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1.
Biomed Res Int ; 2021: 6800294, 2021.
Article in English | MEDLINE | ID: mdl-34746306

ABSTRACT

The main dose-limiting side effect of cisplatin is nephrotoxicity. The utilization of cisplatin is an issue of balancing tumour toxicity versus platinum-induced nephrotoxicity. In this study, we focused on intraorgan distribution of common essential trace elements zinc, copper, and iron in healthy mouse kidneys and distribution of platinum after cisplatin treatment. Renal distribution in 12 nontreated Nu-Nu mice (males) was assessed by laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). Furthermore, 9 Nu-Nu mice were treated with cisplatin. The order of elements concentration in kidneys was as follows: Fe > Zn > Cu. All three metals showed the higher concentrations at the cortex and medulla (28.60, 3.35, and 93.83 µg/g for Zn, Cu, and Fe, respectively) and lower concentration at the pelvis and the urinary tract (20.20, 1.93, and 62.48 µg/g for Zn, Cu, and Fe, respectively). No statistically significant difference between cortex and medulla was observed for these elements. After platinum treatment, the concentration of platinum in kidneys was enhanced more than 60-times, p < 0.001. Platinum significantly showed the highest accumulation in cortex (2.11 µg/g) with a gradient distribution. Platinum was less accumulated in medulla and pelvis than in cortex, and the lowest accumulation occurred in the urinary tract (1.13 µg/g). Image processing has been successfully utilized to colocalize metal distribution using LA-ICP-MS and histological samples images.


Subject(s)
Cisplatin/toxicity , Kidney/metabolism , Kidney/pathology , Animals , Cisplatin/adverse effects , Cisplatin/pharmacology , Copper/analysis , Humans , Iron/analysis , Kidney/drug effects , Male , Mass Spectrometry/methods , Mice , Mice, Nude , PC-3 Cells , Platinum/analysis , Spectrum Analysis/methods , Zinc/analysis
2.
Molecules ; 26(3)2021 Jan 26.
Article in English | MEDLINE | ID: mdl-33530345

ABSTRACT

Immunochemical methods are used not only in clinical practice for the diagnosis of a wide range of diseases but also in basic and advanced research. Based on the unique reaction between the antibody and its respective antigens, it serves to specifically recognize target molecules in biological complex samples. Current methods of labelling antibodies with elemental labels followed by detection by inductively coupled plasma mass spectrometry (ICP-MS) allow detection of multiple antigens in parallel in a single analysis. Using the laser ablation (LA) modality (LA-ICP-MS), it is also possible to monitor the spatial distribution of biogenic elements. Moreover, the employment of metal nanoparticle-labeled antibodies expands the applicability also to molecular imaging by LA-ICP-MS. In this work, conjugates of model monoclonal antibody (DO-1, recognizing p53 protein) with various metal nanoparticles-based labels were created and utilized in dot-blot analysis in order to compare their benefits and disadvantages. Based on experiments with the p53 protein standard, commercial kits of gold nanoparticles proved to be the most suitable for the preparation of conjugates. The LA-ICP-MS demonstrated very good repeatability, wide linear dynamic range (0.1-14 ng), and limit of detection was calculated as a 1.3 pg of p53 protein.


Subject(s)
Antibodies, Monoclonal/pharmacology , Cadmium/chemistry , Europium/chemistry , Gold/chemistry , Silver/chemistry , Antibodies, Monoclonal/chemistry , Humans , Immunoblotting , Lasers , Limit of Detection , Mass Spectrometry , Metal Nanoparticles/chemistry , Quantum Dots/chemistry , Tumor Suppressor Protein p53/antagonists & inhibitors
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