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Merck
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57281-U

Supelco

SPME LC 光纤探针，C18

df 45 μm(C18, pkg of 5 ea

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About This Item

分類程式碼代碼:
41115724
NACRES:
NB.21

材料

metal alloy fiber
plain red hub

針尺寸

22 ga

包裝

pkg of 5 ea

df

45 μm (C18)

技術

solid phase microextraction (SPME): suitable

針長

25 mm (1 in.)

基質活性組

C18 coating

應用

food and beverages

相容性

for use with solvent desorption

分離技術

reversed phase

一般說明

该固相微萃取-液相色谱萃取探针作为一次性设备用于在溶剂解吸和液相色谱分析之前从液体中萃取小分子。

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Barbara Bojko et al.
Analytica chimica acta, 803, 75-81 (2013-11-13)
Metabolomics and biomarkers discovery are an integral part of bioanalysis. However, untargeted tissue analysis remains as the bottleneck of such studies due to the invasiveness of sample collection, as well as the laborious and time-consuming sample preparation protocols. In the
Florin Marcel Musteata et al.
Journal of pharmaceutical and biomedical analysis, 47(4-5), 907-912 (2008-05-13)
Pharmacokinetic (PK) studies in rats typically involve removal of serial blood samples following dosing. This research illustrates the development of a fast in vivo microextraction technique that has the potential to partly replace current sampling techniques based on blood draws
Joanne Chung Yan Yeung et al.
Analytica chimica acta, 665(2), 160-166 (2010-04-27)
The success of in vivo solid phase microextraction (SPME) depends significantly on the selection of calibration method. Three kinetic in vivo SPME calibration methods are evaluated in this paper: (1) on-fibre standardization (OFS), (2) dominant pre-equilibrium desorption (DPED), and (3)
Dajana Vuckovic et al.
Journal of chromatography. A, 1217(25), 4041-4060 (2009-12-25)
The primary objective of this review is to discuss recent technological developments in the field of solid-phase microextraction that have enhanced the utility of this sample preparation technique in the field of bioanalysis. These developments include introduction of various new
Xu Zhang et al.
Journal of chromatography. A, 1216(45), 7664-7669 (2009-09-22)
Solid-phase microextraction (SPME) has been demonstrated to be useful for in vivo sampling in pharmacokinetic studies. In this study, a single time-point kinetic calibration for in vivo dynamic monitoring was developed by simplification of the laborious multiple time-point kinetic calibration
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Biocompatible SPME devices employ C18 bonded porous silica sorbent particles, in a binder which resists fouling by biological matrix components

Rapid Determination of Protein Binding Affinity Using Solid Phase Microextraction

Accurate protein binding affinities were measured using bioSPME more rapidly than membrane dialysis (RED) techniques. Binding affinities correlated to the reference values.

相关内容

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Biocompatible SPME devices employ C18 bonded porous silica sorbent particles, in a binder which resists fouling by biological matrix components

Rapid Determination of Protein Binding Affinity Using Solid Phase Microextraction

Accurate protein binding affinities were measured using bioSPME more rapidly than membrane dialysis (RED) techniques. Binding affinities correlated to the reference values.

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