Editor-in-Chief
Hatice Kübra Elçioğlu
Vice Editors
Levent Kabasakal
Esra Tatar
Online ISSN
2630-6344
Publisher
Marmara University
Frequency
Bimonthly (Six issues / year)
Abbreviation
J.Res.Pharm.
Former Name
Marmara Pharmaceutical Journal
Journal of Research in Pharmacy
2022 , Vol 26 , Issue 2
Development of validation of a rapid and simple analytical separation method for anticancer alkylating agents using application of total error concept
1Department of Pharmaceutical Chemistry, College of Pharmaceutical Sciences, Karnataka, Bengaluru-560078, India
DOI :
10.29228/jrp.140
A simple and sensitive high-performance liquid chromatographic (HPLC) method is established to
separate and quantify the related substance present in two alkylating agents. The use of the traditional approach of
analytical validation, in practice or in the literature, is communal. However, statistical verification, that looks separately
the two errors (such as absolute bias and repeatability) to make a decision, presents a risk to declare that an analytical
method is valid while it is not, or equally. To minimize this peril, a new approach based on the concept of total error
was proposed. In this paper, we reveal the applicability and simplicity of the both methods based on the total error
approach: accuracy profile and uncertainty profile. Proposed study demonstrated by validation case of a liquid
chromatographic LC method for the quantification of related compounds present in two alkylating agents. Both
methods showed good linearity response (> 0.995) with repeatability (%relative standard deviation less than 2%) and
accuracy (94 to 106%). Accuracy profile was found within the range of ±10% and risk profile ±5% between the two series
respectively. The excellence of the total error approach was presented since it enables successfully to validate the
analytical procedure as well the calculation of the measurement uncertainty at each concentration level.
Keywords :
Related substances; Quantification; Total error; HPLC; Validation