scholarly journals  Simple, selective, and sensitive measurement of urea in body fluids of mammals by reversed-phase ultra-fast liquid chromatography

2012 ◽  
Vol 57 (No. 1) ◽  
pp. 19-27 ◽  
Author(s):  
M. Czauderna ◽  
J. Kowalczyk

Ultra-fast liquid chromatography with a photodiode array detector for simple and rapid determination of urea in body fluids of farm animals is described. Blood plasma, milk, and urine samples are treated with trichloroacetic acid and then centrifuged. Supernatants are derivatized at room temperature using p-dimethylaminobenzaldehyde. Samples are separated using a ternary gradient of methanol in buffer and water. Derivatized urea in standards and biological samples is analyzed using a Phenomenex C<sub>18</sub>-column (Synergi 2.5 &micro;m, Hydro-RP, 100&Aring;, 100 &times; 2 mm). The photodiode detector is set to 370 and/or 254 nm for detection. Temperature is maintained at 27&deg;C by a column heater. Clear separation of derivatized urea from the endogenous species present in assayed biological samples was achieved in less than 6 min. The urea adduct peak eluted at 4.36 &plusmn; 0.05 min. Average recoveries of the urea standards added to assayed biological materials were satisfactory (i.e. 100.2 &plusmn; 4.1%). Our chromatographic method with photodiode detection at 370 nm and at 254 nm, in particular, offers low detection (L<sub>D</sub>) and quantification limits (L<sub>Q</sub>) (<sup>370nm</sup>L<sub>D</sub> = 0.47&nbsp;ng, <sup>254nm</sup>L<sub>D</sub> = 0.027 ng and <sup>370nm</sup>L<sub>Q</sub> = 1.41 ng, <sup>254nm</sup>L<sub>Q</sub> = 0.080 ng, respectively). Our liquid chromato-graphy based on detection at 370 nm is the most versatile analytical tool that assures sensitive, accurate, and precise analysis of urea in urine, milk, and plasma samples, and selected diets for mammals. The presented chromatographic procedure is especially suitable for preparation of reference sample sets, very accurate and precise research purposes or rapid clinical diagnostic with smaller sample sets. Urea in urine can be also determined using our liquid chromatography with detection at 254 nm. Detection of urine urea at 254 nm is more sensitive and precise compared with monitoring at 370 nm. Our chromatographic method based on photodiode detection at 370 nm and especially at 254 nm is suitable for the non-invasive analysis of urea in only urine of humans and animals. &nbsp; &nbsp;

2002 ◽  
Vol 776 (2) ◽  
pp. 251-254 ◽  
Author(s):  
Anna Pastore ◽  
Anna Lo Russo ◽  
Fiorella Piemonte ◽  
Liliana Mannucci ◽  
Giorgio Federici

1993 ◽  
Vol 218 (2) ◽  
pp. 159-168 ◽  
Author(s):  
Tom Teerlink ◽  
Marcel W.T. Hennekes ◽  
Paul A.M. van Leeuwen ◽  
Alexander Houdijk

1993 ◽  
Vol 76 (1) ◽  
pp. 92-94 ◽  
Author(s):  
Paolo Cabras ◽  
Marinella Melis ◽  
Lorenzo Spanedda

Abstract A liquid chromatographic method is described for the determination of cymiazole residues in honey. This acaricide is determined on a reversed-phase (C18) column, with a CH3CN-O.OOIN HCI-NaCI mixture (950 mL + 50 mL + 0.3 g/L) as the mobile phase, and UV detection at 265 nm. Cymiazole is extracted with n-hexane from aqueous alkalinized (pH 9) honey solutions. No further cleanup of the honey extract was required before chromatographic analysis. Recoveries on control samples fortified with 0.01,0.10, and 1.00 ppm cymiazole ranged from 92 to 102%. The limit of determination was 0.01 ppm.


Author(s):  
Kanan G Gamit ◽  
Niraj Y Vyas ◽  
Nishit D Patel ◽  
Manan A Raval

Objective: A study was aimed to estimate guggulsterone-Z (GZ) in Gokshuradi Guggulu (GG).Methods: An analytical method was developed and validated using Waters Alliance high-performance liquid chromatography system (Empower software), equipped with photodiode array detector. Separation was achieved using Phenomenex, C-18 (250 mm×4.6 mm, 5 μ) column. Mobile phase consisted of acetonitrile:water (70:30,v/v). Flow rate was set to 1 ml/min and detection was performed at 251 nm.Results and Discussion: Validation parameters such as linearity, precision, accuracy, limit of detection, limit of quantification, and robustness were performed. Amount of GZ was estimated using linearity equation.Conclusion: GG was found to contain 0.815±0.03 g% w/w GZ. Validated method may be used as one of the parameters to standardize the formulation.


1999 ◽  
Vol 82 (4) ◽  
pp. 809-813 ◽  
Author(s):  
Mamun M Or-Rashid ◽  
Ryoji Onodera ◽  
Shaila Wadud ◽  
Mohamed-Emad A Nasser ◽  
Mohammad R Amin

Abstract A simple, rapid, and sensitive method was developed for detection and quantitation of lysine (Lys) in various biological samples by isocratic liquid chromatography (LC). Samples containing Lys and other amino acids were derivatized with 9-fluorenylmethyl chloroformate (FMOC-CI). The mobile phase used for isocratic elution was 50 mmol/L sodium acetate buffer (pH 4.20)-acetonitrile (43 + 57, v/v). Lys was detected with a UV detector at 265 nm. The derivatized Lys eluted from a LiChrospher 100 RP-18 (150× 4.0 mm id) column at a retention time of 5.6 min. The limit of detection was 0.73 μmol/L (signal-to-noise [S/N] ratio, 3:1), and the limit of quantitation was 2.37 μmol/L (S/N ratio, 10:1). Lys recoveries from fortified biological samples were &gt;97.5%. Average Lys contents found in rumen fluid samples collected before the morning feeding and at 2.0,4.0, and 6.0 h after feeding were 4.26,3.34,3.58, and 3.82 μmol/L, respectively. The hydrolysate of a sample of mixed rumen microorganisms collected before the morning feeding was determined to contain 1.372 μmol/mg microbial nitrogen in the form of Lys. The Lys concentrations of human plasma, goat plasma, human urine, and goat urine were 140.0, 102.0,58.0, and 32.0 μmol/L, respectively.


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