Abstract
Poly(Thioether-Ester) nanoparticles synthetized via thiol-ene polymerization from a renewable castor oil monomer are produced by miniemulsion polymerization and emulsification/evaporation of pre-formed polymer. Its antioxidant activity, probably due to the oxidation of sulfide groups, is confirmed by 2,2-diphenyl-1-picryl hydrazyl (DPPH) free radical-scavenging and β-carotene/linoleic acid assays, with an amount of polymer required to reduce the initial concentration of DPPH· radicals by 50% of ~195 µg.ml-1 promoting hydrogen or electron exchange and the capability to prevent lipid peroxidation of ~55%. The results show a promising application in food packing.
Keywords:
Polymer nanoparticles; antioxidant activity; thiol-ene polymerization; poly (thioether-ester)
INTRODUCTION
Some conductive polymers, such as polypyrrole (PPy), poly (3,4-ethylenedioxythiophene) (PEDOT) and polyaniline have been reported to have radical scavenging properties and the antioxidant activity of these polymers have been studied (Hsu et al., 2008Hsu, C. F., Zhang, L., Peng, H., Travas-Sejdic, J., and Kilmartin, P. A., Free radical scavenging properties of polypyrrole and poly(3,4-ethylenedioxythiophene). Current Applied Physics, 8, 316-319 (2008). doi: 10.1016/j.cap.2007.10.049
https://doi.org/10.1016/j.cap.2007.10.04...
; ,Gizdavic-Nikolaidis et al., 2004Gizdavic-Nikolaidis, M., Travas-Sejdic, J., Bowmaker, G. A., Cooney, R. P., Thompson, C., and Kilmartin, P. A., The antioxidant activity of conducting polymers in biomedical applications. Current Applied Physics, 4(2-4), 347-350 (2004). doi: 10.1016/j.cap.2003.11.045
https://doi.org/10.1016/j.cap.2003.11.04...
). Also polysaccharides chemically modified to obtain sulfated derivatives have been studied for their antioxidant activities recently (Xie et al., 2016Xie, J. H., Wang, Z. J., Shen, M. Y., Nie, S. P., Gong, B., Li, H. S., Zhao, Q., Li, W.J., and Xie, M.Y.. Sulfated modification, characterization and antioxidant activities of polysaccharide from Cyclocarya paliurus. Food Hydrocolloids, 53, 7-15 (2016). doi: 10.1016/j.foodhyd.2015.02.018
https://doi.org/10.1016/j.foodhyd.2015.0...
). However, the antioxidant activity of poly(thioether-ester)s synthetized by thiol-ene reactions has never been reported.
Thiol-ene addition reactions have been known for more than a century and studied throughout the years (Türünç and Meier, 2010Türünç, O., and Meier, M. A. R., Fatty Acid Derived Monomers and Related Polymers Via Thiol-ene (Click) Additions. Macromolecular Rapid Communications, 31(20), 1822-1826 (2010). doi: 10.1002/marc.201000291
https://doi.org/10.1002/marc.201000291...
). The reaction is simply the thiol and ene group combination, with or without photo- or thermo-initiators, which proceeds via a radical addition mechanism, followed by chain transfer to a thiol end group, thus reinitiating the cycle (Hoyle and Bowman, 2010Hoyle, C. E., and Bowman, C. N., Thiol-Ene Click Chemistry. Angewandte Chemie International Edition, 49(9), 1540-1573 (2010). doi: 10.1002/anie.200903924
https://doi.org/10.1002/anie.200903924...
). Thiol-ene polymerization presents some advantages such as rapid polymerization rates, high overall functional group conversion, and little sensitivity to oxygen inhibition (Cramer et al., 2010Cramer, N. B., Couch, C. L., Schreck, K. M., Boulden, J. E., Wydra, R., Stansbury, J. W., and Bowman, C. N., Properties of methacrylate-thiol-ene formulations as dental restorative materials. Dental Materials, 26(8), 799-806 (2010). doi: 10.1016/j.dental.2010.04.005
https://doi.org/10.1016/j.dental.2010.04...
).
A wide range of enes with activated and non-activated species and multiply-substituted olefinic bonds can be used as suitable substrates (Lowe, 2010Lowe, A. B., Thiol-ene “click” reactions and recent applications in polymer and materials synthesis. Polym. Chem., 1(1), 17-36 (2010). doi: 10.1039/B9PY00216B
https://doi.org/10.1039/B9PY00216B...
). However, some attention has been given to renewable feedstocks, like plant oils (Cardoso et al., 2014Cardoso, P. B., Musyanovych, A., Landfester, K., Sayer, C., De Araújo, P. H. H., and Meier, M. A. R., ADMET reactions in miniemulsion. Journal of Polymer Science, Part A: Polymer Chemistry, 52(9), 1300-1305 (2014). doi: 10.1002/pola.27118
https://doi.org/10.1002/pola.27118...
; ,Türünç and Meier, 2010Türünç, O., and Meier, M. A. R., Fatty Acid Derived Monomers and Related Polymers Via Thiol-ene (Click) Additions. Macromolecular Rapid Communications, 31(20), 1822-1826 (2010). doi: 10.1002/marc.201000291
https://doi.org/10.1002/marc.201000291...
), due to the minimization of hazards, and the generation of substances with as little toxicity as possible, plus the biodegradable nature of the products (Salimon et al., 2012Salimon, J., Salih, N., and Yousif, E., Industrial development and applications of plant oils and their biobased oleochemicals. Arabian Journal of Chemistry, 5(2), 135-145 (2012). doi: 10.1016/j.arabjc.2010.08.007
https://doi.org/10.1016/j.arabjc.2010.08...
).
Thiol-ene polymers have been successfully synthesized from different kinds of multifunctional enes and thiols, finding application in the biomedical field as polymeric nanoparticles and hydrogels for drug-delivery systems, biomimetic hydrogels, and dental restorative resins (Machado et al., 2016). For polymeric nanoparticle production, some researchers have been producing nanoparticles with pre-formed polymers from “click” thiol-ene reactions using emulsification/evaporation techniques (Durham et al., 2015Durham, O. Z., Norton, H. R., and Shipp, D. A., Functional polymer particles via thiol-ene and thiol-yne suspension “click” polymerization. RSC Adv., 5(82), 66757-66766 (2015). doi: 10.1039/C5RA12553G
https://doi.org/10.1039/C5RA12553G...
.; Poetz et al. 2015Poetz, K. L., Durham, O. Z., and Shipp, D. A., Polyanhydride nanoparticles by "click" thiol-ene polymerization. Polymer Chemistry, 5464-5469 (2015). doi: 10.1039/c5py00843c
https://doi.org/10.1039/c5py00843c...
). Moreover, as a fresh field, thiol-ene polymers have also shown potential to be synthetized in dispersed media, like miniemulsion polymerization, and some works are reported in the literature using different enes and thiols in photopolymerization (Amato et al., 2015Amato, D. N. V. N. D. V. D., Flynt, A. S., and Patton, D. L. D., Functional, sub-100 nm polymer nanoparticles via thiol-ene miniemulsion photopolymerization. Polymer Chemistry, 6(31) 5625-5632 (2015). doi: 10.1039/C4PY01449A
https://doi.org/10.1039/C4PY01449A...
; Durham et al., 2017Durham, O. Z., Poetz, K. L., and Shipp, D. A., Polyanhydride Nanoparticles: Thiol - Ene “Click” Polymerizations Provide Functionalized and Cross-Linkable Nanoparticles with Tuneable Degradation Times. Australian Journal of Chemistry, 70(6), 735-742 (2017), doi: 10.1039/c5ra12553g
https://doi.org/10.1039/c5ra12553g...
; Jasinski et al., 2014Jasinski, F., Lobry, E., Tarablsi, B., Chemtob, A., Nouen, D. Le, and Criqui, A., Light-Mediated Thiol - Ene Polymerization in Miniemulsion: A Fast Route to Semicrystalline Polysul fi de Nanoparticles. ACS Macro Letters, 3, 958-962 (2014). doi: dx.doi.org/10.1021/mz500458s
dx.doi.org/10.1021/mz500458s...
). In this way, polymeric nanoparticles can be synthetized by different techniques, which depend of the origin of the polymeric material used as matrix material, which can be synthetized in situ or by preformed polymers.
The objective of this work was to synthesize poly(thioether-ester) (PTEE) nanoparticles from a renewable α,ω-diene diester monomer, derived from castor oil and isosorbide. Dianhydro-D-glucityl diundec-10-enoate (DGU) was copolymerized with 1,4-butanedithiol (Bu(SH)2) via thiol-ene polymerization in bulk and miniemulsion, resulting in poly-co-dianhydro-D-glucytil-diundec-10-enoate-co-1,4-butanedithiol. The obtained nanoparticles were individually assessed for their possible antioxidative capacities by employing DPPH free radical-scavenging and β-carotene/linoleic acid assays.
MATERIALS AND METHODS
Materials
10-Undecenoic acid (Sigma-Aldrich, 98%), dianhydro-D-glucitol (Aldrich, 98%), p-toluenesulfonic acid monohydrate (Sigma-Aldrich, 98.5%), 1,4-butanedithiol (Bu(SH)2), Sigma Aldrich), azobisisobutyronitrile (AIBN, Vetec, 98%), Crodamol GTCC (Crodamol, Alpha Química), a saturated triglyceride from coconut oil, Lutensol AT 80 (Lut. AT80, BASF), dichloromethane (DCM, MARCA), Poly Vinyl Alcohol (PVA, MARCA), and distilled water were used for all formulations.
Synthesis of the renewable monomer
Dianhydro-D-glucityl diundec-10-enoate (DGU) synthesis was conducted by esterification of 10-undecenoic acid (318.9 mmol), dianhydro-D-glucitol (107.8 mmol) and (15.7 mmol) p-toluenesulfonic acid. For that, 200 mL of toluene were added to the mixture and heated to 135 ºC under magnetic stirring; the resultant mixture was cooled down and toluene was evaporated. Purification was realized by filtration in a short pad of aluminum oxide and silica gel (using hexane as eluent). After hexane evaporation the final product was dissolved in diethyl ether and washed twice with 1N NaHCO3 solution and once with distilled water. Finally, the organic fraction was dried with anhydrous MgSO4 and the solvent was removed under reduced pressure.
Nanoparticles production
For the production of the PTEE nanoparticles, two techniques were employed: Miniemulsion polymerization (i) and Emulsification/ evaporation (ii).
-
Miniemulsion polymerization was conducted by stirring in an adequate flask the organic phase, composed of 1000 mg of DGU as monomer, 123 mg of Crodamol as coestabilizer and 3.4 mg of AIBN as initiator, with an aqueous phase containing the surfactant Lutensol AT 80 at 3% (w/v) and 5.5 mL of water, during 15 min, followed by the addition of the second monomer dithiol (Bu(SH)2) in quantities of 240 mg and stirred again for 5 min. The final emulsion was submitted to ultrasonication using a Fischer Scientific Sonic Dismembrator (Model 500) in an ice bath during 2 min (10 s on, 5 s off) at 70% of amplitude. Finally, the solution was transferred to an ampoule and immersed in a thermal bath at 80 ºC for 4 h producing NP 1.
-
For the emulsification/evaporation technique, PTEE was synthesized by bulk polymerization immersing an ampoule containing DGU, Bu(SH)2 and AIBN (at the same concentration cited previously for the miniemulsion polymerization technique) in a thermal bath at 80 ºC for 4 h. A quantity of 100 mg of the resulting polymer was solubilized in 4 mL of dichloromethane and, after complete dissolution of PTEE, the organic phase was dripped into 20 mL of aqueous phase composed of a poly(vinyl alcohol) (PVA) solution at 0.3 wt.%, and stirred at room temperature for 15 min, followed by application of ultrasonication in an ice bath at an amplitude of 70% during 2 min (15 s on, 10 s off) to reduce the droplets to submicrometric range. After obtaining the dispersion, the solvent was evaporated under magnetic stirring at room temperature and atmospheric pressure for 12 h, producing NP 2.
Particle size measurements
Particle size distribution measurements of intensity average particle size (Dp) and polydispersity index (PdI) were realized by dynamic light scattering (DLS) using a Zeta Sizer Nano S equipment from Malvern Instruments. Analyses were performed after dispersion in water to 0.5% of total solids and measured at 25 ºC in a glass cuvette.
Chemical analysis
The absorption spectra of dried samples were determined using Fourier Transform Infrared Spectroscopy with a Shimadzu spectrophotometer (IRPrestige-21) using a conventional KBr pellet method; samples were ground and compressed with anhydrous KBr to form pellets. The scanning range was 400-4000 cm-1 and the resolution was 4 cm-1.
1H NMR analyses were recorded in deuterated chloroform (CDCL3), using a Bruker Ascend 600 spectrophotometer at 600 MHz. Chemical shifts (δ) are reported in part per million (ppm) relative to the internal standard tetramethylsilane (TMS, δ = 0 ppm) used to calibrate the chemical shift.
Molar mass measurements
The molecular weight distribution measurements of the PTEE nanoparticles were carried out by gel permeation chromatography (GPC) using a High Performance Liquid Chromatography equipment (HPLC, model LC 20-A) and Shim Pack GPC800 Series Columns (GPC 801, GPC 804 and GPC 807) both from Shimadzu. After complete dissolution of 0.02 g of each dried sample in 4 mL of tetrahydrofuran (THF), the solutions were filtered through a nylon syringe filter with 0.45 µm pore size and 33 mm diameter. THF was used as eluent with a volumetric flow rate of 1 mL.min-1 at 40 ºC. The GPC system was calibrated using polystyrene standards with molecular weight ranging from 580 to 9.225x106 g.mol-1.
Particles Morphology
Transmission Electron Microscopic analyses using a JEM-1011 TEM (100 kV) were conducted to provide information about particle morphology. Samples NP 1 and 2 were diluted in distilled water up to 0.1% of solids; one drop of each sample was placed on a carbon-coated grid and dried under room conditions overnight.
Antioxidant activity
The DPPH free radical scavenging measurements were used to determine the scavenging capacity of NP 1 and 2. With minor modification, the method previously described (Blois, 1958Blois, M. S., Antioxidant Determination by the Use of a Stable Free Radical. Nature, 181, 1199-1200 (1958). doi: 10.1038/1811199a0
https://doi.org/10.1038/1811199a0...
; Brand-Williams et al., 1995Brand-Williams, W., Cuvelier, M. E., and Berset, C., Use of a free radical method to evaluate antioxidant activity. LWT - Food Science and Technology, 28(1), 25-30 (1995). doi: 10.1016/S0023-6438(95)80008-5
https://doi.org/10.1016/S0023-6438(95)80...
) was employed. Briefly, 500 µL of NP samples were mixed with 1000 µL of ethanolic DPPH solution (0.125 mM) and incubated in a dark room for 1 h at room temperature. Then, the tubes were centrifuged at 10.000 rpm for 30 min and the supernatant was taken for measurement at 517 nm using a Hitachi (U-1900) UV-vis spectrophotometer. Blank samples were prepared by mixing 500 µL of distilled water with 1000 µL of DPPH ethanolic solution. The percentage of DPPH scavenging activity (SA%) of NP samples was calculated following Equation 1.
where, As and A0 are the absorbance of sample and absorbance of blank, respectively.
The β-carotene/ linoleic acid assay was conducted by evaluation of the inhibition of the peroxidation effects of NP 1 and NP 2, using a linoleic acid system determined by the β-carotene bleaching test (Matthäus, 2002Matthäus, B., Antioxidant activity of extracts obtained from residues of different oilseeds. Journal of Agricultural and Food Chemistry, 50(12), 3444-3452 (2002). doi: 10.1021/jf011440s
https://doi.org/10.1021/jf011440s...
; ,Kang et al., 2006Kang, H. J., Chawla, S. P., Jo, C., Kwon, J. H., and Byun, M. W., Studies on the development of functional powder from citrus peel. Bioresource Technology, 97(4), 614-620 (2006). doi: 10.1016/j.biortech.2005.03.037
https://doi.org/10.1016/j.biortech.2005....
), quantifying the difference between the initial and final (after 120 min) amount of β-carotene discolored by spectrophotometric measurements at 470 nm. First, an emulsion with 3.4 mg of β-carotene and 44 µL of linoleic acid was prepared using 364 µL of Tween 20 and 1 mL of chloroform for better solubilization; the solution was shaken and the chloroform was evaporated in a rotaevaporator at 40 ºC. After that, 100 mL of water was added and homogenized. A blank emulsion was also done containing just 44 µL of linoleic acid, 364 µL of Tween 20 and 100 mL of distilled water. Samples were prepared at a concentration of 1.6 mg.mL-1 of polymer nanoparticles. Tests were performed by adding 200 µL of sample (NP 1 and NP 2) and 5 mL of β-carotene emulsion in test tubes, and 200 µL of sample with blank emulsion, The tubes were then placed in a thermal bath at 50 ºC and the absorbance measured at 470 nm in 0, 15, 30, 60 and 120 min. Control samples were prepared with 200 µL of ethanol and 5 mL of β-carotene emulsion and 200 µL of ethanol with 5 mL of blank emulsion. The antioxidant activity of samples was determined using Equation 2.
where, Act120 and Act0 are the absorbance of the control after 120 and 0 min, respectively, and Ast120 and Ast0 are the absorbance of the sample after 120 and 0 min, respectively.
RESULTS AND DISCUSSION
Particle size was evaluated by both techniques used, as seen in Table 1. NP 1 and NP 2 presented Dp between 206 and 261 nm, with a PdI below 0.2. Both samples analyzed remained stable after the storage time of 30 days, with a slight change in Dp and PdI for NP1, from 207.1 ± 1.1 to 238.8 ± 1.2, and from 0.150 ± 0.030 to 0.190 ± 0.010, respectively.
Particle size (Dp), Polydispersity index (PdI), stability evaluation of the formed NPs by DLS on day 1 and day 30 and Molar mass (Weight average molecular-Mw, Mean average-Mn) of the formed polymers.
Molar mass results expressed in terms of Mn and Mw are exposed in Table 1. The formation of the polymer by both techniques employed, miniemulsion and bulk, achieved polymers of low molecular weights with Mw of 7.48 and 13.99 kDa, respectively.
Chemical analyses were realized to prove PTEE formation. Fourier Transform Infrared (FT-IR) spectra of the dried samples of NP 1 and NP 2 are presented in Figure 1. Results for both samples show characteristic peaks of DGU at 2930 cm-1 corresponding to CH antisymmetric and symmetric stretching of -CH3 and CH2, at 2850 cm-1 to the presence of CH stretching modes from -CH3 attached to oxygen, and at 1740 cm-1 to C=O stretch of esters, as well as peaks at 1162 and 1095 cm-1 corresponding respectively to C-O-C antisymmetric stretch in esters and C-O-C symmetric stretch in ethers. A specific peak at 720 cm-1 indicates the presence of sulfide bonds (S-C) formed during the thiol-ene polymerization reaction, which were formed by the consumption of double bonds of vinyl compounds (CH=CH2) in the region of 910 cm-1 and also the double bonds of DGU at 1640 cm-1 (C=C stretch), resulting in the addition of the thiyl radicals across the ene group. The similar results for FT-IR suggest that both polymerization methods, miniemulsion and bulk, were able to produce PTEE with similar characteristics.
FT-IR spectra of nanoparticles obtained by: (a) Miniemulsion polymerization (NP 1); and (b) Emulsification/evaporation (NP 2).
To complement these results and prove PTEE formation, 1H NMR analyses were also used. Figure 2a shows the chemical structure and 1H NMR spectrum of DGU monomer before polymerization with characteristic peaks in the region 5.81-5.74, 4.98-4.89 and 2.00 corresponding to the CH=CH2 bonds. In contrast, Figure 2b shows the 1H NMR spectrum of the polymer formed, showing a reduction of the relative intensities of the three peaks attributed to CH=CH2, which indicates the consumption of double bonds of diene monomer during thiol-ene reaction of polymerization and suggesting the formation of PTEE.
1H NMR spectra for (a) monomer DGU and (b) Poly(thioether-ester), indicating the composition and consumption of the double bonds after polymerization for the miniemulsion sample. (a) 1H-NMR (600 MHz, CDCl3, δ): 5.81-5.74 (m, 2H, 2x-CH=CH2), 5.16 (d, 1H, -COO-CH-), 5.11 (q, 1H, -COO-CH-), 4.98-4.89 (m, 4H, 2x-CH=CH2), 4.79 (t, 1H, -CH2 -O-CH-), 4.43 (d, 1H, -CH2-O-CH-), 3.97-3.94 (dd, 1H, -CH2-O-CH-), 3.93-3.89 (m, 2H, -CH2-O- CH-), 3.76 (dd, 1H, -CH2-O-CH-), 2.33 (t, 2H, CH2COO-), 2.27 (t, 2H, CH2COO-), 2.00 (q, 4H, 2xCH2-CH=CH2), 1.63- 1.53 (m, 4H, 2xCH2CH2COO-), 1.36-1.31 (m, 4H, 2xCH2) 1.29-1.23 (br.s, 16H, 2x[4CH2]) ppm. (b) Peaks equal to those of a of lower intensity at 5.81-5.74 (o), 4.98-4.89 (l) and 2.00 (d), with additional peaks at 3.60, 2.50-2.40 and 1.55-1.45, which can be attributed to the presence of surfactant and water in the miniemulsion sample.
Transmission Electron Microscopy (TEM) was conducted to provide information about nanoparticle morphology and shape. TEM images show that particles obtained by miniemulsion polymerization (NP 1) presented spherical shape with particle diameters around 200-400 nm (Figure 3a), whereas particles produced by emulsification/evaporation (NP 2) also presented spherical shape, but with some imperfections on the surface and particles diameters around 80-150 nm (Figure 3b). The imperfections observed on the particle surface in NP 2 could be attributed to coalescence of smaller particles during the evaporation step. The results of FTIR and TEM showed that the different techniques affected the particle size but did not change polymer properties.
TEM images of nanoparticles obtained by: (a) Miniemulsion polymerization (NP 1); and (b) Emulsification/evaporation (NP 2).
The antioxidant activity of PTEE nanoparticles was evaluated by its capability as a hydroxyl radical scavenger through the use of 2,2-diphenyl-1-picryl hydrazyl (DPPH), via a spectrophotometric assay. When a hydrogen atom or electron is transferred to the odd electron in DPPH·, the absorbance decreases due the DPPHH non-radical formation, which can be detected at 517 nm. Figure 4 shows the scavenging activity of PTEE nanoparticles, with PTEE concentrations varying from 5 to 500 µg.ml-1. It is possible to note that increasing PTEE concentration led to an increase of the antioxidant activity for both samples (NP 1 and NP 2). The EC50 was also determined, denoting the amount of polymer required to reduce the initial concentration of DPPH· radicals by 50%. As shown in Table 2, EC50 for NP 1 and NP 2 was respectively 177.97±3.29 µg.mL-1 and 212.28±2.36 µg.mL-1 after 30 min of exposure. Similar results were found by Gizdavic-Nikolaidis et al. (2004)Gizdavic-Nikolaidis, M., Travas-Sejdic, J., Bowmaker, G. A., Cooney, R. P., Thompson, C., and Kilmartin, P. A., The antioxidant activity of conducting polymers in biomedical applications. Current Applied Physics, 4(2-4), 347-350 (2004). doi: 10.1016/j.cap.2003.11.045
https://doi.org/10.1016/j.cap.2003.11.04...
for polyaniline grafted with lignin at 20 wt% in an antioxidant test with methanolic DPPH·assay. As a result, a concentration of 200 µg.mL-1 was enough to reduce the level of 72 µM of DPPH· radicals by close to 50%. These results indicated that PTEE has potential as a scavenger of the DPPH free radical. Its activity is probably due to an inevitable polymer oxidation during the process, and the oxidation product may involve positively charged centers, with consequent donation of one or more protons from the polymer to form DPPHH (Gizdavic-Nikolaidis et al., 2004Gizdavic-Nikolaidis, M., Travas-Sejdic, J., Bowmaker, G. A., Cooney, R. P., Thompson, C., and Kilmartin, P. A., The antioxidant activity of conducting polymers in biomedical applications. Current Applied Physics, 4(2-4), 347-350 (2004). doi: 10.1016/j.cap.2003.11.045
https://doi.org/10.1016/j.cap.2003.11.04...
).
DPPH scavenging activity after 30 min of exposure at different PTEE concentrations. Results for PTEE nanoparticles obtained by: Miniemulsion polymerization (NP 1); and Emulsification/evaporation (NP 2).
Antioxidant Activity of Poly (thioether-ester) nanoparticles by DPPH free radical scavenging activity and β-carotene/linoleic acid assay.
Inhibiting peroxidation effects of nanoparticles was also determined on a linoleic acid system determined with the β-carotene bleaching test. The free radical is formed from linoleic acid and a hydrogen atom removed from a methyl group of the β-carotene molecule followed by a discoloration of β-carotene. The effect of the presence of PTEE nanoparticles in the β-carotene/linoleic acid assay was evaluated and the results are displayed in Table 2. The antioxidant activities in percentage for NP 1 and NP 2 were found to be 53.41±0.62 and 57.45±2.25, respectively. These results show that the polymer at the concentration of 1.6 mg.ml-1 was able to prevent the β-carotene discoloration by almost 60%. This result showed that the polymer had the capability of inhibiting the free-radical induction, Preventing the hydrogen atom exchange, lipid molecules cannot be converted into lipid hydroperoxide and, consequently, the lipid peroxidation is interrupted. However, the present antioxidant activity can be due to electron transfer, where a compound can deactivate a free radical by first forming a radical cation followed by rapid and reversible deprotonation in solution (Wright et al., 2001Wright, J. S., Johnson, E. R., and DiLabio, G. A., Predicting the activity of phenolic antioxidants: Theoretical method, analysis of substituent effects, and application to major families of antioxidants. Journal of the American Chemical Society, 123(6), 1173-1183 (2001). doi: 10.1021/ja002455u
https://doi.org/10.1021/ja002455u...
).
CONCLUSION
Results show that the poly (thioether-ester) nanoparticles obtained by miniemulsion polymerization or emulsification/ evaporation presented antioxidant activity, confirmed by DPPH free radical scavenging activity and β-carotene/linoleic acid assay, probably due to polymer oxidation during the process, which is able to donate hydrogen or an electron to the free radical. This property of PTEE polymers indicates their potential as a functional barrier material in the packing industry to avoid food or lipid degradation by oxidation, besides acting as a physical barrier in the composition of the polymer film.
ACKNOWLEDGEMENTS
The authors thank the financial support from CNPq (Conselho Nacional de Desenvolvimento Científico e Tecnológico), CAPES (Coordenação de Aperfeiçoamento de Pessoal de Nível Superior), TEM analyses from Laboratório Central de Microscopia Eletrônica (LCME) of Universidade Federal de Santa Catarina (UFSC) and 1H NMR analyses from Laboratório de Ressonância Magnética Nuclear (LRMN) of Universidade de Brasília-UnB, Brazil.
REFERENCES
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» https://doi.org/10.1039/C4PY01449A - Blois, M. S., Antioxidant Determination by the Use of a Stable Free Radical. Nature, 181, 1199-1200 (1958). doi: 10.1038/1811199a0
» https://doi.org/10.1038/1811199a0 - Brand-Williams, W., Cuvelier, M. E., and Berset, C., Use of a free radical method to evaluate antioxidant activity. LWT - Food Science and Technology, 28(1), 25-30 (1995). doi: 10.1016/S0023-6438(95)80008-5
» https://doi.org/10.1016/S0023-6438(95)80008-5 - Cardoso, P. B., Musyanovych, A., Landfester, K., Sayer, C., De Araújo, P. H. H., and Meier, M. A. R., ADMET reactions in miniemulsion. Journal of Polymer Science, Part A: Polymer Chemistry, 52(9), 1300-1305 (2014). doi: 10.1002/pola.27118
» https://doi.org/10.1002/pola.27118 - Durham, O. Z., Poetz, K. L., and Shipp, D. A., Polyanhydride Nanoparticles: Thiol - Ene “Click” Polymerizations Provide Functionalized and Cross-Linkable Nanoparticles with Tuneable Degradation Times. Australian Journal of Chemistry, 70(6), 735-742 (2017), doi: 10.1039/c5ra12553g
» https://doi.org/10.1039/c5ra12553g - Cramer, N. B., Couch, C. L., Schreck, K. M., Boulden, J. E., Wydra, R., Stansbury, J. W., and Bowman, C. N., Properties of methacrylate-thiol-ene formulations as dental restorative materials. Dental Materials, 26(8), 799-806 (2010). doi: 10.1016/j.dental.2010.04.005
» https://doi.org/10.1016/j.dental.2010.04.005 - Durham, O. Z., Norton, H. R., and Shipp, D. A., Functional polymer particles via thiol-ene and thiol-yne suspension “click” polymerization. RSC Adv., 5(82), 66757-66766 (2015). doi: 10.1039/C5RA12553G
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Publication Dates
-
Publication in this collection
Apr-Jun 2018
History
-
Received
28 Oct 2016 -
Reviewed
21 Mar 2017 -
Accepted
06 Apr 2017