What is use of LOD and LOQ in validtion and give range and in calculation why we use 3.3* LOD here why we use 3.3
Answer Posted / nikkosthiru@gmail.corai12
LOD is Limit of detection. We can dedect the peak but cant quantify
LOQ Limit od quaantification. We quantify also this is known as reporting thereshold.
During the RS analysis Below LOQ level we cant included in the total impurities calculation.
LOD and LOQ Determination three methods
1.S/N Ratio method
3 or 2 ratio for LOD
NLT 10 ratio for LOQ
2. Slope Method
Plot the linearity for active and impurities through serial dilution at lower level
Formula for LOD
3.3*Slope/Std.dev
Formula for LOQ
10*Slope/Std.Dev
3. Visualization method
It will be using for only identification and TLC Method
| Is This Answer Correct ? | 1 Yes | 0 No |
Post New Answer View All Answers
What is the difference between Discriminating media and DPDM(Dissolution Profile with Different Media)
Explain the relations between number of carbon atoms in alkanes and retention time ?
in sampling of raw material which side is pasted sampled labels
Why we use potassium dichromate in uv calibration Exact reason behind it??
how can give the expiry period and restadardisation of volumetric solution
how to select short coloum and long coloumn for new molecule
cefoperozone and sulbactam inj. hplc test method
WHAT IS THE PURPOSE WE USE HCL, CHOPPER, BURNER, MONOCHROMATOR in AAS? PLEASE EXPLAIN BRIEFLY
What is dose dumping? why require to do?
some product having water content method with pyridine and ethylene glycol mixture instead of methanol? how they are selecting and methanol is not suitable solvent how ?
How to calculation of residual solvent methanol (3000 ppm) standard solution, and how many quantity used of test sample
why require to add enzymes in capsules dissolution only? is it require to tablet also?
why require the ph, buffer during hplc mobile phase?
I have compare C2H2-air and C2H2-N2O flame AAS on determination calcium. Both use same range of std to plot calibration curve. (2-6ppm) When i measure the sample with phosphate, KCl and LaCl, C2H2-N2O flame give false positive result, around 0.5ppm. When i measure the sample with phosphste, KCl and EDTA. C2H2-N2O flame also give 0.5ppm false positive. But both above mentioned sample would not give false positive when measured by C2H2-air flame. What is the reason?
What is the accrptance criteria in RSD for RS method precision on basis of impurity percentages?