Advertisement

Problem with LC analysis of Vilazodone

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

4 posts Page 1 of 1
Presently we are working on a drug vilazodone (Antidepressant) and we are having a difficulty with LC analytical method. The peak shape obtained for drug is very broad (peak width around 2 minute) as well as tailing & fronting effect. We had numerous trials using different mobile phases like methanol: phosphate buffer pH 3 adjusted by orthophosphoric acid (80:20), Acetonitrile : methanol (90:10). Also we worked at different pH (Acidic as well as Alkaline), yet could not get sharp peak. Kindly suggest solution.
what is your analyte concentration?
How many ul you inject?
What column you use?
Fronting is a problem in general issued by extra column effects, bad connections, dead volume etc.!
What is the pK of your drug?
Can you use also some volatile buffers, instead of phosphate buffer?
What column material you use, particle size etc.?
Dimension of your column can also play a role. Maybe another separation mode can do the job, like HILIC!
Gerhard Kratz, Kratz_Gerhard@web.de
4 posts Page 1 of 1

Who is online

In total there are 2 users online :: 1 registered, 0 hidden and 1 guest (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: Bing [Bot] and 1 guest

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.

Liquid Chromatography

Gas Chromatography

Mass Spectrometry