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. 2010 Dec 10;26(7):2281–2289. doi: 10.1093/ndt/gfq709

Table 3.

Laboratory analysis methods and their sensitivity and linearity

Substance Measurement method Linearity Sensitivity Dialysate (mean ± SD) [min–max] Blood (mean ± SD) [min–max]
Urea (mmol/L) UV cinetic 0.8–50 0.38 4.6 ± 1.4 [1.3–9.3] 12 ± 8 [1.6–31]
Creatinine (μmol/L) Compensated Jaffe 5–2000 2.4 85 ± 2 [23–173] 406 ± 230 [73–939]
β2 microglobulin (mg/L) Immunoturbidimetry 0.5–16 0.06 6.5 ± 7.1 [0.06–37] 13.5 ± 5.6 [3.2–23]
Total proteins (dialysate) (g/L) Photometric colour 0.01–2.00 0.007 0.10 ± 0.06 [0.01–0.44]
Total proteins (dialysate) (mg/L) Bradford 0–500 0.002 98 ± 60 [0.002–272]
Total proteins (serum) (g/L) Photometric colour 30–120 0.77 67 ± 7 [52–84]
Albumin ‘micro’ assays (mg/L) Immunoturbidimetry 5–300 0.46 12 ± 14 [0.1–113]
α1-Antitrypsin (g/L) Immunoturbidimetry 0.3–5.0 0.01 1.5 ± 0.3 [0.84–2.44]
Leptin (μg/L)a ELISA 0.0156–1 0.0078 25 ± 47 [0.6–386]
RBP (mg/L)a ELISA 1.56–100 0.224 13 ± 7 [1.4–44] 178 ± 96 [55–667]
a

Leptin and RBP were diluted before measurement in order to be in the linearity range.