The elemental changes occurring in the rat liver after exposure to PEG-coated iron oxide nanoparticles: total reflection x-ray fluorescence (TXRF) spectroscopy study
Abstract:The main goal of this study was to evaluate in vivo effects of low dose of PEG-coated magnetic iron oxide nanoparticles (IONPs) on the rat liver. The IONPs was intravenously injected into rats at a dose equaled to 0.03 mg of Fe per 1 kg of an animal body weight. The elemental composition of liver tissue in rats subjected to IONPs action and controls were compared. Moreover, in order to determine the dynamics of nanoparticles (NPs) induced elemental changes, the tissues taken from animals 2 hours, 24 hours, and… Show more
“…The most common techniques used today for the quantification of Cu and Fe from biological samples in vitro and ex vivo include inductive coupling plasma mass spectrometry (ICP-MS) [209][210][211][212], atomic absorption spectrometry (AAS) [212,213], total reflection X-ray fluorescence (TXRF) [214,215], and colorimetric assays by UV-Vis measurements [216,217]. ICP-MS is a highly sensitive tool that allows the precise quantification of metal content down to sub parts per billion (ppb) levels using internal standards [218,219].…”
Section: Techniques To Quantify Cu and Fe Levelsmentioning
A very promising direction in the development of anticancer drugs is inhibiting the molecular pathways that keep cancer cells alive and able to metastasize. Copper and iron are two essential metals that play significant roles in the rapid proliferation of cancer cells and several chelators have been studied to suppress the bioavailability of these metals in the cells. This review discusses the major contributions that Cu and Fe play in the progression and spreading of cancer and evaluates select Cu and Fe chelators that demonstrate great promise as anticancer drugs. Efforts to improve the cellular delivery, efficacy, and tumor responsiveness of these chelators are also presented including a transmetallation strategy for dual targeting of Cu and Fe. To elucidate the effectiveness and specificity of Cu and Fe chelators for treating cancer, analytical tools are described for measuring Cu and Fe levels and for tracking the metals in cells, tissue, and the body.
“…The most common techniques used today for the quantification of Cu and Fe from biological samples in vitro and ex vivo include inductive coupling plasma mass spectrometry (ICP-MS) [209][210][211][212], atomic absorption spectrometry (AAS) [212,213], total reflection X-ray fluorescence (TXRF) [214,215], and colorimetric assays by UV-Vis measurements [216,217]. ICP-MS is a highly sensitive tool that allows the precise quantification of metal content down to sub parts per billion (ppb) levels using internal standards [218,219].…”
Section: Techniques To Quantify Cu and Fe Levelsmentioning
A very promising direction in the development of anticancer drugs is inhibiting the molecular pathways that keep cancer cells alive and able to metastasize. Copper and iron are two essential metals that play significant roles in the rapid proliferation of cancer cells and several chelators have been studied to suppress the bioavailability of these metals in the cells. This review discusses the major contributions that Cu and Fe play in the progression and spreading of cancer and evaluates select Cu and Fe chelators that demonstrate great promise as anticancer drugs. Efforts to improve the cellular delivery, efficacy, and tumor responsiveness of these chelators are also presented including a transmetallation strategy for dual targeting of Cu and Fe. To elucidate the effectiveness and specificity of Cu and Fe chelators for treating cancer, analytical tools are described for measuring Cu and Fe levels and for tracking the metals in cells, tissue, and the body.
“…Wrobel et al [24] combine TXRF with μXRF for quantitative Fe, Cu, and Zn imaging in rat kidney, spleen, and liver tissues. Matusiak et al [23] apply TXRF for Ca, Fe, Cu, and Zn quantification in rat liver tissues. However, for the latter, no validation experiments are given.…”
Section: Analytical Figures Of Merit and Comparison With Other Methodsmentioning
confidence: 99%
“…Furthermore, TXRF is costeffective and does not require any gas or cooling media. Examples for valid trace determination by TXRF cover a broad variety of different biological samples, from isolated proteins and nuclei acids to fluids, cells, bacteria, hair, and tissues such as the liver, placenta, chest, kidney, lung, prostate, or colon [2,13,[20][21][22][23][24][25][26][27][28][29][30][31][32][33]. Besides the above-mentioned advantages, highly convenient and reliable multi-element quantification can be performed by adding an internal standard for a one-point calibration [20,21,27,30,31].…”
Trace elements are essential for life and their concentration in cells and tissues must be tightly maintained and controlled to avoid pathological conditions. Established methods to measure the concentration of trace elements in biological matrices often provide only single element information, are time-consuming, and require special sample preparation. Therefore, the development of straightforward and rapid analytical methods for enhanced, multi-trace element determination in biological samples is an important and raising field of trace element analysis. Herein, we report on the development and validation of a reliable method based on total reflection X-ray fluorescence (TXRF) analysis to precisely quantify iron and other trace metals in a variety of biological samples, such as the liver, parenchymal and non-parenchymal liver cells, and bone marrow-derived macrophages. We show that TXRF allows fast and simple one-point calibration by addition of an internal standard and has the potential of multi-element analysis in minute sample amounts. The method was validated for iron by recovery experiments in homogenates in a wide concentration range from 1 to 1600 μg/L applying well-established graphite furnace atomic absorption spectrometry (GFAAS) as a reference method. The recovery rate of 99.93 ± 0.14% reveals the absence of systematic errors. Furthermore, the standard reference material "bovine liver" (SRM 1577c, NIST) was investigated in order to validate the method for further biometals. Quantitative recoveries (92-106%) of copper, iron, zinc, and manganese prove the suitability of the developed method. The limits of detection for the minute sample amounts are in the low picogram range. Keywords Total reflection X-ray fluorescence spectrometry. Iron trace analysis. Biometal trace analysis. Bone marrow-derived macrophages. Liver cells. Liver tissues Published in the topical collection featuring Female Role Models in Analytical Chemistry.
“…As an internal standard, gallium solution in concentration of 10 ppm was used at 0.3 ml per 1 ml of digested tissue sample. A detailed protocol of the whole procedure can be found elsewhere [20,22].…”
Section: Experimental Animals and Sample Preparationmentioning
confidence: 99%
“…The evidence gained through such a study points out that IONPs may accumulate within organs such as liver, brain, heart, or kidneys, leading to transient histopathological and functional changes [11][12][13][14][15][16][17]. One of the possible ways to obtain information about the biodistribution and biokinetics of IONPs as well as the range of their effects is exploration of elemental changes occurring in organs of NPs-treated animals [9,[18][19][20][21][22]. In combination with multivariate statistical analyses, this approach may allow to determine elemental markers of biological effects following exposure to nanoparticles.…”
The systemic influence of iron oxide nanoparticles on the elemental homeostasis of key organs was examined in male rats. In tissues taken at different intervals from nanoparticles injection, the dynamics of elemental changes was analyzed. The organ metallome was studied using total reflection X-ray fluorescence. The obtained data were processed with advanced cluster and discriminant analyses-to classify the tissues according to their organs of origin and to distinguish accurately the nanoparticletreated and normal rats. Additionally, in the case of liver and heart, it was possible to determine the elements of highest significance for different treatments, which may serve as markers of exposure to iron oxide nanoparticles.
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