Famotidine Tablet Analyzed with HPLC - AppNote
August 12, 2012
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API Separation from Matrix Component

This Method for Analysis of Famotidine Tablets is easy to perform and produces a Symmetrical Peak Shape for the API. This compound has numerous amines which can be problematic in terms of Peak Shape with conventional Columns. Separation from a component from the tablet extract matrix is obtained as well, illustrating specificity of the Method.

Reproducibility is shown by the overlay of runs from two different Column lots.


 
Famotidine Tablet Chromatogram

Famotidine Chemical Structure

Peaks:
1. Matrix Component,   2. Famotidine

Method Conditions
Column: Cogent Diamond Hydride™, 4 μm, 100Å
Catalog No.: 70000-7.5P
Dimensions: 4.6 x 75 mm

Mobile Phase:
-- A: DI Water with 0.1% Trifluoroacetic Acid (TFA) v/v
-- B: Acetonitrile with 0.1% Trifluoroacetic Acid (TFA) v/v

Gradient:
Time (minutes) %B
0 95
2 95
6 50
7 95

Post Time
: 3 minutes
Injection vol.: 1 μL
Flow rate: 1.0 mL / minute
Detection: UV @ 265 nm

Sample Preparation: 10 mg strength Famotidine tablet was ground and added to a 25 mL volumetric flask. A portion of 50:50 Solvent A / Solvent B diluent was added and the flask was sonicated 10 minutes. It was then diluted to mark and filtered with a 0.45 μm Nylon Syringe Filter (MICROSOLV Tech Corp.).

t 0 : 0.9 minutes

 

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