Hemorrhoidal Compositions

The present invention relates to a method of treating the symptoms of hemorrhoids. More specifically, the invention relates to a method of treating the symptoms of hemorrhoids by the application of an anti-inflammatory, antipruritic, astringent composition to the affected area. All three pharmacologic effects are provided in a single composition which is capable of delivering the active ingredients in a biologically effective state to the external hemorrhoidal tissue.

Hemorrhoids or piles result from a varicose condition of the external hemorrhoidal veins which causes painful swellings at the anus. When the dilated veins form tumors to the outer side of the external sphincter, or are covered by the skin of the anal canal, the condition is called external hemorrhoids; when the swollen veins are beneath the mucous membrane within the sphincter it is called internal hemorrhoids. The condition is often accompanied by bleeding, itching, burning and soreness.

Current preparations generally used to treat hemorrhoid symptoms involve the use of ointments, creams and suppositories that provide traditional medicinal ingredients such as local anesthetics, vasoconstrictors, antiseptics and emollient protectants. Medicated pads are also employed but these provide only mild astringent and antiseptic actions.

Four types of drugs are currently used to alleviate hemorrhoid symptoms: anesthetics, astringents, anti-inflammatory agents and lubricant softeners. The anesthetic is used to relieve the pain and itching of hemorrhoids. The astringent is used to contract, or draw together, the swollen tissues while the antiseptic is used to prevent infection. The lubricant softener is added to the product base to make it a more nonirritating vehicle. These drugs are available in many dosage forms. For intrarectal use, suppositories, creams, ointments, gels and foams are used along with applicators. Creams, ointments, gels, pads, liquids and foams are used externally. Some of the available products used for treating hemorrhoid symptoms contain one or two of these drugs but none of the available formulations combines all four effects in a biologically available form. Part of the problem is due to the fact that the bioavailability of drugs from anorectal dosage forms is a result of complex interplay among physiochemical, physiological, manufacturing, dosage form, dosage and application variables. Absorption from anorectal dosage forms involves release of the drug from the vehicle, dissolution into the surrounding medium, diffusion to a membrane and penetration of the membranes. Steroids have been employed in anorectal dosage formulations but the bioavailability of the drug is limited by the relative insolubility of steroids.

One object of the present invention is to provide a method of treating the symptoms of hemorrhoids.

A further object of this invention is to provide an anorectal dosage form which offers the sufferer of external hemorrhoids biologically active anti-inflammatory, antipruritic and astringent pharmacologic activity to relieve the disease state and the symptoms.

Applicants' invention is based upon the discovery that hydrocortisone dissolves in a solvent mixture of dimethyl isosorbide and an alcohol to form a stable solution. The solution is compatible with hamamelis extract, commonly known as witch hazel, and the resulting solvent mixture forms a biologically active solution from which the drug is readily available for quick absorption at the site of application. The solution is then absorbed on a suitable carrier in superwetted condition and when applied to the inflamed hemorrhoidal tissues, the superwetted carrier preferentially releases the hydrocortisone to provide anti-inflammatory and antipruritic activity while the hamamelis extract solution provides the astringent action. The superwetted state is achieved by the incorporation of an amphoteric surfactant into the liquid portion of the composition. This combination of ingredients provides, for the first time, a unique composition which offers four necessary pharmacologic actions for external hemorrhoid treatment in a biologically active system.

The composition of this invention is comprised of hydrocortisone dissolved in a liquid solution containing dimethyl isosorbide, an alcohol, hamamelis extract, a fungicide-bactericide, a film-former, an amphoteric surfactant and water.

Therapeutically effective amounts of hydrocortisone are employed in the formulation. Generally, amounts in the range of about 0.001 to 0.5 percent by weight have been found to be effective. The dimethyl isosorbide is present in an amount ranging from about 0.5-25 percent by weight. The preferred range is from about 15-25 percent. As the alcohol component alcohols such as propylene glycol, isopropyl alcohol, polyethylene glycol-400 or ethyl alcohol (190 proof) may be employed. The alcohol is present in the formulation in an amount ranging from about 0.5-15 percent by weight. The preferred range is about 5-15 percent. The hamamelis extract (86.0% witch hazel extract - 14% alcohol) is present in the solution in amounts ranging from about 43.0 to 58.45 percent by weight.

Methyl paraben can be employed as the fungicide-bactericide in the formulation. It may be present in an amount ranging from about 0.1-0.25 percent by weight; the preferred amount is 0.25 percent. Other materials which can be employed include the propyl and butyl parabens; cations like benzalkonium chloride and cetyl pyridinium chloride; phenyl mercuric chloride, phenol and derivatives of phenol such as resorcinol.

Film-formers such as polyvinylpyrrolidone having a molecular weight between 38,000 and 40,000, polymer JR-400 (a cationic cellulosic resin sold by Union Carbide having an approximate molecular weight of 400,000), sodium carboxymethyl cellulose and polyvinyl alcohol having a molecular weight between 170,000 and 250,000 may also be employed in the formulation. The film-former may be present in an amount ranging from about 0.075-1.375 percent by weight. The preferred range is from about 0.075-1.00 percent by weight.

As the amphoteric surfactant Miranol C2M-SF Conc., also known as Amphoteric 2 (an essentially salt-free, aqueous, amphoteric surfactant solution derived from coconut fatty acid manufactured by Miranol Chemical Co.) may be employed in concentrations ranging from about 0.1-0.25 percent by weight. The preferred concentration is about 0.25 percent. Other amphoteric surfactants which can be employed include Miranol 2MCA modified (Amphoteric 6--an aqueous salt solution derived from coconut fatty acid); Miranol CM Conc. (Amphoteric 1--an aqueous surfactant solution derived from coconut fatty acid); Miranol MHT (Amphoteric 17--an aqueous salt solution derived from lauric acid); Mirataine CB (an aqueous solution of cocamidoalkyl betaine); Mirataine BB (an aqueous solution of the lauric-myristic amidopropylbetaine) and Mirataine CDMB (an aqueous solution of N-cocoyl-N,N-dimethyl-glycine). The preferred surfactant, however, is Miranol C2M-SF Conc. The remainder of the composition (100% by weight) is water, preferably purified water which serves both as a vehicle for the formulation and a means of further diluting the preparation so as to avoid unnecessary irritation.

Any suitable means may be employed to apply the formulation to the affected areas. The solution can be applied by means of a sponge or commercially available nonwoven materials. Cotton swabs, absorbent wipes, pads and the like or any other absorbent material may also be employed. Care should be taken to use a sterile applicator in order to avoid infection.

The novel compositions can be prepared generally as follows:

The alcohol and the dimethyl isosorbide are thoroughly mixed and the hydrocortisone and methyl paraben are added to the mixture followed by the addition of the surfactant. The film-former is then dissolved in water and the aqueous solution is mixed well with the hamamelis extract. The solution containing the steroid is then added slowly to the solution of the film-former and the hamamelis extract with stirring. When either sodium carboxymethyl cellulose or polyvinyl alcohol is employed as the film-former, it is added to the solution containing the steroid prior to the addition of the aqueous solution in order to obtain a more homogeneous solution.

The following examples illustrate the invention and should not be construed as a limitation thereof: