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jf9b01106 Si 001
jf9b01106 Si 001
Figure SI1: Optimal amount determination of ingredients (chitosan, pectin, TPP and paraquat) for nanoparticle
formation.
Figure SI3: Analysis of the samples using Fourier transform infrared spectroscopy (FTIR).
Table SI 1: Toxicity of NPs, PQ, NP:PQ and commercial PQ on cell line (Adenocarcinomic human alveolar basal
epithelial cells (A549).
Table SI 2: Toxicity of NPs, PQ, NP:PQ and commercial PQ on cell line (Carcinoma of the mouth cells (KB).
Figure SI 1. Optimal amount determination of ingredients (chitosan, pectin, TPP and paraquat) for nanoparticle
formation. In constant concentrations of other parameters, the optimal encapsulation efficiencies were achieved by
0.04%, 0.08% and 0.01% of chitosan, pectin and TPP, respectively. In the optimal amounts of other components, the
most encapsulation efficiency was seen in paraquat amount of 5 mg.
Figure SI 2. The pH of unloaded PEC/CS/TPP nanoparticles (NPs) or nanoparticles containing paraquat (NP:PQ) as
a function of time (0-60 days), at 25◦C.
Figure SI 3. Analysis of the samples using Fourier transform infrared spectroscopy (FTIR): (a) TPP, (b) Pectin, (c)
nanoparticles without paraquat (NPs), (d) nanoparticles containing paraquat (NP:PQ), (e) Chitosan, and (f) Paraquat.
The numbers indicate the wavenumbers of the main groups present in the components of the samples.
Figure SI 4. Differential scanning calorimetry (DSC) thermograms of derivatives of residual weight for chitosan
(CS), pectin (PEC) and tripoly phosphate (TPP) under nitrogen degradation.
Figure SI 5. Soil sorption of paraquat, NP:PQ, PQ and Commercial PQ, at 25◦C and pH 4.5 (n = 3). Application of the pseudo-
second order mathematical model (Aa-Cc) where qt is amount of soluted sorbate at any time t (mg/g).
Table SI 1. Toxicity of NPs, PQ, NP:PQ and commercial PQ on cell line (Adenocarcinomic human alveolar basal epithelial cells
(A549).
Table SI 2. Toxicity of NPs, PQ, NP:PQ and commercial PQ on cell line (Carcinoma of the mouth cells (KB).