J Clin Pathol Qual Control.  1998 Dec;20(2):417-422.

Evaluation of ACS : 180SE Automated Chemiluminescence Immunoassay System

Affiliations
  • 1Department of Clinical Pathology, Yonsei University Wonju College of Medicine, Korea.
  • 2Department of Clinical Pathology, Wonjum and College of Medicine, Hallym University, Choonchun, Korea.

Abstract

BACKGROUND: Radioimmunoassay (RIA) has contributed to diagnostic medicine but the use of radioactive tracer complicates their routine use. Perhaps the most promising candidate is chemiluminescence immunoassay (CLIA), which is based on the detection of light emitted as the result of a chemical reaction, potentially can exhibit even greater sensitivity than RIA.
METHODS
We evaluated the technical performance of the Ciba Corning ACS:180SE automated chemiluminescence immunoassay system for following analytes: trithyroxine, thyroxine, free thyroxine, thyroid simulating hormone, follicle-stimulating hormone, luteinizing hormone, prolactin, alpha-feto protein, carcinoembryonic antigen, carbohydrate antigen 19-9, carbohydrate antigen 125, prostate specific antigen, and ferritin. The characteristics evaluated were linearity, precision, and comparison with the results of radioimmunoassay (RIA).
RESULTS
The within-run precision were from 0.94 to 21.70% and between-run precision 2.75 to 15.19%. The range of linearity was statistically acceptable for all analytes. The correlation coefficient between the value determined by ACS:180SE and RIA was above 0.90.
CONCLUSIONS
We conclude that ACS:180SE system is a rapid and precise, and offers safety and time advantages over conventional RIA techniques.


MeSH Terms

Carcinoembryonic Antigen
Ferritins
Follicle Stimulating Hormone
Immunoassay*
Luminescence*
Luteinizing Hormone
Prolactin
Prostate-Specific Antigen
Radioimmunoassay
Thyroid Gland
Thyroxine
Zea mays
Carcinoembryonic Antigen
Ferritins
Follicle Stimulating Hormone
Luteinizing Hormone
Prolactin
Prostate-Specific Antigen
Thyroxine
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