AU736523B2 - Electro-release systems, modified electrodes and their use - Google Patents

Description

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AUSTRALIA

PATENTS ACT 1990 DIVISIONAL APPLICATION NAME OF APPLICANT: Plant Bioscience Limited ADDRESS FOR SERVICE: DAVIES COLLISON CAVE Patent Attorneys 1 Little Collins Street Melbourne, 3000.

INVENTION TITLE: "Electro-release systems, modified electrodes and their use" The following statement is a full description of this invention, including the best method of performing it known to us: ELECTRO-RELEASE SYSTEMS, MODIFIED ELECTRODES AND THEIR USE BACKGROUND OF THE INVENTION 1. Field of the Invention This invention relates to modified electrodes their manufacture and use, to electro-release systems including modified electrodes for electro-release of compounds, for example medical or veterinary pharmaceutical compounds, and to methods for electro- 10 release. By electro-release is meant that the ooeo o electrochemical release of the compound, or the inhibition of such release, is caused by the application of an appropriate voltage bias to an electrode. Such a system allows accurate control of timing and/or amount 15 of release.

2. Description of Prior Art A naked electrode placed in a conducting solution can be viewed as an infinite sink or source of electrons which behaves as a tunable redox reagent. The rate of oxidation or reduction of molecules close to the electrode can be controlled by varying the interfacial electrode potential. In this way reactions can be switched on or off. Some twenty years ago it was recognised that chemical modification of an electrode surface with functional groups may provide additional degrees of control over the electrochemistry. The types of control sought include: chiral induction, whereby a prochiral molecule is reduced or oxidised to a single optical isomer; electrocatalysis, whereby electrontransfer chemistry is catalysed by binding substrate molecules at catalytic sites; electro-releasing, whereby electrode-bound molecules are released into solution by changing the electrode potential; and electrosensing, whereby selective interaction of an analate with the modified surface gives rise to a measurable electrode response. The design and construction of devices based on modified electrodes have potential application in areas such as controlled drug delivery, bioelectrocatalysis and bioelectronics.

There have been some previous published proposals for an electro-release system. The present inventors have published details of modified electrodes in publications listed at the end of this description.

SUMMARY OF THE INVENTION The present inventors have now developed multilayer modified electrodes carrying electroreleasable compounds and obtained electrically stimulated release.

The background to this development is earlier work carried out by the inventors and other at the Nitrogen Fixation Laboratory, Norwich, England, on electrodes modified by application of a layer of a polymerized pyrrole or thiophene derivative. The Srelevant publications are listed at the end of this specification. Reference should be made to these publications (references 1 5) for details of how to make the functionalized polypyrrole or polythiophene layers used in aspects of the present invention.

According to the invention there is provided a modified electrode structure having an electrode and on the electrode a plurality of conductive polymer layers wherein each polymer layer comprises polymers with monomeric units of the form 0 9 0 0 0 0 0 0

S

S

00..

P'

I

(pnX where P is or NH S and X is a substituent group other than H attached at the 1(N) position or the 3 position in the case where P 15 is and at the 3 position in the case

NH

where P is the substituent X in the two polymer layers being different from each other, thereby providing different functions and/or different reactivities. There may be a plurality of substituents X, the same or different, attached to the monomer unit

P.

This arrangement of two (or more) polymer layers based on pyrrole or thiophene having different 0 functionality allows the production of modified electrodes having useful properties, since the different layer can provide different effects. The use of polymers based on polypyrrole or polythiophene, which provide conductive layers, allows electrochemical reactions to be effected in one or more of the layers, and one or more layers may provide properties adapted for an environment in which the electrode is to be used.

For example a hydrophobic or hydrophilic layer can be S 10 present. One or more layers may also control access of species to another of the layers, e.g. diffusion of the species to or from another layer.

In a preferred embodiment of the invention there i is provided a modified electrode structure for electro- 15 release of compounds having an electrode and on the electrode a plurality of conductive polymer layers as described above, wherein a first one of said polymer layers contains an electro-releasable compound ionically bonded to the substituent X thereof. A second one of said polymer layers has a substituent X adapted to release protons, on application of an appropriate voltage bias to the electrode, said protons effecting the release of said electro-releasable compound. It is also preferred that substituent X in one of said polymer layers provides biocompatibility of the structure.

This system is for example applicable as a transdermal delivery system, for transdermal delivery of *1 an electro-releasable compound which is a medical or veterinary pharmaceutical. Other possible applications are in subcutaneous and intravenous release.

According to another aspect of the invention there is provided a method of making a modified electrode structure comprising forming at least two polymer layers successively on an electrode, each said polymer layer comprising a polymer with monomeric units of the form

I

xn where P is selected from N and NH S and X is a substituent group other than H replacing H at one of the 1(N) position and the 3 position in the case where P is and at the 3 position in the

NH

case where P is the substituent X in

S

two said polymer layers being different from each other thereby providing at least one of different functions and different reactivities.

O0 Preferably at least one of said polymer layers is formed by making a precursor layer by polymerising an unsubstituted or substituted pyrrole or thiophene and thereafter forming said substituent X thereof.

The term "ionic bond" is used to indicate that the electro-releasable compound is bound electrostatically. Other interactions with the electroreleasable compound, such as hydrogen bonding, may occur in addition provided that they do not prevent the desired release of the compound.

Very many pharmaceutical compounds, or their salts, exist in an ionic form which makes them suitable for use in the electro-release system of the invention.

An example of an anionic compound having a carboxylate 10 group is ibuprofen. Examples of cationic compounds are morphine, dopamine and alkaloid salts.

Ionized polypeptides and proteins may also be capable of bonding and release by such a system.

00.i Preferably, the generation of protons by 15 electrochemical oxidation at the substituent X adapted to release protons, on application of an appropriate voltage bias causes breakage of the ionic bond, thereby 0: releasing the electro-releasable species. The protons typically combine with the anion of the ionic bond to neutralize its charge. For example the proton combines with a carboxylate group of the ionic bond. The electro-releasable species may be anionic or cationic.

If it is anionic, e.g. has a carboxylate group, it can combine with a released proton to convert it to the carboxylic acid form which is released into an electrolyte bounding the electrode. In this case the substituent X forming the ionic bond is cationic, e.g.

e0g.

C

C. *0 *0 S0

C

C

C

*0 quaternary ammonium or phosphonium. Conversely, if the electro-releasable compound is cationic, the released proton may combine with the anion of the ionic bond which is provided by the substituent X, e.g. a carboxylate anion, freeing the cation of the electroreleasable compound to pass into the electrolyte bounding the electrode. Suitable anionic species other than carboxylate may be employed, e.g. a sulphonate group (-S0 3 The electrolyte may be a liquid, or may be provided by the skin of a patient in a transdermal delivery system in which a counter-electrode is provided elsewhere on the patient's skin.

The substituent X adapted to release protons on application of an appropriate voltage bias may be for example cysteine groups which are electrochemically converted to a cystine group, or a hydroquinone group.

The release mechanism described, caused by application of voltage bias to the electrode, may be reversible, e.g. on removal of the bias or application of a reverse bias, provided that the reactions at the different substituents X in the two polymer layers are reversible. For pharmaceutical compound release, reversibility is not generally required, but reversibility may permit reloading of an expensive electrode with the electro-releasable compound.

Other conductive polymers may be employed for the

IVI-

0

PPO

polymer layers instead of polypyrrole or polythiophene, provided that they can form the desired layer structure on the electrode and provide a suitable site or sites for substitution.

Preferably the electrode-bound polymer layers are formed in situ, by an electro-polymerization step of a substituted pyrrole or thiophene for each layer to be produced. As mentioned above, references 1-5 give details for the production of polypyrrole derivative 10 single layers. If the nature of the substituent X permits, the polymerizing monomer may be pyrrole or thiophene substituted by X. Alternatively a layer may be formed by polymerizing in situ a substituted pyrrole i*S or thiophene which is subsequently modified in situ to incorporate the desired substituent X. Such modification may take place before or after a subsequent polymer layer has been formed, as is appropriate.

It has been shown that chemical modification of derivatised polypyrrole or polythiophene does not lead to polymer surface modification, but to bulk film transformation (reference Polymer conversions such as quaternisation and cleavage of a disulfide bond (in the formation of cysteinyl groups from polycystinyl pyrroles) have been demonstrated; conversions involving an activating ester group a pentafluorophenyl or 2,4-dinitro phenyl ester) have been developed to produce other esters, amides and amino acid derivatives and in 0 polymer cross-linking. The advantages of functionalisation after polymerization is that groups which are sensitive to the oxidative conditions of polymer growth, or which interfere with the polymerization, can be conveniently introduced; additionally, since minimal amounts of reacting agent are required, the transformations are economic. The formation of methionine-derivated pyrroles illustrates one of these points. Methionine methyl ester reacts 10 rapidly and quantitively with a polymer containing the activating ester group to give the desired functionalised film.

It is for example possible to polymerize in situ *i a substituted pyrrole or thiophene which has a photolabile group. Photoclearage of the photolabile group can be performed subsequently to permit modification of the polypyrrole. This may be carried out selectively, by patterning the application of light for the photoclearage.

In use of the bilayer or multi-layer structures in modified electrodes of the invention, electrical charge may be propagated to the desired sites, e.g. to cause redox reactions through the conducting polymer backbone or by electron-hopping between redox groups.

The electrode used in the electrode systems of this invention may be for example a platinum electrode, or a vitreous carbon electrode. In situ growth of

S

S

S

S

S

S

.555 polypyrrole films on both these electrodes has been demonstrated. Other electrodes based on carbon, such as carbon felt, may be used as an electrode, as may also a conductive ink or conductive paste applied to a substrate.

The invention also consists in the abovedescribed methods of manufacture of the modified electrode.

A base layer of unsubstituted polypyrrole or 10 polythiophene may be applied to the electrode to improve adhesion of the polymer layers, but we have not found this necessary.

Examples of modified electrodes useful in accordance with the invention are now given. The terms "inner" and "outer" refer to layers respectively closer to and further from the electrode.

I. An electrode structure having an inner hydrophobic polymer layer carrying a functional substituent X intended to take part in an electrochemical reaction, such as electro-release as described above or reaction with a species entering the layer structure from the exterior, and an outer hydrophilic layer which makes the electrode structure wettable by an aqueous medium, allowing species to permeate to or from the inner layer.

II. An electrode structure having an electro- 0.k releasable compound ionically bonded to an inner polymer

I

layer as described above, and an outer layer which provides biocompatibility of the electrode structure, e.g. an outer layer having a sugar-type group. Other.

possible types of outer layer providing biocompatibility are based on hydroxyapatite and silicone.

III. An electrode structure in which two layers carry respectively two different functional groups which cooperate to provide an electrochemical reaction, e.g.

the first and second functional groups of the electrorelease system of the invention described above.

Alternatively two or more electro-release systems as described above may be applied as separate layers, permitting controlled selective release of different electro-releasable compounds.

15 IV. An electrode structure in which an outer layer carries a functional group such as phosphocholine which inhibits cell adhesion when the electrode structure is in a biological environment.

Multiple layers can readily be built-up, e.g. two or more layer types in a repeating pattern layer A layer B layer A layer etc. or layer A layer B layer C layer A etc.).

Each layer may be in the range 100 5000nm thick, e.g. about 1000nm.

Functional groups which can be provided in polymer layers of such an electrode structure of the R. invention include peptide groups which allow the ~aN aN pfx assembly of electro-active bio-inorganic structures.

For example the electropolymerization of the compound I including a cystine-linkage: SN+Me 3

NH

NN

H

a a a a a.

NH

Me 3

W

5 and its reduction to the cysteinyl state allows binding of an electro-active ferredoxin centre: polymer 2-/3polymer N+Me 3 Details of the binding of a ferredoxin centre in this way in a polypyrrole single layer are given in references 1, 2 and 3. We have found that a concentration of about 1M of the ferredoxin centres in the polymer film can be achieved. These centres are in redox communication with each other and with the electrode.

Another possibility using such peptide groups is the binding of a cofactor of a protein, such as the "FeMoco" cofactor of nitrogenase, by N-histidine bonding at the Mo atom and S-cysteine bonding at the distal Fe atom. Such a structure may lead the way to electrocatalysts using such a cofactor.

:BRIEF INTRODUCTION OF THE DRAWINGS 0 Figs. 1A and 1B are diagrams illustrating two states of a bilayer modified electrode structure in accordance with the invention.

Figs. 2A and 2B show stages in the formation of a bilayer modified electrode in accordance with the 15 invention.

Figs. 3A, 3B, 3C and 3D show stages in the formation of another bilayer modified electrode in accordance with the invention.

DESCRIPTION OF PREFERRED EMBODIMENTS Electro-release of an ionic compound in accordance with the invention is illustrated in accompanying Figs. 1A and 1B.

These figures illustrate the use 'of pyrrole polymer bilayer electrode structures to perform switchable release of drugs.

A polypyrrole functionalised with reactive groups is electrochemically grown on a conducting material to the desired thickness to form the inner polymer layer in Figs. 1A and 1B. On top of this layer a second functionalised polypyrrole is electrochemically grown to the desired thickness to form the outer polymer layer.

This outer layer possesses either a carboxylic acid group for binding cationic drugs such as metoclopramide or morphine derivatives (Type I) or a cationic group such as NMe 3 for binding carboxylate drugs e.g.

ibuprofen (Type II). Type I is illustrated in Figs. 1A 1. 0 and 1B.

The inner polymer layer is selectively reacted with a group attached to an electro-oxidisable QH n centre to locate this centre in the inner layer. QHn may be for example a hydroquinone or a thiol moiety. Hydroquinone is illustrated in Figs. 1A and lB.

Loading the electrode with cationic drugs is by carboxylate salt formation with the outer Type I layer.

e Loading the electrode with anionic carboxylate drugs is by salt formation with the Type II cationic outer layer.

Figs. 1A and 1B show Type I, with cationic metoclopramide as the ionically bound drug, forming an ionic bond with a carboxylate group in the outer layer.

As mentioned, the inner layer has a hydroquinone group which releases protons. The bound state is shown by Fig. 1A.

The drug is released by electrochemically switching the potential of the electrode to a value which causes QH n to oxidise to Q nH*. This is illustrated in Fig. 1A by the migration of e and H*.

The dose is controlled by the duration and level of the current flow. Protons generated in the inner polymer layer neutralise the carboxylate groups of the Type I outer layer thereby releasing the cationic drug into the surrounding medium, which may be an aqueous solution or another suitable medium such as human or animal tissue.

S: This state is shown by Fig. lB.

10 In the Type II system, protons generated in the inner layer neutralise the carboxylate group of the electrostatically bound anionic drug thereby releasing it in the carboxylic acid form into the surrounding S* medium.

Figs. 2A and 2B show a method for obtaining a modified electrode having a bilayer with a desired derivatised inner layer. A bilayer as shown in Fig. 3A is formed by polymerizing as a first layer on the electrode pyrrole substituted at the 1(N) position with an 2,4-dinitro phenyl propanoic ester group, and as a second layer a 3-nitro phenyl propanoic ester group.

Such films can be grown by electropolymerization of the monomeric pyrrole on Pt discs in a CH 3 CN solution containing [N(C 4 Hg) 4 [BF The monomer concentration is typically 8 to 10 mM. The electrodes were previously polished using diamond paste and then washed with water and CH 3 CN. When this bilayer is contacted with methanol solution, methanol penetrates to the inner layer to provide the methyl ester, as shown in Fig. 2B. The outer layer remains unchanged. This change is detected spectroscopically.

Figs. 3A-3D show another method for obtaining a modified electrode having a polymer bilayer. Fig. 3A shows a first layer formed by polymerizing the 2,4dinitro phenyl propanoic ester pyrrole derivative. Fig.

3B shows the conversion of this to an amide by reaction 10 with histidine methyl ester. Then a second polymer p layer of the 2,4-dinitro phenyl propanoic ester pyrrole p :derivative is formed (Fig. 3C) and then converted (Fig.

3D) by reaction with glucosamine to give a hydrophilic .i outer layer, thus producing a bifunctional bilayer 15 structure on the electrode.

The monomers used in the bilayers of Figs. 2 and 3 were prepared as.follows: p* 2,4-dinitrophenyl 3-(1H -1-pyrrolyl) propanoate Solid dicyclohexylcarbodiimide (1.5g, 7.3 mmol) was added to a cold stirred solution of 3-(pyrrol-l-yl) propanoic acid (Ig, 7.2 mmol) synthesized as described in reference 4 below and 2,4-dinitrophenol (Ig, 7.2 mmol) in ethyl acetate (35 mL). After an hour of stirring precipitated dicyclohexyl urea (DCU) was removed from the solution by filtration. The filtrate 0O was left stirring for an additional 15 hours at room temperature and the solution was again filtered to remove further DCU. The filtrate was evaporated under vacuum to give a crude oil. This was dissolved in acetonitrile and the solution was allowed to stand at -15 0 C for 3 hours. Further DCU was removed by filtration b .o99 9oo.

9 9 10 9 99* f* 9 9 *9 9 9 9 and the resulting filtrate evaporated under vacuum. The oily product was triturated with hexane and a pale yellow solid was formed. The solid was recrystallised from diethyl ether-hexane. Yield 70% (2.30g), m.p.

860C.

Microanalysis Found C, 51.7; H, 4.1; N 12.3. Calc. for C 13 HN30 C, 51.2; H, 3.6; N 13.7.

9 9 3-nitrophenyl 3-(1H -1-pyrrolyl) propanoate This compound was prepared from 3-nitrophenol using the procedure as for the 2,4-dinitrophenyl compound above.

Yield 65% (1.20g), m.p. 68-690C.

Microanalysis Found C, 59.8; H,4.6; N 10.7. Calc. for C 3

H

2

N

2 0 4 C, 60.0; H,4.7; N 10.8.

Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", and variations such as "comprises" and "comprising", will be understood to imply the inclusion of a stated integer or step or group of integers or s 18 steps but not the exclusion of any other integer or step or group of integers or steps.

The reference to any prior art in this specification is not, and should not be taken as, an acknowledgement or any form of suggestion that that prior art forms part of the common general knowledge in Australia.

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References 15 3.

4.

Moutet and C.J. Picket, J. Chem. Soc., Chem. Commun., 1989, 188, "Iron-sulphur clusters in ionic polymers on electrodes".

C.J. Pickett, K.S. Ryder and Moutet, J.

Chem. Soc., Chem. Commun., 1992, 694, "Synthesis and Anodic Polymerisation of an L-Cystine derivatised Pyrrole; Copolymerisation with a Tetraalkylammonium Pyrrole allows Reduction of the Cystinyl Film to a Cysteinyl State that Binds Electroactive {Fe 4

S

4 2 Centres".

C.J. Pickett, K.S. Ryder and Moutet, J.

Chem Soc. Dalton Trans., 1993, 3695, "Ironsulphur clusters in ionic polymers on electrodes".

C.J. Pickett and K.S. Ryder, J. Chem. Soc. Dalton Trans., 1994, 2181, "Bioinorganic Reaction Centres on Electrodes. Modified Electrodes possessing Amino Acid, Peptide and Ferredoxintype Groups on a Poly(pyrrole) Backbone".

S.K. Ibrahim, C.J. Pickett and C. Sudbrake, J.

Electroanalytical, 387 (1995), 139, "Peptide derivatised poly(pyrrole) modified electrodes with built-in ion-exchange functions".

Claims (8)

1. A modified electrode structure having an electrode and on the electrode at least two polymer layers wherein each said polymer layer comprises a polymer with monomeric units of the form where P is selected from and NH S and X is a substituent group other than H replacing H at one of the 1(N) position and the 3 position in the case where P is and at the 3 position in the case where P is the substituent X in S two said polymer layers being different from each other thereby providing at least one of different functions and different reactivities.

2. A modified electrode structure according to claim 1, wherein a first one of said polymer layers contains an electro-releasable compound ionically bonded to the substituent X thereof. ADc

3. A modified electrode structure according to claim 2, wherein a second one of said polymer layers has a substituent X adapted to release protons, on application of an appropriate voltage bias to the electrode, said protons effecting release of said electro-releasable compound.

4. A modified electrode structure according to claim 1, wherein the substitutent X in one of said layers provides biocompatibility of the structure. 0000 0 0 0 00 0 0 0 I.:.0 00% oo 0 .0 0.: 0:01 oo.. oooo 10

5. A method of making a modified electrode structure comprising forming at least two polymer layers successively on an electrode, each said polymer layer comprising a polymer with monomeric units of the form 15 i where P is selected from and NH S and X is a substituent group other than H replacing H at one of the 1(N) position and the 3 position in the case where P is and at the 3 position in the NH case where P is ,the substituent X in two S said polymer layers being different from each other- thereby providing at least one of different functions and different reactivities.

6. A method according to claim 5, wherein at least one of said polymer layers is formed by making a precursor layer by polymerizing an unsubstituted or substituted pyrrole or thiophene and thereafter forming said substituent X thereof.

7. A modified electrode structure according to claim 1, substantially as hereinbefore described with reference to any one of the examples. "i

8. A method of making a modified electrode structure *o according to claim 5, substantially as hereinbefore described with reference to any one of the examples. DATED this 4th day of June, 2001 Plant Bioscience Limited By DAVIES COLLISON CAVE SPatent Attorneys for the Applicants