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lower detection limit

Discussions about HPLC, CE, TLC, SFC, and other "liquid phase" separation techniques.

4 posts Page 1 of 1
Please help
an interview Q I couldn't answer can you please provide answer...

What parrameters do we need to change to lower the detection limit by a factor of 10 in a method??

The general answer is that detectability is ultimately limited by signal/noise ratio. There are only two ways to improve that:
- more signal
- less noise.

Under "more signal":
- inject a 10 x larger volume (this works only if they define detectability in terms of concentration)
- get a 10 x smaller column volume
- get a 10 x longer flow cell
- decrease retention (will help, but not 10 x)
- use smaller particles (will help, but not 10 x)
- find a better wavelength (maybe)
- make a more detectable derivative (maybe)
- find a more sensitive detection technique

Under "less noise":
- improve instrument performance (lamp age, degassing, temperature control) if system not meeting specifications.
- detector time constant (works for short-term noise only)

All of the above may have ramifications in terms of affecting other characteristics of the method, and may not be permissable in the case of a validated method.
-- Tom Jupille
LC Resources / Separation Science Associates
tjupille@lcresources.com
+ 1 (925) 297-5374
Thanks Tom...

I thought of those when i'm home but donno exactly... I appreciate your reply

Regards
Gokul

One thing that may also be worth trying is playing with your sampling rate on your detector. This can have quite drastic effects on your s/n ratio.
4 posts Page 1 of 1

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