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Publication numberUS20070039615 A1
Publication typeApplication
Application numberUS 11/459,798
Publication dateFeb 22, 2007
Filing dateJul 25, 2006
Priority dateNov 8, 1999
Also published asUS8398580, US20100104665
Publication number11459798, 459798, US 2007/0039615 A1, US 2007/039615 A1, US 20070039615 A1, US 20070039615A1, US 2007039615 A1, US 2007039615A1, US-A1-20070039615, US-A1-2007039615, US2007/0039615A1, US2007/039615A1, US20070039615 A1, US20070039615A1, US2007039615 A1, US2007039615A1
InventorsJulia Rasor, Ned Rasor, Gerard Pereira
Original AssigneeCapnia, Incorporated
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Methods and apparatus for treating rhinitis
US 20070039615 A1
Abstract
Apparatus and methods deliver treatment agents simultaneously with capnic gases. The capnic gases can enhance the effectiveness of the treatment agent for treating rhinitis, lower the dosage of drug or concentration of agent necessary to achieve a therapeutic result, or both. Exemplary capnic gases include carbon dioxide, nitric oxide, nitrous oxide, and dilute acid gases.
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Claims(36)
1. A method for treating a patient, said method comprising:
administering a treatment agent selected to treat rhinitis to the patient; and
delivering a capnic gas to a nasal, oral, auricular, or ocular membrane of the patient;
wherein the systemic treatment agent and capnic gas are administered and delivered simultaneously.
2. A method as in claim 1, wherein the treatment agent is selected from the group consisting of antihistamines, corticosteroids, leukotriene receptor antagonists, mast cell stabilizers, and decongestants (e.g., alpha-adrenergic agonists).
3. A method as in claim 2, wherein the treatment agent comprises an antihistamine.
4. A method as in claim 2, wherein the treatment agent comprises an H1 receptor antagonist selected from the group consisting of fexofenadine, cetirizine, loratidine, desloratadine, and azelastine.
5. A method as in claim 2, wherein the treatment agent comprises a corticosteroid selected from the group consisting of fluticasone, mometasone, budesonide, triamcinolone, and flunisolide.
6. A method as in claim 2, wherein the treatment agent comprises montelukast, a leukotriene receptor antagonist.
7. A method as in claim 2, wherein the treatment agent comprises ipratropium, an anticholonergic agent.
8. A method as in claim 2, wherein the treatment agent comprises cromolyn, a mast cell stabilizer.
9. A method as in claim 2, wherein the treatment agent comprises a decongestant selected from the group consisting of oxymetazoline and pseudoephedrine.
10. A method as in claim 2, wherein the treatment agent comprises an alpha-adrenergic agonist.
11. A method as in claim 1, wherein the capnic gas is delivered to a nasal or oral mucosa while the patient refrains from inhaling the capnic gas.
12. A method as in claim 11, wherein the capnic gas is infused through a nostril and exits through a nostril and/or the mouth.
13. A method as in claim 11, wherein the capnic gas is infused through the mouth and exits through at least one nostril and/or the mouth.
14. A method as in any one of claims 11 to 13, wherein the capnic gas comprises carbon dioxide at a concentration of at least 50% by volume and is delivered at a controlled flow rate in the range from 0.5 cc/sec to 30 cc/sec.
15. A method as in claim 1, wherein the gas is selected from the group consisting of carbon dioxide, nitric oxide, nitrous oxide, and dilute acid gases.
16. A method as in claim 15, wherein the gas comprises carbon dioxide.
17. A method as in claim 16, wherein the carbon dioxide is present at a concentration of at least 50% by volume.
18. A method as in claim 17, wherein the carbon dioxide is substantially pure.
19. A method for treating a patient for rhinitis, said method comprising:
administering a treatment agent selected to treat rhinitis in the patient; and
delivering a capnic gas to a nasal, oral, auricular, or optical membrane of the patient;
wherein the rhinitis medication and the capnic gas are administered and delivered within sixty minutes of each other.
20. A method as in claim 19, wherein the treatment agent is selected from the group consisting of antihistamines, corticosteroids, leukotriene receptor antagonists, mast cell stabilizers, and decongestants.
21. A method as in claim 20, wherein the treatment agent comprises an antihistamine.
22. A method as in claim 20, wherein the treatment agent comprises an H1 receptor antagonist selected from the group consisting of fexofenadine, cetirizine, loratidine, desloratadine, and azelastine.
23. A method as in claim 20, wherein the treatment agent comprises a corticosteroid selected from the group consisting of fluticasone, mometasone, budesonide, triamcinolone, and flunisolide.
24. A method as in claim 20, wherein the treatment agent comprises montelukast, a leukotriene receptor antagonist.
25. A method as in claim 20, wherein the treatment agent comprises ipratropium, an anticholonergic agent.
26. A method as in claim 20, wherein the systemic treatment gent comprises cromolyn, a mast cell stabilizer.
27. A method as in claim 20, wherein the treatment agent comprises a decongestant selected from the group consisting of oxymetazoline and pseudoephedrine.
28. A method as in claim 20, wherein the treatment agent comprises an alpha-adrenergic agonist.
29. A method as in claim 19, wherein the capnic gas is delivered to a nasal or oral mucosa while the patient refrains from inhaling the capnic gas.
30. A method as in claim 29, wherein the capnic gas is infused through a nostril and exits through a nostril and/or the mouth.
31. A method as in claim 29, wherein the capnic gas is infused through the mouth and exits through at least one nostril and/or the mouth.
32. A method as in claim 29, wherein the capnic gas comprises carbon dioxide at a concentration of at least 50% by volume and is delivered at a controlled flow rate in the range from 0.5 cc/sec to 30 cc/sec.
33. A method as in claim 19, wherein the capnic gas is selected from the group consisting of carbon dioxide, nitric oxide, nitrous oxide, and dilute acid gases.
34. A method as in claim 33, wherein the gas comprises carbon dioxide.
35. A method as in claim 34, wherein the carbon dioxide is present at a concentration of at least 50% by volume.
36. A method as in claim 35, wherein the carbon dioxide is substantially pure.
Description
CROSS-REFERENCES TO RELATED APPLICATIONS

This application is a continuation-in-part of U.S. application Ser. No. 11/192,852 (Attorney Docket No. 020017-000320US), filed Jul. 29, 2005, which was a continuation-in-part of U.S. application Ser. No. 09/708,186 (Attorney Docket No. 020017-000310US), filed Nov. 7, 2000 (now U.S. Pat. No. 6,959,708), which claimed the benefit of U.S. Provisional Patent Application Nos. 60/185,495, filed on Feb. 28, 2000 60/164,125, filed on Nov. 8, 1999, each of which is incorporated by reference herein.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to drug delivery. More particularly, the present invention relates to methods and apparatus for delivering agents to mucosal and other tissue surfaces, in the presence of capnic gases, particularly for the treatment of rhinitis.

Drug delivery to mucosal surfaces, such as the mucosa of the nose, is well known. While in some cases drugs delivered to the nose and other mucosal surfaces are intended to have local effect, more often such transmucosal drug delivery is intended for systemic administration. In either case, penetration of the drug into or through the mucosa is limited by the ability of the particular drug to pass into or through the mucosal cell structure. Such resistance from the mucosal cell structure can result in slowing of the delivery, the need to use higher dosages of the drug, or in the case of larger molecules, the inability to deliver via a nasal or other mucosal route.

A walk through the cold and allergy section of any pharmacy quickly reveals that there is wide spread interest in remedies for relieving symptoms commonly associated with allergies, colds, asthma, and other common ailments which have symptoms of rhinitis e.g., runny noses and watery eyes. The commonly available therapies include oral medicines, nasal sprays, oral inhalers, nasal inhalers, eye drops, and nose drops, and probably other devices and approaches that have been developed over the years. Still more possible therapies are available from the pharmacy with a prescription from a patient's doctor (e.g., injectables, inhalables). Despite the very large number of therapies which are available, no one therapy meets all patient needs, and many of the therapies suffer from very significant shortcomings. For example, present day therapies are slow-acting, may have numerous adverse side effects (e.g., drowsiness, rebound congestion from decongestant overuse, dizziness, sedation, addiction, and numerous others), have low efficacy, and are contraindicated for a large portion of patients (e.g., those with hypertension, coronary artery disease, cerebrovascular disease, peptic ulcers, pregnancy, concurrent medications that would interact, children, elderly, and others). Suffice it to say that there is a continuing interest in providing improved methods and apparatus for treating such common symptoms and ailments.

Very recently, the use of carbon dioxide and other capnic gases alone and in combination with other gases has been proposed for the treatment of rhinitis and other conditions. The carbon dioxide is preferably delivered to nasal or other mucosa without inhalation. It is believed that the carbon dioxide may cause an intracellular acidosis which inhibits the release of calcitonin gene-related peptide (CGRP) and other neuropeptides which in turn reduces nasal symptoms of rhinitis. It has also been found that the onset of relief with carbon dioxide is usually much more rapid than that achieved with antihistamines, intranasal corticosteroids, leukotriene antagonists, and other drug therapies.

Despite the promise of conventional drug therapies and the newer delivery of capnic gases, neither therapy is effective in all individuals and neither therapy is entirely effective in relieving rhinitis and associated symptoms in all circumstances. It would thus be desirable to provide improved methods and systems for treating rhinitis. In particular, it would be desirable to provide treatments which are more effective, more rapid, more long-lasting, and/or which have other benefits when compared to the administration of either known rhinitis drugs or capnic gases alone.

2. Description of Background Art

Inhalation devices, systems and methods for delivering carbon dioxide and other gases and aerosols to patients, with and without co-delivery of a drug are described in U.S. Pat. Nos. 3,776,227; 3,513,843; 3,974,830; 4,137,914; 4,554,916; 5,262,180; 5,485,827; 5,570,683, 6,581,539; and 6,652,479. While some methods and devices provide for co-delivery of a drug and carbon dioxide or other gases, the purpose is usually not potentiation. For example, carbon dioxide may be used as a safe propellant, as shown in Wetterlin, U.S. Pat. No. 4,137,914. See also copending applications No. 09/614,389 (Attorney Docket No. 020017-000110US); No. 10/666,947 (Attorney Docket No. 020017-000420US); and No. 10/666,562 (Attorney Docket No. 020017-000430US), the full disclosures of which are incorporated herein by reference.

Additional background art may be found in the following references: Guyton A C, Hall J E. Textbook of Medical Physiology. Ninth Ed., W.B. Saunders Co., Philadelphia, 1996; Tang A, Rayner M, Nadel J. “Effect of C0 2 on serotonin-induced contraction of isolated smooth muscle,” Clin Research 20:243, 1972; Qi S, Yang Z, He B. “An experimental study of reversed pulmonary hypertension with inhaled nitric oxide on smoke inhalation injury,” Chung Hua Wai Ko Tsa Chih 35(1):56-8, January 1997; Loh E, Lankford E B, Polidori D J, Doering-Lubit E B, Hanson C W, Acker M A. “Cardiovascular effects of inhaled nitric oxide in a canine model of cardiomyopathy,” Ann Thorac Surg 67(5): 13 80-5, May 1999; Pagano D, Townend J N, Horton R, Smith C, Clutton-Brock T, Bonser R S. “A comparison of inhaled nitric oxide with intravenous vasodilators in the assessment of pulmonary haemodynamics prior to cardiac transplantation,” Eur J Cardiothorac Surg 10(12):1120-6, 1996; and Sterling G, et al. “Effect of CO2 and pH on bronchoconstriction caused by serotonin vs. acetylcholine,” J of Appl Physiology, vol. 22, 1972.

BRIEF SUMMARY OF THE INVENTION

The present invention provides methods and apparatus for treating patients, particularly patients suffering or at risk of suffering from rhinitis, by administering a treatment agent to the patient and simultaneously delivering a capnic gas to a nasal, oral, auricular, or ocular membrane of the patient. By “simultaneously,” it is meant that the treatment agent will be administered and the capnic gas delivered at the same time or within a very short time of each other, typically within 60 minutes, preferably within 30 minutes, and more preferably within 10 minutes. In some instances, it may be desirable to deliver the treatment agent together with the capnic gas, e.g., where the capnic gas can act as a carrier for the treatment agent. It will be more common to deliver the treatment agent separately in a separate dosage form, such as any of the dosage forms which are commonly available for the particular treatment agents described below. While the treatment agent will often be delivered systemically, in other cases it may be delivered orally to the target mucosa and have a local effect in the mucosal tissue.

In preferred protocols, at the onset of a rhinitis attack, the patient would take a dose of the treatment agent and substantially simultaneously initiate delivery of the capnic gas to the target membrane. The capnic gas would provide a rapid onset of action, possibly by inhibiting the release of CGRP as described above, in order to interrupt or delay progression of the rhinitis attack. At the same time, the treatment agent would begin to function by its particular mode of action. The patient would experience a more effective treatment in one of several ways. As the capnic gas would at least slow the progression of the rhinitis attack, the symptoms would be less intense by the time the treatment agent becomes effective. The magnitude of congestion, runny nose, watery eyes, and associated symptoms experienced by the patient should be lessened at all points during the treatment. In other cases, the patient might benefit by reducing the dosage of the treatment agent and thereby reducing side effects.

Rhinitis is the medical term describing irritation and inflammation principally of the nose. Symptoms include a runny nose, sneezing, congestion and irritation in the nose, eyes, throat and ears. Rhinitis is related to and often occurs together with other disorders such as asthma and sinusitis. It is chronic or acute inflammation of the mucous membrane of the nose due to viruses, bacteria or irritants. The inflammation results in excessive mucous production producing a runny nose, nasal congestion and postnasal drip.

Exemplary systemic treatment agents useful in the methods of the present invention include antihistamines; Hi receptor antagonists, such as fexofenadine, cetirizine, loratidine, desloratadine, and azelastine; corticosteroids, such as fluticasone, mometasone, budesonide, triamcinolone, and flunisolide; leukotriene receptor antagonists, such as montelukast; anticholonergics, such as ipratropium; mast cell stabilizers, such as cromolyn; decongestants, such as oxymetazoline, pseudoephedrine and other alpha-adrenergic agonists.

The treatment agents may be delivered in any conventional form, including oral dosage forms (tablets, gels, capsules, and the like), intranasal forms (in which case they could optionally be combined with delivery of the capnic gases), forms intended for pulmonary delivery, injectable forms, and topical forms (for transcutaneous delivery).

Preferred capnic treatment gases include carbon dioxide, nitric oxide, nitrous oxide, and dilute acid gases, such as dilute hydrochloric acid and the like. Particularly preferred are carbon dioxide gases having a relatively high concentration, typically greater than 10% by volume, usually greater than 20% by volume, and preferably greater than 25% by volume and often being as great as 80% by volume, 90% by volume, and in many instances being substantially pure. The capnic gases may be used in combinations of one or more adjuvant gases and/or may be combined with physiologically inert gases such as nitrogen, to control concentration of the capnic gases.

The capnic gas is delivered to a nasal, oral, auricular, or ocular membrane of the patient, typically using a hand-held or other dispenser. Preferably, the capnic gas will be delivered to a nasal or oral mucosa, while the patient refrains from inhaling the capnic gas. In the exemplary embodiments, the capnic gas is infused through a nostril and exits through a nostril and/or the mouth. The patient will refrain from inhaling, typically by holding the velum in the throat closed, while the capnic gas is infused. In other instances, the capnic gas will be infused through the mouth and be allowed to exit through at least one nostril, usually both nostrils. In those instances, the patient will also refrain from inhaling the gas.

The capnic gases will usually be delivered using a dispenser. Typically, the dispenser includes a pressurized source of the capnic gas and a valve assembly for releasing the gas at a controlled flow rate, typically in the range from 0.5 cc/sec to 30 cc/sec in the case of high concentration of carbon dioxide. Optionally, the treatment agent may be dissolved or suspended in the pressurized capnic gas for simultaneous delivery. Alternatively, the treatment agent may be delivered simultaneously from a separate receptacle, either through the same or a different delivery path. Often, the capnic gas and the treatment agent, even when stored in separate receptacles, will be delivered through a common conduit and nozzle to allow for both simultaneous and sequential delivery.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 illustrates an exemplary capnic gas infusion device, illustrating a charge/dose and dose rate adjustment features.

FIG. 2 is a schematic illustration of a delivery system incorporating separate receptacles for the capnic and the treatment agent, where the receptacles are joined through valves into a common delivery conduit.

FIGS. 3A-3E show application of the capnic gas optionally in combination with the treatment agent to the nose, mouth, both nostrils, eye, and ear, using a gas dispenser according to the present invention.

DETAILED DESCRIPTION OF THE INVENTION

An exemplary carbon dioxide dispenser 100 comprising a carbon dioxide cartridge 101 is illustrated in FIG. 1. The embodiment of FIG. 1 is described in greater detail in parent application Ser. No. 09/708,186, now U.S. Pat. No. 6,959,708, the full disclosure of which has previously been incorporated herein by reference. A user delivers a dose of carbon dioxide or other treatment gas, referred to generally as “capnic gases” (optionally carrying the systemic treatment agent to be delivered) by applying the top of the dispenser 608 to the user's nose or mouth and pushing a button 600 which releases an internal mechanism to allow the CO2 to flow from the top of the dispenser 608. The internal mechanism will lower the pressure of CO2 in the cartridge and will control the flow rate within suitable ranges, typically from 0.5 to 30 cc/sec. The flow rate may be maintained for a suitable time period, typically at least 2 seconds when suffusing the nasal and sinus passages. The device is cocked by rotation as shown by arrow 602 and pushing the button 600 to deliver the dose by an automatic counter-rotation. The user may select the specific carbon dioxide flow rate by setting at a set screw through aperture 609.

The dispenser 100 of FIG. 1 may be used to deliver any of the capnic gases in accordance with the principles of the present invention. The capnic gases may be delivered with or without the systemic treatment agent incorporated in the canister 101. In cases where the capnic gas is to be delivered by itself, at some suitable concentration, the systemic treatment agent will have to be delivered systemically in some other manner. The systemic treatment agent could be delivered in any of the conventional dosage forms described above or could be delivered to the target mucosa by suffusion or infusion, by placing a liquid, powder, or the like over the tissue surface, by introducing a vapor, mist, or the like using conventional drug delivery vapor sources and misters, or the like.

FIG. 2 is a schematic illustration showing a system for simultaneous or closely separated sequential delivery of the capnic gas and systemic treatment agent. The capnic gas is held in a separate cartridge or other container 202 while the systemic treatment agent is held in a cartridge or other container 204. Both the gas and the systemic treatment agent will be in a gaseous, vapor, mist, or other flowable form which permits them to pass through associated valves 206 and 208 respectively, and thereafter through a conduit 210 which receives flow from both valves. The valves will be suitable for controlling both flow rate and pressure of the capnic gas and the systemic treatment agent. It will be appreciated that more complex delivery systems can be provided including flow rate measurement, feedback control, temperature control, timers, and the like.

Referring now to FIGS. 3A to 3E, a variety of ways for effecting mucosal infusion with the capnic gas, optionally combined with the systemic treatment agent, are illustrated. The capnic gas is preferably infused at a flow rate in a range from 0.5 cc/sec to 30 cc/sec, depending on the tolerance of the individual being treated. In some instances, the selected drug or other systemic treatment agent can be delivered separately by suffusion, infusion, misting, the application of powder, or the like. As shown in FIG. 3A-B, the individual P infuses oral and nasal mucous membranes by placing the source of low flow rate CO2 (or other mixed gas) or other appropriately physiologically active gas or vapor in or around a facial orifice, such as the mouth or nostril, while substantially inhibiting the flow of the CO2 into the trachea and lungs by limiting inhalation of the CO2. If the mouth is infused the gas is allowed to exit from the nostrils. Alternatively, one or both nostrils may be infused either by using the dispenser head shown in FIG. 3B or by use of a cup or similar device that covers both nostrils as shown in FIG. 3E. The gas is allowed to flow from a remaining open orifice, i.e., either the mouth, the uninfused nostril, or both as appropriate. Completely holding the breath is not necessary to substantially prevent inhalation of the CO2. With practice, it is possible for the individual to breathe through an uninfused orifice. For example, if one nostril is infused and the gas is allowed to exit though the other nostril, it is possible for the individual to breathe through the mouth without substantial inhalation of the infused gas. The eye or eyes may also be infused using a cup as shown in FIG. 3C or merely by holding a hand over the eye and releasing the gas between the hand and the eye. Persons of ordinary skill in the art will appreciate that a double cup could be developed to infuse both eyes simultaneously, and similarly appropriate heads could be developed to infuse the mouth and one nostril. The ear or ears may also be infused as shown in FIG. 3D. Note that a similar process may be used with the first embodiment to infuse a mixture of a drug and gas into various facial orifices.

Infusion can be continued to the limit of tolerance or until the desired potentiation effect is realized. Since most individuals develop a temporary increased tolerance after extended applications or repeated applications, it may be possible and desirable to increase the duration of additional infusions after a few applications when all applications occur within a short time of each other, i.e., approximately 1 to 20 minutes between each application.

While the above is a complete description of the preferred embodiments of the invention, various alternatives, modifications, and equivalents may be used. Therefore, the above description should not be taken as limiting the scope of the invention which is defined by the appended claims.

Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US7827986Sep 21, 2006Nov 9, 2010Capnia, Inc.Methods for treating jaw pain
US7836883Jul 10, 2006Nov 23, 2010Capnia, Inc.Methods for treating rhinitis and conjunctivitis
US7845347Jul 10, 2006Dec 7, 2010Capnia, Inc.Methods for treating headaches
US7845348Jul 10, 2006Dec 7, 2010Capnia, Inc.Methods for treating trigeminal neuralgia
US8096968Feb 18, 2010Jan 17, 2012Capnia, Inc.Methods and apparatus for the enhanced delivery of physiologic agents to tissue surfaces
US8398580Dec 30, 2009Mar 19, 2013Capnia, Inc.Methods and apparatus for treating rhinitis
US8464711Nov 1, 2010Jun 18, 2013Capnia, Inc.Methods for treating headaches
US8763604Nov 26, 2012Jul 1, 2014Capnia, Inc.Methods for treating allergy
Classifications
U.S. Classification128/200.24
International ClassificationA62B7/00
Cooperative ClassificationA61M15/0041, A61H33/14, A61K33/00, A61M37/00, A61H2033/145, A61M15/0065, A61K45/06, A61M15/009, A61M2202/0225, A61M2202/064
European ClassificationA61H33/14, A61M15/00P, A61M37/00, A61K45/06, A61K33/00
Legal Events
DateCodeEventDescription
May 19, 2010ASAssignment
Owner name: CAPNIA, INC.,CALIFORNIA
Free format text: CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE NAME AND TO UPDATE THE ASSIGNEE ADDRESS PREVIOUSLY RECORDED ON REEL 018492 FRAME 0072. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNEE NAME IS CAPNIA, INC. AND THE ASSIGNEE ADDRESS IS 2445 FABER PLACE, SUITE 250, PALO ALTO, CA 94303;ASSIGNORS:RASOR, JULIA S.;RASOR, NED S.;PEREIRA, GERARD F.;SIGNED BETWEEN 20060821 AND 20061102;US-ASSIGNMENT DATABASE UPDATED:20100520;REEL/FRAME:24412/262
Free format text: CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE NAME AND TO UPDATE THE ASSIGNEE ADDRESS PREVIOUSLY RECORDED ON REEL 018492 FRAME 0072. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNEE NAME IS CAPNIA, INC. AND THE ASSIGNEE ADDRESS IS 2445 FABER PLACE, SUITE 250, PALO ALTO, CA 94303;ASSIGNORS:RASOR, JULIA S.;RASOR, NED S.;PEREIRA, GERARD F.;SIGNING DATES FROM 20060821 TO 20061102;REEL/FRAME:024412/0262
Nov 7, 2006ASAssignment
Owner name: CAPNIA, INCORPORATED, CALIFORNIA
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:RASOR, JULIA S.;RASOR, NED S.;PEREIRA, GERARD F.;REEL/FRAME:018492/0072;SIGNING DATES FROM 20060821 TO 20061102