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. 2021 Sep 20;11(49):31047–31057. doi: 10.1039/d1ra05121k

Evaluation of intra-day and inter-day accuracy and precision of the proposed method in case of different serum samplesa.

Serum samples Standard method Proposed method
Intra-day accuracy and precision (n = 3) Inter-day accuracy and precision (n = 3)
Average Average reading ±CL RE (%) RSD (%) Average reading ±CL RE (%) RSD (%)
Patient (1) 10 10.2 ±0.0135 2.00 0.98 10.5 ±0.0133 5.00 0.95
Patient (2) 23 22.9 ±0.0090 0.43 0.44 22.1 ±0.0092 3.91 0.45
Patient (3) 27 27.1 ±0.0083 0.37 0.37 28 ±0.0081 3.70 0.36
Patient (4) 15 15.5 ±0.0109 3.33 0.65 14.5 ±0.0113 3.33 0.69
Patient (5) 18 18.3 ±0.0101 1.67 0.55 18 ±0.0101 0.00 0.56
Patient (6) 99 98.8 ±0.0043 0.20 1.00 100 ±0.0043 1.01 1.00
Patient (7) 78 78.0 ±0.0049 0.00 1.30 79 ±0.0048 1.28 1.31
Patient (8) 130 130.6 ±0.0038 0.46 0.80 129 ±0.0038 0.77 0.80
Patient (9) 210 210.2 ±0.0030 0.10 0.50 212 ±0.0030 0.95 0.50
Patient (10) 105 105.4 ±0.0042 0.38 0.90 103 ±0.0042 1.90 1.00
Patient (11) 222 221.7 ±0.0029 0.14 0.50 225 ±0.0043 1.96 0.10
Patient (12) 102 102.3 ±0.0043 0.29 0.10 100 ±0.0029 1.35 0.40
a

RE: percent relative error, RSD (%): relative standard deviation and CL: confidence limits were calculated from: CL = ±tS/√n (the tabulated value of t is 4.303, at the 95% confidence level; S = standard deviation and n = number of measurements).