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HPLC Analysis of Dermorphin in Horse Plasma on Ascentis® Express F5 after SPE with HybridSPE®

HPLC Analysis of Dermorphin in Horse Plasma on Ascentis® Express F5 after SPE with HybridSPE® application for HPLC, application for SPE

Materials

analytical column

Product No.
Description
Pricing

Ascentis® Express F5, 2.7 μm HPLC Column

2.7 μm particle size, L × I.D. 10 cm × 2.1 mm

CONDITIONS

sample preparation

SPE (Solid Phase Extraction)

sample/matrix

horse plasma spiked at 10 μg/mL

SPE tube/cartridge

[TM"HybridSPE"]-Phospholipid Plate, 50mg/96-Well (575656-U)

sample addition

3:1, (1% formic acid in acetonitrile); plasma

column

Ascentis Express F5, 10 cm x 2.1 mm I.D., 2.7 μm particles (53569-U)

mobile phase

[A] acetonitrile [B] 20 mM ammonium formate; (90:10, A:B); pH 4.5 with formic acid, after mixing A & B

flow rate

0.4 mL/min

pressure

1305 psi (90 bar)

column temp.

35 °C

detector

MS, ESI(+), TIC, m/z 100-1000

injection

1 μL

Description

Analysis Note

Dermorphin is a natural heptapeptide opioid. Because of poor recovery from horse plasma following protein precipitation, alternate methods of extraction are sought. While the HybridSPE protocol successfully removes proteins and phospholipids, dermorphin solubility in plasma remains a limitation. Dermorphin is effectively retained on the pentafluorophenyl phase under aqueous normal phase conditions.

Legal Information

Ascentis is a registered trademark of Merck KGaA, Darmstadt, Germany
HybridSPE is a registered trademark of Merck KGaA, Darmstadt, Germany