-
- Posts: 2
- Joined: Mon Jan 07, 2013 8:18 pm
Advertisement
HELP! Troubleshooting HPLC. Increased concentrations
Discussions about HPLC, CE, TLC, SFC, and other "liquid phase" separation techniques.
6 posts
Page 1 of 1
We are running PCMX/Triclosan on our Varian Pro Star HPLC and are experiencing increased concentrations of both. We changed the cloumn, flow cell, UV lamp, recalibrated numerous times. The method is the same and the same standards are being used that were used before the problem started. We even ran a known of a finished product containing the active ingredients and it also gave spiked concentrations. We are at a complete loss. Can anyone out there shed some light on this? It would be greatly appreciated.
-
- tom jupille
- Site Admin
-
- Posts: 4978
- Joined: Wed Aug 11, 2004 4:55 pm
What you're seeing is consistent with degraded standards.same standards are being used that were used before the problem started
-- Tom Jupille
LC Resources / Separation Science Associates
tjupille@lcresources.com
+ 1 (925) 297-5374
LC Resources / Separation Science Associates
tjupille@lcresources.com
+ 1 (925) 297-5374
-
- Posts: 3594
- Joined: Mon Aug 30, 2004 11:43 pm
Tom is saying that standards lower than the stated value make the samples higher in comparison. That's why the known sample (your control sample) also assayed high.
We assayed samples containing both chloroxylenol and triclosan for years and never had such issues. Make up standards and samples fresh. I assume that you are doing gradient elution so that your triclosan peak isn't too broad, or that your earlier-eluting chloroxylenol is retained adequately.
Waht solvent are you using for samples and standards?
We assayed samples containing both chloroxylenol and triclosan for years and never had such issues. Make up standards and samples fresh. I assume that you are doing gradient elution so that your triclosan peak isn't too broad, or that your earlier-eluting chloroxylenol is retained adequately.
Waht solvent are you using for samples and standards?
-
- Posts: 3594
- Joined: Mon Aug 30, 2004 11:43 pm
OK, now I re-read:
Just for "fun", how much higher were the recent assays? When you look at the chromatograms and peak areas, does that confirm your findings, or are you simply relying on electronic data analysis where someone could've made a mistake with a dilution, calibration table, multiplier, etc.?
We've encountered stuff off because someone used a 200 ml flask and entered it as 250ml, and the reverse. Have a second analyst go through with you, and definitely make up fresh standards. I assume that you make a standard containing both API ingredients, and assay in a single gradient run.
Does this mean that you re-injected the standards or that you used the areas from the past?The method is the same and the same standards are being used that were used before the problem started.
Interesting. Because if my peak shapes are areas were essentially the same as I'd always gotten, I don't think I would've changed any of those, as whatever of those that affected my standards would also affect the samples.We changed the column, flow cell, UV lamp...
Just for "fun", how much higher were the recent assays? When you look at the chromatograms and peak areas, does that confirm your findings, or are you simply relying on electronic data analysis where someone could've made a mistake with a dilution, calibration table, multiplier, etc.?
We've encountered stuff off because someone used a 200 ml flask and entered it as 250ml, and the reverse. Have a second analyst go through with you, and definitely make up fresh standards. I assume that you make a standard containing both API ingredients, and assay in a single gradient run.
-
- Posts: 2
- Joined: Mon Jan 07, 2013 8:18 pm
The solvents we are using are methanol and sodium perchlorate. The peaks are non-linear at the LOQ but had been linear in the past. We are seeing about a %10 increase in PCMX and about %25 increase in Triclosan.
-
- Posts: 3594
- Joined: Mon Aug 30, 2004 11:43 pm
We used water-ACN with a little acetic acid. Sometimes simple is better.
6 posts
Page 1 of 1
Who is online
In total there are 17 users online :: 4 registered, 0 hidden and 13 guests (based on users active over the past 5 minutes)
Most users ever online was 4374 on Fri Oct 03, 2025 12:41 am
Users browsing this forum: Ahrefs [Bot], Amazon [Bot], Baidu [Spider], Google [Bot] and 13 guests
Most users ever online was 4374 on Fri Oct 03, 2025 12:41 am
Users browsing this forum: Ahrefs [Bot], Amazon [Bot], Baidu [Spider], Google [Bot] and 13 guests
Latest Blog Posts from Separation Science
Separation Science offers free learning from the experts covering methods, applications, webinars, eSeminars, videos, tutorials for users of liquid chromatography, gas chromatography, mass spectrometry, sample preparation and related analytical techniques.
Subscribe to our eNewsletter with daily, weekly or monthly updates: Food & Beverage, Environmental, (Bio)Pharmaceutical, Bioclinical, Liquid Chromatography, Gas Chromatography and Mass Spectrometry.
- Follow us on Twitter: @Sep_Science
- Follow us on Linkedin: Separation Science
