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amino acids analysis
Discussions about HPLC, CE, TLC, SFC, and other "liquid phase" separation techniques.
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I am looking for RP HPLC method, using UV detector for lysine concentration determination. Now we are using EC for that, but sample prep is too complicated. Thank you.
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What is your sample? There are several ways to do it through derivatization of Lys. Low wavelength UV will also work without derivatization if your sample is simple enough (which I doubt if you are saying that sample preparation is too complicated when using EC).
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My sample has lipids, dextrose, API and lysine.
I use to use HPLC method for amino acids purity in a past, but forgot details. And I am not sure if I can use this method for my sample now.
I used Luna column, mobile phase A: phosphate buffer with ACN and mobile phase B: ACN or ACN+MeOH.
I use to use HPLC method for amino acids purity in a past, but forgot details. And I am not sure if I can use this method for my sample now.
I used Luna column, mobile phase A: phosphate buffer with ACN and mobile phase B: ACN or ACN+MeOH.
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- Joined: Thu Nov 13, 2008 5:41 am
Ollysa,
You can use our mixed-mode Primesep columns for direct analysis of amino acids with UV detection. Your mobile phase will consist of ACN/water/acid (sulfuric, phosphoric acid and corresponding buffers at pH 2-3):
http://www.sielc.com/application_114.html
http://www.sielc.com/application_085.html
http://www.sielc.com/application_087.html
http://www.sielc.com/application_080.html
http://www.sielc.com/application_105.html
Contact me if you have any questions
P.S. if you API is basic or hydrophobic in nature you can use this approach to quantitate API and lysine in one run, Dextrose is not going to be retained and lypids can be trapped on a guard column similar to this approach:
http://www.sielc.com/pdf/SIELC_September_2004.pdf
You can use our mixed-mode Primesep columns for direct analysis of amino acids with UV detection. Your mobile phase will consist of ACN/water/acid (sulfuric, phosphoric acid and corresponding buffers at pH 2-3):
http://www.sielc.com/application_114.html
http://www.sielc.com/application_085.html
http://www.sielc.com/application_087.html
http://www.sielc.com/application_080.html
http://www.sielc.com/application_105.html
Contact me if you have any questions
P.S. if you API is basic or hydrophobic in nature you can use this approach to quantitate API and lysine in one run, Dextrose is not going to be retained and lypids can be trapped on a guard column similar to this approach:
http://www.sielc.com/pdf/SIELC_September_2004.pdf
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- Posts: 3
- Joined: Tue Nov 11, 2008 6:17 pm
yzelechonok,
Thank you. I will try it.
Thank you. I will try it.
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- Joined: Mon Aug 30, 2004 5:42 pm
In your original conditions Lys would be eluted in the void volume. You can try the Primesep columns or ion pairing chromatography methods or...
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- Joined: Thu Feb 23, 2006 3:15 am
Separation of basic amino acids (including lysine) on Unison UK-Amino:
http://www.silvertonesciences.com/files/TI329E.pdf
http://www.silvertonesciences.com/files/TI329E.pdf
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- Joined: Wed Mar 30, 2005 12:32 am
I have more one some try for you, I bilieve this method is more easyer....and flexible for you condiction...think about this..
Implementing stepwise solvent elution in sequential injection chromatography for fluorimetric determination of intracellular free amino acids in the microalgae Tetraselmis gracilis
doi:10.1016/j.physletb.2003.10.071
Implementing stepwise solvent elution in sequential injection chromatography for fluorimetric determination of intracellular free amino acids in the microalgae Tetraselmis gracilis
doi:10.1016/j.physletb.2003.10.071
Dr. Jose Carlos Penteado
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