Background: Clear cell renal cell carcinoma (ccRCC) comprises the majority, approximately 70–80%, of renal cancer cases and often remains asymptomatic until incidentally detected during unrelated abdominal imaging or at advanced stages. Currently, standardized screening tests for renal cancer are lacking, which presents challenges in disease management and improving patient outcomes. This study aimed to identify ccRCC-specific volatile organic compounds (VOCs) in the urine of ccRCC-positive patients and develop a urinary VOC-based diagnostic model. Methods: This study involved 233 pretreatment ccRCC patients and 43 healthy individuals. VOC analysis utilized stir-bar sorptive extraction coupled with thermal desorption gas chromatography/mass spectrometry (SBSE-TD-GC/MS). A ccRCC diagnostic model was established via logistic regression, trained on 163 ccRCC cases versus 31 controls, and validated with 70 ccRCC cases versus 12 controls, resulting in a ccRCC diagnostic model involving 24 VOC markers. Results: The findings demonstrated promising diagnostic efficacy, with an Area Under the Curve (AUC) of 0.94, 86% sensitivity, and 92% specificity. Conclusions: This study highlights the feasibility of using urine as a reliable biospecimen for identifying VOC biomarkers in ccRCC. While further validation in larger cohorts is necessary, this study’s capability to differentiate between ccRCC and control groups, despite sample size limitations, holds significant promise.

Perfluoroalkyl carboxylic acids (PFCAs) are a significant group of per- and polyfluoroalkyl substances (PFASs). They are persistent organic chemicals manufactured for their resistance to heat, water, and stains. PFCAs are ubiquitous in the environment, particularly in surface water and wastewater, because they are widely used in everyday consumer products. This contamination poses a risk to drinking water supplies and human health, necessitating sensitive and effective analytical methods. Traditional liquid chromatography–tandem mass spectrometry (LC-MS/MS) is commonly used but involves complex sample handling and high costs. In this study, we developed an enhanced stir bar sorptive extraction (SBSE) method coupled with thermal desorption–gas chromatography–mass spectrometry (TD-GC-MS) for the analysis of PFCAs in water. This method demonstrates linearity, with R² values from 0.9892 to 0.9988, and low limits of detection (LOD) between 21.17 ng/L and 73.96 ng/L. Recovery rates varied from 47 to 97%, suggesting efficient extraction. Compared to traditional methods, the developed SBSE technique requires only a 1 mL sample volume and minimal amounts of solvents, enhancing eco-friendliness and reducing potential contamination and handling errors. This method also demonstrated good precision and robustness across various water matrices. Overall, the developed method offers a precise, eco-friendly, and reliable approach for analyzing PFCAs in diverse water samples.

Uranium is a unique element, characterized by its dual role as a valuable resource and a source of significant hazards. Widely used in industry, research, and medicine, uranium has played a pivotal role in shaping modern science and technology. Since the discovery of its fission properties in the early twentieth century, uranium has gained attention as a powerful and influential element. Historically, uranium’s role in the discovery of radioactivity marked a turning point in scientific research, and its ability to release immense energy through nuclear fission has transformed human history. From its destructive potential in warfare to its peaceful applications in electricity generation via nuclear power plants, uranium has had a profound impact. Furthermore, it has advanced medical science through the production of isotopes for diagnostic imaging and therapeutic treatments. However, increased demand for uranium has led to expanded mining and milling processes, which pose public health risks due to environmental contamination. This chapter explores uranium’s legacy, highlighting its scientific significance while balancing the potential benefits with the inherent risks associated with its use. The discussion underscores the need for careful consideration and management of uranium’s dual nature as both a powerful resource and potential source of harm.

In this study, eco-friendly and sustainable alginate-activated carbon (Alg-C)-based beads were synthesized and characterized for the adsorption of nonylphenols (NPs) from aqueous environments under various conditions. The surface characterization, functional groups, and adsorption behavior were analyzed using multiple analytical techniques. The effect of key parameters, including dosage, pH, temperature, and reusability, were evaluated. Isotherm and kinetic studies revealed that the adsorption process followed a pseudo-second-order kinetic model and aligned with the Freundlich isotherm, indicating a heterogeneous surface. The beads exhibited a high removal efficiency of 97% over five reuse cycles in a 50 mL solution of 10 mg L⁻¹ NPs under static conditions, demonstrating their recyclability. Thermodynamic analysis suggested potential electrostatic interactions, supported by positive Gibbs free energy values. The highest removal performance was achieved within 90 min, with adsorption capacities from 0.10 to 0.39 mg g⁻¹. Additionally, the performance of Alg-C beads remained stable across different pH levels, highlighting their robustness. When tested with wastewater samples, Alg-C beads maintained high removal efficiency, with no significant matrix effects observed. These results underscore Alg-C beads as a promising and sustainable solution for the elimination of NPs from contaminated water sources.