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Fig 1.

A: Changes in the absorption maximum of the congo red-polysaccharide complex at various concentrations of sodium hydroxide solution; B: HPTLC analysis for monosaccharide composition of the polysaccharide. L1: L-Arabinose L2: D-Fructose, L3: D-Fucose, L4: D-Galactose, L5: Polysacchaide, L6: D-Glucose, L7: D-Mannose, L8: D-Rhamnose, L9: D-Xylose; C: GC-MS of five standard monosaccharides and D: GC-MS of polysaccharide from P. flabellatus.

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Fig 2.

From left, dispersed and exfoliated graphene oxide, aqueous solution of the polysaccharide, polysaccharide-reduced graphene oxide.

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Fig 2 Expand

Fig 3.

DLS elucidation of the synthesized PR-GO.

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Fig 4.

TEM image of PR-GO.

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Fig 5.

XRD spectrum of PR-GO nanosheets.

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Fig 6.

EDX spectrum of PR-GO nanosheets.

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Fig 7.

Fourier transform infrared spectra of (a) PR-GO; (b) Crude polysaccharide and (c) GO.

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Fig 8.

Raman Spectrum of PRGO (Curve A) and GO (Curve B).

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Fig 9.

Cytotoxicity of PR-GO in terms of MTT, Resazurin and neutral red uptakeassays.

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Fig 10.

Flow cytometry and confocal microscopy of human PBMC treated with different concentrations of PR-GO.

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Fig 11.

Genotoxic effects of different concentrations of PR-GO on human PBMCs.

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Fig 12.

ROS generation in human PBMCs induced by PR-GO.

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