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US20110274743A1 - Medicament for the Treatment of Pain and Inflammation - Google Patents

Medicament for the Treatment of Pain and Inflammation Download PDF

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Publication number
US20110274743A1
US20110274743A1 US13/144,807 US200913144807A US2011274743A1 US 20110274743 A1 US20110274743 A1 US 20110274743A1 US 200913144807 A US200913144807 A US 200913144807A US 2011274743 A1 US2011274743 A1 US 2011274743A1
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Prior art keywords
pain
composition
cholecalciferol
calciol
gram
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Abandoned
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US13/144,807
Inventor
Jan Anne Lyftogt
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Horopito Ltd
ANZAMED INTERNATIONAL Ltd
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PHARMACEUTICAL COMPOUNDING NZ Ltd
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Priority claimed from NZ57423109A external-priority patent/NZ574231A/en
Application filed by PHARMACEUTICAL COMPOUNDING NZ Ltd filed Critical PHARMACEUTICAL COMPOUNDING NZ Ltd
Assigned to PHARMACEUTICAL COMPOUNDING NZ LIMITED reassignment PHARMACEUTICAL COMPOUNDING NZ LIMITED ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: LYFTOGT, JAN ANNE
Publication of US20110274743A1 publication Critical patent/US20110274743A1/en
Assigned to ANZAMED INTERNATIONAL LIMITED reassignment ANZAMED INTERNATIONAL LIMITED ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: PHARMACEUTICAL COMPOUNDING NZ LIMITED
Assigned to HOROPITO LIMITED reassignment HOROPITO LIMITED ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: LYFTOGT, JAN ANNE
Abandoned legal-status Critical Current

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0014—Skin, i.e. galenical aspects of topical compositions
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/59—Compounds containing 9, 10- seco- cyclopenta[a]hydrophenanthrene ring systems
    • A61K31/593—9,10-Secocholestane derivatives, e.g. cholecalciferol, i.e. vitamin D3
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics

Definitions

  • the present invention relates to a medicament for the relief of pain and inflammation, in particular neurogenic inflammation and neuropathic pain.
  • the medicament of the present invention has been found to be especially effective in the relief of peripheral neuropathic pain.
  • Neurogenic inflammation is inflammation of the nerves which is actually caused by the nerves, in the sense that it is caused by the pro-inflammatory neuropeptides released by the nerves when the nerves are irritated, damaged, or injured.
  • the neurogenic inflammation causes the neuropathic pain.
  • Peripheral neuropathic pain is neuropathic pain experienced in the distribution of the peripheral nervous system, i.e. outside the central nervous system (brain and spinal cord). Typical sites for peripheral neuropathic pain are the heels/hands/feet/elbows/knees.
  • Neurogenic inflammation and the resulting neuropathic pain, typically are difficult to treat and often respond poorly to standard pain treatments.
  • Treatments typically used for neurogenic inflammation and neuropathic pain include non-steroidal anti-inflammatory drugs, painkillers, anticonvulsant drugs, antidepressant drugs, electrical nerve stimulation, and corticosteroid/local anaesthetic injections; however, none of these treatments reliably reduces the pain in a majority of cases, and in addition may have undesirable side-effects.
  • An object of the present invention is the provision of a medicament capable of providing a convenient, safe and effective relief for neurogenic inflammation and neuropathic pain (including peripheral neuropathic pain), with minimal risk of undesirable side-effects.
  • the present invention provides the use of vitamin D3 for the manufacture of a medicament for the transdermal treatment of neurogenic inflammation and neuropathic pain (including peripheral neuropathic pain).
  • the present invention further provides a method for the relief of neurogenic inflammation and neuropathic pain (including peripheral neuropathic pain) by the transdermal application of a medicament including vitamin D3.
  • the medicament of the present invention includes a carrier medium suitable for transdermal application, in which vitamin D3 is dispersed or dissolved.
  • vitamin D3 is fat soluble.
  • Vitamin D3 is commercially available either as a powder or dissolved in a plant oil; in either form it can be mixed into the carrier medium.
  • suitable carrier mediums for transdermal application would include aqueous-based creams, massage oils, ointments, gels, pessaries/suppositories, patches, and impregnated bandages or other sheet material, e.g. insoles for footwear.
  • vitamin D3 means cholecalciferol, (i.e. the pro-hormone form of vitamin D3) as opposed to the metabolically active form, calcitriol.
  • the preferred range of concentration of the vitamin D3 in the medicament is in the range 5000 IU/gram to 100,000 IU/gram; a concentration of 40,000 IU/gram has been found particularly effective. (IU is an abbreviation of “International Unit”).
  • Vitamin D3 is of course known as a vitamin necessary for bone health, although the recommended daily intake of vitamin D3 is currently a matter of debate.
  • vitamin D3 would have any anti-inflammatory and/or anaesthetic or pain relieving properties when applied externally.
  • vitamin D3 is applied transdermally
  • a treatment for psoriasis in which a cream containing the active form of vitamin D3 (calcitriol) is used.
  • this cream is ineffective for the relief of neurogenic inflammation or neuropathic pain.
  • FIG. 1 is a visual analogue scale diagram showing progress of pain relief for Patient 1
  • FIG. 2 is a visual analogue scale diagram showing progress of pain relief for Patient 2.
  • FIG. 3 Is a visual analogue scale diagram showing the results of a one-year clinical audit on a number of patients.
  • a cream was prepared using a known pharmaceutical cream base plus 12,000 IU/gram powdered vitamin D3 in the form of cholecalciferol (25 (0H) D3).
  • the cream was designed to be suitable for transdermal application by massaging into the skin.
  • Patient 1 Hisstory: MM, age 46, female, elite masters middle distance runner with 2-month history of right inferior heel pain treated initially with subcutaneous prolotherapy, complicated by infection, complaining of inability to run, difficulty walking, and pain at rest. Past history of bilateral peripatellar pain treated with failed surgical decompression, Achillodynia.
  • Patient 2 Hisstory: JF, age 24, female, fitness trainer with 8-month history of left inferior heel pain, complaining of inability to run, difficulty walking, affecting work. Has prior treatment with physiotherapy and podiatry without effect. Past history of bilateral Osgood Schlatter Disease, right medial shin splints and peripatellar pain.
  • Inferior heel pain (plantar fasciitis) is a difficult to treat condition, causing high levels of pain and disability for up to four years in one prospective study of 100 patients (BMJ Clinical Evidence Concise June 2006)
  • the underlying cause of inferior heel pain is postulated to be due to chronic neurogenic inflammation of the distal Tibial nerves branches known as the medial cutaneous calcaneal nerves.
  • the patients were treated with a cream consisting of a known cream base of a type suitable for transdermal applications of medication to which had been added vitamin D3 in oil base form, at a concentration of 40,000 IU/gram.
  • the cream was gently massaged into the skin over the inflamed portion, at least twice a day.
  • Ten of the 14 patients were treated with the vitamin D3 cream only; four of the patients used the vitamin D3 cream in combination with weekly prolotherapy (injections of 20% glucose, 0.1% lignocaine). All patients were monitored at intervals for blood levels of vitamin D3; all levels were normal.
  • FIG. 3 shows the visual, analogue scores for pain, graphed against time.
  • the solid lines represent the cases treated with vitamin D3 cream only; the broken lines show the four cases treated with the combination of prolotherapy and vitamin D3 cream.
  • FIG. 3 shows that there was little difference in outcome between the two treatments, and also shows that there was a strong correlation between initial pain scores and the length of treatment needed:—patients with high initial pain scores required a longer treatment period. However, there was a consistent and high response rate to the treatment with vitamin D3 cream alone.
  • the medicament of the present invention is successful in relieving a wide range of forms of neurogenic inflammation and neuropathic pain, including peripheral neuropathic pain.
  • the cream has been successful in relieving all of the following conditions:—plantar fascia, tennis elbow, golfers elbow, knee pain, Achilles tendon pain, neck pain (whiplash injury) low back pain, chronic exertional compartment syndrome, osteo arthritis symptoms of hand and fingers, fibromyalgia pains, hip pains and shoulder pains, contact dermatitis (especially contact dermatitis caused by cement/concrete and by Diesel), acute contusions, sprains and strains, purigo, first-degree burns (including sunburn), chilblains and shingles.
  • the condition is treated simply by massaging the cream into the affected area of skin.
  • Many sprains and strains and other injuries causing neuropathic pain can become a cause of chronic pain, and the medicament of the present invention is particularly valuable in that it can be used to treat such pain quickly and effectively, thus preventing the neurogenic inflammation from becoming chronic and hence causing chronic pain.
  • the levels of vitamin D3 in the user's blood have been monitored by a series of regular blood tests and it is interesting that in all cases so far, there have been no significant increases of vitamin D3 levels in the user's blood as a result of the use of the medicament.

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  • Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • Chemical & Material Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Dermatology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
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Abstract

The use of vitamin D3 for the manufacture of a medicament for the transdermal treatment of neurogenic inflammation and neuropathic pain (including peripheral neuropathic pain); also a method for the relief of neurogenic inflammation and neuropathic pain using this medicament.

Description

    FIELD OF THE INVENTION
  • The present invention relates to a medicament for the relief of pain and inflammation, in particular neurogenic inflammation and neuropathic pain. The medicament of the present invention has been found to be especially effective in the relief of peripheral neuropathic pain.
    • BACKGROUND OF THE INVENTION
  • Neurogenic inflammation is inflammation of the nerves which is actually caused by the nerves, in the sense that it is caused by the pro-inflammatory neuropeptides released by the nerves when the nerves are irritated, damaged, or injured. The neurogenic inflammation causes the neuropathic pain. Peripheral neuropathic pain is neuropathic pain experienced in the distribution of the peripheral nervous system, i.e. outside the central nervous system (brain and spinal cord). Typical sites for peripheral neuropathic pain are the heels/hands/feet/elbows/knees.
  • Neurogenic inflammation, and the resulting neuropathic pain, typically are difficult to treat and often respond poorly to standard pain treatments. Treatments typically used for neurogenic inflammation and neuropathic pain (including peripheral neuropathic pain) include non-steroidal anti-inflammatory drugs, painkillers, anticonvulsant drugs, antidepressant drugs, electrical nerve stimulation, and corticosteroid/local anaesthetic injections; however, none of these treatments reliably reduces the pain in a majority of cases, and in addition may have undesirable side-effects.
    • Disclosure of the Invention
  • An object of the present invention is the provision of a medicament capable of providing a convenient, safe and effective relief for neurogenic inflammation and neuropathic pain (including peripheral neuropathic pain), with minimal risk of undesirable side-effects.
  • The present invention provides the use of vitamin D3 for the manufacture of a medicament for the transdermal treatment of neurogenic inflammation and neuropathic pain (including peripheral neuropathic pain).
  • The present invention further provides a method for the relief of neurogenic inflammation and neuropathic pain (including peripheral neuropathic pain) by the transdermal application of a medicament including vitamin D3.
  • Preferably, the medicament of the present invention includes a carrier medium suitable for transdermal application, in which vitamin D3 is dispersed or dissolved. It should be noted that vitamin D3 is fat soluble. Vitamin D3 is commercially available either as a powder or dissolved in a plant oil; in either form it can be mixed into the carrier medium. It is envisaged that suitable carrier mediums for transdermal application would include aqueous-based creams, massage oils, ointments, gels, pessaries/suppositories, patches, and impregnated bandages or other sheet material, e.g. insoles for footwear.
  • It should be noted that, as used herein, the term “vitamin D3” means cholecalciferol, (i.e. the pro-hormone form of vitamin D3) as opposed to the metabolically active form, calcitriol.
  • The preferred range of concentration of the vitamin D3 in the medicament is in the range 5000 IU/gram to 100,000 IU/gram; a concentration of 40,000 IU/gram has been found particularly effective. (IU is an abbreviation of “International Unit”).
  • Vitamin D3 is of course known as a vitamin necessary for bone health, although the recommended daily intake of vitamin D3 is currently a matter of debate.
  • Over the last 10 years, studies carried out in USA and UK have indicated that people suffering from persistent, non-specific musculoskeletal pain syndromes resistant to normal forms of treatment tend to have a deficiency of vitamin D3, and obtain benefit from a vitamin D3 supplement, given either as an intramuscular injection or as an oral dose.
  • Further, a recent study dealing with patients with diabetic neuropathy found that treatments with daily oral doses of vitamin D3 resulted in a significant reduction in the diabetic neuropathic pain.
  • However, none of the studies carried out to date suggest that vitamin D3 would have any anti-inflammatory and/or anaesthetic or pain relieving properties when applied externally.
  • The only known treatment in which vitamin D3 is applied transdermally is a treatment for psoriasis, in which a cream containing the active form of vitamin D3 (calcitriol) is used. However, this cream is ineffective for the relief of neurogenic inflammation or neuropathic pain.
    • BRIEF DESCRIPTION OF THE DRAWINGS
  • By way of example only, preferred embodiments of the present invention are described with reference to the accompanying drawings, in which:
  • FIG. 1 is a visual analogue scale diagram showing progress of pain relief for Patient 1,
  • FIG. 2 is a visual analogue scale diagram showing progress of pain relief for Patient 2; and
  • FIG. 3 Is a visual analogue scale diagram showing the results of a one-year clinical audit on a number of patients.
    •
  • In the visual analogue scale: 0=no pain
      • 10=worst imaginable pain
    DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS
  • A cream was prepared using a known pharmaceutical cream base plus 12,000 IU/gram powdered vitamin D3 in the form of cholecalciferol (25 (0H) D3). The cream was designed to be suitable for transdermal application by massaging into the skin.
    • Example 1
  • Patient 1—History: MM, age 46, female, elite masters middle distance runner with 2-month history of right inferior heel pain treated initially with subcutaneous prolotherapy, complicated by infection, complaining of inability to run, difficulty walking, and pain at rest. Past history of bilateral peripatellar pain treated with failed surgical decompression, Achillodynia.
  • The patient applied the cream by massaging the cream into the painful area twice a day and after any activity, with the massaging followed by the application of heat where possible. This procedure was followed until all pain and tenderness had disappeared from the area. The treatment was continued for three months, and an assessment of pain was recorded every seven days, as shown in FIG. 1. Over this period, the pain reduced from a severe pain to very little pain, with the pattern of pain reduction being a period of steady decrease of pain followed by a plateau, then a further steady decrease followed by another plateau. It is notable that the patient has since continued to run and is pain-free, although continuing to use the cream.
    • Example 2
  • Patient 2—History: JF, age 24, female, fitness trainer with 8-month history of left inferior heel pain, complaining of inability to run, difficulty walking, affecting work. Has prior treatment with physiotherapy and podiatry without effect. Past history of bilateral Osgood Schlatter Disease, right medial shin splints and peripatellar pain.
  • The patient applied the cream by massaging the cream into the painful area twice a day and after any activity, with the massaging followed by the application of heat where possible. This procedure was followed until all pain and tenderness had disappeared from the area. The treatment was continued for two months:—as shown in FIG. 2, over this period the pain steadily diminished from severe pain to no pain. This patient is still using the cream, and continues to run with no pain.
  • The patients from Examples 1 and 2 were monitored for serum vitamin D levels at the end of treatment; both showed normal levels.
    • Example 3
  • A total of 14 patients, all suffering from recalcitrant inferior heel pain (plantar fasciitis) were studied over a period of several months. The patients consisted of three males with a mean age of 56 (range 50 to 60) and 11 females with a mean age of 44 (range 23 to 61).
  • Inferior heel pain (plantar fasciitis) is a difficult to treat condition, causing high levels of pain and disability for up to four years in one prospective study of 100 patients (BMJ Clinical Evidence Concise June 2006)
  • The underlying cause of inferior heel pain is postulated to be due to chronic neurogenic inflammation of the distal Tibial nerves branches known as the medial cutaneous calcaneal nerves.
  • All patients in this study had received prior treatment including physiotherapy, cortison injections and podiatry with taping and orthotics without benefit.
  • The patients were treated with a cream consisting of a known cream base of a type suitable for transdermal applications of medication to which had been added vitamin D3 in oil base form, at a concentration of 40,000 IU/gram. The cream was gently massaged into the skin over the inflamed portion, at least twice a day. Ten of the 14 patients were treated with the vitamin D3 cream only; four of the patients used the vitamin D3 cream in combination with weekly prolotherapy (injections of 20% glucose, 0.1% lignocaine). All patients were monitored at intervals for blood levels of vitamin D3; all levels were normal.
  • Over the study period shown, all patients responded to the treatment with a complete recovery, with only one recorded relapse, and no adverse reactions were observed. The progress of the treatment is shown in FIG. 3 which shows the visual, analogue scores for pain, graphed against time. The solid lines represent the cases treated with vitamin D3 cream only; the broken lines show the four cases treated with the combination of prolotherapy and vitamin D3 cream. FIG. 3 shows that there was little difference in outcome between the two treatments, and also shows that there was a strong correlation between initial pain scores and the length of treatment needed:—patients with high initial pain scores required a longer treatment period. However, there was a consistent and high response rate to the treatment with vitamin D3 cream alone.
  • Further testing on individual cases indicates that the medicament of the present invention is successful in relieving a wide range of forms of neurogenic inflammation and neuropathic pain, including peripheral neuropathic pain. The cream has been successful in relieving all of the following conditions:—plantar fascia, tennis elbow, golfers elbow, knee pain, Achilles tendon pain, neck pain (whiplash injury) low back pain, chronic exertional compartment syndrome, osteo arthritis symptoms of hand and fingers, fibromyalgia pains, hip pains and shoulder pains, contact dermatitis (especially contact dermatitis caused by cement/concrete and by Diesel), acute contusions, sprains and strains, purigo, first-degree burns (including sunburn), chilblains and shingles. In all cases, the condition is treated simply by massaging the cream into the affected area of skin. Many sprains and strains and other injuries causing neuropathic pain can become a cause of chronic pain, and the medicament of the present invention is particularly valuable in that it can be used to treat such pain quickly and effectively, thus preventing the neurogenic inflammation from becoming chronic and hence causing chronic pain.
  • Whenever the medicament of the present invention has been used, the levels of vitamin D3 in the user's blood have been monitored by a series of regular blood tests and it is interesting that in all cases so far, there have been no significant increases of vitamin D3 levels in the user's blood as a result of the use of the medicament.

Claims (15)

1. A composition for the treatment of at least one selected from the group consisting of neurogenic inflammation, and neuropathic pain, and combinations thereof, wherein the composition comprises calciol (cholecalciferol) and wherein the composition is formulated for transdermal application.
2. The composition as claimed in claim 1, wherein the composition further comprises a carrier medium suitable for transdermal application, in which calciol (cholecalciferol) is dispersed or dissolved.
3. The composition as claimed in claim 2, wherein the carrier medium is selected from the group consisting of: aqueous-based cream, massaging oil, gel base, ointment, patches, impregnated sheet material, pessaries and suppositories.
4. The composition as claimed in claim 1, wherein the calciol (cholecalciferol) is present in a concentration in the range of 5000 IU/gram to 100,000 IU/gram.
5. The composition as claimed in claim 4, wherein the calciol (cholecalciferol) is present in a concentration of 40,000 IU/gram.
6. The composition as claimed in claim 1, wherein the calciol (cholecalciferol) is in the form of a powder.
7. The composition as claimed in claim 1, wherein the calciol (cholecalciferol) is dissolved in a plant oil.
8. A method for relieving at least one selected from the group consisting of neurogenic inflammation, neuropathic pain, and combinations thereof, said method comprising the step of transdermally administering a composition comprising calciol (cholecalciferol) to a subject in need thereof.
9. The method as claimed in claim 8, wherein the composition further comprises a carrier medium suitable for transdermal application, in which calciol (cholecalciferol) is dispersed or dissolved.
10. The method as claimed in claim 9, wherein the carrier medium is selected from the group consisting of: aqueous-based cream, massaging oil, gel base, ointment, patches, impregnated sheet material, pessaries and suppositories.
11. The method as claimed in claim 8, wherein the calciol (cholecalciferol) is present in a concentration in the range of 5000 IU/gram to 100,000 IU/gram.
12. The composition as claimed in claim 2, wherein the carrier medium is selected from the group consisting of aqueous-based cream, massaging oil, gel base, ointment, patches, impregnated sheet material, pessaries, suppositories, aerosol sprays, non-aerosol sprays and combinations thereof.
13. The composition as claimed in claim 1, wherein the calciol (cholecalciferol) is present in a concentration in the range of 5000 IU/gram to 200,000 IU/gram.
14. The method as claimed in claim 9, wherein the carrier medium is selected from the group consisting of aqueous-based cream, massaging oil, gel base, ointment, patches, impregnated sheet material, pessaries, suppositories, aerosol sprays, non-aerosol sprays and combinations thereof.
15. The method as claimed in claim 8, wherein the calciol (cholecalciferol) is present in a concentration in the range of 5000 IU/gram to 200,000 IU/gram.
US13/144,807 2009-01-16 2009-08-13 Medicament for the Treatment of Pain and Inflammation Abandoned US20110274743A1 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
NZ57423109A NZ574231A (en) 2009-01-16 2009-01-16 Transdermal medicament containing cholecalciferol (vitamin D3) for the treatment of pain and inflammation
NZ574231 2009-01-16
NZ57537909 2009-03-06
NZ575379 2009-03-06
PCT/NZ2009/000167 WO2010082837A1 (en) 2009-01-16 2009-08-13 Medicament for the treatment of pain and inflammation

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WO2021252292A1 (en) * 2020-06-08 2021-12-16 Nova Neura, Llc Systems and methods for treating persistent pain of neurogenic origin and complex injury

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