2019
DOI: 10.1016/j.jtemb.2018.09.009
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Quantitative dried blood spot analysis for metallodrugs by laser ablation-inductively coupled plasma-mass spectrometry

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Cited by 17 publications
(9 citation statements)
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“…In this work, in-house solid matrix-matched standards were prepared from uranium-spiked kidney homogenate. Nevertheless, further calibration strategies are found in the literature including the solution-based calibration [27], fabrication xerogel solid calibration standards which are more suitable for the calibration of glasses and silicate matrices [28], the synthesis of metal-spiked polymer films [29], the use of dried droplets or dried matrix spots (DMS) deposited on different substrates [30][31][32][33][34], and the spiking and sectioning of gelatine droplets, whose use has increased noticeably in recent years for the quantitative analysis of biological tissues [35][36][37][38][39][40][41]. For internal standardization, three different approaches are mainly described in the literature for the quantitative elemental imaging of biological samples: (i) the simultaneous nebulization of a standard solution [42], (ii) the use of an element naturally occurring in the sample [43][44][45], and (iii) the addition of an internal standard-spiked layer between the sample and support or on the sample [46][47][48][49][50][51].…”
Section: Introductionmentioning
confidence: 99%
“…In this work, in-house solid matrix-matched standards were prepared from uranium-spiked kidney homogenate. Nevertheless, further calibration strategies are found in the literature including the solution-based calibration [27], fabrication xerogel solid calibration standards which are more suitable for the calibration of glasses and silicate matrices [28], the synthesis of metal-spiked polymer films [29], the use of dried droplets or dried matrix spots (DMS) deposited on different substrates [30][31][32][33][34], and the spiking and sectioning of gelatine droplets, whose use has increased noticeably in recent years for the quantitative analysis of biological tissues [35][36][37][38][39][40][41]. For internal standardization, three different approaches are mainly described in the literature for the quantitative elemental imaging of biological samples: (i) the simultaneous nebulization of a standard solution [42], (ii) the use of an element naturally occurring in the sample [43][44][45], and (iii) the addition of an internal standard-spiked layer between the sample and support or on the sample [46][47][48][49][50][51].…”
Section: Introductionmentioning
confidence: 99%
“…Other approaches for the study of Gd deposition were developed by Löhofer et al [26], which combined MRI and LA-ICP-MS for the detection and quantification of Gadofluorine P deposition in scar formation and myocardial remodeling in the heart after myocardial infarction. Kröger et al [23] employed a dried blood spot method to quantify the metallodrugs gadopentetate and gadoterate.…”
Section: Gadolinium Distributionmentioning
confidence: 99%
“…Other laboratories used LA-ICP-MSI or related techniques to analyze the composition of human kidney stones [54], identify inflammatory hotspots associated with elevated metal quantities in placental tissue from low-birth-weight pregnancy [55], map trace and bulk elements in tumor tissue obtained from an individual previously treated with cisplatin [56], and define contaminations in human hair or teeth resulting from occupational exposure or unfavorable dental fillings [57][58][59]. Likewise, the first studies analyzed element distribution in human eye lenses, brain tissue, or skin biopsies from patients suffering from renal insufficiency [60][61][62], optimized radiodosages in treatment of tumors [63], or determined individual metals or metal-containing contrast agents in human blood or serum [64][65][66][67][68]. In addition, there are many inborn errors of metal and metalloid metabolism human trace elements disorders, in which LA-ICP-MSI offers advantages.…”
Section: Translational Aspects Of La-icp-msimentioning
confidence: 99%