Title of Invention

"A PROCESS FOR THE MANUFACTURE OF A PHARAMACEUTICAL PREPARATION"

Abstract

The invention relates to the use of moxonidine and the physiologically compatible acid additional salts thereof for producing pharmaceutical preparations for the treatment of myocardial infarction damages of the myocardium. Moxonidine and pharmaceutical preparations which contain physiologically compatible acid additional salts of moxonidine are suitable for use in acute myocardial infarction treatment and/or postmyocardial infarction treatment.

Full Text

Description The present, invention concerns the process for the manufacture of a pharmaceutical preparation and use of 4-chloro-5-[(4,5-dihydro-lH-itnidazol-.2-yl)-ammo]-6-methoxy-2-methyl-pyrirmidine(- moxonidine) and its physiologically compatible acid addition salts for the treatment of myocardial damage secondary to myocardial infarction and for the manufacture of drugs suitable for this'treatment. The object of the invention is to provide novel pharmaceutical preparations that exert a beneficial influence, promoting recovery and/or rehabilitation, on the myocardial status of myocardial infarction patients and which are therefore .suitable for the" treatment of mypcardial damage secondary to myocardial infarction within the context of myocardial infarction and/or postmyocardial infarction management. According to the invention, 4-chloro-5-[(4,5-dihydro-lH-imidazol-2-yl) -amino] -6-methpxy-2-methylpyrimidine of Formula I (Formula Removed) and its physiologically compatible acid addition salts are used for the manufacture of pharmaceutical preparations for the treatment of myocardial damage secondary to myocardial infarction. Suitable physiologically compatible acid addition salts of moxonidine include salts with inorganic acids, for example hydrohalic acids, or with organic acids, for example lower aliphatic mono- or dicarboxylic acids such as acetic acid, fumaric acid or tartaric acid or aromatic carboxylic acids such as e.g. salicylic acid. The compounds used according to the invention fall within the scope of the 5-[(2-imidazolin-2-yl)-amino]-pyri-midine derivatives with blood pressure-lowering properties described in German Patent Application No. 28 49 537, and are known from this patent application. Pharmaceutical i preparations containing moxonidine are commercially available as antihypertensive medications under the trade name Physiotens® and are used medically as antihypertensive agents. The compounds can be manufactured in a manner knowfr in the art according to the processes described in the aforementioned patent application or in a manner analogous to these processes. It has now surprisingly been found that moxonidine and its physiologically compatible acid addition salts exert a beneficial effect, promoting recovery and/or rehabilitation, on the myocardial status following myocardial infarction and are therefore suitable for the treatment of myocardial damage secondary to myocardial infarction in man and larger mamma1s. A myocardial infarction is generally understood to mean necrosis of a circumscribed area of heart muscle due to persisting complete interruption or critical reduction of blood supply to this area. In addition to general therapeutic measures (analgesia and sedation, oxygen administration, bed rest and diet) the management of acute myocardial infarction comprises especially thrombolytic or fibrinolytic therapy with the aim of preserving as much (primary) ischaemic myocardium as possible from final cell death (e.g. definitive necrosis) by reperfusing the ischaemic area and thereby restricting the infarct size to the smallest possible area. Further (supportive) measures can contribute to improving myocardial status, especially in the region of the infarct area, both in the acute phase of myocardial infarction and in the postmyocardial infarction phase. The compounds used according to the invention for the treatment of myocardial damage secondary to myocardial infarction are suitable for general use in the management of myocardial infarction. They can therefore already be used for the treatment of acute myocardial infarction and especially for postmyocardial infarction management both in patients who have already received fibrinolytic treatment and in patients without such lysis. In postinfarction patients with lysis, treatment with the compounds used according to the invention in particular also has the effect of preventing the development of cardiac insufficiency of myocardial origin (myocardial heart failure). This also applies to those patients who have already been treated with p-adrenoceptor blocking drugs. fostinfarction patients who have not undergone lysis pass into the chronic phase of myocardial infarction. For postinfarction patients in the chronic stage, the important role played by the sympathetic nervous system (SNS) in cardiovascular regulation is of particular significance. For example, sympathetic stimulation is the primary mechanism for increasing cardiac output, since this stimulation causes an increase both in myocardial contractility and heart rate. Acute myocardial infarction results, among other things, in activation of the SNS to maintain perfusion pressure and tissue perfusion. This acute situation can develop into a more chronic phase in which the sympathetic activation contributes to hypertrophy and remodelling processes in the non-infarcted myocardium. This process, however, can progress beyond the desired degree and the continued SNS activation may become harmful for various reasons: 1) Chronic activation of the central sympathetic nervous system is to be regarded as unfavourable as regards the progression of heart failure. Persisting adrenergic stimulation results in a compensatory reduction of adrenergic receptors in the heart. The consequence of this protective mechanism of the heart against persistently elevated catecholamine levels, however, is significant impairment of the regulation of heart rate and the force of myocardial contraction via the autonomic nervous system. 2) The SNS stimulation increases vascular tone and consequently the afterload of the heart. 3) Increased circulating catecholamine levels induce focal necrosis in the heart and contribute to the development of cardiac hypertrophy. 4) Elevated plasma catecholamine levels contribute to the unfavourable increase of the heart rate and to the development of sometimes life-threatening cardiac arrhythmias. The prevention and abolition of excessive sympathetic activation can therefore represent a desirable strategy for the management of myocardial infarction patients, especially also with the aim of preventing the progression of heart failure after myocardial infarction. It has now surprisingly been found that moxonidine used according to the invention for myocardial infarction and/or postmyocardial infarction management is distinguished by a surprising beneficial influence, promoting recovery and/or rehabilitation, on the functional status of the myocardium of myocardial infarction patients, especially of postmyocardial infarction patients in the chronic stage. Administration of moxonidine after myocardial infarction causes a reduction of cardiac weight and a reduction of sympathetic activation, as demonstrated by measurement of plasma noradrenaline levels. Moxonidine is therefore suitable for the reduction of excessive cardiac hypertrophy, especially in later phases of postmyocardial infarction treatment. Furthermore, moxonidine decreases plasma noradrenaline levels, allowing sympathetic activation after myocardial infarction to be effectively normalised. For the treatment of myocardial damage secondary to myocardial infarction according to the invention, moxonidine and its physiologically compatible acid addition salts can be administered orally, intravenously or transdermally in conventional pharmaceutical preparations. For example, moxonidine and its physiologically compatible acid addition salts may be included, in an amount effective in promoting recovery and/or rehabilitation of myocardial status, with conventional pharmaceutical auxiliaries and/or vehicles in solid or liquid pharmaceutical preparations. Examples of solid formulations, which can be formulated for immediate or sustained release of the active ingredient, are preparations suitable for oral administration such as tablets, coated tablets, capsules, powders or granules, but also suppositories and patches (transdermal therapeutic systems). These solid formulations may contain conventional pharmaceutical inorganic and/or organic vehicles such as lactose, talc or starch as well as conventional pharmaceutical auxiliaries such as lubricants or tablet disintegrants. In the case of patches the active ingredient is placed in an active ingredient reservoir, in particular e.g. in an active ingredient matrix (e.g. a polymeric matrix). Liquid preparations such as solutions, suspensions or emulsions of the active ingredients can contain the usual diluents such as water, oils and/or suspending agents such as polyethylene glycols and the like. Further auxiliaries may also be added, such as preservatives, flavouring agents and the like. The active ingredients can be mixed and formulated with the pharmaceutical auxiliaries and/or vehicles in a manner known to the art. To manufacture solid dosage forms, the active ingredients may for example be mixed with the auxiliaries and/or vehicles in the usual manner and be wet or dry granulated. The granules or powder can be filled directly into capsules or compressed into tablet cores in the usual manner. If desired, these cores can be coated in the manner known to the art. Patches or transdermal therapeutic systems can be composed in the conventional manner, e.g. of cover layer, active ingredient reservoir (self-adhesive or with additional adhesive layer) and strip-off layer, as matrix-controlled systems as well as membrane-controlled systems (e.g. equipped with additional control membrane). Description of tests and results The beneficial actions of moxonidine in the management of myocardial infarction and especially postmyocardial infarction can be demonstrated in standard tests for the determination of pharmacological indicators of the effect of substances on factors that influence the functional status of the myocardium after myocardial infarction. A suitable animal model for demonstrating effects on factors that influence the functional status of the myocardium especially in the chronic stage of myocardial infarction are, for example, Wistar rats with chronic myocardial infarction (MI) . In this animal model (MI rats) it was found that plasma noradrenaline levels increase acutely after myocardial infarction. In the advanced stages of heart failure the plasma noradrenaline level can increase further. Close observation of the MI rats revealed that even three weeks after the infarction, i.e. after the "healing period", heart rate (measured in vivo on unconfined, conscious rats) appeared to be elevated, while the remaining plasma noradrenaline level was still about 50% higher than in sham rats (see below: sham-operated rats without ligation of the coronary artery). The central nervous system of these animals was also found to have increased metabolic activity in the paraventricular hypothalamus and the locus coeruleus, in which the sympathetic effects on the peripheral vessels are regulated. Behavioural studies showed increased anxiety levels in infarct rats. These observations therefore show that chronically elevated sympathetic activation was present in this infarct rat model. Experimental animals and dosage: The following studies were performed on male Wistar rats (270 to 320 q, Harlan Zeist, Netherlands). The rats were kept in rooms with a 12 h light/dark cycle and had free access to standard rat diet and water. The animals underwent coronary artery ligation (MI rats) or sham operation without ligation (sham rats). After 24 hours the MI rats were randomised and implanted with osmotic minipumps (Alzet, Model 2001) in order to administer moxonidine in a dose of 3 or 6 mg/kg-day s.c. (subcutaneously) or only vehicle. The moxonidine treatment was continued up to the end of the experiment three weeks after the surgical procedure. Coronary artery ligation: The left anterior descending coronary artery was ligated under pentobarbital anaesthesia (60 mg/kg, i.p.). Brief description: after intubation of the trachea, an incision was made in the skin over the 4th intercostal space. The overlying muscles were separated and kept aside. The animals were then placed on positive pressure ventilation (rate 65 to 70/min, stroke volume 3 ml) and the thoracic cavity was opened by cutting the intercostal muscles. The pericardium was opened. The heart was left in situ and a 6-0 silk suture was placed below the left coronary artery close to the origin of the pulmonary artery. The suture was tightened. Sham rats were subjected to the same procedure but without actual ligation. The ribs were pulled together with 3-0 silk suture. The muscles were then returned to their original position and the skin was sutured. Preparation and collection of blood samples: 19 days after the surgical procedure for coronary artery ligation the rats were again anaesthetised with pentobarbital and a catheter (PE-10, heat-sealed with PE-50) was introduced through the femoral artery and placed in the abdominal aorta. The catheter was advanced subcutaneously as far as the animal's neck, where it was allowed to exit and was fixed and closed at the exit site. The rats were allowed a 2-day recovery period. On the day of sampling the catheter was lengthened with a heparin-treated, saline-filled tube and two 1-ml blood samples were collected after at least 60 minutes. The blood was collected in pre-cooled sample pots (syringes) prepared with 10 ul EDTA (0.1M). After centrifugation the plasma was collected in pre-cooled tubes containing either 1.2 mg glutathione or 10 ul aprotinin (100 KIU; KIU = kilo international units) in order to determine either catecholamines or atrial natriuretic factor (ANF). The tubes were stored at -80 °C. The plasma concentrations of noradrenaline, adrenaline and dopamine were determined by HPLC, whereas the concentrations of ANF were analysed using an RIA test. Measurement of cardiac collagen: The quantity of interstitial collagen was determined on 6 to 7 hearts randomly selected from each experimental group. For this purpose the hearts were fixed by perfusion with 3.6% by weight phosphate-buffered formaldehyde. After removal of the atria and large vessels, the ventricles were cut into four slices from the apex to the base of the heart and the slices were kept for at least 24 hours in formaldehyde. After fixation the slices were dehydrated and embedded in paraffin. Deparaffinised 5 µm sections were incubated for 5 min with 0.2% by weight/vol. aqueous phosphomolybdic acid, and then for 45 min with 0.1% by weight Sirius red F3BA (Polysciences Inc., Northampton, UK) in saturated picric acid, then washed for 2 min with 0.01 M hydrochloric acid, dehydrated and embedded in Entellan (Merck, Darmstadt, Germany) for microscopic analysis. Interstitial collagen was determined, distant from the infarct site, in the interventricular septum of each heart as a Sirius red positive area at 40-fold magnification. Data analysis: The data obtained were expressed as group means ± SEM (standard error of the mean) unless otherwise stated. Only data of infarcted hearts with an infarct area covering the major portion of the free heart wall of the left ventricle were included in the evaluation since smaller infarct areas are usually fully compensated haemodynamically. The data were analysed by one-way analysis of variance (ANOVA) followed by post-hoc Bonferroni analysis. Differences in the structural parameters of the vessels in moxonidine-treated and untreated infarcted hearts were determined by Student t-test independently for the two groups. Results: Four groups of rats were studied: 2 groups of moxonidine-treated infarct rats (dosage 3 and 6 mg/kg-day), untreated infarct rats and sham-operated control rats (SHAM rats). Coronary artery ligation produced a main infarction in the free wall of the left ventricle. Total mortality of the experimental animals was 29% and was the same in both infarct groups. Data of five rats of the 6 mg/kg-day group had to be excluded since their infarct area was too small. The results of the tests are summarised in Table 1 for experiments with a dosage of 6 mg/kg-day and for a dosage of 3 mg/kg-day, and are explained in the following. The results shown in Table 1 comprise the data of groups of 7 to 14 rats with the exception of the collagen measurements, for which the data refer to groups of 6 to 7 rats. Although the body weight of the test animals was similar at the beginning of the tests, moxonidine-treated infarct rats had a slightly lower body weight than the untreated infarct rats, but a significantly lower body weight than the sham rats. The cardiac weight of the moxonidine-treated infarct rats was significantly lower than the cardiac weight of untreated infarct rats. These effects were dosage-dependent in the range from approximately 3 to 6 mg/kg-day (see Table 1). It can be concluded from the data that excessive cardiac hypertrophy was prevented by moxonidine administration. Neurohumoral activity measured on the basis of plasma noradrenaline and ANF levels was significantly elevated in untreated infarct rats. Plasma ANF levels of moxonidine treated rats were unchanged compared to those of untreated infarct rats. Plasma noradrenaline levels were reduced by moxonidine treatment to about half the value found for the sham rats. The plasma noradrenaline levels measured were found to be significantly increased in untreated infarct rats/ reaching up to three times the value of the sham rats. Plasma noradrenaline levels were reduced by treating infarct rats with moxonidine in the 6 mg/kg-day group to almost half the values of the sham rats. In the 3 mg/kg-day group the plasma noradrenaline levels were clearly reduced. This shows that the dose of 3 or 6 mg moxonidine/kg daily can effectively reduce sympathetic activation after myocardial infarction in rats . The results of the measurement of the cardiac collagen are also evident from Table 1 for the 3 and 6 mg/kg-day groups. Heart rate measured in conscious animals was markedly increased in infarct rats compared to sham rats. This tachycardia was not only prevented by moxonidine administration, but the treated infarct rats even showed a slowing of cardiac activity (bradycardia) compared to the sham rats. Table 1: Test results for sham-operated control animals (SHAM), untreated infarct rats (INFARCT) and moxonidine-treated infarct rats (INF + MOX); dose 3 mg/kg daily and dose 6 mg/kg daily (Table Removed) Abbreviations: MAP = mean arterial pressure; NA = noradrenaline; ANF = atrial natriuretic factor * = significantly different from sham rats # = significantly different from untreated infarct rats These experimental results clearly suggest that the functional status of the myocardium can be beneficially influenced by the administration of moxonidine in the context of myocardial infarction treatment and especially postmyocardial infarction treatment. From the measured plasma catecholamine levels it can be concluded that moxonidine can effectively normalise sympathetic activation in infarct rats. This result is confirmed by the heart rate data (in vivo, on conscious rats) since heart rate in moxonidine-treated rats was even below the levels found for sham rats. This is presumably due more to a chronic than an acute effect of moxonidine, since in acute treatment the reduced heart rate is accompanied by a rise in mean arterial blood pressure not observed during chronic treatment. As regards the effect of moxonidine [words missing] complex. Although the positive effects observed on the cardiac weight/body weight ratio (hypertrophy) appear not to be significant and the measurement of interstitial collagen suggests at most a minor remodelling effect, these results do reveal a recognisable trend towards a preventive effect of moxonidine against excessive cardiac hypertrophy and undesired remodelling. The above experimental results therefore show that moxonidine and its acid addition salts exert a beneficial influence, promoting recovery and/or rehabilitation, on myocardial status after myocardial infarction and are therefore suitable for the treatment of myocardial damage secondary to myocardial infarction in humans and larger mammals, both in the management of acute myocardial infarction and especially also postmyocardial infarction management. Particularly in postmyocardial infarction management, moxonidine can also have a preventive effect on the progression of heart failure after myocardial infarction. The dosages of moxonidine or its acid addition salts to be administered may differ between individuals and naturally vary depending on the type of condition to be treated and the form of administration. The daily dosages for myocardial infarction and postmyocardial infarction management in man are generally in the range from 0.05 to 5 mg, preferably about 0.25 to 3.0 mg on oral administration. Moxonidine or its acid addition salts can be administered in pharmaceutical preparations designed for immediate, prolonged, controlled and/or regulated active substance release. In this context it goes without saying for those skilled in the art that preparations for prolonged, controlled and/or regulated drug release may contain higher amounts of active substance than preparations for immediate active substance release. The following example is provided to illustrate the manufacture of a pharmaceutical preparation containing moxonidine suitable for myocardial infarction and/or postmyocardial infarction treatment, without however restricting the scope of the application. Example 1; Film-coated tablets containing moxonidine Composition: Cores: Moxonidine Lactose Povidone USP Crospovidone USP Magnesium stearate (Water Total solids 0.025 parts 9.575 parts 0.070 parts 0.300 parts 0.030 parts 0.750 parts) 10.000 parts Film coating: Hydroxypropylmethylcellulose 30% aqueous ethylcellulose dispersion (= solid) Polyethylene glycol 6000 Titanium dioxide Talc Red iron oxide 0.156 parts 0.480 parts (0.144) parts 0.030 parts 0.150 parts 0.1197 parts 0.0003 parts (Water 3.864 parts) Total solids 0.600 parts Total film-coating suspension 4.800 parts 4.8 kg of the above film coating suspension is used to coat 10,000 cores weighing 100 rug each. Production of cores: The moxonidine and lactose were mixed. The mixture was thoroughly moistened with a solution of the binder povidone in water, thoroughly kneaded and the resulting product was spread out on trays and dried at a temperature of about 50°C to a moisture content of not more than 0.5%. The dried product was passed through a 0.75 mm sieve (Frewitt machine). After mixing the resulting granules with Crospovidone and magnesium stearate, cores with a weight of 100 mg were compressed such that each core contained 0.25 mg active ingredient. Preparation of film-coating suspension: The hydroxypropylmethylcellulose and the polyethylene glycol 6000 were dissolved in part of the water. A suspension of talc, titanium dioxide and iron oxide in the remaining water was added to this solution whilst stirring. The resulting suspension was diluted with the 30% aqueous ethylcellulose dispersion with gentle stirring. Film coating of cores: The film coating suspension was sprayed onto the cores in a film coating apparatus while warm air at about 70 °C heated the cores to a temperature of about 45 °C. The film-coated tablets were then dried for 16 hours at a temperature of about 45 °C. WE CLAIM: 1. A process for the manufacture of a pharmaceutical preparation for the treatment of myocardial damage secondary to myocardial infarction which comprises-4-chloro-5-[(4,5-dihydro-1H-jmidazoIr2-yl)"amino]-6'-methoxy-2-methylpyrimidine of Formula I (Formula Removed) or a physiologically compatible acid addition salt thereof and a conventional pharmaceutical auxiliary, wherein a core is formed by mixing the compound of Formula I or a physiologically compatible acid addition salt thereof with an aqueous solution of povidone as a binder, drying the resultant mixture, mixing the resulting granules with further conventional pharmaceutical auxiliaries and compressing the mixture; as film-coating suspension is formed by mixing a conventional film-forming agent with water; the cores are heated; the film coating suspension is sprayed onto the cores; and the resultant film coated tablets are dried.

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