material
metal alloy fiber, plain red hub
needle size
22 ga
packaging
pkg of 5 ea
df
45 μm (C18)
technique(s)
solid phase microextraction (SPME): suitable
needle L
25 mm (1 in.)
matrix active group
C18 coating
application(s)
food and beverages
compatibility
for use with solvent desorption
separation technique
reversed phase
General description
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。
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
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
In Vivo Sampling of Environmental Organic Contaminants in Fish by Solid-Phase Microextraction
Zhang, X., et al.
TrAC, Trends in Analytical Chemistry, 32, 31-39 (2012)
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
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)
商品
Biocompatible SPME devices employ C18 bonded porous silica sorbent particles, in a binder which resists fouling by biological matrix components
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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A demonstration of the use of innovative BioSPME fibers for the selective extraction of drugs and polar metbolites from biological matrices.
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