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Flame control accessory for GC-FID operation with autosampler injection

✍ Scribed by Helmig, Detlev ;Schwarzer, Norbert ;Steinhanses, Jürgen


Book ID
102348369
Publisher
John Wiley and Sons
Year
1990
Tongue
English
Weight
292 KB
Volume
13
Category
Article
ISSN
0935-6304

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✦ Synopsis


of 79LN35R.D i I I ( b ) 5 10 15 20 25 Time ( m i n . ) Figure 4 HPLC chromatograms of degraded Nicardipine samples ( 2 mg/ml in mobile phase): (a) after three weeks under daylight and at room temperature; (b) after three months at 50 "C; (c) control sample.

4 Conclusions

This work describes a chromatographic method which is applicable to the quantitation of Nicardipine and its related compounds (present as minor impurities). Although the method is simple, and requires neither derivatization nor sophisticated apparatus, the chromatographic parameters must be set with care. The system suitability test should be run before each analysis to guard against deviation from the original conditions.

Both assay and purity methods have been shown to be good indicators of stability. The method is being applied to samples prepared from raw materials and excellent results have been obtained.