2021
DOI: 10.1016/j.aca.2020.11.056
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Rapid determination of tacrolimus and sirolimus in whole human blood by direct coupling of solid-phase microextraction to mass spectrometry via microfluidic open interface

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Cited by 37 publications
(18 citation statements)
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References 47 publications
(76 reference statements)
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“…For applications where SPME is directly coupled to mass spectrometry (SPME-MS) with the aim of achieving rapid analysis, the mass transfer resistance in the extraction phase is a significant issue, as the desorption times used are in the order of seconds (microfluidic open interface and coated blade spray) or lower (probe electrospray ionization). When using a thick extraction phase, it is simply not enough to obtain the best possible desorption efficiency. Therefore, the extraction phase must be modified in response to the increase in surface area; specifically, this modification largely entails carefully optimizing the percentage of sorbent in the extraction phase and reducing the extraction phase thickness.…”
Section: Resultsmentioning
confidence: 99%
“…For applications where SPME is directly coupled to mass spectrometry (SPME-MS) with the aim of achieving rapid analysis, the mass transfer resistance in the extraction phase is a significant issue, as the desorption times used are in the order of seconds (microfluidic open interface and coated blade spray) or lower (probe electrospray ionization). When using a thick extraction phase, it is simply not enough to obtain the best possible desorption efficiency. Therefore, the extraction phase must be modified in response to the increase in surface area; specifically, this modification largely entails carefully optimizing the percentage of sorbent in the extraction phase and reducing the extraction phase thickness.…”
Section: Resultsmentioning
confidence: 99%
“…With regard to instrumental analysis, there are many options for the direct coupling of the SPME probe with analytical instrumentation, particularly mass spectrometers [ 61 ]. A strategy which seems to be specifically suitable for this purpose is the microfluidic open interface, presented lately for the fast monitoring of drugs [ 62 , 63 , 64 ].…”
Section: Discussionmentioning
confidence: 99%
“…The commercial fibers can be directly bought with good repeatability and satisfactory enrichment capacity, which are usually selected for the extraction of VOCs and metabolites with different physicochemical properties. , Hydrophilic–lipophilic balance (HLB) particles have been explored by the group of Prof. Janusz Pawliszyn as novel SPME coating materials, which can be mixed with polyacrylonitrile dimethylformamid to produce bio-SPME fibers. These prepared bio-SPME fibers have been used for the therapeutic drug monitoring of tranexamic acid (TXA) from plasma and urine of patients with chronic renal dysfunction, as well as the rapid determinations of four relevant immunosuppressive drugs (tacrolimus, sirolimus, everolimus, and cyclosporine A) in whole human blood . The emerging functional materials provide a good chance for the steadily enhanced extraction of target analytes in human urine and serum, including perylene diimide-POSS network, chitosan nanocomposite incorporated with polyoxomolibdate nanocluster/graphene oxide, HKUST-1, polypyrrole, magnetic Fe 3 O 4 @MIL-101­(Cr) nanoparticles/polyaniline nanocomposite, and molecularly imprinted polymers. Moreover, the extraction efficiency of self-made SPME fiber can be further enhanced by designing the adsorbents based on the structure property of the target analytes.…”
Section: Spme In Biological Analysismentioning
confidence: 99%