How to Perform Linearity and Range in Analytical Method Validation

Introduction and outcome

Linearity and Range is one of the important parameter of analytical method. In this article, I will discuss procedure to perform linearity and range with case study

Procedure to perform Linearity and Range

Linearity for Related substances test

Prepare two stock solutions A and B. Now prepare five solutions in the concertation range of 50% to 150% using stock solution A and B. Inject each of these five solutions (once) and generate the chromatogram. Plot the linearity graph using concentrations in the X axis and their corresponding responses in the Y axis Calculate correlation coefficient (R2) and slope. R2 should be more than or equal to 0.997

Case studies

A drug substance D having the following specifications for related substances:

  • Impurity A NMT: 0.20%
  • Any unknown impurity NMT: 0.10%
  • Total impurity NMT 0.50%

Sample concentration is 1.0mg/ml to perform related substances test and QL of the method is 0.05%

The following concentrations (≥5) can be prepared to perform linearity:

Impurity A solution concentration for Linearity calculation

The level of linearity and value of impurity A and their corresponding concertation have been calculated in the following table

Level (L)Impurity value (I)
(0.20 x L/100 )
Impurity solution concentration
( 1000 x I/100)
QL(0.05%)0.05%0.5mcg/ml
50%0.10%1.0mcg/ml
70%0.14%1.4mcg/ml
100%0.20%
2.0mcg/ml
130%0.26%
2.6mcg/ml
150%0.30%
3.0mcg/ml
Impurity A level and their corresponding concentration

Inject Impurity A solution at each concertation as given in the above table and generate the chromatogram and note down the area response

Impurity A ( mcg/ml)Area response
0.515457
1.031904
1.443400
2.061830
2.680380
3.092750
Slope30746
Correlation coefficient (R2)0.9993 ≥ 0.997

Acceptance Criteria: R2 is 0.9993 ≥ 0.997 and it passes the linearity criteria

Linearity and Range; linearity plot for impurity A
Image source: phramaknowledgeforum

Range

Impurity A is linear between 0.05% to 0.30% (QL to 150% of the specification limit).

Conclusion

Linearity is one of the important parameter of the Analytical method validation. It gives range in which method gives accurate and precise result. For any opinion or suggestions related to this article, you can write in the comment section. For any further assistance you can contact me using contact form.

References
  • https://www.chromatographyonline.com/view/limit-detection
  • https://database.ich.org/sites/default/files/Q2%28R1%29%20Guideline.pdf
Abbreviations
  • mcg: microgram
  • ml: milli liter
  • QL: Quantitation limit

Disclaimer: The numerical data used in the tables or calculations are not actual data. It is designed to explain the topic.

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