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
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.