Detection of polystyrene nanoplastics in biological samples based on the solvatochromic properties of Nile red: application in Hydra attenuata exposed to nanoplastics

Francois Gagne*, Joelle Auclair, Brian Quinn

*Corresponding author for this work

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

The release of nanoplastics (NP) from the weathering of microplastics is a major concern for the environment. Methods for the detection of NP in biological tissues are urgently needed because of their ability to penetrate not only in tissues but also in cells. A simple fluorescence-based methodology for the detection of polystyrene NP in biological tissues is proposed using the solvatochromic properties of Nile red. Although NPs alone increased somewhat Nile red fluorescence, a characteristic hypsochromic shift in the emission spectra was found when the dye and NP were incubated with subcellular tissue fraction. To explain this, the probe and NPs (50 and 100 nm) were prepared in the presence of increasing concentrations of two detergents (Tween-20, Triton X-100) as a proxy to phospholipids. The data revealed that both detergents readily increased fluorescence values when added to the NP and Nile red. The addition of NPs in tissue extracts blue-shifted further the emission spectra to 623 nm from the normal Nile red-lipid peak at 660 nm. The fluorescence intensity was proportional to the NP concentration. A methodology is thus proposed for the detection of NPs in laboratory-exposed organisms based on the solvatochromic properties of Nile red. The methodology was used to detect the presence of NP and changes in polar lipid contents in Hydra attenuata exposed to polystyrene NP.
Original languageEnglish
Pages (from-to)33524-33531
Number of pages8
JournalEnvironmental Science and Pollution Research
Volume26
Issue number32
Early online date2 Oct 2019
DOIs
Publication statusE-pub ahead of print - 2 Oct 2019

Keywords

  • Polystyrene
  • Nanoplastic
  • Nile red
  • Fluorescence
  • Detection

Cite this

@article{6554f913a2d84fce8de8de48d4261de4,
title = "Detection of polystyrene nanoplastics in biological samples based on the solvatochromic properties of Nile red: application in Hydra attenuata exposed to nanoplastics",
abstract = "The release of nanoplastics (NP) from the weathering of microplastics is a major concern for the environment. Methods for the detection of NP in biological tissues are urgently needed because of their ability to penetrate not only in tissues but also in cells. A simple fluorescence-based methodology for the detection of polystyrene NP in biological tissues is proposed using the solvatochromic properties of Nile red. Although NPs alone increased somewhat Nile red fluorescence, a characteristic hypsochromic shift in the emission spectra was found when the dye and NP were incubated with subcellular tissue fraction. To explain this, the probe and NPs (50 and 100 nm) were prepared in the presence of increasing concentrations of two detergents (Tween-20, Triton X-100) as a proxy to phospholipids. The data revealed that both detergents readily increased fluorescence values when added to the NP and Nile red. The addition of NPs in tissue extracts blue-shifted further the emission spectra to 623 nm from the normal Nile red-lipid peak at 660 nm. The fluorescence intensity was proportional to the NP concentration. A methodology is thus proposed for the detection of NPs in laboratory-exposed organisms based on the solvatochromic properties of Nile red. The methodology was used to detect the presence of NP and changes in polar lipid contents in Hydra attenuata exposed to polystyrene NP.",
keywords = "Polystyrene, Nanoplastic, Nile red, Fluorescence, Detection",
author = "Francois Gagne and Joelle Auclair and Brian Quinn",
year = "2019",
month = "10",
day = "2",
doi = "10.1007/s11356-019-06501-3",
language = "English",
volume = "26",
pages = "33524--33531",
journal = "Environmental Science and Pollution Research",
issn = "1614-7499",
publisher = "Springer International Publishing AG",
number = "32",

}

TY - JOUR

T1 - Detection of polystyrene nanoplastics in biological samples based on the solvatochromic properties of Nile red

T2 - application in Hydra attenuata exposed to nanoplastics

AU - Gagne, Francois

AU - Auclair, Joelle

AU - Quinn, Brian

PY - 2019/10/2

Y1 - 2019/10/2

N2 - The release of nanoplastics (NP) from the weathering of microplastics is a major concern for the environment. Methods for the detection of NP in biological tissues are urgently needed because of their ability to penetrate not only in tissues but also in cells. A simple fluorescence-based methodology for the detection of polystyrene NP in biological tissues is proposed using the solvatochromic properties of Nile red. Although NPs alone increased somewhat Nile red fluorescence, a characteristic hypsochromic shift in the emission spectra was found when the dye and NP were incubated with subcellular tissue fraction. To explain this, the probe and NPs (50 and 100 nm) were prepared in the presence of increasing concentrations of two detergents (Tween-20, Triton X-100) as a proxy to phospholipids. The data revealed that both detergents readily increased fluorescence values when added to the NP and Nile red. The addition of NPs in tissue extracts blue-shifted further the emission spectra to 623 nm from the normal Nile red-lipid peak at 660 nm. The fluorescence intensity was proportional to the NP concentration. A methodology is thus proposed for the detection of NPs in laboratory-exposed organisms based on the solvatochromic properties of Nile red. The methodology was used to detect the presence of NP and changes in polar lipid contents in Hydra attenuata exposed to polystyrene NP.

AB - The release of nanoplastics (NP) from the weathering of microplastics is a major concern for the environment. Methods for the detection of NP in biological tissues are urgently needed because of their ability to penetrate not only in tissues but also in cells. A simple fluorescence-based methodology for the detection of polystyrene NP in biological tissues is proposed using the solvatochromic properties of Nile red. Although NPs alone increased somewhat Nile red fluorescence, a characteristic hypsochromic shift in the emission spectra was found when the dye and NP were incubated with subcellular tissue fraction. To explain this, the probe and NPs (50 and 100 nm) were prepared in the presence of increasing concentrations of two detergents (Tween-20, Triton X-100) as a proxy to phospholipids. The data revealed that both detergents readily increased fluorescence values when added to the NP and Nile red. The addition of NPs in tissue extracts blue-shifted further the emission spectra to 623 nm from the normal Nile red-lipid peak at 660 nm. The fluorescence intensity was proportional to the NP concentration. A methodology is thus proposed for the detection of NPs in laboratory-exposed organisms based on the solvatochromic properties of Nile red. The methodology was used to detect the presence of NP and changes in polar lipid contents in Hydra attenuata exposed to polystyrene NP.

KW - Polystyrene

KW - Nanoplastic

KW - Nile red

KW - Fluorescence

KW - Detection

U2 - 10.1007/s11356-019-06501-3

DO - 10.1007/s11356-019-06501-3

M3 - Article

VL - 26

SP - 33524

EP - 33531

JO - Environmental Science and Pollution Research

JF - Environmental Science and Pollution Research

SN - 1614-7499

IS - 32

ER -