1993
DOI: 10.1515/cclm.1993.31.10.701
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Comparison of the Automated Random Access Immunoassay Analysers, ACS-180 (Ciba Corning) and AIA-1200 (Tosoh)

Abstract: Summary:Two random access immunoassay analysers, the ACS-180 (Ciba Corning) and the AIA-1200 (Tosoh Corp.) were compared with respect to performance and user-friendliness. Precision studies revealed an almost equal intra-assay variation coefficient, but day-to-day reproducibility was better on the AIA-1200. Recovery of dilution series of tumour markers was too high with the ACS-180. Both systems were free from carry-over effects, on account of the extra wash step in the ACS-180 (for thyrotropin, carcinoembryon… Show more

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“…Results were evaluated by the non-parametric regression procedure of Passing & Bablok (8). Tlie concentrations were distributed within the expected clinical thyrotropin range, and they included low and high values.…”
Section: Limit Of Detectionmentioning
confidence: 99%
“…Results were evaluated by the non-parametric regression procedure of Passing & Bablok (8). Tlie concentrations were distributed within the expected clinical thyrotropin range, and they included low and high values.…”
Section: Limit Of Detectionmentioning
confidence: 99%
“…To avoid tedious chromatographic separations, a rapid and precise immunoassay was developed based on enzymatic conversion of Hcy to S-adenosyl-L-homocysteine (SAH) by the action of SAH hydrolase, followed by quantification of SAH in a competitive immunoassay with use of an anti-SAH antibody [15]. Moreover, this principle has been used in an automated tHcy assay on the Abbott IMx intstrument and AxSYM analyzer [16][17][18]. These completely automated methods use expensive equipments while those need less time and have good accuracy and precision.…”
Section: Introductionmentioning
confidence: 99%
“…Sample carryover is a potential hazard for laboratory parameters sharing a large dynamic range. Published reports in regard to the determination of TSH describe no significant carryover (Costongs and Janson, 1993, Khalil et al, 1991, Hebles-Duvison et al, 1995, Stockmann et al, 1998, Letellier et al, 1996, Forrest et al, 1998, Knedel et al, 1988, DCosta et al, 1993. An estimated specimen carryover of 1:1250 to 1:1160 has been reported for pipetting stations using fixed pipettes (Sadler et al, 1996, European Committee for Clinical Laboratory Standards.…”
Section: Introductionmentioning
confidence: 99%