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Polyphenol-Conjugated Bimetallic [email protected] for Improved Wound Healing

Authors Orlowski P, Zmigrodzka M, Tomaszewska E, Ranoszek-Soliwoda K, Pajak B, Slonska A, Cymerys J, Celichowski G, Grobelny J, Krzyzowska M

Received 9 March 2020

Accepted for publication 10 June 2020

Published 13 July 2020 Volume 2020:15 Pages 4969—4990

DOI https://doi.org/10.2147/IJN.S252027

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 2

Editor who approved publication: Prof. Dr. Thomas J. Webster

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Piotr Orlowski,1 Magdalena Zmigrodzka,2 Emilia Tomaszewska,3 Katarzyna Ranoszek-Soliwoda,3 Beata Pajak,4 Anna Slonska,5 Joanna Cymerys,5 Grzegorz Celichowski,3 Jaroslaw Grobelny,3 Malgorzata Krzyzowska1

1Laboratory of Nanobiology and Biomaterials, Military Institute of Hygiene and Epidemiology, Warsaw, Poland; 2Department of Pathology and Veterinary Diagnostics, Institute of Veterinary Medicine, Warsaw University of Life Sciences (WULS-SGGW), Warsaw, Poland; 3Department of Materials Technology and Chemistry, Faculty of Chemistry, University of Lodz, Lodz, Poland; 4Laboratory of Genetics and Molecular Biology, Military Institute of Hygiene and Epidemiology, Warsaw, Poland; 5Division of Microbiology, Department of Preclinical Sciences, Institute of Veterinary Medicine, Warsaw University of Life Sciences, Warsaw 02-786, Poland

Correspondence: Malgorzata Krzyzowska Email [email protected]

Background: Polyphenols possess antioxidant, anti-inflammatory and antimicrobial properties and have been used in the treatment of skin wounds and burns. We previously showed that tannic acid-modified AgNPs sized > 26 nm promote wound healing, while tannic acid-modified AgNPs sized 13 nm can elicit strong local inflammatory response. In this study, we tested bimetallic [email protected] sized 30 nm modified with selected flavonoid and non-flavonoid compounds for wound healing applications.
Methods: Bimetallic [email protected] were obtained by growing an Ag layer on AuNPs and further modified with selected polyphenols. After toxicity tests and in vitro scratch assay in HaCaT cells, modified lymph node assay as well as the mouse splint wound model were further used to access the wound healing potential of selected non-toxic modifications.
Results: Tannic acid, gallic acid, polydatin, resveratrol, catechin, epicatechin, epigallocatechin, epicatechin gallate, epigallocatechin gallate and procyanidin B2 used to modify [email protected] exhibited good toxicological profiles in HaCaT cells. [email protected] modified with 15 μM tannic acid, 200 μM resveratrol, 200 μM epicatechin gallate, 1000 μM gallic acid and 200 μM procyanidin B2 induced wound healing in vivo and did not lead to the local irritation or inflammation. Tannic acid-modified [email protected] induced epithelial-to-mesenchymal transition (EMT) – like re-epithelialization, while other polyphenol modifications of [email protected] acted through proliferation and wound closure.
Conclusion: Bimetallic [email protected] can be used as a basis for modification with selected polyphenols for topical uses. In addition, we have demonstrated that particular polyphenols used to modify bimetallic nanoparticles may show different effects upon different stages of wound healing.

Keywords: polyphenols, bimetallic nanoparticles, wound healing, mouse model

Introduction

Polyphenols are a class of naturally occurring compounds having multiple numbers of hydroxyl groups attached to aromatic rings.13 They are synthesized as secondary metabolites and are divided into flavonoid and non-flavonoid compounds. Flavonoids consist of flavonols, flavones, flavanones, flavan-3-ols, isoflavones and anthocyanidins. The non-flavonoid metabolites include phenolic acids, lignans, stilbenes, tannins and lignins.14 Polyphenols exhibit a large and diverse array of biological properties, with a great potential for the treatment of lifestyle-related diseases, such as type 2 diabetes, obesity, and metabolic syndrome.5,6 They have been also reported to prevent from aging, Alzheimer’s disease, cardiovascular diseases, and cancer.79 The most common properties of polyphenols—antioxidant, anti-inflammatory and antimicrobial indicate that they may be used in the treatment of various skin damages, such as wounds and burns.10,11

Wound healing is a process which aims to restore the integrity of the skin as rapidly as possible. It is divided into four stages that overlap in time and space: hemostasis, inflammation, new tissue formation (granulation and angiogenesis) and tissue remodeling. Various cell types such as leukocytes, fibroblasts and keratinocytes, which are controlled by several factors, including cytokines, chemokines, growth factors and enzymes interact with each other at each stage of wound healing.12,13 Prolonged inflammation delays wound closure. Chronic wounds represent a major health burden and remain a challenging clinical problem.13,14 Many studies have been focused on wound healing improvement and development of new drugs and/or dressings that promote wound healing.

In our previous papers, we demonstrated that tannic acid-modified AgNPs sized above 30 nm showed a good toxicological profile in human HaCaT and VK2-E6/E7 keratinocyte cell lines and possessed immunomodulatory and antimicrobial properties useful for potential dermal applications.15 Tannic acid-modified AgNPs sized >30 nm also promoted wound healing in the mouse model.16

AuNPs and AgNPs are the most widely used nanomaterials in biomedical applications. AuNPs exhibit chemical stability and biocompatibility, while AgNPs show good antimicrobial effects.17 However, AgNPs are less stable under identical biological and chemical conditions than AuNPs, and may show toxic effects in biological systems. Therefore, a combination of gold and silver in one bimetallic nanostructure helps to obtain a new set of properties resulting from both metals.

Bimetallic gold-silver nanostructures exhibit unique electronic,18 optical,19 and biological properties.20 Bimetallic core–shell NPs are nanostructures where one metal element forms an inner core and is surrounded by a shell from another metal. Core-shell structures containing both gold and silver material (for example, [email protected] – a gold core and a silver shell) have already been investigated.1924 [email protected] were first synthesized by Morriss and Collins19 for plasmonic applications. Core-shell [email protected] show antibacterial properties and excellent photothermal activity.22 Antibacterial activity of bimetallic gold and silver NPs was detected against both Gram-negative (Escherichia coli and Pseudomonas aeruginosa) and Gram-positive (Enterococcus faecalis and Pediococcus acidilactici) bacteria with more efficacy against Gram-negative bacteria.20 [email protected] were also used as optical biosensors to detect staphylococcal enterotoxin.23

The potential wound healing of bimetallic core–shell NPs still remains unexplored. Taking into account polyphenol usefulness in wound healing, the combined use of bimetallic NPs and polyphenols may create new possible drugs or dressings which can prove new or better properties.

In this paper, [email protected], sized 30 nm, were modified with different polyphenolic compounds: gallic acid (a building unit of tannic acid), gallic acid derivatives (epicatechin gallate, epigallocatechin gallate), and compared with other compounds containing the epicatechin core: epicatechin and epigallocatechin. The polyphenols were selected based on the analysis of the composition of the green tea extract, which has been known for its bioactive and wound healing properties.25 As the structural references two more tannins: i) resveratrol and ii) procyanidin B2 were selected. Resveratrol is the smallest polyphenol molecule with a well-known bioactivity26 in the pure form and as a complex with glucose – polydatin (naturally present in grapes). Both compounds are commercially available both in the pure form and in many extracts. Procyanidin B2 is the most basic example of non-hydrolysable tannins, commercially available in the pure form. This tannin contains two condensed epicatechin derivative substructures similar to those present in the green tea extract.

This paper uses in vitro and in vivo model to test wound healing properties of bimetallic [email protected] modified with different polyphenols.

Materials and Methods

Synthesis of Nanoparticles

Chemicals

All chemical reagents used for the synthesis and functionalization of nanoparticles were purchased from commercial suppliers: gold (III) chloride hydrate (HAuCl4·xH2O, Au ≥49, Sigma-Aldrich, Saint Louis, MO, USA), silver nitrate (AgNO3, purity 99.999%, Sigma-Aldrich), sodium citrate dihydrate (C6H5Na3O7·2H2O, ≥99.0%, Sigma-Aldrich), polyphenols (Extrasynthese, Genay, Cedex, France). For all preparations, deionized water was used (Deionizer Millipore Simplicity UV system, specific resistivity of water was equal to 18.2 MΩ·cm).

Nanoparticle Synthesis and Functionalization

[email protected] were prepared by the seeded growth-mediated method. AuNPs with the size of about 13 nm were synthesized in water according to chemical reduction method and used as crystallization seeds for the growth of AgNPs by reduction of Ag+ ions with sodium citrate. The AuNPs were synthesized by the standard citrate method with HAuCl4 reported in our previous work.27 Briefly, chloroauric acid aqueous solution (95.4 g, 1.81·10-2% wt.) was heated under reflux with vigorous stirring to the boiling point. Next, a solution of sodium citrate (4.6 g, 1% wt.) was added into the flask and the mixture was heated for additional 15 min and next cooled down to room temperature. The molar ratio of HAuCl4 to sodium citrate was 1:3.5 and the concentration of gold in colloid was 100 ppm.

The synthesis of silver shell on AuNPs seeds ([email protected]) was as follow: 10.3 g of AuNPs seed solution, 37.6 g of deionized water and 6 g sodium citrate solution (1%) were heated to the boiling point under reflux. Next, 6 g of silver nitrate aqueous solution (0.13%) was added to the reaction flask through a capillary tube with syringe pump (the flow rate equal 6 mL h−1; syringe diameter 10 mm). After the addition of all reagents, the mixture was heated for additional 15 min, and next was cooled down to room temperature in the water bath.

[email protected] were functionalized with polyphenols by incubation of aqueous modifier solution at appropriate concentration (15–1000 μm/l). The diagram showing the work-flow is presented in Supplementary Figure 1.

Nanoparticle Characterization Techniques

The hydrodynamic size and colloidal stability of [email protected] before and after polyphenol functionalization were investigated by dynamic light scattering (DLS) measurements (Anton Paar; laser wavelength 658 nm; scattering angle 173°; measurement temperature 25°C; medium viscosity 0.8903 mPa s−1; medium refractive index 1.330; silver refractive index 0.280). All measurements were performed in a quartz microcuvette.

The size of [email protected] was measured with High Resolution-Scanning Transmission Electron Microscopy (HR-STEM, Nova NanoSEM 450, FEI) using the transmission mode (STEM II) at accelerating voltage of 30 kV. Samples for measurements were prepared by placing a drop of colloid onto carbon-coated copper grid and left for 2h for solvent evaporation.

Cell Culture and Toxicity Tests

Human HaCaT keratinocytes were obtained from CLS Cell Lines Service GmbH (Eppelheim, Germany) and propagated in Dulbecco’s modified MEM (DMEM) supplemented with 10% fetal calf serum, 10 U/mL penicillin and 100 μg/mL streptomycin (Gibco by Thermo Fisher Scientific, Carlsbad, CA, USA). The cells were seeded into 24 well plates at the density of 5x104/mL cells and cultured for 24 h before exposure to nanoparticles at the concentration range of 0.5–10 µg/mL. After another 24 h cells were used for further analyses.

Toxicity of polyphenol-modified [email protected] was accessed using a cationic dye, 5,5ʹ,6,6ʹ-tetrachloro1,1ʹ,3,3ʹ-tetraethyl-benzimidazolylcarbocyanine iodide (JC-1) (Sigma-Aldrich, Saint Louis, Missouri, USA), as described previously.15,16 The stained cells were analysed in FACS Calibur using CellQuest program (BD Biosciences, USA).

ROS Production

The ROS generation was determined by a fluorometric assay with 2ʹ,7ʹ-dichlorofluorescein diacetate (DCFH-DA) (Sigma-Aldrich), as described previously.15,16 The dye-loaded cells were harvested and the fluorescence was measured at 520 nm emission wavelengths in FACS Calibur flow cytometer.

Wound Assay in vitro

HaCat cells were plated in 24-well dishes and cultured to 100% confluence. Scratches were produced using a 200 µL pipette tip, as described by Liang et al28 and Orlowski et al.16

Visualization of [email protected]

For microscopy detection of nanoparticles, cells were grown on coverslips at a density of 1 x 105/mL for 18 h before exposure to nanoparticles. After 24h of exposure to 10 µg/mL of [email protected], the medium was discarded and cells were fixed with 4% paraformaldehyde (PFA) in PBS, washed twice with PBS and covered with PBS containing 2 µg/mL Hoechst 33342 (Sigma-Aldrich). Confocal images were acquired using a Fluoview FV10i laser scanning confocal microscope (Olympus Polska Sp. z o.o.) with a 10x air lens and a 60x water immersion lens, using ultraviolet/visible light LD lasers with excitation at 638 nm. Nanoparticles were visualized in the reflection mode.

Western Blotting

Cells were collected from 6-well dishes and lysed on ice in RIPA buffer (1x PBS, 10 mL/L Igepal CA-630, 5 g/L sodium deoxycholate, 1 g/L SDS, 0.4 mM PMSF, 10 μg/mL of aprotinin and 10 μg/mL of sodium orthovanadate, Sigma Aldrich) for 30 min. After centrifugation (10,000 g, 5 min) whole-cell protein levels were quantified with Bradford assay using solution of commercial Bradford reagent (Bio-Rad) (1:4 v/v) in water. Samples containing equal amounts of protein (20 µg) were separated by SDS-PAGE and transferred to PVDF membranes. After blocking in 5% skimmed milk in TBST (NaCl 137 mM, KCl 2.7 mM, Tris base 19 mM, 0.1% Tween), membranes were probed overnight at 4°C with primary antibodies against: e-cadherin (1:200, mouse, sc-8426, Santa Cruz Biotechnology), PCNA (1:200, mouse, sc-56, Santa Cruz Biotechnology), MMP-9 (1:500, rabbit, ab38898, Abcam), involucrin (1:500, rabbit, ab53112, Abcam) and actin (1:500, goat, sc1516, Santa Cruz Biotechnology). Membranes were then incubated with an HRP conjugated secondary antibody: goat anti-rabbit (Cell Signaling Technology, 7074S) or donkey anti-mouse (Sigma Aldrich) or donkey anti-goat (Sigma Aldrich) for 1 h at room temperature (RT). Chemiluminescence detection of proteins was obtained using ECL (Thermo Fisher Scientific, 32209) and standard x-ray film developing. Subsequent quantification of band images was performed using analysis software – Image Studio Lite Version 5.2.5 (LI-COR Biotechnology – GmbH, Hamburg, Germany).

Ethical Statement

The study was performed in accordance with the recommendations of the Polish Act of 21 January 2005 on animal experiments (OJ no 33, item 289) and Directive 2010/63/EU of the European Parliament and the Council of 22 September 2010 on the protection of animals used for scientific purposes. The protocol was approved by the 4th Local Committee on the Ethics of Animal Experiments in Warsaw, Poland (permit Number: 76/2015 and WAW2/059/2018).

Wound Model in vivo

Female C57BL6 mice (Medical University of Bialystok, Bialystok, Poland), 8 weeks of age, were assigned to groups (5 animals per group). Mice were anesthetized by intraperitoneal injection of 85 mg/kg ketamine (Biowet, Pulawy, Poland) and 10 mg/kg xylazine (Xylopan, Polypharm S.A., Warsaw, Poland). Hair removal and skin wounding were performed as described previously.16 Modified [email protected] nanoparticles or corresponding polyphenol solutions were applied at 5 µg/mL in saline in the volume of 100 µL to one wound, and a vehicle control to the other. The wound was covered with a transparent occlusive dressing (3M Health Care, Neuss, Germany). 5 mg/kg of meloxicam (Loxicom, ScanVet, Gniezno, Poland) was administered once daily via subcutaneous injection for the post-operative pain relief during first 3 days. At 3, 6 and 14 days, mice were given euthanasia, wounds were excised and used for further tests.

Morphological Analysis of Wound Re-Epithelialization and Inflammatory Infiltration

Skin specimens were fixed in 4% paraformaldehyde buffered with PBS (pH 7.4) and embedded in paraffin. Tissue sections were stained with hematoxylin/eosin and Gomori’s Trichome Special Stain Kit according to the manufacturer’s instructions (Leica Biosystems, Kawaska, Zalesie, Poland). The images were captured with the Zeiss Axio Imager.M2 (Zeiss GmbH, Oberkochen, Germany). Wounds were assessed as described previously,16 ie the wound closure was calculated as the percentage of wound area at the time point in comparison to the initial wound area. The epithelial sheet area (re-epithelialization) was measured in the cross-sections stained with hematoxylin/eosin using ZEN software. Neutrophils were counted in five randomly selected microscope fields per section in the wound cavity at 400-fold magnification (0.234 mm2).

Local Lymph Node Assay (LLNA)

Female BALB/c mice (Medical University of Bialystok, Bialystok, Poland), 8 weeks of age, were assigned to groups (3 animals per group) using a stratified random grouping method based on individual body weights. Ears were stripped 10 times with an ordinary adhesive tape (Polopor, Viscoplast, Polfa Warszawa, Poland), as described before.16 After tape stripping, a vehicle negative control (acetone: olive oil, 3:1), a positive control – 25% w/v citral in vehicle (Sigma-Aldrich) and 25% w/v of polyphenol-modified [email protected] in vehicle or corresponding tannin solution in vehicle were applied to the dorsum of each ear (25 μL/ear) once daily for three consecutive days. To access lymphocyte proliferation in auricular lymph nodes, Cell Proliferation ELISA, BrdU colorimetric kit (Sigma-Aldrich) was used. Shortly, cells were seeded in 96-well round bottom plates at 104 cells per well in RPMI medium without phenol red supplemented with 10% FBS, 10 U/mL penicillin, 100 μg/mL streptomycin (Gibco), 2 µg/mL concanavalin A (Sigma-Aldrich) and at 72h, BrdU was added and the cells were incubated for another 24h. BrdU incorporation was further detected according to the manufacturer’s protocol. The absorbance was measured using FLUOstar Omega counter (BMG Labtech, Ortenberg, Germany).

Quantitative Reverse Transcriptase-Polymerase Chain Reaction (RT2-PCR)

Total RNA was isolated from the wound tissues preserved in RNAlater (Sigma Aldrich) using Universal RNA Purification Kit (EURx, Gdansk, Poland). Transcripts of TNF-α, VEGF-α, PDGF-β, IL-1α and TGF-β1 were quantified using Taqman Gene Expression Assays (Thermo Fisher Scientific). All PCR reactions were carried out with QuantiFast Probe RT-PCR Kit (Qiagen, Hilden, Germany) using a real-time PCR instrument Stratagene MX4000 Real-Time qPCR System (Agilent Technologies) according to the manufacturer’s protocol. The 2-∆∆Ct method was used in calculating the relative ratio to control uninfected tissue.

Statistical Methods

Data are shown as the mean ± standard error of the mean (SEM) from at least three independent experiments. Data were analysed using a two-tailed paired Student’s t-test (normal distribution) or with non-parametric Kruskal–Wallis and Wilcoxon's tests were applied using Biostat software (AnalystSoft Inc., CA, USA). In every analysis values of p ≤ 0.05 were considered significant.

Results

Characterisation of [email protected] Modified with Polyphenols

Figure 1A represents the schematic illustration of the [email protected] core-shell structure used for further functionalization and biological experiments. The [email protected] were designed as spherical silver nanoparticles with the size equal to 30 nm containing gold core with the size equal to 13 nm. To confirm the core-shell structure of nanoparticles, [email protected] were tested with the high-resolution scanning transmission electron microscopy (HR-STEM). The bright-field (BF), darkfield (DF) and high angle annular dark-field (HAADF) detectors were used. The BF detector in HR-STEM is located within the cone of illumination of the transmitted beam and it allows to obtain high-quality morphological images (Figure 1B) while the DF detects the scattered electrons which lie outside of the path of the directly transmitted beam (Figure 1C). The most informative for the core-shell structures is the HAADF detector, detecting incoherently scattered electrons and allowing to obtain a Z-contrast image. The Z-image is directly related to the atomic number, hence, it is useful for determination of not only the size and shape of the core-shell structure but it also helps to distinguish two types of materials with different atomic numbers. The high resolution of HAADF gives an advantage over the detection of back scattered electrons (BSE), which can also be used to detect materials with different atomic number, but with a lower resolution for core-shell nanoparticles. The HR-STEM images of synthesized [email protected] core-shell structures are presented in Figure 1BD.

Figure 1 Schematic representation of the [email protected] synthesis strategy (A) and HR-STEM images of synthesized [email protected] (BD) bright field (B); dark field (C); and high angle annular dark field (D).

The HR-STEM revealed that [email protected] are uniform with spherical shape and the mean size is 30 nm. Furthermore, HR-STEM images confirmed the core-shell structure of [email protected] Based on the image contrast, a silver shell around the gold core can be observed. AuNPs used as seeds for the growth of AgNPs are clearly visible inside the nanoparticles structure as darker areas while the silver shell is visible as a lighter coating. A silver shell of the thickness approx. 8 nm is apparent in the STEM images (Figure 1BD). In HAADF image of [email protected] (Figure 1D) the AuNPs seeds are seen as white structures. It is known that HAADF images are formed by collection of only very high angle, incoherently scattered electrons. As a result, HAADF detector is highly sensitive to atomic number of atoms present in the material (Z-contrast). For elements with a larger atomic number, the electrostatic interactions between the nucleus and the electron beam are higher, hence more electrons are scattered at higher angles. As a result, the HAADF detects more signals from atoms with higher atomic number and these elements can be seen as brighter areas in the resulting image – AuNPs seeds with ZAu = 79, while the Ag shell (ZAg = 47) on the same image is seen as darker areas (Figure 1D).

The hydrodynamic size and the colloidal stability of [email protected] were investigated with DLS measurements. The DLS size distribution histogram is presented in Figure 2A. The mean hydrodynamic size of citrate [email protected] is equal to 33 nm. Colloid was stable and any aggregates were not observed. [email protected] were functionalized with different polyphenols and characterized by DLS technique. The DLS size distribution histograms of [email protected] after functionalization with gallic acid (GAL), resveratrol (RES), epigallocatechin gallate (EGC), procyanidin B2 (PRO) and tannic acid (TAN) are presented in Figure 2BF.

Figure 2 The DLS size distribution histograms with the mean hydrodynamic size of nanoparticles: citrate [email protected] (A), [email protected] (B); [email protected] (C); [email protected] (D); [email protected] (E); [email protected] (F) with the respective chemical structure of compounds used for the functionalization. Abbreviations: ECG, epicatechin gallate modified; GAL, gallic acid modified; PRO, procyanidin B2 modified; RES, resveratrol modified; TAN, tannic acid modified.

All [email protected] colloids were stable after functionalization. The mean size of hydrodynamic diameter increased after the [email protected] modification and was: 36 nm, 45 nm, 61 nm, 63 nm and 38 nm for [email protected], [email protected], [email protected], [email protected] and [email protected], respectively. The increase of the hydrodynamic size of particles results from the size of the modifier molecule, ie, the larger the modifier molecule, the larger is the hydrodynamic diameter of the nanoparticle. Such a relationship was not observed for [email protected] because the amount of TAN used to modify was much smaller compared to other polyphenols (15 μmol/l for tannic acid, 1000 μmol/l for gallic acid; 200 μmol/l for resveratrol, epigallocatechin gallate, procyanidin B2).

Toxicity of [email protected] Modified with Polyphenols in vitro

At 24h of incubation with [email protected], the mitochondrial potential (ΔΨm) was measured using the JC-1 assay. As shown in Table 1, the cytotoxic effect of [email protected] modified with polyphenols upon the mitochondrial potential was minimal, except for modification with (15–340 μM) tannic acid and 200 μM epigallocatechin gallate (p ≤ 0.05) (Table 1). All corresponding polyphenol solutions did not induce any toxicity, except for 340 μM tannic acid causing mitochondrial toxicity already at 5 µg/mL (p ≤ 0.05) (Table 1). [email protected] modified with 200 μM epigallocatechin gallate significantly decreased mitochondrial potential at 10 µg/mL, in comparison to 200 μM epigallocatechin gallate reference solution (p ≤ 0.05) (Table 1), while 100 μM epigallocatechin gallate had no significant toxic effects (Table 1).

Table 1 Cytotoxicity of Polyphenol-Conjugated [email protected] in Human HaCaT Keratinocytes. HaCaT Cell Line Was Exposed to Polyphenol-Conjugated [email protected] at 2.5–10 µg/Ml for 24 h and Subjected to Measurement of Mitochondrial Potential with JC-1. TheResults are Expressed as the Percentage of Cells with Decreased Mitochondrial Potential from 3 Separate Experiments ± SEM

We previously showed that tannic acid-modified AgNPs sized 13 and 33 nm induced production of reactive oxygen species in HaCaT cells.15 The concentration of the tannic acid used in this work was 340 μM. Here, we used lower concentrations for modifications, such as 15 and 170 μM to found that the latter actually significantly decreased ROS production by HaCaT cells, when used at 5 μg/mL (p ≤ 0.05) (Table 2). Also, polydatin, resveratrol and epicatechin reduced production of ROS in a concentration-dependent manner (p ≤ 0.05) (Table 2). On the other hand, 340 μM of tannic acid and 100 µM epigallocatechin significantly increased ROS production (p ≤ 0.05) (Table 2).

Table 2 ROS Production by HaCaT Cell Exposed to Polyphenol-Modified [email protected] HaCaT Cell Line Was Exposed to Polyphenol-Conjugated [email protected] at 5 and 10 µg/Ml for 24 h and Subjected to ROS Measurement (Materials and Methods). The Results are Expressed as the Mean Green Fluorescence from 3 Experiments ± SEM

Wound Healing Potential Depends on the Type and Concentration of a Polyphenol Used for Modification of [email protected]

Next, we decided to find if modification of bimetallic nanoparticles with polyphenols leads to an additive effect on the migration of keratinocytes in cell culture. The scratch assay using human HaCaT cell line is a well-characterized method to measure keratinocyte migration in vitro.28 The scratch area of HaCaT cells treated with modified bimetallic nanoparticles at 5 μg/mL or with a corresponding concentration of a polyphenol used for modification appeared to have a greater number of keratinocytes present within the scratch region when compared to control cells (Figure 3) but also to cells treated with unmodified [email protected] (p ≤ 0.05) (Figure 3). For tannic acid (TAN), the migration of keratinocytes was inversely proportional to its concentration used for modification, with the [email protected] μM TAN conjugate showing significantly higher migration of keratinocytes in comparison to the polyphenol solution (p ≤ 0.01) (Figure 3A). However, only TAN-modified [email protected] showed a significant increase of cell migration (p ≤ 0.05) (Figure 2A).

Figure 3 Keratinocyte migration in response to polyphenol-modified [email protected] Quantitative analysis of scratch assay in HaCaT cell line exposed to [email protected], and [email protected] modified with different concentrations of (A) tannic acid and gallic acid; (B) resveratrol and its precursor, polydatin and (C) hydrolysable and nonhydrolyzable flavanols at 5 µg/mL for 24 h. Migration of cells is expressed as % increase in relation to control, unexposed culture with scratch. Each bar represents the mean from 5 experiments (N = 5) ± S.E.M., *represents significant differences with p ≤ 0.05, while **p ≤ 0.01. Abbreviations: S.E.M., standard error of mean.

Gallic acid (GAL), a structural unit of gallotannins such as tannic acid, significantly better induced cell migration when used for [email protected] modification in comparison to its solution (p ≤ 0.01) (Figure 3A). This effect was concentration-dependent, with [email protected] μM GAL conjugate inducing the highest cell migration (Figure 3A).

Modification of [email protected] with resveratrol or its glucoside form – polydatin showed that modifications with those two stilbenoids induced significantly higher migration of keratinocytes in comparison to unmodified [email protected] (p ≤ 0.05) (Figure 3B). However, only modification with resveratrol (RES) at 200 μM led to a significant additive effect in comparison to resveratrol solution at the same concentration (p = 0.01) (Figure 3B).

Next, we tested modification of [email protected] with flavan-3-ols for stimulation of keratinocyte migration. We found that while epicatechin at 50 and 100 μM significantly increased cell migration (p ≤ 0.05) (Figure 3C), only modification of [email protected] with 100 μM epicatechin (EPI) led to a significantly increased keratinocyte migration in comparison to unmodified [email protected] (p = 0.03) (Figure 3C). On the other hand, modification of [email protected] with its optical isomer, catechin (CAT) at 200 μM induced scratch healing in contrast to the catechin solution itself, although insignificant (p > 0.05) (Figure 3C). Epigallocatechin (EGC) as well as its gallate ester, epigallocatechin gallate (EGCG) induced significant cell migration leading to a scratch closing (p ≤ 0.05) (Figure 3C), but when used to modify [email protected], they did not produce any additive effect upon healing in comparison to [email protected] (p > 0.05) (Figure 3C). However, the gallate ester of epicatechin (ECG) used to modify [email protected] at 200 μM induced a significant additive effect upon cell migration (p = 0.001) (Figure 3C). Procyanidin B2 (PRO), a natural oligomer of epicatechin showed a significant additive effect upon cell migration within the scratch when used to modify [email protected] at 200 μM in comparison to unmodified [email protected] and procyanidin B2 itself (p ≤ 0.05) (Figure 3C). Therefore, we decided to use [email protected] modified with 1000 μM gallic acid (GAL), 15 μM tannic acid (TAN), 200 μM resveratrol (RES), 200 μM procyanidin B2 (PRO) and 200 μM epicatechin gallate (ECG) for further tests. Figure 4 shows representative images of HaCaT keratinocytes with internalised nanoparticles (turquoise). We observed no differences in the levels of internalised modified nanoparticles and in general, HaCaT cells showed very low uptake of nanoparticles (Figure 4). Supplementary Figure 1 shows the work-flow for polyphenol modification choice and further tests.

Figure 4 Keratinocytes do not significantly internalize polyphenol-modified [email protected] Confocal microscopy images showing polyphenol modified and unmodified [email protected] inside the cells (dark blue). (A) control, untreated cells, cells treated at 5 µg/mL with (B) citrate [email protected], (C) [email protected], (D) [email protected], (E) [email protected], (F) [email protected] and (G) [email protected], Nuclei were stained with Hoechst 33342 (turquoise). Images were captured using 63 x objective lens and 1.5 x digital zoom. Abbreviations: TAN, tannic acid modified; GAL, gallic acid modified; ECG, epicatechin gallate modified; RES, resveratrol modified; PRO, procyanidin B2 modified.

Polyphenol-Modified [email protected] Differently Influence Proliferation and Re-Epithelization by Keratinocytes in vitro

To test the direct effects of polyphenol-modified [email protected] upon keratinocyte biology we first tested the expression of the proliferation marker, PCNA in HaCaT cells. We found that all tested polyphenols, either alone or in conjugation with [email protected] induced significantly higher proliferation of HaCaT cells (p ≤ 0.05) (Figure 5, Table 3), except for unmodified [email protected], tannic acid or [email protected] cultures (p > 0.05) (Figure 5, Table 3).

Table 3 Quantitative Immunoblotting Results of Involucrin, E-Cadherin (80 and 120 kDa), PCNA and MMP-9 in HaCaT Cells Treated with Unmodified and Polyphenol-Modified [email protected] Cells Were Treated at 5 µg/Ml with Citrate, Unmodified [email protected], [email protected], [email protected], [email protected], [email protected] and [email protected] for 24h and Subjected to Western Blotting Assay. The Results are Expressed as Density Measurements from 3 Experiments ± SEM

Figure 5 Representative immunoblotting results of involucrin, E-cadherin (80 and 120 kDa), PCNA and MMP-9 in HaCaT cells treated with unmodified and polyphenol-modified [email protected] Cells were treated at 5 µg/mL with citrate, unmodified [email protected], [email protected], [email protected], [email protected], [email protected] and [email protected] for 24h and subjected to Western blotting assay. Abbreviations: ECG, epicatechin gallate modified; GAL, gallic acid modified; PRO, procyanidin B2 modified; RES, resveratrol modified; TAN, tannic acid modified; PCNA, proliferating cell nuclear antigen; MMP-9, matrix metalloproteinase 9.

In comparison to untreated control and cells treated with unmodified [email protected], [email protected] as well as with tannic acid itself, all other modified nanoparticles and corresponding polyphenol solutions significantly up-regulated expressions of E-cadherin (120 kDa) (p ≤ 0.05) (Figure 5, Table 3), while down-regulated production of soluble E-cadherin form (80 kDa) (p ≤ 0.05) (Figure 5, Table 3). Interestingly, [email protected] conjugates showed lower up-regulation of E-cadherin expression in comparison to corresponding polyphenol solutions (Figure 5, Table 3). Although high expression of E-cadherin is related to keratinocyte differentiation, the process characteristic for the end stage of wound healing, only epicatechin gallate, but not [email protected], caused significant up-regulation of involucrin, another marker of keratinocyte differentiation (p = 0.01, Figure 5). Matrix metalloproteinase-9 (MMP-9) is a type IV collagenase that is transiently expressed in the process of normal wound healing. Here, we found that [email protected] modified with gallic acid (GAL), procyanidin B2 (PRO), epicatechin gallate (ECG) and resveratrol (RES) or corresponding polyphenol solutions (except for resveratrol) significantly up-regulated expression of MMP-9 (p ≤ 0.05) (Figure 5). Unmodified [email protected] down-regulated expression of MMP-9 (p = 0.01, Figure 5), while [email protected] and tannic acid had no significant influence upon MMP-9 expression (p ≥ 0.05) (Figure 5).

Tannin-Ag/AuNP Conjugates Improve Wound Healing in vivo

Wound closure was observed in all treatment groups within 14 days, albeit with different characteristics (Figure 6). All tested animals formed scabs at the wound site, which lasted for several days and left residual lesions on the skin tissue after they fell off. All tested polyphenol conjugates with [email protected] showed significantly better wound closure at day 6 in comparison to untreated control and unmodified [email protected] (p ≤ 0.05) (Figures 6A and 7). However, the highest increase in thickness was observed at day 6 for [email protected] (p ≤ 0.05) (Figures 6B and 7). The corresponding polyphenol solutions did not significantly influence epithelial thickness at day 6 (Figures 6B and 7). The [email protected], tannic acid, resveratrol and epigallocatechin gallate-treated wounds showed significantly lower epithelial sheet thickness at day 14 (p ≤ 0.05) (Figures 6B and 7), while all conjugates showed similar thickness as control wounds, or higher (Figures 6B and 7). For [email protected] wounds, significantly higher epithelial sheet thickness was observed already at day 3 and 6, in comparison to wounds treated with unmodified [email protected] (p ≤ 0.05) (Figure 6B). Similarly, wounds treated with [email protected] showed earlier increase in re-epithelialization at day 6 in comparison to control and [email protected] treatment (p ≤ 0.05) (Figure 6B). Epithelial sheet thickness observed at day 6 and 14 for GAL-, RES- and [email protected] were significantly higher than that measured in wounds treated with unmodified [email protected] (p ≤ 0.05) (Figure 6B). However, these measurements did not differ from those performed for control, untreated wounds (Figure 6B).

Figure 6 [email protected] modified with selected polyphenols (tannic acid, gallic acid, resveratrol, epicatechin gallate and procyanidin B2) improve healing in a mouse wound model. Modified and unmodified [email protected] as well as solutions of polyphenols used for modification were applied at 5 µg/mL in saline and the wounds were subjected to further tests at 3, 6 and 14 days from injury. Each bar represents the mean from 5 animals ± S.E.M (N=5). (A) Percentage of the original wound size at day 6 from wounding. (B) Re-epithelialization, expressed as the epithelial sheet thickness in µm measured in hematoxylin-eosin stained tissue sections at respective days after injury. (C) Numbers of neutrophils per field in the skin sections subjected to hematoxylin-eosin staining at respective days after injury (magnification 400 x). *p ≤ 0.05 versus untreated control. Abbreviations: NPs, [email protected]; ECG, epicatechin gallate modified; GAL, gallic acid modified; PRO, procyanidin B2 modified; RES, resveratrol modified; TAN, tannic acid modified; S.E.M., standard error of mean.

Figure 7 General morphology of wounds after treatment with unmodified and polyphenol-modified [email protected] Representative microphotographs of the Tri-chrome Masson stained wound sections at 6 and 14 day post-injury. Modified and unmodified [email protected] as well as solutions of polyphenols used for modification were applied at 5 µg/mL in saline. Magnification x 400. Abbreviations: NPs, [email protected]; ECG, epicatechin gallate modified; GAL, gallic acid modified; PRO, procyanidin B2 modified; RES, resveratrol modified; TAN, tannic acid modified.

Figure 7 shows the wound healing histology for each treatment group at day 6, and 14 after wounding, stained with Masson’s trichrome procedure. This staining shows stained collagen fibers in pale blue, the cytoplasm in pale purple, the nuclei in blue, and the red blood cells in cherry red. At the early stage of the healing processes (day 6), wounds in all groups displayed evident inflammatory cell infiltration, granulation tissue formation, and epidermal proliferation. However, wounds treated with polyphenol [email protected] conjugates showed stronger and early collagen deposition and wound closure in comparison to control and [email protected] group (Figure 7).

To evaluate inflammation in wounds, we calculated the numbers of neutrophils per field (Figure 6C, Supplementary Figure 2). At day 3, we did not find any significant differences in neutrophil infiltration in comparison to control group. Interestingly, starting at day 6 neutrophil infiltration increased significantly for [email protected] wounds in comparison to control group, and it continued at day 14, also for and [email protected] (p ≤ 0.05) (Figure 6C, Supplementary Figure 2).

Polyphenol-Modified Ag/AuNPs Do Not Induce Toxic Dermal Reaction

The basic principle underlying the murine local lymph node assay (LLNA) is that sensitizers induce proliferation of lymphocytes in the lymph nodes draining the site of substance application (auricle). This proliferation is proportional to the dose applied, and provides means of obtaining an objective, quantitative measurement of sensitization. Here, we used a nonradiolabelled 5-bromo-2-deoxyuridine (BrdU) with detection by an enzyme-linked immunosorbent assay (ELISA) to assess lymphocyte proliferation. In lymph nodes isolated from ears treated with a sensitizer – citral, we found a significant proliferative response (p = 0.009), while lymphocyte proliferation in [email protected], RES- and [email protected] animals was at the level similar to control mice (Figure 8). Interestingly, corresponding polyphenol – resveratrol (RES) and epicatechin gallate (ECG) caused significant down-regulation of lymphocyte proliferation (p ≤ 0.01) (Figure 8). Similarly, other polyphenol conjugates as well as corresponding polyphenol solutions, such as GAL-, TAN- and [email protected] caused a significant decrease of lymphocyte proliferation (p ≤ 0.05) (Figure 8).

Figure 8 Polyphenol-modified [email protected] do not induce toxic dermal reaction. The murine local lymph node assay (LLNA) was used to test inflammatory ear reaction upon Ag/AuNPs exposure. Mice were subjected to ear stripping followed by three applications of unmodified and tannin-modified [email protected] (25 µg per each ear, every 24 h). Citral was used as a positive control. Proliferative response of lymphocytes isolated from auricle lymph nodes was measured by BrdU test at 72 h after stimulation with concanavalin A. Each bar represents the mean from 3 animals ± S.E.M (N=3), *means significant differences with p ≤ 0.05, while **means p ≤ 0.001 in comparison to negative control (vehicle). Abbreviations: NPs, [email protected]; ECG, epicatechin gallate modified; GAL, gallic acid modified; PRO, procyanidin B2 modified; RES, resveratrol modified; TAN, tannic acid modified; S.E.M., standard error of mean.

Polyphenol-Modified Ag/AuNPs Differently Modulate Expression of Cytokines in Wounds

The mRNA levels of tumour necrosis factor-α (TNF-α), transforming growth factor β1 (TGF-β1), interleukin 1β (IL-1β), vascular endothelial growth factor-α (VEGF-α) and platelet-derived growth factor-β (PDGF-β) were measured by qRT-PCR (Figure 9). In general, mRNA expressions of detected cytokines were increased in all treated groups at day 3 of wound repair in comparison to control wounds (Figure 9). However, the levels of mRNAs upregulation differed between the treatment groups. At day 3, wounds treated with ECG- or [email protected] and the corresponding polyphenol solutions showed the highest up-regulation of mRNA for TNF-α (Figure 9), while only [email protected] and their modifications with RES and ECG caused significant up-regulation of TGF-β1 mRNA (p ≤ 0.05) (Figure 9). Similarly, polyphenol modifications of [email protected] showed higher up-regulation of PDGF-β mRNA levels in comparison to corresponding polyphenol solutions (p ≤ 0.05) (Figure 9), except for procyanidin B2 modification. For IL-1β mRNA, the highest levels were detected at day 3 for ECG- or [email protected] The levels of mRNA for TNF-α, IL-1β, TGF-β1 and PDGF-β decreased until day 6, except for unmodified [email protected], showing high levels of TNF-α mRNA at day 14 (Figure 9). The levels of mRNA for VEGF-α were significantly up-regulated at day 14 for the wounds treated with unmodified [email protected] and modified with resveratrol and epicatechin gallate (p ≤ 0.05) (Figure 9).

Figure 9 Cytokine expression changes in wounds subjected to treatment with unmodified and polyphenol-modified [email protected] at 3, 6 and Comment: Dear author, please advise should 7 day be changed to 14 day instead as per figure images. 14 day from injury. mRNA levels of TNF-α (A), PDGF-β (B), IL-1β (C), TGF-β1 (D) and VEGF (E) were expressed as expression relative to control on the basis of the 2ΔCt method. mRNA levels were counted from three PCR reactions for each sample. N=3. *Means significant differences with p ≤ 0.05, while **means p ≤ 0.001 in comparison to control.Abbreviations: NPs, [email protected]; TAN, tannic acid modified; GAL, gallic acid modified; ECG, epicatechin gallate modified; RES, resveratrol modified; PRO, procyanidin B2 modified.

Discussion

Polyphenols have been widely used in traditional medicine to treat several chronic skin diseases, such as psoriasis and vitiligo, and they are also known to be therapeutically beneficial in wound healing and show anti-inflammatory effects when applied topically.29,30 Each bioactive agent may have specific function on wound healing properties, influencing different stages of this process. Wound dressings containing AgNPs can effectively protect an injury from bacterial infection and promote tissue regeneration during the healing process.31,32 Previously, we showed that AgNPs sized >26 nm modified with 340 μM tannic acid (TA-AgNPs) promoted wound healing both in vivo and in vitro by accelerating re-epithelialization.16 We reported that TA-AgNPs sized >26 nm induced little cytotoxicity in both mouse and human keratinocytes as well as fibroblasts in vitro. However, an increased toxicity was found in mouse monocytes, showing intensive internalization of TA-AgNPs.15,33 The internalisation-related toxicity was size-dependent, with 13 nm TA-AgNPs being the strongest inducers of ROS production.15,33

In this study, we used bimetallic [email protected], sized 30 nm, to reduce previously observed cytotoxicity and to test if we can combine wound healing properties of nanoparticles with particular properties of different polyphenols (Supplementary Figure 1). First, we chose polyphenols from the green tea extracts, known to influence skin healing on the basis of the literature review. Next, we prepared conjugates of selected polyphenols with 30 nm [email protected] and used for toxicity screening. Out of approx. 100 polyphenols used to modify [email protected], only several showed little, or no toxicity, depending on the concentration used for modification. These polyphenols included: tannic acid, gallic acid, polydatin, resveratrol, catechin, epicatechin, epigallocatechin, epicatechin gallate, epigallocatechin gallate and procyanidin B2 at different concentrations (Table 1). The toxicity of both [email protected] and polyphenol-modified [email protected] was very low, except for the highest concentrations of modification with tannic acid (340 μM) and epigallocatechin gallate (200 μM) (Table 1). This toxicity was related to ROS production (Table 2). Furthermore, polyphenol-conjugated [email protected] showed little internalization by HaCaT cells, which was related to low toxicity (Figure 4). Low toxicity of bimetallic [email protected] was also shown by other authors for HaCat cells, red blood cells34 and HEK293 cells.35

In order to select the most promising conjugates for further studies, we used in vitro scratch assay to screen for the ability to stimulate keratinocyte migration (Figure 3). We found that migration of keratinocytes into the wounded area was dependent on the type of the polyphenol used to modify [email protected], but also on its concentration. Our goal was to select modifications of [email protected], showing the highest additive effect for wound healing in comparison to polyphenol solution itself. Only five combinations fulfilled this requirement: 15 μM tannic acid, 200 μM resveratrol, 200 μM epicatechin gallate, 1000 μM gallic acid and 200 μM procyanidin B2 (Figure 3) and were used for further in vitro and in vivo studies.

Epithelial-to-mesenchymal transition (EMT) is a tightly regulated physiological process in which epithelial cells undergo multiple morphologic, biochemical and genetic changes enabling them to acquire a mesenchymal phenotype.36,37 The process of re-epithelialization is sometimes termed as “partial EMT”.38 A hallmark of EMT is cell-cell dissociation and acquisition of motility. During re-epithelialization keratinocytes at the wound edge lose their intercellular adhesions and migrate across the wound.38 EMT is also characterised by the loss of epithelial cell markers, such as E-cadherin.36,37 The cell then progresses towards a mesenchymal phenotype, accompanied by a temporally regulated expression of proteins including neural cadherin (N-cadherin), vimentin, integrin, fibronectin, and matrix metalloproteinases (MMPs).3639 Pathological EMT is present in many inflammatory diseases and leads to tissue fibrosis, loss of organ function, cancer progression and metastasis.36,37 Gliga et al, used a model of non-tumorigenic, SV40 transformed human lung BEAS-2B cells to show that repeated low-dose, long-term exposure of these cells to AgNPs sized 10 and 75 nm is pro-fibrotic, induces EMT and cell transformation.40 On the other hand, many polyphenols have been shown to regulate excessive EMT, such as tannic acid, gallic acid, epicatechin gallate, procyanidin B2 and resveratrol.41

Here, we found that polyphenols and polyphenol-modified [email protected] induced proliferation of HaCaT cells, except for unmodified [email protected] and TA-AuAgNPs (Figure 5). Interestingly, while other conjugates up-regulated expression of E-cadherin (Figure 5, Table 3), they also down-regulated production of a soluble E-cadherin form (80 kDa). Up-regulation of E-cadherin by certain polyphenols has been shown before.41 Epicatechin gallate and resveratrol can reverse TGF-β1-induced epithelial-to-mesenchymal transition by up-regulation of E-cadherin and involucrin.42,43 Metalloproteinases (MMPs) are zinc-dependent endopeptidases and key molecules in the healing process and tissue remodelling. They are capable of degrading all kinds of extracellular matrix proteins, thus helping in cell migration and wound closure. However, increased levels of MMPs are also found in chronic wounds, such as diabetic ulcers, characterised with excessive inflammation.44 AgNPs have been shown to have no influence upon MMP-2 and MMP-9 secretion45,46 and we also found that unmodified [email protected] as well as [email protected] did not influence MMP-9 expression (Figure 5). Other tested polyphenol conjugates induced expression of MMP-9 (Figure 5).

Taken together, we can conclude that wound healing by [email protected] is mediated through a presumably different process than this induced by other tested polyphenols (RES-, GAL-, ECG- and [email protected]). [email protected] induce more EMT-like re-epithelialization than other polyphenol modifications of [email protected], acting through proliferation and wound closure rather than migration of keratinocytes. Previous studies showed that TAN might directly interact with TGF-β1, thereby repressing TGF-β signalling and subsequent EMT process in epithelial cells.47 However, it is also possible that upon conjugation with NPs, especially in low doses, this activity of TAN is diminished.

Previously, we showed that treatment of the same in vivo model with 33 and 46 nm TAN-AgNPs led to a faster wound closure and increased re-epithelialization compared with control mice.16 Similarly as here, we did not observe better wound healing with uncoated AgNPs. However, other authors showed that uncoated AgNPs sized 5–15 nm but also those with a diameter of ~20 nm accelerated re-epithelialization, enhanced migration of fibroblasts and reduced neutrophil and macrophage infiltration at the wound site in rodent models.48,49 In this study, we found that modification of bimetallic nanoparticles with selected polyphenols leads to the improvement of wound healing, although particular polyphenols may show different effects upon its subsequent stages. Additionally, application of polyphenol-modified [email protected] onto the stratified ear skin in LLNA test did not lead to the local irritation or inflammation. Furthermore, some modifications also showed anti-inflammatory potentials, such as GAL-, TAN- and [email protected] (Figure 8).

Tannic acid (TAN) is a plant polyphenol found abundantly in the galls of Quercus species, and it is categorized as an antioxidant, antimicrobial, antiviral, and anti-inflammatory agent.50,51 Structurally, TAN has a glucose moiety as a core, and the hydroxyl groups of glucose are esterified with five digallic acids.50,51 Chen et al, demonstrated that TAN can accelerate wound healing through modulation of inflammatory cytokines and growth factors as well as through activation of ERK1/2 pathway.52 We also found that TAN-modified but not unmodified AgNPs down-regulated inflammatory response in HaCaT keratinocytes subjected to TNF-α and LPS, as well as induced ERK 1/2 pathway.15 We previously used AgNPs modified with 340 μM TAN, while here we managed to obtain a similar healing effect with a decreased concentration of tannic acid, and without toxicity. Previously, we also showed that expression of VEGF-α, TGF-1β and PDGF was induced by both tannic acid modified and unmodified AgNPs early during wound healing. However, this effect could be contributed to the AgNPs rather than tannic acid modification.16 [email protected] modified with 15 μM tannic acid showed up-regulation of only PDGF-α only early during proliferative phase and again, this should be contributed to the activity of nanoparticles (Figure 9).

As mentioned, TAN is a polymer of gallic acid (GA).50,51 Gallic acid is a 3,4,5-trihydoxybenzoic acid, a phenolic acid found in almost all plants including fruits, leaves, and wild flowers.53 It has been reported to possess antioxidant, anti-inflammatory, analgesic, and anticancer properties.5355 Kapoor et al, showed that GA induced cell cycle arrest at G1 phase and promoted apoptosis in fibroblasts derived from keloids.56 GA inhibited AKT and ERK1/2 activity in fibroblasts in a dose-dependent manner.56 Here we found that GA did not show any inhibitory effects upon keratinocyte proliferation, which is consistent with other studies by Yang et al demonstrating that GA is beneficial to wound healing by promoting the migration of keratinocytes and fibroblasts under normal and hyperglucidic conditions.57 However, [email protected] showed no significant up-regulation of cytokines related to wound healing, except for PDGF-α (Figure 9).

Catechins are naturally occurring polyphenolic compounds with putative anti-inflammatory, antioxidant and free radical scavenging effects in vitro.5860 By using a full-thickness incisional model of wound healing in rats Kapoor et al showed a significant improvement in the quality of scar formation and an increase in the number of new blood vessels in the ECG-treated group, correlating with high levels of VEGF.56 In our study, ECG-modified [email protected] showed the highest wound healing potential. [email protected] also induced expression of TNF-α, IL-1β and PDGF early during wound healing (inflammation phase) and this effect could be contributed to ECG itself rather than NPs. TGF-1β and VEGF levels were increased by [email protected] during inflammation and proliferative phases of healing, respectively (Figure 9). TGF-β1 plays an important role in almost all stages of wound healing and scar formation and AgNPs can upregulate TGF-β1 early during wound healing process.61 Gurunathan et al have demonstrated that AgNPs inhibited VEGF-induced cell proliferation, migration, and capillary-like tube formation of bovine retinal endothelial cells as well as effectively inhibited the formation of new blood microvessels induced by VEGF.62 Both here and previously,16 we observed an opposite effect, with [email protected] inducing VEGF upregulation during wound healing. However, this effect seems to be specifically related to the silver nanoparticle core/shell rather than a specific polyphenol modification.

Resveratrol (RES) consists 3,5,40-trihydroxytrans-stilbene, and it is one of the best-studied phytophenols with pleiotropic properties.63,64 Resveratrol inhibits VEGF-induced angiogenesis in endothelial cells65 and inhibits TNF-α-induced keratinocyte proliferation and matrix metalloproteinase (MMP-9) expression by inhibiting nuclear factor (NF)-kappa B and activator protein-1 (AP-1).65 RES also suppresses type I collagen deposition and keloid fibroblast proliferation.66 In this study, RES did not influence keratinocyte proliferation but it inhibited MMP-9 and TNF-α expression (Figure 5, Table 3). RES can inhibit EMT in colorectal cancer through the TGF-β1/Smads signaling pathway67 as well as PDGF-β-induced migration of retinal pigment epithelial cells.68 Here, [email protected] induced expression of TGF-β1 and PDGF-β expression during inflammatory phase of wound healing (Figure 9). Furthermore, [email protected] also induced expression of VEGF in the remodelling phase (Figure 9). This implies that the presence of silver in this particular conjugate modifies polyphenol properties related to EMT and angiogenesis. Still, [email protected] showed anti-inflammatory properties, as found in LLNA test.

Proanthocyanidins are a species of phenolic compounds that take the form of polymers or oligomers built of flavan-3-ol units, such as catechin, epicatechin, gallocatechin, epigallocatechin, afzelechin, and epiafzelechin.69 The most ubiquitous proanthocyanidin present in natural source is the procyanidin B2, where the flavan-3-ols are linked via an interflavan bond between the benzylic C-4 carbon of the heterocyclic ring of the upper unit and the C-8 carbon of the flavan-3-ol A-ring of the lower unit (4→8).70 Procyanidin B2 possesses anti-microbial and antioxidant properties and it induces anti-inflammatory M2 polarization of macrophages.71 Takahashi et al found that procyanidin oligomers promote the proliferation of mouse hair epithelial cells.72 Here, procyanidin B2 promoted wound healing both in vitro and in vivo, and showed anti-inflammatory activity (Figures 3, 68). Surprisingly, [email protected] up-regulated neutrophil accumulation late during wound healing (14 d) despite no up-regulation of pro-inflammatory cytokines.

Conclusion

The results of this study have demonstrated, for the first time, that treatment with bimetallic [email protected] modified with selected polyphenols results in a significant improvement of wound healing both in vitro and in vivo. In addition, we have demonstrated that particular polyphenols used to modify bimetallic nanoparticles may show different effects upon different stages of wound healing. Taking into account the ability of bimetallic nanoparticles to penetrate injured skin and interact with the skin immune system, we can assume that combining [email protected] with selected polyphenols allows to prepare a new type of nanomaterials, precisely tailored for the requirements of different types of injuries, such as chronic, infected or hyperproliferative wounds.

Acknowledgments

This work was supported by the National Science Centre Poland grant no. 2014/13/B/NZ5/01356.

Author Contributions

All authors made substantial contributions to conception and design, acquisition of data, or analysis and interpretation of data; took part in drafting the article or revising it critically for important intellectual content; gave final approval of the version to be published; and agree to be accountable for all aspects of the work.

Disclosure

The authors report no conflicts of interest in this work.

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