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1 - 9 of 9 results
Analysis of five nitrosamines in sartan drugs using the published GC-MS/MS FDA method
| Chinese (Simplified) (China) | Complete (PDF) |
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| Korean (Korea) | Complete (PDF) |
| Japanese (Japan) | Complete (PDF) |
Describes the use of the Agilent 8890 GC to analyze impurities in sartan products according to a United States Food and Drug Administration (US FDA) method.
A GC/FID/MSD method for the residual solvents.
| Korean (Korea) | Complete (PDF) |
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| Chinese (Simplified) (China) | Complete (PDF) |
Extractables were identified in pressurized metered dose inhaler components using two Agilent 5977A Series GC/MSD Systems.
GC/Q-TOF MS data was used for identification and quantitation, while MSMS data was used to predict the impuriy fragment structures using MSC software.
| Korean (Korea) | Complete (PDF) |
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Plasticizers were identified in drug suspension using headspace GC/MS and MMI GC/MS. SIM confirmed the identification of phthalate and fatty acid plasticizers.
| Korean (Korea) | Complete (PDF) |
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| Chinese (Simplified) (China) | Complete (PDF) |
propylene oxide impurities were analyzed with low method-detection limit, good resolution, sample recovery, and repeatability using Agilent J&W PoraBOND U.
The analysis of Class1, Class 2A, and Class 2B residual solvents are demonstrated at USP 467 limit concentrations using the 5977 MSD with the 7890B and 7697A Headspace sampler
| Publication Part Number | 5991-2079EN | ||||
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USP residual solvents were analyzed by static headspace on the Agilent 7697A Headspace Sampler combined with the Agilent 7890B Gas Chromatograph.
| Publication Part Number | 5991-1834EN | |||
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