High-performance liquid selectivity

For selective estimation of phenols pollution of environment such chromatographic methods as gas chromatography with flame-ionization detector (ISO method 8165) and high performance liquid chromatography with UV-detector (EPA method 625) is recommended. For determination of phenol, cresols, chlorophenols in environmental samples application of HPLC with amperometric detector is perspective. Phenols and chlorophenols can be easy oxidized and determined with high sensitivity on carbon-glass electrode. 

Selectivity of chromatographic separation is known to be varied by changing both the nonstationary phase composition and adsorbent nature. It is shown that the less are the values of the reached selectivity coefficient the higher are the requirements to column effectiveness. In this connection the choice of stationai y phase with high and predicted selectivity coefficient for the compounds being separated is still remains a topical problem of high-performance liquid chromatography. 

The value of for calcium hydroxyapatite can be defined by charge of Ca + and PO ions. From this point of view calcium hydroxyapatite can be used as high-selective adsorbents for high performance liquid chromatography because with increasing of will be rise a selectivity coefficient a. 

High performance liquid chromatography (HPLC) is an excellent technique for sample preseparation prior to GC injection since the separation efficiency is high, analysis time is short, and method development is easy. An LC-GC system could be fully automated and the selectivity characteristics of both the mobile and stationary... 

Demeter J, Heyndrickx A. 1979. Selection of a high-performance liquid chromatographic cleanup procedure for the determination of organochlorine pesticides in fatty biological extracts. Vet Hum Toxicol 21 151-155. 

DALLUGE J J, NELSON B c, THOMAS J B and SANDER L 0 (1998) Selection of column and gradient elution system for the separation of catechins in green tea using high-performance liquid chromatography , J Chromatogr A, 793, 265-74. 

MAiANi G, SERAFiNi M, SALUCCi M, AZZiNi E and FERRO-Luzzi A (1997) Application of a new high-performance liquid chromatographic method for measuring selected polyphenols in hiunan plasma , J of Chromatog B, 692, 311-17. 

Tian, Q. et al., Screening for anthocyanins using high-performance liquid chromatography coupled to electrospray ionization tandem mass spectrometry with precursor-ion analysis, product-ion analysis, common-neutral-loss analysis, and selected reaction monitoring, J. Chromatogr. A, 1091, 72, 2005. 

B. Waiczak, L. Morin-Allory, M. Chrdtien, M. Lafosse and M. Dreux, Factor analysis and experiment design in high-performance liquid chromatography. III. Influence of mobile phase modifications on the selectivity of chalcones on a diol stationary phase. Chemom. Intell. Lab. Syst., I (1986) 79-90. 

High-performance liquid chromatography (HPLC) with a micellar mobile phase or with a selective pre-column or reaction detection system has also been used to determine alkylenebis(dithiocarbamaes). ° Zineb and mancozeb residues in feed were determined by ion-pair HPLC with ultraviolet (UV) detection at 272 nm. These compounds were converted to water-soluble sodium salts with ethylenediaminetetra-acetic acid (EDTA) and sodium hydroxide. The extracts were ion-pair methylated with tetrabuthylammonium hydrogensulfate (ion-pair reagent) in a chloroform-hexane solvent mixture at pH 6.5-8.S. The use of an electrochemical detector has also been reported. ... 

Brinkman, U. A. Th., de Jong, G. J., and Gooijer, C., Use of luminescence techniques for sensitive and selective determinations in HPLC (high-performance liquid chromatography), Pure Appl. Chem., 59, 625, 1987. 

Jandera, P., Correlation of retention and selectivity of separation in reversed-phase high-performance liquid chromatography with interaction indices and with lipophilic and polar structural indices, J. Chromatogr. A, 656, 437, 1993. 

Snyder L. R., Changing reversed-phase high performance liquid chromatography selectivity which variables should be tried first , ]. Chromatogr. B, 689(1), 105, 1997. 

Nagels, L.J., Creten, W.L. (1985). Evaluation of the glassy carbon electrochemical detector selectivity in high-performance liquid chromatographic analysis of plant material. Anal. Chem. 57, 2706. 

Chloupek, R.C., Hancock, W.S., Marchylo, B.A., Kirkland, J.J., Boyes, B.E., Snyder, L.R. (1994). Temperature as a variable in reversed-phase high-performance liquid chromatographic separations of peptide and protein samples, n. Selectivity effects observed in the separation of several peptide and protein mixtures. J. Chromatogr. A 686, 45-59. 

High performance liquid chromatography-mass spectrometric methods Nitin et al. [75] developed and validated a sensitive and selective liquid chromatography-tandem mass spectrometric method (LC MS MS) for the simultaneous estimation of bulaquine and its metabolites primaquine in monkey plasma. The mobile phase consisted of acetonitrile ammonium acetate buffer (20 mM, pH 6) (50 50, v/v) at a flow rate of 1 mL/min. The chromatographic separations were achieved on two Spheri cyano columns (5 pm, 30 cm x 4.6 mm), connected in... 

Rao et al. [87] developed a high performance liquid chromatographic method for the determination of primaquine phosphate in pharmaceutical dosage form. A /(-Bondapak NH2 column with chloroform-methanol (60 40) as eluent was selected with sulfalene as internal standard. The method was convenient with recovery of approximately 100% for primaquine. 

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