Topical amlodipine salts for the treatment of anorectal diseases

Abstract

Provided is a topical pharmaceutical gel composition of an amlodipine salt and methods for its use in the treatment of anorectal disease.

Claims

1. A stable topical pharmaceutical gel composition of amlodipine besylate comprising: about 0.01-1% w/w of amlodipine besylate, as measured as the free base, wherein said amlodipine besylate is present in a dissolved state in said gel, and wherein the degradation impurities of said amlodipine besylate is less than about 2.5% for a storage period of at least 24 months at a temperature of about 2-8° C.; about 5-75% w/w of at least one glycol solvent; about 0.1-10% w/w of hydroxyethyl cellulose; about 30-50% w/w of glycerin; about 5-15% w/w of ethanol; and about 15-35% w/w of water.

2. The stable topical pharmaceutical gel composition according to claim 1, wherein said at least one glycol solvent is chosen from propylene glycol, polyethylene glycol, ethylene glycol, butylene glycol, hexylene glycol, and mixtures thereof.

3. The stable topical pharmaceutical gel composition according to claim 2, wherein said glycol solvent is propylene glycol.

4. The stable topical pharmaceutical gel composition according to claim 1, wherein said amlodipine besylate is present at a concentration of 0.01-1% w/w as measured as the free base, wherein said at least one glycol solvent is propylene glycol and is present at a concentration of 5-75% w/w, wherein said hydroxyethyl cellulose is present at a concentration of 0.1-10% w/w, wherein said glycerin is present at a concentration of 30-50% w/w, wherein said ethanol is present at a concentration of 5-15% w/w, wherein said water is present at a concentration of 15-35% w/w, wherein said stable topical pharmaceutical gel composition further comprises methyl parahydroxybenzoate, and wherein said methyl parahydroxybenzoate is present at a concentration of 0.01-5% w/w.

5. The stable topical pharmaceutical gel composition according to claim 1, wherein said amlodipine besylate is present at a concentration of about 0.1-1% w/w, as measured as the free base.

6. The stable topical pharmaceutical gel composition according to claim 4, wherein the degradation impurities of said amlodipine besylate is less than 2.5% for a storage period of at least 24 months at a temperature of about 2-8° C.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) The novel features of the invention are set forth with particularity in the appended claims. A better understanding of the features and advantages of the present invention will be obtained by reference to the following detailed description that sets forth illustrative embodiments, in which the principles of the invention are utilized, and the accompanying drawings (also “FIGURE” and “FIG.” herein) of which:

(2) The FIGURE shows the mean±SD plasma level curves for amlodipine in female Göttingen minipigs on day 28 when administered orally (Oral) or topically as 0.2% topical pharmaceutical gel (Topical).

DESCRIPTION

(3) While preferred embodiments of the present invention have been shown and described herein, it will be obvious to those skilled in the art that such embodiments are provided by way of example only. Numerous variations, changes, and substitutions will now occur to those skilled in the art without departing from the invention. It should be understood that various alternatives to the embodiments of the invention described herein may be employed in practicing the invention. It is intended that the following claims define the scope of the invention and that methods and structures within the scope of these claims and their equivalents be covered thereby.

(4) In the following description, certain specific details are set forth in order to provide a thorough understanding of various embodiments. However, one skilled in the art will understand that the invention may be practiced without these details. In other instances, well-known structures have not been shown or described in detail to avoid unnecessarily obscuring descriptions of the embodiments. Unless the context requires otherwise, throughout the specification and claims which follow, the word “comprise” and variations thereof, such as, “comprises” and “comprising” are to be construed in an open, inclusive sense, that is, as “including, but not limited to.” Further, headings provided herein are for convenience only and do not interpret the scope or meaning of the claimed invention.

(5) Reference throughout this specification to “one embodiment” or “an embodiment” or “some embodiments” or “a certain embodiment” means that a particular feature, structure or characteristic described in connection with the embodiment is included in at least one embodiment. Thus, the appearances of the phrases “in one embodiment” or “in an embodiment” or “in some embodiments” or “in a certain embodiment” in various places throughout this specification are not necessarily all referring to the same embodiment. Furthermore, the particular features, structures, or characteristics may be combined in any suitable manner in one or more embodiments.

(6) Amlodipine is a dihydropyridine calcium antagonist that inhibits the transmembrane influx of calcium ions into vascular smooth muscle and cardiac muscle. Experimental data suggest that amlodipine binds to both dihydropyridine and nondihydropyridine binding sites. The contractile processes of cardiac muscle and vascular smooth muscle are dependent upon the movement of extracellular calcium ions into these cells through specific ion channels. Amlodipine inhibits calcium ion influx across cell membranes selectively, with a greater effect on vascular smooth muscle cells than on cardiac muscle cells. Negative inotropic effects can be detected in vitro but such effects have not been seen in intact animals at therapeutic doses. Serum calcium concentration is not affected by amlodipine. Within the physiologic pH range, amlodipine is an ionized compound (pKa=8.6), and its kinetic interaction with the calcium channel receptor is characterized by a gradual rate of association and dissociation with the receptor binding site, resulting in a gradual onset of effect.

(7) Amlodipine is a peripheral arterial vasodilator that acts directly on vascular smooth muscle to cause a reduction in peripheral vascular resistance and reduction in blood pressure.

(8) Following administration of therapeutic doses to patients with hypertension, amlodipine produces vasodilation resulting in a reduction of supine and standing blood pressures. These decreases in blood pressure are not accompanied by a significant change in heart rate or plasma catecholamine levels with chronic dosing. Although the acute intravenous administration of amlodipine decreases arterial blood pressure and increases heart rate in hemodynamic studies of patients with chronic stable angina, chronic oral administration of amlodipine in clinical trials did not lead to clinically significant changes in heart rate or blood pressures in normotensive patients with angina.

(9) With chronic once daily oral administration, antihypertensive effectiveness is maintained for at least 24 hours. Plasma concentrations correlate with effect in both young and elderly patients. The magnitude of reduction in blood pressure with amlodipine is also correlated with the height of pretreatment elevation; thus, individuals with moderate hypertension (diastolic pressure 105-114 mmHg) had about a 50% greater response than patients with mild hypertension (diastolic pressure 90-104 mmHg). Normotensive subjects experienced no clinically significant change in blood pressures (+1/−2 mmHg).

(10) Amlodipine does not change sinoatrial nodal function or atrioventricular conduction in intact animals or man. In patients with chronic stable angina, intravenous administration of 10 mg did not significantly alter A-H and H-V conduction and sinus node recovery time after pacing. Similar results were obtained in patients receiving amlodipine and concomitant beta-blockers. In clinical studies in which amlodipine was administered in combination with beta-blockers to patients with either hypertension or angina, no adverse effects on electrocardiographic parameters were observed. In clinical trials with angina patients alone, amlodipine therapy did not alter electrocardiographic intervals or produce higher degrees of AV blocks.

(11) After oral administration of therapeutic doses of amlodipine, absorption produces peak plasma concentrations between 6 and 12 hours. Absolute bioavailability has been estimated to be between 64 and 90%. The bioavailability of amlodipine is not altered by the presence of food.

(12) Amlodipine is extensively (about 90%) converted to inactive metabolites via hepatic metabolism with 10% of the parent compound and 60% of the metabolites excreted in the urine. Ex vivo studies have shown that approximately 93% of the circulating drug is bound to plasma proteins in hypertensive patients Elimination from the plasma is biphasic with a terminal elimination half-life of about 30-50 hours. Steady-state plasma levels of amlodipine are reached after 7 to 8 days of consecutive daily dosing.

(13) The pharmacokinetics of amlodipine are not significantly influenced by renal impairment. Patients with renal failure may therefore receive the usual initial dose.

(14) Elderly patients and patients with hepatic insufficiency have decreased clearance of amlodipine with a resulting increase in AUC of approximately 40-60%, and a lower initial dose may be required. A similar increase in AUC was observed in patients with moderate to severe heart failure

(15) Amlodipine is indicated for the treatment of hypertension to lower blood pressure, symptomatic treatment of chronic stable angina, confirmed or suspected vasospastic angina and to reduce the risk of hospitalization for angina and to reduce the risk of a coronary revascularization procedure.

(16) The usual initial antihypertensive oral dose of Amlodipine is 5 mg once daily, and the maximum dose is 10 mg once daily. The recommended dose for chronic stable or vasospastic angina is 5-10 mg, with the lower dose suggested in the elderly and in patients with hepatic insufficiency. Most patients will require 10 mg for adequate effect. The effective antihypertensive oral dose in pediatric patients ages 6-17 years is 2.5 mg to 5 mg once daily. Doses in excess of 5 mg daily have not been studied in pediatric patients.

(17) As used herein, “amlodipine salt” refers to an acid addition salt of amlodipine. Acid addition salts may be prepared by methods well known in the art, and may be formed from organic and inorganic acids. Suitable acids include 1-hydroxy-2-naphthoic acid, 2,2-dichloroacetic acid, 2-hydroxyethanesulfonic acid, 2-oxoglutaric acid, 4-acetamidobenzoic acid, 4-aminosalicylic acid, acetic acid, adipic acid, ascorbic acid (L), aspartic acid (L), benzenesulfonic acid, benzoic acid, camphoric acid (+), camphor-10-sulfonic acid (+), capric acid (decanoic acid), caproic acid (hexanoic acid), caprylic acid (octanoic acid), carbonic acid, cinnamic acid, citric acid, cyclamic acid, dodecylsulfuric acid, ethane-1,2-disulfonic acid, ethanesulfonic acid, formic acid, fumaric acid, galactaric acid, gentisic acid, glucoheptonic acid (D), gluconic acid (D), glucuronic acid (D), glutamic acid, glutaric acid, glycerophosphoric acid, glycolic acid, hippuric acid, hydrobromic acid, hydrochloric acid, isobutyric acid, lactic acid (DL), lactobionic acid, lauric acid, maleic acid, malic acid (−L), malonic acid, mandelic acid (DL), methanesulfonic acid, naphthalene-1,5-disulfonic acid, naphthalene-2-sulfonic acid, nicotinic acid, nitric acid, oleic acid, oxalic acid, palmitic acid, pamoic acid, phosphoric acid, proprionic acid, pyroglutamic acid (−L), salicylic acid, sebacic acid, stearic acid, succinic acid, sulfuric acid, tartaric acid (+L), thiocyanic acid, toluenesulfonic acid (p), and undecylenic acid.

(18) Also, as used in this specification and the appended claims, the singular forms “a,” “an,” and “the” include plural referents unless the content clearly dictates otherwise.

(19) As used herein, “amlodipine besylate” may be referred to as 3-ethyl-5-methyl (±)-2-[(2-aminoethoxy)methyl]-4-(2-chlorophenyl)-1,4-dihydro-6-methyl-3,5-pyridinedicarboxylate, monobenzenesulphonate. Its empirical formula is C.sub.20H.sub.25CIN.sub.2O.sub.5.C.sub.6H.sub.6O.sub.3S, and its structural formula is:

(20) ##STR00001##

(21) Amlodipine besylate is a white crystalline powder with a molecular weight of 567.1. It is slightly soluble in water and sparingly soluble in ethanol. Amlodipine besylate tablets are formulated as white tablets equivalent to 2.5, 5, and 10 mg of amlodipine for oral administration. In addition to the active ingredient, amlodipine besylate, each tablet contains the following inactive ingredients: microcrystalline cellulose, dibasic calcium phosphate anhydrous, sodium starch glycolate, and magnesium stearate. Amlodipine besylate is instable in aqueous solution. Various attempts were made in order to develop orally available liquid formulations (M. Friciu et. al. CJHP, 2016, 69(4), pp 327; I. Kasagić Vujanović, et. al., Contemporary Materials, 2014, V-2 (2014), pp 214; Z. Ž. Stoiljkovi□ et. al., Chem. Ind. Chem. Eng. Q., 2014, 20(2) pp 295; C. Milap et. al., Nahata, J Am Pharm Assoc., 1999, 39, pp 375; A. Abdoh et. al., Pharm. Dev. Tecnol., 2004, 9(1), pp. 15), however stable liquid based formulations have not been developed to date.

(22) There has been work done on the development of transdermal systems for calcium channel antagonists (Zeng, et al., Drug Development and Industrial Pharmacy, 2010, 36(6), pp 724; Y. Jiang, et al., Pharmazie, 2008, 63, pp 356; Patel, et al., Asian Journal of Pharmaceutical and Clinical Research, 2010, 3(1), pp 31). McDaid et. al. (International Journal of Pharmaceutics, 1996, 133, pp 71) investigated the topical absorption of amlodipine besylate and confirmed that the compound was too hydrophilic for adequate transdermal delivery using a convenient area of device, despite the use of penetration enhancers and increase in the thermodynamic gradient across various rate-controlling membranes by ethanol. Permeation of amlodipine from a range of hydrophilic and hydrophobic bases through hairless mouse skin was studied and the influence of the penetration enhancers, sodium lauryl sulphate 1% and propylene glycol 20% in a sodium carboxymethylcellulose 3% gel base was examined. In vivo studies using rabbits were performed to assess the suitability of a reservoir-type device. Employing data obtained from in vitro studies involving human abdominal skin, it was possible to predict the plasma profile resulting from the application of a similar device onto human skin over a period of 1 week and was found to be inadequate for clinical use. No adverse local effects in the animal model arising from the application of the transdermal device were observed. The therapeutic plasma level of amlodipine was in the range 3-10 ng/ml. The average absorption rate of 1.24 μg/cm.sup.2 per h would result in a daily dose of 0.59 mg amlodipine being delivered using an exposure area of 20 cm.sup.2. This dosage falls short of the desired level of ˜3.2 mg. Both application sites in rabbits were examined visually for signs of local irritation after wearing the device for 3 days. No local irritation was observed at either application site, confirming that the device was well tolerated on dermal application even after several days of wear. These results are not surprising as the Ca.sup.2+ antagonists inhibition activity in acute and chronic models of inflammation in a dose-dependent manner is widely known.

(23) The subject invention is based on the discovery that anorectal diseases can be treated by topical formulations comprising a calcium channel blocker, such as amlodipine salts. Moreover, this treatment can be directed to the site of application and immediate surrounding area without a significant similar systemic effect.

(24) Provided is a topical pharmaceutical gel composition comprising an amlodipine salt and a carrier.

(25) In one aspect, the topical pharmaceutical gel compositions comprise an amlodipine salt and a carrier, with an amlodipine salt present at a concentration chosen from about 1% w/w, about 0.5% w/w, about 0.2% w/w, about 0.1% w/w, about 0.05% w/w and 0.01% w/w, as measured as the free base.

(26) In an embodiment, the carrier comprises at least one glycol solvent, at least one gelling agent, and at least one diluent.

(27) In an embodiment, the carrier further comprises one or more components chosen from preservatives and antioxidants.

(28) In an embodiment, the carrier comprises one or more components chosen from hydroxyethyl cellulose, methyl parahydroxybenzoate, ethanol, water, propylene glycol, and glycerin.

(29) Also provided is a topical pharmaceutical gel composition of an amlodipine salt comprising:

(30) about 0.01-1% w/w of an amlodipine salt, as measured as the free base;

(31) about 5-75 w/w of at least one glycol solvent;

(32) about 0.1-10% w/w of at least one gelling agent; and

(33) about 0.001-5 w/w of at least one preservative.

(34) Also provided is a topical pharmaceutical gel composition of an amlodipine salt comprising:

(35) about 0.01-1% w/w of an amlodipine salt, as measured as the free base;

(36) about 5-75 w/w of at least one glycol solvent;

(37) about 0.1-10% w/w of at least one gelling agent;

(38) about 0.001-5% w/w of at least one preservative; and

(39) at least one diluent.

(40) In an embodiment, the amlodipine salt is chosen from amlodipine besylate, amlodipine maleate, amlodipine mesylate, amlodipine adipate, amlodipine camsylate and amlodipine nicotinate. In an embodiment, the amlodipine salt is chosen from amlodipine besylate, amlodipine maleate, and amlodipine mesylate. In an embodiment, the amlodipine salt is amlodipine besylate.

(41) In an embodiment, the amlodipine salt is present at a concentration chosen from about 0.01% w/w to about 1% w/w, as measured as the free base. In an embodiment, the amlodipine salt is present at a concentration chosen from about 1% w/w, about 0.5% w/w, about 0.2% w/w, about 0.1% w/w, about 0.05% w/w and 0.01% w/w, as measured as the free base.

(42) In an embodiment, the at least one glycol solvent is chosen from propylene glycol, polyethylene glycol, ethylene glycol, butylene glycol, hexalylene glycol, and mixtures thereof.

(43) In an embodiment, the glycol solvent is polyethylene glycol.

(44) In an embodiment, the at least one glycol solvent is present in an amount of about 5-75% w/w. In an embodiment, the at least one glycol solvent is present in an amount of about 5-50% w/w. In an embodiment, the at least one glycol solvent is present in an amount of about 10-40% w/w. In an embodiment, the at least one glycol solvent is present in an amount of about 15-30% w/w, such as about 20-30% w/w, for example about 25% w/w.

(45) In an embodiment, the at least one gelling agent is chosen from carbomers, xanthan gum, acacia, tragacanth, sodium alginate, gelatin, modified starches, hydroxypropyl cellulose, hydroxyethyl cellulose, hydroxypropyl methylcellulose, carboxymethyl cellulose, carboxymethyl cellulose sodium, hydroxypropyl methylcellulose phthalate, methyl cellulose, co-polymers formed between maleic anhydride and methyl vinyl ether, methacrylate derivatives, polyethylene oxides, polyoxyethylene-polyoxypropylene copolymers, polyvinyl alcohol and mixtures thereof.

(46) In an embodiment, the at least one gelling agent is chosen from carbomers, xanthan gum, acacia, tragacanth, sodium alginate, gelatin, modified starches, hydroxypropyl cellulose, hydroxyethyl cellulose, hydroxypropyl methylcellulose, hydroxypropyl methylcellulose phthalate, methyl cellulose, carboxymethyl cellulose, co-polymers formed between maleic anhydride and methyl vinyl ether, methacrylate derivatives, polyethylene oxides, polyoxyethylene-polyoxypropylene copolymers, polyvinyl alcohol and mixtures thereof.

(47) In an embodiment, the gelling agent is hydroxyethyl cellulose.

(48) In an embodiment, the at least one gelling agent is present in an amount of about 0.1-10% w/w. In an embodiment, the at least one gelling agent is present in an amount of about 0.1-5% w/w. In an embodiment, the at least one gelling agent is present in an amount of about 1-% w/w. In an embodiment, the at least one gelling agent is present in an amount of about 1-4% w/w. In an embodiment, the at least one gelling agent is present in an amount of about 1, about 2, about 3, or about 4% w/w.

(49) In an embodiment, the at least one preservative is chosen from methyl paraben, propyl paraben, chlorocresol, thomersal, sorbic acid, potassium sorbate, methyl parahydroxybenzoate and mixtures thereof.

(50) In an embodiment, the preservative is methyl parahydroxybenzoate.

(51) In an embodiment, the preservative is present in an amount of about 0.001-5% w/w. In an embodiment, the preservative is present in an amount of about 0.001-1% w/w. In an embodiment, the preservative is present in an amount of about 0.001-0.005% w/w, such as about 0.001, about 0.002, about 0.003, about 0.004, or about 0.005% w/w.

(52) In an embodiment, the topical pharmaceutical gel composition further comprises at least one diluent.

(53) In an embodiment, the at least one diluent is chosen from ethanol, propanol, 2-propanol, water, glycerin, and mixtures thereof.

(54) In an embodiment, the at least one diluent comprises about 5-75% w/w of glycerin, such as about 5-70% w/w, about 5-65% w/w, about 5-60% w/w, about 5-55% w/w, about 5-50% w/w, about 5-45% % w/w, or about 4-40% w/w.

(55) In an embodiment, the at least one diluent comprises about 1-20% w/w of ethanol, such as about 1-15% w/w or about 5-15% w/w, for example, about 5, about 6, about 7, about 8, about 9, about 10, about 11, about 12, about 13, about 14, or about 15% w/w.

(56) In an embodiment, the at least one diluent comprises about 10-40% w/w of water, such as about 10-35% w/w or 15-30% w/w, for example, about 15, about 16, about 17, about 18, about 19, about 20, about 21, about 22, about 23, about 24, about 25, about 26, about 27, about 28, about 29, or about 30% w/w.

(57) In an embodiment, the at least one diluent is a mixture of glycerin, ethanol, and water. In an embodiment, the at least one diluent is a mixture of about 5-75% w/w of glycerin; about 1-20% w/w of ethanol; and about 10-40% w/w of water. In an embodiment, the at least one diluent is a mixture of about 30-50% w/w of glycerin, about 5-15% w/w of ethanol, and about 15-35% w/w of water. In an embodiment, the at least one diluent is a mixture of about 20-30% w/w of glycerin, about 5-15% w/w of ethanol, and about 15-35% w/w of water. In an embodiment, the at least one diluent is a mixture of about 40% w/w of glycerin, about 9-10% w/w of ethanol, and about 20-25% w/w of water.

(58) In an embodiment, the topical gel composition further comprises a local anesthetic such as lidocaine or anti-inflammatory agent such as COX, COX-1 or COX-2 inhibitors or their mixtures.

(59) In an embodiment, the topical gel composition further may comprise at least one or more additional ingredients or excipients selected from antioxidants, alkalizers or alkalizing agents, buffering agents, moisturizing agents, humectants, surfactants, neutralizing agents, chelating agents, and emollients. In an embodiment, the topical gel composition further may comprise at least one or more additional ingredients or excipients selected from buffering agents, moisturizing agents, humectants, surfactants, neutralizing agents, chelating agents, and emollients.

(60) In an embodiment, the topical pharmaceutical gel composition further comprises at least one antioxidant. In an embodiment, the at least one antioxidant is chosen from edetate disodium, sodium sulphite, sodium metabisulfite, propyl gallate, edetate trisodium, tocopherol derivatives, butylated hydroxyl toluene, butylated hydroxyl anisole, ascorbic acid, fumaric acid, malic acid, citric acid, and mixtures thereof.

(61) In an embodiment, the at least one antioxidant is present in an amount equal to or less than 5% w/w. In an embodiment, the pharmaceutical gel composition does not include at least one antioxidant.

(62) In an embodiment, the topical pharmaceutical gel composition further comprises at least one alkalizer or alkanizing agent.

(63) In an embodiment, the at least one alkalizer or alkanizing agent include organic and inorganic basic compounds. Examples of inorganic basic salts include ammonium hydroxide, alkali metal salts, and alkaline earth metal salts such as magnesium oxide, magnesium hydroxide, calcium hydroxide, sodium hydroxide, potassium hydroxide, lithium hydroxide, aluminum hydroxide, potassium carbonate, sodium bicarbonate and combinations thereof.

(64) In an embodiment, the alkalizer or alkanizing agent is aqueous sodium hydroxide solution.

(65) In an embodiment, the topical pharmaceutical gel compositions further comprise or are co-administered with steroids such as prednisolone, busenonide or hydrocortisone, anesthetics such as acetylsalicylic acid, locally acting lignocaine, and soothants.

(66) In an embodiment, the topical pharmaceutical gel compositions further comprise typical components used in existing fissure or hemorrhoidal treatment, such as zinc oxide, benzyl benzoate, bismuth oxide, bismuth subgallate or Peru balsam.

(67) In one aspect, the topical pharmaceutical gel composition comprises an amlodipine salt, hydroxyethyl cellulose, methyl parahydroxybenzoate, ethanol, water, propylene glycol, and glycerin with the amlodipine salt present at a concentration chosen from about 1 w/w, about 0.5% w/w, about 0.2% w/w, about 0.1% w/w, about 0.05% w/w and 0.01% w/w, as measured as the free base.

(68) In one aspect, the topical pharmaceutical gel composition consists essentially of amlodipine salt, hydroxyethyl cellulose, methyl parahydroxybenzoate, ethanol, water, propylene glycol, and glycerin with the amlodipine salt present at a concentration chosen from about 1% w/w, about 0.5% w/w, about 0.2% w/w, about 0.1% w/w, about 0.05% w/w and 0.01% w/w, as measured as the free base.

(69) Also provided is a topical pharmaceutical gel composition of an amlodipine salt comprising:

(70) about 0.01-1% w/w of an amlodipine salt, as measured as the free base;

(71) about 5-75 w/w of at least one glycol solvent;

(72) about 0.1-10% w/w of at least one gelling agent;

(73) about 0.001-5% w/w of at least one preservative;

(74) about 5-75% w/w of glycerin;

(75) about 1-20% w/w of ethanol; and

(76) about 10-40% w/w of water.

(77) Also provided is a topical pharmaceutical gel composition of an amlodipine salt comprising:

(78) about 0.01-1% w/w of an amlodipine besylate, as measured as the free base;

(79) about 5-75 w/w of at least one glycol solvent;

(80) about 0.1-10% w/w of at least one gelling agent;

(81) about 0.001-5% w/w of at least one preservative;

(82) about 5-75% w/w of glycerin;

(83) about 1-20% w/w of ethanol; and

(84) about 10-40% w/w of water.

(85) Also provided is a topical pharmaceutical gel composition of an amlodipine salt comprising:

(86) about 0.01-1% w/w of an amlodipine salt, as measured as the free base;

(87) about 5-75 w/w of propylene glycol;

(88) about 0.1-10% w/w of at least one gelling agent;

(89) about 5-75% w/w of glycerin;

(90) about 1-20% w/w of ethanol; and

(91) about 10-40% w/w of water.

(92) Also provided is a topical pharmaceutical gel composition of an amlodipine salt comprising:

(93) about 0.01-1% w/w of amlodipine besylate, as measured as the free base;

(94) about 5-75 w/w of propylene glycol;

(95) about 0.1-10% w/w of at least one gelling agent;

(96) about 5-75% w/w of glycerin;

(97) about 1-20% w/w of ethanol; and

(98) about 10-40% w/w of water.

(99) Also provided is a topical pharmaceutical gel composition of an amlodipine salt comprising:

(100) about 0.01-1% w/w of an amlodipine salt, as measured as the free base;

(101) about 5-75 w/w of propylene glycol;

(102) about 0.1-10% w/w of hydroxyethyl cellulose, carbomers, carboxymethyl cellulose, or a mixture thereof;

(103) about 0.01-5% w/w of methyl parahydroxybenzoate;

(104) about 5-75% w/w of a glycerin;

(105) about 1-20% w/w of ethanol; and

(106) about 10-40% w/w of water.

(107) Also provided is a topical pharmaceutical gel composition of an amlodipine salt comprising:

(108) about 0.01-1% w/w of an amlodipine besylate, as measured as the free base;

(109) about 5-75 w/w of propylene glycol;

(110) about 0.1-10% w/w of hydroxyethyl cellulose, carbomers, carboxymethyl cellulose, or a mixture thereof;

(111) about 0.01-5% w/w of methyl parahydroxybenzoate;

(112) about 5-75% w/w of a glycerin;

(113) about 1-20% w/w of ethanol; and

(114) about 10-40% w/w of water.

(115) Also provided is a topical pharmaceutical gel composition of an amlodipine salt comprising:

(116) about 0.01-1% w/w of an amlodipine salt, as measured as the free base;

(117) about 5-75 w/w of propylene glycol;

(118) about 0.1-10% w/w of hydroxyethyl cellulose;

(119) about 0.01-5% w/w of methyl parahydroxybenzoate;

(120) about 5-75% w/w of a glycerin;

(121) about 1-20% w/w of ethanol; and

(122) about 10-40% w/w of water.

(123) Also provided is a topical pharmaceutical gel composition of an amlodipine salt comprising:

(124) about 0.01-1% w/w of amlodipine besylate, as measured as the free base;

(125) about 5-75 w/w of propylene glycol;

(126) about 0.1-10% w/w of hydroxyethyl cellulose;

(127) about 0.01-5% w/w of methyl parahydroxybenzoate;

(128) about 5-75% w/w of glycerin;

(129) about 1-20% w/w of ethanol; and

(130) about 10-40% w/w of water.

(131) Also provided is a topical pharmaceutical gel composition of an amlodipine salt comprising:

(132) about 0.01-1% w/w of amlodipine salt, as measured as the free base;

(133) about 5-75 w/w of at least one glycol solvent;

(134) about 0.1-10% w/w of hydroxyethyl cellulose;

(135) about 5-75% w/w of glycerin;

(136) about 1-20% w/w of ethanol; and

(137) about 10-40% w/w of water.

(138) Also provided is a topical pharmaceutical gel composition of an amlodipine salt comprising:

(139) about 0.01-1% w/w of amlodipine besylate, as measured as the free base;

(140) about 5-75 w/w of at least one glycol solvent;

(141) about 0.1-10% w/w of hydroxyethyl cellulose;

(142) about 5-75% w/w of glycerin;

(143) about 1-20% w/w of ethanol; and

(144) about 10-40% w/w of water.

(145) In an embodiment, the topical pharmaceutical gel formulation of an amlodipine salt is storage stable at room temperature for a period of at least 24 months with 95-105% assay criterion limit.

(146) In an embodiment, the topical pharmaceutical gel formulation of an amlodipine salt is storage stable at a temperature of 2-8° C. for a period of at least 24 months with 95-105% assay criterion limit.

(147) In another aspect, degradation impurities (related substances) of an amlodipine salt in the topical pharmaceutical gel formulation is less than about 2.5% for a storage period of at least 24 months at room temperature.

(148) In another aspect, degradation impurities (related substances) of an amlodipine salt in the topical pharmaceutical gel formulation is less than about 2.5% for a storage period of at least 24 months at a temperature of about 2-8° C.

(149) In another aspect, relative bioavailability of topically applied amlodipine salt in the topical pharmaceutical gel formulation is less than 10% compared to oral administration. The topical administration of the pharmaceutical gel formulation for 28 days resulted in no local tolerance of histopathological findings.

(150) In an embodiment, the shear viscosity of the topical pharmaceutical gel composition is in the range of about 5 to 30 Pas measured at 10 s.sup.−1 shear rate by Kinexus Pro rheometer (Malvern Instruments Ltd.).

(151) In an embodiment, the pH of the topical pharmaceutical gel composition is in the range of about 4.0-8.0.

(152) In an embodiment, the density of the topical pharmaceutical gel composition is in the range of about 0.9-1.5 g/ml.

(153) In an embodiment, the topical pharmaceutical gel composition is formulated as ointments, creams, suspensions, lotions, powders, solutions, pastes, gels, sprays, foam, oils, aerosols, suppositories or enemas.

(154) In an embodiment, the topical pharmaceutical gel composition is applied to the affected areas of the skin to a patient suffering from anorectal diseases such as hemorrhoids, anal fissure and painful conditions after anorectal surgery.

(155) Disclosed herein are topical pharmaceutical gel compositions for use in treating anorectal diseases such as hemorrhoids, anal fissure (acute and chronic), painful conditions after anorectal surgery, perianal abscess, prolapsed thrombosed piles, perianal haematoma, cancer invading the sphincters (anorectal cancer), anal herpes, anal warts, anal itching, proctalgia fugax, constipation, anal bleeding and Crohn's disease or another inflammatory bowel disease related anorectal disorders.

(156) Also provided is a method for the treatment of an anorectal disease comprising topically applying a topical pharmaceutical gel composition of any one of claims 1 to 15 to a skin surface of a patient in need thereof.

(157) In an embodiment, the anorectal disease is chosen from hemorrhoids, anal fissure (acute and chronic), painful conditions after anorectal surgery, perianal abscess, prolapsed thrombosed piles, perianal haematoma, cancer invading the sphincters (anorectal cancer), anal herpes, anal warts, anal itching, proctalgia fugax, constipation, anal bleeding and Crohn's disease or another inflammatory bowel disease related anorectal disorders.

(158) Also disclosed herein is a method for the manufacture of topical gel formulation of an amlodipine salt. The method of manufacture comprises the following steps: stirring the at least one diluent, the at least one glycol solvent, the amlodipine salt, the at least one preservative and the at least one gelling agent to form a gel; and adding water up to the total weight/volume desired.

(159) In an embodiment, the method of manufacture comprises the following steps: mixing and homogenizing ethanol, glycol solvent and water; dissolving an amlodipine salt and preservative in ethanol, glycol solvent and water; adding the gelling agent to the dissolved solution; mixing and homogenizing the solution to obtain a gel; adding glycerin to the gel under continuous stirring; adding water up to the total weight/volume desired.

(160) In an embodiment, the method for the manufacture of a topical gel formulation of an amlodipine salt comprises the following steps: mixing and homogenizing ethanol, glycol solvent and water; dissolving an amlodipine salt and methyl parahydroxybenzoate in ethanol, glycol solvent and water; adding hydroxyethyl cellulose to the completely dissolved (b) solution; mixing and homogenizing the solution to obtain a gel; adding glycerin to the gel under continuous stirring; adding water up to the total weight/volume desired.

(161) The examples, which follow, are not intended to be limiting of the scope of the present invention but read in conjunction with the detailed and general description above, provide further understanding of the present invention and an outline of a process for preparing the compositions of the invention.

EXAMPLES

Example 1

(162) Preparation of Amlodipine Besylate Topical Pharmaceutical Gel Compositions Using Carbomer

(163) Amlodipine besylate topical pharmaceutical gel compositions were prepared using carbomer as gelling agent. Compositions of the prepared gels are summarized in Table 1.

(164) TABLE-US-00001 TABLE 1 Topical pharmaceutical gel compositions prepared using carbomer Sample No. #1 #2 #3 pH 7 6 5 Component Quantity (% w/w) Amlodipine besylate 0.100-0.200 0.100-0.200 0.100-0.200 Carbomer (980 NF or 1.000 1.010 0.950 971 or Ultrez 10) Ethanol 5.910 4.950 5.510-5.610 Methyl 0.002 0.002 0.002 parahydroxybenzoate Glycerin 5.000 5.060 4.760 Sodium hydroxide 0.410 0.270 0.120 Water 87.470-87.570 88.500-88.600 88.460 

(165) Process of example #1: 0.2-0.4 g amlodipine besylate was dissolved in 9.8 g ethanol. 87.8-87.6 g water was added to the solution and mixed well. 2 g Carbomer was added to the prepared solution and stirred well until completely dissolved. Separately, 0.828 g sodium hydroxide was dissolved in 107.2 g water and 2 mL 0.2% methyl parahydroxibenzoate ethanolic solution was added. The two solutions were mixed together to form gel. 10 g glycerol was added to the gel and homogenized well.

(166) Process of example #2: 0.2-0.4 g amlodipine-besylate was dissolved in 9.8 g ethanol. 87.8-87.6 g water was added to the solution and mixed well. 2 g Carbomer was added to the prepared solution and stirred well until completely dissolved. Separately, 0.540 g sodium hydroxide was dissolved in 107.5 g water and 2 mL 0.2% methyl parahydroxibenzoate ethanolic solution was added. The two solutions were mixed together to form gel. 10 g glycerol was added to the gel and homogenized well.

(167) Process of example #3: 0.2 g Carbomer was dissolved in 100 g water. 0.25 g sodium hydroxide was dissolved in 86 g water. The two solutions were mixed together to form gel. 2 mL 0.2% methyl parahydroxibenzoate ethanolic solution, 10 g glycerol and 9.9-10 g 2-4% amlodipine-besylate ethanolic solution were added to the gel and homogenized well.

Example 2

(168) Preparation of Amlodipine Besylate Topical Pharmaceutical Gel Compositions Using Carboxymethyl Cellulose

(169) Amlodipine besylate topical pharmaceutical gel compositions were prepared using carboxymethyl cellulose as gelling agent. Compositions of the prepared gels are summarized in Table 2.

(170) TABLE-US-00002 TABLE 2 Topical pharmaceutical gel compositions prepared using carboxymethyl cellulose Sample No. #4 pH 7 Component Quantity (% w/w) Amlodipine besylate  0.100-0.200 Carboxymethyl cellulose 2.090 Ethanol 6.150 Methyl parahydroxybenzoate 0.001 Glycerin 5.210 Water 86.3400-86.440

(171) Process of example #4: 0.1-0.2 g amlodipine-besylate was dissolved in 4.9 g ethanol and then 5 g 0.2% methyl parahydroxibenzoate ethanolic solution and 87.8-87.9 g water was added to the solution. 2 g carboxymethyl cellulose was added to the solution to form a gel. 5 g glycerol was homogenized in the gel.

Example 3

(172) Preparation of Amlodipine Besylate Topical Pharmaceutical Gel Compositions Using Hydroxyethyl Cellulose

(173) Amlodipine besylate topical pharmaceutical gel compositions were prepared using hydroxyethyl cellulose as gelling agent. Compositions of the prepared gels are summarized in Table 3.

(174) TABLE-US-00003 TABLE 3 Topical pharmaceutical gel compositions prepared using hydroxyethyl cellulose Sample No. #5 #6 #7 pH 7 7 7 Component Quantity (% w/w) Amlodipine besylate 0.10-0.20 0.14-0.28 0.14-0.28 Hydroxyethyl cellulose 2.00 2.00 2.00 Ethanol 5.91 10.86 9.60 Methyl 0.002 0.002 0.100 parahydroxybenzoate Glycerin 5.00 40.00 40.00 Propylene glycol 0 0 25.00 Water 86.89-86.99 46.86-47.00 23.02-23.16

(175) Process of example 5: 0.2-0.4 g amlodipine-besylate was dissolved in 9.8 g ethanol and then 2 g 0.2% methyl parahydroxybenzoate ethanolic solution and 173.6-173.8 g water was added to the solution. 4 g hydroxyethyl cellulose was added to the prepared solution and mixed well to form a gel. 10 g glycerol was homogenized in the gel.

(176) Process of example 6: 0.14-0.28 g amlodipine-besylate was dissolved in 9.86 g ethanol and then 1 g 0.2% methyl parahydroxybenzoate ethanolic solution and 46.95-47.00 g water was added to the solution. 2 g hydroxyethyl cellulose was added to the solution and mixed well to form a gel. 40 g glycerol was homogenized in the gel.

(177) Process of example 7: 9.6 g ethanol, 25 g propylene glycol and 23.02-23.16 g water was mixed well. 0.14-0.28 g amlodipine-besylate and 0.1 g methyl parahydroxybenzoate was dissolved in the solvent mixture. 2 g hydroxyethyl cellulose was added to the solvent mixture and mixed well to form a gel. 40 g glycerol was homogenized in the gel.

Example 4

(178) Preparation of Amlodipine Maleate and Amlodipine Mesylate Topical Pharmaceutical Gel Compositions Using Hydroxyethyl Cellulose

(179) Amlodipine maleate and amlodipine mesylate topical pharmaceutical gel compositions were prepared using hydroxyethyl cellulose as gelling agent. Compositions of the prepared gels are summarized in Table 4.

(180) TABLE-US-00004 TABLE 4 Topical pharmaceutical gel compositions prepared using hydroxyethyl cellulose but different amlodipine salts, not amlodipine besylate Sample No. #8 #9 pH 7 7 Component Quantity (% w/w) Amlodipine maleate 0.13-0.26 0 Amlodipine mesylate 0 0.12-0.25 Hydroxyethyl cellulose 2.00 2.00 Ethanol 9.60 9.60 Methyl parahydroxybenzoate 0.004 0.004 Glycerin 40.00 40.00 Propylene glycol 25.00 25.00 Water 23.14-23.27 23.15-23.27

(181) Process of example 8: 9.6 g ethanol, 25 g propylene glycol and 23.14-23.27 g water was mixed well. 0.13-0.26 g amlodipine-maleate and 0.004 g methyl parahydroxybenzoate was dissolved in the solvent mixture. 2 g hydroxyethyl cellulose was added to the solvent mixture and mixed well to form a gel. 40 g glycerol was homogenized in the gel.

(182) Process of example 9: 9.6 g ethanol, 25 g propylene glycol and 23.15-23.27 g water was mixed well. 0.12-0,258 g amlodipine-mesylate and 0.004 g methyl parahydroxybenzoate was dissolved in the solvent mixture. 2 g hydroxyethyl cellulose was added to the solvent mixture and mixed well to form a gel. 40 g glycerol was homogenized in the gel.

Example 5

(183) Amlodipine besylate topical pharmaceutical gel compositions prepared according to Example 1-4 were stored in a closed vial at RT and 4° C. in order to investigate the stability. At different time points related substances tests were performed by RP-HPLC method. Amlodipine besylate topical pharmaceutical gel compositions prepared using hydroxyethyl cellulose were more stable compared to the composition prepared using carbomer. Topical pharmaceutical gels of different amlodipine salts prepared using hydroxyethyl cellulose showed different decomposition profile after 1 month storage at 4° C. and RT. Only the amlodipine besylate gel prepared using hydroxyethyl cellulose had satisfying degradation profile in both storage conditions. (Table 5).

(184) TABLE-US-00005 TABLE 5 Amlodipine decomposition in different topical pharmaceutical gel compositions in time. Amlodipine besylate content of sample #1-5 is 0.1%. Amlodipine content of sample #6- 9 is 0.1%. Degradation after storage at 4° C. Degradation after storage at RT (%) (%) Sample 1 2 1 2 3 1 2 1 2 3 No. week weeks month months months week weeks month months months #1 — — 0.50 — 1.18 — — 2.07 — 5.22 #2 — — 0.21 — 1.71 — — 1.85 — 6.79 #3 0.53 — — — — 2.60 — — — — #4 — 0.14 — — — — 12.07 — — — #5 — — 0.19 0.38 — — — 0.46 0.98 — #6 — — 0.24 — — — — 0.31 — — #7 — — 0.19 — 0.32 — — 0.44 — 0.68 #8 — — 0.20 — — — — 0.93 — — #9 — — 0.28 — — — — 0.33 — —

Example 6

(185) In Vitro Permeability of Amlodipine Besylate Topical Pharmaceutical Gel Compositions

(186) In vitro permeability of amlodipine besylate, amlodipine mesylate and amlodipine maleate gels was investigated using dialysis measurement. The donor compartment contained 4000 mg topical pharmaceutical gel composition, while the receiver medium was phosphate buffer, pH 7.4 (100 ml). The measurement was performed at 37±0.5° C. The dialysis membrane was SnakeSkin Dialysis Tubing, 3.5K MWCO (35 mm dry I.D.). Amlodipine besylate topical pharmaceutical gel composition prepared using hydroxyethyl cellulose showed significantly higher in vitro permeability compared to the compositions prepared with different amlodipine salts or using carbomer as gelling agent. Amlodipine content of the receiver compartment was 1.7 times higher for the amlodipine besylate topical pharmaceutical gel compositions prepared using hydroxyethyl cellulose compared to other gels' (Table 6).

(187) TABLE-US-00006 TABLE 6 In vitro permeability of amlodipine besylate, amlodipine mesylate and amlodipine maleate gels Permeability of gel example #1 Permeability of gel example #7 t Dissolved API in receiver Dissolved API in receiver (min) compartment (%) compartment (%) 15 2.15 1.21 30 4.92 7.04 60 11.21 19.53 120 26.90 48.02 180 40.64 68.49 240 51.08 86.44 Permeability of gel example #8 Permeability of gel example #9 t Dissolved API in receiver Dissolved API in receiver (min) compartment (%) compartment (%) 15 0.77 0.54 30 3.25 2.75 60 10.19 9.35 120 29.29 28.78 180 42.00 40.47 240 56.11 52.64

Example 7

(188) 28-Day Dermal Tolerance Study Followed by an 8-Day Recovery Period in Minipigs Methods

(189) The purpose of this study was to obtain information on the dermal local tolerance and dermal irritation of the 0.2% w/w amlodipine topical pharmaceutical gel composition in minipigs administered twice daily topically (dermal) over a period of 28 days and to assess reversibility of any effect after an 8-day recovery period. In addition, the pharmacokinetic profile of the systemic exposure was investigated.

(190) Amlodipine gel or placebo was measured onto plastic spatulas and was homogenously smeared on the left and right treatment sites (treatment area: approx. 20 cm.sup.2). The application sites were non-occluded.

(191) Pharmacokinetic investigation: Approx. 3 mL blood was collected into plastic vials containing K3-EDTA as anticoagulant at the following time points after last treatment: 0 min, 1 h, 2 h, 4 h, 6 h, 8 h, 12 h, 16 h, 24 h, 36 h and 48 h after treatment (11 samples/animal). Amlodipine was quantified in minipig plasma using a reliable LC-MS/MS method developed in ATRC. Deuterated analogue of amlodipine (Amlodipine-d4) served as internal standard (IS). The plasma proteins were precipitated with methanol and the supernatant subjected to reverse phase chromatographic separation with gradient elution. Following electrospray ionization in positive mode the analyte was detected in MRM mode at the following transitions: Amlodipine: 409.10.fwdarw.238.15 m/z, IS: 413.10.fwdarw.238.15 m/z, Calibration range: 50 pg/mL-50 ng/mL, LLOQ: 50 pg/mL. Pharmacokinetic analysis was performed using a validated Phoenix WinNonlin® software version 6.3 (Pharsight Corporation, USA). The individual and mean plasma level versus time curves were evaluated using noncompartmental method. The results are shown in the FIGURE and Table 7. It was be concluded that 28-day repeated topical administration of 0.2% amlodipine gel resulted in very low total systemic exposure. At the end of the repeated administration all measured plasma concentrations remained below 300 pg/mL and both the average C.sub.max and AUC.sub.0-24 h values were around than 5% of those obtained after repeated oral administration at the same dose.

(192) TABLE-US-00007 TABLE 7 Pharmacokinetic parameters following oral administration of amlodipine tablets or topical administration of 0.2% topical pharmaceutical gel in female Göttingen minipigs. Animal No. #1 #2 #3 #4 Mean S.D. Oral, day 28, AUC 36.3495 46.079 62.522 55.6115 50.1405 11.4006 2 mg/day t.sub.max 4.0 4.0 6.0 4.0 4.5 1 C.sub.max 2.39 3.48 3.52 4.05 3.36 0.6969 Topical, day 28, AUC 0.918 3.9941 3.744 1.015 2.417775 1.6794 2 mg/day t.sub.max 36.0 0.0 4.0 4.0 4.0 16.7730 C.sub.max 0.0765 0.265 0.276 0.0683 0.17145 0.1145

(193) Viability, mortality and clinical signs: Viability, mortality and clinical signs were recorded three times daily (once before and twice after the first treatment) on the treatment days and twice on the treatment-free days. No mortality occurred during the course of the study. No clinical signs were observed related to the amlodipine gel during the study.

(194) Body weight: Measurement of body weight was performed twice during the acclimatization period and then on the treatment days before administration. There was no difference related to the test item in the body weight gain between the animals treated with placebo and amlodipine gel.

(195) Local tolerance: The treated skin area of the animals (on both side) was observed twice daily during treatment (before treatments) and recovery periods in order to evaluate the local tolerance with special regard to erythema, edema, inflammation, hypersensitivity, infection, biofilm formation, ischemia, necrosis, erysipelas and cellulitis. No local tolerance findings related to amlodipine gel or placebo were observed on the treatment sites during the entire study

(196) Necropsy: At the end of the recovery period (on study day 37). No amlodipine gel or placebo related macroscopic findings were observed in any animals during necropsy.

(197) Histopathology: Full histopathological examinations of samples from treatment sites from all animals. Treatment-related effects or toxicity was not seen following 28 days dermal exposition and 8 days recovery with placebo or amlodipine gel

(198) In conclusion the dermal tolerance study with twice daily topical (dermal) amlodipine gel at dose level of 2 mg/animal/treatment to minipigs over a period of 28 days resulted in no adverse effects. According to the results, the 2 mg/animal/treatment dose was well tolerated in all animals.

(199) From the foregoing description, one skilled in the art can easily ascertain the essential characteristics of this invention, and without departing from the spirit and scope thereof, can make various changes and modifications of the invention to adapt it to various usages and conditions.