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Sorbent tested

FIGURE 9.10 Result of PSS SEC sorbent tests selectivity vs molecular size determined by inverse SEC. [Pg.288]

IgE allergies can be detected in two different ways. The more modern is the radio aller go sorbent test (RAST). Here, a small sample of the patient s blood is collected and the serum is tested for the binding of IgE to food protein bound to a solid matrix using radiolabelled or enzyme-linked antihuman IgE. [Pg.51]

Polystyrene-divinylbenzene resins are the most efficient solid sorbents tested for the accumulation of mutagenic agents from water. This greater efficiency recommends their use in bioassay programs for the preliminary assessment of health risks associ-... [Pg.95]

Another use of the RIA is to measure the quantities of serum IgE antibodies specific for various allergens in a patient s serum, in which case it is called a Radio Allergo Sorbent Test (RAST) (Nalebuff 1985). In this case, the test is performed similar to an ELISA for Ab, using radiolabeled antiglobulins specific for IgE, rather enzyme-labeled antiglobulins. However, this test has been almost completely replaced by ELISA. [Pg.174]

Numerous examples of the ulitity and selectivity of these sorbents are. given below. Table 2.3 lists nine steroids that were tested for their retentiveness on five different sorbents [31]. The steroid standards at 1 mg/ml were dissolved in methanol-water for the evaluation of a C,8 sorbent. For all the other sorbents, the steroids were dissolved in methylene chloride. At the polarity extremes for these steroids, cholesterol (the least polar) is retained only on C18, whereas hydrocortisone (most polar) is retained on all five of the sorbents tested. [Pg.281]

Breakthrough Experiments. For the breakthrough experiments the sorbents were packed in 100-mg beds, 4 mm in diameter, and inserted into the six ports in the manifold. The effluent ends of the tubes were connected to a common line leading to the flame ionization detector. While the flame ionization detector, calibrated with the challenge atmosphere, monitored the concentration of vinyl acetate in the combined bed effluents, the pump in the detector drew the challenge atmosphere through each bed at approximately 0.2 L/min. The output from the detector, the breakthrough curve, was recorded with a strip-chart recorder. Most of the porous polymer sorbents tested were first washed with acetone and dried. [Pg.174]

Quantitative blood test For some allergens a skin-prick test is not sufficient. In these cases blood tests are used to determine the level of specific antibodies that target the allergen. The most commonly used technique is the Radio Allergo Sorbent Test (RAST) that measures the amount of immunoglobulin E (IgE) antibodies, which trigger histamine release and the body s immune response. [Pg.33]

Development of reliable in-vitro predictive tests, e.g. employing serum or lymphocytes, is a matter of considerable importance, not merely to remove hazard but to avoid depriving patients of a drug that may be useful. Detection of drug-specific circulating IgE antibodies by the radioallergo-sorbent test (RAST) is best developed for penicillins and succinyl choline. [Pg.145]

Renin-angiotensin-aldosterone system Radio-allergo-sorbent test Retinol-binding protein... [Pg.905]

FAST functional assessment staging (of Alzheimer s disease) fluoro-allegro sorbent test fetal acoustical stimulation test... [Pg.238]

Immunoassay is an application of the substoichiometric principle ( 9.3.4) developed by Yalow (Nobel laureate in 1977) for protein analysis. In the United States tens of millions radioimmunoassays are made annually in hospitals to measure hormones, enzymes, viruses, serum proteins, drugs, and so forth. Only a drop of the patient s blood is needed, reflecting the versatility and smisitivity of this technique, which can be performed automatically. Commercial RAST-kits (Radio Allergy Sorbent Tests) are used for rapid diagnosis of allergic reactions. [Pg.268]

For the removal of hpids, various silica-based (C8 and C18) and polymeric (PS-DVB) sorbents were tested. Recently Lehotay et al. [10] also showed the effectiveness of C18 for the removal of hpids from QuEChERS extracts. Although PS-DVB type sorbents are regarded as more hpophihc than C18 (ODS) sorbents, the PS-DVB sorbents tested were found to be less efficient in removing fatty hpids than ODS-type sorbents, with the exception of a PS-DVB with 1500 m surface from Interchim , which showed a similar effect to ODS. The better efficiency of ODS in this respect is obviously related to the fact that triglycerides are structurally very closely related to ODS, both containing fatty acid chains. Nevertheless,... [Pg.452]

Eor the selective pre-concentration of deactivated phenols a new silica-based material with the grafted 2,3,5-triphenyltetrazole was proposed. This method is based on the formation of molecular chai ge-transfer comlexes of 2,3,5-triphenyltetrazole (7t-acceptor) with picric acid (7t-donor) in the phase of the sorbent. Proposed SPE is suitable for HPEC analysis of nitrophenols after their desorption by acetonitrile. Test-system for visual monitoring of polynitrophenols under their maximum concentration limits was developed using the proposed adsorbent. [Pg.254]

BBT solution on unmodified sorbents of different nature was studied. Silica gel Merck 60 (SG) was chosen for further investigations. BBT immobilization on SG was realized by adsoi ption from chloroform-hexane solution (1 10) in batch mode. The isotherm of BBT adsoi ption can be referred to H3-type. Interaction of Co(II), Cu(II), Cd(II), Ni(II), Zn(II) ions with immobilized BBT has been studied in batch mode as a function of pH of solution, time of phase contact and concentration of metals in solution. In the presence of sodium citrate absorbance (at X = 620 nm) of immobilized BBT grows with the increase of Cd(II) concentration in solution. No interference was observed from Zn(II), Pb(II), Cu(II), Ni(II), Co(II) and macrocomponents of natural waters. This was assumed as a basis of soi ption-spectroscopic and visual test determination of Cd(II). Heavy metals eluted from BBT-SG easily and quantitatively with a small volume of HNO -ethanol mixture. This became a basis of soi ption-atomic-absoi ption determination of the total concentration of heavy metals in natural objects. [Pg.292]

One question of chief interest concerns the number of runs that can be run with one individual SEC column. The lifetime of the sorbent itself must be tested as well as the maximum run number for the packed column. Because column packing procedures for SEC columns are rather time-consuming and all SEC columns have to be checked very carefully with respect to performance, very frequent repacking of the column is unreasonable. Therefore, CIP protocols are generally necessary. The CIP protocol should be developed as part of the process validation program. [Pg.237]

All packing materials produced at PSS are tested for all relevant properties. This includes physical tests (e.g., pressure stability, temperature stability, permeability, particle size distribution, porosity) as well as chromatographic tests using packed columns (plate count, resolution, peak symmetry, calibration curves). PSS uses inverse SEC methodology (26,27) to determine chromatographic-active sorbent properties such as surface area, pore volume, average pore size, and pore size distribution. Table 9.10 shows details on inverse SEC tests on PSS SDV sorbent as an example. Pig. 9.10 shows the dependence... [Pg.288]

Some authors have suggested the use of fluorene polymers for this kind of chromatography. Fluorinated polymers have attracted attention due to their unique adsorption properties. Polytetrafluoroethylene (PTFE) is antiadhesive, thus adsorption of hydrophobic as well as hydrophilic molecules is low. Such adsorbents possess extremely low adsorption activity and nonspecific sorption towards many compounds [109 111]. Fluorene polymers as sorbents were first suggested by Hjerten [112] in 1978 and were tested by desalting and concentration of tRN A [113]. Recently Williams et al. [114] presented a new fluorocarbon sorbent (Poly F Column, Du Pont, USA) for reversed-phase HPLC of peptides and proteins. The sorbent has 20 pm in diameter particles (pore size 30 nm, specific surface area 5 m2/g) and withstands pressure of eluent up to 135 bar. There is no limitation of pH range, however, low specific area and capacity (1.1 mg tRNA/g) and relatively low limits of working pressure do not allow the use of this sorbent for preparative chromatography. [Pg.167]

Universal anti-Rh sera deprived of anti-A or B-antibodies were prepared by contacting A and B-immunoadsorbents with human blood sera. To achieve zero titer in the Coombs agglutination test a portion of immunoadsorbent (80-160 mg) proportional to the initial serum titer (1 8-1 64, 1 ml) is required. The incorporation of A-immunoadsorbent into anti-B sera did not interfere with their titer and vice versa, Under the same circumstances an anti-Rh serum titer is lowered by one step or remains unchanged [125], Properties of this composite sorbent are therefore promising for its use in extracorporal hemisorption processes. [Pg.171]

Various physical, chemical, and biological methods have been used for the treatment of dye-containing wastewater. However, these conventional technologies have disadvantages like poor removal efficiency and high running cost. Therefore, low-cost sorbents which can bind dye molecules and be easily regenerated have been extensively searched and tested [3-7]. [Pg.161]

The remaining weight of dry sorbents with time is shown in Fig. 2. For every dry sorbent, attrition mainly still occurs in the early stage of fluidization and A1 test on the basis of the weight after 5 hours shows that Als of molecular sieve 5A and molecular sieve 13X presented 2.1 4.0 times higher than those of activated carbon and activated alumina. Therefore, the use of molecular sieve 5A and 13X in a fluidized bed can cause high maintenance cost and problems in the operating the process. [Pg.550]

Many types of matrices have been used in the past to measure the field stability of the test substance. Cotton gloves, cellulose patches, face wipe handkerchiefs and/or gauze face wipe matrices, long underwear (inner dosimeters), pants, shirts, coveralls (outer dosimeters), sorbent tubes, urine, and other matrices are common matrices that have been used for this purpose. [Pg.1007]


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See also in sourсe #XX -- [ Pg.354 , Pg.356 ]




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