Detection Limit Calculator Formula

Understand the math behind the detection limit calculator. Each variable explained with a worked example.

Formulas Used

Limit of Detection (LOD, 3sigma)

lod = 3 * blank_std / slope

Limit of Quantitation (LOQ, 10sigma)

loq = 10 * blank_std / slope

Variables

VariableDescriptionDefault
blank_stdStandard Deviation of Blank (sigma)0.005
slopeCalibration Slope (m)2500

How It Works

Limit of Detection and Quantitation

LOD is the lowest analyte concentration that can be reliably detected (S/N ≈ 3). LOQ is the lowest concentration that can be quantified with acceptable precision (S/N ≈ 10).

Formulas (ICH Method)

LOD = 3.3 × sigma / S (often simplified to 3 × sigma / S)

LOQ = 10 × sigma / S

where sigma is the standard deviation of the blank response and S is the slope of the calibration curve. This is the most common approach in pharmaceutical and environmental analysis.

Worked Example

Blank standard deviation = 0.005, calibration slope = 2500 signal/M.

blank_std = 0.005slope = 2500
  1. 01LOD = 3 × 0.005 / 2500 = 0.015 / 2500 = 6.0 × 10⁻⁶ M = 6.0 uM
  2. 02LOQ = 10 × 0.005 / 2500 = 0.05 / 2500 = 2.0 × 10⁻⁵ M = 20 uM

Frequently Asked Questions

What is the difference between LOD and LOQ?

LOD answers "is the analyte present?" (qualitative). LOQ answers "how much is present?" (quantitative). LOQ is about 3× higher than LOD because greater S/N is needed for reliable quantitation.

How is the blank standard deviation determined?

Measure the response of 10-20 blank samples (same matrix as unknowns but without analyte). The standard deviation of these measurements is sigma. Use the same instrumental conditions as actual samples.

Are there other methods to determine LOD?

Yes. Visual evaluation (lowest visible S/N ≈ 3), signal-to-noise method (directly measuring S/N at low concentrations), and EPA method detection limit (MDL) using t-distribution statistics on replicate measurements.

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