The role of Nd3+ concentration in the modulation of the thermometric performance of Stokes/anti-Stokes luminescence thermometer in NaYF4:Nd3.

The growing popularity of luminescence thermometry observed in recent years is related to the high application potential of this technique. However, in order to use such materials in a real application, it is necessary to have a thorough understanding of the processes responsible for thermal changes in the shape of the emission spectrum of luminophores. In this work, we explain how the concentration of Nd3+ dopant ions affects the change in the thermometric parameters of a thermometer based on the ratio of Stokes (4F3/2 → 4I9/2) to anti-Stokes (4F7/2,4S3/2 → 4I9/2) emission intensities in NaYF4:Nd3+. It is shown that the spectral broadening of the 4I9/2 → 4F5/2, 2H9/2 absorption band observed for higher dopant ion concentrations enables the modulation of the relative sensitivity, usable temperature range, and uncertainty of temperature determination of such a luminescent thermometer.

Modulation of thermometric performance of single-band-ratiometric luminescent thermometers based on luminescence of Nd3+ activated tetrafluorides by size modification.

Due to a number of its advantages, luminescence thermometry has been a strongly developed strand of temperature metrology over a period of time. Although there are several different types of luminescent thermometers, recently attention has been focused on a new single-band ratiometric approach, which is based on the excited state absorption phenomenon. Nevertheless, since this process is nontrivial and has not been studied extensively in the context of thermometry to date, a number of studies are necessary to enable the intentional development of highly sensitive thermometers based on this method. One of the important aspects is to investigate the influence of material size and the associated occurrence of surface effects, which is considered in this work. In addition, the research in this paper has been extended to explore the aspect of host material composition. Accordingly, nanocrystals and microcrystals of ß-NaYF4:2%Nd3+, ß-NaGdF4:2%Nd3+, and LiGdF4:2%Nd3+ were investigated in this work. The influence of surface effects on thermometric parameters was proved, with special emphasis on the useful temperature range. Thus, by increasing the particle size, it was possible to intentionally extend the useful range by even more than 100 K.

Correlation between the Covalency and the Thermometric Properties of Yb3+/Er3+ Codoped Nanocrystalline Orthophosphates.

Lanthanide-doped NaYF4 nanoparticles are most frequently studied host materials for numerous biomedical applications. Although efficient upconversion can be obtained in fluoride nanomaterials and good homogeneity of size and morphology is achieved, they are not very predestined for extensive material optimization toward enhanced features and functions. Here, we study the impact of rare-earth metals RE = Y, Lu, La, and Gd ions within Yb3+/Er3+ codoped nanocrystalline REPO4 orthophosphates. The enhanced luminescent thermometry features were found to be in relation to the covalency of RE3+-O2- bonds being modulated by these optically inactive rare-earth ion substitutes. Up to 30% relative sensitivity enhancement was found (from ca. 3.0 to ca. 3.8%/K at -150 °C) by purposefully increasing the covalence of the RE3+-O2- bond. These studies form the basis for intentional optimization thermal couple-based luminescent thermometers such as Yb3+-Er3+ upconverting ratiometric thermometer.

NIR luminescence lifetime nanothermometry based on phonon assisted Yb3+-Nd3+ energy transfer.

Luminescence thermometry in biomedical sciences is a highly desirable, but also highly challenging and demanding technology. Numerous artifacts have been found during steady-state spectroscopy temperature quantification, such as ratiometric spectroscopy. Oppositely, the luminescence lifetime is considered as the most reliable indicator of temperature thermometry because this luminescent feature is not susceptible to sample properties or luminescence reabsorption by the nanothermometers themselves. Unfortunately, this type of thermometer is much less studied and known. Here, the thermometric properties of Yb3+ ions in Nd0.5RE0.4Yb0.1PO4 luminescent temperature probes were evaluated, aiming to design and optimize luminescence lifetime based nanothermometers. Temperature dependence of the luminescence lifetimes is induced by thermally activated phonon assisted energy transfer from the 2F5/2 state of Yb3+ ions to the 4F3/2 state of Nd3+ ions, which in turn is responsible for the significant quenching of the Yb3+:2F5/2 lifetime. It was also found that the thermal quenching and thus the relative sensitivity of the luminescent thermometer can be intentionally altered by the RE ions used (RE = Y, Lu, La, and Gd). The highest relative sensitivity was found to be S R = 1.22% K-1 at 355 K for Nd0.5Y0.4Yb0.1PO4 and it remains above 1% K-1 up to 500 K. The high sensitivity and reliable thermometric performance of Nd0.5La0.4Yb0.1PO4 were confirmed by the high reproducibility of the temperature readout and the temperature uncertainty being as low as δT = 0.05 K at 383 K.

Synthesis, Cytotoxicity Assessment and Optical Properties Characterization of Colloidal GdPO4:Mn2+, Eu3+ for High Sensitivity Luminescent Nanothermometers Operating in the Physiological Temperature Range.

Herein, a novel synthesis method of colloidal GdPO4:Mn2+,Eu3+ nanoparticles for luminescent nanothermometry is proposed. XRD, TEM, DLS, and zeta potential measurements confirmed the crystallographic purity and reproducible morphology of the obtained nanoparticles. The spectroscopic properties of GdPO4:Mn2+,Eu3+ with different amounts of Mn2+ and Eu3+ were analyzed in a physiological temperature range. It was found that GdPO4:1%Eu3+,10%Mn2+ nanoparticles revealed extraordinary performance for noncontact temperature sensing with relative sensitivity SR = 8.88%/°C at 32 °C. Furthermore, the biocompatibility and safety of GdPO4:15%Mn2+,1%Eu3+ was confirmed by cytotoxicity studies. These results indicated that colloidal GdPO4 doped with Mn2+ and Eu3+ is a very promising candidate as a luminescent nanothermometer for in vitro applications.

Enhancing the sensitivity of a Nd3+,Yb3+:YVO4 nanocrystalline luminescent thermometer by host sensitization.

Numerous methods are known to improve the relative temperature sensitivity of luminescent thermometers. These methods include optimization of the host material, the size of the nanoparticles, the dopant ion type and concentration, or the excitation intensity and operation mode of the excitation source. Here we propose a new approach, which exploits temperature dependent host sensitized emission from Nd3+ and Yb3+ lanthanide ions in a YVO4 matrix. We found out that the emission ratio of these two activators strongly depends on temperature, the size of the nanocrystals and the relative dopant concentration. The novelty comes from the fact that CT → Nd3+ and CT → Yb3+ are temperature dependent, and therefore helps to double the relative temperature sensitivity from ∼0.12% K-1 up to 0.25% K-1 for the smallest nanocrystals. Based on the temperature dependent luminescence lifetimes of Nd3+ and Yb3+ activators, we also found out that Nd3+→ Yb3+ ET has 70-75% efficiency and is temperature dependent.

Adaptive down-regulation of the serotonin transporter in the 6-hydroxydopamine-induced rat model of preclinical stages of Parkinson's disease and after chronic pramipexole treatment.

Our recent study has indicated that a moderate lesion induced by bilateral 6-hydroxydopamine (6-OHDA) injections into the ventrolateral region of the caudate-putamen (CP) in rats, modeling preclinical stages of Parkinson's disease, induces a "depressive-like" behavior which is reversed by chronic treatment with pramipexole (PRA). The aim of the present study was to examine the influence of the above lesion and chronic PRA treatment on binding to the serotonin transporter (SERT) in different brain regions. As before, 6-OHDA (15 µg/2.5 µl) was administered bilaterally into the CP. PRA (1mg/kg) was injected subcutaneously twice a day for 2 weeks. Serotonergic and dopaminergic neurons of the dorsal raphe (DR) were immunostained for tryptophan hydroxylase and tyrosine hydroxylase, respectively, and were counted stereologically. Binding of [(3)H]GBR 12,935 to the dopamine transporter (DAT) and [(3)H]citalopram to SERT was analyzed autoradiographically. Intrastriatal 6-OHDA injections decreased the number of dopaminergic, but not serotonergic neurons in the DR. 6-OHDA reduced the DAT binding in the CP, and SERT binding in the nigrostriatal system (CP, substantia nigra (SN)), limbic system (ventral tegmental area (VTA), nucleus accumbens (NAC), amygdala, prefrontal cortex (PFCX), habenula, hippocampus) and DR. A significant positive correlation was found between DAT and SERT binding in the CP. Chronic PRA did not influence DAT binding but reduced SERT binding in the above structures, and deepened the lesion-induced losses in the core region of the NAC, SN, VTA and PFCX. The present study indicates that both the lesion of dopaminergic neurons and chronic PRA administration induce adaptive down-regulation of SERT binding. Moreover, although involvement of stimulation of dopaminergic transmission by chronic PRA in its "antidepressant" effect seems to be prevalent, additional contribution of SERT inhibition cannot be excluded.

Association of chemokine receptor gene variants with HIV-1 genotype predicted tropism.

OBJECTIVES: As a switch from chemokine (C-C motif) receptor 5 [CCR5 (R5)] to chemokine (C-X-C motif) receptor 4 [CXCR4 (X4)] HIV-1 tropism is associated with symptomatic and AIDS stages of infection, while chemokine receptor gene variants modify the tempo of HIV disease progression, we aimed to analyse the association between pretreatment HIV-1 tropism and chemokine polymorphisms known to restrict disease progression. METHODS: V3 genotype tropism prediction was performed in a group of 221 treatment-naïve patients, with subsequent CCR5 Δ32 (rs333), CCR2 V64I (rs1799864), CCR5 promoter (-627 C/T; rs1799988) and CX3CR1 V249I (rs3732378) genotyping performed in 206 patients. Alleles with a protective effect were assigned positive values while risk alleles were assigned negative values to calculate genetic scores. χ(2) tests, Mann-Whitney U-tests and logistic and linear regression models were used for statistical analyses. RESULTS: R5 tropism was found in 85.5% of patients (n = 189) using a false positive rate (FPR) of 5.75% and in 72.8% of patients (n = 161) using an FPR of 10%. A higher frequency of the 5.75% FPR predicted R5 tropism was associated with the CX3CR1 A allele (P = 0.027). Lower additive genetic scores were associated with an increased frequency of 5.75% FPR predicted R5 tropism (P = 0.0059), with the trend confirmed by logistic regression [odds ratio (OR) 0.5819; 95% confidence interval (CI) 0.3457-0.9795; P = 0.0416]. Viral load tended to increase with decreasing genetic score in the logistic regression analysis (slope = -0.127 ± 0.076; P = 0.095; r(2) = 0.161). CONCLUSIONS: The CX3CR1 A allele and lower genetic scores may restrict the switch of HIV-1 tropism from R5 to X4. This effect may be associated with the amount of co-receptor on the cell surface. Chemokine receptor gene polymorphisms influence both disease progression and tropism variability.

Role of endogenous zinc in bones of newborn rats.

Concentration of abundant elements e.g. calcium as well as of elements present in trace amount e.g. zinc in mandibles of 7, 14 an 28 day old newborn rats were determined by X-ray fluorescence analysis. The measurements were carried out by using a measurement system containing X-ray tube ECLIPSE-III and X-ray and gamma ray detector XR-100T-CdTe (Amptek Inc.). Concentration of calcium and zinc depended on the region of interest on the rat's mandible due to mineralization degree conditioned by its function. Increasing age produced a remarkable increase in Ca content in contrast to Zn content in the bone tissue obtained from 7, 14 and 28 day old newborn rats. The calculated Zn/Ca concentration ratio was the biggest for 7 day old newborns and successively decreased with age indicating the important role of zinc at the beginning of bone ontogenesis.

Interference of psychotropic drugs with the injuring action of ethanol on gastric mucosal barrier.

The aim of this study was to establish whether some psychotropic drugs, applied to patients under influence of alcohol, may potentiate its damaging action on gastric mucosal barrier. A sensitive index of such damage is a decline of the potential difference (PD) across the stomach wall. The experiments were carried out on Wistar rats of either sex, anesthetized with urethane-chloralose. The PD values were assayed with an apolarization method. The investigated solutions were administered intragastrically by gavage. Ethanol at a concentration of 40% v/v depressed PD by 39%. The investigated psychotropic drugs did not change PD by themselves but given in combination with ethanol caused significant decline of PD: diazepam (0.4 mg/kg) by 58%, chlorpromazine (6.7 mg/kg) by 59%, imipramine (2 mg/kg) by 48%, amitriptyline (4 mg/kg) by 49%, phenytoin (4 mg/kg) by 53%, pyridinol (0.3 mg/kg) by 58%. Intragastric administration of water did not change PD. The results indicate that while psychotropic drugs given alone do not affect significantly the gastric mucosal barrier, they may potentiate the damaging action of ethanol on this barrier.

[Changes in electrical potentials of gastric mucosa during various types of experimental hypoxia]. / Zmiany potencjalów elektrycznych blony sluzowej zoladka w warunkach doswiadczalnej hipoksji wywolanej róznymi czynnikami.

In experiments performed on anaesthetized male and female Wistar rats the effects of different types of hypoxia on the electrical potential difference (PD) between the inner and the outer sides of the gastric wall were examined. The PD was determined by mean of the Digital Multimeter VC-10T, Unitra, and the calomel electrodes connected with the KCl-agar bridges. There were four series of experiments carried out in which hypoxia was produced by: I--low atmospheric pressure (hypobaric hypoxia) corresponding with the altitudes of 2500, 5500, 8500 and 10,500 m above sea level, II--1 min. nitrogen breathing (anoxic anoxia), III--bleeding ca. 1% of the body weight (anemic hypoxia), IV--the gastric vessels ligation (ischemic hypoxia). There were also performed the adequate control experiments of each series. In all types of hypoxia (I--IV) a decrease in the PD was observed. The value and rate of this decrease were dependent on the type, grade, duration and rate of hypoxia. In the conditions of the hypobaric hypoxia simulated altitude 10,500 m only evoked the statistically significant PD drops, by 31%. The nitrogen breathing caused the PD decrease by 23% and the anemic hypoxia by 18%. In the ischemic hypoxia the total disappearance of the potential difference (PD = 0 mV) was observed. In the control experiments small non significant fluctuations, not exceeding 4%, occurred only. The decrease in the PD of the gastric wall observed during hypoxia could be explained by the changes in the membrane transport e.g. the back-diffusion of Na+, Cl-, and H+ ions.