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一般說明
HybridSPE-Phospholipid磷脂去除技术是一种简单且通用的样本制备平台,设计用于在 LC-MS 或 LC-MS/MS 分析之前,从生物血浆和血清中总体去除内源性蛋白和磷脂干扰。首先通过加入和混合酸化乙腈使生物血浆或血清发生蛋白沉淀。然后通过离心除去沉淀蛋白,并将所得上清液上样至 HybridSPE-Phospholipid 96 孔板或固相萃取柱上,其作为化学过滤器,专门靶向去除内源性样品磷脂。截留磷脂的原理是HybridSPE-Phospholipid固定相键合的专有氧化锆离子和所有磷脂都具有的磷酸根发生高度选择性的路易斯酸碱相互作用。得到的洗脱液可立即用于 LC-MS 或 LC-MS-MS 分析。
HybridSPE-Phospholipid 96 孔板和Ultra固相萃取柱有“孔内”/“柱内”沉淀法可供选择。即先将生物血浆/血清加入孔内或柱内,接着加入酸化乙腈(沉淀剂)。短暂混合/涡旋后,抽真空。96孔板和 Ultra固相萃取柱含有一系列低孔隙率疏水滤膜/筛板,这些填充柱床的滤膜/筛板组件作为深层过滤器,有助于在提取过程中同时去除磷脂和沉淀蛋白。标准 HybridSPE-Phospholipid磷脂固相萃取小柱需要采用“离柱”沉淀法。
HybridSPE-Phospholipid 96 孔板和Ultra固相萃取柱有“孔内”/“柱内”沉淀法可供选择。即先将生物血浆/血清加入孔内或柱内,接着加入酸化乙腈(沉淀剂)。短暂混合/涡旋后,抽真空。96孔板和 Ultra固相萃取柱含有一系列低孔隙率疏水滤膜/筛板,这些填充柱床的滤膜/筛板组件作为深层过滤器,有助于在提取过程中同时去除磷脂和沉淀蛋白。标准 HybridSPE-Phospholipid磷脂固相萃取小柱需要采用“离柱”沉淀法。
HybridSPE-磷脂96孔板必需试剂盒,包括以下每种试剂:
- 96孔HybridSPE-磷脂板(575656-U)
- 96方孔收集板,2 mL,聚丙烯
- 96方孔可刺穿的环垫
特點和優勢
- 融合了蛋白质沉淀的简单性和固相萃取(SPE)定向除去磷脂的选择性
- 通过完全除去磷脂和沉淀蛋白,减少离子抑制
- 2-3 步通用流程
- 方法开发最少,甚至不需要方法开发
- 有 96 孔和 1 mL 萃取柱规格可供选择
法律資訊
HybridSPE is a registered trademark of Merck KGaA, Darmstadt, Germany
套裝中的組件也可單獨購買
產品號碼
描述
SDS
- 575656-UHybridSPE®-Phospholipid, 96-well Plate, bed wt. 50 mg, volume 2 mL, pk of 1SDS
- 575655-U96 Square Well Pierceable Cap Mats, configured for sealing Discovery SPE and square well collection plates, pk of 50SDS
- 575653-USPE 96-Deep Square Well Collection Plate, well volume 2 mL, polypropylene, pk of 50SDS
Determination of carboplatin in human plasma using HybridSPE-precipitation along with liquid chromatography-tandam mass spectrometry
Hongliang, J,, et al.
Journal of Chromatography. B, Biomedical Applications, 879 (22), 2162-2170 (2011)
Nora Unceta et al.
Journal of pharmaceutical and biomedical analysis, 70, 529-533 (2012-06-01)
This work proposes a liquid chromatography-electrospray ionization ion trap mass spectrometry (LC-ESI-ITMS) method, for the quantification of sildenafil (SDF), tadalafil (TDF) and vardenafil (VDF) and their metabolites N-desmethylSDF, O-desethylSDF and N-desethylVDF, preceded by a sample preparation step based on protein
C Ferreiro-Vera et al.
Journal of chromatography. A, 1240, 21-28 (2012-04-17)
Fractionation of biological fluids for proper analysis by LC-MS of low-abundance metabolites in the presence of high-abundant endogenous metabolites is of interest, particularly when the latter cause undesirable phenomena such as ionization suppression, as is the case with phospholipids (PLs).
Improved sensitivity of sedimentary phospholipid analysis resulting from a novel extract cleanup strategy
Zhu, Z., et al.
Organic Geochemistry, 65, 46-52 (2013)
Identification and elimination of ion suppression in the quantitative analysis of sirolimus in human blood by LC/ESI-MS/MS
Mano, N., et al.
Journal of Chromatography. B, Biomedical Applications, 879 (13-14), 968-974 (2011)
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