On-chip integrated metasystem for spin-dependent multi-channel color holography.

On-chip integrated metasurface driven by in-plane guided waves is of great interests in various light-field manipulation applications such as colorful augmented reality and holographic display. However, it remains a challenge to design colorful multichannel holography by a single on-chip metasurface. Here we present metasurfaces integrated on top of a guided-wave photonic slab that achieves multi-channel colorful holographic light display. An end-to-end scheme is used to inverse design the metasurface for projecting off-chip preset multiple patterns. Particular examples are presented for customized patterns that were encoded into the metasurface with a single-cell meta-atom, working simultaneously at RGB color channels and for several different diffractive distances, with polarization dependence. Holographic images are generated at 18 independent channels with such a single-cell metasurface. The proposed design scheme is easy to implement, and the resulting device is viable for fabrication, promising plenty of applications in nanophotonics.

Identifying the Epitopes of Bacillus thuringiensis Cry2Aa Toxin Involved in Cadherin Interaction by a Monoclonal Antibody.

Antibodies are a useful tool for assistance to map the binding epitopes in Bacillus thuringiensis Cry toxins and their receptors, and even determine how receptors promote toxicity. In this work, a monoclonal antibody (mAb-1D2) was produced by the hybridoma cell line raised against Cry2Aa toxins, with a half inhibition concentration (IC50) of 9.16 µg/mL. The affinity constant of two recombinant toxin-binding fragments derived from Helicoverpa armigera and Plutella xylostella cadherin-like protein (HaCad-TBR or PxCad-TBR) to Cry2Aa toxin was measured to be 1.21 µM and 1.24 µM, respectively. Competitive ELISA showed that mAb-1D2 competed with HaCad-TBR or PxCad-TBR binding to Cry2Aa. Meanwhile, the toxicity of the Cry2Aa toxin to the H. armigera and P. xylostella larvae were greatly reduced when the toxin was mixed with mAb-1D2, which indicated that cadherin may play an important functional role in the toxicity of Cry2Aa. After transforming mAb-1D2 to a single-chain variable fragment (scFv), the hot spot residues of Cry2Aa with 1D2-scFv, PxCad-TBR, and HaCad-TBR were analyzed by molecular docking. It was demonstrated that the hot spot residues of Cry2Aa involving with 1D2-scFv interaction were mainly in Domain II, and some residues in Domain I. Moreover, mAb-1D2 and the two cadherin fragments shared the common hot spot residues on Cry2Aa, which could explain mAb-1D2 inhibited Cry2Aa binding with cadherin fragments. This monoclonal antibody could be a useful tool for identifying the binding epitopes between Cry2Aa and cadherin, and even assist to analyze the roles of cadherin in Cry2Aa toxicity.

Knockdown of Long Noncoding RNA LUCAT1 Inhibits Cell Viability and Invasion by Regulating miR-375 in Glioma.

Recently, long noncoding RNAs (lncRNAs) have emerged as new gene regulators and prognostic markers in several cancers, including glioma. Here we focused on lncRNA LUCAT1 on the progression of glioma. qRT-PCR was used to determine the expression of LUCAT1 and miR-375 in glioma tissues and cells. MTT and Transwell invasion assays were performed to determine the function of LUCAT1 in glioma progression. The bioinformatics tool DIANA was used to predict the targets of LUCAT1. Pearson's correlation analysis was performed to explore the correlation between LUCAT1 and miR-375. In the present study, we showed that LUCAT1 was substantially upregulated in glioma tissues and cells. LUCAT1 inhibition significantly suppressed the proliferation and invasion of glioma cells. Subsequently, DIANA showed that miR-375 was predicted to contain the complementary binding sites to LUCAT1. Luciferase reporter assay showed that miR-375 directly targeted LUCAT1. In addition, we found that miR-375 was downregulated in glioma tissues and negatively correlated with LUCAT1 expression in glioma tissues. Furthermore, the results showed that miR-375 could rescue the function of LUCAT1 in glioma progression. The lncRNA LUCAT1 was critical for the proliferation and invasion of glioma cells by regulating miR-375. Our findings indicated that LUCAT1 might offer a potential novel therapeutic target for the treatment of glioma.

Isolation of a peptide from Ph.D.-C7C phage display library for detection of Cry1Ab.

Traditional ELISA methods of using animal immunity yield antibodies for detection Cry toxin. Not only is this incredibly harmful to the animals, but is also time-intensive. Here we developed a simple method to yield the recognition element. Using a critical selection strategy and immunoassay we confirmed a clone from the Ph.D-C7C phage library, which has displayed the most interesting Cry1Ab-binding characteristics examined in this study (Fig. 1). The current study indicates that isolating peptide is an alternative method for the preparation of a recognition element, and that the developed assay is a potentially useful tool for detecting Cry1Ab.

Suppression of Chlorantraniliprole Sorption on Biochar in Soil-Biochar Systems.

The sorption behavior of chlorantraniliprole (CAP) by biochar and effect of soil extracts on sorptivity in soil-biochar systems were examined. The results showed that biochar amendment could enhance the sorption of CAP in soils. The values of K F increased significantly when the soils were amended with 0.5 % BC850, which were from 1.54 to 196.5. The indigenous sorptivity of biochar was suppressed after it was applied to the soils. The degree of biochar sorptivity attenuation in different soil-biochar systems varied with the properties of soil water soluble matters. Sorption of CAP by biochar from the five soil extracts was found to be lower than that from a CaCl2 solution. The calculated K d values at C w of 0.01 mg kg(-1) for biochar sorption of CAP from CaCl2 solution were 21.4-26.6 times of that from soil extracts. Aging of biochar in soil extract reduced CAP sorption by up to 85 %.

Artificial liver support system improves short- and long-term outcomes of patients with HBV-associated acute-on-chronic liver failure: a single-center experience.

For patients with acute-on-chronic liver failure (ACLF), artificial liver support system (ALSS) may help prolong lifespan and function as a bridge to liver transplantation (LT), but data on its long-term benefit are lacking. We conducted this prospective, controlled study to determine the efficacy of ALSS and the predictors of mortality in patients with hepatitis B virus (HBV)-associated ACLF.From January 2003 to December 2007, a total of 234 patients with HBV-associated ACLF not eligible for LT were enrolled in our study. They were allocated to receive either plasma exchange centered ALSS plus standard medical therapy (SMT) (ALSS group, n=104) or SMT alone (control group, n=130). All the patients were followed-up for at least 5 years, or until death.At 90 days, the survival rate of ALSS group was higher than that of the control group (62/104 [60%] vs 61/130 [47%], respectively; P<0.05). Median survival was 879 days in the ALSS group (43% survival at 5 years) and 649 days in the control group (31% survival at 5 years, log-rank P<0.05). ALSS was found to be associated with favorable outcome of these patients by both univariate and multivariate analysis. Multivariate Cox regression analysis also revealed that lower serum sodium levels, higher grades of encephalopathy, presence of cirrhosis, hepatorenal syndrome, and higher model for end-stage liver disease scores were independent predictors for both 90-day and 5-year mortality due to ACLF.Our findings suggest that ALSS is safe and may improve the short- and long-term prognosis of patients with HBV-associated ACLF.

Treatment with ginseng total saponins improves the neurorestoration of rat after traumatic brain injury.

ETHNOPHARMACOLOGICAL RELEVANCE: Ginseng, the root of Panax ginseng C.A. Meyer, is a traditional medicinal herb that has been widely used in Asia for the treatment of many diseases through its effects of reinforcing vitality, strengthening the bodily resistance to pathogenic factors, engendering body liquids and allaying thirst, relieving uneasiness of the body and mind and benefiting intelligence, reducing body weight and prolonging life. Ginsenosides are the most important biologically active substances in ginseng. Many reports have suggested that ginsenosides could exert prominent neuroprotective and neurotrophic effects, promote neural stem/progenitor cell (NSC) proliferation and promote neurite outgrowth and neuronal network formation. The present study aimed to investigate whether treatment with ginsenosides could facilitate NSC proliferation in the hippocampal formation after traumatic brain injury (TBI) and contribute to the recovery of neurological functions including learning and memory. MATERIALS AND METHODS: The modified Feeney׳s method was used to induce a TBI in rats. Ginseng total saponins (GTS) were treated intraperitoneally twice a day for 1 week after the TBI. The neurological functions, morphology of the hippocampus, expression of nerve growth-related factors and number of NSCs in the hippocampal formation ipsilateral to the trauma were determined. RESULTS: We determined 1) GTS (5-80 mg/kg) treatment after a TBI improved the recovery of neurological functions, including learning and memory, and reduced cell loss in the hippocampal area. The effects of GTS at 20, 40, 60, and 80 mg/kg were better than the effects of GTS at 5 and 10 mg/kg. 2) GTS treatment (20 mg/kg) after a TBI increased the expression of NGF, GDNF and NCAM, inhibited the expression of Nogo-A, Nogo-B, TN-C, and increased the number of BrdU/nestin positive NSCs in the hippocampal formation. CONCLUSIONS: GTS treatment in rats after a TBI alleviated the secondary brain injury and ameliorated the neurological functions with an effective dose limit of 5-80 mg/kg. GTS regulated the expression of nerve growth-related factors and improved the proliferation of neural stem/progenitor cells, which might facilitate neural regeneration and tissue repair, and might contribute to the recovery of neurological functions, including learning and memory. These effects of GTS might provide a foundation for the use of ginseng as a medicinal herb to enhance intelligence, reduce the aging process and prolong life in the traditional medicine.

Persistence and dissipation of chlorpyrifos in Brassica chinensis, lettuce, celery, asparagus lettuce, eggplant, and pepper in a greenhouse.

The residue behavior of chlorpyrifos, which is one of the extensively used insecticides all around the world, in six vegetable crops was assessed under greenhouse conditions. Each of the vegetables was subjected to a foliar treatment with chlorpyrifos. Two analytical methods were developed using gas chromatography equipped with a micro-ECD detector (LOQ = 0.05 mg kg(-1)) and liquid chromatography with a tandem mass spectrometry (LOQ = 0.01 mg kg(-1)). The initial foliar deposited concentration of chlorpyrifos (mg kg(-1)) on the six vegetables followed the increasing order of brassica chinensis

Gambogic acid induces EGFR degradation and Akt/mTORC1 inhibition through AMPK dependent-LRIG1 upregulation in cultured U87 glioma cells.

Glioblastoma multiforme (GBM) is the most common malignant tumor in adults' central nervous system (CNS). The development of novel anti-cancer agents for GBM is urgent. In the current study, we found that gambogic acid induced growth inhibition and apoptosis in cultured U87 glioma cells, which was associated with Akt/mTORC1 (mTOR complex 1) signaling in-activation. To restore Akt activation by introducing a constitutively active (CA) Akt attenuated gambogic acid-induced cytotoxicity against U87 cells. For mechanism study, we found that gambogic acid induced LRIG1 (leucine-rich repeat and Ig-like domain-containing-1) upregulation, which was responsible for EGFR (epidermal growth factor receptor) degradation and its downstream Akt/mTORC1 inhibition. Further, we provided evidence to support that AMPK (AMP-activated protein kinase) activation mediated gambogic acid-induced LRIG1 upregulation, U87 cell apoptosis and growth inhibition, while AMPK inhibition by shRNA or compound C reduced gambogic acid-induced EGFR/Akt inhibition and cytotoxicity in U87 cells. We here proposed novel signaling mechanism mediating gambogic acid-induced cytotoxic effects in glioma cells.

Washing effects of limonene on pesticide residues in green peppers.

BACKGROUND: The presence of pesticide residues in food has caused much concern. The low health risks and environmental impacts of limonene make it a very interesting solvent for use in green chemistry. Washing effects of limonene on pesticide residues of methyl chlorpyrifos, chlorothalonil, chlorpyrifos, fenpropathrin and deltamethrin were investigated in green pepper. RESULTS: Results showed that washing with a low concentration of limonene for 5 min (where LOQ is limit of quantitation) caused 53.67%,

Effect of biochar amendment on the bioavailability of pesticide chlorantraniliprole in soil to earthworm.

To evaluate the effect of biochar amendment on the bioavailability of chlorantraniliprole (CAP) in soils with different physico-chemical properties, the uptake of CAP from various soils by earthworms was studied. It was observed that the biochar amendment of the soils affected the sorption of CAP, but the magnitude of the sorption enhancement by biochar amendment among the soils was varied, presumably due to the attenuation of the sorptivity of the biochar when amended in the soil. The amendment with biochars leads to a decrease in the bioavailability of CAP in the soils to earthworms, and more prominent for biochar BC850 amendment. In the soil with a CAP concentration of 10 mg kg(-1), the residue of CAP in the earthworm tissues was found to be 9.65 mg kg(-1), in comparison with that the CAP residue was 4.05 mg kg(-1) in BC450 amended soil and 0.59 mg kg(-1) in BC850, respectively. The degree of bioavailability reduction by same level of biochar amendment was different among soils with different properties. The results demonstrate that the properties of soils are important to performance of biochar in soil.

Recent developments in the detection of melamine.

In recent years, there were two reported outbreaks of food borne illness associated with melamine. The presence of melamine and its related compounds in milk, feed, and other foods has resulted in the need for reliable methods for the detection and accurate quantification of this class of contaminants. The sample pretreatment for melamine in a complex matrix usually involves a liquid extraction by a polar solvent, followed by a further clean-up with solid phase extraction. Analyses of melamine and related compounds are commonly carried out by liquid or gas chromatographic methods conjugated with mass spectrometry. Other innovative screening methods, which use antibodies, molecularly imprinted polymers, capillary electrophoresis, and gold nanoparticles, are also used to develop assays and biosensors to melamine. However, many of these methods have been hindered by matrix effects, the solubility of melamine-cyanuric acid complex, and background contamination. This article reviews recent developments for detecting melamine and discusses future directions.

[Impact of biochar amendment on the sorption and dissipation of chlorantraniliprole in soils].

The effects of biochar amendment on sorption and dissipation of chlorantraniliprole (CAP) in 5 different agricultural soils were studied. Red gum wood (Eucalyptus spp.) derived biochar was amended into a black soil, a yellow soil, a red soil, a purplish soil, and a fluvo-aquic soil at the rate of 0.5% (by weight). The sorption and dissipation behaviors of CAP in soils with and without biochar amendment were measured by batch equilibration technique and dissipation kinetic experiment, respectively. The objective was to investigate the impact of biochar application on the environmental fate of pesticides in agricultural soils with different physical-chemical properties, and evaluate the potential ecological impacts of field application of biochar materials. The results showed that biochar application in soils could enhance the sorption of CAP, but the magnitudes were varied among soils with different properties. Amendment of 0.5% (by weight) biochar in the black soil, which have high content of organic matter (4.59%), resulted in an increase of sorption coefficient (K(d)) by 2.17%; while for the fluvo-aquic soil with organic matter content of 1.16%, amendment of biochar at the same level led to an increase of 139.13%. The sorption capacity of biochar was partially suppressed when biochar was mixed with soils. The calculated K(Fbiochar) of biochar after mixed in the black soil, yellow soil, red soil, purplish soil, and fluvo-aquic soil were decreased by 96.94%, 90.6%, 91.31%, 68.26%, and 34.59%, respectively, compared to that of the original biochar. The half-lives of CAP in black soil, yellow soil, red soil, purplish soil, and fluvo-aquic soil were 115.52, 133.30, 154.03, 144.41 and 169.06 d, respectively. In soils amended with biochar, the corresponding half-lives of CAP were extended by 20.39, 35.76, 38.51, 79.19, and 119.75 d, respectively. Similar to the effects of biochar on CAP sorption, in soil with higher content of organic matter, the retardation of CAP dissipation by amending biochar was smaller than that in soil with lower content of organic matter. Our results suggested that application of biochar in soils could enhance the sorption and sequestration of CAP, and retard its soil dissipation, but the magnitudes depended on the organic matter content of the soils.

Dissipation of chlorpyrifos and residue analysis in rice, soil and water under paddy field conditions.

The analytical method for the residues of chlorpyrifos in rice plants, water and soil was developed and dissipation of chlorpyrifos under field conditions was studied. The limit of detection (LOD) of chlorpyrifos was 0.006 mg kg(-1) and the limit of quantification (LOQ) was found to be 0.04 mg kg(-1) in rice plant (water) and 0.02 mg kg(-1) in the other substrates, respectively. The results showed that the initial residues of chlorpyrifos in Nanjing and Guangxi were 4.99 and 6.05 mg kg(-1) (rice plant), 1.35 and 1.58 mg kg(-1) (water) and 0.51 and 0.63 mg kg(-1) (soil), respectively. The half-lives of chlorpyrifos in rice plant, water and soil from Nanjing were 4.28, 0.58 and 1.35 day, respectively, and the half-lives of those from Guangxi were 3.86, 0.52 and 1.21 day, respectively. The husked rice, rice hull and straw samples were found to contain chlorpyrifos well below the maximum residue limit (MRL) following the recommended dosage, the residues of chlorpyrifos in soil were undetectable under all application levels and frequencies after 28 day of applications.

Impact of woodchip biochar amendment on the sorption and dissipation of pesticide acetamiprid in agricultural soils.

Pyrolysis of vegetative biomass into biochar and application of the more stable form of carbon to soil have been shown to be effective in reducing the emission of greenhouse gases, improving soil fertility, and sequestering soil contaminants. However, there is still lack of information about the impact of biochar amendment in agricultural soils on the sorption and environmental fate of pesticides. In this study, we investigated the sorption and dissipation of a neonicotinoid insecticide acetamiprid in three typical Chinese agricultural soils, which were amended by a red gum wood (Eucalyptus spp.) derived biochar. Our results showed that the amendment of biochar (0.5% (w/w)) to the soils could significantly increase the sorption of acetamiprid, but the magnitudes of enhancement were varied. Contributions of 0.5% newly-added biochar to the overall sorption of acetamiprid were 52.3%, 27.4% and 11.6% for red soil, paddy soil and black soil, respectively. The dissipation of acetamiprid in soils amended with biochar was retarded compared to that in soils without biochar amendment. Similar to the sorption experiment, in soil with higher content of organic matter, the retardation of biochar on the dissipation of acetamiprid was lower than that with lower content of organic matter. The different effects of biochar in agricultural soils may attribute to the interaction of soil components with biochar, which would block the pore or compete for binding site of biochar. Aging effect of biochar application in agricultural soils and field experiments need to be further investigated.

Acute toxicity to zebrafish of two organophosphates and four pyrethroids and their binary mixtures.

BACKGROUND: Environmental pollutants, including metals, pesticides and other organics, pose serious risks to many aquatic organisms. The acute toxicities to zebrafish (Brachydanio rerio Hamilton & Buchanan) were determined for two organophosphorus insecticides, four pyrethroid insecticides and 50:50 binary mixtures. RESULTS: At 24, 48, 72 and 96 h after treatment, LC(50) of permethrin, tetramethrin, bifenthrin, etofenprox, dichlorvos and phoxim to zebrafish were 0.0052-0.0025, 0.0782-0.0460, 0.0065-0.0032, 0.0969-0.0791, 51.3-13.0 and 1.28-0.469 mg L(-1) respectively. LC(50) of permethrin + dichlorvos, permethrin + phoxim, tetramethrin + dichlorvos, tetramethrin + phoxim, bifenthrin + dichlorvos, bifenthrin + phoxim, etofenprox + dichlorvos and etofenprox + phoxim were 0.0082-0.0046, 0.0078-0.0042, 0.264-0.124, 0.141-0.121, 0.0251-0.0154, 0.0154-0.0087, 0.396-0.217 and 0.213-0.0391 mg L(-1). CONCLUSION: Toxicity levels of all pyrethroid insecticides to the zebrafish were high or very high. The organophosphate dichlorvos showed low toxicity, but phoxim showed high or intermediate toxicities to zebrafish, and the toxicities of binary mixtures of permethrin and dichlorvos or phoxim, bifenthrin and dichlorvos or phoxim and etofenprox and phoxim (48, 72 and 96 h exposure) were very high. The toxicities of binary mixtures of tetramethrin and dichlorvos or phoxim, etofenprox and dichlorvos and etofenprox and phoxim (24 h exposure) were high.

[Screening of anti-Cry1Ac scFv from A phage display antibody library.].

AIM: To clone human anti-Cry1Ac single-chain antibodies (scFv) from Tomlinson J phage antibody library. METHODS: A human large phage antibody library was panned for four rounds of "adhesion-elution-amplification". The specificity of the antigen binding activity of the selected clones was identified by ELISA and the variable genes were analyzed and identified. RESULTS: After the panning, 2 positive clones were obtained, which could bind Cry1Ac specifically. DNA sequence analysis showed that they had different antibody V region encoding genes. CONCLUSION: By-passing immunization, the specific human anti-Cry1Ac scFv also can be prepared by using phage antibody library.

Development of an enzyme-linked immunosorbent assay for toosendanin.

Enzyme-linked immunosorbent assays (ELISAs) were developed by using polyclonal antibody for toosendanin (TSN), a biopesticide from Melai toosendan Sieb. et Zucc. Their application in the determination of this analyte in spiked cabbage, tomato and apple samples was studied. The haptens, 28-hemisuccinyl-TSN (TSN-S) and 28-hemiglutaryl-TSN (TSN-G) were synthesized by using esterification. Immunogen and coating antigen were synthesized by using the mixed anhydride reaction and active ester protocol, respectively. Rabbits were immunized with TSN-G-BSA and TSN-S-BSA. Using the selected antibody and coating antigen, an indirect competitive ELISA for TSN was developed, which showed an IC(50) value of 1.023 microg mL(-1), with a detection limit of 0.009 microg mL(-1). A direct competitive ELISA using an enzyme tracer was also developed. The assay showed an IC(50) value of 0.840 microg mL(-1) with a detection limit of 0.014 microg mL(-1). Both assays displayed high cross-reactivity to a closely structurally related compound. Recoveries of TSN from both immunoassays of fortified samples ranged from 76.4% to 113.2% and 75.1% to 132.3%, respectively. Linear regression analysis showed good correlation between the TSN concentrations derived from ELISA and HPLC analyses, which suggested that the ELISA is a convenient supplementary analytical tool for monitoring TSN.

Acute toxicity of organophosphorus and pyrethroid insecticides to Bombyx mori.

Acute toxicities of two organophosphorus insecticides (dichlorvos and phoxim), four pyrethroid insecticides (permethrin, tetramethrin, bifenthrin, and ethofenprox), and their combined uses to the third instar of the silkworm, Bombyx mori (L.), were determined by feeding the insect with the insecticide-treated mulberry, Morus albus (L.), leaves. Twenty-four and 48 h after treatment, toxicity levels of all insecticides to the silkworm were in the very high or high range, and the LC50 values of permethrin, tetramethrin, bifenthrin, ethofenprox, dichlorvos, and phoxim were 1.60 and 0.75, 3.86 and 2.83, 0.09 and 0.06, 2.87 and 0.80, 6.63 and 4.11, and 1.05 and 0.45 mg liter(-1), respectively. The toxicity levels of 50:50 binary mixtures of organophosphorus and pyrethroid insecticides to the silkworm were in the high or middle range. Twenty-four and 48 h after treatment, the LC50 values of 50:50 binary mixtures permethrin + phoxim, permethrin + dichlorvos, tetramethrin + phoxim, tetramethrin + dichlorvos, bifenthrin + phoxim, bifenthrin + dichlorvos, ethofenprox + phoxim, and ethofenprox + dichlorvos to the silkworm were 1.49 and 0.85, 1.24 and 0.79, 2.20 and 1.08, 14.62 and 13.16, 0.33 and 0.13, 0.12 and 0.10, 2.81 and 1.37, and 4.82 and 3.00 mg liter(-1), respectively. Based on the combinations coefficient values, the toxicities of binary mixtures of organophosphorus and pyrethroid insecticides had additive effect except for the binary mixture of etramethrin + dichlorvos, which showed antagonism effect.

Synthesis of three haptens for the class-specific immunoassay of O,O-dimethyl organophosphorus pesticides and effect of hapten heterology on immunoassay sensitivity.

A general and broad class-specific enzyme-linked immunosorbent assay was developed for the O,O-dimethyl organophosphorus pesticides, including malathion, dimethoate, phenthoate, phosmet, methidathion, fenitrothion, methyl parathion and fenthion. Three haptens with different spacer-arms were synthesized. The haptens were conjugated to bovine serum albumin (BSA) for immunogens and to ovalbumin (OVA) for coating antigens. Rabbits were immunized with the immunogens and six polyclonal antisera were produced and screened against each of the coating antigens using competitive indirect enzyme-linked immunosorbent assay for selecting the proper antiserum. The effect of hapten heterology on immunoassay sensitivity was also studied. The antibody-antigen combination with the most selectivity for malathion was further optimized and tested for tolerance to co-solvent, pH and ionic strength changes. The IC(50) values, under optimum conditions, were estimated to be 30.1microgL(-1)for malathion, 28.9microgL(-1) for dimethoate, 88.3microgL(-1) for phenthoate, 159.7microgL(-1) for phosmet, 191.7microgL(-1) for methidathion, 324.0microgL(-1) for fenitrothion, 483.9microgL(-1) for methyl parathion, and 788.9microgL(-1) for fenthion. Recoveries of malathion, dimethoate, phenthoate, phosmet and methidathion from fortified Chinese cabbage samples ranged between 77.1% and 104.7%. This assay can be used in monitoring studies for the multi-residue determination of O,O-dimethyl organophosphorus pesticides.