PROCESS FOR THE PREPARATION OF BIOCOMPATIBLE, FREE-STANDING

NANOFILMS OF CONDUCTIVE POLYMERS

DESCRIPTION

Field of the invention

The present invention refers to a process for the preparation of biocompatible, free-standing nanofilms of conductive polymers that, thanks to their characteristics of flexi bi l ity, strength , abi l ity to ad h ere to d ifferent substrates and excellent biocompatibility, are useful for different technological applications, in particular in the biomedical field, for example for use as a support for seeding and proliferation of cells.

State of the Art

In the latest decades conductive polymers have been the subject of a very large number of studies for their interesting properties of stability and conductivity, which make them potential replacements for conventional inorganic conductive materials in electrical and electronic devices. For such applications, materials able to be obtained in the form of thin films are particularly sought after, whereas conductive polymers, since they scarcely soluble in common solvents, are not easy to manipulate to obtain thin conductive films and their dispersion and/or solubilisation is difficult due to the lack of adequate solubilisation media and techniques that are simple and cost-effective. In order to avoid this problem, these polymers are often prepared in situ directly on the desired substrates, starting from the respective monomers with ch em ical or electrochemical processes. In this case, however, the subsequent removal of the film, or its transferal onto other substrates, are particularly difficult, if not actually impossible, whereas for many applications it is required to have films without support, so-called "free-standing" films.

Thanks to the good conductivity and the exceptional chemical stability, one of the most successful conductive polymers is poly(3,4-ethylendioxytiophene), or PEDOT, in particular in the form of a complex with polystyrene sulphonate, or PSS (S. Kirchmeyer et al., J. of Materials Chemistry 2005, 15, 2077) an aqueous dispersion of which can be found on the market, which has been used for some time to produce conductive coatings on different substrates, as described for example in EP1616893. Such a material is used for example as a conductive coating in optoelectronic multi-layer structures, or in electrolytic condenser, or also as active material in transducers based on its properties of responsiveness to externa l physical sti m u l i. The h ig h biocompatibility of this material has also been recently demonstrated and has led to its application for the development of microelectrodes for neural interface as well as for building supports for the adhesion and proliferation of epithelial cells controlled by the electrochemical modulation of surface properties [M. H. Bolin et al., Sensors and Actuators, B: Chemical 2009, 142, 451 ; and K. Svennerstenet al., Biomaterials 2009, 30, 6257].

However, as far as the Applicants are aware, up to now there has been no description in literature of any simple and cost-effective process, capable of producing biocompatible, free-standing nanofilms of PEDOT, as well as of other conductive polymers. Recently, techniques have been described for obtaining free-standing films of PEDOT or PEDOT/PSS, but of substantial thickness, comprised between 5-10 μηη and a few cm [see for example H. Okuzaki et al., J. Phys. Chem. B 2009, 113, 1 1378]. Such methods refer mainly to techniques of deposition of film by solvent casting, which are intrinsically not very specific for obtain ing films with nanometric thickness. Moreover, the control of the thickness able to be obtained with such methods is difficult and not very accurate; and, even when these methods could be used with suitable modifications to obtain nanofilms, the possible release from the substrate and transferal would be impossible given their extreme fragility.

K. S. Choi et al., Langmuir 2010, 26 (15), 12902-12908 describe a nanofilm that can be released in water, consisting of three alternate layers of graphene, PEDOT and graphene; but the process for its preparation is very long and complicated, as well as very wasteful both in terms of materials used and in terms of equipment. Moreover, the use i n th is process of solvents and chemical reactants that are certainly not biocompatible can have a negative impact upon the biocompatibility of the nanofilm obtained, which is not however investigated in the article in question.

T. Fujie et al., Adv. Funct. Mater. 2009, 19, 2560-2568 describe a process for preparing free-standing polysaccharide nanofilms, for biomedical applications, consisting of deposition by spin-coating directly on a support of Si0 ₂ of aqueous solutions of polysaccharides, such as chitosan and sodium alginate, followed by the deposition of a layer of polyvinyl alcohol (PVA) by "drop-casting". The bi-layer film consisting of polysaccharide and PVA is then removed from the Si0 ₂ support with tweezers and d ipped i n water where the layer of PVA dissolves, releasing a polysaccharide nanofilm. In this article there is no mention of intermediate layers between support for growth of Si0 ₂ and polysaccharide layer, and nor reference is made to conductive polymers, and in general to the possibility of using a similar method to produce nanofilms of different polymers to the polysaccharide ones given as an example.

A similar method was also described by Stroock et al., Langmuir, 2003, 19, 2466-

2472, where polyacrylic acid (PAA) was however used as water-soluble sacrificial layer instead of polyvinyl alcohol (PVA), for deposition on a multi-layer film where many different polymers were cross-linked and in turn deposited on a printed support. The surface of the films obtained with this process was very small.

Therefore, the technical problem is still felt of having a simple and cost-effective process for the production of biocompatible nanofilms of conductive polymers, which are free-standing, i.e. capable of supporting themselves and of keepi ng thei r characteristics of stability and conductivity even when released from the support on which they were prepared.

Summary of the invention

Now the Applicants have found a simple and cost-effective process, suitable for the preparation of free-standing nanofilms of conductive polymers, which also does not compromise the biocompatibility of the polymer used, so that the films obtained are highly biocompatible, and therefore particularly suitable for biomedical applications, for example for use as supports for the seeding and proliferation of cells.

Subject of the i nvention is therefore a process for the preparation of biocompatible, free-standing nanofilms of conductive polymers, characterised in that it comprises the following steps:

a) sequential deposition on a support for growth of a layer of a first polymer and of a layer of conductive polymer, wherein the deposition of said layer of conductive polymer is carried out by spin-coating, to obtain a film consisting of said layer of a first polymer and said layer of conductive polymer on said support for growth;

b) thermal treatment of the film coming from step a);

c) deposition of a layer of a second polymer, soluble in water and such that said layer of conductive polymer adheres to said layer of a second polymer;

d) peel off of said layer of conductive polymer on said layer of second polymer, from said layer of a first polymer on a support for growth;

e) release of said layer of conductive polymer as a free-standing nanofilm by immersion in water of said layer of conductive polymer on said layer of a second polymer coming from step d), and dissolving said layer of a second polymer.

A further subject of the invention is films comprising a layer of conductive polymer on a layer of said second polymer coming from step d) of the aforementioned process; and their use for the preparation of free-standing nanofilms of the invention by dissolving the layer of said second polymer.

The films obtained with the process of the invention have a high surface area/thickness ratio and, although they have no support, they remain flexible and strong, with high adhesiveness; they are also highly stable and easy to manipulate in aqueous environment or in biological fluids, and thus suitable for a wide range of applications, including those in the biomedical field. The present films are also characterised by a high homogeneity and equipped with conductive properties, which make them useful for example for the preparation of supports for cell cultures in which growth and cell proliferation can be stimulated by electrical impulses. At the same time, with the process of the invention, it is also possible to obtain nanofilms with a conductive layer that is not homogeneous but comprises conductive areas and non- conductive areas, according to a predetermined pattern; such films allow to achieve differences in potential on the film itself in a localised manner, for example finding advantageous applications in cell stimulation, and i n maki ng sensors and/or biosensors.

Further characteristics of the process according to the present invention are given in the attached claims.

Brief description of the drawings

Further characteristics and advantages of the process according to the invention will become clearer from the following description of embodiments thereof given as a non-limiting example with reference to the attached Figures, in which:

- Figure 1 is a schematic representation of an intermediate film according to the invention, before dissolving the sacrificial layer of cellulose acetate;

- Figure 2 illustrates the progression of the surface resistivity of the PEDOT/PSS nanofilms obtained as described in Examples 1 to 4, as a function of the rotation speed applied in the step of deposition of the conductive layer of PEDOT/PSS. The values indicated with— o— refer to the data obtained using the commercial product Clevios™ P AG as precursor of the layer of PEDOT/PSS, whereas the values indicated with— ·— refer to the data obtained using the Clevios™ PH1000 product.

- Figure 3 illustrates the progression of the values of surface resistance detected as a function of the rotation speed, for both the two series of films obtained from the two different commercial precursors of the layer of PEDOT/PSS, again supported on Si/PDMS. The values indicated with — o— refer to the data obtained using the commercial product Clevios™ P AG, whereas the values indicated with— ·— refer to the data obtained using the Clevios™ PH1000 product.

- Figure 4 illustrates the progression of the values of surface resistance detected for three different series of nanofilms all prepared from Clevios™ PH1000, as a function of the different rotation speeds applied. The values indicated with— ·— refer to the data obtained using the film of PEDOT/PSS again supported on Si/PDMS, the values indicated with—■— refer to the free-standing films of PEDOT/PSS transferred on glass, whereas the values indicated with—□— refer to the same films transferred on glass but also subjected to thermal treatment at a temperature of 170°C for 1 hour.

- Figure 5 illustrates a histogram that compares the values of conductivity detected for four different types of PEDOT/PSS nanofilms:

• PAG@PDMS: nanofilms prepared from Clevios™ P AG again supported on Si/PDMS (obtained in step c) of the present process);

• PH1000@PDMS: nanofilms prepared from Clevios™ PH1000 again supported on Si/PDMS (obtained in step c));

· PH1000@Glass: free-standing nanofilms prepared from Clevios™

PH1000 transferred on glass (obtained in step e) then transferred on glass); • PH1000@Glass ^* : free-standing nanofilms prepared from Clevios PH1000 transferred on glass and subjected to thermal treatment at the temperature of 170°C for 1 hour (obtained in step e), then transferred on glass and subjected to thermal treatment);

- Figure 6 shows the photographic image of a free-standing nanofilm, floating in water, consisting of a layer of polylactic acid (PLA) and of a layer of PEDOT:PSS, obtained as described in Example 8.

Detailed description of the invention

In the process according to the invention a layer of a first polymer is deposited on a support for growth, for example selected among the planar supports commonly used in preparations of supported films, like for example supports made of Silicon, Silicon nitride, quartz, glass, Indium oxide doped with tin (ITO), and ceramic materials.

The deposition of the layer of conductive polymer is carried out in the present process by "spin-coating", a technique of deposition of polymeric films on supports that is well known in the field and described for example in D. Meyerhofer, Journal of Applied Physics 1978, 49, 3993-3997. Preferably, the deposition of the layer of first polymer is also carried out with this technique, even though other techniques known in the field, like for example spray-coating, inkjet printing, screen printing, and similar, could be used.

For the preparation of the intermediate layer between support for growth and layer of conductive polymer, as first polymer it is possible to select any hydrophobic polymer that can be deposited on a support creating a perfectly planar thin layer, for example by spin-coating of a precursor thereof, and the surface of which can be made hydrophilic by plasma treatment. The first polymer in the present process can for example be selected among epoxy resins, such as the formulations used in UV photolithography processes available on the market with the name SU8 (Microchem, USA), and silicon polymers, for example those that can be obtained using chlorosilanes a s p re c u rs o rs, i n p a rt i c u l a r methylchlorosilanes, ethylchlorosilanes, phenylchlorosilanes, and similar. A silicon polymer that is particularly preferred for use in the present process is poly(dimethyl siloxane) (PDMS), for example able to be prepared from a mixture containing prepolymer and cross-linking agent, and available on the market with the trademark Sylgard (Dow Corp, USA).

When the deposition is carried out by spin-coating of PDMS or of another high- viscosity silicon polymer, a suitable solvent, for example selected among n-alkanes, like n-hexane or n-heptane, is mixed preferably with the polymer or with a precursor thereof, in a quantity comprised for example between 5 and 140% by weight with respect to the weight of the mixture, so as to lower its viscosity and obtain a low thickness of the layer by spin-coating.

Moreover, according to the material selected as first polymer, before carrying out the deposition of the layer of conductive polymer, a further treatment can be carried out in order to increase the surface wettability of the layer of the first polymer; for example, when PDMS is selected as first polymer, a plasma treatment of 0 ₂ is preferably carried out before proceeding to the deposition of the layer of conductive polymer.

The process of the invention can be carried out using any conductive polymer or mixtures/complexes of conductive polymers, provided that they are available in the form of a solution or an aqueous dispersion. In general terms by "conductive polymer" it is meant an organic polymer capable of conducting electrical charges (ion and electronic), generally defined as a polymer having electrical conductivity σ comprised between 10 ^"3 and 10 ⁵ S/cm; typically, the conductive polymers used in the present invention have an electrical conductivity comprised between 0.1 and 1000 S/cm, which is maintained by the nanofilm obtained at the end of the present process. Suitable conductive polymers are selected for example among so-called "conjugated polymers " or "intrinsically conductive polymers" (ICP), polymers consisting of molecules with conjugated bonds that owe their conductivity to the particular structure, possibly complexed with suitable dispersants to make them available in the form of an aqueous dispersion. Examples of these polymers include polypryyol, polythiophene, polyaniline, and their derivatives. Du e to their characteristics of high durability and high conductivity, polythiophene and its derivatives are the preferred conductive polymers according to the invention.

These conjugated polymers can have one or more substituents, the same or different from one another, for example selected from the group consisting of alkyl, alkylene, alkynyl, alkoxy, alkylthio and amino groups. When there are two substituents, bound together, they can form a ring adjacent to the thiophene ring; for example, two alkoxy groups ca n fo rm a dioxane ring. According to a particularly preferred embodiment of the present invention, the conductive polymer is indeed a derivative of polyth ioph ene i n wh ich th e two substituents form a dioxane ring: poly(3,4- ethylendioxytiophene) commonly known by the acronym PEDOT, in the form of a complex with a dispersing agent, for example with polystyrene sulphonate (PSS). Preferred conductive polymers according to the invention are the complexes commonly ind icated by the acronym PEDOT/PSS, i n wh ich the weight ratio of the two components can be comprised between 1/2,5 and 1/20, and it is for example equal to 1/2,5 like in the commercial products Clevios™ PAG and Clevios™ PH1000 (H. C. Starck GmbH, Leverkusen, Germany), respectively.

The film coming from step a) consisting of the layer of first polymer and of the layer of conductive polymer deposited on the support for growth, is then subjected to a thermal treatment, carried out for example at a temperature comprised between 90 and 200°C, preferably subjecting the film for 1 hour to the temperature of 170°C.

Polymers suitable for the preparation of the layer of the second polymer according to the present process are water-soluble polymers, for example selected from the grou p consisting of polyvinyl alcohol (PVA), polyvinylpyrrolidone (PVP), polyethylene glycol (PEG), and water-soluble cellulose ethers, and preferably it is a layer of PVA, prepared by drop-casting deposition of an aqueous solution of PVA having a concentration for example comprised between 5 and 20 % by weight of PVA with respect of the total weight of the solution.

In the present invention, by "water-soluble polymer" we mean in general a polymer that can be dissolved in water as defined for example by Graham S. et al. in Requirements for biodegradable water-soluble polymers, Polymer Degradation and Stability, 1998, 59, 19-24; more specifically, we mean those polymers that can have solubility in water up to values of 10-20% by weight at room temperature; when deposited in layers of typical thickness like that described here, these polymers can be completely dissolved in water, without leaving any residue and without the use of agitation, in a short time period (comprised for example between 60 and 600 seconds) and at a temperature of 25°C.

In step c) of the present process the deposition of the layer of second polymer is carried out with a technique selected among those known and commonly used in the field of the production of polymeric films, with which the layer of conductive polymer adheres preferentially with respect to the layer of first polymer, then in the next step d) the layer of conductive polymer adhered on the layer of second polymer peels off from the layer of first polymer on the support for growth; such a peeling off operation can be made easier by cutting the surface with a thin blade and/or by lifting the film with the help of tweezers.

Thanks to the process of the invention, the release in water of the nanofilm of conductive polymer can be carried out simply by dissolving in water the support layer. The use of mechanical stirring and/or of water at a temperature of between 35 and 40°C may facilitate and speed up the release in water of the nanofilm, and therefore constitutes a preferred embodiment of step e) of the present process.

The transferal of the nanofilm in other aqueous solutions or biological fluids can be easily carried out for example by suction and expulsion with a pipette, without the film suffering any damages. The nanofilms obtained with the process of the invention can therefore be redeposited on solid substrates of various kinds and geometries according to the required application, for example on substrates made from glass, paper, steel, metals, plastic, elastomers, but also on samples of human skin, in all cases displaying excellent adhesion, since the great flexibility and the nanometric thickness of the film allow it to adapt to the microcorrugations and porosities present on the surface of the materials. The deposition on such substrates can be carried out directly or by means of perforated meshes of metal wire, preventing the film from drying out completely before it is deposited on the substrate. Only at this point is it possible to proceed to drying for example with a jet of compressed air and/or thermal treatments, to eliminate any residual water from the surface and to improve the adhesion to the substrate that will finally be complete. Once deposited on the substrate, the film can also be cut with the help of a suitable metallic blade.

The process of the present invention thus makes it possible to obtain strong polymeric films, equipped with limited degradability over time, homogeneity and conductive properties, and of the desired dimensions, with thickness typically comprised between 40 and 200 nm, and preferably comprised between 45 and 100 nm, and a large surface, for example greater than 1 cm ² . Within these ranges the thickness of the present polymeric films can be varied according to requirements, by acting on some parameters of the process, for example speed and rotation times of the spin-coating steps or type of polymers used.

The nanofilms obtained with the present process also have great chemical and structural stability and resistance when released in the form of free-standing films in water, aqueous solutions or biological fluids; in particular, thanks to the present process, the release from the support and transferal in water does not compromise the stability and integrity even of polymeric films with a surface of a few cm ² .

The process of the invention, in a particular embodiment, which will be described in detail hereafter, also makes it possible to prepare nanofilms with the aforementioned dimensions and properties, having a conductive layer that is not homogeneous, but rather comprising both conductive areas and non-conductive areas according to a predetermined pattern, which makes such films particularly suitable for application as supports for cellular growth, stimulation and differentiation thanks to the ability to control in a localised manner the electric potential and cellular adhesiveness on the surface of the substrate; such films are also suitable for use as substrates for making sensors and biosensors.

In such an embodiment, the process of the invention also comprises a step b') of irreversible and localised oxidation of the layer of conductive polymer in the film coming from step b) described above. By the term "localised oxidation" we mean oxidation that is not extensive, but in areas, able to be carried out with various oxidants and various techniques, provided that they are suitable for carrying out an irreversible oxidation of the conductive layer, and selective in certain areas so as to create a sort of definite "design" or "pattern". The irreversible oxidation causes a substantial decrease in electrical conductivity with consequent "deactivation" of the oxidised area that takes on the properties of an electrical insulator. In the present process, as well as the localised "deactivation" of conductivity, a further consequence of the process of irreversible oxidation is the change in colour of the film, which from blue (or light blue, depending o n th e thickness) becomes colourless, with a consequent change in optical transmittance over the entire spectral range of the visible light. The oxidised areas, whilst showing a slight reduction in roughness at the nanometric level with respect to those not oxidised, do not however show significant alterations in thickness.

Oxidising treatments suitable for carrying out the invention are selected from treatments with oxygen plasma, or with an aqueous solution of sodium hypochlorite or of hydrogen peroxide, using printing techniques commonly used in the field of nanotechnology, suitable for printing in areas, like for example so-called micro Contact Printing (μΟΡ), inkjet printing, electrochemical excess oxidation or the photolithographic technique. In the latter suitable photolithographic resins are used, to be deposited on the conductive layer with the function of a protective mask carrying the predetermined pattern, before proceeding to the oxidising treatment by areas in a bath of oxidising solution. Examples of photolithographic resins suitable for the purposes of the invention are th e prod ucts kn own by the trade n ame Shipley Microposit S1800 Series Photoresists, positive tone resists, the residues of which are then removed from the surface after the oxidising treatment. Other similar photoresists, positive or negative, can be used in this step without departing from the scope of the present process.

According to a preferred embodiment of the invention, before proceeding to the deposition of the second polymer soluble in water in step c) described above, the process comprises a step b") in wh ich there is the deposition on the oxidised conductive polymer by areas, of a layer of an additional polymer, and only afterwards the second polymer is deposited, thus creating a water-soluble layer on the layer of additional polymer, instead of directly on the layer of conductive polymer. Additional polymers suitable for use in the present process are polymers soluble in solvents, such as water and chloroform, which do not degrade the underlying conductive polymer, which can easily be deposited in uniform layers by spin-coating and that are insoluble in water after deposition; such polymers are for example selected from polylactic acid and photosensitive resin known with the name SU8, an epoxy-based photoresist. Through the peeling off of the layer of first polymer on the support for growth, and the dissolving in water of the layer of second polymer according to steps d) and e) described above, a nanofilm is finally obtained comprising the layer of additional polymer on which a pattern is created having micrometric resolution, of conductive areas derived from the localised oxidation of the layer of conductive polymer.

Thanks to the characteristics described above, the nanofilms of the present invention have numerous applications, like for example in the field of the development of new sensors and actuators, as "smart material" in the locomotion in water or other biological fluids of objects in the micro- and meso-scale, in the manufacture of multilayer and/or multifunctional structures, in the deposition of nanometric conductive films on microfabricated artefacts, on biological samples or other objects even characterised by non-planar and complicated geometries.

All of the nanofilms prepared with the process of the invention are biocompatible.

The term "biocompatible" in the present invention refers to those products that, when placed in direct contact with organisms, such as cells, microorganisms, tissues, etc., do not cause harmful effects on their vital functions and/or are effectively metabolised by them. In particular the biocompatibility in vitro of the present nanofilms has been demonstrated with respect to maintaining cell viability by means of adhesion tests and viability of cell cultures with cells of various kinds, in the short, medium and long term. The materials used in the preparation of the present nanofilms have also proven to be biocompatible in in vivo tests on animals, and in the application to the construction and coating of neural electrodes, where a total absence of harmful effects, even in the long term, has been confirmed.

Thanks to these properties, the present films can be used as substrates for the adhesion, growth, differentiation and electrical and mechanical stimulation of cells, also in order to develop bio-hybrid devices and actuators. In such micro-devices the use of cell lines capable of contracting spontaneously (for example cardiomyocites) or when subjected to electrical stimuli (for example myoblasts) as active elements for actuation, can be com bi ned with m icro-electronic systems, as described for example in A.W.Feinberg et al., Science 2007, 317, 1366.

The present nanofilms are particularly suitable as a support for the adhesion of cells and for the preparation of these devices, since they can be manipulated in an aqueous environment, characterised by nanometric thickness, controllable flexibility and high modulus of elasticity. The possibility of electrical conduction also ensures the direct and controlled stimulation of muscle cells, making the nanofilms of the invention suitable as components for making muscles in vitro and for the development of new bio-hybrid devices.

Other biomedical applications of the present nanofilms are in the field of regenerative medicine, in tissue engineering, and in the development of devices for the controlled release of drugs.

The following examples are provided in order to illustrate the present invention without however constituting a limitation thereof.

Example 1

On a silicon substrate of dimensions 30x30 mm, 1 ,5 ml of a product prepared by mixing 12 mg of silicon prepolymer (component A) and 1 ,2 mg of cross-linking agent (component B) of the commercial bi-component product Sylgard ^® 184 (Dow Corp., USA) and n-hexane in a quantity equal to 10% by weight with respect to the total weight of the mixture, were deposited. Before deposition on the substrate, the mixture was vigorously mixed for a few minutes and then subjected to a vacuum degassing treatment for a few minutes, to eliminate the air bubbles that form during the mixing of the components.

The substrate was then made to rotate at a rotation speed of 6000 rpm for 150 seconds, then placed in an oven at a temperature of 95°C for 1 hour for the cross- linking and formation of the layer of PDMS. The surface of PDMS thus obtained was then subjected to treatment with air plasma at a pressure of 250 mTorr with a power of 6.8 W for 1 minute and 20 seconds, with the help of the Plasma Cleaner PDC-32G apparatus, produced by Harrick Plasma Inc.

On the layer of PDMS thus obtained a layer of PEDOT/PSS was then deposited, again by spin-coating, using the commercial product Clevios™ P AG (H. C. Starck GmbH, Germany), consisting of an aqueous dispersion of PEDOT/PSS in which the weight ratio PEDOT/PSS is 1/2.5; the substrate was set in rotation for 1 minute at a speed of 1000 rpm, with an acceleration of 500 rpm/s.

On the product thus obtained, after having been subjected to thermal treatment for 1 hour at a temperature of 170°C, the deposition was carried out, by drop casting, of an aqueous solution of PVA of concentration equal to 10% by weight with respect of the total weight of the solution. After air drying, at room temperature, for about 8 hours, the surface of PVA was cut with a suitable thin blade and the film was peeled off the substrate for growth by lifting it with the help of tweezers. The layer of PVA was peeled off going behind the conductive layer of PEDOT/PSS, thanks to the greater adhesion of the latter to PVA with respect to PDMS. The film of PVA and PEDOT/PSS was then placed in water where the layer of PVA completely dissolved, releasing the desired free-standing film of PEDOT/PSS in water.

In order to evaluate the thickness of the film so obtained, it was deposited on the surface of a Silicon substrate and dried there with the help of a flow of nitrogen. The thickness of the film obtained was measured with an atomic force microscope (AFM), and found to be equal to 121 nm.

Example 2

The preparation described in Example 1 was repeated in a totally analogous manner to what has been shown above but using, instead of Clevios™ P AG, the commercial product Clevios™ PH1000, again consisting of an aqueous dispersion of PEDOT/PSS, having a weight ratio PEDOT/PSS equal to 1/2.5.

At the end of preparation the thickness of the film was measured as described above in Example 1 , and found to be equal to 92 nm.

Example 3

The preparations described above in Example 1 and in Example 2 have been repeated in a totally analogous manner to what said above, but varying the rotation speed in the step of deposition of the layer of PEDOT/PSS, and using the following speed values: 1500 rpm, 2000 rpm, 2500 rpm, 3000 rpm, 3500 rpm, 4000 rpm, 4500 rpm, 5000 rpm, 5500 rpm, and 6000 rpm. At the end of each experiment the thickness of the film obtained was measured, as described above in Example 1. The following Table 1 illustrates the values obtained, whereas Figure 2 illustrates the progression thereof as the rotation speed varies:

Table 1

rotation speed (rpm) film thickness (nm)

Clevios'™ P AG Clevios ¹ ™ PH1000

1000 120.9 92.4

1500 91 .1 87.6

2000 78.6 79.6

2500 67.6 66.2 3000 53.6 55.3

3500 47.9 50.8

4000 46.7 43.2

4500 38.9 43.4

5000 40.5 43.8

5500 37.0 45.3

6000 37.3 42.2

Example 4

The films of PEDOT/PSS again supported on Si/PDMS obtained as described in Examples 1 -3 before the deposition of th e layer of PVA, were subjected to measurement of the surface resistance with a four-point method, using a 4-Point Probe Head (Jandel Engineering Ltd., GB). The fall in voltage at the two internal pins of the measurement head in contact with the sample was measured with a multimeter in conditions of application of a current equal to 1 mA through the external pins with the help of a potentiostat (mod. 7050, Amel Instruments, IT). Figure 3 shows the progression of the surface resistance values detected as a function of the rotation speed, and for both of the two series of films obtained using the two different commercial precursors of the layer of PEDOT/PSS.

Example 5

The films of PEDOT/PSS, released in water and obtained as described in Examples 1 -3 given above, were transferred onto glass supports and subjected to thermal treatment for 1 hour at a temperature of 170°C until elimination of the residual water.

The films thus obtained were subjected to measurement of the surface resistance with the same method and under the same conditions described above in Example 4. Figure 4 shows the progression of the values of surface resistance detected for two series of films of PEDOT/PSS prepared starting from Clevios™ PH1000 and transferred on glass and, as a comparison, the progression of the values detected for the films supported on Si/PDMS prepared from Clevios™ PH1000 and already given in Figure 3.

Example 6

Two samples of the nanofilm prepared as described above in Example 2, using the commercial product Clevios™ PH1000 in the step of deposition of the layer of PEDOT/PSS, with a rotation speed of 1500 rpm, were subjected to an 0 ₂ plasma treatment for a time equal to 45 seconds, followed by the formation of a fibronectin coating. On the thus treated samples two types of cells were seeded, muscle skeletal cells C2C12 and cardiac cells H9c2, so as to obtain a concentration equal to 25.000 cells/cm ² .

The biocompatibility and the cellular adhesion were verified with a test that makes it possible to evaluate the cell viability measured through Live/Dead ^® fluorescent colouring, in which particular dyes are used to distinguish, in fluorescent microscope images, the live cells - green in colour - from the dead ones - red in colour. The evaluation of the cellular material with this method was carried out 24 hours after seeding, and 7 days after seeding, for both types of cells, in both cases verifying the excellent biocompatibility of the nanofilm of the invention coated with fibronectin, and the high adhesion of the cells both in the short and in the long term.

Example 7

On a sample of the nanofilm prepared as described above in Example 2, using the commercial product Clevios™ PH1000 in the step of deposition of the layer of PEDOT/PSS, with a rotation speed of 1500 rpm, without the fibronectin coating and in the absence of any treatment suitable for modifying its surface properties, muscle skeletal cells C2C12 were seeded at a concentration equal to 10.000 cells/cm ² and the test with Live/Dead ^® fluorescent colouring was carried out 24 hours after seeding. Also in this case it was found that almost all of the cells seeded on the nanofilm of the invention adhered and was alive, thus demonstrating the biocompatibility of this material.

Example 8

On a silicon substrate of dimensions 30x30 mm, 1 .5 ml of a product prepared by mixing 12 mg of silicon prepolymer (component A) and 1 .2 mg of cross-linking agent (component B) of the commercial bi-component product Sylgard ^® 184 (Dow Corp., USA) and n-hexane in a quantity equal to 15% by weight with respect to the total weight of the mixture, were deposited. Before deposition on the substrate, the mixture was vigorously mixed for a few minutes and then subjected to a vacuum degassing treatment for a few minutes, to eliminate the air bubbles that form during the mixing of the components. The substrate was then made to rotate at a rotation speed of 6000 rpm for 150 seconds, then placed in an oven at a temperature of 95°C for 1 hour for the cross- linking and formation of the layer of PDMS. The surface of PDMS thus obtained was then subjected to treatment with air plasma at a pressure of 250 mTorr with a power of 7 W for 30 seconds, with the help of the Plasma Cleaner P DC-32G apparatus, produced by Harrick Plasma Inc.

On the layer of PDMS thus obtained a layer of PEDOT/PSS was then deposited, again by spin-coating, using the commercial product Clevios™ PH1000 (H. C. Starck GmbH, Germany), consisting of an aqueous dispersion of PEDOT/PSS in which the weight ratio PEDOT/PSS is 1 /2.5; the substrate was set in rotation for 1 minute at a speed of 2000 rpm, with an acceleration of 500 rpm/s. The product was then subjected to thermal treatment for 1 hour at a temperature of 170°C.

On the product thus obtained a layer of photoresist resin MICROPOSIT ^® S1813 ^® PHOTO RESIST, Shipley Company, USA was deposited by spin-coating, putting the substrate in rotation for 30 seconds at a speed of 4500 rpm, then placed on a heating plate at a temperature of 100°C for 1 m i n ute, placed in tight contact with a photolithographic mask carrying the pattern to be transferred by using a Mask Aligner MA6 Suss Microtec (SUSS MicroTec Lithography GmbH, Germany), and exposed for 13.6 seconds to UV rays.

The immersion in a solution of Microposit ^® MF ^® - 319 Developer (Shipley

Company, USA) for 1 minute and subsequent rinsing with deionised water makes it possible to define the desired pattern on the photoresist, obtaining the photoresist mask, i.e. the localised covering of the layer of conductive polymer.

Then the oxidation treatment takes place through immersion of the product for 2 minutes in an aqueous solution of sodium hypochlorite at 10% by weight, followed by washing with deionised water and drying with a gun spraying a jet of nitrogen or compressed air. Such oxidation treatment deactivates the conductive properties in the exposed areas of the PEDOT:PSS film, according to the desired pattern.

The photoresist mask is then completely removed through immersion at room temperature for 2 minutes in a suitable product called Microposit ^® 1 165 Remover (Shipley Company, USA), followed by washing with water and drying with a nitrogen or compressed air gun.

On the so obtained product a layer of poly(lactic acid) (PLA) was deposited by spin-coating from a solution thereof (20 mg/ml in chloroform), setting the substrate in rotation for 20 seconds at a speed of 3000 rpm, then placed on a heating plate at a temperature of 200°C for 10 minutes and finally cooled quickly through immersion in deionised water at a temperature of 15°C and subsequent drying with a nitrogen or compressed air gun.

On the product thus obtained the deposition of an aqueous solution of PVA with concentration equal to 10% by weight with respect of the total weight of the solution, was carried out, by drop casting. After air drying, at room temperature, for about 8 hours, the surface of PVA was cut with a suitable thin blade and the film was peeled off from the preparation substrate lifting it with the help of tweezers. The film consisting of the layer of PVA, the layer of PLA and the "patterned" conductive layer of PEDOT/PSS was then peeled off from the substrate of PDMS, thanks to the greater adhesion of the conductive layer to PLA with respect to PDMS. The film of PVA/PLA and PEDOT/PSS was then placed in water where the layer of PVA completely dissolved, releasing a nanofilm consisting of a uniform layer of PLA and a "patterned" layer of PEDOT/PSS in water.

Figure 6 shows the photographic image of this free-standing nanofilm, floating in water; in this image it is also possible to distinguish the predetermined pattern formed by localised oxidation of the surface of the conductive layer.