Evaluation of the CELL-DYN (R) 3500 haematology instrument for the analysis of the mouse and rat blood

Citation
J. Kieffer et al., Evaluation of the CELL-DYN (R) 3500 haematology instrument for the analysis of the mouse and rat blood, COMP HAEMAT, 9(2), 1999, pp. 92-106
Citations number
16
Categorie Soggetti
Cardiovascular & Hematology Research
Journal title
COMPARATIVE HAEMATOLOGY INTERNATIONAL
ISSN journal
09387714 → ACNP
Volume
9
Issue
2
Year of publication
1999
Pages
92 - 106
Database
ISI
SICI code
0938-7714(1999)9:2<92:EOTC(3>2.0.ZU;2-K
Abstract
The objective of this study was to evaluate the performance of the CELL-DYN (R) 3500 for rat and mouse blood analysis in a routine environment. The WBC (white blood cells), RBC (red blood cells), PLT (platelets) counts and the WBC differential were determined. In addition, the following aspects were studied: within-run precision, day-to-day precision, bias-free paired diffe rence precision; extended ranges of linearity for RBC, HCT (haematocrit), W BC, PLT; carry-over, the effect of blood ageing, cell stability with differ ent anticoagulants; and the normal ranges, the out of range flagging and so me typical pathology cases. The CELL-DYN(R) 3500 is a multiparameter flow cytometer which counts and di fferentiates WBC, based on the principle of multi-angle polarised light sca tter separation. RBC and PLT are determined by the impedance method. The WB C count is evaluated by both, optical and impedance methods. Reference meth ods used were according to the ICSH recommendations on blood cell analysis, including manual counts of WBC and platelets, a centrifugal microhaematocr it method and a haemoglobin measurement by spectrophotometry using the WHO haemoglobin standard. All cell counts were compared with the results obtain ed by our routine blood cell analyser (Contraves AL820), and the WBC differ ential was compared with the manual microscopic differentiation of the 400 WBC (200 cells differentiated by two technicians). The following coefficients of vartiation were obtained: within-run precisio n was 1.2% and 2.7% for WBC; 1.0% and 1.0% for RBC; 1.3% and 0.9% for haema tocrit; 2.1% and 2.7% for platelets (rats and mice respectively)., Day-to-d ay precision was performed using human tri-level control blood, and the CVs were found to be <1.7% for WBC, <1.4% for RBC, <1.2% for haemoglobin and < 6.3% for platelets. The following ranges of measurement were found to be linear in the rat: WBC : 0.10-20.20x10(3)/mu l; RBC: 0.016-14.3 x 10(6)/mu l; haemoglobin: 0.08-26 .8,g/dl; haematocrit: 5.0%-77%; platelets: 14.0-1670.0x 10(3)/mu l. Equal r anges were observed for mouse blood. Carryover in rat blood was found to be 0.12% for WBC, 0.05% for RBC, 0.15% for haemoglobin and 0.46% for platelet s. In mice, similar carry-over results were obtained. The correlation coeff icients (Pearson, correlation coefficient) between the CELL-DYN(R) 3500 and Contraves AL 820 using linear regression analysis were as follows: 0.988 a nd 0.997 for BC; 0.986 and 0.920 for RBC; 0.995 and 0.984 for haemoglobin; 0.958 and 0.85 for haematocrit; 0.958 and 0.963 for platelets, for rats and mice, respectively. Correlation coefficients between the CELL-DYN(R) 3500 and the manual differential of NEU (neutrophils) and LYM (lymphocytes) were higher than 0.8 in rats and higher than 0.9 in mice. Due to the relatively low absolute counts of MONO (monocytes), EOS (eosinophils) and BASO (basop hils), only moderate correlation of methods was found. The CELL-DYN(R) 3500 was judged to be reliable, accurate and easy-to-use fo r counting and identifying normal and most of the pathological blood specim ens obtained from mice and rats. By using the CELL-DYN(R) 3500, the time fo r blood sample analysis can be shortened significantly and provides extensi ve opportunities to characterise pathological samples. Evaluation of the CELL-DYN 3500 for Analysis of Rodent Blood.