55267-U
HybridSPE®-Phospholipid solid phase extraction (SPE) Cartridge
Cartridge, bed wt. 500 mg, volume 6 mL, pk of 30
Synonyme(s) :
HybridSPE (phospholipid and protein removal) 96-well plate, 15 mg
About This Item
Produits recommandés
product name
HybridSPE®-Phospholipid, Cartridge, bed wt. 500 mg, volume 6 mL, pk of 30
Matériaux
PE frit (20/40 μm)
polypropylene hardware
Gamme de produits
HybridSPE®
Composition
bed wt., 500 mg
Conditionnement
pk of 30
Technique(s)
solid phase extraction (SPE): suitable
Volume
6 mL
Groupe de la matrice active
zirconia-based phase
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Catégories apparentées
Description générale
The "In-well" and "In-cartridge" precipitation methods are available for the HybridSPE-Phospholipid 96-well version and HybridSPE-Phospholipid Ultra cartridge in which biological plasma/serum is first added to either the well or cartridge, followed by acidified acetonitrile (precipitation agent). After a brief mixing/vortexing step, vacuum is applied. Because the 96-well and Ultra cartridge versions contain a series of low porosity hydrophobic filters/frits, the packed-bed filter/frit assembly acts as a depth filter facilitating the concurrent removal of both phospholipids and precipitated proteins during the extraction process. Standard HybridSPE-Phospholipid cartridges require an "off-line" precipitation method.
Application
- Rapid analysis of 65 pharmaceuticals and 7 personal care products in plasma and whole-body tissue samples of fish using acidic extraction, zirconia-coated silica cleanup, and liquid chromatography-tandem mass spectrometry.: This study presents a method incorporating HybridSPE-Phospholipid for efficient cleanup in the analysis of various substances in biological matrices, showcasing its application in environmental toxicology (Tanoue et al., 2020).
- Multi LC-MS/MS and LC-HRMS Methods for Determination of 24 Mycotoxins including Major Phase I and II Biomarker Metabolites in Biological Matrices from Pigs and Broiler Chickens.: Demonstrates the use of HybridSPE-Phospholipid in multi-residue mycotoxin analysis, enhancing the detection capabilities in complex sample matrices (Lauwers et al., 2019).
- Liquid chromatography mass spectrometry determination of perfluoroalkyl acids in environmental solid extracts after phospholipid removal and on-line turbulent flow chromatography purification.: Explores the effectiveness of HybridSPE-Phospholipid in removing interfering substances from environmental samples, aiding in the accurate analysis of perfluoroalkyl substances (Mazzoni et al., 2016).
- Development and validation of a liquid chromatography-tandem mass spectrometry method for the quantitative determination of gamithromycin in animal plasma, lung tissue and pulmonary epithelial lining fluid.: Illustrates the adaptability of HybridSPE-Phospholipid in veterinary medicine for quantifying antibiotics, ensuring precision in therapeutic monitoring (De Baere et al., 2015).
Caractéristiques et avantages
- Merges the simplicity of protein precipitation and the selectivity of SPE via the targeted removal of phospholipids
- Reduce ion-suppression through the complete removal of phospholipids and precipitated proteins
- 2-3 step generic procedure
- Minimal to no method development
- Available in 96-well and 1 mL cartridge dimensions
Informations légales
Produit(s) apparenté(s)
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
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Les clients ont également consulté
Articles
This Sigma-Aldrich article continues to detail new methodology for the analysis of Vitamin D metabolites using HybridSPE-Phospholipid technology.
An article focusing on ion-suppression and phospholipid contamination and some of their major causes and difficulties.
This Sigma-Aldrich article discusses how the HybridSPE-Phospholipid Technology works and how the phospholipids are removed.
Protocoles
A simple method to enrich phospholipids from plasma samples, involving a HybridSPE-PPT 96-well plate that both retains phospholipids and removes precipitated proteins.
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