Microextraction versus exhaustive extraction approaches for simultaneous analysis of compounds in wide range of polarity

2013-11-05
Mirnaghi, Fatemeh S.
Gorynski, Krzysztof
Rodriguez-Lafuente, Angel
Boyacı, Ezel
Bojko, Barbara
Pawliszyn, Janusz
This article discusses comparison of microextraction versus exhaustive extraction approaches for simultaneous extraction of compounds in wide range of polarity at low and high volumes of sample by comparing solid phase extraction (SPE) and solid phase microextraction (SPME). Here, both systems are discussed theoretically and evaluated based on experimental data. Experimental comparisons were conducted in terms of extraction recovery, sensitivity, and selectivity for the extraction of doping agent compounds (logP: 0.14-4.98), using C18 as the extraction phase. The extraction recovery of both systems was studied at different volumes of phosphate buffered saline (PBS). The distribution constant of SPME in thin-film geometry (i.e., thin-film microextraction/TFME) as well as the retention factor and breakthrough volume for the SPE system were evaluated for the simultaneous extraction of polar and non-polar compounds. Using 1 mL of sample, the extraction recovery and sensitivity of the SPE system (100 mg sorbent) was comparable with that of TFME format of SPME (15 mg sorbent) for all analytes, with the exception of most polar compounds, due to the smaller amount of the extraction phase in SPME. Breakthrough in the SPE system was observed for more polar compounds in a 25 mL sample; however, this situation did not affect the quantitation of TFME, as this technique operates in equilibrium mode. Experimental values for breakthrough volume were in good match with the calculated theoretical values. Results indicate that the microextraction approach is more suitable for untargeted determinations, where the breakthrough volume cannot be determined prior to the experiment. In addition, when both methods are at optimum conditions, findings suggest that, despite the smaller volume of the extraction phase in TFME, the sensitivity of TFME can exceed that of SPE for samples where the target analytes vary substantially in polarity.
JOURNAL OF CHROMATOGRAPHY A

Suggestions

Pressure Dependence of the Raman Modes Related to the Phase Transitions in Cyclohexane
Yurtseven, Hasan Hamit (2015-03-01)
The pressure dependence of the Raman frequencies for the v(21) mode is studied by using the volume data at room temperature close to the transitions among the phases of III, IV and V in cyclohexane. By determining the pressure dependence of the mode Gruneisen parameter gamma T in the phases and taking the average values, the Raman frequencies of those modes associated with the phase transitions are predicted through the volume data in cyclohexane. Our predicted Raman frequencies agree with those observed ex...
Single pellet reactor for the dynamic analysis of gas-solid reactions ''reaction of SO2 with activated soda''
Kopac, T; Dogu, G; Doğu, Timur (1996-05-01)
Single-pellet moment technique which was initially proposed for the measurement of effective diffusivities in porous catalysts and adsorption rate and equilibrium constants was modified for the analysis of gas-solid reactions. In this technique dynamic version of the Wicke-Kallenbach single-pellet cell was used A pulse of a tracer gas was introduced into stream flowing over one end face of the pellet. In the modified pulse-double response procedure, experimental moments of the response peaks of both reactan...
Photoexcitation Dynamics in Films of C-60 and Zn Phthalocyanine with a Layered Nanostructure
Lane, Paul A.; Cunningham, Paul D.; Melinger, Joseph S.; Kushto, Gary P.; Esentürk, Okan; Heilweil, Edwin J. (2012-02-15)
We elucidate photoexcitation dynamics in C-60 and zinc phthalocyanine (ZnPc) from picoseconds to milliseconds by transient absorption and time-resolved terahertz spectroscopy. Autoionization of C-60 is a precursor to photocarrier generation. Decay of the terahertz signal is due to decreasing photocarrier mobility over the first 20 ps and thereafter reflects recombination dynamics. Singlet diffusion rates in C-60 are determined by modeling the rise of ground state bleaching of ZnPc absorption following C-60 ...
Rapid ionic liquid-supported nano-hybrid composite reinforced hollow-fiber electromembrane extraction followed by field-amplified sample injection-capillary electrophoresis: An effective approach for extraction and quantification of Imatinib mesylate in human plasma
Forough, Mehrdad; Farhadi, Khalil; Eyshi, Ali; Molaei, Rahim; Khalili, Hedayat; Kouzegaran, Vahid Javan; Matin, Amir Abbas (2017-09-01)
The focus of this study is development of a new, convenient, rapid and sensitive electromembrane extraction approach (based on an ionic liquid-supported MWCNTs/ZnO reinforced hollow fiber, for the first time) as an off-line sample clean-upipreconcentration method coupled with capillary electrophoresis (CE-UV) using field-amplified sample injection (FASI) for quantification of Imatinib mesylate in human plasma. The nano-hybrid sorbent, coated by 1-octyl-3-methylimidazolium bromide ionic liquid (E0M1m]Br) in ...
Synthesis and characterization of poly(dibromophenylene oxide)s through thermal decomposition of various transition metal complexes in solid state.
Şanlı, Pınar; Kısakürek, Duygu; Aras, Leyla; Department of Chemistry (2002)
In this study, synthesis and characterization of poly(dibromophenylene oxide)s though thermal decomposition of bis(2,4,6-tribromophenolato)di(N- methyl imidazole) Cu(II), bis(2,4,6-tribromophenolato)di(N-methyl illimidazole)Co(II) and bis(2,4,6-tribromophenolato)di(N-methyl imidazole)Ni(II) complexes in solid state was examined. For the characterization of complexes FTIR, DSC, mass spectroscopy, magnetic susceptibility and C, H,N elemental analysis were performed. Syntheses of the polymer were achieved by t...
Citation Formats
F. S. Mirnaghi, K. Gorynski, A. Rodriguez-Lafuente, E. Boyacı, B. Bojko, and J. Pawliszyn, “Microextraction versus exhaustive extraction approaches for simultaneous analysis of compounds in wide range of polarity,” JOURNAL OF CHROMATOGRAPHY A, pp. 37–43, 2013, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/36658.