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Uric Acid

The document provides detailed information on uric acid testing, including product catalog numbers, package sizes, reference values for different age groups and genders, and the enzymatic method used for measurement. It also outlines the reagent composition, precautions, sample requirements, and stability of the reagents. Additionally, performance data such as analytical range, detection limits, precision, and correlation with other methods are included.
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0% found this document useful (0 votes)
65 views2 pages

Uric Acid

The document provides detailed information on uric acid testing, including product catalog numbers, package sizes, reference values for different age groups and genders, and the enzymatic method used for measurement. It also outlines the reagent composition, precautions, sample requirements, and stability of the reagents. Additionally, performance data such as analytical range, detection limits, precision, and correlation with other methods are included.
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© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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URIC ACID

Mono liquid

Cat.No Package Sizes REFERENCE VALUES


Serum/Plasma
UA450S45 4 x 50 mL + Standard (3 mL)
Female Male
UA4100S83 4 x 100 mL + Standard (3 mL) mg/dl (µmol/l) mg/dl (µmol/l)
UA2125S144 2 x 125 mL + Standard (3 mL) Adults 2,3–6,1 (137–363) 3,6-8,2 (214-488)
UA200H145 Hit I 4 x 50 mL Children
0 – 5 Days 1,9-7,9 (113-470) 1,9-7,9 (113-470)
UA400H245 Hit II 4 x 100 mL
1 – 4 Years 1,7-5,1 (101-303) 2,2-5,7 (131-340)
5 – 11 Years 3,0-6,4 (178-381) 3,0-6,4 (178-381)
METHOD 12 – 14 Years 3,2-6,1 (190-363) 3,2-7,4 (190-440)
15 – 17 Years 3,2-6,4 (190-381) 4,5-8,1 (268-482)
Enzymatic – colorimetric. Trinder, End Point.
Urine
Uricase -PAP
≤ 800 mg/d (4,76 mmol/d) with normal food
≤ 600 mg/d (3.57 mmol/d) with reduced purine food
PRINCIPLE Note: It is recommended for each laboratory to establish and
Enzymatic determination of uric acid according to maintain its own reference values. The given data here are only
the following reactions: an indication.

UricAcid + H2O + O2 Uricase> Allantoin + CO2 + H2O2 PROCEDURE


This reagent can be used manually (see method
TBHBA+ 4-Aminoantipyrin + 2 H2O2 POD> Chinonimine+ 3H2O
below) and on most analyzers. The applications are
(TBHBA= 2,4,6-Tribrom3-hydroxybenzoic acid) available on request.
Wavelength : 550 nm
REAGENT COMPOSITION Temperature : 37°C
R1: Phosphatebuffer pH 7,0 100 mmol/l Cuvette : 1 cm light path
TBHBA 1 mmol/l
4-Aminoantipyrine 0,3 mmol/l
K4[Fe(CN)6] 10 µmol/l Read against reagent blank (RBL)
Peroxidase (POD) ≥ 2 kU/l .
Uricase ≥ 30 U/l • Monoreagent procedure
Standard: 6 mg/dl (357 µmol/l)
Monoreagent 1 mL
PRECAUTIONS Sample 20 µL
- For in vitro diagnostic use only. Mix and after a 5 minutes incubation, measure the
- The reagent contains less than 0,95g/L sodium change of absorbance (A) within 60 minutes against
azide. Avoid contact with skin and/or mucous reagent blank
membranes !
- Use clean or single use glass material only to
avoid contaminations. CALCULATION
A Sample mg/L C = 60
STABILITY OF REAGENT xC mg/dL C = 6
A Standard µmol/L C = 357
When stored at 2-8° C and protected from light,
the unopened reagent and standard are stable until C = standard concentration.
the expiry date printed on the labels .
Take the dilution factor into account for the calculation of
Reagent and standard are ready for use. uric acid concentration in urine!
Stability after opening the bottles :
3months at 2 – 8 °C
4 weeks at 18 – 25 °C
(contamination has to be avoided !)

SAMPLE
Serum free of hemolysis , plasma (EDTA/heparine)
Urine diluted 1/10 in distilled water.

L-S 04/2009 page 1/2


CALIBRATORS & CONTROLS BIBLIOGRAPHY
For calibration Inmesco Multicalibrator Introcal may
st
be used alternatively , for quality control use 1. Thomas L. Clinical Laboratory Diagnostics. 1
Inmesco normal and abnormal control, ed. Frankfurt: TH-Books Verlagsgesellschaft;
Intronorm I and Intronorm II . 1998. p. 208-14.
2. Newman DJ, Price CP. Renal function and
nitrogen metabolites. In: Burtis CA, Ashwood
PERFORMANCE DATA ER, editors. Tietz Textbook of Clinical
rd
- Analytical range Chemistry. 3 ed. Philadelphia: W.B Saunders
The reagent is linear from 0,07 – 20 mg/dl (4,2 - Company; 1999. p. 1204-70.
1190 µmol/l)
- Detection limit
The detection limit is equal to 0,07 mg/dl (4,2 µmol/l)
-
Precision SYMBOLS USED
Within-run reproducibility
n = 20
Mean SD CV Unit For in vitro diagnostic medical use
Control 1 4,37 0,021 0,49 mg/dl
Control 2 10,74 0,032 0,30 mg/dl
Patient 5,46 0,044 0,81 mg/dl Batch Code

Between-run reproducibility
n = 20 Use by
Mean SD CV Unit
Control 1 4,42 0,037 0,84 mg/dl
Temperature limitation
Control 2 10,82 0,058 0,54 mg/dl
Patient 5,41 0,051 0,99 mg/dl

- Correlation
A comparative study has been performed between
the Inmesco method and another commercial
reagent on 70 human serum samples.
The parameters of linear regression are as follows:

y = 0,948 x + 0,44 mg/dl r= 0,995

INTERFERENCES

Interferences are found according to literature

L-S 04/2009 page 2/2

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