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LC/MS Analysis of Phospholipids in Milk on Ascentis® Express HILIC after SPE using Supelclean Si, Shotgun HPLC Analysis

LC/MS Analysis of Phospholipids in Milk on Ascentis® Express HILIC after SPE using Supelclean™ Si, Shotgun HPLC Analysis application for HPLC

材料

SPE管或板

产品编号
说明
价格

Supelclean LC-Si 固相萃取管

bed wt. 1 g, volume 6 mL, pkg of 30 ea

分析柱

产品编号
说明
价格

Ascentis® Express HILIC, 2.7 μm HPLC色谱柱

2.7 μm particle size, L × I.D. 15 cm × 4.6 mm

標準品

产品编号
说明
价格

L-α-磷脂酰-L-丝氨酸 来源于大豆

≥97%

鞘髓磷脂

from chicken egg yolk, ≥95%

L-α-磷脂酰胆碱

egg yolk, Type XVI-E, ≥99% (TLC), lyophilized powder

L-α-磷脂酰乙醇胺 来源于鸡蛋黄

Type III, ≥97% (TLC), lyophilized powder

Phosphatidylinositol ammonium salt solution

from soybean, ≥98.0% (TLC)

CONDITIONS

sample/matrix

Phospholipids from 10 mL cow’s milk (Folch method extraction)

SPE tube/cartridge

Supelclean LC-Si, 1 g/6 mL (57051)

condition

hexane

sample addition

1 mL extract in chloroform/methanol (2:1, v/v)

washing

3 mL of hexane/diethylether (8:2, v/v) and 3 mL of hexane/diethylether (1:1, v/v) to remove nonpolar lipids

elution

1 x 4 mL methanol, followed by 1 x 2 mL methanol, followed by 1 x 2 mL chloroform/methanol/water (3:5:2, v/v/v).

eluate post-treatment

dry under a gentle stream of nitrogen, redissolved residue in chloroform/methanol (2:1, v/v)

column

Ascentis Express HILIC, 15 cm x 4.6 mm I.D., 2.7 μm particles (53981-U)

mobile phase

[A] acetonitrile; [B] acetonitrile:water (2:1)

gradient

0% B held for 5 min; to 30% B in 5 min; to 100% B in 20 min; held at 100% B for 10 min; to 0% B in 1 min

flow rate

0.7 mL/min

column temp.

ambient

detector

ELSD. nebulizing gas (nitrogen) flow: 2 mL/min (180 KPa); drift tube temperature: 50 °C

injection

5 μL

说明

分析報告

Extraction of the lipid fraction was carried out from 10 mL of the cow′s milk sample, according to the Folch method to ensure the exhaustive extraction of the whole lipid content. The total extract was evaporated under vacuum, and the final dry residue (400 mg) was re-dissolved in chloroform/methanol 2:1 (v/v). Lipid extract (100 mg) was afterward dissolved in 1 mL mixture of chloroform/methanol (2:1, v/v). After the cartridge has been conditioned with hexane, the non-polar lipids were eluted with 3 mL of hexane/diethyl-ether (8:2, v/v) and 3 mL of hexane/diethyl-ether (1:1, v/v). Recovery of PLs from the cartridge was obtained by two-step elution, using 4 mL of methanol as first extraction solvent, and subsequently 2 mL of methanol followed by 2 mL of chloroform/methanol/water (3:5:2, v/v/v). The recovered fraction was dried under a gentle stream of nitrogen, yielding 49.7 mg dry residue. The residue was finally re-dissolved in chloroform/methanol (2:1, v/v).

法律資訊

Ascentis is a registered trademark of Merck KGaA, Darmstadt, Germany
Supelclean is a trademark of Sigma-Aldrich Co. LLC