Formulations of magnesium chloride to treat muscle spasm, strain and sprain

Abstract

The present invention describes the use of a pharmaceutically-acceptable formulation of magnesium chloride to treat muscle spasm, strain and sprain.

Claims

1. A method for the treatment of an animal or human in need of treatment for muscle spasm, strain or sprain by use of a pharmaceutically-acceptable formulation consisting of applying to the animal or human, as a roll-on, an effective amount of an aqueous formulation of about 45-55% w/w of magnesium chloride in the total formulation, propylene glycol, aloe, and one or more pharmaceutically-acceptable additives or excipients, including water in about 50% to about 55% w/w of the total formulation, to treat muscle spasm, strain or sprain.

2. The method of claim 1, wherein the formulation used in the method has a net weight of components of about 130 g or 3 oz. consisting of the following pharmaceutically-acceptable components: a) MgCl.sub.2 at about 60 g to about 65 g or about 45% to about 50% w/w of the total formulation; b) Propylene glycol of about 0.2% to about 0.3% w/w of the total formulation; c) Aloe of about 5% to about 6% v/v of the total formulation; d) One or more pharmaceutically-acceptable additives or excipients, including water of about 50% to about 55% w/w of the total formulation; and e) Optional aroma additive of about 0.5% to about 2% v/v of the total formulation.

3. A process for preparing the formulation as defined in claim 2 comprising: A. Adding the MgCl.sub.2 of claim 2 a) to distilled water in a vessel and heating, optionally stirring or shaking the mixture, until the MgCl.sub.2 is dissolved; B. After cooling the solution from step A to about room temperature, transferring the MgCl.sub.2 solution to the individual dispensing device(s); C. Adding the propylene glycol of claim 2 b) to each device; D. Microwave or heating each device to cause the propylene glycol to complex with the MgCl.sub.2 in solution; E. After the device cools to about room temperature, adding the aloe of claim 2 c) to each device; and F. Optionally adding any pharmaceutically-acceptable additives of claim 2 d) to each device; and G. Optionally adding the aroma of claim 2 e) to each device; and H. Final assembly of the device and labeling.

4. The method of claim 1, wherein the pharmaceutically-acceptable additives or excipients is an aroma additive.

5. The method of claim 2, wherein the aroma additive is musk, lavender or citrus.

Description

DETAILED DESCRIPTION OF THE INVENTION

(1) The increased solubility of this formulation where the active ingredient is magnesium chloride (MgCl.sub.2), compared to Epsom salts (MgSO.sub.4), allows for a higher concentration of the magnesium ion to penetrate into the muscle.

(2) In a review article (Adrian C. Williams and Brian W. Berry, “Penetration enhancers”, Advanced Drug Delivery Reviews, 56 (2004), 603-618) the penetration enhancers use is discussed. It is well known that improving transdermal drug delivery often advocates penetration enhancers (also called sorption promoters or accelerants). These agents penetrate into skin to reversibly decrease the barrier resistance to drugs. Numerous compounds have been evaluated for penetration enhancing activity, including sulphoxides (such as dimethylsulphoxide, DMSO), Azones (e.g. laurocapram), pyrrolidones (for example 2-pyrrolidone, 2P), alcohols and alkanols (ethanol, or decanol), glycols (for example propylene glycol (PG), a common excipient in topically applied dosage forms), surfactants (also common in dosage forms) and terpenes. Some of these agents are more useful than others or work better in some formulations.

(3) Many potential sites and modes of action have been identified for agents that serve as such skin penetration enhancers. Examples of some sites are the intercellular lipid matrix in which the accelerants may disrupt the packing motif, the intracellular keratin domains or through increasing drug partitioning into the tissue by acting as a solvent for the permeant within the membrane. Further potential mechanisms of action, for example with the enhancers acting on desmosomal connections between corneocytes or altering metabolic activity within the skin, or exerting an influence on the thermodynamic activity/solubility of the drug in its vehicle are also thought feasible.

(4) The present formulation also includes other additives to aid in the penetration of the muscle, the flow of the formulation, provide aroma, soothing ingredients such aloe, and excipients to make the formulation apply as a roll-on, spray, gel or cream; especially useful is the roll-on formulation for direct application to the desired site.

(5) Epsom salt is not very soluble in water (26.9 g/100 mL), whereas the present formulation with MgCl.sub.2 is much more soluble in water (4.2 g/100 mL). This improved solubility is important in the present formulation. Other forms of magnesium salts have different solubility and toxic concerns.

(6) Other known MgCl.sub.2 preparations, commonly known as magnesium oils, are sticky to touch and leave a residue on the skin once they are applied. Because they do not contain the propylene glycol as an excipient, their absorbency into the muscle is less effective. These known preparations also do not contain aloe, which is needed to prevent dry skin caused from the magnesium ions from MgCl.sub.2. Because the present formulation is a roll-on formulation or spray, it dries quickly, whereas the known formulations are wet and gooey and may not dry at all or only after a longer time interval. Creams or gels frequently require that they are rubbed in and can make the person's hands gooey or sticky. The present roll-on formulation is very convenient to take with you and apply with no sticky hands, without soiling the clothes or having time delays to have it dry. The amount applied varies depending on the site of the muscle area having the spasm, strain or sprain.

(7) The following formulations are included within the present formulation.

(8) A present roll-on formulation is applied from a device having a net weight of components of the formulation of about 130 g or 3 oz. comprising the following pharmaceutically-acceptable components: a) MgCl.sub.2 at about 60 g to about 65 g or about 45% to about 50% w/w (weight/weight) of the total formulation; b) Propylene glycol of about 0.2% to about 0.3% w/w of the total formulation; c) Aloe of about 5% to about 6% v/v (volume/volume) of the total formulation; d) One or more pharmaceutically-acceptable additives and/or excipients, including water of about 50% to about 55% w/w of the total formulation; and e) Optional aroma additive such as musk, lavender, citrus, floral, etc. of about 0.5% to about 2% v/v of the total formulation.

(9) The roll-on formulation is a liquid at room temperature. These formulations have an estimated shelf life of about 2 years.

(10) The present above formulation described above is prepared by: A. Adding the MgCl.sub.2 to distilled water in a vessel and heating, optionally stirring or shaking the mixture, until the MgCl.sub.2 is dissolved; B. After cooling the solution from step A to about room temperature, transferring the MgCl.sub.2 solution to the individual dispensing device(s); C. Adding the propylene glycol of b) in the formulation described above to each device; D. Microwave or heating each device to cause the propylene glycol to complex with the MgCl.sub.2 in solution; E. After the device cools to about room temperature, adding the aloe of c) in the formulation described above to each device; and F. Optionally adding any pharmaceutically-acceptable additives d) in the formulation described above to each device; and G. Optionally adding the aroma e) in the formulation described above to each device; and H. Final assembly of the device and labeling.

(11) The heating can be done by microwave or other conventional means.

(12) Because of its improved properties, the present formulation of MgCl.sub.2 could be used in a device like a spray, including an aerosol spray. The method of making such sprays from the above components is well known in this art.

(13) General Procedure

(14) In the following examples, the data is antidotal but told to the inventor. In some cases he has actual knowledge of the before and after statements.

(15) Materials and Methods

(16) The various components were purchased commercially. These components can be purchased from any suitable source.

(17) MgCl.sub.2 from Pure Organic LLC

(18) Propylene glycol from CVS Health

(19) Aloe from Warren laboratories LLC

(20) Aroma ingredients such as lavender from CVS health

(21) Pharmaceutically-acceptable additives such as distilled water

(22) The product was tested as a roll-on application using the above formulation made by the process as described above.

EXAMPLES

Example 1

(23) A 35 year old male, who is an avid kick boxer, takes whirlpool baths with Epsom salts after competition to relieve his pain. After using this present preparation, he no longer adds Epsom salt to his whirlpool, but prefers to apply the present preparation directly to his sore muscles.

Example 2

(24) A 45 year old woman, who is an occupational therapist, finds it difficult to work because of severe chronic pain in her deltoid muscles. Being under a doctor's care, the only remedy that seemed to help her was prescription strength lidocaine patches. After using the present preparation, the pain and stiffness are now gone.

Example 3

(25) A 55 year old woman, who is a housekeeper, had a rotator cuff injury. After surgery she was incapacitated and in a lot of pain. Using the present preparation immediately mitigated her pain. Over one month of use she was able to return to work.

Example 4

(26) A 65 year old retired nurse was in worsening chronic shoulder pain. Although palliative treatments such as oral NSAIDS's and GABA agonists temporally helped, nothing was slowing the progression of the pain. One day she realized that this worsening chronic pain was now preventing her from combing her hair. After using the present preparation, the pain started to subside. Now after several months of use, she is pain free and has recovered almost full range of motion.

Example 5

(27) A 30 year old male is a recreational runner but has a history of chronic muscle injury due to his forgetfulness to warm up before his runs. Now he uses the present preparation before his runs and is without muscle injury.

(28) Although the invention has been described with reference to its preferred embodiments, those of ordinary skill in the art may, upon reading and understanding this disclosure, appreciate changes and modifications which may be made which do not depart from the scope and spirit of the invention as described above or claimed hereafter. All such modifications that fall within the spirit and broad scope of the appended claims are included.