4.8 Article

Effect of Nanoparticle Size and Natural Organic Matter Composition on the Bioavailability of Polyvinylpyrrolidone-Coated Platinum Nanoparticles to a Model Freshwater Invertebrate

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 55, Issue 4, Pages 2452-2461

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.0c05985

Keywords

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Funding

  1. US National Science Foundation NSF-EPSCoR Fellowship [1738340]
  2. NSF [EAR-1629698]
  3. DOE Office of Science [DE-AC02-06CH11357]

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Laboratory experiments using the model freshwater snail Lymnaea stagnalis characterized the bioavailability of dissolved Pt(IV) and polyvinylpyrrolidone-coated platinum nanoparticles (PtNPs) of different sizes. The results showed that PtNPs had higher bioavailability than dissolved forms, and this bioavailability increased with nanoparticle diameter. The study also found that natural organic matter (NOM) suppressed the bioavailability of PtNPs, with a positive correlation between reduced sulfur content in NOM and PtNP bioavailability. The elimination of accumulated platinum after PtNP exposures exhibited a triphasic pattern, indicating potential in vivo PtNP dissolution.
The bioavailability of dissolved Pt(IV) and polyvinylpyrrolidone-coated platinum nanoparticles (PtNPs) of five different nominal hydrodynamic diameters (20, 30, 50, 75, and 95 nm) was characterized in laboratory experiments using the model freshwater snail Lymnaea stagnalis. Dissolved Pt(IV) and all nanoparticle sizes were bioavailable to L. stagnalis. Platinum bioavailability, inferred from conditional uptake rate constants, was greater for nanoparticulate than dissolved forms and increased with increasing nanoparticle hydrodynamic diameter. The effect of natural organic matter (NOM) composition on PtNP bioavailability was evaluated using six NOM samples at two nanoparticle sizes (20 and 95 nm). NOM suppressed the bioavailability of 95 nm PtNPs in all cases, and DOM reduced sulfur content exhibited a positive correlation with 95 nm PtNP bioavailability. The bioavailability of 20 nm PtNPs was only suppressed by NOM with a low reduced sulfur content. The physiological elimination of Pt accumulated after dissolved Pt(IV) exposure was slow and constant. In contrast, the elimination of Pt accumulated after PtNP exposures exhibited a triphasic pattern likely involving in vivo PtNP dissolution. This work highlights the importance of PtNP size and interfacial interactions with NOM on Pt bioavailability and suggests that in vivo PtNP transformations could yield unexpectedly higher adverse effects to organisms than dissolved exposure alone.

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