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In this study we critically examined with both field and laboratory experiments key components of extant methods for measurement of aerosol soluble platinum in ambient air and workplace environments. Our goal was to develop an improved method for soluble platinum measurement that could be readily implemented in the field and laboratory using readily available modern analytical tools, and in parallel provide insight into factors influencing the robustness of specific aspects of measurement methods for soluble platinum. Experiments addressed sampler type, filter media and pre-cleaning, extraction solvent and volume, extraction time & energy and materials composition, with the objective of optimizing each specific component and promulgating strategies for improving signal/noise and precision. We used basic clean-room protocols and applied ICPMS tools to address these objectives. We document a method that provides for measurement of soluble platinum at the 0.02 ng/m level (8-h sample at 2 L/min). Of the four samplers evaluated (IOM, closed-face cassette, and two parallel particle impactors), the IOM exhibited the best precision. The three filter substrates evaluated (Teflon, MCE, PVC) performed similarly in most challenges, however, overall, we conclude that MCE media is the most robust collection substrate for soluble platinum measurements. To achieve the lowest detection levels, it is critical to pre-clean the filter substrates. The use of a 0.07 M HCl extractant (in preference to a water extractant) is recommended - platinum recoveries, particularly from real-world samples, are higher and more consistent with the HCl extractant. The outcomes of the extraction kinetics experiments suggest that an extraction time of 60 min may improve the method performance with 0.07 M HCl but degrade the performance with water, in comparison with a 30-min extraction period. The use of sonication in preference to a table-top shaker is recommended for energy input during extraction.
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http://dx.doi.org/10.1016/j.scitotenv.2021.152657 | DOI Listing |
Acta Crystallogr C Struct Chem
September 2025
School of Chemistry, Monash University, VIC 3800, Australia.
The crystal structure of the ortho-isomer trans-[N-(2-bromo-3,4,5,6-tetrafluorophenyl)-N',N'-diethylethane-1,2-diaminato(1-)]chloridopyridineplatinum(II), [PtBr(CHBrFN)Cl(CHN)][PtBr(CHBrFN)Cl(CHN)] or [Pt{(o-BrCF)N(CH)NEt}Cl(py)], 1o, revealed syn and anti rotamers in a 1:1 ratio in the solid state. 1o crystallizes in the centrosymmetric space group P1. The Pt-coordinated Cl ligand exhibits partial occupancy with Br, predominantly in the syn-rotamer.
View Article and Find Full Text PDFDalton Trans
August 2025
Department of Chemistry, School of Advanced Sciences (SAS), Vellore Institute of Technology, Vellore-632014, Tamil Nadu, India.
Metallic compounds have shown great promise as anticancer treatments because of their varied mechanisms of action, decreased side effects, and ability to overcome drug resistance. The search for alternative metal-based therapies has been driven by the severe toxicity, drug resistance, and poor selectivity of platinum-based complexes like cisplatin, carboplatin, and oxaliplatin, despite their notable clinical effectiveness. Their clinical translation is made difficult by issues such as off-target toxicity, low absorption, and poor solubility.
View Article and Find Full Text PDFDalton Trans
September 2025
Department of Chemistry and Industrial Chemistry, University of Pisa, Pisa, Italy.
Platinum(IV) prodrugs offer a promising strategy to overcome the limitations of cisplatin and oxaliplatin, including systemic toxicity and acquired resistance. In this study, two novel α-tocopherol succinate-functionalized Pt(IV) complexes, [Pt(oxalato)(DACH)(OAc)(α-TOS)] (4) and [PtCl(NH)(OAc)(α-TOS)] (5), were synthesized and characterized to enhance the efficacy and selectivity of platinum-based chemotherapy. Functionalization with α-TOS (3) was designed to increase lipophilicity and enable selective intracellular reduction.
View Article and Find Full Text PDFRecurrent ovarian cancer (OC) remains a major cause of mortality due to chemoresistance and metastasis. Epigenetic dysfunction, particularly involving microRNAs (miRNAs), contributes to disease progression. Extracellular vesicles (EVs) are key modulators of tumor epigenetic profiles by delivering bioactive cargo to recipient cells.
View Article and Find Full Text PDFChem Commun (Camb)
August 2025
Donostia International Physics Center (DIPC), Donostia-San Sebastián, Euskadi, Spain.
The influence of choline and geranic acid-based ionic liquids (CAGE ILs) on the anticancer activity of selected Pt(II) and Pt(IV) complexes was investigated. All complexes exhibited appreciable solubility in CAGE ILs, with Pt(II) complexes 2 and 4 undergoing immediate ligand substitution. In contrast, the hydrophobic derivative 3 demonstrated remarkable stability for up to 48 hours.
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