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AssigneeAobiome LLC
InventorsTodd Krueger, David R. Whitlock, Lauren Nicole Ambrogio, Larry Weiss
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A method of treating diaper rash in a subject is provided. A method of treating athlete's foot in a subject is provided. A method of treating contact dermatitis in a subject is provided. A method of treating perspiration and body odor in a subject is provided. The method comprises administering an effective amount of a preparation comprising ammonia oxidizing microorganisms to the subject, thereby treating the diaper rash, athlete's foot, contact dermatitis, or perspiration and body odor. Related preparations, kits, and devices are also provided.
A method of treating diaper rash in a subject, comprising:
The method of any of the preceding claims, wherein the diaper rash is associated with irritant dermatitis, candida dermatitis, allergic dermatitis, fungal dermatitis, or bacterial dermatitis.
The method of any of the preceding claims, wherein treating the diaper rash comprises reducing dermatitis in the genital region, thigh, lower abdomen, and/or buttock of the subject.
The method of any of the preceding claims, wherein treating the diaper rash reduces the incidence of at least one of:
The method of any of the preceding claims, wherein the subject has a mild diaper rash prior to treatment.
The method of any of the preceding claims, wherein the subject has a moderate diaper rash prior to treatment.
The method of any of the preceding claims, wherein the subject has a severe diaper rash prior to treatment.
The method of any of the preceding claims, wherein the subject wears a diaper.
The method of any of the preceding claims, wherein the subject is a newborn, infant, or toddler.
The method of any of the preceding claims, wherein the subject is a child or adolescent.
The method of any of the preceding claims, wherein the subject is an adult or senior.
The method of any of the preceding claims, wherein the subject has sensitive skin and/or a history of diaper rash.
The method of any of the preceding claims, wherein the preparation is administered for prevention of diaper rash.
The method of any of the preceding claims, wherein the preparation is administered prior to onset of the diaper rash.
The method of any of the preceding claims, wherein the preparation is administered during incidence of the diaper rash.
The method of any of the preceding claims, wherein the preparation is administered subsequent to relief of the diaper rash.
The method of any of the preceding claims, wherein the preparation is administered in response to a diaper rash symptom, trigger or warning sign, e.g. family history, diaper use, skin irritation, allergic reaction, or contact with urine and/or stool.
The method of any of the preceding claims, further comprising determining whether the subject is in need of treatment for diaper rash.
A method of treating athlete's foot in a subject, comprising:
The method of any of the preceding claims, wherein the athlete's foot is associated with Trichophyton mentagrophytes, Trichophyton rubrum, a toe web infection, a moccasin type infection, a vesicular type infection, or onychomycosis.
The method of any of the preceding claims, wherein treating the athlete's foot comprises reducing a fungal infection in the leg, foot, toe, and/or toe nail of the subject.
The method of any of the preceding claims, wherein treating the athlete's foot reduces the incidence of at least one of:
The method of any of the preceding claims, wherein the subject has a mild athlete's foot prior to treatment.
The method of any of the preceding claims, wherein the subject has a moderate athlete's foot prior to treatment.
The method of any of the preceding claims, wherein the subject has a severe athlete's foot prior to treatment.
The method of any of the preceding claims, wherein the subject has a history of fungal infections or an impaired immune system.
The method of any of the preceding claims, wherein the subject qualifies for chemotherapy, radiation therapy, an organ transplant, or an organ removal surgery.
The method of any of the preceding claims, wherein the preparation is administered prior to onset of the athlete's foot.
The method of any of the preceding claims, wherein the preparation is administered during incidence of the athlete's foot.
The method of any of the preceding claims, wherein the preparation is administered subsequent to relief of the athlete's foot.
The method of any of the preceding claims, wherein the preparation is administered in response to an athlete's foot symptom, trigger or warning sign, e.g. exposure to warm and/or damp climates, alcohol and/or drug use and/or withdrawal, exposure to chemotherapy and/or radiation therapy, use of poorly ventilated footwear, or use of public or shared showers and/or locker rooms.
The method of any of the preceding claims, further comprising determining whether the subject is in need of treatment for athlete's foot.
A method of treating perspiration in a subject, comprising:
The method of any of the preceding claims, wherein the perspiration is associated with focal hyperhidrosis or generalized hyperhidrosis.
The method of any of the preceding claims, wherein treating the perspiration comprises reducing perspiration on the hands, feet, armpits, thighs, genital region, buttock, back, chest, or abdomen of the subject.
The method of any of the preceding claims, wherein treating the perspiration reduces the incidence of at least one of:
The method of any of the preceding claims, wherein the subject has a mild condition of perspiration prior to treatment.
The method of any of the preceding claims, wherein the subject has a moderate condition of perspiration prior to treatment.
The method of any of the preceding claims, wherein the subject has a severe condition of perspiration, e.g., excessive perspiration, prior to treatment.
The method of any of the preceding claims, wherein the subject is exercising or in a hot environment.
The method of any of the preceding claims, wherein the subject has a history of perspiration.
The method of any of the preceding claims, wherein the preparation is administered prior to onset of the perspiration.
The method of any of the preceding claims, wherein the preparation is administered during incidence of the perspiration.
The method of any of the preceding claims, wherein the preparation is administered subsequent to relief of the perspiration.
The method of any of the preceding claims, wherein the preparation is administered in response to a perspiration symptom, trigger or warning sign, e.g. family history, body odor, body type, exercise, stress, anxiety, diet, or alcohol and/or drug use.
A method of treating body odor in a subject, comprising:
The method of any of the preceding claims, wherein the body odor is associated with perspiration, diet, alcohol use, drug use, or composition of skin flora e.g., Corynebacterium, Propionibacterium, Staphylococcus hominis, and Staphylococcus epidermis.
The method of any of the preceding claims, wherein treating the body odor comprises reducing perspiration on the hands, feet, armpits, thighs, genital region, buttock, back, chest, or abdomen of the subject.
The method of any of the preceding claims, wherein treating the body odor reduces the incidence of at least one of:
The method of any of the preceding claims, wherein the subject has a mild condition of body odor prior to treatment.
The method of any of the preceding claims, wherein the subject has a moderate condition of body odor prior to treatment.
The method of any of the preceding claims, wherein the subject has a severe condition of body odor prior to treatment.
The method of any of the preceding claims, wherein the subject is obese or overweight.
The method of any of the preceding claims, wherein the subject has a history of body odor.
The method of any of the preceding claims, wherein the preparation is administered prior to onset of the body odor.
The method of any of the preceding claims, wherein the preparation is administered during incidence of the body odor.
The method of any of the preceding claims, wherein the preparation is administered subsequent to relief of the body odor.
The method of any of the preceding claims, wherein the preparation is administered in response to a body odor symptom, trigger or warning sign, e.g. family history, perspiration, body type, exercise, stress, anxiety, diet, or alcohol and/or drug use.
The method of any of the preceding claims, further comprising determining whether the subject is in need of treatment for perspiration.
The method of any of the preceding claims, further comprising determining whether the subject is in need of treatment for body odor.
A method of treating contact dermatitis in a subject, comprising:
A method of treating occupational contact dermatitis or occupational dermatitis in a subject, comprising:
The method of any of the preceding claims, wherein the contact dermatitis is associated with a source of an irritant, a non-irritant, or an allergen.
The method of any of the preceding claims, wherein treating the contact dermatitis comprises at least one of:
The method of any of the preceding claims, wherein treating the contact dermatitis reduces the incidence of at least one of:
The method of any of the preceding claims, wherein the subject has mild contact dermatitis prior to treatment.
The method of any of the preceding claims, wherein the subject has moderate or severe contact dermatitis prior to treatment.
The method of any of the preceding claims, wherein the subject wears, e.g., routinely wears, latex gloves, makeup, jewelry, dermal adhesive, or products held with dermal adhesive, e.g., a bandage.
The method of any of the preceding claims, wherein the subject has sensitive skin and/or a history of contact dermatitis.
The method of any of the preceding claims, wherein the preparation is administered prior to onset of contact dermatitis.
The method of any of the preceding claims, wherein the preparation is administered during incidence of the contact dermatitis.
The method of any of the preceding claims, wherein the preparation is administered subsequent to relief of the contact dermatitis.
The method of any of the preceding claims, wherein the preparation is administered in response to a contact dermatitis symptom, trigger or warning sign, e.g. skin irritation, allergic reaction, or contact with soap, detergent, chemical, cosmetic, fragrance, or jewelry.
The method of any of the preceding claims, further comprising determining whether the subject is in need of treatment for contact dermatitis.
The method of any of the preceding claims, wherein the preparation is administered within 30, 60, 90, 120, 150, or 180 minutes of the subject waking from sleep.
The method of any of the preceding claims, wherein the preparation is administered within 30, 60, 90, 120, 150, or 180 minutes prior to the subject sleeping.
The method of any of the preceding claims, wherein the preparation is administered within 30, 60, 90, 120, 150, or 180 minutes of the subject eating.
The method of any of the preceding claims, wherein the preparation is administered 30, 60, 90, 120, 150, or 180 minutes before or after the subject cleanses or showers.
The method of any of the preceding claims, wherein the preparation is administered 30, 60, 90, 120, 150, or 180 minutes before or after application or removal of a diaper.
The method of any of the preceding claims, wherein the preparation is administered concurrently with application or removal of a diaper.
The method of any of the preceding claims, wherein the preparation is administered 30, 60, 90, 120, 150, or 180 minutes before or after application or removal of footwear.
The method of any of the preceding claims, wherein the preparation is administered concurrently with the application or removal of footwear.
The method of any of the preceding claims, wherein the preparation is administered 30, 60, 90, 120, 150, or 180 minutes before or after application or removal of a glove, jewelry, or makeup.
The method of any of the preceding claims, wherein the preparation is administered concurrently with the application or removal of a glove, jewelry, or makeup.
The method of any of the preceding claims, further comprising administering a second amount of the preparation to the subject.
The method of any of the preceding claims, wherein the preparation is administered topically.
The method of any of the preceding claims, wherein the preparation is administered to the body of the subject, e.g., to one or more of the face, neck, scalp, limb, hand, foot, back, buttock, torso, genitals, and chest of the subject.
The method of any of the preceding claims, wherein the preparation is administered to the body of the subject, e.g., to one or more of the face, neck, scalp, limb, hand, foot, back, buttock, torso, genitals, and chest of the subject.
The method of any of the preceding claims, wherein the preparation is administered to the body of the subject, e.g., to one or more of the face, neck, scalp, limb, hand, foot, back, buttock, torso, genitals, perineum, abdomen, and chest of the subject.
The method of any of the preceding claims, wherein the preparation is administered intranasally.
The method of any of the preceding claims, wherein the preparation is administered via inhalation.
The method of any of the preceding claims, wherein the preparation is administered as a spray, aerosol, or mist.
The method of any of the preceding claims, wherein the preparation is administered as part of a combination therapy.
The method of any of the preceding claims, further comprising administering a second treatment in combination with the preparation.
The method of any of the preceding claims, wherein the preparation is administered for a period of time prior to initiating the second treatment.
The method of any of the preceding claims, wherein the preparation is administered concurrently with the second treatment.
The method of any of the preceding claims, wherein the preparation is administered for a period of time subsequent to ceasing the second treatment.
The method of any of the preceding claims, wherein the preparation is administered in combination with an antifungal agent, a steroid, e.g., topical or oral steroid, e.g., hydrocortisone, or an anti-histamine.
The method of any of the preceding claims, wherein the preparation is administered in combination with a zinc oxide, petroleum, petrolatum, paraffin, dimethicone, or lanolin.
The method of any of the preceding claims, wherein the preparation is administered in combination with a steroid, e.g., topical or oral steroid, e.g., hydrocortisone, an anti-histamine, or aluminum subacetate.
The method of any of the preceding claims, wherein the preparation is administered in combination with an antifungal agent, e.g., ketoconazole, clotrimazole, miconazole, terbinafine, tolnaftate, butenafine, naftifine, fluconazole, or itraconazole, or an antibiotic agent.
The method of any of the preceding claims, wherein the preparation is administered in combination with an anti-itch lotion, cold compress, lanolin, sunscreen, moisturizer, barrier cream, or avobenzone.
The method of any of the preceding claims, wherein the preparation is administered in combination with a steroid, antibiotic, topical antiseptic, antihistamine, anesthetic, depigmenting agent, or antifungal agent.
The method of any of the preceding claims, wherein the preparation is administered in combination with an anti-anxiety or an antidepressant.
The method of any of the preceding claims, wherein the preparation is administered in combination with an antiperspirant (e.g., aluminum salt), a deodorant, iontophoresis therapy, botulinum toxin A, or an anticholinergic agent.
The method of any of the preceding claims, wherein the preparation is administered in conjunction with nitrite, nitrate, and/or NO, e.g., inhaled NO.
The method of any of the preceding claims, wherein the second treatment is administered orally, subcutaneously, intravenously, or intramuscularly.
The method of any of the preceding claims, wherein the subject has a therapeutic level of a second treatment.
The method of any of the preceding claims, wherein the effective amount is a therapeutically effective dose of AOM.
The method of any of the preceding claims, wherein the therapeutically effective dose of AOM is about or greater than about 1×103, 104, 105, 106, 107, 108, 109, 1010, 1011, 1012, 1013, or 1014 CFU.
The method of any of the preceding claims, wherein the preparation is administered as an analgesic.
The method of any of the preceding claims, wherein the preparation is administered as a prophylactic.
The method of any of the preceding claims, wherein the preparation is self-administered.
The method of any of the preceding claims, wherein the subject has an allergy, a fungal infection, e.g. yeast infection, a bacterial infection, e.g., a Staphylococcusaureus infection or a Streptococcus infection, a viral infection, or contact dermatitis.
The method of any of the preceding claims, wherein the subject has a fungal infection, diabetes, cancer, HIV/AIDS, an autoimmune disorder, or has had an organ surgically removed and/or transplanted (e.g., splenectomy).
The method of any of the preceding claims, wherein the subject has a profession that renders the subject prone to contact dermatitis.
The method of any of the preceding claims, wherein the subject has high stress, anxiety, diabetes, hyperthyroidism, Parkinson's disease, Rheumatoid arthritis, Lymphoma, Gout, an infection, is undergoing menopause, is obese or overweight, or is pregnant.
The method of any of the preceding claims, wherein the preparation is administered about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, or 24 times per day.
The method of any of the preceding claims, wherein the preparation is administered for about 1-3, 3-5, 5-7, 7-9, 5-10, 10-14, 12-18, 12-21, 21-28, 28-35, 35-42, 42-49, 49-56, 46-63, 63-70, 70-77, 77-84, or 84-91 days.
The method of any of the preceding claims, wherein the subject is female.
The method of any of the preceding claims, wherein the subject is male.
The method of any of the preceding claims, wherein the subject is characterized as one of the following ethnicity/race:
The method of any of the preceding claims, wherein the subject is of an age of less than 1, or between 1-5, 5-10, 10-20, 20-30, 30-40, 40-50, 50-60, or over 60 years.
The method of any of the preceding claims, wherein the subject is of an age of less than 1, or between 1-3 years.
The method of any of the preceding claims, wherein the subject is of an age between 50-60, 60-70, 70-80, 80-90, or over 90 years.
The method of any of the preceding claims, wherein the preparation comprises AOM in a buffer solution, e.g., an aqueous buffer solution.
The method of any of the preceding claims, wherein the buffer solution, e.g., aqueous buffer solution, comprises disodium phosphate and magnesium chloride, for example, 50 mM Na2HPO4 and 2 mM MgCl2 in water.
The method of any of the preceding claims, wherein the buffer solution e.g., aqueous buffer solution, consisting essentially of disodium phosphate and magnesium chloride, for example, 50 mM Na2HPO4 and 2 mM MgCl2 in water.
The method of any of the preceding claims, wherein the buffer solution, e.g., aqueous buffer solution, consists of disodium phosphate and magnesium chloride, for example, 50 mM Na2HPO4 and 2 mM MgCl2 in water.
The method of any of the preceding claims, wherein the preparation comprises at least one of ammonia, ammonium salts, and urea.
The method of any of the preceding claims, wherein the preparation comprises a controlled release material, e.g., slow release material.
The method of any of the preceding claims, wherein the preparation further comprises an excipient, e.g., a pharmaceutically acceptable excipient.
The method of any of the preceding claims, wherein the excipient is a surfactant.
The method of any of the preceding claims, wherein the preparation is administered before or after a surgical or diagnostic procedure.
The method of any of the preceding claims, wherein the preparation is administered before or after a procedure, e.g. a desensitization or dermatological procedure.
The method of any of the preceding claims, wherein the preparation is administered before or after application or removal of a diaper.
The method of any of the preceding claims, wherein the preparation is administered before or after application or removal of clothing, e.g., footwear.
The method of any of the preceding claims, wherein the preparation is administered before or after application or removal of clothing.
The method of any of the preceding claims, wherein the excipient comprises an anti-adherent, binder, coat, disintegrant, filler, flavor, color, lubricant, glidant, sorbent preservative, chelator, or sweetener.
The method of any of the preceding claims, wherein the preparation is substantially free of other organisms.
The method of any of the preceding claims, wherein the preparation is provided as a liquid, droplet, powder, solid, cream, lotion, gel, stick, aerosol, spray, mist, salve, wipe, or bandage.
The method of any of the preceding claims, wherein the preparation comprises a moisturizing agent, deodorizing agent, scent, colorant, insect repellant, cleansing agent, or UV-blocking agent.
The method of any of the preceding claims, wherein the preparation comprises between about 1×103 CFU/mL to about 1×1014 CFU/mL AOM.
The method of any of the preceding claims, wherein the preparation comprises between about 1×109 CFU/mL to about 10×109 CFU/mL AOM.
The method of any of the preceding claims, wherein the AOM comprise ammonia oxidizing bacteria (AOB).
The method of any of the preceding claims, wherein the AOM consist essentially of AOB.
The method of any of the preceding claims, wherein the AOM consist of AOB.
The method of any of the preceding claims, wherein the AOM comprise Nitrosomonas, Nitrosococcus, Nitrosospira, Nitrosocystis, Nitrosolobus, Nitrosovibrio, and combinations thereof.
The method of any of the preceding claims, wherein the AOM is Nitrosomonas eutropha (N. eutropha).
The method of any of the preceding claims, wherein the AOM is N. eutropha D23, having ATCC accession number PTA-121157.
The method of any of the preceding claims, wherein the AOM comprise ammonia oxidizing archaea (AOA).
The method of any of the preceding claims, wherein the AOM are capable of converting ammonia or ammonium to nitrite at a rate of at least about 1 pmol/min/mg protein, e.g., at least about 0.1 nmol/min/mg protein.
The method of any of the preceding claims, wherein the subject is relieved of the diaper rash in about 24 hours subsequent to treatment.
The method of any of the preceding claims, wherein the subject is recovered from the diaper rash in about 24 hours subsequent to treatment.
The method of any of the preceding claims, wherein the subject is relieved of the athlete's foot in about 24 hours subsequent to treatment.
The method of any of the preceding claims, wherein the subject is recovered from the athlete's foot in about 24 hours subsequent to treatment.
The method of any of the preceding claims, wherein the subject is relieved of the perspiration in about 24 hours subsequent to treatment.
The method of any of the preceding claims, wherein the subject is recovered from the perspiration in about 24 hours subsequent to treatment.
The method of any of the preceding claims, wherein the subject is relieved of the body odor in about 24 hours subsequent to treatment.
The method of any of the preceding claims, wherein the subject is recovered from the body odor in about 24 hours subsequent to treatment.
The method of any of the preceding claims, wherein the subject is relieved of or recovered from contact dermatitis in about 24 hours subsequent to treatment.
The method of any of the preceding claims, further comprising removing or eliminating the source of the irritant or allergen.
The method of any of the preceding claims, wherein a target percentage of administered AOM are transferred to the subject.
The method of any of the preceding claims, wherein the preparation is administered in conjunction with an anti-inflammatory agent.
The method of any of the preceding claims, wherein the preparation is administered in conjunction with a medical approach that treats, e.g., is approved to treat or is commonly used to treat diaper rash or a symptom of diaper rash.
The method of any of the preceding claims, wherein the preparation is administered in conjunction with a medical approach that treats, e.g., is approved to treat or is commonly used to treat athlete's foot or a symptom of athlete's foot.
The method of any of the preceding claims, wherein the preparation is administered in conjunction with a medical approach that treats, e.g., is approved to treat or is commonly used to treat perspiration or a symptom of perspiration.
The method of any of the preceding claims, wherein the preparation is administered in conjunction with a medical approach that treats, e.g., is approved to treat or is commonly used to treat body odor or a symptom of body odor.
The method of any of the preceding claims, wherein the preparation is administered in conjunction with a medical approach that treats, e.g., is approved to treat or is commonly used to treat contact dermatitis or a symptom of contact dermatitis.
The method of any of the preceding claims, wherein the subject has a disrupted microbiome.
The method of any of the preceding claims, wherein the preparation further comprises or is administered concurrently with a compound that promotes growth or metabolism of the AOM, NO production, and/or urease activity.
The method of any of the preceding claims, wherein a biome-friendly product is used in connection with the administered preparation comprising AOM.
The method of any of the preceding claims, wherein administering the effective amount of the preparation changes or alters a level of nitrite or NO in the subject, e.g. at a target tissue or in circulation.
The method of any of the preceding claims, wherein administering the effective amount of the preparation modulates a microbiome associated with the subject.
The method of any of the preceding claims, wherein the preparation is administered concurrently with a change of diaper.
The method of any of the preceding claims, wherein the preparation is administered concurrently with a change of garment, e.g., sock or footwear.
The method of any of the preceding claims, wherein the preparation is administered concurrently with a change of clothing.
The method of any of the preceding claims, wherein the preparation is administered concurrently with a change of glove.
The method of any of the preceding claims, wherein the preparation is administered in response to exposure to poison oak or poison ivy.
A preparation comprising AOM, as recited in any of the preceding claims, for the treatment of diaper rash in a subject.
A preparation comprising AOM, as recited in any of the preceding claims, for the treatment of athlete's foot in a subject.
A preparation comprising AOM, as recited in any of the preceding claims, for the treatment of perspiration in a subject.
A preparation comprising AOM, as recited in any of the preceding claims, for the treatment of body odor in a subject.
A preparation comprising AOM, as recited in any of the preceding claims, for the treatment of contact dermatitis in a subject.
The preparation of any of the preceding claims, wherein the preparation is packaged for single use.
The preparation of any of the preceding claims, wherein the preparation is packaged for multiple use.
The preparation of any of the preceding claims, wherein the preparation is packaged as a pretreated diaper.
The preparation of any of the preceding claims, wherein the preparation is packaged as a pretreated garment, e.g., footwear.
The preparation of any of the preceding claims, wherein the preparation is packaged as a pretreated garment.
The preparation of any of the preceding claims, wherein the preparation is packaged as a pretreated glove.
The preparation of any of the preceding claims, comprising AOM and other organisms, e.g., a community of organisms.
A device for administering a preparation comprising AOM, as recited in any of the preceding claims, to a subject for treatment.
The device for administering a preparation comprising AOM, as recited in any of the preceding claims, wherein the device is a diaper pretreated with the preparation.
The device for administering a preparation comprising AOM, as recited in any of the preceding claims, wherein the device is a garment, e.g., footwear, a sock, or a glove, pretreated with the preparation.
The device for administering a preparation comprising AOM, as recited in any of the preceding claims, wherein the device comprises a garment pretreated with the preparation.
A kit comprising a preparation comprising AOM as recited in any of the preceding claims.
Dependencies are inferred from the claim text.