| Molecular Formula | C52H100NO8P |
|---|---|
| Molecular Weight | 898.3 |
| InChI Key | SDEURMLKLAEUAY-JFSPZUDSSA-N |
| LogP | 18.1 |
| Synonyms |
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Applications:
ELSD-HPLC Method for Analysis of Phospholipids on Lipak Colulm
November 22, 2024
ELSD-HPLC Method for Phospholipids on Lipak by SIELC Technologies
High Performance Liquid Chromatography (HPLC) Method for Analysis of DEPC, DSPG
Phospholipids are vital components of cell membranes, playing key roles in cell signaling, energy storage, and protective functions. They are essential for maintaining cellular structure and function, making them crucial in biological processes and industrial applications such as drug delivery and cosmetic formulations.
Over time, phospholipids can degrade into various biologically active products, including lysophospholipids and fatty acids, which are involved in cellular signaling and inflammation. Monitoring both phospholipids and their degradation products provides valuable insights into metabolic health, lipid metabolism, and the stability of lipid-based formulations.
Our high-resolution chromatograms ensure accurate and reliable analysis of both phospholipids and their degradation products, supporting applications in clinical diagnostics, pharmaceuticals, and food quality control.
Furosemide can be retained, and analyzed using a Lipak mixed-mode stationary phase column. The analysis utilizes an gradient method with a simple mobile phase consisting of water, methanol (MeOH), ammonium formate and formic acid as a buffer. Detection is achieved using ELSD
| Column | Lipak, 4.6 x 150 mm, 5 µm, 100 A |
| Mobile Phase | Gradient MeOH –90-100% 20 min, 10 min hold |
| Buffer | AmFm– 10 mM, FA – 0.05% |
| Flow Rate | 1.0 ml/min |
| Detection | ELSD, the nebulizer and evaporator temperatures 40°C, with a gas flow rate of 1.6 Standard Liters per Minute (SLM) |
Application Column
DSPG
