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Biomedical trace analysis

For biomedical trace analysis, three types of detectors are currently popular—the absorption photometric detector, the fluorescence detector, and the electrochemical detector. Although there are other kinds of detectors, only these have the ability to detect 10 -10 g of analyte, the kind of detectability needed in biomedical analysis, especially where small amounts of drugs are concerned. [Pg.199]

Delaunay Bertoncini, N., and Hennion, M. C. (2004) Immunoaffinity solid phase extraction for pharmaceutical and biomedical trace analysis coupling with HPLC and CE perspectives. Journal of Pharmaceutical and Biomedical Analysis, 34, 717 736. [Pg.378]

Dunges, W. The HPLC and TLC determination of acidic compounds after their fluorescence labeling with 4-bromomethyl-7-methoxycoumarin a new tool for biomedical trace analysis. W Spectrom. Group Bull. 1977,5, 38 5. [Pg.97]

Leis HJ, Fauler G, Rechberger GN, Windischhofer W. 2004. Electron-capture mass spectrometry a powerful tool in biomedical trace level analysis. Curr Med Chem 11 1585. [Pg.172]

A convenient method is the spectrometric determination of Li in aqueous solution by atomic absorption spectrometry (AAS), using an acetylene flame—the most common technique for this analyte. The instrument has an emission lamp containing Li, and one of the spectral lines of the emission spectrum is chosen, according to the concentration of the sample, as shown in Table 2. The solution is fed by a nebuhzer into the flame and the absorption caused by the Li atoms in the sample is recorded and converted to a concentration aided by a calibration standard. Possible interference can be expected from alkali metal atoms, for example, airborne trace impurities, that ionize in the flame. These effects are canceled by adding 2000 mg of K per hter of sample matrix. The method covers a wide range of concentrations, from trace analysis at about 20 xg L to brines at about 32 g L as summarized in Table 2. Organic samples have to be mineralized and the inorganic residue dissolved in water. The AAS method for determination of Li in biomedical applications has been reviewed . [Pg.324]

The hydrolysis products (23-25) of the three nitrogen mustards listed in Schedule 1 of the CWC were included in the general LC/APCI/MS screening procedures of Black and Read, 14 26 . These procedures, and those of other laboratories, have successfully identified Af-methyldiethanolamine (23) and N-clhyldiclhanolaminc (24) in OPCW proficiency tests. More specific methods based on LC/ESI/MS have been reported for the trace analysis of ethanolamines in environmental residues (66) and biomedical samples (67). [Pg.308]

More than a dozen mass spectrometric methods have been reported for the trace analysis of alkyl MPAs in environmental and biomedical samples. [Pg.419]

SFE is an efficient and fast extraction technique that fits well with green chemistry strategies. The broadest applications of SFE can be found in food, environmental, and pharmaceutical analysis, in industrial and biomedical laboratories, and in speciation analysis [86, 88, 93-97]. Table 6.13 presents selected examples of the use of SFE in trace analysis. [Pg.146]

In the modem world, trace analysis plays an important role in such areas as ecology, chemical engineering, food processing, biomedical analysis, and dmg chemistry. Advanced, sensitive, and precise analytical methods allow identification and quantification of different compounds, both organic and inorganic, including macro-molecular complexes. All these methods present very good detection and quantification levels, up to parts per trillion (ppt) or parts per quadrillion (ppq). [Pg.197]

The big advantage of splitless injection is the improved sensitivity over split. Typically 20- to 50-fold more sample enters the column and the result is improved trace analysis for environmental, pharmaceutical, or biomedical samples. [Pg.56]

Naturally the likelihood of any such project being undertaken is essentially zero in real life chemists are faced with one or several of literally hundreds of thousands of possible compounds present in a wide range of matrices in Chapter 11a handful of examples out of literally tens of thousands of possibilities are discussed. There is no useful purpose to a physics-style effort to measure a trace level amount of substance to the utmost precision and accuracy that analytical technologies could conceivably provide. In fact, the spectacular success of chemical metrology applied to trace analysis is not the 1 in 10 precision that is routinely achieved, but the analyte levels of one in 10 —10 for which such levels of precision (and accuracy) can be achieved on a high throughput basis for a wide range of, e.g., biomedical and environmental samples, despite their inherent complexity. [Pg.13]

The determination of molecular formulas via accurate mass measurements relies on isotopic masses accurate to at least 1 in 10 [10]. Elemental trace analysis is required for the detection of radioactive nuclides in the environment, of transition metals such as Pt in exhaust fumes from automobiles [11], and in the quality control of low-sulfur fuels for the same. All electronic devices demand for high-purity semiconductors and the properties of alloys are critically influenced by trace elements [12]. Age determinations from isotope ratios are applied in archeology, paleontology, and geology [4,13,14]. More recently, elemental MS and biomedical MS are jointly employed to unveil the presence and preferably location of metals in proteins or DNA as well as their lateral distribution in tissues [15-18], a field of research basically going back to seminal work by Houk in 1980... [Pg.685]

Pietra, R., Fortaner, S., and Sabbioni, E. (1993). Use of Chelex 100 resin in preconcentration and radiochemical separation neutron activation analysis applied to environmental toxicology and biomedical research. /. Trace Microprobe Tech. 11, 235-250. [Pg.132]

With the introduction of modern electronics, inexpensive computers, and new materials there is a resurgence of voltammetric techniques in various branches of science as evident in hundreds of new publications. Now, voltammetry can be performed with a nano-electrode for the detection of single molecular events [1], similar electrodes can be used to monitor the activity of neurotransmitter in a single living cell in subnanoliter volume electrochemical cell [2], measurement of fast electron transfer kinetics, trace metal analysis, etc. Voltammetric sensors are now commonplace in gas sensors (home CO sensor), biomedical sensors (blood glucose meter), and detectors for liquid chromatography. Voltammetric sensors appear to be an ideal candidate for miniaturization and mass production. This is evident in the development of lab-on-chip... [Pg.662]

Iyengar G. 1989. Elemental analysis of biological systems. Vol. 1 Biomedical, environmental, compositional, and methodological aspects of trace elements. Boca Raton, FL CRC Press, 173-174. [Pg.237]

Aitio, A., Jarvisalo, J., Stoeppler, M. Sampling and sample storage, in Trace Metal Analysis in Biological Specimens (ed.) Stoeppler, M., Foster City, California, Biomedical Publications, in preparation... [Pg.170]

Speciation analysis comes into its own mainly in environmental, nutritional, and biomedical research. The sample matrices are generally highly complex and the requirements for reliable (trace) element determinations are stringent (even for total amounts). The most important challenges in this context involve... [Pg.438]

Schramel P. 1988. ICP and DCP emission spectrometry for trace element analysis in biomedical and environmental samples A review. Spectrochim Acta 43 881-896. [Pg.124]


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