| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2507953 | Journal of Pharmaceutical Analysis | 2012 | 5 Pages |
Objective: To develop the representative fingerprint for the quality control of placenta polypeptide injection.MethodsThe chromatographic separation was performed using a Phenomenex Gemini C18 column (250 mm×4.6 mm, 5 μm) maintained at 30 °C. 0.1% aqueous trifluoroacetic acid (Solvent A) and acetonitrile contained 0.1% TFA (Solvent B) were used as mobile phase with a gradient elution. Detection wavelength was 280 nm with the sample injection volume of 50 μL; the flow rate was 1.0 mL/min. The fingerprints of different samples were investigated by similarity analysis.ResultsNine peaks were identified as the characteristic common peaks. The similarities of the fingerprints of the 10 batches of samples were above 0.992.ConclusionThis method showed high precision and good repeatability, and provided the basis for the improvement of the quality control of placenta polypeptide injection.
