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Results for “selective extraction”

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At least 109 records · Page 6Linked to original sources
PubMed1979

Selective extraction of desmosomal proteins by low ionic strength media.

Desmosomes, isolated using an acidic buffer, have been subjected to extraction at low ionic strength. This treatment removes more than 35% of their protein in the form of two polypeptide chains of molecular weight 210 000 and 230 000, but the desmosomes show only subtle changes in ultrastructure. It is concluded that the use of low ionic strength media for desmosome isolation yields residual structures specifically depleted in high molecular weight proteins.

Animals↗
PubMed1995

Selective extraction of quercetrin in vegetable drugs and urine by off-line coupling of boronic acid affinity chromatography and high-performance liquid chromatography.

Quercetrin, quercetin and chlorogenic acid were measured in urine or in drugs by combination of boronic acid affinity chromatography and HPLC. Simple reversed-phase HPLC with UV detection was used to determine quercetrin in five different Solidago virgaurea drugs. For determination of quercetrin in human urine immobilized boronic acid was applied for sample pretreatment. this procedure leads to a determination limit of 0.01 micrograms/ml with a recovery rate of 95.3%. The first results using this method for quercetrin pharmacokinetics are presented.

Boronic Acids↗
PubMedDate not supplied

Immobilized phenylboronic acids for the selective extraction of beta-blocking drugs from aqueous solution and plasma.

The use of phenylboronic acid (PBA) solid-phase extraction cartridges for the extraction of a range of beta-blockers from aqueous buffer and plasma has been investigated and compared with other phases commonly used for solid-phase extraction. PBA was found to provide an efficient means for the extraction of this class of compound from simple aqueous buffer systems. Extraction from buffers was pH-dependent and gave optimum results at approximately pH 8. Extraction from plasma was less efficient for some of the test compounds; this matrix effect was probably due to protein binding. Chromatography showed that plasma extracts were free of major sources of interference.

Adrenergic beta-Antagonists↗
PubMed2005

Prediction of [3-(14)C]phenyldodecane biodegradation in cable insulating oil-spiked soil using selected extraction techniques.

This study investigated the use of an aqueous hydroxypropyl-beta-cyclodextrin (HPCD) shake extraction in predicting microbial mineralisation and total loss of [3-(14)C]phenyldodecane associated activity in soils spiked with cable insulating oil; phenyldodecane represents a major constituent of cable insulating oil. Direct comparisons were made between freshly spiked and aged soils, and following composting. Soil was spiked with [3-(14)C]phenyldodecane (10mg kg(-1)) and stored in microcosms and aged for 1, 23, 44, 65, 90 and 153 d. At each sample time point, a variety of analyses were performed to assess the relationship between chemical and biological techniques in determining mineralisation and loss of (14)C-activity in soils under composting and non-composting conditions. Methods included determination of total (14)C-activity remaining, dichloromethane (DCM) and HPCD extractions. Mineralisation assays were also carried out to quantify the fraction of (14)C-phenyldodecane associated activity available for degradation in the soil at each time point. DCM and HPCD extractability were compared to contaminant mineralisation and to total loss of (14)C-phenyldodecane associated activity from the microcosms, after 153 d incubation. Poor relationships were found between (i) the amount of (14)C-activity mineralised and the fraction removed from the soils using DCM extraction and (ii) DCM extraction and total loss of [(14)C]phenyldodecane associated activity from the soil systems. Good relationships were observed between (i) the amount of (14)C-activity mineralised and the fraction removed from the soils using the HPCD extraction and (ii) HPCD extraction and total loss of [(14)C]phenyldodecane associated activity from the soil systems. The results of this study indicate that an aqueous HPCD extraction may be a useful tool in assessing the microbial availability of phenyldodecane in freshly and aged spiked soils.

Alkanes↗
PubMed2005

Development and application of a multi-target immunoaffinity column for the selective extraction of natural estrogens from pregnant women's urine samples by capillary electrophoresis.

In this paper, a methodology for the determination of three naturally occurring estrogens (estradiol, estrone and estriol) in pregnant women's urine has been described. The procedure included immunoaffinity column (IAC) extraction of 4 mL of urine sample and subsequent analysis of the extraction by micellar electrokinetic chromatography (MEKC). A multi-target polyclonal antibody that has high affinity to three estrogens was produced. Then the IAC was developed by coupling polyclonal antibody to CNBr-activated Sepharose 4B. The IAC showed high affinity for these estrogens. Recoveries of three estrogens from human serum matrix were greater than 92% with R.S.D. less than 4.5%. The final elute of urine sample was diluted with running buffer and then quantitated with MEKC. The experimental results demonstrated that IAC was a useful technique for extraction and concentration of estrogens from biological samples. Three estrogens levels in six pregnant women's urine were measured by both the present method and enzyme-linked immunoadsorbent assay (ELISA). The results of this method have been found to correlate well with those of ELISA.

Chromatography, Affinity↗
PubMed2002

New procedure for selective extraction of polycyclic aromatic hydrocarbons in plants for gas chromatographic-mass spectrometric analysis.

A new solid-phase extraction method for the clean-up and the quantitation by GC-MS of regulated polycyclic aromatic hydrocarbons (PAHs) from lettuce was developed and the experimental conditions were optimized. After ultrasonic extraction using toluene and saponification of samples, a clean-up of extracts through solid-phase extraction was performed. Samples were finally analyzed by gas chromatography-mass spectrometry (GC-MS) using an internal deuterated standard. Saponification by KOH in methanol-water (80:20) was successful allowing a good elimination of the interfering chlorophylls from the extracts containing the PAHs. The average recovery of the 16 regulated PAHs was 70, 74, 79 and 89%, respectively, for naphthalene, acenaphthylene, acenaphthene and chrysene and higher than 94% for the others.

Gas Chromatography-Mass Spectrometry↗
PubMed2003

Selective extraction of salbutamol from human plasma with the use of phenylboronic acid.

An investigation was conducted on the usage of a single-step extraction procedure involving the retention of a phenylboronate-salbutamol complex on an end-capped C18 solid-phase sorbent to determine the level of salbutamol in human plasma samples. Propranolol, a beta-blocker, was chosen as the internal standard for this assay. In this solid-phase clean-up method, 50 mM sodium carbonate buffer, pH 9.60, was used for conditioning the column as well as washing the endogenous interference. Under the optimal conditions, the recovery of salbutamol from spiked plasma samples was found to be high and reproducible with mean recoveries (n = 3) of more than 90% after elution by using 50% 1 M trifluoroacetic acid in methanol. This sample clean-up step was effectively analyzed under reversed-phase high-performance liquid chromatography with fluorimetric detection. The method was successfully applied to the routine measurement of salbutamol in human plasma from the bioequivalence study on the different administration route of salbutamol. Quantification of salbutamol was convincingly reported with the correlation of coefficient of 0.9980 for the concentration range from 0 to 1000 ng ml(-1). An adequate precision was achieved with both between- and within-day precisions of less than 10% (n = 6) for 100 and 1000 ng ml(-1) and less than 15% (n = 6) for 10 ng ml(-1).

Adrenergic beta-Agonists↗