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Fluorescent tracer dyes represent an important class of sub-cellular probes and allow the examination of cellular processes in real-time with minimal impact upon these processes. Such tracer dyes are becoming increasingly used for the examination of membrane transport processes, as they are easy-to-use, cost effective probe substrates for a number of membrane protein transporters. Rhodamine 123, a member of the rhodamine family of flurone dyes, has been used to examine membrane transport by the ABCB1 gene product, MDR1. MDR1 is viewed as the archetypal drug transport protein, and is able to efflux a large number of clinically relevant drugs. In addition, ectopic activity of MDR1 has been associated with the development of multiple drug resistance phenotype, which results in a poor patient response to therapeutic intervention. It is thus important to be able to examine the potential for novel compounds to be MDR1 substrates. Given the increasing use rhodamine 123 as a tracer dye for MDR1, a full characterisation of its spectral properties in a range of in vitro assay-relevant media is warranted. Herein, we determine λmax for excitation and emission or rhodamine 123 and its metabolite rhodamine 110 in commonly used solvents and extraction buffers, demonstrating that fluorescence is highly dependent on the chemical environment: Optimal parameters are 1% (v/v) methanol in HBSS, with λex = 505 nm, λem = 525 nm. We characterise the uptake of rhodamine 123 into cells, via both passive and active processes, and demonstrate that this occurs primarily through OATP1A2-mediated facilitated transport at concentrations below 2 µM, and via micelle-mediated passive diffusion above this. Finally, we quantify the intracellular sequestration and metabolism of rhodamine 123, demonstrating that these are both cell line-dependent factors that may influence the interpretation of transport assays.

Carbon Quantum dot (CQDs) is one of the newest materials in carbon-based nanomaterials. It is pertinent to study the synthesis and the application of these carbon dots. Here we have studied the effect of precursor on the optical, morphological, and photocatalytic properties of CQDs. We have synthesized CQDs using pyrolysis method using the precursors citric acid, urea, polyethyleneimine. We have synthesized two samples: CQD-S1; synthesized using urea and polyethyleneimine, and CQD-S2; synthesized using citric acid and polyethyleneimine. In optical properties study two distinct peaks have been obtained at 243 nm and 345 nm for CQD-S1, and at 265 nm and 335 nm for CQD-S2. In fluorescence study, the maximum emission was found at excitation wavelength of 340 nm for CQD-S1 and at excitation wavelength of 350 nm for CQD-S2. In morphological studies, Transmission Electron Microscope (TEM) revealed particle size of sample CQD-S1 and CQD-S2 were 1.91 nm and 1.61 nm, respectively. EDX confirmed the elemental composition in both samples. The rhodamine B (RhB) dye degradation percentages in dark and under visible and UV light were found to 6, 13, and 98.4% respectively for CQD-S1. Similarly, dye degradation for CQD-S2 were 7, 11, and 99.63%, respectively. Effective degradation of photocatalysis performed under UV-light within 100 min using mineralization process.

Rhodamine derivatives have been widely investigated for their mitochondrial targeting and chemotherapeutic properties that result from their lipophilic cationic structures. In previous research, we have found that conversion of Rhodamine 6G into nanoGUMBOS, i.e., nanomaterials derived from a group of uniform materials based on organic salts (GUMBOS), led to selective chemotherapeutic toxicity for cancer cells over normal cells. Herein, we investigate the chemotherapeutic activity of GUMBOS derived from four different rhodamine derivatives, two bearing an ester group, i.e., Rhodamine 123 (R123) and SNAFR-5, and two bearing a carboxylic acid group, i.e., rhodamine 110 (R110) and rhodamine B (RB). In this study, we evaluate (1) relative hydrophobicity via octanol–water partition coefficients, (2) cytotoxicity, and (3) cellular uptake in order to evaluate possible structure–activity relationships between these different compounds. Intriguingly, we found that while GUMBOS derived from R123 and SNAFR-5 formed nanoGUMBOS in aqueous medium, no distinct nanoparticles are observed for RB and R110 GUMBOS. Further investigation revealed that the relatively high water solubility of R110 and RB GUMBOS hinders nanoparticle formation. Subsequently, while R123 and SNAFR-5 displayed selective chemotherapeutic toxicity similar to that of previously investigated R6G nanoGUMBOS, the R110 and RB GUMBOS were lacking in this property. Additionally, the chemotherapeutic toxicities of R123 and SNAFR-5 nanoGUMBOS were also significantly greater than R110 and RB GUMBOS. Observed results were consistent with decreased cellular uptake of R110 and RB as compared to R123 and SNAFR-5 compounds. Moreover, these results are also consistent with previous observations that suggest that nanoparticle formation is critical to the observed selective chemotherapeutic properties as well as the chemotherapeutic efficacy of rhodamine nanoGUMBOS.

Live-cell fluorescence nanoscopy is a powerful tool to study cellular biology on a molecular scale, yet its use is held back by the paucity of suitable fluorescent probes. Fluorescent probes based on regular fluorophores usually suffer from a low cell permeability and an unspecific background signal. Here we report a general strategy to transform regular fluorophores into fluorogenic probes with an excellent cell permeability and a low unspecific background signal. Conversion of a carboxyl group found in rhodamines and related fluorophores into an electron-deficient amide does not affect the spectroscopic properties of the fluorophore, but allows us to rationally tune the dynamic equilibrium between two different forms: a fluorescent zwitterion and a non-fluorescent, cell-permeable spirolactam. Furthermore, the equilibrium generally shifts towards the fluorescent form when the probe binds to its cellular targets. The resulting increase in fluorescence can be up to 1,000-fold. Using this simple design principle, we created fluorogenic probes in various colours for different cellular targets for wash-free, multicolour, live-cell nanoscopy.It is difficult to develop suitable fluorescent probes for live-cell nanoscopy, but a general strategy is now reported that can transform regular fluorophores into fluorogenic probes with excellent cell permeability and low unspecific background signals. Using this approach, probes in a variety of colours were developed for different cellular targets and used for wash-free, multicolour, live-cell confocal and STED microscopy.

A multifunctional system comprised of hyaluronic acid microneedles was developed as an effective transdermal delivery platform for rapid local delivery. The microneedles can regulate the filling amount on the tip, by controlling the concentration of hyaluronic acid solution. Ultrasonication induces dissolution of the HA microneedles via vibration of acoustic pressure, and AC iontophoresis improves the electrostatic force-driven diffusion of HA ions and rhodamine B. The effect of ultrasound on rhodamine release was analyzed in vitro using a gelatin hydrogel. The frequency and voltage dependence of the AC on the ion induction transfer was also evaluated experimentally. The results showed that the permeability of the material acts as a key material property. The delivery system based on ultrasonication and iontophoresis in microneedles increases permeation, thus resulting in shorter initial delivery time than that required by delivery systems based on passive or ultrasonication alone. This study highlights the significance of the combination between ultrasonic waves and iontophoresis for improving the efficiency of the microneedles, by shortening the reaction duration. We anticipate that this system can be extended to macromolecular and dependence delivery, based on drug response time.

The Rhodamine B adsorption was realized in batch using calcined bentonite clay. The effects of Rhodamine B initial concentration, pH, and temperature were evaluated and the conditions where the adsorption was favored were in 500 mg L −1 , pH 3, and 35 °C. The equilibrium isotherms studied were from Langmuir and Freundlich. The coefficients of determination ( R 2  > 0.99) were found to confirm the best fitted to Langmuir isotherm, with a monolayer adsorption capacity ( q max ) of 552.49 mg g −1 . The kinetic data agreed well with the pseudo-second order model ( R 2  > 0.99). The in natura and calcined clay were characterized by the techniques of X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), N 2 physisorption (BET), and scanning electron microscopy (SEM). Thermodynamic parameters including Gibbs free energy (ΔG°), enthalpy change (ΔH°), and entropy change (ΔS°) were calculated to estimate the nature of Rhodamine B adsorption in clay. The results suggested that the adsorption was endothermic and spontaneous, with the enthalpy adsorption increasing with the increase of temperature. Therefore, calcined bentonite can be used as an efficient adsorbent for discoloration of large volume of residual water, presenting low-cost and high adsorptive capacity.

This study explores the dual applications of a greenly synthesized ZnO@CTAB nanocomposite for the efficient remediation of Rhodamine B (RhB) and lead (Pb). The synthesis method involves a sustainable approach, emphasizing environmentally friendly practices. FT-IR, XRD, FESEM, zeta potential, and particle size analyzer (PSA), BET, and UV–VIS were used to physically characterize the zinc oxide and CTAB nanocomposite (ZnO@CTAB). The size and crystalline index of ZnO@CTAB are 77.941 nm and 63.56% respectively. The Zeta potential of ZnO@CTAB is about − 22.4 mV. The pore diameter of the ZnO@CTAB was 3.216 nm, and its total surface area was 97.42 m 2 /g. The mechanism of adsorption was investigated through pH ZPC measurements. The nanocomposite’s adsorption performance was systematically investigated through batch adsorption experiments. At pH 2, adsorbent dose of 0.025 g, and temperature 50 °C, ZnO@CTAB removed the most RhB, while at pH 6, adsorbent dose of 0.11 g, and temperature 60 °C, ZnO@CTAB removed the most Pb. With an adsorption efficiency of 214.59 mg/g and 128.86 mg/g for RhB and Pb, the Langmuir isotherm model outperforms the Freundlich isotherm model in terms of adsorption. The pseudo-2nd-order model with an R 2 of 0.99 for both RhB and Pb offers a more convincing explanation of adsorption than the pseudo-1st-order model. The results demonstrated rapid adsorption kinetics and high adsorption capacities for RhB and Pb. Furthermore, there was minimal deterioration and a high reusability of ZnO@CTAB till 4 cycles were observed. Graphical Abstract

A silver phosphate/hydroxyapatite (Ag PO /HA) composite was produced from phosphate waste rocks, firstly by the valorization of these wastes to HA and then by the treatment of this prepared HA with a silver nitrate solution. A type of response surface methodology, Box-Behnken experimental design, was used to find optimum synthesis parameters (silver to HA weight ratios, calcination temperature and calcination time). The visible light photodegradation of Rhodamine B in aqueous solution was used as the experimental response. The analysis of variance for the results showed that silver weight ratio is the most influential parameter on photoactivity of the synthesized photocatalyst. The optimum conditions were predicted to give an RhB degradation yield of 98.609%/4 hours under visible light conditions. In this context, a Ag/HA weight ratio of 14%, a calcination temperature of 300 °C, and a calcination time of 30 min were found to be the optimum conditions. Samples synthesized under the optimum condition were characterized by the use of X-ray diffraction, X-ray fluorescence spectrometer, Fourier transform infrared spectrum analysis, scanning electron microscopy, transmission electron microscopy and ultraviolet-visible diffuse reflection spectroscopy. By comparison with pure HA, the characterization results clearly showed the successful synthesis of the Ag PO /HA composite.

Alterations in glutathione (GSH) homeostasis are associated with a variety of diseases and cellular functions, and therefore, real-time live-cell imaging and quantification of GSH dynamics are important for understanding pathophysiological processes. However, existing fluorescent probes are unsuitable for these purposes due to their irreversible fluorogenic mechanisms or slow reaction rates. In this work, we have successfully overcome these problems by establishing a design strategy inspired by Mayr's work on nucleophilic reaction kinetics. The synthesized probes exhibit concentration-dependent, reversible and rapid absorption/fluorescence changes ( t 1/2  = 620 ms at [GSH] = 1 mM), as well as appropriate K d values (1–10 mM: within the range of intracellular GSH concentrations). We also developed FRET-based ratiometric probes, and demonstrated that they are useful for quantifying GSH concentration in various cell types and also for real-time live-cell imaging of GSH dynamics with temporal resolution of seconds. Reversible fluorescent probes for intracellular glutathione (GSH) imaging have now been designed and synthesized based on Si-rhodamine fluorophores. These probes are shown to be capable of quantifying the GSH concentration in various living cell types and also for monitoring real-time live-cell imaging of GSH dynamics with a temporal resolution of seconds.

Bismuth oxyhalides (BiOXs, X = Cl, Br and I) are emerging photocatalytic materials with unique layered structure, flexible band structure and superior photocatalytic activity. The purpose of this study was to develop a facile alcoholysis route to prepare BiOCl I nanosheet solid solutions at room temperature. X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), UV-vis diffuse reflectance spectroscopy (UV-vis DRS), photoluminescence emission spectroscopy (PL) and Brunauer-Emmett-Teller (BET) surface area analyzer were used to characterize the as-prepared photocatalysts. These results revealed that two-dimension BiOCl I nanosheet solid solutions could be obtained with high percentage of {001} crystal facets exposed. Moreover, the formation of solid solution could regularly change the optical absorption thresholds and band gaps of BiOCl I photocatalysts. The photocatalytic experiments indicated that BiOCl I exhibited the highest photocatalytic performance for the degradation of Rhodamine B (RhB) under simulated sunlight irradiation and the photocatalytic process followed a pseudo-first-order kinetic equation. A possible mechanism of RhB photodegradation over BiOCl I solid solutions was proposed based on the structural properties of BiOCl I solid solutions and RhB photosensitization.