RESUMO
Benzene is associated with diverse occupational and public health hazards. It exhibits an ability to rapidly permeate the skin and contaminate water and food sources, leading to dermal and ingestion exposures. Despite numerous studies examining the associations between benzene and various indicators of harm, the findings have yielded inconsistent results. Furthermore, relying solely on air concentration as a measure of benzene exposure is limited, as it fails to account for internal exposure dose and individual susceptibility. This study aimed to conduct a comprehensive review in order to present current knowledge on benzene biomarkers and their significance in evaluating exposure levels and associated health hazards. The search methodology adhered to the PRISMA guidelines and involved the application of specific inclusion and exclusion criteria across multiple databases including PubMed, Embase, and Web of Science. Two researchers independently extracted and evaluated the relevant data based on predetermined criteria. Following the screening process, a total of 80 articles were considered eligible out of the initially retrieved 1053 articles after undergoing screening and assessment for inclusion. As the level of exposure decreased, specific biomarkers demonstrated a gradual increase in limitations, including heightened background concentrations and vulnerability to confounding factors. The advancement of sampling and analysis techniques will yield new biomarkers. Additionally, when conducting practical work, it is crucial to employ a comprehensive utilization of diverse biomarkers while excluding individual metabolic variations and combined exposure factors.
RESUMO
The identification of noninvasive volatile biomarkers for lung cancer is a significant clinical challenge. Through in vitro studies, the recognition of altered metabolism in cell volatile organic compound (VOC) emitting profile, along with the occurrence of oncogenesis, provides insight into the biochemical pathways involved in the production and metabolism of lung cancer volatile biomarkers. In this research, for the first time, a comprehensive comparative analysis of the volatile metabolites in NSCLS cells (A549), SCLC cells (H446), lung normal cells (BEAS-2B), as well as metabolites in both the oxidative stress (OS) group and control group. Specifically, the combination of eleven VOCs, including n-dodecane, acetaldehyde, isopropylbenzene, p-ethyltoluene and cis-1,3-dichloropropene, exhibited potential as volatile biomarkers for lung cancer originating from two different histological sources. Furthermore, the screening process in A549 cell lines resulted in the identification of three exclusive biomarkers, isopropylbenzene, formaldehyde and bromoform. Similarly, the exclusive biomarkers 1,2,4-trimethylbenzene, p-ethyltoluene, and cis-1,3-dichloropropene were present in the H446 cell line. Additionally, significant changes in trans-2-pentene, acetaldehyde, 1,2,4-trimethylbenzene, and bromoform were observed, indicating a strong association with OS. These findings highlight the potential of volatile biomarkers profiling as a means of noninvasive identification for lung cancer diagnosis.
RESUMO
La-modified RHBCs (La-RHBCs) were fabricated by immobilizing La(OH)3 nanoparticles on mesoporous rice husk biochars (RHBCs) using a co-precipitation method. Specifically, the effects of the pore structure of the RHBCs, solution pH, and coexisting substances on phosphate adsorption by the La-RHBCs were studied. The results showed that the La loading of the La-RHBCs was positively correlated with the mesoporosity of the RHBCs. La-modified RHBCs with higher mesoporosity hosts showed faster adsorption rates and lower leaching of La during phosphate adsorption. The adsorption process could be described by a pseudo second-order kinetic model, and the reaction rate was controlled by intraparticle diffusion. The Langmuir isotherm model fitted the adsorption process better, and the theoretical maximum adsorption capacities were 41.22, 43.26, and 45.62 mg·g-1, respectively. The high P/La molar ratios of more than 1.5 indicated the high utilization efficiencies of the La in the La-immobilized RHBCs. Moreover, phosphate could be effectively removed by the La-modified RHBCs over a wide pH range of 3-9. The La-modified RHBCs also exhibited good adsorption selectivity towards phosphate in the presence of coexisting anions and humic acids. Phosphate adsorption by the La-RHBCs was enhanced in the presence of Ca2+, while it was inhibited in the presence of Mg2+.
RESUMO
Immobilizing La(OH)3 nanoparticles (NPs) to porous hosts has been widely applied to inhibiting their inherent aggregation as well as the subsequent low utilization efficiency of La. In this study, a series of rice husk biochars (RHBCs) with high mesoporous rates were prepared and the effects of host pore structure and point of zero charge (pHpzc) on phosphate adsorption by La-modified RHBCs was particularly focused. Characterization results confirmed that La(OH)3 NPs were both confined in the pore channel and external surface of RHBCs. Adsorption kinetics and isotherms showed that La-modified RHBCs with higher mesoporous rates of the host showed a faster adsorption rate and La-modified RHBCs exhibited superior La utilization efficiency than many reported La-incorporated adsorbents. Phosphate could be effectively captured over a wide pH of 3-10 due to the high pHpzc of La-modified RHBCs. Moreover, the La-modified RHBCs showed satisfactory affinity towards phosphate in the presence of coexisting anions and the phosphate adsorption by La-RHBC9 was enhanced in the presence of Ca2+, while it was inhibited in the presence of Mg2+. The mesoporous structure of RHBCs strengthened the stability of La-modified RHBCs and weakened the inhibition of coexisting humic substances on phosphate adsorption through the "shielding effect".
