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Rapid Count of Microbial Cells in Dialysate
Author(s) -
Shimakita Tomonori,
Yamamoto Hidenori,
Naramura Tomotaka,
Fujimori Akira,
Ide Takao,
Tashiro Yoshikazu,
Saito Mikako,
Matsuoka Hideaki
Publication year - 2007
Publication title -
therapeutic apheresis and dialysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.415
H-Index - 53
eISSN - 1744-9987
pISSN - 1744-9979
DOI - 10.1111/j.1744-9987.2007.00500.x
Subject(s) - medicine , intensive care medicine
An apparatus for the non‐culture method (NCM) of microbial cell count was formerly developed and named a bioplorer. The bioplorer NCM is based on the double staining of cells with 4′, 6‐diamidino‐2‐phenylindole (DAPI) and propidium iodide (PI) and the automatic analysis of their fluorescent microscopic images. Viable cells can be stained with DAPI, while dead cells can be stained with DAPI and PI. In this study, the bioplorer NCM has been applied to the dialysate. The viable and dead cells in dialysate could be counted within 20 min. The detection limit expressed by log 10 [cells/100 mL] was 2.0. When cell‐spiked dialysate samples containing prescribed number of Bacillus subtilis cells were assayed, the numbers of cells determined by the bioplorer NCM (N VIA (NCM)) and a conventional culture method (CM) on R2A medium (N VIA (R2A‐CM)) were similar in the range of 2.6–4.6 within the 95% confidence interval (NCM‐CM equivalent range). When test solutions sampled from a practical facility in a hospital were assayed, N VIA (NCM) was greater than, but comparable to, N VIA (R2A‐CM). The endotoxin (ET) in the test samples were assayed as well using a test kit for limulus amoebocyte lysate assay. The results of microbial cells and ET concentration indicated that the dialysate supplying line was clean and well maintained. The bioplorer NCM can determine if the microbial contamination of dialysate supplying facilities is greater than 2.6 (398 cells/100 mL).