Small Molecule Pharmaceutical

Formulation

• Determination of Counterions (Cations) by Ion Chromatography
• Determination of Counterions (Anions) by Ion Chromatography
• Analysis of Organic Acid Counterions by Ion Exclusion Chromatography

Pharmacokinetics

• Analysis and Evaluation of Chiral Drugs in Biological Samples Using the Nexera UC-MS/MS System
• Comprehensive Monitoring Method for Analyzing 158 Lipid Mediator Species Using the Ultra-Fast LCMS-8050
• High-Speed Analysis of Itraconazole in Plasma Using Triple Quadrupole LC/MS/MS (LCMS-8050)
• Improved Analytical Workflow for Phospholipids by Nexera-e and Co-Sense for Impurities
• Simultaneous Analysis of 97 Primary Metabolites By PFPP: Pentafluorophenylpropyl Column
• Analysis of Favipiravir in Human Plasma Using Fully Automated Sample Preparation LC/MS/MS System
• Analysis of Favipiravir in Human Plasma_8060
• High Sensitivity Analysis of Aldosterone in Human Serum Using LCMS™-8060NX

Toxicity Evaluation

• A Study of Toxicity Evaluation Using the iMScope TRIO - Analysis of Localization of Amiodarone in Rat Lungs -

Cleaning Validation

• Analytical Instruments and Methods for Cleaning Validation
• Cleaning Validation | Measurement of Drug Component Residues (Swab Method)

Impurities, Genotoxic Impurities and Elemental Impurities

• Analysis by ICP Atomic Emission Spectrometry in Accordance with the ICH Q3D Guideline for Elemental Impurities
• Analysis of Decomposition Products in Drugs (LC/MS)
• Analysis of Nitrosamines in Sartan-Type Bulk Drug Substances
• Impurities and Foreign Matter | Easy Elemental Analysis of Pills (EDX)
• Quantitative Analysis of Trace Impurities in Drugs (LC/MS)
• Structural Estimation of Impurities in Drugs Using MSn Data
• LC/MS/MS Analysis of Impurities in Active Pharmaceutical Ingredients Using the Co-Sense for Impurities System
• Method Transfer and High-Speed Analysis of Impurities of Drug by Prominence-i
• Impurities and Foreign Matter | Analysis of Colored Components on the Surface of Pills (FTIR)

Other

• Recovery Test of Sodium Dodecylbenzenesulfonate by TOC-LCPH
• 15 Second Screening Analysis of Cyanide in Blood Serum Without Pretreatment
• Technologies for Enhanced LC and SFC Workflow

Method development

• Analysis of Irbesartan Using an Integrated LC System - Nexera-i MT
• Ultra-High Speed Analysis of Ibuprofen by Nexera in Accordance with USP 621
• i-DReC, a New Photodiode Array Detector Function; Impurity Analysis Application
• High-Speed Analysis of Pramipexole following the Draft Guidance of International Harmonization of Pharmacopoeias

Physical Properties and Observations

• Diffusion of Metal into Bone Tissue
• Interactions between Benzoic Acid and Magnesium Oxide
• Melting of Aspirin
• Physical Properties and Observations | Internal Observations of Pills
• Push-Out Test for Pills in Push-Through-Packs
• Strength Testing of Pill Score Marks

Residual Solvents in Pharmaceuticals

• GC Analysis Data Collection for Residual Solvents in Pharmaceuticals
• GCMS Qualitative Analysis of Impurities Detected in Tests for Residual Solvents in Pharmaceuticals
• Simultaneous Analysis of Class 1, 2A and 2B Residual Solvents in Pharmaceuticals via HS-GCMS
• Analysis of Residual Solvents in Pharmaceuticals Using Headspace GC-FID/MS Detector Splitting System
• Analysis of Residual Solvents in Pharmaceuticals by Water-Soluble Samples Using N₂ Carrier
• Analysis of Residual Solvents in Pharmaceuticals by Nexis GC-2030 + HS-20 (JP17 Supplement II, USP 467)
• Analysis of Residual Solvents in Drugs (Headspace GC)
• Measurement of Residual Solvents in Pharmaceuticals by Headspace GC - USP <467> Residual Solvents Procedure A-

• Related Information

Drug development and quality control

• Amino Acid Composition Analysis"Pre-Colum HPLC"
• HPLC Analysis of biomolecules
• Simultaneous Analysis of Cell Culture
• Structural characterization of biomolecules