AU612975B2 - Compositions for treating the symptoms of or preventing the common cold - Google Patents

Description

AU5TR3k-IA Form 1 PATENTS ACT 1952 COMPLETE SPECIFICATION

(ORIGINAL)

FOR OFFICE USE Short Title: Int. Cl: Application Number: Lodged: 7 .2 S715/ '7 a Complete Specification-Lodged: Accepted: Lapsed: Published: S Priority: Related Art: t TO BE COMPLETED BY APPLICANT Name of Applicant: T R CHEMICALS, INC.

f ft Address of Applicant: 700 CELLUM ROAD

CLINT

TEXAS 79836

USA

Actual Inventor: Address for Service: CLEMENT HACK CO., 601 St. Kilda Road, Melbourne, Victoria 3004, Australia.

Complete Specification for the invention entitled: COMPOSITIONS FOR TREATING THE SYMPTOMS OF OR PREVENTING THE COMMON COLD The following statement is a full description of this invention including the best method of performing it known to me:- 6: i: t COMPOSITIONS FOR TREATING THE SYMPTOMS OF OR PREVENTING THE COMMON COLD This invention relates to the treatment of the common cold either by ameliorating the symptoms of the common cold or by preventing the rhinoviruses from causing colds or by preventing the cold symptoms from worsening. The invention includes the treatment of the common cold or head cold in mammals, especially man, and describes methods of treatment and pharmaceutical compositions for use in carrying out such treatments.

000o o ooooao 0 0 000 0 0f0 0 I Q 4t ft i o i ofp ft 0 ft 000 0 0 ft 0*e ftp 0 at~f ft* a 9 o0 o t ft 0 ft<,0A Common colds appear to be caused by a number of viruses or at least a number of strains of viruses which explains the remarkably transient immunity to colds and the fact that reinfection can take place within as little as three weeks of an apparent recovery. No ailment is quite so universal as the common cold and, indeed, it is probably the commonest of all infectious diseases.

0c 4 *o 4, 4r 4 An institution that has played a major role in the investigation of the cold is The Medical Research Council, Common Cold Unit, Salisbury, England.

Investigations and tests at MRC during the past forty years have proven that the common cold is caused by rhinoviruses that enter the body mainly by the nostrils, and are usually transmitted by an infected person, sometimes by a simple handshake, that will often carry the virus to the facial cavities and there contact the mucus membranes. A good sneeze from an 10 infected person in a public place will disseminate a vast number of droplets among those present, some of whom will quite likely acquire an upper respiratory tract infection.

15 The infection produced by the rhinovirus is an acute one, and like other acute infections, it may clear up in the course of only a few days.

Frequently, however, secondary invaders follow upon the primary infection, and these convert an otherwise acute infection into a chronic disease which may drag on for several unpleasant weeks. These secondary invaders attack first the nose and throat and may later spread to the larynx, trachea, bronchi and up into the sinuses which open into the nose. For the first day or so, the mucus membrane lining of the :r4 4 4- 4 4 -L nose and throat is swollen, red and dry, giving the all too well known symptoms of feeling "stuffed-up".

Soon the nose secretes a watery fluid which runs from the nose continually. Secondary invaders change the nature of the inflammation from a watery secretion to one that is more purulent which may continue to be discharged for several weeks.

Folk medicine through the years has suggested the uses of endless numbers of remedies, including pine-needle, honeysuckle, chrysanthemum and licorice S0 teas. Some people believe in sweating the cold out, Po or taking a hot alcoholic beverage and acetylsalicylic acid before going to bed at night are useful, although 000 15 there is a theory that acetylsalicylic aggravates the oo 0 o common cold.

More recent treatments for the common cold include the use of topically-applied sympathomimetic 0 I1 drugs which exert a vasoconstrictor action directly on the mucus membrane to which they are applied. An example of such a drug is epinephrine, although other more recently developed longer-acting drugs are preferred. All of these have the disadvantage that t ar a ar ii

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a a their use may be followed by "after congestion" and that prolonged use over a period of time often results in chronic rhinitis. Ephedrine and pseudoephedrine, also sympathomimetic drugs, have been given orally as nasal decongestants either by themselves or in combination with a variety of other agents including antihistamines, analgesics, caffeine, antitussives or antimuscarinic drugs. Of this last-mentioned category, atropine and belladonna alkaloids are the most commonly used to reduce 10 secretions in both the upper and lower respiratory tract, including reducing the volume of bronchial secretion. It is recognized that this therapy does not affect the natural courses of the condition for which the drugs are administered; see Goodman and Gilman, The Pharmacological Basis of Therapeutics (1975), at page 529. All of these drug substances discussed above are used to treat the symptoms of the infection and, to make the patient more comfortable while the infection runs its normal course of several days to over a week.

Despite extensive discussion in the literature of folk medicine and current therapeutics, little has i i i;-f si it k It

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i-: i.i i i 1:i i c r II been written about the fact that some individuals' nasal acid system destroys invading rhinoviruses. The germ-destroying properties of such acidic conditions are particularly useful in the nasal passages which, under normal conditions, provide secretions that are only slightly on the acid side. It is believed that this acidic-type environment makes the nasal passages and mucus membranes an inhospitable environme for invading rhinoviruses.

It has now been discovered, and hereby disclosed, a means for adjusting the pH of the nasal cavity, including the involved mucus membranes, by administering to that cavity ions of a family of pharmaceutical agents defined in more detail below.

These agents and this course of administration treats the preliminary symptoms of the common cold and thus, it is believed, serve to abort development of these initial symptoms into a full-blown rhinovirus common cold infection.

While not wishing to be bound by any particular theory or mode of operation, it appears that to a certain degree the normal (non-viral infected) state

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-6acidity in the nose is effective to prevent propogation of invading rhinoviruses. However, there comes a time when nasal acidity is no longer sufficient to inhibit rhinovirus replication. It is at this point that the nasal secretions shift from acidity to alkalinity. An alkaline environment is hospitable and facilitates propogation of these rhinoviruses and this, in turn, initiates the all too well known syndrome developing into a head cold or o common cold. In changing from acidic to alkaline 10 conditions, the body attempts to defend itself, via a o o pseudo "immunization" (for lack of a more precise 0 o0 0"o word) but in the meantime, the cold symtoms almost always continue to mount and may last from 4 to up to 14 days to subside assuming, of course, that no 0 60A 00o"0 15 further complications, such as secondary invaders, occur.

o Almost every individual feels certain symptoms that foretell the person that the symptoms of a cold are about to set in. These may manifest themselves in many forms, depending upon the individual, but it usually starts as an itching sensation inside of the nose, often accompanied by sneezing. It is believed j -7that these preliminary symptoms at the outset of a cold are the turning point from the normal acidity to alkalinity conditions in the mucus membranes lining the nasal passages and sinus cavities. The present invention is based on the discovery thac when the released ions of a family of pharmaceutical agents, identified in more detail below, are administered to a mammal, including man, in the affected area, these preliminary cold symptoms do not further develop, a 0 0 10 full blown cold does not result and the person o receiving such therapy is spared many unpleasant days 1 a and nights of discomfort.

*4 0 0 o o It has been discovered that sodium bisulfite, either as such or in an aqueous solution of sulfite a ions (S0 3 is useful in the treatment of the symptoms of the common cold and related conditions r when administered to humans in a suitable form or vehicle such as in aqueous dilute solution.

S' This invention thus includes the treatment and amelioration of symptoms of the progressive onset of rhinovirus infection of a person suffering from such an infection. Conceptually the method results in an i adjustment membrane.

I person in u rhinovirui -8t of the pH of the person's nasal mucosal This is accomplished by administering to the the nasal mucosa a pH-adjusting and 3-inhibiting quantity of an isotonic, buffered solution of an alkali metal, alkaline earth metal or ammonium sulfite or bisulfite, such as the sodium, potassium, calcium or magnesium salts, or mixture thereof. Preferably the salt administered is sodium bisulfite or sodium metabisulfite, and the isotonic, buffered solution is administered drop-wise either as a nasal solution or it is sprayed into the patient's nostrils as a nasal spray. The concentration of active ingredient in the solution usually ranges from 1 to preferably and is generally about by weight.

Also included within the invention is a nasal spray containing an aqueous isotonic buffered solution comprising as the sole active ingredient an alkali metal, alkaline earth metal or ammonium sulfite or bisulfite or mixture thereof.

Usually, the said solution is administered by spraying into or dropping down drops in one of the nostrils of a patient in a lying position. After one minute the same administration is repeated in the other nostril. After an additional minute, the patient can iif r 9: -9blow his or her nose (both nostrils). When the solution is first applied in the manner indicated, there is a transitory burning sensation inside the sinus area and possibly as far down as the throat; this may last from twenty to thirty seconds.

The rational and the biological mechanism by which the pharmaceutical agents function is not presently known and cannot now be explained to a high degree of accuracy. However, it is theorized with no intention to be bound by such theory, that this family of agents, after administration to the nostrils of a patient dissolve the incipient viral colonies in the sinus cavity area, because of their mucolytic properties (hydrolyzation of mucopolysaccharides), resulting in the release of bisulfite and/or sulfite ions. Once these viral colonies are actively deprived of their polysaccharide food source and consequently drained in or :ut or otherwise removed from the body, alkalinity is stopped and acidity returns to the sinus area, thus aborting the common cold. The bisulfite and/or sulfite ions appear to be responsible for the observed beneficial therapeutic effects.

The use of this invention is preferably practiced at present using a dilute aqueous solution of sodium ii r^ bisulfite. Because of the tendency for sodium bisulfite to undergo oxidation when in aqueous solution when oxygen is present, it is presently common and even preferred in using this invention to employ a solution which comprises on a 100% by weight total solution basis:from about 1 to 10% by weight of dissolved inorganic solids, and the balance up to 100% by weight of any given solution being water.

The water used in such solution is preferably purified filtered, deionized, distilled or the like) and, for purposes of nasal application, is preferably isotonic and may contain small quanitities of preservatives such as 0.001% thiomersal. After preparation, such a solution is preferably stored in a closed container to reduce oxidation.

i 20 Sodium bisulfite, usually shown by formula to be 11 NaHS0 3 has been used for many commercial purposes, as a preservative for prevention of the deterioration of liquids, such as food-stuffs and pharmaceutical solids and solutions, and has been used medically externally for parasitic skin diseases and internally as a gastrointestinal antiseptic.

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The sodium bisulfite of commerce consists chiefly of sodium metabisulfite, Na 2 S205 for purposes of this invention such is believed to possess the same properties as (and to be equivalent to) the true sodium bisulfite when di.-olved in an aqueous solution.

The use of-sodium bisulfite and metabisulfite in the treatment of hypertension is described in U.S.

Patent No. 4,327,083 and is also described as an antithrombotic agent useful for prolonging both prothrombin time (PT) and partial thromboplastin time (PTT) of blood or blood plasma in U.S. Patent 4,401,654.

The use of sulfite and/or bisulfite ions for the treatment of epilepsy and epileptic conditions as well as arthritis and arthritic conditions are described in U.S. Patent 4,532,131. To the best of our knowledge, sulfite and bisulfite ions have not previously been used or otherwise described in the art for the treatment of the symptoms of the common cold (rhinovirus-originated) or for preventing further common cold symptoms from i developing.

The present invention is further illustratud by the following Example and Case Histories.

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_I I -12- EXAMPLE I A solution of sodium bisulfite is prepared by dissolving pharmaceutical grade Grade) powdered sodium bisulfite (sodium metabisulfite) in distilled water at room temperature to form a 5% by weight aqueous solution.

This solution is then placed into a series of plastic squeeze bottles, each with a volumetric capacity of about 50-52 ml. Each bottle is provided with a cap permitting drop-wise dispensing of solution from such bottle at an estimated rate of 15 drops per ml. This solution was used in each of the Case Histories that follow.

Case History I A woman, aged 64, weight 71 had an itching sensation inside the nose, one of the preliminary symptoms of the common cold. She lay down and applied two drops of the pharmaceutical solution as prepared above to her left nostril and after one minute, two more drops to her right nostril. About one minute later, she blew her nose. Soon after her itching sensation had disappeared.

Case History II A man, aged 40, weight 82 Kg, had a slight w 6 *6 600 06 66* 16or 13 runny nose, one of the preliminary symptoms of the common cold. He lay down and applied two drops of the pharmaceutical solution in each of his nostrils with one minute intervals. Two minutes later he blew his nose. His symptom disappeared immediately.

Case History III A boy, age 10, weight 39 Kg, had two of the 10 preliminary symptoms of the common cold sneezing and a stuffy feeling in the head. He lay down and one drop of the pharmaceutical solution was applied to each one of his nostrils with one minute intervals.

Soon after he blew his nose. He sneezed no more and about one hour later he said his head was clear.

Case History IV A girl, age 6, weight 25 Kg, had some preliminary symptoms of the common cold itching sensation in the nose, watery eyes and a slight fever. Before going to sleep at night, one drop of the pharmaceutical solution was put in each of her nostrils, while she was in a lying position, with one minute intervals.

She then blew her nose. The next day she felt fine.

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Claims (9)

1. A nasal spray containing an aqueous isotonic buffered solution for treating the common cold or other rhinovirus infection, said solution comprising as the sole active ingredient an alkali metal, alkaline earth metal or ammonium sulfite or bisulfite or mixture thereof.

2. A nasal spray as claimed in Claim 1, wherein said -active ingredient is sodium bisulfite.

3. A nasal spray as claimed in Claim 2, wherein said sodium bisulfite is sodium metabisulfite. i

4. A nasal spray as claimed in any one of the Ireceding Claims, wherein said composition contains i to by weight of said sulfite or bisulfite salt.

5. A nasal spray as claimed in Claim 1, wherein the composition is substantially as hereinbefore S'described in Example 1.

6. A method of treating the common cold or other rhinovirus infection in a patient comprising I -vC V j administering to the patient's nasal mucosa a pH-adjusting and rhinovirus-inhibiting quantity of an aqueous isotonic buffered solution of an alkali metal, alkaline earth metal or ammonium sulfite or bisulfite or mixture thereof.

7. A method as claimed in Claim 6, wherein the said compound is sodium bisulfite.

8. A method as claimed in Claim 7, wherein the sodium bisulfite is sodium metabisulfite.

9. A method as claimed in any one of Claims 6 to 8, wherein the solution is administered as a nasal spray. A method as claimed in any one of Claims 6 to 8, wherein the compound is administered drop-wise as a nasal solution. DATED this 7th day of May, 1991 T. R. CHEMICALS, INC. By Its Patent Attorneys GRIFFITH HACK CO. Fellows Institute of Patent Attorneys of Australia