SODIUM BUTYRATE FOR USE IN THE PREVENTION OR TREATMENT OF RHINOVIRUS INFECTION
20230190687 · 2023-06-22
Inventors
Cpc classification
A61K31/59
HUMAN NECESSITIES
A61K31/592
HUMAN NECESSITIES
A61K2300/00
HUMAN NECESSITIES
A61K2300/00
HUMAN NECESSITIES
A61K9/0073
HUMAN NECESSITIES
A61K31/593
HUMAN NECESSITIES
A61K9/127
HUMAN NECESSITIES
A61K9/5068
HUMAN NECESSITIES
A61K31/593
HUMAN NECESSITIES
International classification
A61K31/59
HUMAN NECESSITIES
A61K9/00
HUMAN NECESSITIES
A61K9/127
HUMAN NECESSITIES
Abstract
A composition comprising sodium butyrate for the prevention and/or treatment of a viral infection caused by Rhinovirus. The composition may further comprise Vitamin D. The composition may be administered in the form of a tablet or capsule, in the form of an inhaler, or provided as a dietary supplement.
Claims
1. A composition comprising sodium butyrate for use in the prevention and/or treatment of a viral infection caused by Rhinovirus.
2. A composition according to claim 1, for use in the prevention and/or treatment of an acute Rhinovirus infection.
3. A composition according to claim 1 or claim 2, wherein the composition stimulates the immune cells of an individual to release substances that kill Rhinovirus and/or inhibit its replication.
4. A composition according to any preceding claim, wherein the composition further comprises Vitamin D.
5. A composition according to any preceding claim, wherein the composition is administered by mouth.
6. A composition according to claim 8, wherein the composition is administered in the form of a tablet or capsule.
7. A composition according to any one of claims 1 to 4, wherein the composition is administered in the form of an inhaler.
8. A composition according to any one of claims 1 to 6, wherein the composition is coated with a material such as a lipid or sugar, or a combination thereof.
9. A composition according to any one of the preceding claims, wherein the composition comprises at least one acceptable carrier and may be carried within a vesicle, micelle, liposome, nanoparticle or other suitable vehicle.
10. A composition according to any preceding claim, wherein the composition is provided as a dietary supplement.
11. A composition according to any preceding claim, wherein the composition is incorporated into a food or drink.
12. A dietary supplement comprising a composition comprising sodium butyrate for the prevention and/or treatment of a viral infection caused by Rhinovirus.
13. A dietary supplement according to claim 12, wherein the composition further comprises Vitamin D.
14. A tablet comprising a composition comprising sodium butyrate for the prevention and/or treatment of a viral infection caused by Rhinovirus.
15. A tablet according to claim 14, wherein the composition further comprises Vitamin D.
16. An inhaler comprising a composition comprising sodium butyrate for the prevention and/or treatment of a viral infection caused by Rhinovirus.
17. An inhaler according to claim 16, wherein the composition further comprises Vitamin D.
18. An inhaler according to claim 16 or 17, wherein the inhaler is a nasal inhaler.
19. A method for preventing and/or treating a viral infection caused by Rhinovirus using a composition comprising sodium butyrate in accordance with any one of claims 1 to 11.
20. A method according to claim 19, for the prevention and/or treatment of acute Rhinovirus infection using a composition comprising sodium butyrate in accordance with any one of claims 1 to 11.
21. A method according to claim 19 or 20, comprising the use of a composition comprising sodium butyrate and Vitamin D.
Description
[0030] The invention will be further described by way of example and with reference to the following FIGURES, in which:
[0031]
[0032] Advantageously, the use of the composition comprising sodium butyrate and/or Vitamin D results in the reduction and/or removal of Rhinovirus infection within an individual.
[0033] The composition in accordance with the present invention acts through the stimulation of the immune response within an individual, wherein the composition stimulates the immune cells of an individual to release one or more substances that kill/inactivate Rhinovirus and/or inhibit its replication.
[0034] In one embodiment, the composition is provided as a dietary supplement. Advantageously, dietary supplementation with sodium butyrate enhances the host's immune response to Rhinovirus. Preferably, the composition is provided in the form of a dietary supplement in pill form and marketed as an over the counter dietary supplement.
[0035] In another embodiment, the composition may be administered in the form of a tablet or capsule. In this embodiment, the composition may be coated with a material such as a lipid or sugar, or a combination thereof. Typically, the coating or target-guiding material dissolves to allow efficient and sufficient delivery of the conjugate to the cells, tissues or organs.
[0036] Pharmaceuticals, food supplements or dietary supplements often contain compounds and/or other ingredients derived from a natural source or from a synthetic source. The natural or synthetic ingredient may be an active ingredient that provides a beneficial effect or may be an inactive ingredient.
[0037] Inactive ingredients, often termed excipients, are typically present within a pharmaceutical or a food or dietary supplement formulation. The choice of excipient or excipients in a formulation is dependent upon whether the active ingredients are to be delivered in a tablet form, a capsule form, in a liquid form or the manufacturing process.
[0038] The active or inactive ingredient may be a compound considered as “Generally Regarded As Safe” (GRAS) for human or animal consumption.
[0039] Excipients may be derived from a natural source or from a synthetic source. Excipients have a wide range of physical or chemical properties that are dependent on their structure. Excipient properties include but are not limited to anti-adhesion, binding, bulking, providing a protective or enteric coating, aiding dissolution or disintegration, providing a colouring, a flavouring or a sweetening effect, providing a flow or glidant effect, solvation, a sorbent effect or a lubricating effect that is beneficial in formulation, manufacturability or the delivery of the active ingredients.
[0040] An example of the composition according to the invention is described below and contains both active ingredients and excipient ingredients that are common within pharmaceuticals and food or dietary supplements:
[0041] Active Ingredients:
TABLE-US-00001 Vitamin D (CAS No: 69-97-0) 25 micrograms (1000 IU or 25 ug) Sodium Butyrate 300 milligrams (mg) (CAS No: 156-54-7)
[0042] Excipients/Inactive Ingredients:
TABLE-US-00002 Microcrystalline Cellulose 350 milligrams (mg) (CAS No: 9004-34-6) Calcium Diphosphate (CAS no: 7758-87-4) 300 milligrams (mg) Silica SiO2 (CAS No: 7631-86-9) 20 milligrams (mg) Magnesium Stearate (CAS No: 557-04-0) 30 milligrams (mg)
[0043] The above example formulation is for a single, solid dose to be given orally.
[0044] Those skilled in the art will understand the benefit in varying the ratio of the ingredients within the above example formulation to enable volume manufacturing of tablets or capsules for human or animal consumption.
[0045] In another embodiment, the composition may be prepared comprising sodium butyrate as an active ingredient and the excipients/inactive ingredients microcrystalline cellulose, calcium diphosphate, silica SiO.sub.2 and magnesium stearate in the amounts as mentioned above.
[0046] With reference to
[0047] The leukocyte cells were incubated for a period of time to allow them to release proteins into the surrounding cell culture media (referred to as ‘conditioned media’). The conditioned media was then incubated with HRV1B Rhinovirus. The leukocyte cells were incubated with a solution comprising 0.5 mM sodium butyrate, a solution comprising 0.5 mM Vitamin D, and with a solution comprising both 0.5 mM sodium butyrate and 0.5 mM Vitamin D.
[0048] The results shown in
[0049] The data shown is an average of n=3 independent biological replicates (the titration is an average of ten fold reductions quantified over the three replicates).
[0050] Sodium butyrate and Vitamin D have effects on different intracellular mediators and/or signalling molecules in order to provide an effective response to viral infection. Thus, the provision of a composition comprising both sodium butyrate and Vitamin D would be advantageous since some individuals may be more responsive, in the context of their innate immunity, to either sodium butyrate or Vitamin D. Thus, administering a composition comprising both sodium butyrate and Vitamin D would provide an effective reduction in viral infection in a broader range of people.
[0051] Butyrate has been shown to increase cathelicidin production (Schauber et al, Gut 2003, 52(5), 735-741 and Hase et al, Infect Immun 2002, 70 (2), 953-963).
[0052] With reference to the present invention, it is understood that the sodium butyrate reduces the level of Rhinovirus titre through the stimulation of cathelicidins.
[0053] In addition, downregulation of inflammation in the context of viral infection can be an additional beneficial outcome since in Rhinovirus infection, much of the symptomology can be attributed to virus induced inflammation (Greenberg, Arch Int Med, 2003 163(3), 278-284). It has been shown in mouse models of influenza infection that exogenous LL-37 (a human member of the cathelicidin family) can decrease inflammation (Barlow et al, PLos One, 2011, 6(10)), thus resulting in enhanced survival rates. It has also been demonstrated that exogenous LL-37 can reduce Rhinovirus induced inflammatory cytokine release in cell models (Casanova et al, Front Immunol 2020, 11 (85).
[0054] With reference to the present invention, it is understood that sodium butyrate can reduce inflammation caused by viral infection through a reduction in NFkappa B signalling which would be of benefit for relief of the symptoms of Rhinovirus infection.