Farmaceutické analýzy - přehled aplikačního použití GC a GCMS systémů 2019-2020
Pixabay/Mizianitka: Farmaceutické analýzy - přehled aplikačního použití GC a GCMS systémů 2019-2020
Podívejte se na nejnovější trendy v oblasti analýz spojených s produkcí léčiv s využitím plynových chromatografů (GC), headspace autosamplerů (HS), GC/MS, GC/QQQ nebo spojenení plynové chromatografie s hmotnostními spektrometry s vysokým rozlišením (HRMS).
Nejnovější technologie posouvají hranice detekčních limitů ve všech aplikačních oblastech - od analýzy zbytkových rozpouštědel, přes v dnešní době kritické analýzy nitrosaminů až k analýzám extrahovatelných a vyluhovatelných látek např. z obalových materiálu.
Díky možnostem naší unikátní databáze s pokročilým vyhledáváním jste schopni ve vteřině vyhledávat a filtrovat dle přesné konfigurace systému, výrobce nebo zaměření.
GC/HRMS (2)
Analytical solutions for challenges in headspace GC-MS analysis of volatile extractable and leachable compounds |2019| Thermo Fischer Scientific
Extractables & LeachablesAnalysis of Pharmaceutical Nasal Spray Samples using the Hi-Resolution Accurate Mass GC/QTOF |2019| Agilent Technologies
GC/QQQ (7)
Combined Direct Injection N-Nitrosodimethylamine (NDMA),N-Nitrosodiethylamine (NDEA), N-Nitrosoethylisopropylamine (NEIPA), N-Nitrosodiisopropylamine (NDIPA), and N-Nitrosodibutylamine (NDBA)Impurity Assay by GC-MS/MS | 2019 | Ostatní
Analysis of Five Nitrosamine Impurities in Drug Products and Drug Substances Using Agilent GC/MS/MS Instrumentation | 2020 | Agilent Technologies
Analysis of Pharmaceuticals’ Impurity - Regulations and Analysis for Carcinogenic Substances | 2020 | Shimadzu
Nitrosamine Impurities Application Guide - Confidently Detect and Quantify Mutagenic Impurities in APIs and Drug Products | 2020 | Agilent Technologies
Quantification of Nitrosamine Impurities in Metformin Using Agilent GC/MS/MS Instrumentation | 2020 | Agilent Technologies
Overcoming the challenges of nitrosamine impurities in drugs | 2020 | Thermo Fischer Scientific
Determination of 33 pesticide residues in Ginseng using gas chromatography-triple quadrupole mass spektrometry | 2020 | Shimadzu
GC/SQ (12)
Determination of genotoxic nitrosamines in Valsartan with gas chromatography and mass spektrometry | 2019 | Thermo Fischer Scientific
Analysis of N-Nitrosodimethylamine and N-Nitrosodiethylamine Using the Agilent 7697A Headspace Sampler, 8890/5977 GC/MSD Systém | 2019 | Agilent Technologies
Analysis of USP <467> Residual Solvents of Class 1, Class 2, and Class 3 using the Agilent 8890 GC/ FID /5977B MSD Systém | 2019 | Agilent Technologies
Selective and Sensitive Analysis of 20 Category I and II Residual Solvents for Cannabis Application using Headspace-GCMS | 2020 | Shimadzu
Analysis of Terpene and Terpenoid Content in Cannabis Sativa Using Headspace with GC/MSD | 2020 | Agilent Technologies
Analysis of NDMA and NDEA in Sartan Drugs and Drug Products by GC-MS on a Zebron™ ZB-624PLUS™ | 2019 | Phenomenex
Agilent ASMS 2020 Posters Book | 2020 | Agilent Technologies
Analysis of Pharmaceuticals’ Impurity - Regulations and Analysis for Carcinogenic Substances | 2020 | Shimadzu
Nitrosamine Impurities Application Guide - Confidently Detect and Quantify Mutagenic Impurities in APIs and Drug Products | 2020 | Agilent Technologies
Overcoming the challenges of nitrosamine impurities in drugs | 2020 | Thermo Fischer Scientific
Thermal Desorption – GCMS Method for Screening Analysis of Extractables in Drug Packaging Materials | 2020 | Shimadzu
GC (15)
Analysis of Residual Solvents in Pharmaceuticals An Analysis Method for Class 2 Solvents (Water- Soluble Samples) Unsuited to Headspace GC Methods | 2019 | Shimadzu
Analytical solutions for challenges in headspace GC-MS analysis of volatile extractable and leachable compounds | 2019 | Thermo Fischer Scientific
Analysis of USP Method <467> Residual Solvents on the Agilent 8890 GC System | 2019 | Agilent Technologies
Analysis of USP <467> Residual Solvents of Class 1, Class 2, and Class 3 using the Agilent 8890 GC/ FID /5977B MSD System | 2019 | Agilent Technologies
Enhanced Productivity for Residual Solvent Analysis in Pharmaceutical Products According to USP 467 by Using a New Valve and Loop Static Headspace Sampler | 2019 | Thermo Fischer Scientific
Investigation of Key Parameters for a Smooth Method Transfer to a New Optimized Valve and Loop Headspace Autosampler | 2019 | Thermo Fischer Scientific
Investigation of key parameters for a smooth method transfer to the new Thermo Scientific TriPlus 500 Headspace Autosampler | 2019 | Thermo Fischer Scientific
System Suitability Test of Low-Substituted Hydroxypropyl Cellulose for USP42-NF37 | 2020 | Shimadzu
Analysis of Residual Solvents in Pharmaceuticals by Nexis™ GC-2030 + HS-20 (JP17 Supplement II, USP 467) | 2020 | Shimadzu
Analysis of Residual Solvents in Pharmaceuticals by Water-Soluble Samples Using N2 Carrier (JP17 Supplement II, USP 467) | 2020 | Shimadzu
Analysis of Residual Solvents in Pharmaceuticals by Water-Insoluble Samples Using N2 Carrier (JP17 Supplement II, USP 467) | 2020 | Shimadzu
Analysis of Volatile Impurities in Anhydrous Ethanol and Ethanol for Disinfection in Accordance with the Purity Test set by the Pharmacopoeias (JP, USP, EP) | 2020 | Shimadzu
Alcohol Determination of Sanitizer Gel in accordance with USP<611> | 2020 | Shimadzu
Analysis of Residual Solvents in Pharmaceutical Products by Headspace-GC-FID with Nitrogen Carrier Gas Following USP<467> - Procedure B | 2020 | Shimadzu
Packed Column Analysis of Alcohol Number Determination Conforming to Japanese Pharmacopoeia Using Nexis™ GC-2030 (FID) | 2020 | Shimadzu