Title of Invention	IONTOPHORETIC DELIVERY OF AN ANTIMIGRAINE DRUG
Abstract	The present invention relates to the iontophorctic delivery to a patient, more in particular to a migraine patient, of a compound of formula (I) as shown hereinunder. The invention also relates to a device for the iontophoretic delivery of a compound of formula (I), as well as to a composition containing a compound of formula (I), which can be applied in a device for iontophoretic delivery. Said compounds are benzopyranalkylaminoalkyl substituted guanidines having the formula the pharmaceuticaliy acceptable acid addition salts thereof, and the stereochemically isomeric forms thereof, wherein R1 is hydrogen orCl-6alkyl; R2 is hydrogen, C1-6alkyl, C3-6alkenyl or C3-6alkynyl; R3 is hydrogen or C1-6alkyl; or R2 and R3 taken together form a bivalent radical of formula -(CH2)m- wherein m is 4 or 5; or R1 and R2 taken together form a bivalent radical of formula -CH=CH-or of formula -(CH2)n- wherein n is 2, 3 or 4; or R3 may represent a bond when R1 and R2 taken together form a bivalent radical of formula -CH=CH-CH=; R4 and R5 each independently are hydrogen orC1-6alkyl; Alk1 is a bivalent C1-3alkanediyl radical; Alk2 is a bivalent C2-15alkanediyl radical; and R6and R7 each independently are hydrogen, halo, Cl-6alkyl, C3-6alkenyl, C3-6alkynyl, hydroxy, C1-6alkyloxy or cyano.

Title of Invention

IONTOPHORETIC DELIVERY OF AN ANTIMIGRAINE DRUG

Abstract

The present invention relates to the iontophorctic delivery to a patient, more in particular to a migraine patient, of a compound of formula (I) as shown hereinunder. The invention also relates to a device for the iontophoretic delivery of a compound of formula (I), as well as to a composition containing a compound of formula (I), which can be applied in a device for iontophoretic delivery. Said compounds are benzopyranalkylaminoalkyl substituted guanidines having the formula the pharmaceuticaliy acceptable acid addition salts thereof, and the stereochemically isomeric forms thereof, wherein R1 is hydrogen orCl-6alkyl; R2 is hydrogen, C1-6alkyl, C3-6alkenyl or C3-6alkynyl; R3 is hydrogen or C1-6alkyl; or R2 and R3 taken together form a bivalent radical of formula -(CH2)m- wherein m is 4 or 5; or R1 and R2 taken together form a bivalent radical of formula -CH=CH-or of formula -(CH2)n- wherein n is 2, 3 or 4; or R3 may represent a bond when R1 and R2 taken together form a bivalent radical of formula -CH=CH-CH=; R4 and R5 each independently are hydrogen orC1-6alkyl; Alk1 is a bivalent C1-3alkanediyl radical; Alk2 is a bivalent C2-15alkanediyl radical; and R6and R7 each independently are hydrogen, halo, Cl-6alkyl, C3-6alkenyl, C3-6alkynyl, hydroxy, C1-6alkyloxy or cyano.

Full Text	The present invention relates to the iontophoretic delivery to a patient, more in particular to a migraine patient, of a compound of formula (I) as shown hereinunder. The invention also relates to a device for the iontophoretic delivery of a compound of formula (I), as well as to a composition containing a compound of formula (I), which can be applied in a device for iontophoretic delivery. Although in general, oral administration of a drug is considered as most convenient, this route poses particular problems when administering a drug, more in particular an anti-migraine drug, to patients suffering from a migraine attack. Migraine patients often feel nauseous, sometimes resulting in violent vomiting, thus hampering the oral administration of the anti-migraine drug. The successful oral delivery of some anti-migraine substances is also impeded by its susceptibility to degradation by the acid environment of the stomach and by the digestive activity of several enzymes in the gastrointestinal tract. Other disadvantages of the oral route are the often poor absorption due to gastroparesis and the extensive first-pass elimination in the liver (the hepatic first-pass effect), whereby a compound is transformed in the liver into a metabolite more prone for excretion. Along with convenient administration, it is essential for an effective treatment of a migraine attack that the activity of the drug sets on immediately, or at least very rapidly, after administration and that the effect lasts long enough. Hence a means of directly inserting the drug into the bloodstream should be a method of choice for the administration of an anti-migraine drug. An obvious way of doing so is by injecting a solution of the drug either intravenously or subcutaneously. However, the consequent pain, risk of infection, the complex procedures of self-administration and potential for low patient compliance make such parenteral administration undesirable. Transdermal delivery is an attractive alternative because : (a) it avoids gastrointestinal degradation and the hepatic first-pass effect; (b) it lends itself to a controlled and/or sustained release; (c) it allows for convenient and simple self-administration and encourages patient compliance, since a transdermal formulation would be easy to apply or to remove. Traditional transdermal drug delivery systems are based on the transport of drugs into the skin by diffusion through the outermost layer of the epidermis, i.e. the stratum comeum. The number of solutes which can be delivered by this route are limited due to the excellent barrier properties of the said stratum corncum. Hence, attainment of a therapeutically effective level is therefore difficult without some form of facilitation. One means of facilitation is the delivery of the drug by electrokinetic action, more in particular -2- by iontophoretic action. The principle of iontophoresis is that ionized (or polar) drug molecules can be driven into the skin if an appropriate electrical potential is applied across the skin. Iontophoresis may be due solely to electromigration, i.e. the movement of ionized drug molecules across an electrical field per se, or it may be due to a combined effect of elcctromigration and electroosmosis. The latter is a transdermal flux of liquid solvent containing the drug by the presence of an electricaJ field. The problem 10 be solved is to find or develop compounds and compositions, which have the desired anti-migraine activity and which are susceptible for said convenient iontophoretic delivery. Recently, it was discovered that the compounds of formula (I) show 5HTi-iJke agonistic activity and, more in particular, anti-migraine activity. Unexpectedly it has been found that these compounds of formula (I) can be delivered via iontophoretic action. Said compounds arc dihydrobcnzopyranalkylaminoalkyl substituted guanidincs having the formula the pharmaccutically acceptable acid addition salts thereof, and the stercochcmically isomeric forms thereof, wherein Rl is hydrogen or Cl-6alkyl; R2 is hydrogen, C1-6alkyl, C3-6alkenyl or C3-6alkynyl; R3 is hydrogen or C1-6alkyl; or R2 and R3 taken together form a bivalent radical of formula -(CH2)nr wherein m is 4 or 5; or Rl and R2 taken together form a bivalent radical of formula -CII=CH- or of formula -(CH2)n-. wherein n is 2, 3 or 4; or R3 may represent a bond when R1 and R2 taken together form a bivalent radical of formula -CH=CH-CH=; R4 and R5 each independently are hydrogen orC1-6 alkyl; Alk 1 is a bivalent C1 -3alkanediyl radical; Alk2 is a bivalent C2-15 alkanediyl radical; and R6 and R7 each independently are hydrogen, halo, C1-6alkyl, C3-6alkenyl, C3-6alkynyl, hydroxy, C1-6alkyloxy or cyano. In the foregoing definitions, the term "halo" is generic to fluoro, chloro, bromo, -3- iodo; the term "C1-6alkyl" means straight or branched saturated hydrocarbon radicals having from 1 to 6 carbon atoms, such as, methyl, ethyl, propyl, butyl, pentyl, hexyl, and the like; "C3-6alkenyl" defines straight and branch chained hydrocarbon radicals containing one double bond and having from 3 to 6 carbon atoms, such as, for example, 2-propcnyl, 3-butenyl, 2-buteny1, 2-pcntenyl, 3-pcntenyl, 3-methyl-2-butenyl and the like; and the carbon atom of said C3-6alkenyl being connected to a nitrogen atom preferably is saturated, "C3-6alkynyl" defines straight and branch chained hydrocarbon radicals containing one triple bond and having from 3 to 6 carbon atoms, such as, for example, 2-propynyl, 3-butynyl, 2-butynyl, 2-pcntynyl, 3-pentynyl, 3-hexynyl, and the like; and the carbon atom of said C3-6alkynylradicaI being connected to a nitrogen atom preferably is saturated; "Ci^alkanediyl" is meant to comprise straight or branched saturated hydrocarbon radicals containing 1 to 3 carbon atoms, such as, methylenc, cthanediyl, propanediyl, and the like; "C2-15alkancdiyl" is meant to comprise straight or branched saturated hydrocarbon radicals having from 2 to 15 carbon atoms, such as, ethanediyl, propancdiyl, butanediyl, pentanediyl, hexanediyl, heptanediyl, octanediyl, nonanediyl, decanediyl, undecancdiyl, dodecanediyl, tridecanediyl, tetradecanediyl, pcntadecanediyl and the branched isomers thereof. Pharmaceutically acceptable acid addition salts as mentioned hereinabove comprise the therapeutically active non-toxic acid addition salt forms which the compounds of formula (I) are able to form. Said salt forms can conveniently be obtained by treating the base form of the compounds of formula (I) with appropriate acids such as inorganic acids, for example, hydrohalic acid, e.g. hydrochloric, hydrobromic and the like acids, sulfuric acid, nitric acid, phosphoric acid and the like; or organic acids, such as, for example, acetic, propanoic, hydroxyacetic, 2-hydroxypropanoic, 2-oxopropanoic, ethancdioic, propanedioic, butanedioic, (Z)-2-butenedioic, (E)-2-butenedioic, 2-hydroxybutancdioic, 2,3-dihydroxybutanedioic, 2-hydroxy-1,2,3-propanetri-carboxylic, mcthanesulfonic, ethanesulfonic, benzenesulfonic, 4-methylbenzenesulfonic, cyclohexanesulfamic, 2-hydroxybenzoic, 4-amino-2-hydroxybenzoic and the like acids. Conversely the salt form can be convened by treatment with alkali into the free base form. The term "stercochcrnically isomcric forms" as used hereinbefore and hereinafter defines all the possible isomeric forms which the compounds of formula (I) may possess. Unless otherwise mentioned or indicated, the chemical designation of compounds denotes the mixture of all possible stereochemically isomeric forms, said mixtures containing all diastereomers and enantiomers of the basic molecular structure. More in particular, stercogenic centers may have the R- or S-configuration. The present -4- invention clearly intends to embrace in its scope both the individual stereochemically isorneric forms and the mixtures thereof. It has to be understood that, when mixtures of enantiomers are present, they may be separated according to classical resolution methods, e.g. by fractional crystallization of their acid addition salts with a suitable chiral acid or by the separation by chromatography using a chiral phase. Moreover, some of the compounds of formula (I) may also exist in their tautomeric forms. Such forms although not explicitly indicated in the above formula (I) are intended be included within the scope of the present invention. K 1 is suitably hydrogen or methyl; R2 is suitably hydrogen or methyl; R3 is suitably hydrogen or methyl; preferably R1 and R2 are taken together to form a bivalent radical of formula -CH=CH-, -(CH2)2- or -(CH2)3-; or when R3 is a free bond R1 and R2 taken together form a bivalent radical or formula -CH=CH-CH= ; R4 is suitably methyl or hydrogen, preferably hydrogen; R5 is suitably methyl or hydrogen, preferably hydrogen; R6 and R7 suitably are hydrogen, halo, or Cl-6alkyl, preferably hydrogen, fluoro, methyl or ethyl. Interesting compounds of formula (I) arc those compounds of formula (I) wherein Alk 1 is C1-2alkanediyl> especially mcthylcne. Other interesting compounds are those compounds of formula (I) wherein Alk2 is C2-6alkanediyl, particularly, ethanediyl, propanediyl, butanediyl, pentancdiyl, hcxanediyl, preferably 1,3-propanediyl. Most preferred compounds are N-\|(3,4-dihydro-2H-l-benzopyran-2-yl)methyl]-N'-( 1,4,5,6-tetrahydro-2-pyrimidinyl)-l,3-propanediamine, the stereochemical isomers thereof, particularly the R-isomer, and the pharmaceutically acceptable acid addition salts thereof. The compounds of formula (I) may be prepared following art-known procedures. The process of iontophoretic drug delivery is performed in general by putting a composition containing the drug onto intact skin. This composition may for instance be a solution (absorbed onto some porous material, for instance a piece of filter paper or a -5- piecc of hydrophilic polyurethane) or a gel. The composition is then covered by an electrode. A second electrode is placed elsewhere on the skin, and a direct current source is connected between the electrodes in such a way that the electrode in contact with the drug solution assumes the same charge as the ionized drug. Under influence of the electric field present, drug molecules migrate through the skin. A current flows between the electrodes, part of which is carried by the drug. Iontophoretic devices as such arc known in the art, for instance from, WO-A 9116946, WO-A 9116944, WO-A 9116943, WO-A 9115261, WO-A 9115260, WO-A 9115259, WO-A 9115258, WO-A 9115257, WO-A 9115250, WO-A 9109645, WO-A 9108795, WO-A 9004433, WO-A9004432, WO-A 9003825, EP-A 254965, US 4717378, EP-A 252732 and GB-A 2239803. As a first aspect of this invention an iontophoretic drug delivery system for administering a compound of formula (I) is provided. Basically, said iontophoretic drug delivery system, also called an electrotransdermal drug delivery system (ETS), is a device containing four components : a power source, e.g. batteries; control circuitry; electrodes; and reservoirs. The device itself may be a one-part or a two-part device; in the latter case a first part may contain the control circuitry and an associated power source, while the second part may consist of an electrode unit containing the above-mentioned active ingredient. The housing of the device or of the parts of the device arc usually moldings normally made of electrically nonconductive material, such as hydrophobic non-conducting polymeric materials, e.g.polyethylene or polypropylene. The opening at the base of the molding, which is in contact with the skin may optionally be covered by a microporous membrane which is attached to the bottom of the molding and is preferably made of electrically nonconductive material, such as stretched polyethylene or polypropylene film. The membrane can be coated with a surfactant if necessary for the purpose of wettability. The microporous membrane allows electrical migration of ions but inhibits leakage of fluid. The material of which the microporous membrane is made can vary with the actual active ingredient used in the device. The electrode system consists of an anode, a cathode, and two reservoirs, one containing drug ions and the other containing, for instance, a biocompatible salt, such as sodium chloride, alkaline salts of inorganic acids, e.g. chlorides, sulfates, nitrates, carbonates, phosphates, or of organic acids, e.g. ascorbatcs, citrates, acetates. Delivery of a positive drug salt, as is the case here, requires that the drug salt be placed during actual delivery in the anode reservoir, while delivery of a negative drug requires -6- placement of the drug salt in the cathode reservoir. Delivery of the same drug out of both reservoirs in an alternating fashion can also be accomplished by periodically reversing the polarity of the electrodes. Electrodes may be metal foils, polymer matrix loaded with metal powder, powdered graphite, carbon fibers or other suitable electrically conductive material. Suitable metals for use in electrodes arc for instance platinum, silver, aluminium, copper, lead, iron, tin, chromium or zinc. Also metal / insoluble salt electrodes may be used, such as silver/silverhalidc electrodes, particularly silvcr/silverchloride electrodes. Interesting electrodes are platinum electrodes. Preferably silver/silverchloride electrodes are used. The configuration of electrodes can be very simple or may comprise a plurality of spaccd-apart and isolated electrodes arranged on a first surface adapted for contact with the skin. The arrangement of electrodes can be alligned, for instance, side-by-side or concentrically. The concentric allignment of the electrodes can be circular, elliptical, rectangular or any of a variety of geometric configurations. Said arrangement of a plurality of electrodes may facilitate delivery of the active ingredient by minimizing current requirements for such delivery as well as minimizing any skin irritation that might be associated with the use of the device. The combined skin contacting areas of electrode assemblies can vary from less than 1 cm-" to greater than 2(X) cm2. The average device will have a contacting area from about 5 cm2 to about 50 cm2. The power source can be batteries or a galvanic couple. Preferred power sources are batteries. Batteries to be used in these drug delivery systems will usually be the conventional miniature or "light-weight" batteries. For example, conventional sheet batteries and microbatteries may be used. Suitable batteries arc alkaline batteries and lithium batteries of the type used in hearing aids and watches. The iontophoretic system further consists of an electronic control module including an ON/OFF switch. The control circuitry of the iontophoretic system can be as simple as a resistor, which would limit the applied current to some maximum value, or as complex as an integrated circuit, which would allow for time varying or feed back-con trolled drug delivery. In this manner the iontophoretic delivery system may for instance reduce the chance of under- or overdosing as a result of said possibility to preprogram the drug delivery at the required therapeutic rate. An interesting preprogrammed delivery scheme in this case of administering an anti-migraine drug may be : first the administration of a bolus of the compound of formula (I) to alleviate the instant pain immediately and after -7- some time a sustained delivery of smaller amounts of the compound to avoid the possibility of break-through head-aches. The device may also include an electrical circuit with means for indicating that an active ingredient is being actively delivered. This feature is desirable for example to reassure the patient that he or she is receiving medication. Compositions suitable for introducing in a iontophoretic device containing a compound of formula (I) provide a further aspect of this invention. Said compositions may for instance be a in a liquid form contained in a reservoir having a membrane which is permeable for active ingredient . Alternatively, the active ingredient may be dispersed in a matrix of a solid, semi-solid or mucilaginous material and optionally having an active ingredient permeable membrane associated therewith. The matrix material is suitably a hydrogel, polyurethane, silicone or other material known in the art for holding a drug in a stable condition prior to release to the skin. The drug may also be contained in the reservoir using an ion-exchange resin or a ligand affinity medium as the drug reservoir matrix. Suitable materials for forming a matrix for use in an electrode for the device according to the invention include, for example, plant extracts, vegetable oils, gums, synthetic or natural polysaccharides, polypeptides, alginates, hydrocarbons, synthetic polymers, mineral and silicon compounds and mixtures thereof. Such materials are solidifying or gel-forming agents which upon mixing and/or heating with the active ingredient and optionally one or more auxiliary material(s) in a solvent or a mixture of solvents form a matrix with the active ingredient and auxiliary material(s), if present, dispersed therethrough. The term "solidifying agent" as used herein also embraces thickening, hardening, setting, suspending or the like agents. Suitable plant extracts include agar-agar, ispaghula, psyllium, cydonia and ceratonia or a mixture thereof. A suitable vegetable oil is hydrogenated castor oil. Examples of suitable gums include guar gum, acacia gum, ghatti gum, karaya gum and tragacanth gum or a mixture thereof. Suitable synthetic and natural polysaccharides include alkylcelluloses, hydroxyalkylcelluloses, cellulose ethers, cellulose esters, nitro celluloses dextrin, carrageenan, pectin, furcellaran and starch or starch derivatives. An example of a preferred starch derivative is sodium starch glycolate. Synthetic polymers include polyvinylalcohol, polyacrylamide, polyacrylic acid, polyvinylpyrrolidone, hydroxyethylmethyiacrylate, polyethyleneoxides, polyethylene, polypropylene, polyisoprcncs, polytsobutylene, polyvinylacctate. Suitable polypcptidcs include 7ein, gelatin, collagen and polygelinc or mixtures thereof. Suitable alginates include alginic acid, propylcne glycol alginate and sodium alginate or a mixture thereof. Preferred hydrocarbons include soft paraffin and hard paraffin, especially white petiolatum. Especially preferred synthetic polymers arc carbovinyl polymer or polyurethanc. Suitable minerals include bentonite, hectorite, aluminium magnesium silicate and magnesium silicate or a mixture thereof. Suitable compounds based on silicon include colloidal silicon dioxide, siliconcs, polysiloxanes and silica gels or a mixture thereof. In the case of a hydrogel the solvent used is preferably water. The solvent used may suitably be an alcohol such as eihanol or stcaryl alcohol, glycerol, propylene glycol. polyethylene glycol or silicone or a mixture thereof, including mixtures with water. Penetration enhancers may also be used. Such penetration enhancers are preferably neither toxic nor irritating nor allergcnic. Suitable penetration enhancers are, for instance, ethanol and higher alcohols, N-dccylmethylsulfoxide, polyethylene glycol monolaurate, dilaurate and related esters, glycerol monolaurate and related mono-, di-and rrifunctional glycerides, diethyl toluamidc, N,N-dimelhyl lauramide, N,N-dimcthyl lauramine oxide, sodium lauryl sulfate, sodium dodecylsarcosinate, cholesterol hemisuccinatc, sodium cetyl sulfate, sodium dodccylbenzenesulfonatc, sodium dioctylsulfosuccinate, and quaternary ammonium compounds, such as cetyl trimethylammonium chloride, and the like. Suitable auxiliary materials may include one or more of the following : an antimicrobial agent, a.prcservative, a.anti-oxidant, a.plastizer, a.tackifier, a.surfactant, a.humectant, a.rhcological agent, a.local anaesthetic, a.chelating agent, or a.rubefacient. 'ihe pH of the solution containing the active ingredient may range from about 3 up to about 12. An even more interesting pH-range is between about 4 and about 11. Preferably the pi I of the solution containing the active ingredient is between about 8 and about 10. Most preferred pH-valuc is from about 8.5 to9.5. Any buffer system capable of sustaining a pH as mentioned hercinabovc can be used. Interesting examples are buffers on the basis of phosphoric acid, boric acid, citric acid, ethanolamine, tris(hydroxymcthyl)-aminomethanc. sodium bicarbonate, and the like or mixtures thereof. These buffer solutions can be prepared in an art-known manner. The choice of buffer solution is dependent upon the electrodes used and upon the other components of the composition containing the compound of formula (1). For instance in the case where the electrodes used are silver/silverchloride electrodes, the buffer solution preferably -9-contains chloride ions. The ionic strength of the solution may range from about 0.001 M to about I M, particularly the range is between about 0.01 M and about 0.5 M, especially between about 0.05 M and about 0.1 M. The amount of active ingredient in the ionized form in solution ranges preferably from about 0.1 mg/ml to about 100 mg/ml, preferably between about 1 mg/ml and about 50 mg/ml, especially between about 2 mg/ml and about 8 mg/ml. The reservoir in contact with the counter electrode comprises a solution containing a biocompatible salt. Suitable salts include sodium chloride or alkali metal salts and alkaline earth metal salts such as chlorides, sulfates, nitrates, carbonates, phosphates, and organic salts such as ascorbates, citrates, acetates and mixtures thereof. The current density used can be in the region of 0.01-10 mA per cm2. For example, the device most usually will operate at about 0.1 to about 0.7 mA per cm2, preferably at about 0.2 to about 0.4 mA per cm2. The current may be constant, variable or pulsed according to a given program of active ingredient delivery. Preferably the applied current is constant. The device and composition according to the invention and as described hereinabovc may be used in a method of delivering a compound of formula (I) by the iomophoretic route, which comprises applying said device to a patient. In practice, a patient suffering from a migraine attack would apply the iontophoretic delivery device somewhere on the body, for instance, on the arm or on the chest and switch on the device. When suffering from a recurrent headache, the patient can, at his option, again tum on the device and receive another dose of the antimigraine drug. The iontophorctic delivery can be sustained for an uninterrupted period of time. It may be appropriate to intersperse a period of active iontophoretic delivery (i.e. a period wherein the iontophoretic device is turned on) with current-free intervals. An uninterrupted application period ranges from about 5 minutes up to about 120 minutes , particularly from about 10 to about 60 minutes, especially from about 15 to about 40 minutes. Current-free intervals may vary from about 5 minutes to 3 hours, particularly from about 15 minutes to about 2 hours, especially from about 30 minutes to 1 hour. Experimental part In vitro experiments In the following examples a two chamber polycarbonate cell was used. The two -10- compartments were separated from each other by a horizontally fixed piece (3 cm2) of freshly excised full thickness abdominal skin of hairless rats. The donor compartment contained 1.4 ml of a solution of the test compound, i.e. R-N-[(3,4-dihydro-2H-1 -benzopyran-2-yl)methyl]-N'-( 1,4,5,6-tctrahydro-2-pyrimidinyl)-1,3-propanediamine (hereinafter referred to as "test compound"), spiked with 3H-Iabelled compound. The radiolabclled spike was introduced at a concentration of 1 ?Ci/ml. The receptor compartment was filled with a phosphate buffer (0.024 M) at a pH of 7.4 isotonized with glucose. In both compartments electrodes were fixed, connected with each other via a power supply. The concentration of test compound migrated through the skin was measured at set points in rime. Said concentration was determined by measuring the radioactivity in a liquid scintillation counter. The ratio of cumulated quantities detected in the receptor compartment to the skin area (3 cm^) are shown as a function of time hcreinundcr. The results are expressed as mean value of at least three experiments. The standard error (SFi) of the mean is also given. Example 1 The test compound was introduced into to the donor compartment at a concentration of 5 mg/ml in a borate buffer (0.1 M) at a pH of 9.5. Platinum electrodes were fixed in both compartments. The applied conditions are enumerated hereinunder and the results are shown in Table 1. - No current was applied (column A). - A direct current of 0.2 mA/cm^ for 1 hour was applied (column B). - A direct current of 0.4 mA/cm^ for 1 hour was applied (column C). - A pulsed current (2 kHz) at a mean current density of 0.4 mA/cm2 for 1 hour was applied (column D). Table 1 -11- Example 2 The test compound was introduced in the donor compartment at different concentrations in different buffersystems at a pH of 9.5. Silvcr/silverchloride electrodes were fixed in both compartments. A direct current of 0.4 mA/cm^ was applied for one hour. The applied conditions are enumerated hereinunder and the results are shown in Table 2. - The concentration of test compound was 5 mg/ml in a borate buffer (0.05 M) containing 0.007 M NaCl (column A). - The concentration of test compound was 7.5 mg/ml in a borate buffer (0.05 M) containing 0.007 M NaCl (column B). - The concentration of test compound was 5 mg/ml in a ethanolamine buffer (0.05 M) (column C). -12- Example 3 The test compound was introduced in the donor compartment at different concentrations in different buffcrsystems. Platinum electrodes were fixed in both compartments. A direct current of 0.4 mA/cm2 was applied for one hour. The applied conditions are enumerated hcreinundcr and the results are shown in Table 3. - The concentration of test compound was 5 mg/ml in a citrate buffer (0.05 M) at a pH of 5.5 (column A). - The concentration of test compound was 5 mg/ml in a citrate buffer (0.1 M) at a pH of 5.5 (column B). Tablee 3 -13- In vivo experiment Example 4 Hydrophilic polyurcihane 10 cm2 foam patches (Allevyn, Smith & Nephew) were soaked with a solution of the test compound, i.e. R-N-[(3,4-dihydro-2H-l-bcnzopyran-2-yl)methyl]-N'-(l,4,5,6-tetrahydro-2-pyrimidinyl)-l,3-propanediamine (7.5 mg/ml of the test compound in ethanolamine buffer (0.05 M) at a pH of 9.5). Ag/AgCl electrodes were inserted in the foam patch and connected to a direct current generator. On the drug treatment day, volunteers were administered the test compound by an electrotransdermal drug delivery system (ETS) with a direct current of 0.2 mA/cm2 applied for two consecutive 30 min periods (periods were separated by a current-free interval of 90 min). The drug delivery system (foam patch) was applied on the ventral side of the forearm of the volunteer and remained in place until 90 min after the second current application period (=240 min after start of 1 st current application). Blood samples, blood pressure measurements and electrocardiogram recordings were performed ai several time points during the ETS application period and at specific time points until 6 hours thereafter. The volunteers remained in the clinical pharmacology unit until 4 hours after start of the first current application period. To evaluate tolerability, the volunteers saw the investigator for a follow-up visit, which was scheduled between 1 and 7 days after drug administration. Venous blood samples (5ml) were taken from an anticubital vein (opposite to administration site) immediately before and at 30 (end of 1st current application period), 60, 90, 120 (before 2nd current application period), 150 (end of 2nd current application period), 180, 210, 240, 300 and 360 min after start of the 1st current application period. The blood samples were collected in heparinized tubes. Plasma concentrations of the test compound were determined by radio-immunoassay. -14- Eight volunteers participated in the experiment and the mean value of the plasma concentration (in ng/ml) in the blood samples is given in Table 4. ND : not detectable by the RIA-mcthod ( 15-We Claim: 1. A iontophoretic drug delivery device comprising (a) a power source, (b) control circuitry, (c) electrodes, and (d) reservoirs, characterized in that it contains as active ingredient a compound of formula the pharmaceutically acceptable acid addition salts thereof, and the stereochemically isomeric forms thereof, wherein R1 is hydrogen or C1-6 alkyl; R2 is hydrogen, C1-6 alkyl, C3-6 alkenyl or C3-6 alkynyl; R3 is hydrogen or C1-6 alkyl; or R2 and R3 taken together form a bivalent radical of formula -(CH2)m- wherein m is 4 or 5; or Rl and R2 taken together form a bivalent radical of formula -CH=CH- or of formula-(CH2)n-, wherein n is 2, 3 or 4; or R3 may represent a bond when R1 and R2 taken together form a bivalent radical of formula -CH-CH-CH=; - 16- R4 and R5 each independently are hydrogen or C1-6 alkyl; Alk1 is a bivalent C1-3 alkanediyl radical; Alk2 is a bivalent C2-15 atkanediyl radical; and R6 and R7 each independently are hydrogen, halo, C1-6 alkyl, C3-6 alkenyl, C3-6 alkynyl, hydroxy, C1-6 alkyloxy or cyano. 2. A device as claimed in claim 1 wherein it contains as an active ingredient N-[(3,4-dihydro-2H-l-benzopyran-2-yl)methyl]-N'- (1,4,5,6-tetrahydro-2-pyrimidinyl)-l,3-propanediamine, a stereochemically isomenc form thereof or a pharmaceutically acceptable acid addition salt form thereof. 3. A device as claimed in claims 1 or 2 wherein the active ingredient is in liquid form contained in a reservoir, having an active ingredient permeable membrane. 4. A device as claimed in claims 1 or 2 wherein the active ingredient is dispersed in a matrix of a solid, semi-solid or mucilaginous m aterial. 5. A device as claimed in claims 1 or 2 wherein at least one of the electrodes is a silver/silverchloride electrode. - 17- 6. A composition containing a compound of formula (I) suitable for applying in a iontophoretic drug delivery device. 7. ' A composition as claimed in claim 6 wherein it contains a compound of formula (I) in an amount ranging from about 1 mg/mito about 50 mg/ml. 8. A composition as claimed in claim 7 wherein it has a pH ranging from 4 to 11. 9. A composition as claimed in claim 8 wherein it has a pH range from about 8.5 to 9.5. The present invention relates to the iontophorctic delivery to a patient, more in particular to a migraine patient, of a compound of formula (I) as shown hereinunder. The invention also relates to a device for the iontophoretic delivery of a compound of formula (I), as well as to a composition containing a compound of formula (I), which can be applied in a device for iontophoretic delivery. Said compounds are benzopyranalkylaminoalkyl substituted guanidines having the formula the pharmaceuticaliy acceptable acid addition salts thereof, and the stereochemically isomeric forms thereof, wherein R1 is hydrogen orCl-6alkyl; R2 is hydrogen, C1-6alkyl, C3-6alkenyl or C3-6alkynyl; R3 is hydrogen or C1-6alkyl; or R2 and R3 taken together form a bivalent radical of formula -(CH2)m- wherein m is 4 or 5; or R1 and R2 taken together form a bivalent radical of formula -CH=CH-or of formula -(CH2)n- wherein n is 2, 3 or 4; or R3 may represent a bond when R1 and R2 taken together form a bivalent radical of formula -CH=CH-CH=; R4 and R5 each independently are hydrogen orC1-6alkyl; Alk1 is a bivalent C1-3alkanediyl radical; Alk2 is a bivalent C2-15alkanediyl radical; and R6and R7 each independently are hydrogen, halo, Cl-6alkyl, C3-6alkenyl, C3-6alkynyl, hydroxy, C1-6alkyloxy or cyano.

Full Text

The present invention relates to the iontophoretic delivery to a patient, more in particular to a migraine patient, of a compound of formula (I) as shown hereinunder. The invention also relates to a device for the iontophoretic delivery of a compound of formula (I), as well as to a composition containing a compound of formula (I), which can be applied in a device for iontophoretic delivery.
Although in general, oral administration of a drug is considered as most convenient, this route poses particular problems when administering a drug, more in particular an anti-migraine drug, to patients suffering from a migraine attack. Migraine patients often feel nauseous, sometimes resulting in violent vomiting, thus hampering the oral administration of the anti-migraine drug. The successful oral delivery of some anti-migraine substances is also impeded by its susceptibility to degradation by the acid environment of the stomach and by the digestive activity of several enzymes in the gastrointestinal tract. Other disadvantages of the oral route are the often poor absorption due to gastroparesis and the extensive first-pass elimination in the liver (the hepatic first-pass effect), whereby a compound is transformed in the liver into a metabolite more prone for excretion. Along with convenient administration, it is essential for an effective treatment of a migraine attack that the activity of the drug sets on immediately, or at least very rapidly, after administration and that the effect lasts long enough. Hence a means of directly inserting the drug into the bloodstream should be a method of choice for the administration of an anti-migraine drug. An obvious way of doing so is by injecting a solution of the drug either intravenously or subcutaneously. However, the consequent pain, risk of infection, the complex procedures of self-administration and potential for low patient compliance make such parenteral administration undesirable.
Transdermal delivery is an attractive alternative because : (a) it avoids gastrointestinal degradation and the hepatic first-pass effect; (b) it lends itself to a controlled and/or sustained release; (c) it allows for convenient and simple self-administration and encourages patient compliance, since a transdermal formulation would be easy to apply or to remove.
Traditional transdermal drug delivery systems are based on the transport of drugs into the skin by diffusion through the outermost layer of the epidermis, i.e. the stratum comeum. The number of solutes which can be delivered by this route are limited due to the excellent barrier properties of the said stratum corncum. Hence, attainment of a therapeutically effective level is therefore difficult without some form of facilitation. One means of facilitation is the delivery of the drug by electrokinetic action, more in particular

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by iontophoretic action. The principle of iontophoresis is that ionized (or polar) drug molecules can be driven into the skin if an appropriate electrical potential is applied across the skin. Iontophoresis may be due solely to electromigration, i.e. the movement of ionized drug molecules across an electrical field per se, or it may be due to a combined effect of elcctromigration and electroosmosis. The latter is a transdermal flux of liquid solvent containing the drug by the presence of an electricaJ field.
The problem 10 be solved is to find or develop compounds and compositions, which have the desired anti-migraine activity and which are susceptible for said convenient iontophoretic delivery.
Recently, it was discovered that the compounds of formula (I) show 5HTi-iJke agonistic activity and, more in particular, anti-migraine activity. Unexpectedly it has been found that these compounds of formula (I) can be delivered via iontophoretic action. Said compounds arc dihydrobcnzopyranalkylaminoalkyl substituted guanidincs having the formula

the pharmaccutically acceptable acid addition salts thereof, and the stercochcmically isomeric forms thereof, wherein
Rl is hydrogen or Cl-6alkyl;
R2 is hydrogen, C1-6alkyl, C3-6alkenyl or C3-6alkynyl;
R3 is hydrogen or C1-6alkyl; or
R2 and R3 taken together form a bivalent radical of formula -(CH2)nr wherein m is 4
or 5; or
Rl and R2 taken together form a bivalent radical of formula -CII=CH- or of formula
-(CH2)n-. wherein n is 2, 3 or 4; or
R3 may represent a bond when R1 and R2 taken together form a bivalent radical of
formula -CH=CH-CH=;
R4 and R5 each independently are hydrogen orC1-6 alkyl;
Alk 1 is a bivalent C1 -3alkanediyl radical;
Alk2 is a bivalent C2-15 alkanediyl radical; and
R6 and R7 each independently are hydrogen, halo, C1-6alkyl, C3-6alkenyl, C3-6alkynyl, hydroxy, C1-6alkyloxy or cyano.
In the foregoing definitions, the term "halo" is generic to fluoro, chloro, bromo,

-3-
iodo; the term "C1-6alkyl" means straight or branched saturated hydrocarbon radicals having from 1 to 6 carbon atoms, such as, methyl, ethyl, propyl, butyl, pentyl, hexyl, and the like; "C3-6alkenyl" defines straight and branch chained hydrocarbon radicals containing one double bond and having from 3 to 6 carbon atoms, such as, for example, 2-propcnyl, 3-butenyl, 2-buteny1, 2-pcntenyl, 3-pcntenyl, 3-methyl-2-butenyl and the like; and the carbon atom of said C3-6alkenyl being connected to a nitrogen atom preferably is saturated, "C3-6alkynyl" defines straight and branch chained hydrocarbon radicals containing one triple bond and having from 3 to 6 carbon atoms, such as, for example, 2-propynyl, 3-butynyl, 2-butynyl, 2-pcntynyl, 3-pentynyl, 3-hexynyl, and the like; and the carbon atom of said C3-6alkynylradicaI being connected to a nitrogen atom preferably is saturated; "Ci^alkanediyl" is meant to comprise straight or branched saturated hydrocarbon radicals containing 1 to 3 carbon atoms, such as, methylenc, cthanediyl, propanediyl, and the like; "C2-15alkancdiyl" is meant to comprise straight or branched saturated hydrocarbon radicals having from 2 to 15 carbon atoms, such as, ethanediyl, propancdiyl, butanediyl, pentanediyl, hexanediyl, heptanediyl, octanediyl, nonanediyl, decanediyl, undecancdiyl, dodecanediyl, tridecanediyl, tetradecanediyl, pcntadecanediyl and the branched isomers thereof.
Pharmaceutically acceptable acid addition salts as mentioned hereinabove comprise the therapeutically active non-toxic acid addition salt forms which the compounds of formula (I) are able to form. Said salt forms can conveniently be obtained by treating the base form of the compounds of formula (I) with appropriate acids such as inorganic acids, for example, hydrohalic acid, e.g. hydrochloric, hydrobromic and the like acids, sulfuric acid, nitric acid, phosphoric acid and the like; or organic acids, such as, for example, acetic, propanoic, hydroxyacetic, 2-hydroxypropanoic, 2-oxopropanoic, ethancdioic, propanedioic, butanedioic, (Z)-2-butenedioic, (E)-2-butenedioic, 2-hydroxybutancdioic, 2,3-dihydroxybutanedioic, 2-hydroxy-1,2,3-propanetri-carboxylic, mcthanesulfonic, ethanesulfonic, benzenesulfonic, 4-methylbenzenesulfonic, cyclohexanesulfamic, 2-hydroxybenzoic, 4-amino-2-hydroxybenzoic and the like acids. Conversely the salt form can be convened by treatment with alkali into the free base form.
The term "stercochcrnically isomcric forms" as used hereinbefore and hereinafter defines all the possible isomeric forms which the compounds of formula (I) may possess. Unless otherwise mentioned or indicated, the chemical designation of compounds denotes the mixture of all possible stereochemically isomeric forms, said mixtures containing all diastereomers and enantiomers of the basic molecular structure. More in particular, stercogenic centers may have the R- or S-configuration. The present

-4-
invention clearly intends to embrace in its scope both the individual stereochemically isorneric forms and the mixtures thereof.
It has to be understood that, when mixtures of enantiomers are present, they may be separated according to classical resolution methods, e.g. by fractional crystallization of their acid addition salts with a suitable chiral acid or by the separation by chromatography using a chiral phase.
Moreover, some of the compounds of formula (I) may also exist in their tautomeric forms. Such forms although not explicitly indicated in the above formula (I) are intended be included within the scope of the present invention.
K 1 is suitably hydrogen or methyl;
R2 is suitably hydrogen or methyl;
R3 is suitably hydrogen or methyl;
preferably R1 and R2 are taken together to form a bivalent radical of formula
-CH=CH-, -(CH2)2- or -(CH2)3-; or when R3 is a free bond R1 and R2 taken together
form a bivalent radical or formula -CH=CH-CH= ;
R4 is suitably methyl or hydrogen, preferably hydrogen;
R5 is suitably methyl or hydrogen, preferably hydrogen;
R6 and R7 suitably are hydrogen, halo, or Cl-6alkyl, preferably hydrogen, fluoro, methyl
or ethyl.
Interesting compounds of formula (I) arc those compounds of formula (I) wherein Alk 1 is C1-2alkanediyl> especially mcthylcne.
Other interesting compounds are those compounds of formula (I) wherein Alk2 is C2-6alkanediyl, particularly, ethanediyl, propanediyl, butanediyl, pentancdiyl, hcxanediyl, preferably 1,3-propanediyl.
Most preferred compounds are N-|(3,4-dihydro-2H-l-benzopyran-2-yl)methyl]-N'-( 1,4,5,6-tetrahydro-2-pyrimidinyl)-l,3-propanediamine, the stereochemical isomers thereof, particularly the R-isomer, and the pharmaceutically acceptable acid addition salts thereof.
The compounds of formula (I) may be prepared following art-known procedures.
The process of iontophoretic drug delivery is performed in general by putting a composition containing the drug onto intact skin. This composition may for instance be a solution (absorbed onto some porous material, for instance a piece of filter paper or a

-5-
piecc of hydrophilic polyurethane) or a gel. The composition is then covered by an electrode. A second electrode is placed elsewhere on the skin, and a direct current source is connected between the electrodes in such a way that the electrode in contact with the drug solution assumes the same charge as the ionized drug. Under influence of the electric field present, drug molecules migrate through the skin. A current flows between the electrodes, part of which is carried by the drug.
Iontophoretic devices as such arc known in the art, for instance from, WO-A 9116946, WO-A 9116944, WO-A 9116943, WO-A 9115261, WO-A 9115260, WO-A 9115259, WO-A 9115258, WO-A 9115257, WO-A 9115250, WO-A 9109645, WO-A 9108795, WO-A 9004433, WO-A9004432, WO-A 9003825, EP-A 254965, US 4717378, EP-A 252732 and GB-A 2239803.
As a first aspect of this invention an iontophoretic drug delivery system for administering a compound of formula (I) is provided. Basically, said iontophoretic drug delivery system, also called an electrotransdermal drug delivery system (ETS), is a device containing four components : a power source, e.g. batteries; control circuitry; electrodes; and reservoirs. The device itself may be a one-part or a two-part device; in the latter case a first part may contain the control circuitry and an associated power source, while the second part may consist of an electrode unit containing the above-mentioned active ingredient. The housing of the device or of the parts of the device arc usually moldings normally made of electrically nonconductive material, such as hydrophobic non-conducting polymeric materials, e.g.polyethylene or polypropylene. The opening at the base of the molding, which is in contact with the skin may optionally be covered by a microporous membrane which is attached to the bottom of the molding and is preferably made of electrically nonconductive material, such as stretched polyethylene or polypropylene film. The membrane can be coated with a surfactant if necessary for the purpose of wettability. The microporous membrane allows electrical migration of ions but inhibits leakage of fluid. The material of which the microporous membrane is made can vary with the actual active ingredient used in the device.
The electrode system consists of an anode, a cathode, and two reservoirs, one containing drug ions and the other containing, for instance, a biocompatible salt, such as sodium chloride, alkaline salts of inorganic acids, e.g. chlorides, sulfates, nitrates, carbonates, phosphates, or of organic acids, e.g. ascorbatcs, citrates, acetates. Delivery of a positive drug salt, as is the case here, requires that the drug salt be placed during actual delivery in the anode reservoir, while delivery of a negative drug requires

-6-
placement of the drug salt in the cathode reservoir. Delivery of the same drug out of both reservoirs in an alternating fashion can also be accomplished by periodically reversing the polarity of the electrodes.
Electrodes may be metal foils, polymer matrix loaded with metal powder, powdered graphite, carbon fibers or other suitable electrically conductive material. Suitable metals for use in electrodes arc for instance platinum, silver, aluminium, copper, lead, iron, tin, chromium or zinc. Also metal / insoluble salt electrodes may be used, such as silver/silverhalidc electrodes, particularly silvcr/silverchloride electrodes. Interesting electrodes are platinum electrodes. Preferably silver/silverchloride electrodes are used.
The configuration of electrodes can be very simple or may comprise a plurality of spaccd-apart and isolated electrodes arranged on a first surface adapted for contact with the skin. The arrangement of electrodes can be alligned, for instance, side-by-side or concentrically. The concentric allignment of the electrodes can be circular, elliptical, rectangular or any of a variety of geometric configurations. Said arrangement of a plurality of electrodes may facilitate delivery of the active ingredient by minimizing current requirements for such delivery as well as minimizing any skin irritation that might be associated with the use of the device.
The combined skin contacting areas of electrode assemblies can vary from less than 1 cm-" to greater than 2(X) cm2. The average device will have a contacting area from about 5 cm2 to about 50 cm2.
The power source can be batteries or a galvanic couple. Preferred power sources are batteries. Batteries to be used in these drug delivery systems will usually be the conventional miniature or "light-weight" batteries. For example, conventional sheet batteries and microbatteries may be used. Suitable batteries arc alkaline batteries and lithium batteries of the type used in hearing aids and watches.
The iontophoretic system further consists of an electronic control module including an ON/OFF switch. The control circuitry of the iontophoretic system can be as simple as a resistor, which would limit the applied current to some maximum value, or as complex as an integrated circuit, which would allow for time varying or feed back-con trolled drug delivery. In this manner the iontophoretic delivery system may for instance reduce the chance of under- or overdosing as a result of said possibility to preprogram the drug delivery at the required therapeutic rate. An interesting preprogrammed delivery scheme in this case of administering an anti-migraine drug may be : first the administration of a bolus of the compound of formula (I) to alleviate the instant pain immediately and after

-7-
some time a sustained delivery of smaller amounts of the compound to avoid the possibility of break-through head-aches.
The device may also include an electrical circuit with means for indicating that an active ingredient is being actively delivered. This feature is desirable for example to reassure the patient that he or she is receiving medication.
Compositions suitable for introducing in a iontophoretic device containing a compound of formula (I) provide a further aspect of this invention. Said compositions may for instance be a in a liquid form contained in a reservoir having a membrane which is permeable for active ingredient .
Alternatively, the active ingredient may be dispersed in a matrix of a solid, semi-solid or mucilaginous material and optionally having an active ingredient permeable membrane associated therewith. The matrix material is suitably a hydrogel, polyurethane, silicone or other material known in the art for holding a drug in a stable condition prior to release to the skin. The drug may also be contained in the reservoir using an ion-exchange resin or a ligand affinity medium as the drug reservoir matrix.
Suitable materials for forming a matrix for use in an electrode for the device according to the invention include, for example, plant extracts, vegetable oils, gums, synthetic or natural polysaccharides, polypeptides, alginates, hydrocarbons, synthetic polymers, mineral and silicon compounds and mixtures thereof. Such materials are solidifying or gel-forming agents which upon mixing and/or heating with the active ingredient and optionally one or more auxiliary material(s) in a solvent or a mixture of solvents form a matrix with the active ingredient and auxiliary material(s), if present, dispersed therethrough.
The term "solidifying agent" as used herein also embraces thickening, hardening, setting, suspending or the like agents.
Suitable plant extracts include agar-agar, ispaghula, psyllium, cydonia and ceratonia or a mixture thereof. A suitable vegetable oil is hydrogenated castor oil. Examples of suitable gums include guar gum, acacia gum, ghatti gum, karaya gum and tragacanth gum or a mixture thereof. Suitable synthetic and natural polysaccharides include alkylcelluloses, hydroxyalkylcelluloses, cellulose ethers, cellulose esters, nitro celluloses dextrin, carrageenan, pectin, furcellaran and starch or starch derivatives. An example of a preferred starch derivative is sodium starch glycolate. Synthetic polymers include polyvinylalcohol, polyacrylamide, polyacrylic acid, polyvinylpyrrolidone, hydroxyethylmethyiacrylate, polyethyleneoxides, polyethylene, polypropylene,

polyisoprcncs, polytsobutylene, polyvinylacctate. Suitable polypcptidcs include 7ein, gelatin, collagen and polygelinc or mixtures thereof. Suitable alginates include alginic acid, propylcne glycol alginate and sodium alginate or a mixture thereof.
Preferred hydrocarbons include soft paraffin and hard paraffin, especially white petiolatum. Especially preferred synthetic polymers arc carbovinyl polymer or polyurethanc.
Suitable minerals include bentonite, hectorite, aluminium magnesium silicate and magnesium silicate or a mixture thereof.
Suitable compounds based on silicon include colloidal silicon dioxide, siliconcs, polysiloxanes and silica gels or a mixture thereof.
In the case of a hydrogel the solvent used is preferably water. The solvent used may suitably be an alcohol such as eihanol or stcaryl alcohol, glycerol, propylene glycol. polyethylene glycol or silicone or a mixture thereof, including mixtures with water.
Penetration enhancers may also be used. Such penetration enhancers are preferably neither toxic nor irritating nor allergcnic. Suitable penetration enhancers are, for instance, ethanol and higher alcohols, N-dccylmethylsulfoxide, polyethylene glycol monolaurate, dilaurate and related esters, glycerol monolaurate and related mono-, di-and rrifunctional glycerides, diethyl toluamidc, N,N-dimelhyl lauramide, N,N-dimcthyl lauramine oxide, sodium lauryl sulfate, sodium dodecylsarcosinate, cholesterol hemisuccinatc, sodium cetyl sulfate, sodium dodccylbenzenesulfonatc, sodium dioctylsulfosuccinate, and quaternary ammonium compounds, such as cetyl trimethylammonium chloride, and the like.
Suitable auxiliary materials may include one or more of the following : an antimicrobial agent, a.prcservative, a.anti-oxidant, a.plastizer, a.tackifier, a.surfactant, a.humectant, a.rhcological agent, a.local anaesthetic, a.chelating agent, or a.rubefacient.
'ihe pH of the solution containing the active ingredient may range from about 3 up to about 12. An even more interesting pH-range is between about 4 and about 11. Preferably the pi I of the solution containing the active ingredient is between about 8 and about 10. Most preferred pH-valuc is from about 8.5 to9.5. Any buffer system capable of sustaining a pH as mentioned hercinabovc can be used. Interesting examples are buffers on the basis of phosphoric acid, boric acid, citric acid, ethanolamine, tris(hydroxymcthyl)-aminomethanc. sodium bicarbonate, and the like or mixtures thereof. These buffer solutions can be prepared in an art-known manner. The choice of buffer solution is dependent upon the electrodes used and upon the other components of the composition containing the compound of formula (1). For instance in the case where the electrodes used are silver/silverchloride electrodes, the buffer solution preferably

-9-contains chloride ions.
The ionic strength of the solution may range from about 0.001 M to about I M, particularly the range is between about 0.01 M and about 0.5 M, especially between about 0.05 M and about 0.1 M.
The amount of active ingredient in the ionized form in solution ranges preferably from about 0.1 mg/ml to about 100 mg/ml, preferably between about 1 mg/ml and about 50 mg/ml, especially between about 2 mg/ml and about 8 mg/ml.
The reservoir in contact with the counter electrode comprises a solution containing a biocompatible salt. Suitable salts include sodium chloride or alkali metal salts and alkaline earth metal salts such as chlorides, sulfates, nitrates, carbonates, phosphates, and organic salts such as ascorbates, citrates, acetates and mixtures thereof.
The current density used can be in the region of 0.01-10 mA per cm2. For example, the device most usually will operate at about 0.1 to about 0.7 mA per cm2, preferably at about 0.2 to about 0.4 mA per cm2. The current may be constant, variable or pulsed according to a given program of active ingredient delivery. Preferably the applied current is constant.
The device and composition according to the invention and as described hereinabovc may be used in a method of delivering a compound of formula (I) by the iomophoretic route, which comprises applying said device to a patient. In practice, a patient suffering from a migraine attack would apply the iontophoretic delivery device somewhere on the body, for instance, on the arm or on the chest and switch on the device. When suffering from a recurrent headache, the patient can, at his option, again tum on the device and receive another dose of the antimigraine drug.
The iontophorctic delivery can be sustained for an uninterrupted period of time. It may be appropriate to intersperse a period of active iontophoretic delivery (i.e. a period wherein the iontophoretic device is turned on) with current-free intervals. An uninterrupted application period ranges from about 5 minutes up to about 120 minutes , particularly from about 10 to about 60 minutes, especially from about 15 to about 40 minutes. Current-free intervals may vary from about 5 minutes to 3 hours, particularly from about 15 minutes to about 2 hours, especially from about 30 minutes to 1 hour.
Experimental part In vitro experiments
In the following examples a two chamber polycarbonate cell was used. The two

-10-
compartments were separated from each other by a horizontally fixed piece (3 cm2) of freshly excised full thickness abdominal skin of hairless rats. The donor compartment contained 1.4 ml of a solution of the test compound, i.e. R-N-[(3,4-dihydro-2H-1 -benzopyran-2-yl)methyl]-N'-( 1,4,5,6-tctrahydro-2-pyrimidinyl)-1,3-propanediamine (hereinafter referred to as "test compound"), spiked with 3H-Iabelled compound. The radiolabclled spike was introduced at a concentration of 1 ?Ci/ml. The receptor compartment was filled with a phosphate buffer (0.024 M) at a pH of 7.4 isotonized with glucose. In both compartments electrodes were fixed, connected with each other via a power supply. The concentration of test compound migrated through the skin was measured at set points in rime. Said concentration was determined by measuring the radioactivity in a liquid scintillation counter. The ratio of cumulated quantities detected in the receptor compartment to the skin area (3 cm^) are shown as a function of time hcreinundcr. The results are expressed as mean value of at least three experiments. The standard error (SFi) of the mean is also given.
Example 1
The test compound was introduced into to the donor compartment at a concentration of 5 mg/ml in a borate buffer (0.1 M) at a pH of 9.5. Platinum electrodes were fixed in both compartments. The applied conditions are enumerated hereinunder and the results are shown in Table 1.
- No current was applied (column A).
- A direct current of 0.2 mA/cm^ for 1 hour was applied (column B).
- A direct current of 0.4 mA/cm^ for 1 hour was applied (column C).
- A pulsed current (2 kHz) at a mean current density of 0.4 mA/cm2 for 1 hour was
applied (column D).
Table 1

-11-

Example 2
The test compound was introduced in the donor compartment at different concentrations in different buffersystems at a pH of 9.5. Silvcr/silverchloride electrodes were fixed in both compartments. A direct current of 0.4 mA/cm^ was applied for one hour. The applied conditions are enumerated hereinunder and the results are shown in Table 2.
- The concentration of test compound was 5 mg/ml in a borate buffer (0.05 M)
containing 0.007 M NaCl (column A).
- The concentration of test compound was 7.5 mg/ml in a borate buffer (0.05 M)
containing 0.007 M NaCl (column B).
- The concentration of test compound was 5 mg/ml in a ethanolamine buffer (0.05 M)
(column C).

-12-

Example 3
The test compound was introduced in the donor compartment at different concentrations in different buffcrsystems. Platinum electrodes were fixed in both compartments. A direct current of 0.4 mA/cm2 was applied for one hour. The applied conditions are enumerated hcreinundcr and the results are shown in Table 3.
- The concentration of test compound was 5 mg/ml in a citrate buffer (0.05 M) at a pH of
5.5 (column A).
- The concentration of test compound was 5 mg/ml in a citrate buffer (0.1 M) at a pH of
5.5 (column B).
Tablee 3

-13-

In vivo experiment Example 4
Hydrophilic polyurcihane 10 cm2 foam patches (Allevyn, Smith & Nephew) were soaked with a solution of the test compound, i.e. R-N-[(3,4-dihydro-2H-l-bcnzopyran-2-yl)methyl]-N'-(l,4,5,6-tetrahydro-2-pyrimidinyl)-l,3-propanediamine (7.5 mg/ml of the test compound in ethanolamine buffer (0.05 M) at a pH of 9.5). Ag/AgCl electrodes were inserted in the foam patch and connected to a direct current generator.
On the drug treatment day, volunteers were administered the test compound by an electrotransdermal drug delivery system (ETS) with a direct current of 0.2 mA/cm2 applied for two consecutive 30 min periods (periods were separated by a current-free interval of 90 min). The drug delivery system (foam patch) was applied on the ventral side of the forearm of the volunteer and remained in place until 90 min after the second current application period (=240 min after start of 1 st current application).
Blood samples, blood pressure measurements and electrocardiogram recordings were performed ai several time points during the ETS application period and at specific time points until 6 hours thereafter. The volunteers remained in the clinical pharmacology unit until 4 hours after start of the first current application period. To evaluate tolerability, the volunteers saw the investigator for a follow-up visit, which was scheduled between 1 and 7 days after drug administration.
Venous blood samples (5ml) were taken from an anticubital vein (opposite to administration site) immediately before and at 30 (end of 1st current application period), 60, 90, 120 (before 2nd current application period), 150 (end of 2nd current application period), 180, 210, 240, 300 and 360 min after start of the 1st current application period. The blood samples were collected in heparinized tubes.
Plasma concentrations of the test compound were determined by radio-immunoassay.

-14-
Eight volunteers participated in the experiment and the mean value of the plasma concentration (in ng/ml) in the blood samples is given in Table 4.

ND : not detectable by the RIA-mcthod (
15-We Claim:
1. A iontophoretic drug delivery device comprising (a) a power source, (b) control circuitry, (c) electrodes, and (d) reservoirs, characterized in that it contains as active ingredient a compound of formula

the pharmaceutically acceptable acid addition salts thereof, and the
stereochemically isomeric forms thereof, wherein
R1 is hydrogen or C1-6 alkyl;
R2 is hydrogen, C1-6 alkyl, C3-6 alkenyl or C3-6 alkynyl;
R3 is hydrogen or C1-6 alkyl; or
R2 and R3 taken together form a bivalent radical of formula -(CH2)m-
wherein m is 4 or 5; or
Rl and R2 taken together form a bivalent radical of formula -CH=CH- or
of formula-(CH2)n-, wherein n is 2, 3 or 4; or
R3 may represent a bond when R1 and R2 taken together form a bivalent
radical of formula -CH-CH-CH=;

- 16-
R4 and R5 each independently are hydrogen or C1-6 alkyl;
Alk1 is a bivalent C1-3 alkanediyl radical;
Alk2 is a bivalent C2-15 atkanediyl radical; and
R6 and R7 each independently are hydrogen, halo, C1-6 alkyl, C3-6 alkenyl,
C3-6 alkynyl, hydroxy, C1-6 alkyloxy or cyano.
2. A device as claimed in claim 1 wherein it contains as an active
ingredient N-[(3,4-dihydro-2H-l-benzopyran-2-yl)methyl]-N'-
(1,4,5,6-tetrahydro-2-pyrimidinyl)-l,3-propanediamine, a
stereochemically isomenc form thereof or a pharmaceutically
acceptable acid addition salt form thereof.
3. A device as claimed in claims 1 or 2 wherein the active ingredient
is in liquid form contained in a reservoir, having an active
ingredient permeable membrane.
4. A device as claimed in claims 1 or 2 wherein the active ingredient
is dispersed in a matrix of a solid, semi-solid or mucilaginous
m aterial.
5. A device as claimed in claims 1 or 2 wherein at least one of the
electrodes is a silver/silverchloride electrode.

- 17-
6. A composition containing a compound of formula (I) suitable for
applying in a iontophoretic drug delivery device.
7. ' A composition as claimed in claim 6 wherein it contains a
compound of formula (I) in an amount ranging from about 1
mg/mito about 50 mg/ml.
8. A composition as claimed in claim 7 wherein it has a pH ranging
from 4 to 11.
9. A composition as claimed in claim 8 wherein it has a pH range
from about 8.5 to 9.5.

The present invention relates to the iontophorctic delivery to a patient, more in particular to a migraine patient, of a compound of formula (I) as shown hereinunder. The invention also relates to a device for the iontophoretic delivery of a compound of formula (I), as well as to a composition containing a compound of formula (I), which can be applied in a device for iontophoretic delivery.
Said compounds are benzopyranalkylaminoalkyl substituted guanidines having the formula

the pharmaceuticaliy acceptable acid addition salts thereof, and the stereochemically isomeric forms thereof, wherein R1 is hydrogen orCl-6alkyl; R2 is hydrogen, C1-6alkyl, C3-6alkenyl or C3-6alkynyl; R3 is hydrogen or C1-6alkyl; or R2 and R3 taken together form a bivalent radical of formula -(CH2)m- wherein m is 4 or 5; or R1 and R2 taken together form a bivalent radical of formula -CH=CH-or of formula -(CH2)n- wherein n is 2, 3 or 4; or R3 may represent a bond when R1 and R2 taken together form a bivalent radical of formula -CH=CH-CH=; R4 and R5 each independently are hydrogen orC1-6alkyl; Alk1 is a bivalent C1-3alkanediyl radical; Alk2 is a bivalent C2-15alkanediyl radical; and R6and R7 each independently are hydrogen, halo, Cl-6alkyl, C3-6alkenyl, C3-6alkynyl, hydroxy, C1-6alkyloxy or cyano.

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Patent Number

209227

Indian Patent Application Number

00195/CAL/1995

PG Journal Number

34/2007

Publication Date

24-Aug-2007

Grant Date

23-Aug-2007

Date of Filing

24-Feb-1995

Name of Patentee

JANSSEN PHARMACEUTICA N.V.

Applicant Address

TURNHOUTSEWEG 30, B-2340-BEERSE, BELGIUM

Inventors:

#	Inventor's Name	Inventor's Address
1	GUSTAAF VAN REET,	POPULIERENLAAN 14, B-2460-KASTERLEE, BELGIUM
2	FRANK MARIA JOZEF DE BEUKELAAR,	RENIER SNIEDERSSTRAAT 38, B-2340-BEERSE, BELGIUM
3	JEAN LOUIS MESENS,	MOEREIND 17, B-2275-WECHELDERZANDE, BELGIUM

PCT International Classification Number

A61K 31/35

PCT International Application Number

N/A

PCT International Filing date

PCT Conventions:

#	PCT Application Number	Date of Convention	Priority Country
1			NA