Modulating the Antioxidant Activity of Thin Layer-by-Layer Films with Polyphenols

Plants and fruits contain many antioxidant molecules among them polyphenols [1]. Such natural antioxidants can find applications in food science [2] and in particular for food packaging when the molecules of interest are integrated in a film or a membrane. Many polyphenols, among them tannic acid (Figure 1) deposit spontaneously at solid liquid interfaces in a versatile manner. The deposition of TA and other polyphenols occurring spontaneously on glasses from wine or from tea has been exploited recently in materials science [3,4]. Polyphenols contain redox active groups which can also act as coordination centers for metal cations like Fe3+. This chemical modality allows the deposition from polyphenol-metal cation mixtures to yield conformal coatings [5] or to obtain films by alternating adsorption steps of the polyphenol and metal cations according to a Layer-by-Layer (LBL) deposition method [6]. The same deposition strategy can be used to deposit polyphenol containing films by alternating their adsorption with that of a polymer [7], a polyelectrolyte [8] or proteins [9]. In these cases, the interactions responsible for the cohesion of the films are due to hydrogen bonding or to electrostatic interactions (polyphenols containing also weakly acidic groups able to become anionic at high enough pH). The deposition of films made from proteins and polyphenols is due to the interplay of many kinds of interactions among them some specific interactions with amino acids like L-proline [10]. Films containing TA and other polyphenols display some antioxidant activity [11]. The advantage of the LBL deposition method of a material with respect to direct functionalization by contact with a polyphenol containing solution, leading mostly to a deposited monolayer, is an increased stability and durability of the coating. Herein, it will be shown, that LBL films made from a polycation and TA are characterized by an amount of TA which is proportional to the number of deposition steps. The antioxidant activity of those (PAH-TA)n films (where n denotes the number of deposition cycles of the polycation and the polyphenol) scales also proportionally with the number of the deposition steps, as in other studies [11]. This means that all the polyphenol molecules in the film are accessible to the used probe, 2,2-diphenyl-1-picrylhydrazyl (Figure 1). The antioxidant properties of the films can be suppressed by depositing two capping bilayers made from poly (allylamine hydrochloride) (PAH) and poly (sodium 4-styrene sulfonate) (PSS). This new finding will be discussed in terms of possible applications in food packaging.


Copyright © Vincent Ball
SBB.MS.ID.000560. 3 (2).2019 1 , Mw=70000g.mol -1 obtained by means of gel permeation chromatography as given by the furnisher) were purchased from Sigma Aldrich and used without further purification. All solutions were prepared before use in 50mM sodium acetate buffer. The buffer was made from double distilled and deionized water (Millipore D8 system, ρ=18.2 MΩ.cm). TA, PAH and PSS were dissolved in the sodium acetate buffer at a concentration of 1mg.mL -1 . DPPH (ref. D9132, Sigma-Aldrich) was dissolved at 10 -4 M in absolute ethanol and stored at 4 °C in the absence of light to ensure its stability. The chemical structure of TA and DDPH, as well as the reaction of DDPH with an oxidant are shown in Figure 1. The adsorption substrates were 4cmx1cm quartz slides (Thuet, Blodelsheim, France) cleaned with ethanol, dried under a stream of filtered air and subjected to 5min of plasma cleaning in an air plasma (PDC-32G-2, Harrick Scientific, USA). The LBL deposition was performed as described in ref. [12]. Briefly: the cleaned quartz slide was dipped during 5min in the PAH solution, in sodium acetate buffer, in the TA solution and again in sodium acetate buffer. The contact with buffer allowed to remove weakly bound molecules from the surface. The successive deposition of a PAH and TA led to the deposition of one-layer pair. This deposition step was repeated n times. The as obtained (PAH-TA) n films were then rinsed with distilled water and dried under a stream of filtered air, in order to avoid crystallization of salt from the buffer.

Oxydant+H
Reduced molecule-H A B The absorbance of the quartz slide was then measured between 250 and 700nm using a double beam spectrophotometer (UV-mc², Safas, Monaco) against a cleaned quartz slide taken as the reference. The films were then immersed in a 10 -4 M DPPH solution dissolved in absolute ethanol which constitutes time t=0 of the DPPH quenching kinetics. To follow that kinetics as a function of the number of PAH-TA layer pairs, the absorbance of the solution with the immersed quartz slide+film was measured every 15s during 15min at λ=517nm with the mc² spectrophotometer. In these kinetic experiments, the reference cuvette contained the ethanolic DPPH solution and an uncoated quartz slide. Hence, the spontaneous quenching of DDPH by oxygen is taken into account. The absorbance will appear as negative values since the films induce a faster quenching than dissolved oxygen. To characterize the film deposition, water contact angles were measured with 5µL water droplets using the sessile drop method with an attention theta goniometer (Biolin Scientific, Sweden). The obtained contact angle values correspond to the average of 5 regularly spaced locations along the quartz slide and the error bar corresponds to one standard deviation. The water contact angle of LBL films characterizes their surface composition and a last layer effect is often observed for relatively stratified films [13].

Result and Discussion
The deposition of (PAH-TA) n films (5min per adsorption and rinsing step as in ref. [12]) was characterized by means of UV-vis spectroscopy ( Figure 2) and by contact angle goniometry ( Figure  3). The film growth is of linear type, meaning that the absorbance increases at λ=300nm, due to TA (PAH does not absorb light above λ=200nm), scales in proportion to the number of deposited layer pairs ( Figure 2). In addition, the interaction of the film with tiny water droplets reflects the nature of the last deposited layer ( Figure  3). The films are more hydrophilic (static water contact angle close to 8 °) when they are made from TA as the last deposited layer than from PAH as the last layer (contact angle close to 12 °). The behavior found for (PAH-TA) n films is typical of linearly growing LBL films [6,11,13]. The morphology of the (PAH-TA) n films has also been characterized by means of Atomic Force Microscopy and some typical images acquired in the contact mode and in the dry state can be found in Figure 4 of ref. [12]. Absorbance spectra of (PAH-TA)n films with n = 1 (_ _ _ _), n = 2 (_____), n=4 (_____), n = 6 (______) and n=8 (______) deposited layer pairs. The inset displays the absorbance increase at λ=300nm as a function of the number of deposited layer pairs. The full and dotted lines represent the linear regression to the data and the limit of the 95% confidence interval respectively. The (PAH-TA)n films were deposited on quartz slides and their spectra were measured against a plasma cleaned quartz slide.  The (PAH-TA) n films display some antioxidant activity as quantified through a decrease in absorbance at λ=517nm, typical of the transformation of the purple DPPH into the yellowish DPPH-H (Figure 1). From a qualitative point of view, one observes indeed a reduction in the purple color of a 10 -4 M DPPH solution when a quartz slide covered with a (PAH-TA) 4 film on both its faces is immersed in it during 15min ( Figure 4A). After 15min the reservoir of active TA in the films seems not yet exhausted as shown by the kinetic runs in Figure 4B. But for convenience we stopped the assays after 15min, and all films were compared for their antioxidant activity after this given reaction time with DPPH. It appears that the antioxidant activity of the (PAH-TA) n films is proportional to the number of deposited layer pairs ( Figure 4A) and hence to the amount of incorporated TA (Figure 2). This means that the films are permeable to DPPH which can reach all TA molecules in the film irrespective of their position, either close to the film/solution or to the quartz/film interface. This result is in perfect agreement with the data reported in ref. [11].
There is however a single way to suppress access of DPPH to the TA present in the (PAH-TA) n films by capping them with (PAH-PSS) layer pairs ( Figure 5A&5B). Such layer pairs are known to be of compact nature and to suppress the diffusion of a polyelectrolyte like poly-L-Lysine (PLL) from a superior (PLL-HA) m1 stratum (HA represents hyaluronic acid) to a previously deposited (PLL-HA) m2 stratum [14]. Hence (PAH-PSS) n layer pairs are able to stratify an otherwise un-stratified (exponentially growing) (PLL-HA) m film. In the present investigation we show that an extremely thin (PAH-PSS) 2 film (about 5-6nm in thickness [15]) is able to almost quantitatively suppress the diffusion of a small molecule like DPPH in the underlying (PAH-TA) 3 film. This is the major finding of the present investigation. It could have some applications in packaging: when a (PAH-TA) n -(PAH-PSS) 2 film is deposited on a package (for instance by alternated spray deposition to speed up the process with respect to alternated dipping) no color change of a drop of deposited DDPH is found as long as the coating has not undergone damage. But as soon as the package has been damaged, the (PAH-PSS) 2 capping layer contains some cracks and becomes permeable to DPPH which then undergoes a visible and fast color change.

Figure 5:
A: Reduction of the antioxidant activity of (PAH-TA)3 films after deposition of PAH-PSS "capping layers" as indicated in the inset. Each kinetic curve corresponds to an independently prepared film. B: Evolution of the relative antioxidant activity after 15min of contact with the 10-4M DPPH solution as a function of the number of (PAH-PSS) capping layer pairs. The relative activity of 1 corresponds to that of the (PAH-TA) film.

Conclusion
It has been shown that the antioxidant activity of (PAH-TA) n films can be modulated through an increase in the number of deposited layer pairs and hence with an increase in the amount of TA, the antioxidant polyphenol, incorporated in the film. The addition of only two (PAH-PSS) capping layer pairs totally suppresses the access of DPPH to the underlying TA highlighting the compact and impermeable nature of those very thin capping layers. A practical application in possible sensing of packaging integrity is proposed on the basis of those findings.