1. Field of the Invention
This invention relates generally to the field of veterinary medication. More particularly, the invention relates to an improved L-lysine mixture and an apparatus and method for administering L-lysine to a pet.
2. Description of the Related Art
Feline herpesvirus type I (“FHV-1”) is a common viral infection in cats which can affect the eyes and respiratory tract. Most cats are initially infected as kittens and a significant number of cats become chronic carriers without displaying evidence of clinical disease. In a recent study, 97% of cats tested positive for an antibody reaction to FHV-1, 95% of which were higher than the vaccine alone would elicit. The most common signs of FHV-1 include upper respiratory infection and ocular diseases such as conjunctivitis and corneal ulceration.
One strategy to assist in the treatment of FHV-1 identified in the last few years is the oral administration of L-lysine. It is hypothesized that L-lysine inhibits herpesvirus growth through competitive inhibition of arginine, which is required for viral multiplication. Recent reports suggest that maintenance of cats on L-lysine will result in a longer period of time between ocular viral flare-ups. Moreover, if signs of the virus reoccur, the infection is typically milder and of a shorter duration. L-lysine is typically administered to cats at a dosage of 250-1000 mg daily.
L-lysine supplements have been prescribed for humans for many years to reduce the effects of Human Herpes Simplex 1 (“HSV-1”). It is estimated that between 60% and 90% of humans have HSV-1, the most common clinical sign of which is a fever blister around the mouth. Current over-the-counter L-lysine formulations prescribed for human treatment include tablets, capsules, gel caps and powders.
To treat FHV-1, cat owners are currently expected to purchase and administer one of the over-the-counter L-lysine preparations designed for human consumption. There are several problems with this scenario. Cats are not amenable to “pilling” or forced liquids, particularly on a long term basis. Moreover, mixing medications such as L-lysine with food provides for unreliable dosing, particularly in households with multiple cats.
Accordingly, what is needed is an improved apparatus and method for administering L-lysine to cats and/or other pets. What is also needed is a mixture of L-lysine and a base substance which is palatable to cats and/or other pets.
A mixture is described comprising L-lysine and a base substance palatable to cats. Also described is a improved method and apparatus for administering L-lysine using an oral syringe.
A better understanding of the present invention can be obtained from the following detailed description in conjunction with the following drawings, in which:
In the following description, for the purposes of explanation, numerous specific details are set forth in order to provide a thorough understanding of the present invention. It will be apparent, however, to one skilled in the art that the invention may be practiced without some of these specific details.
In one embodiment, L-lysine is mixed into a flavored gel, paste or other base substance known to be palatable to cats. Different flavored base substances may be used to achieve the desired effect. A malt or fish flavor has been found to be particularly suitable for cats. However, various different flavorings may be used while still complying with the underlying principles of the invention including, but not limited to, beef, chicken, liver, lamb, turkey, cheese, duck, shrimp, crab, tuna, salmon, seafood, whitefish, sardine, cod, and catfish.
The base may be created from various substances including, but not limited to, malt syrup, corn syrup, soybean oil, cod liver oil, cane molasses, glycerin, gelatin byproducts, methylcellulose, digest of poultry and tuna by-products, safflower oil, barley malt syrup, white petrolatum & light mineral oil and/or any combination thereof. In one embodiment, the following specific base ingredients are used (listed in order of decreasing concentration): corn syrup, malt syrup, soybean oil, water, cane molasses, methylcellulose, and sodium benzoate (preservative). In another very specific embodiment, the palatable base is comprised of 47% corn syrup, 30% malt syrup, and 23% liquid petroleum. It should be noted, however, that the underlying principles of the invention are not limited to any particular set of palatable base substances or any particular concentration thereof.
L-lysine may also be added to other known remedies such as hairball remedies and vitamin supplements. For example, in one embodiment, the base substance, in addition to containing palatable compounds, includes elevated percentages of liquid petroleum, glycerine, light mineral oil, and/or any other compounds known to aid cats in expelling hairballs. In one specific embodiment, the following components are used for the base, in the following proportions: 47% malt syrup, 44% liquid petroleum, 7% glycerine, 2% Acacia and less than 0.5% of Vitamin B1.
The L-lysine used in the mixture may be a raw form of L-lysine such as, for example, an L-lysine powder (e.g., 78-99% pure with 85%<1 mm granulation size). In one embodiment, the L-lysine used in the mixture is 2,6-Diaminohexanoic acid monohydrochloride (C6H14N202.HCL). Different forms of L-lysine may be used while still complying with the underlying principles of the invention.
Various different concentrations of L-lysine may be used in the mixture. In one embodiment, L-lysine is initially dissolved in water at a concentration of 500 mg/ml. The L-lysine/water solution is then mixed with the palatable base substance at a 1:1 ratio (i.e., 50% solution and 50% palatable base), resulting in an L-lysine concentration of 250 mg/ml. Given that the current recommended dosage of L-lysine is 250 to 1000 mg daily, two 2 ml doses may be administered daily. Alternatively, a single 4 ml dose may be administered (if the cat is willing to consume the 4 ml dose). It should be noted, however, that the underlying principles of the invention are not confined to any particular concentration of L-lysine or any particular dosage. For example, any concentration up to the maximum amount capable of being dissolved in water may be used (e.g., 64.2 gm/100 ml water @ 20□ C, or approximately 650 mg/ml). Moreover, the L-lysine solution may then be added to the palatable base at various different ratios, based on the desired L-lysine concentration and/or the desired consistency of the final mixture (e.g., 2:1, 3:1, 1:2, . . . etc).
In one embodiment, the mixture containing L-lysine is packaged and/or administered with an oral syringe 100 such as the one illustrated in
In one embodiment, a special type of oral syringe, sometimes referred to as a “dial-a-dose” oral syringe is used to administer the L-lysine mixture. As illustrated in
In operation, the user rotates the dose dialing knob 102 with a counter-clockwise rotation to move the dose dialing knob 102 along the plunger 101, away from the dispensing chamber 104. Volume markings 103 on the plunger indicate the volume of the L-lysine mixture associated with the distance moved by the dialing knob 102 along the plunger. When the dialing knob 102 is positioned at the desired volume marking (e.g., indicating 500 mg of L-lysine for a cat), the user may then push the plunger into the chamber, dispensing the desired amount of L-lysine. When the correct amount of L-lysine has been dispensed, the dose dialing knob 102 is positioned directly adjacent to the dispensing chamber 104, thereby preventing the plunger from being pushed further into the dispensing chamber 104.
Throughout the foregoing description, for the purposes of explanation, numerous specific details were set forth in order to provide a thorough understanding of the invention. It will be apparent, however, to one skilled in the art that the invention may be practiced without some of these specific details. For example, while the embodiments described above focus on the treatment of cats, the invention may be used to treat various other animals. Moreover, while the embodiments described above mention specific components used to create a palatable base, and specific concentrations of L-lysine, the underlying principles of the invention are not limited to any particular palatable base composition or any particular L-lysine concentration. Finally, while the embodiments described above focus on dispensing L-lysine with a dial-a-dose oral syringe, various alternate dispensing mechanisms may be employed. Thus, the scope and spirit of the invention should be judged in terms of the claims which follow.
This application is a divisional application of U.S. patent application Ser. No. 10/290,586, filed Nov. 7, 2002.
Number | Date | Country | |
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Parent | 10290586 | Nov 2002 | US |
Child | 11360328 | Feb 2006 | US |