Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0406810 (NAME)
 13,345 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

A direct immersion solid-phase microextraction coupled with gas chromatography-electron capture detection (SPME-GC-ECD) method was optimized and validated for the quantitative determination of 18 organochlorine pesticides in ground water. Ionic strength, stirring speed, adsorption and desorption time and pH were some of the parameters investigated in order to select the optimum conditions for SPME with a 50/30 DVB/CAR/PDMS fiber coating. The SPME-GC/ECD method showed good linear response below 10 ng L(-1) with R(2) values in the range of 0.9950-0.9997. The repeatability of the measurements were lower than 10%. Values of relative recoveries located within the acceptable range (80-120%). Limits of quantification (LOQ) from 4.5x10(-3) to 1.5 ng L(-1) were obtained. On average 8 organochlorines were found per sample, even so all the 18 organochlorines were quantified among them. Substances such as endrin ketone, gamma-BHC and beta-BHC were the pesticides determined in larger concentration (0.06-305 ng L(-1)), while methoxychlor and aldrin in smaller amounts (0.151-1.55 ng L(-1)). Measured levels of organochlorine pesticides were above the limits established by Brazilian regulations.
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PMID:Determination of organochlorine pesticides in ground water samples using solid-phase microextraction by gas chromatography-electron capture detection. 1907 40

Solid phase microextraction (SPME) has been optimized and applied to the determination of the volatile halogenated compounds (VHCs) and semi-volatile halogenated compounds (SVHCs). Three types of SPME fiber coated with different stationary phases (PDMS-100 mum, CAR/PDMS-75 mum, PDMS/DVB-65 mum) were used to examine their extraction efficiencies for the compounds tested. Experimental parameters such as the selection of SPME coatings, extraction time, and addition of salts were studied. The carboxen-polydimethylsiloxane (CAR/PDMS) fiber appears to be the most suitable for the determination of VHCs. Analytical parameters such as linearity, limit of detection, and precision were also evaluated. Application of ECD detector for the determination of VHCs and SVHCs allows their determination on the low concentration level, ranging from 0.005 to 0.8 mug/L(-1). The HS-SPME-GC/ECD procedure gave good analytical precision expressed as relative standard deviation (RSD) (ranged from 5.08% to 8.07%) for a concentration level of 5 mug/L(-1) and good linearity (r(2) > 0.98) in a wide calibration range. The applied HS-SPME-GC/ECD method was found to be a quick and effective technique for the determination of microtrace amounts of volatile and semi-volatile halogenated compounds in samples containing high amounts of various organic compounds.
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PMID:Application of Headspace Solid-Phase Microextraction for Determination of Chloro-Organic Compounds in Sewage Samples. 1969 11

The transmembrane protein CD19 is exclusively expressed on normal and malignant B cells and therefore constitutes the target of approved CAR-T cell-based cancer immunotherapies. Current efforts to assess CAR-T cell functionality in a quantitative fashion both in vitro and in vivo are hampered by the limited availability of the properly folded recombinant extracellular domain of CD19 (CD19-ECD) considered as "difficult-to-express" (DTE) protein. Here, we successfully expressed a novel fusion construct consisting of the full-length extracellular domain of CD19 and domain 2 of human serum albumin (CD19-AD2), which was integrated into the Rosa26 bacterial artificial chromosome vector backbone for generation of a recombinant CHO-K1 production cell line. Product titers could be further boosted using valproic acid as a chemical chaperone. Purified monomeric CD19-AD2 proved stable as shown by non-reduced SDS-PAGE and SEC-MALS measurements. Moreover, flow cytometric analysis revealed specific binding of CD19-AD2 to CD19-CAR-T cells. Finally, we demonstrate biological activity of our CD19-AD2 fusion construct as we succeeded in stimulating CD19-CAR-T cells effectively with the use of CD19-AD2-decorated planar supported lipid bilayers.
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PMID:Getting CD19 Into Shape: Expression of Natively Folded "Difficult-to- Express" CD19 for Staining and Stimulation of CAR-T Cells. 3211 29