April 29, 2024, 08:06:17 AM
Forum Rules: Read This Before Posting


Topic: Validating a method...impurity of analyte  (Read 3509 times)

0 Members and 1 Guest are viewing this topic.

Offline Peacock

  • Regular Member
  • ***
  • Posts: 16
  • Mole Snacks: +0/-0
Validating a method...impurity of analyte
« on: December 15, 2010, 07:43:28 AM »
Dear all,

While developing an analytical method for GC, I have realised that one of the reagents contains traces of my analyte from the factory. It seems impossible to get this reagent impurity free.
Therefore my question is:

How valid would it be as a method if I subtract the blank peak area from any sample?

Does this impair the whole method and, therefore I should be thinking of finding another one?

Would it be ok if I draw a calibration curve crossing the ordinate axis above 0?

What would you do in my situation?

Regards

Offline Stepan

  • Chemist
  • Full Member
  • *
  • Posts: 358
  • Mole Snacks: +39/-4
  • Gender: Male
  • Air Chemistry Man
    • Supplier of air sampling equipment and services
Re: Validating a method...impurity of analyte
« Reply #1 on: December 15, 2010, 05:12:30 PM »
This is very common. You need to subtract solvent blank from your result. Be sure you take it into account when you estimate your detection limit.

Offline vijayak

  • New Member
  • **
  • Posts: 3
  • Mole Snacks: +0/-0
Re: Validating a method...impurity of analyte
« Reply #2 on: January 16, 2011, 04:01:59 AM »
 :)

Offline ruthfabiny

  • Very New Member
  • *
  • Posts: 1
  • Mole Snacks: +0/-0
Re: Validating a method...impurity of analyte
« Reply #3 on: January 18, 2011, 12:05:33 AM »
This was helpful. Thanks ,
Ruth Fabiny

Sponsored Links