Lipase (LPS) is a pancreatic enzyme necessary for the absorption and digestion of
nutrients that catalyzes the hydrolysis of glycerol esters of fatty acids. Determination of
LPS is used for diagnosis of diseases of pancreas such as acute and chronic
pancreatitis and obstruction of the pancreatic duct1,7,8. Clinical diagnosis should not be
made on a single test result; it should integrate clinical and other laboratory data.
PREPARATION
The reagents are ready to use.
STORAGE AND STABILITY
All the components of the kit are stable until the expiration date on the label when stored
tightly closed at 2-8ºC, protected from light and contaminations prevented during their
use. Do not use reagents over the expiration date.
Signs of reagent deterioration:
- Presence of particles and turbidimetry (note 1)
- Blank absorbance (A) at 570 nm 1,00.
- R2 is a turbid orange-colored micro-emulsion, discard if turning to red.
ADDITIONAL EQUIPMENT
- SPINLAB 180 Autoanalyzer.
- General laboratory equipment (note 2)
SAMPLES
Fresh serum samples are recommended.
Spinreact does not recommend the use of EDTA and citrate plasma samples. These
sample types could only be used if different reference ranges are established by each
laboratory using different sample types other than fresh serum.
Avoid repeated freezing and thawing. Stability: 14 days at 2-8ºC and at -20ºC.
QUALITY CONTROL
Control sera are recommended to monitor the performance of assay procedures:
SPINTROL H Normal and Pathologic (Ref. 1002120 and 1002210).
If control values are found outside the defined range, check the instrument, reagents
and technique for problems.
Each laboratory should establish its own Quality Control scheme and corrective actions
if controls do not meet the acceptable tolerances.
REFERENCE VALUES
the normal range for pancreatic lipase when measured by the DGGR method is 13-60
U/L8
These values are for orientation purpose; each laboratory should establish its own
reference range.
INTERFERENCES
Bilirubin up to 75 mg/dL, hemoglobin up to 110 mg/dL and ascorbic acid up to 120 mg/dL
do not interfere at the tested Lipase concentrations (40 U/L). 600 mg/dL Intralipid (1300
mg/dL triglycerides) do not interfere.
A list of drugs and other interfering substances with lipase determination has been
reported2, 3
.
NOTES
1. In some storage conditions (i.e. storage at a temperature lower that the one
indicate) a precipitate may appear in the vial, it is not recommended to resuspend
the precipitate as it could alter the functionality.
2. In order to avoid contamination, it is recommended to use disposable material.
BIBLIOGRAPHY
1. McNeely M. Lipase. Kaplan A et al. Clin Chem The C.V. Mosby Co. St Louis. Toronto.
Princeton 1984; 1130-1134, 892.
2. Neumann U et al. Comptes Rend. 4 colloque de Pont-a-Musson, Masson 627-634 (1979)
3. Junge W et al. J.Clin.Chem.Clin.Biochem., 21 445-451 (1983).
4. Neumann U et al. Methods of Enzymatics Analysis, 3rd ed. Vol.4, 26-34 (1984)
5. Young DS. Effects of drugs on Clinical Lab. Tests, 4th ed AACC Press, 1995.
6. Young DS. Effects of disease on Clinical Lab. Tests, 4th ed AACC 2001.
7. Burtis A et al. Tietz Textbook of Clinical Chemistry, 3rd ed AACC 1999.
8. A. H. B. Wu, Tietz clinical guide to Laboratory Tests, Fourth Edi. Saunders Elsevier, 2006.
