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Identification of Drug Degradation Products in Pharmaceutical Formulations by Liquid Chromatography-Mass Spectrometry (LC-MS) (CAT#: STEM-CT-1631-CJ)

Introduction

Degradation products are unwanted chemicals that can develop during the manufacturing, transportation, and storage of drug products and can affect the efficacy of pharmaceutical products.




Principle

Liquid chromatography (LC) is a technique widely used to separate compounds from a sample prior to analysis and is frequently coupled to mass spectrometry (MS). With LC, separation of the sample components is based on the interactions of the compounds with the mobile and stationary phases, and the degree of compound separation is related to each compound's affinity for the mobile phase. Following chromatographic separations, compounds elute off of the column, desolvated into the gas phase and ionized at an ionization source, and are then introduced into the mass spectrometer for mass analysis.

Applications

Biomedical; Biopharmaceuticals

Procedure

1. Sample Collection
2. Sample Preparation
3. Standardization and Calibration
4. Chromatographic Separation and Analysis

Materials

• Sample: Blood; Urine; Plasma; Crops; Livestock tissues; Milk; Eggs; Soil; Water; Sediment; Nucleotides; Peptides; Steroids; Hormones; Dyes; Fatty acids; Alcohols
• Equipment: Liquid-phase separation system; Mass spectrometer; Liquid chromatograph mass spectrometers
• LC-MS grade water; Acetonitrile
• Ion pairing agents: Trifluoroacetic acid (TFA); Formic acid (FA); Heptafluorobuteric acid (HFBA)

Notes

1. LC-MS is a dominant analytical technique that has a very high accuracy, sensitivity, and specificity.
2. Although known for its key features in providing rapid analysis of complex mixtures and quality performance, LC-MS is an expensive instrument.