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Phosphorus LS Mono-Test: Molybdate U.V. Method

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Phosphorus LS Mono-test

Molybdate U.V. Method


50 x 1 mL
Store at 2-8C

Quantitative determination of Phosphors by means of Molybdate U. V. Test.


Phosphorus in mg/dL = (Abs. T) - (Abs. B) x 5 (Standard)
Only for in vitro use in clinical laboratory (IVD). (Abs. S) - (Abs. B)
Application sheets for automated systems are available on request.
Intended Use: Phosphorus(Inorganic) test reagent/kits is a medical device
intended for the estimation of Phosphorus(Inorganic) in serum, plasma or
Calibrators and Controls
urine.
It is recommended that appropriate quality control sera and/or controls be run with
Clinical Significance each assay batch to monitor procedural parameters.
Phosphorus is an essential mineral for tissue bone formation and is required by every
cell in the body for normal function. Approximately 85% of the body phosphorus is
found in bone and in teeth. Low levels of phosphorus can be caused by hyper Reference Range
vitaminosis D, primary hyper parathyroidism, renal tubular disorders, antacids or
Serum or plasma
malabsorption. High levels of phosphorus can be caused by diet, bone metastases,
Children 4.0 – 6.50 mg/dL
liver disease, alcohol ingestion, diarrhea and vomiting.
Adults 2.5 – 5.0 mg/dL
Urine
Principle Adults 0.3 – 1.0 gm /24 hours
When Inorganic phosphorus reacts with ammonium molybdic, in an acidic medium, it
form Phosphomolybdate complex, which is measured in the U.V. range i.e. 340nm. These values are for orientation purpose; each laboratory should
The absorbance of this complex is directly proportional to the amount of inorganic establish its own reference range.
phosphorus present in the sample.
Performance Characteristics
Linearity: Up to 20 mg/dL
Reagents
Reagent 1: Molybdate Reagent : 50 x 1 mL When values exceed this range the samples should be diluted
Reagent 2: Phosphorus Standard (05mg/dL) :1 x 2 mL appropriately with Distilled water and the result multiplied by the dilution
Prewashed yellow Micropipette tips : 50 nos. factor.

Storage Instructions and Reagent Stability


The reagent is stable up to the end of the indicated month of expiry, if stored at 2–8 Mode End point
°C, protected from light and contamination is avoided. Do not freeze the reagents Wavelength (nm) 340 nm

Reagent Preparation & Stability Sample Volume (l) 10 µL


Reagent 1 is ready for use. Working Reagent Volume(l) 1000 µL

Specimen and Stability Lag time (Sec.) 5 sec


Serum or plasma: Free of hemolysis, should be removed from the clot as quickly as Standard(mg/dl) 5 mg/dl
possible to avoid elevation of serum phosphorus from hydrolysis or leakage of
phosphate present in erythrocytes. Incubation Time (sec) 5 minutes
Urine: acidify the urine with few drops of concentrated HCl and dilute the sample 1/10 Reaction Temperature ( C) R.T.
with distilled water. Mix. Multiply the result by 10 (dilution factor).
Reaction Direction Increasing
Stability in serum /plasma : 7 days at 2 – 8 °C Linearity (mg/dl) 20 mg/dl
Urine : 10 days at 2 – 8 °C
Additional Equipment Blank with Reagent
- Spectrophotometer or colorimeter measuring at 340 nm. Units mg/dl
- Matched Cuvette 1.0 cm light path.
- General laboratory equipment

Assay Procedure Literature


1. Assay conditions: 1. Goodwin. J.F. (1970) Clin Chem16919) : 776
Wavelength: . . . . . . . . . . . . . . . . . . . . . . . ... 340 nm
Cuvette: . . . . . .. . . . . . . . . . . . . . .. . .. 1 cm. light path
Temperature . . . . . . . . . . . . . . . . . . . .. 37 / 30 / 25ºC For in vitro Diagnostic use only.
2. Adjust the instrument to zero with distilled water
3. Pipette into a Cuvette
Dispense Blank Standard Samples
Reagent 1000 µL 1000 µL 1000 µL
Distilled Water 10 µL -
Sample - - 10 µL
Standard - 10 µL -
4. Mix, incubate for 5 min. at Room Temperature.
5. Read absorbance against Reagent blank.

Calculation

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