Cochylis hospes. Fractionation of a sunflower head extract, by normal-phase flash column chromatography, resulted in an early eluting fraction exhibiting significant activity in an egg-laying bioassay. Compounds 1 and 2, along with ent-trachyloban-19-oic acid (3) and ent-kaur-16-en-19-oic acid (4), were isolated as the major components of this fraction and identified by their NMR and mass spectra. The purified compounds were individually tested for ovipositional activity in dose-response bioassays. In these bioassays, compounds 1 and 2 gave linear dose responses, with increasing numbers of eggs laid as the dosage of either increased. Compounds 3 and 4 failed to stimulate significant egglaying at any of the dosages tested. A factorial design bioassay, using compounds 1 and 2, showed that 1 was relatively more stimulatory than 2, and that there was no synergistic effect on oviposition when the two compounds were combined.


Subject(s)
Diterpenes/isolation & purification , Helianthus/chemistry , Moths/physiology , Animals , Diterpenes/pharmacology , Female , Male , Moths/drug effects , Oviposition/drug effects , Plant Extracts/chemistry , Stimulation, Chemical
4.
J Nat Prod ; 68(1): 26-30, 2005 Jan.
Article in English | MEDLINE | ID: mdl-15679312

ABSTRACT

A novel beta-lactone, vittatalactone (1), was isolated from collections of airborne volatile compounds from feeding male striped cucumber beetles, Acalymma vittatum. The structure of 1 was determined to be (3R,4R)-3-methyl-4-(1,3,5,7-tetramethyloctyl)oxetan-2-one by microderivatization, GC-MS, and NMR studies. The absolute configurations at C-2 and C-3 on the beta-lactone ring were assigned by use of the modified Mosher method, applied to the beta-hydroxy acid methyl ester resulting from methanolysis of 1. Biological activity of 1, possibly as an aggregation pheromone for A. vittatum, was indicated by electrophysiological studies using beetle antennae and by the production of 1 by feeding male, and not female, beetles.


Subject(s)
Coleoptera , Lactones/isolation & purification , Sex Attractants/isolation & purification , Animals , Female , Lactones/chemistry , Lactones/pharmacology , Male , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular , Sex Attractants/chemistry , Sex Attractants/pharmacology , Stereoisomerism
5.
J Chem Ecol ; 29(11): 2439-46, 2003 Nov.
Article in English | MEDLINE | ID: mdl-14682525

ABSTRACT

The female-produced sex pheromone of the scarab beetle Phyllophaga lanceolata was identified as the methyl ester of an essential amino acid, L-leucine. During field testing, 239 male P. lanceolata were caught in traps baited with L-leucine methyl ester. L-Isoleucine and L-valine methyl esters, similar in structure to L-leucine methyl ester and previously identified as female-produced sex pheromone compounds employed by other Phyllophaga species, were also tested. Addition of L-valine or L-isoleucine methyl esters to the L-leucine methyl ester in 1:1 ratios completely inhibited attraction of P. lanceolata males. Males of P. squamipilosa were also captured using L-leucine methyl ester. This is the first record of P. squamipilosa from Kansas.


Subject(s)
Coleoptera/physiology , Leucine/analogs & derivatives , Leucine/pharmacology , Sex Attractants/chemistry , Sex Attractants/pharmacology , Animals , Female , Leucine/chemistry , Leucine/isolation & purification , Male , Movement
6.
J Chem Ecol ; 29(2): 503-7, 2003 Feb.
Article in English | MEDLINE | ID: mdl-12737273

ABSTRACT

Chemical investigation of a female balloon-like organ of the European chafer, Rhizotrogus majalis (Razoumowsky), with GC-EAD has resulted in the identification of female-specific compounds, (R)-3- hydroxybutan-2-one, (2R,3R)-2,3-butanediol, and meso-2,3-butanediol that are specifically EAD-active with male antennae. No behavioral role for any of the EAD active compounds could be discerned with this species.


Subject(s)
Butylene Glycols/analysis , Coleoptera/chemistry , Pheromones/isolation & purification , Pheromones/pharmacology , Animals , Butylene Glycols/chemistry , Butylene Glycols/pharmacology , Chemoreceptor Cells/physiology , Chromatography, Gas , Electrophysiology , Female , Male
SELECTION OF CITATIONS
SEARCH DETAIL
...