2020
DOI: 10.1016/j.aca.2020.09.016
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Copper nanoparticles for SERS-based determination of some cephalosporin antibiotics in spiked human urine

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Cited by 36 publications
(19 citation statements)
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“…Therapeutic drug monitoring (TDM) involves assessing the drug concentration in a biological matrix (most commonly plasma or serum) at a known time related to administration and interpreting these concentrations in terms of relevant clinical parameters (target range and pharmacokinetics of the drug) (Jaworska et al, 2016). In TDM experiments, the easiest approach is simply to investigate the recorded SERS spectra of the body fluid (urine, blood, and blood plasma) that contains the drug of interest and monitor the intensity of the bands assigned to that drug (Markina et al, 2020). Unfortunately, due to the complexity of the sample, this procedure requires a bit of luck as spectral signatures of the drug are not necessarily seen in the recorded spectra because of the interference from the signals from the body fluid.…”
Section: Therapeutic Drug Monitoringmentioning
confidence: 99%
“…Therapeutic drug monitoring (TDM) involves assessing the drug concentration in a biological matrix (most commonly plasma or serum) at a known time related to administration and interpreting these concentrations in terms of relevant clinical parameters (target range and pharmacokinetics of the drug) (Jaworska et al, 2016). In TDM experiments, the easiest approach is simply to investigate the recorded SERS spectra of the body fluid (urine, blood, and blood plasma) that contains the drug of interest and monitor the intensity of the bands assigned to that drug (Markina et al, 2020). Unfortunately, due to the complexity of the sample, this procedure requires a bit of luck as spectral signatures of the drug are not necessarily seen in the recorded spectra because of the interference from the signals from the body fluid.…”
Section: Therapeutic Drug Monitoringmentioning
confidence: 99%
“…For example, the authors demonstrated that the modification with β-CD-SH does not enable elimination of the negative effect of some metabolites (creatinine and corticosterone) which remarkably compete with the target analyte reducing its SERS signal. However, because the analysis of body fluids by SERS is really a challenging task due to strong competitive interactions with intrinsic body fluid components [ 5 , 7 ], more studies in this direction (particularly with real samples) are required before concluding the suitability of CD-SERS assays for such analysis and capability of CDs to improve selectivity.…”
Section: Analytical Performancementioning
confidence: 99%
“…Low selectivity significantly restricts application of SERS for analysis of complex mixtures such as body fluids, and several approaches have been proposed to overcome this limitation. The simplest one is the adjustment of pH, ionic strength, and/or dielectric constant of the analyzed solution to maximize interaction of analyte molecules with SERS substrate and minimize such interaction for admixtures [3][4][5]. The next approach implies preliminary separation of the analyte by chromatographic separation or by solid-phase/ liquid-liquid extraction [6][7][8].…”
Section: Introductionmentioning
confidence: 99%
“…The SERS enhancement mostly relies on the amplification of the electromagnetic field-i.e., electromagnetic (EM) hot spots generated by the excitation of the localized surface plasmon resonance (LSPR) of the metal nanostructures [17]. Therefore, plasmonic metallic nanostructures including Au, Ag, and Cu have been fabricated to prepare an excellent SERS substrate for sensing molecules [18][19][20]. Designing and optimizing the geometry of a plasmonic nanostructure, such as its size [21], sharp corners [22], tips [23], surface roughness [24], and interparticle gaps [25], is essential in order to provide a strong EM hotspot and hence enhance SERS signal intensities.…”
Section: Introductionmentioning
confidence: 99%