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Plasma pre-treatment

The pre-treatment plasma concentration of natriuretic peptide type B may be a good marker for pioglitazone-induced congestive heart failure but this needs confirmation (99). [Pg.465]

Although his pre-treatment plasma uric acid level was only modestly elevated (7 3 mg/100 ml.) his urinary excretion was 1,140 mg in 2k hours His creatinine clearance was 155 mg/min He had been satisfactorily treated with Allopurinol which was stopped one month prior to the commencement of the present study. With kOO mg of thiopurinol per day the plasma uric acid fell in one week from 7 2 to 5 0 mg/100 ml., a drop of 315 . At the same time the urinary uric acid excretion fell by 52%, with no change in the urinary excretion of xanthine or hypo-xanthine or in their ratio ... [Pg.230]

Case 2 A 35 year old man with a history or recurrent gouty arthritis commencing in 1957 He weighed 99 kilograms and was mildly hypertensive (B.P. 160/100). His pre-treatment plasma uric acid level had been 10.2 mg/100 ml. with a uric excretion of 1.100 mg. per day. The creatinine clearance was 1 9 ml/min. In 1969 he had been placed on Allopurinol 00 mg. a day and this had adequately corrected his hyperuricaemia and controlled his gouty attacks. In 197" he volunteered to take part in a study of Thiopurinol which took place after Allopurinol had been left off for one week. This may have been an inadequate period of time as shown in Table 2. The plasma uric acid at the commencement of the study was only 5 7 rag/100 ml. Nevertheless, there was a 57% fall in plasma uric acid level following the introduction of Thiopurinol in a dose of hOO mg. per day. In this case however, there was no comparable fall in the urine uric acid level, and no change in the oxypurine excretion. [Pg.231]

The pre-treatment plasma folate concentration was substantially higher in fortified populations compared with that in non-fortified populations, and allocation to B vitamin treatment was associated with a greater proportional reduction in homocysteine concentrations in non-fortified compared with that in fortified populations (Clarke et al. 2010). The meta-analysis assessed the effects of B vitamins on risk of vascular and non-vascular events assodated with about a 25% reduction in homocysteine levels for about five years (Clarke et al. 2010). [Pg.791]

Drug resistance A small study in 20 NVP exposed infants found that low frequencies of several NVP resistance mutations including K103N and Y181C in pre-treatment plasma samples were significantly associated with virologic failure [263 ]. [Pg.423]

Pre-treatment Plasma gas helium fed at 2000 seem AC-voltage frequency 20 KHz Deposition Precursor Uquid fluoroacrylate monomer (with 5% Irgacure-184 photoinitiator)... [Pg.213]

Pre-treatment Plasma gas helium with 10% oxygen fed at 3000 seem AC-voltage Erequency 20 KHz... [Pg.213]

Generally, SCR of NO works effectively at temperatures above 500-550 K, but the performance for NO removal decreases considerably at lower temperatures [90], At low temperature, it is known that the efficiency of the SCR of NO strongly depends on N02 concentration in the gas stream. About 30-50% of N02 in the gas stream could greatly enhance the performance of SCR. However, in real conditions, the fraction of N02 present in the total NO does not exceed 5%. Hence, an oxidation pre-treatment is necessary to increase the concentration of N02. Plasma-assisted SCR is currently being studied by many researchers. It was reported that the presence of plasma greatly enhances the performance of SCR catalyst to achieve high NO removal efficiencies even at low gas temperatures [36,82,91-96],... [Pg.384]

The oxidation of NO to N02 can be considered an advantage when combining plasma with selective catalytic reduction, as it is well-known that at low temperature the efficiency of NO reduction by SCR strongly depends on the N02 concentration in the gas. An oxidation pre-treatment of the gas by non-thermal plasma, prior to the SCR reactor greatly enhances the performance of SCR at temperatures below 500 K. Therefore, the PE-SCR technique is very promising for efficient NO reduction. [Pg.390]

Demidouk, V., Ravi, V., Chae, J.-O. et al. (2005) Pt-Al203 catalyst and discharge plasma pre-treatment techniques for enhancing selective catalytic reduction of nitrogen oxides A comparative study, React. Kinet. Catal. Lett. 85, 239-44. [Pg.395]

An internal standard should always be used for every analysis carried out. This is an amino acid that is known to be absent from the sample under investigation. For instance in blood plasma analysis either of the non-physio-logical amino acids, nor-leucine or a-amino-/3-guanidinobutyric acid, may be used. This should be added in a known amount to the sample prior to any sample pre-treatment (for example, removal of protein). [Pg.379]

Bayliss and co-workers [10] combined ultra-high flow rates, parallel LC columns, a multiplex electrospray source, and mass spectrometric detection for the rapid determination of pharmaceuticals in plasma using four narrow bore (50 mm x 1 mm, 30 pm Oasis HLB) or capillary (50 mm x 0.18 mm, 25 pm Oasis HLB) HPLC columns with large particle sizes (to avoid high system back-pressure) in parallel with a multiple probe injector and a MUX MS interface. Small sample aliquots were injected directly into the system without sample pre-treatment procedure, obtaining very low limits of quantification (from 1 to 5 ng/mL). [Pg.51]

Gluing is difficult, needing pre-treatments such as, for example, chemical etching (sulfo-chromic acid etching), flame oxidation or hot-air (500°C) treatment, corona discharge, plasma or UV treatments. The exposure must be brief and superficial and the original and aged properties must be tested. [Pg.231]

Pomerleau CS, Pomerleau OF, Majchrzak MJ (1987) Mecamylamine pre-treatment increases subsequent nicotine self-administration as indicated by changes in plasma nicotine level. Psychopharmacology 91 391-393... [Pg.399]

A fully automated on-line SPE-HPLC-MS-MS method was developed and validated for the direct analysis of 14 antidepressants and their metabolites in plasma by de Castro et al. [75]. After direct injection of 50pL of plasma without prior sample pre-treatment, gradient RP separation was completed in 14 min, with a sample throughput of 3h. LOQs were estimated to be at 10 ng/ mL. Analytes proved to be stable during sample process with the exception of clomipramine and norclomipramine. [Pg.670]

The choice of an appropriate derivatisation of BAs is a crucial point for a good GC analysis [15]. Unconjugated BAs are commonly analysed as methyl ester-trimethyl-silyl (TMS) ether derivatives, although interference from plasma sterols may occur at the LCA retention time. Use of -butyl ester-TMS ether derivatives allows a better chromatographic separation between BAs, which elute later, and sterols. The advantage of this derivative procedure is the simplification of plasma pre-treatment. [Pg.612]

Plastics for which the adhesion of coatings may be improved by plasma pre-treatment are reported to be polyethylene, polypropylene, polycarbonates, polyacetals, polyaromatic esters, polyimides, polyamides, polyphenylene ether, polyacrylates, acetal homopolymer, and poly(ether imide). [Pg.245]

Y. S. Chung, R. M. Barnes, Determination of gold, patinum, palladium and silver in geological samples by inductively coupled plasma atomic emission spectrometry after poly(dithiocarbamate) resin pre-treatment,. /. Anal. Atom. Spectrom., 3 (1988), 1079D 1082. [Pg.378]

C. M. R. Almeida, M. T. S. D. Vasconcelos, Determination of lead isotope ratios in port wine by inductively coupled plasma mass spectrometry after pre-treatment by UV-irradiation, Anal. Chim. Acta, 396 (1999), 45-53. [Pg.497]

Conventional coating approaches to TPO, which rely on the use of substrate pretreatments such as flaming, corona discharge, plasma or chemical pre-treatment, have led to a substantial oxidation of the surface, which enhances adhesion. These pretreatments, however, have a limited service life before the surface reverts to its unoxidized, apolar condition. [Pg.1303]


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See also in sourсe #XX -- [ Pg.28 ]




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