Different natures of surface electronic transitions of carbon nanoparticles.

The photoluminescence behaviour of carbon-based nanodots is still debated. Both core and surface structures are involved in the emission mechanism, and the electronic transitions can be modified by external agents such as metal ions or pH, but the general relation between the structure and the optical function is poorly understood. Here, we report a comparative study on the effects of these variables, changing the core structure from crystalline to amorphous, and modifying the surface structure by different passivation procedures. Our results highlight that the emission mechanism of the tunable visible fluorescence is identical for crystalline and amorphous samples, indicating the independence of the emission from the core structure. Furthermore, surface functionalization weakly influences the emission peak position, but has large consequences on their interaction with different metal ions. This suggests the involvement of quasi-degenerate electronic states originating from the high density of different interacting groups on the surface. Finally, we report the presence of an unusual ultraviolet emission band for the amorphous sample, likely involving localized molecular-type chromophores with carboxyl ends. Our findings provide new information on the emission mechanisms of CDs and can be used to engineer sub-types of CDs displaying very similar emission features, but specifically tailored for different sensing applications.

Development of a biosensing system for tacrine based on nitrogen-doped graphene quantum dots and acetylcholinesterase.

This work presents a novel fluorescent sensor for the determination of tacrine by combining the magnificent fluorescence properties of nitrogen-doped graphene quantum dots (N-GQDs) with the high potential of acetylcholinesterase (AChE) enzyme for screening its inhibitors. Tacrine was the first drug approved for Alzheimer's disease and it is currently being used in several therapeutic treatments given its activity as a reversible inhibitor of AChE. The principle of the developed biosensor relies on the fact that the native fluorescence of the synthesized N-GQDs is quenched by interaction with enzymatic reaction products, and the inclusion of tacrine in assay solution results in the gradual recovery of the original fluorescence in an inhibitor concentration-dependent manner. While N-GQD fluorescence was not directly affected by tacrine, the inclusion of an AChE based-enzymatic system allowed for its determination with a detection limit (S/N = 3) of 1.22 µM. This biosensor was demonstrated to be simple, rapid and reproducible (%RSD 4.87, n = 7) for analysis of tacrine in aqueous solutions.

Raman spectroscopic characterization of single walled carbon nanotubes: influence of the sample aggregation state.

Raman spectroscopy has been employed in analytical sciences for purity determination of carbon nanotube samples based on the consideration of G-/D-band intensity ratios. This work demonstrates the role of aggregation in these feature bands, which, in the case of single walled carbon nanotubes (SWNTs), has proved to be crucial for G-/D-band intensity ratio measurements. We have found variation in the relative intensities of G- and D-bands across a sample of SWNTs without any other treatment, discarding the possible influence of the laser beam or sample focusing. In the case of multiwalled carbon nanotubes (MWNTs), this effect is less notorious. Thus, to achieve a good representativeness of Raman measurements, it is important to consider the sample preparation procedure in order to avoid aggregation, which has an effect over the signals, making difficult the subsequent interpretation of results.

Sustainable cultivation of melon landraces: Effects of grafting on the accumulation of flavor-related compounds.

Melon landraces are highly appreciated by consumers who pay price premiums to compensate for lower yields, enabling on-farm conservation. However, they are highly susceptible to soilborne diseases. This study analyses the impact of Cucurbita and Cucumis rootstocks on the accumulation of flavor-related metabolites in Spanish landraces of the Ibericus melon group, as a strategy to promote their sustainable cultivation. Scion genotype was the main factor conditioning the accumulation of sugars and acids both under standard and saline organic farming conditions. The effects of grafting on organic acid accumulation were negligible, while the effects on sugar content were significant. The latter effects were dependent on specific scion-rootstock combinations, though wild Cucumis (e.g. Fian) rootstocks represent an alternative that should be further studied. The effect on the accumulation of volatiles was limited, and again depended on specific scion-rootstock combinations. The rootstock effect even differed between populations of the same landrace.

Is trimodal therapy the current standard for muscle-invasive bladder cancer?

OBJECTIVE: The aim of this review is to summarize the current evidence and future perspectives of bladder-sparing treatment for MIBC. METHODS: A non-systematic literature search in Medline/Pubmed was performed in October 2023 with the following keywords "bladder cancer", "bladder-sparing", "trimodal therapy", "chemoradiation", "biomarkers", "immunotherapy", "neoadjuvant chemotherapy", "radiotherapy". RESULTS: Urology guidelines recommend radical cystectomy as the standard curative treatment for muscle-invasive urothelial bladder cancer, reserving radiotherapy for patients who are unfit or who want to preserve their bladder. Given the morbidity and mortality of cystectomy and its impact on quality of life and bladder function, modern oncologic therapies are increasingly oriented toward organ preservation and maximizing functional outcomes while maintaining treatment efficacy. Trimodal therapy, which incorporates maximal transurethral resection followed by radiotherapy with concurrent radiosensitizing chemotherapy, is an effective regimen for bladder function preservation in well-selected patients. Despite the absence of comparative data from randomized trials, the two approaches seem to provide comparable oncologic outcomes. Studies are evaluating the expansion of eligibility criteria for trimodal therapy, the optimization of radiotherapy and immunotherapy delivery to further improve outcomes, and the validation of biomarkers to guide bladder preservation. CONCLUSIONS: Trimodal therapy has shown acceptable outcomes for bladder preservation; therefore, it provides a valid treatment option in well-selected patients.

Recommendations on the treatment of metastatic hormone-sensitive prostate cancer: Patient selection.

The standard treatment for metastatic hormone-sensitive prostate cancer (mHSPC) is now a combination of androgen deprivation therapy plus an androgen receptor-targeted therapy (abiraterone, apalutamide, enzalutamide or darolutamide), with or without chemotherapy (docetaxel). The selection of suitable patients for each therapeutic approach has become a determining factor to ensure efficacy and minimize side effects. This article combines recent clinical evidence with the accumulated experience of experts in medical oncology, radiation oncology and urology, to provide a comprehensive view and therapeutic recommendations for mHSPC.

Teaching social responsibility in analytical chemistry.

Analytical chemistry is key to the functioning of a modern society. From early days, ethics in measurements have been a concern and that remains today, especially as we have come to rely more on the application of analytical science in many aspects of our lives. The main aim of this Feature is to suggest ways of introducing the topic of social responsibility and its relation to analytical chemistry in undergraduate or graduate chemistry courses.

Qualitative detection and quantitative determination of single-walled carbon nanotubes in mixtures of carbon nanotubes with a portable Raman spectrometer.

The main aim of this work is to develop a one-step method for the characterization of mixtures of single- and multi-walled carbon nanotubes using a simple and inexpensive tool, a portable Raman spectrometer. In order to overcome the problem of heat dissipation in solid samples, the suitability of three surfactants-SDS, Triton X-100 and CTAB-to disperse nanotubes has been evaluated. A systematic study of the wavelength and relative intensity of the D and G bands has been carried out with six samples of multiwalled carbon nanotubes (MWNTs) and one of single-walled carbon nanotubes (SWNTs) dispersed in these surfactants, and this has been compared with solid samples. Finally, the possibility has been demonstrated to identify and (semi)quantify the presence of SWNTs in a mixture containing MWNTs.

Solid phase extraction-capillary electrophoresis determination of sulphonamide residues in milk samples by use of C18-carbon nanotubes as hybrid sorbent materials.

The exceptional sorption capabilities of carbon nanotubes were used to preconcentrate trace sulphonamides from milk samples. To this end, single walled carbon nanotubes (SWNTs) and multi-walled carbon nanotubes (MWNTs) dispersed in the ionic liquid 1-hexyl-3-methylimidazolium hexafluorophosphate were retained on a C18 stationary phase to obtain a hybrid material in a simple manner. In this approach ionic liquids are an excellent alternative to improve the dispersion of CNTs, without chemical modification or the use of solid substances or organic solvents. MWNTs provided better results than SWNTs. Carbon nanotubes retained in the C18 sorbent matrix were found to confer aromatic character, increasing its preconcentration capacity as a result. The conventional C18 stationary phase played a two-fold role: as a support to retain carbon nanotubes in the cartridge and as a medium to prevent their aggregation. The modified MWNT/C18 and SWNT/C18 materials were used to preconcentrate residual sulphonamides (SAs) in milk samples for their determination at concentrations as low as 0.03-0.069 mg L(-1) by capillary electrophoresis. Analyte recoveries from spiked samples ranged from 103.2 to 98.8% and precision, as RSD, from 8.2 to 5.4%.

Magnetically confined hydrophobic nanoparticles for the microextraction of endocrine-disrupting phenols from environmental waters.

In this article, a solid-phase extraction approach, which takes advantage of the good extraction capabilities of hydrophobic magnetic nanoparticles (MNPs), is presented. The new approach involves the deposition of a thin layer of MNPs in a dedicated stirring unit based on the dual function of a mini-magnet. The system allows the extraction of the analytes in a simple and efficient way. The approach, which reduces the negative effect of the aggregation tendency of hydrophobic MNPs, is characterized for the resolution of a model analytical problem: the determination of some endocrine-disrupting phenols in water by liquid chromatography-photometric detection. All the variables involved in the extraction process have been clearly identified and optimized. The new extraction mode allows the determination of these compounds with limits of detection in the range from 0.15 µg/L (for 4-tert-octylphenol) to 2.7 µg/L (for 4-tert-butylphenol) with a relative standard deviation lower than 5.3 % (for 4-tert-butylphenol).

Evaluation of hippuric acid content in goat milk as a marker of feeding regimen.

Organic producers, traders, and consumers must address 2 issues related to milk: authentication of the production system and nutritional differentiation. The presence of hippuric acid (HA) in goat milk samples has been proposed as a possible marker to differentiate the feeding regimen of goats. The objective of this work is to check the hypothesis that HA could be a marker for the type of feeding regimen of goats by studying the influence of production system (conventional or organic) and feeding regimen (with or without grazing fodder). With this purpose, commercial cow and goat milk samples (n=27) and raw goat milk samples (n=185; collected from different breeds, localizations, and dates) were analyzed. Samples were grouped according to breed, feeding regimen, production system, and origin to compare HA content by ANOVA and honestly significant difference Tukey test at a confidence level of ≥95%. Hippuric acid content was obtained by analyzing milk samples with capillary electrophoresis. This method was validated by analyzing part of the samples with HPLC as a reference technique. Sixty-nine raw goat milk samples (of the total 158 samples analyzed in this work) were quantified by capillary electrophoresis. In these samples, the lowest average content for HA was 7±3 mg/L. This value corresponds to a group of conventional raw milk samples from goats fed with compound feed. The highest value of this group was 28±10 mg/L, corresponding to goats fed compound feed plus grass. Conversely, for organic raw goat milk samples, the highest concentration was 67±14 mg/L, which corresponds to goats fed grass. By contrast, the lowest value of this organic group was 26±10 mg/L, which belongs to goats fed organic compounds. Notice that the highest HA average content was found in samples from grazing animals corresponding to the organic group. This result suggests that HA is a good marker to determine the type of goats feeding regimen; a high content of HA represents a diet based mainly or exclusively on eating green grass (grazing), independently of the production system. Hence, this marker would not be useful for the actual organic policies to distinguish organic milk under the current regulations, because organic dairy ruminants can be fed organic compound feed and conserved fodder without grazing at all.

Rapid analysis of gold nanoparticles in liver and river water samples.

This paper describes a simple approach to determine gold nanoparticles in liver and river water samples. The method of purification of nanoparticles from the matrix is based on the stabilization of gold nanoparticles with a cationic surfactant followed by a microliquid-liquid extraction in ionic liquid. Finally, the extracted nanoparticles can be analysed by UV/Vis detection or Raman spectroscopy. The precision of the proposed method for the analysis of liver tissue and river water samples was 9.7% and 18% respectively for UV/Vis analysis. The sensitivity was 1.17 × 10(-12) M for the analysis of 3 mL of liver homogenate or river water sample.

Coiled carbon nanotubes combined with ionic liquid: a new soft material for SPE.

For the first time a soft material formed from coiled carbon nanotubes and 1-hexyl-3-methylimidazolium hexafluorophosphate has been used as sorbent material. The soft material has high stability as well as a high capacity to adsorb analytes. In this work we propose using a natural cotton fiber impregnated with the soft material to miniaturize the system. The system was tested for the analysis of polycyclic aromatic hydrocarbons in spiked river water samples. The absolute recovery ranged between 97.5 and 105.5%, demonstrating the usefulness of the soft material. The limit of detection ranged from 2.5 to 6.1 µg/L and the precision expressed as the relative standard deviation for the analysis of five consecutive analyses ranged between 2.5 and 5.8%.

Determination of non-steroidal anti-inflammatory drugs in urine by the combination of stir membrane liquid-liquid-liquid microextraction and liquid chromatography.

A stir membrane liquid phase microextraction procedure working under the three-phase mode is proposed for the first time for the determination of six anti-inflammatory drugs in human urine. The target compounds are isolated and preconcentrated using a special device that integrates the extractant and the stirring element. An alkaline aqueous solution is used as extractant phase while 1-octanol is selected as supported liquid membrane solvent. After the extraction, all the analytes are determined by liquid chromatography (LC) with ultraviolet detection (UV). The analytical method is optimized considering the main involved variables (e.g., pH of donor and acceptor phases, extraction time, stirring rate) and the results indicate that the determination of anti-inflammatory drugs at therapeutic and toxic levels is completely feasible. The limits of detection are in the range from 12.6 (indomethacin) to 30.7 µg/L (naproxen). The repeatability of the method, expressed as relative standard deviation (RSD, n = 5) varies between 3.4% (flurbiprofen) and 5.7% (ketoprofen), while the enrichment factors are in the range from 35.0 (naproxen) to 72.5 (indomethacin).

Analytical potential of hybrid nanoparticles.

The growing use of nanoparticles in the analytical process in recent years has set a new trend towards the simplification of analytical methods and improvement of their performance. Miniaturization and nanotechnology have allowed new analytical challenges to be met. Hybrid nanoparticles in particular possess exceptional properties enabling further improvement of analytical methods. Despite the continuous developments in their synthesis and characterization, hybrid nanomaterials have scarcely been used in analytical chemistry, however. This paper discusses the analytical potential of hybrid nanoparticles in terms of their special characteristics and properties, and describes their analytical applications.

The potential of carbon nanotube membranes for analytical separations.

Advances in nanotechnology have enabled the development of nanoporous membranes based on carbon nanotubes, which, by virtue of their exceptional properties, constitute excellent supports for analytical processes, including the selective separation of some molecules.

Highly selective and non-conventional sorbents for the determination of biomarkers in urine by liquid chromatography.

Urine is one of the most extensively analysed biological fluids in clinical and toxicological investigations owing to its high availability and non-invasive collection. The chemical nature of the analytes involved (polarity and thermal instability) makes liquid chromatography the separation technique of choice for compound determination. Moreover, sample treatment based on solid-phase extraction is usually carried out owing to its flexibility and the availability of new sorbent materials with increased selectivity and versatility towards the target compounds. Taking into account these three fundamental points, this review focuses on recent developments in urine pretreatment using highly selective and non-conventional sorbents in solid-phase extraction such as affinity sorbents (immunosorbents and molecularly imprinted polymers), restricted access materials and carbon nanotubes, with emphasis on the new synthesis methods. Their main advantages and shortcomings are presented, together with representative examples in this context.

Sensitive in-surface infrared monitoring coupled to stir membrane extraction for the selective determination of total hydrocarbon index in waters.

In this paper, the direct coupling between stir membrane extraction and infrared spectroscopy working under transmission mode is presented for the sensitive and selective determination of the total hydrocarbon index in waters. For this purpose, a new extraction unit was built using stainless steel in order to maximize the adsorption of the target analytes in the 40-microm-thick polytetrafluoroethylene membrane. The method allows the determination of hydrocarbons in the presence of grease, using hexadecane and stearic acid as model compounds, respectively. The proposal is optimized in depth, taking into account the main experimental variables such as membrane thickness, extraction time, and stirring and sample volume. Later on, the method was characterized on the basis of its linearity, precision, and limits of detection. The combination allows the determination of the hydrocarbon index with a limit of detection of 18 microg L(-1), the precision being (expressed as relative standard deviation) better than 4.3%. The analytical method provides a high sample throughput since some extractions can be performed in parallel, the relative standard deviation between devices being better than 8%. The proposed analytical method is finally compared in terms of analytical figures with counterpart ASTM method, recently presented.

Dispersive solid phase extraction for in-sorbent surface attenuated total reflection infrared detection.

The combination of dispersive solid phase extraction (DSPE) and attenuated total reflection (ATR) infrared spectroscopy is presented using the joint determination of sorbic and benzoic acids in juice samples as a model analytical problem. The dispersive extraction process allows the selective extraction of the target analytes from the sample matrix allowing their preconcentration prior to their infrared detection. The extraction efficiency is improved compared to the conventional procedures since the interaction between sorbent and analytes is favored with the stirring process. Moreover, the extracted analytes are directly determined in the sorbent. As no elution step is required, analyte dilutions and consumption of organic solvents are avoided. The proposed approach has been qualitative and quantitative studied. The hierarchical cluster analysis permits the sample classification according to the relative concentration of the analytes. The precision of the quantitative analysis was better than 6% with analyte recoveries in the range 87-90%. The proposed method was applied to the analysis of different commercial fruit juice samples. Finally, the main advantages and limitations of the new proposal are presented and compared with existing alternatives.

Stir membrane extraction: a useful approach for liquid sample pretreatment.

In this paper, a novel extraction approach based on the use of a polymeric membrane as the extraction medium is described. For this aim, an original unit which allows the magnetic stirring of the membrane during the extraction process has been designed, optimized, and practically evaluated. On one hand, the main variables affecting the extraction process such as the unit design, the stirring rate, the extraction time, the sample volume, and the elution conditions were deeply studied. Once optimized, a model analytical problem, the determination of polycyclic aromatic hydrocarbons in water samples, was selected for practical evaluation of the stir membrane extraction procedure. The method was characterized on the basis of its linearity, precision, and limits of detection. The novel approach was sensitive and precise enough for the detection of the target analytes in the low nanogram per liter range using 25 mL of sample. In fact, limits of detection ranged from 0.8 ng/L (fluoranthene) to 7.6 ng/L (benzo-anthracene) with relative standard deviations lower than 8%.