MilliporeSigma
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52798-U

Supelco

HybridSPE®-Phospholipid

Small Volume 96-well Plate, bed wt. 15 mg, volume 0.8 mL, pk of 20

NACRES:
NB.21

Quality Level

form

solid

composition

bed wt., 15 mg

packaging

pk of 20

technique(s)

solid phase extraction (SPE): suitable

volume

0.8 mL

matrix active group

zirconia-based phase

application(s)

food and beverages

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This Item
52794-U575657-U575656-U
HybridSPE®-Phospholipid Small Volume 96-well Plate, bed wt. 15 mg, volume 0.8 mL, pk of 20

Supelco

52798-U

HybridSPE®-Phospholipid

HybridSPE®-Phospholipid Small Volume 96-well Plate, bed wt. 15 mg, volume 0.8 mL, pk of 1

Supelco

52794-U

HybridSPE®-Phospholipid

HybridSPE®-Phospholipid 96-well Plate, bed wt. 50 mg, volume 2 mL, pk of 20

Supelco

575657-U

HybridSPE®-Phospholipid

HybridSPE®-Phospholipid 96-well Plate, bed wt. 50 mg, volume 2 mL, pk of 1

Supelco

575656-U

HybridSPE®-Phospholipid

packaging

pk of 20

packaging

pk of 1

packaging

pk of 20

packaging

pk of 1

technique(s)

solid phase extraction (SPE): suitable

technique(s)

solid phase extraction (SPE): suitable

technique(s)

solid phase extraction (SPE): suitable

technique(s)

solid phase extraction (SPE): suitable

matrix active group

zirconia-based phase

matrix active group

zirconia-based phase

matrix active group

zirconia-based phase

matrix active group

zirconia-based phase

application(s)

food and beverages

application(s)

-

application(s)

-

application(s)

-

form

solid

form

-

form

solid

form

solid

General description

HybridSPE-Phospholipid technology is a simple and generic sample prep platform designed for the gross level removal of endogenous protein and phospholipid interferences from biological plasma and serum prior to LC-MS or LC-MS/MS analysis. Biological plasma or serum is first subjected to protein precipitation via the addition and mixing of acidified acetonitrile. Precipitated proteins are then removed by centrifugation and the resulting supernatant is loaded on the HybridSPE-Phospholipid 96-well plate or cartridge which acts as a chemical filter that specifically targets the removal of endogenous sample phospholipids. The phospholipid retention mechanism is based on a highly selective Lewis acid-base interaction between the proprietary zirconia ions functionally bonded to the HybridSPE-Phospholipid stationary phase and the phosphate moiety consistent with all phospholipids. The resulting eluent is ready for immediate LC-MS or LC-MS-MS analysis.

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.

Features and Benefits

  • 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

Legal Information

HybridSPE is a registered trademark of Sigma-Aldrich Co. LLC

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Pankaj K Kanaujia et al.
Journal of chromatography. A, 1218(38), 6612-6620 (2011-08-25)
Selective extraction and enrichment of nerve agent degradation products has been achieved using zirconia based commercial solid-phase extraction cartridges. Target analytes were O-alkyl alkylphosphonic acids and alkylphosphonic acids, the environmental markers of nerve agents such as sarin, soman and VX.
A high-throughput method for liquid chromatography-tandem mass spectrometry determination of plasma alkylresorcinols, biomarkers of whole grain wheat and rye intake
Ross, A.B., et al.
Analytical Biochemistry, 499, 1-7 (2016)
Development and validation of an HPLC-MS/MS method to determine clopidogrel in human plasma. Use of incurred samples to test back-conversion
Silvestro, L., et al.
Journal of Chromatography. B, Biomedical Applications, 878 (30), 3134-3142 (2010)
Quantitative determination of capecitabine and its six metabolites in human plasma using liquid chromatography coupled to electrospray tandem mass spectrometry
Deenen, M, et al.
Journal of Chromatography. B, Biomedical Applications, 913-914, 30-40 (2013)
Solid-phase extraction of phosphorous-containing amino acid herbicides from biological specimens with a zirconia-coated silica cartridge
Watanabe, D., et al.
Journal of Chromatography. B, Biomedical Applications, 969, 69-76 (2014)

Articles

Ion-Suppression & Phospholipid Contamination

We are presenting an article focusing on ion-suppression and phospholipid contamination and some of their major causes and difficulties.

Protocols

Enrichment of Phospholipids in Biological Samples Using HybridSPE-PL

A simple method to enrich phospholipids from plasma samples, involving a HybridSPE-PPT 96-well plate that both retains phospholipids and removes precipitated proteins.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service