CA2522294A1

CA2522294A1 - Formulations and methods for treating rhinosinusitis

Info

Publication number: CA2522294A1
Application number: CA002522294A
Authority: CA
Inventors: Imtiaz Chaudry
Original assignee: Individual
Current assignee: Mylan Specialty LP
Priority date: 2003-04-16
Filing date: 2004-03-29
Publication date: 2004-10-28
Anticipated expiration: 2024-03-29
Also published as: RU2005135333A; CA2522294C; US9180126B2; RU2410083C2; US20040209852A1; WO2004091576A1; JP4718445B2; US8663695B2; US20080058296A1; BRPI0409348B1; US8309061B2; KR101396262B1; MX364708B; EP1613282B1; US20120237559A1; PL377855A1; MXPA05011106A; BRPI0409348A; US20050180925A1; JP2006523631A

Abstract

The invention involves methods and formulations for treating or preventing rhinosinusitis, including fungus-induced rhinosinusitis in mammals. In one embodiment, the formulation of the present invention comprises a steroidal anti-inflammatory agent having a specific particle size distribution profile . The formulation may also comprise an antifungal agent, antibiotic or antivir al agent.

Description

FORMULATIONS AND METHODS FOR TREATING RHINOSINUSITIS
I. RELATED APPLICATIONS
The present application is a continuation-in-part of Application Serial Nos.
141414,682 and Application Serial No. 10/414,756. Both applications were filed April 16, 2003. Each application is incorporated herein by reference in its entirety.
II. FIELD OF THE INVENTION
The present invention relates to formulations and methods for treating rhinosinusitis in mammals (e.g., humans), including but not limited to fungus induced rhinosinusitis. . The formulations of the present invention comprise a steroidal agent, such as fluticasone or beclomethasone, wherein the steroidal agent has a specific particle size distribution profile. The formulations may also comprise an antibiotic, antifungal agent or an antiviral agent, or any combination thereof. While the formulations of the present invention may take any form, preferably they are provided as a sterile, aqueous suspension or solution which can be administered intranasally to the nasal-paranasal mucosa via spray pump. Also, the steroidal agent may be administered alone or in conjunction with an antifungal agent, antibiotic or antiviral agent.
III. BACKGROUND OF THE INVENTION
Rhinosinusitis is generally described as an inflammation of the nasal cavity andlor paranasal sinuses and involves the nasal mucosa. Chronic rhinosinusitis (CRS) is diagnosed when signs or symptoms of inflammation persist for 8-12 weeks or longer. It is estimated that one out of every seven Americans suffers from chronic rhinosinusitis (CRS}. Symptoms of CRS include nasal obstruction, loss of sense of smell, nasal or postnasal discharge, nasal congestion, and facial painlpressure (typically over the affected sinus area).
CRS impairs normal physical and social functioning, and patients with CRS
typically suffer from an overall poor quality of life. Moreover, CRS is often associated with other co-morbid conditions such as asthma, eczema and other media. Asthma is found in 20-35% ofpatients with CRS, and CRS is found in up to 75% ofmoderate-to severe asthmatics.
It is now known that rhinosinusitis may be caused by fungi found in mucus. It is believed that some persons have an immunologic response to certain fungi found in most, if not all, persons' mucus. This immunologic response causes activated white blood cells, eosinophils, to enter the mucus. The activated eosinophils release a major basic toxic protein into the mucus which attacks and kills the fungi, but damages the nose and sinus membranes as well.. The major basic protein also injures the epithelium, which allows bacteria to infect the tissues.
One type of fungus-induced rhinosinusitis is allergic fungus rhinosinusitis (AFS).
AFS is generally diagnosed by: (1) the presence of nasal polyps; (2) allergic mucin; (3) CRS evidenced by CT scan; (4) positive fungal culture or histology; and/or (5) allergy to fungi by history, skin prick test or serology., AFS often leads to or is associated with CRS.
Current treatments for fungus induced rhinosinusitis include antifungal medications to remove the antigenic burden. A topical or systenuc corticosteroid may also be prescribed to control inflammation of the mucosal tissue associated with CRS.
This inflammation is thought to contribute to tissue and bone destruction associated with

2 CRS. Recently, it has been discovered that steroidal anti-inflammatories such as fluticasone propionate (FP) and beclomethasone dipropionate (BDP) having a particular particle size distribution profile provide increased bioavailability, increased efficacy and/or prolonged therapeutic effect when administered intranasally.
CRS may also be characterized by or associated with a chronic bacterial infection of the sinuses (nasal-paranasal region) which is often superimposed upon a self perpetuating, eosinophii-rich inflammatory process in the sinuses. Currently, antibiotic therapy is indicated for up to six weeks or more for the treatment~and elimination of the bacterial infection associated with CRS.
IV. SUMMARY OF INVENTION
' The present invention relates generally to formulations and methods for treating rhinosinusitis in mammals (e.g., humans), including, but not limited to fungus-induced rhinosinusitis. In one embodiment, the formulations of the present invention comprise a steroid, alone or in combination with an antifungal agent or antibiotic. It is believed that treating the patient with an antifungal agent will sufficiently reduce the level of fungal organisms in the patient's mucus such that the one ore more of the symptoms of rhinosinusitis are prevented from developing or are lessened, or are prevented from worsening.
In an embodiment, the present formulations comprise about 4 mg to about 30 mg of the anti-fungal agent ~amphotericin ~. In an alternative embodiment, the formulation of the present invention comprises about 20 to about 70 mg of the anti-fungal agent fluconazole or itraconazole.

3 The present invention is also based on the realization that a patient or individual may have already developed one or more symptoms of rhinosinusitis, possibly CRS, when he or she first seeks the help of a physician or by the time that treatment is started.
Thus, it would also be beneficial to provide an anti-inflammatory steroid to the patient to treat inflammation of the mucosal tissue associated with rhinosinusitis, since such inflammation might lead to or contribute to tissue and bone destruction in the nasal-paranasal region.
It has recently been discovered that certain steroidal anti-inflammatories having a specific particle size distribution profile provide increased bioavailability, increased efficacy or prolonged therapeutic effect when administered intranasally. In one embodiment, the formulation of the present invention comprises about 25 to about 400 mcg of the steroidal anti-inflammatory agent, including but not limited to, fluticasone, or a pharmaceutically acceptable derivative thereof, having the following particle size distribution profile: about 10% of the drug substance particles have a particle size of about 0.90 microns; about than.25% of the drug substance particles have a particle size of less than 1.6 microns;.about 50% of the drug substance particles have a particle size of less than 3.2 microns; about 75% of the drug substance particles have a particle size of less than 6.10 microns; about 90% of the drug substance particles have a particle size of less than 10.0 microns.
In an alternative embodiment, the formulation of the present invention comprises about 0.2 to about 3 mg of the steroidal anti-inflammatory beclomethasone, or a pharmaceutically acceptable derivative thereof, having the following particle size distribution profile: about 10% of the drug substance particles have a particle size of

4 about 0.75 microns; about than 25% of the drug substance particles have a particle size of Iess than 1.5 microns; about 50% of the drug substance particles have a particle size of less than 2.0 microns; about 75% of the drug substance particles have a particle size of less than 3.5 microns; about 90% of the drug substance particles have a particle size of less than 5.0 microns; and, greater than 90% or about 100% of the drug substance particles have a particle size of less than 10 microns.
In many instances the fungus-induced rhinosinusitis may be accompanied by, or associated with, a bacterial infection of the nasal-paranasal mucosa. In one embodiment, the fonnulations of the present invention comprise an antibiotic. In an alternative embodiment, the present formulations comprise about 1 to about 800 mg of the antibiotic neomycin sulfate.
The formulations of the present invention may be provided in any form which directly contacts the formulation with the nasal-paranasal mucosa. In one embodiment, the present formulation is provided as a sterile aqueous solution or.
suspension. In an alternative embodiments the formulation is in a metered dose spray pump.
The.present invention also generally relates to methods for treating rhinosinusitis, including fungus-induced rhinosinusitis. In one alternative embodiment, an individual suffering from rhinosinusitis may be administered a steroidal agent of the, present invention alone, or in combination or conjunction with an anti-fungal agent, antibiotic or antiviral agent. For example, the steroidal agent may be administered separately from the anti-fungal agent or antibiotic, or each of these ingredients may be administered simultaneously (e.g., in a single formulation) or individually, concurrently, in tandem or subsequently relative to each other, or in any combination thereof.

Y. DETAILED DISCUSSION OF THE IIVYENTION
The present invention is directed to formulations for the treatment of one or more symptoms of rhinosinusitis in an individual, lZhinosinusitis occurs in the nasal paranasal region. Symptoms of rhinosinusitis include, without limitation, facial pain, pressure, and/or fullness; loss of smell; nasal obstruction or blockage; nasal or postnasal discharge;
rhinorrhea; hyposimia/ansomnia; fever; headaches; halitosis; fatigue; dental pain; cough;
and ear pain, pressure, and/or fullness. Upon examination, the presence of thick mucus or the visual identification of nasal or paranasal obstruction with mucus or polyps often indicates a rhinosinusitis condition.
Nasal polyps may also be associated with or indicative of rhinosinusitis.
Nasal polyps are outgrowths from the nasal-paranasal mucosa that are typically smooth, gelatinous, semitranslucent, round or pear shaped, and pale. In general, nasal polyps are located on the lateral wall of the nose, usually in the middle meatus or along the middle and superior tuxbinates. Most nasal polyps arise from the ethmoid sinus but some polyps originate in the maxillary sphenoid sinuses. The mass of a nasal.polyp is composed mainly of edematous fluid with sparse fibrous cells and a few mucous glands.
The surface epithelium of nasal and paranasal polyps generally reveals squamous metaplasia.
Eosinophils are usually present in polyps in moderate to large numbers, and it is now known that nasal polyp fluid contains greater than normal concentrations of IgA, IgE, IgG, and IgM antibodies as well as abnormally high concentrations of IL-5, a cytokine that contributes to eosinophil activation and survival.
It is understood that the scope of the invention is directed to the treatment of rhinosinusitis including, but.not limited to, any rhinosinusitis condition, including, but not limited to, acute, subacute, recurrent acute and chronic rhinosinusitis, which may be accompanied by, aggravated by, associated with or caused by (in whole or in part) fungi, viruses, or microorganisms in the mucosa. For example, rhinosinusitis may include fungus-induced rhinosinusitis caused by, for example, an immunologic response to mucosal fungi or other organism. In one alternative enibodiment, the fungus-induced rhinosinusitis is allergic fungal rhinosinusitis, or AFS.
Formulation In one alternative embodiment, the present invention is directed to formulations for the treatment of rhinosinusitis. In one embodiment, the formulations comprise a steroidal anti-inflammatory, alone or in combination with an antifungal agent, antibiotic or antiviral~ agent. As used herein, treatment means the prophylaxis, prevention or amelioration of one or more symptoms of, or associated with, rhinosinusitis, or any manner in which one or more of the symptoms of, or associated with, rhinosinusitis are beneficially altered or are prevented from worsening. . As used herein, amelioration means any lessening, whether permanent or temporary, lasting or transient, of one or more symptoms of rhinosinusitis, including but not limited to fungus-induced rhinosinusitis.
Antifun~al Aeent Antifungal agents for use herein include any agent effective in treating rhinosinusitis, including fungus-induced rhinosinusitis. Preferably, the antifungal agent of the present formulations reduces the presence of fungal organisms within mucus to a level such that the characteristic inflammatory responses and resulting damages associated with fungal induced rhinosinusitis are lessened, whether permanent or temporary, lasting or transient, stopped, treated, or prevented.
For example, in one alternative embodiment of the present invention, an antifungal agent for. use herein may include any agent that prevents the growth of or kills a fungal organism such as antifungal polyene macrolides, tetraene macrolides, pentaenic macrolides, fluorinated pyrimidines, imidazoles, triazoles, azoles, halogenated phenolic ethers, thiocarbamates, and allylamines, and other. In addition, antifungal agents can be agents that interpolate fungal cell wall components or act as sterol inhibitors. Specific antifungal agents within the scope of the invention include, without limitation, amphotericin Vii, flucytosine, ketoconazole, miconazole, itraconazole, fluconazole, griseofulvin, clotrimazole, econazole, terconazole, butoconazole, oxiconazole, sulconazole, saperconazole, voricona2ole, ciclopirox olamine, haloprogin, tolnaftate, naftifine, nystatin, natamycin, terbinafine hydrochloride, morpholines, butenafine undecylenic acid, Whitefield's ointment, propionic acid, and caprylic acid as well as those agents that can be identified as antifungal agents using methods well known in the art.
Preferably, the antifungal agent of the present formulations is amphotericin (3 or fluconazole.
It is noted that a particular patient may possess a fungal organism acting as the etiological agent that is resistant to a particular antifungal agent. In such a case, an embodiment of this invention involves treating that patient with an effective antifungal agent (e.g., an antifungal agent that prevents the growth of, or kills, the fungal organism acting as the etiological agent). Such fungal organisms acting as etiological agents can be identified using collection and culture methods known in the art.

In one alternative embodiment, the formulation of the present invention may comprise any mount of antifungal agent that reduces, prevents, or eliminates one or more symptoms of, or associated with, fungus-induced rhinosinusitis without producing significant toxicity. In one embodiment, an effective amount rnay be any amount greater than or equal to th.e minimum inhibitory concentration (MIC) fox a fungal organism or isolate present within a particular individual's mucus that does not induce significant toxicity to the individual upon administration. Some antifungal agents may have a relatively large concentration range that is effective while others may have a relatively narrow effective concentration range. In addition, the effective amount can vary depending upon the specific fungal organism or isolate since certain organisms and isolates are more or less susceptible to particular antifungal agents. Such effective amounts can be determined for individual antifungal agents using commonly available or easily ascertainable information involving antifungal effectiveness concentrations, animal.
toxicity concentrations, and tissue permeability rates.
For example, non-toxic antifungal agents typically can be directly or indirectly administered in any amount that exhibits antifungal activity within mucus. In addition, antifungal agents that do riot permeate mucosal epithelium typically can be directly administered to the mucus in any amount that exhibits antifungal activity within mucus.
Using the information provided herein, such effective amounts also can be determined by routine experimentation in vitro or in vivo. For example, a patient having a fungus-induced rhinosinusitis can receive direct administration of an antifungal agent in an amount close to the MIC calculated from in vitro analysis. If the patient fails to respond, then the amount can be increased by, for example, ten fold. After receiving this higher .

concentration, the patient can be monitored for both responsiveness to the treatment and toxicity symptoms, and adjustrnents made accordingly.
In one embodiment, the present formulations comprise about O.OI ng to about 1000 mg per kg of body weight of the mammal per administration of formulation, where the formulation is administered directly to the nasal-paranasal mucose.
Antifungal agent particularly suitable for administration are itraconazole, ketoconazole, or voriconazole.
The MIC values for voriconazole range from about 0.003 µg/mL to about 4 :mu.glniL
depending upon the specific fungal organism or isolate tested. For fluconazole, the MIC
values range from about 0.25 µg/mL to greater than about 64 µglmL.
Various factors can influence the actual amount of antifungal agent in the formulations provided herein. For example, the frequency of administration of the formulations, duration of treatrnent, combination of other antifungal agents, site of administration, degree of inflammation, and the anatomical configuration of the treated area may require an increase or decrease in the actual amount of antifungal agent in the present formulations.
Table 1 sets forth preferable ranges and dosages of the antifungal agent of the presentinvention.
Table 1 Antifungal Agents and Dosages Brand PreferableMore Most Most Generic Class PreferablePreferablePreferable Name Name ~nge Ran a Ran a Dose Am hotericinFun Antifun0.5-150 4-30 m 7.5-IS 10 m 'zone al m m 12H

FluconazoleDiflucanAntifun0.5-150 20-70 25-50 10 m al m m m 12H

ltraconazoleS oranoxAntifun0.5-150 20-70 25-50 30 m al m m m 12H

Steroidal Anti-Inflarnmatory Steroidal anti-inflammatories for use herein include fluticasone, beclomethasone, any pharmaceutically acceptable derivative thereof, and any combination thereof. As used herein, a pharmaceutically acceptable derivative includes any salt, ester, enol ether, enol ester, acid, base, solvate or hydrate thereof. Such derivatives may be prepared by those of skill in the art using known methods for such derivatization.
In one alterative embodiment, the steroidal anti-inflammatory agents have a specific particle size distribution profile. As used herein, particle size refers to an average particle size as measured by conventional particle size measuring techniques well known to those skilled in the art, such as, for examples sedimentation field flow fractionation, photon correlation spectroscopy, or disk centrifugation, among other techniques.
Fluticasone Preferably, the intranasal steroid of the present formulations is fluticasone propionate. Fluticasone propionate is a synthetic corticosteroid and has the empirical formula CZSH31F3~SS~ It has the chemical name S-(fluromethyl)6a,9-difluoro-11(3-17-dihydroxy 16a-methyl-3-oxoandrosta-1,4-diene-17~i-carbothioate,17-propionate.
Fluticasone propionate is a white to off white powder with a molecular weight of 500.6 and is practically insoluble in water, freely soluble in dimethyl sulfoxide and dimethylformamide, and slightly soluble in methanol and 95% ethanol.
In an embodiment, the formulations of the present invention may comprise a stervidal anti-inflammatory (e.g., fluticasone propionate) having the following particle size distribution profile: about 10% or less of the steroid particles have a particle size of less than 0.90 microns; about 25% or less of the steroid particles have a particle size of less than 1.6 microns; about 50% or less of the steroid particles have a particle size of less than 3.2 microns; about 75% or less of the steroid particles have a particle size of less than 6.10 microns; about 90% or less of the steroid particles have a particle size of less than 10 microns.
In an alternative embodiment, the formulation of the present invention comprises a steroidal anti-inflammatory having the following particle size distribution profile; about 10% of the steroid particles have a particle size of less than 0.70 microns;
about 25% of the steroid particles have a particle size of less than 1.30 microns; about 50% of the steroid particles have a particle size of less than 2.5 microns; about 75% of the steroid particles have a particle size of less than 4.0 microns; about 90% of the steroid particles have a particle size of less than 6.0 microns; and greater than 90% or about 100% of the steroid particles have aparticle size of less than 10 microns. Preferably, the steroid is fluticasone propionate.
In one preferred embodiment, the formulation of the present invention comprises a steroid having the following particle size distribution profile: about 10%
of the steroid particles have a particle size less than 0.50 microns; about 25% of the steroid particles have a particle size less than 0.90 microns; about 50% of the steroid particles have a particle size less than 1.7 microns; about 75% of the steroid particles have a particle size less than 3.5 microns; about 90°l0 of the steroid particles have a particle size less than 5.5 microns.

In another alternative embodiment, greater than 90% or about 100% of the steroid particles have a particle size less than 15 microns, preferably less than 10 microns, more preferably less than 8 microns, most preferably less than 7 microns.
Beclomethasone Also preferably, the steroidal anti-inflammatory of the present formulations is beclomethasone dipropionate or its monohydrate. Beclomethasone dipropionate has the chemical name 9-chloro-llb,I7,21-trihydroxy 16b-methylpregna-1,4-diene-3,20-doine17,21-dipropionate. The compound may be a white~powder with a molecular weight of 521.25; and is very slightly soluble in water (Physicians' Desk Reference.RTl~, very soluble in chloroform, and freely soluble in acetone and in alcohol. ~ ' The formulations of the present invention may comprise a steroidal anti-inflammatory (e.g., beclometasone diproprionate) having the following particle size distribution profile: about 10% or less of the steroid particles have a particle size of less than 0.75 microns; about 25% or less of the steroid particles have a particle size of less than 1.5 microns; about 50% or less of the steroid particles have a particle size of less than 2.0 microns; about 75% or less of the steroid particles have a particle size of less than 3.5 microns; about 90% or less of the steroid particles have a particle size of less than 5.0 microns; and greater than 90% or about 100% of the steroid particles have a particle size of less than 10 microns.
In an alternative embodiment, the formulation of the present invention comprises a steroidal anti-inflammatory having the following particle size distribution profile: about 10% of the steroid particles have a particle size of less than 0.35 microns;
about 25% of the steroid particles have a particle size of less than 0.70 microns; about 50% of the steroid particles have a particle size of less than 1.25 microns; about 75% of the steroid panicles have a particle size of less than 2.0 microns; about 90% of the steroid particles have a particle size of less than 3.0 microns; and greater than 90% or about 100% of the steroid particles have a particle size of less than 6.5 microns. Preferably, the steroid is beclomethasone dipropionate.
In one preferred embodiment, the formulation of the present invention comprises a steroidal anti-inflammatory having the following particle size distribution profile: about 10% of the steroid particles have a particle size less than 0.40 microns;
about 25°/ of the steroid particles have a particle size less than 0.70 microns; about 50% of the steroid particles have a particle size less than 1.3 microns; about 75% of the steroid particles have a particle size less than 2.0 microns; about 90% of the steroid particles have a particle size less than 3.0 microns; greater than 90% or about 100% of the steroid particles have a particle size less than 6.O~microns.
In another alternative embodiment, the formulation of the present invention comprises a steroidal anti-inflammatory having the following particle size distribution profile: about 10% of the steroid particles have a particle size less than 0.60 microns;
25% of the steroid particles have a particle size less than 0.90 microns;
about 50% of the steroid particles have a particle size less than 1.5 microns; about 75% of the steroid particles have a particle size less than 2.5 microns; about 90% of the steroid particles have a particle size less than 3.5 nucrons; greater than 90% or about 100% of the steroid particles have aparticle size~less than 6.0 microns.

In another alternative embodiment, greater than 90% or about 100% of the steroid particles have a particle size less than 15 microns, preferably less than 10 microns, more preferably less than 8 microns, most preferably less than 7 microns. In another preferred embodiment, greater than 90% or about 100% of the steroid particles have a particle size between 4 and 7 microns or 5 and 6 microns. In another embodiment, greater than 90% or about 100% of the steroid particles have a particle size less than 10 microns, preferably less than 7 microns; less than 6 microns; less than 5 microns, or less than 4 microns.
Providing steroidal anti-inflammatories according to the present invention is believed to be a more effective way to provide the medication to the nasal-paranasal region, thereby increasing bioavailability and efficacy of the steroid. It is understood that each of the particle size distribution profiles described in Serial Appl. Nos.
10/41,682 and lOl4I4,756 may be suitable for.any of the anti-inflammatory agents described herein.
The preferred anti-inflammatory agents are fluticasone and beclomethasone.
Also, the dosages described in these applications may also be suitable for use in the present invention. Each of these applications are incorporated herein by reference in their entirety.
Additionally, the formulations of the present invention may comprise fluticasone or beclomethasone alone or in combination with one or more other steroidal anti-inflammatories. Examples of steroidal anti=inflammatories for use herein include,'but are not limited to, betamethasone, triamcinolone, dexamethasone, prednisone, mometasone, flunisolide and budesonide. ' Other anti-inflammatory for use herein are listed below in Table 2.

Table 2 Steroidal Anti-inflammatory Agents and Dosages Most Most Preferable More PreferablePreferablePreferable Generic Brand NameClass Ran Ran a Ran a Dose Name a Ace 1c steineMucomist Mucol 125-S00 150-450 200-400 30D m Mucosil 'cs m m m 12H

Amikacin Amikin Aminoglycoside50-500 75-300 100-200 166 mg mg mg mg Q8-A hotericinFun izone Antifun 2.5-45 4-30 m 7.5-15 10 m 12H
H al m m Atro ine Anticoliner10-700 25-400 75-30 200 me 'c me me me 12H

Azelastine Astelin Antihistamine137-1096 204-822 382-616 411 mcg mcg mcg Q12H

me Azithro Zithromax Macrolide50-400 75-300 150-200 167 m in m m m 12H

Aztreonan Aaactam Monobactam250-1 300-900 475 750 450 m ODO m m 8H
m HeclamethasoneVanceril Steroidal0.1-4 0.2-3 0.2-2 0.8 mg Beclovent Anti- mg mg mg QI2H

inflammato HetamethasoneCelestone Steroidai0.1-4 0.2-3 0.2-2 0.8 mg . Anti- mg mg mg Q12H

inflammato Cefazolin Ancef, Cephlasporin250-1000 300-900 575-700 650 mg FCefzol mg mg mg Q8H

Gen Cefepine Maxipime Cephlasporin12S-1000 200-900 575-700 650 mg mg rng mg QI2H

Gen Cefonicid Moniacid Cephlasporin250-1000 300-900 575-700 600 mg mg mg mg Q24H

Gen CefaperazoneCefobid Cephlasporin250-1000 300-900 575-700 600 mg mg mg mg Q12H

Gen Cefotaxime Claforan Cephlasporin250-1000 300-900 575-700 600 mg mg mg mg Q8-Gen H ' 12H

Cefotetan Cefotan Cephlasporin250-1000 300-900 575-700 600 mg mg mg mg Q8-C ham 12H
cin Cefoxitin Mefoxiri Cephlasporin250-1000 300-900 575-700 600 mg ~ mg mg mg Q12H
-Ceoham cin CeRazidime Fortaz, Cephlasporin250-1000 300-900 475-750 550 mg Ceptaz mg mg mg Q12H

Gen II

CeflizoximeCeflzox Cephlasporin250.1000 300-900 575-?OD 600 mg mg mg mg Q8-Gen 12H

CeftriaxoneRocephin Cephtasporin250-1000 300-900 575-700 650 mg mg mg mg QI2H

Gen II

Cefuroxime Ceftin Cephlasporin100-600 200-520 250-400 285 mg mg mg mg Q8H

Gen II

Cephapirin Cefadyl Cephlasporin250-1000 300-900 575-700 650 mg mg mg mg Q12H

Gen Ci rofloxacinCi o uinolone25-200 50-175 75-110 90 m 12H
m m m Clind cin Cleocin Lincosamide50-600 75-500 125-300 225 m m rn m 12H

Cromolyn lntaIINasalcromMast 5-100 7.5-75 10-50 20 mg Sodium cell mg mg mg Q12H
.

stabilizer DexamethasoneDecadron Steroidal0.1-4 0.2-3 0.2-2 D.8 mg Anti- mg mg mg Q12H

inflammato Domase a1 Pulmo a Mucot 0.5-5 1-4. m 2-3 m 1.5 m ha 'c m 12H

Do c cline Vibra cin Tetrac 10-100 15-80 25-65 Z7 m 12H
cline m m m ErythromycinErythrocinMacrotide50-600 60-350 100-300 150 mg mg mg mg Q8H

Lactobionate FluconazoleDiflucan Antifun 12.5-150 20-70 25-50 30 m 12H
al m m m FlunisolideAerobid Steroidal0.1-4 0.2-3 0.2 2 0.8 mg Nasalide Anti- mg mg mg Q12H

inflammato FlurbiprofenOcofen Nonsteroidal0.01-2 0.05-I 0.1-0.S D.15 mg mg mg mg Q12H

Anti-inflammato FluticasoneFlonase Steroidal10-700 25-400 75-300 200 meg Anti- mcg mcg mcg Q24H

inflammato Gentam cin Garam cin Amino 10-200 30-150 80-120 95 m 8-12H
I oside m m m Ibuprofen Motrin Nonsteroidal25-400 30-300 50150 100 rng mg mg mg Q12H

Anti-inflammato I ratro Atrovent Anticholiner10 25-400 75-300 200 me ium 'c 700 mo me 12H
me ItraconazoleS oranox Antifungal12.5--I5020-70 mg 25-50 30 m 12H
m m Ketorolac Acular Nonsteroidal0.05-4 0.1-2 mg 0.3-I 0.5 mg mg mg QI2H

Anti-inflamatto LevofloxacinLeva uin uinolone40-200 50-150 60-80 70 m 12H
m rn m Linezolid Zyvox Miscellaneous50-600 7S-450 100-300 200 mg mg mg ng QI2H

anti-bacterial Loratidine Clarion Antihistamine0.5-10 1-7.5 m I-5 m 2 m 12H
m Mero enem Merrin Carba 200-75 250-700 300-500 33 m 8H
enem m m m~

MezlacillinMezlin Penicillin 300-1500375-1000 - 833 m m m ?50-950 H
m Miconazole Monistat Antifun 12.5-30030-200 50-100 60 m 12H
al m rii m MontelukastSin ulair Anoleukatriene 0.5-15 2-25 m 3-15 10 m 12H
m m Mu irocin Bactroban Antibacterial 1-25 1.5-20 2-15 10 m 6-8H
m m m Nafcillin Uni en Penicillin 250-1000300-900 575-700 600 m m m m 8H

Nedocromil Tilade Mast 1-25 3-IS mg 5-12 7 mg QI2H
cell rng mg stabilizer Ofloxacin Floxin uinolone 25-200 50-175 75-110 90 m 12H
m m m Oxacillin Prosta Penicillin Z50-1000300-900 575-700 600 m hin m m m 8H

OxymetazolinoAfiin Decongestant 0.05--0.50.075-0.4 0.1-0.3 0.2 mg mg mg QI2H

m Phen 1 herineNeo-S hineDecon 5-50 10-35 m 1S-20 10 m 12H
estant m m Pi eracillinPi racil Penicillin 100-1000125-750 250-600 460 m m m m H

Potassium Antis 30-20 40-150 50-80 60 m 12H
Iodide tic 0 m m m Rifa in ltifadin Miscellaneous _ 1000-4000 1500-35002250 m 500-5000m m 12H
m Taurolin TaurolidineNon 5-200 20-150 40-t20 80 mg antibiotic mg mg mg ' Q12H

antimicrobial Tetrah drozolidineTizine Decon 0.05-D.50.06-0.4 0.1-0.3 0.15 m estant m m m 12H

TicarcillinTimentin Penicillin 500-50001000-4000 1500-35002250 mg + mg mg mg Q6-Clavulanatc gH

Tobra cin Nebcin Aminooside10-200 30-150 80-120 95 m 812H
I m m m TriamcinaloneAsthmacor Steroidal 0.05-3 0.2-2.5 0.5-2 0.6 mg,Ql2H
Anti- mg mg mg Aristacortinflammato Vancomycin Vancocin Antibiotic- 50-400 75-325 125.250 166 mg mg mg mg Q6-8H

miscellaneous X lometazoline~ Otrivin Decon 0.05-0.40.075-03 0.1-0.Z 0125 m estant m m m 12H

ZafirlukastAccolate Antileukotriene 2-60 4-50 m 6-30 20 m 12H
m m Ant1b10tiC
The formulations of the present invention may further comprise an antibiotic.
Additionally, since more than one bacterial organism may be associated with the bacterial infection of the nasal-paranasal region, the present formulations may comprise a broad-spectrum antibiotic such as amoxycillin, erythromycin, or cefadroxil.
Alternatively, a combination of anti-bacterial agents with differing spectra of activity may also be used.
Examples of antibiotics for use in the present invention are shown in Table 3.

Antibiotic Agents and Dosages PreferableMare Most Most Generic Brand . Class gauge PreferablePreferablePreferable Flame Name Itan Ran a Dose a Anukacin Amikin amino 1 1-800 5-500 50-300 I50 m coside m m m SH

~ AzithromycinZithromaxMacrolide 25-400 ~ 75-300L150-200~ 167 ~ ~ ~ mg mg mg mg Q12H

AztreonanAzactam Monobactam150-1000300-900 475-750 450 m CefazolinAncef, Cephlasporinm m m 8H
Kefzol (Gen 150-1000300-900 575-700 650 mg Cefepine I mg mg mg QSH
Maxipime Cephlasporin Cefonicid (Gen 75-1000 200-900 575-?00 650 mg Moniacid IV mg mg mg Q12H
Cefaperazone Cephlasporin Cefobid (Gen 150-1000300-900 575-700 600 mg I mg mg mg Q24H
Cephlasporin (Gen 150-1000300-900 575-700 600 mg ItI mg mg mg Q12H

CefotaximeClaforan Cephlasporin150-1000300-900 575-700 600 mg (Gen mg mg mg Q8-IlI I2H

CefotetanCefotetanCephlasporin150-1000300-900 575-700 600 mg mg mg mg Q8-C ha cin I2H

CefoxitinMefoxia' Cephlasporin150-1000300-900 575-700 600 mg mg mg mg Q12H

C h in Ceftazidime1ortaz, Cephlasporin150-1000300-900 475-750 550 mg Ceptaz (Gen mg mg mg Q12H

CeftizoximeCeBzox Cephiasporin150-1000300-900 575-700 600 mg . (Gen mg mg mg , Q8-CeflriaxoneRocephin Cephlasporin150-1000300-900 575-700 650 mg (Gen mg mg mg Qt2H

n CefuroximeCeftin Cephlasporin50-600 200-520 250-400 285 mg (Gen mg mg mg Q8H

I

CephapirinCefadyl Cephlasporin150-1000300-900 575-700 650 mg (Gen mg mg mg Qt2H

I

Ci rotloxacinCi ro uinolone 15-200 50-175 750110 90 m m m m 12H

Clinda Cleocin Lincosamide25-600 75-500 125-300 225 m cin m m m . 12H

Do line Vibra Tetrac 10-100 15-80 25-65 27 m cin cline m m m 12H

ErythromycinErythtocinMacrolide25-600 60-350 100-300 I50 mg mg mg mg Q8H

Lactobionate GentamicinGaram Amino I-80D 5-500 50-300 150 m cin 1 oside m m m 8H

Kana cin ICantrex Amino 1-800 5-500 50-300 150 m 1 oside m m m 8H

LinezotidZyvox Miscellaneous25-600 75-450 100-300 200 mg mg mg ng Q12H

anti-bacterial MealocillinMezlin Penicillin10D-1500375-1000 750-950 833 m ~ m m m H

M irocin BactrobanAntibacterial1-25 1.520 2-15 10 m m m m d-8H

NafcillinUni en Penicillin150-1000300-900 575-700 600 m m m m 8H

NetilmicinNetro Amino I-800 5-500 50-300 i50 m cin 1 oside m m m 8H

Neom cin M cifradinAmino 1-800 5-500 50-300 I50 m 1 oside m m m SH

OxacillinProsta Penicillin150-1000300-900 575-700 600 m hin m m m 8H

Paromo Humatin Amino I-800 5-500 50-300 150 m cin 1 oside m m m 8H

Pi eracillinPi cil Penicillin50-1000 125-750 250600 460 m m m m H

S to cin Amino 1-800 5-500 50-300 150 m 1 oside m m m 8H

TicarcillinTimentin Penicillin200-50001000-40001500-35002250 + mg mg mg mg Q6-Clawlanaic 8H

Tobra Amino 1-800 5-500 50-300 150 m cin 1 coside m m m 8H

VancomycinVancocin Antibiotic-25-400 75-325 125.250 166 mg mg mg mg Q6-8H

miscellaneous Antiviral Agents The formulations of the present invention may comprise a therapeutically effective amount of one or more antiviral agents. These agents can be administered individually or simultaneously with the steroidal agent of the present invention. The antiviral agent may also include Acyclovir, Famciclovir, Valacyclovir, edoxudine, ganciclovir, foscarnet, cidovir (vistide), Vitl-asert, Formivirsen, HPMPA (9-(3 hydroxy-2-phosphonomethoxypropyl)adenine), PMEA (9-(2-phosphonomethoxyethyl)adenine), IiPMPG (9-(3-Hydroxy-2-(Phosphonomethoxy)propyl)guanine), PMEG (9-[2-(phosphonomethoxy)ethyl]guanine), HPMPC (1-(2-phosphonomethoxy-3-hydroxypropyl)-cytosine), ribavirin, EICAR (5-ethynyl-1-beta-D-ribofuranosylimidazole-4-carboxamine), pyrazofurin (3-[beta-D-ribofuranosyl]-4-hydroxypyrazole-5-carboxamine), 3-Deazaguanine, GR-92938X (1-beta-D-ribofuranosylpyrazole-3,4-dicarboxamide), LY253963 (1,3,4-thiadiazol-2-yl-cyanamide), RD3-0028 (1,4-dihydro-2,3-Benzodithiin), CL387626 (4,4'-bis[4,6-di[3-aminophenyl-N,N-bis(2-carbamoylethyl)-sulfonilimino]-1,3,5-triazin-2-ylamino-biphenyl-2,2'-disulfonic acid disodium salt), BABIM (Bis[5-Amidino-2-benzimidazolyl]methane), and N1H351.
Other suitable dosages and methods of treatment of the ingredients described herein are described in US 2001/0006944AI, pub. date July 5, 2001, which is incorporated herein by reference in its entirety. .
Other Components The formulation of the present invention may be in any form piovided the formulation can be administered to a mammal in an amount, at a frequency, and for a duration effective to prevent, reduce, or eliminate one or more symptoms associated with Rhinosinusitis, including fungus induced Rhinosinusitis. For example, a formulation within the scope of the invention can be in the form of a solid, liquid, and/or aerosol including, without limitation, powders, crystalline substances, gels pastes, ointments, salves, creams, solutions, suspensions, partial liquids, sprays, nebulae, mists, atomized vapors, tinctures, pills, capsules, tablets, and gelcaps. In addition, the formulation can contain a cocktail of other ingredients, particularly those described herein.
For example, a formulation within the scope of the invention can contain, without limitation, one, two, three, four, five, or more different antifungal agents, antibiotics, antiviral agents, or the other ingredients described herein. Further, formulations within the scope of the invention can contain additional ingredients including, without limitation, pharmaceutically acceptable aqueous vehicles, pharmaceutically acceptable solid vehicles, steroids, mucolytic agents, antibacterial agents,.anti-inflammatory agents, immunosuppressants, dilators, vaso-constrictors, decongestants, leukotriene inhibitors, anti-cholinergics, anti-histamines, therapeutic compounds and combinations thereof.
Such antiviral agents may include IIVIPDH inhibitors, inhibitors of virus adsorption entry, inhibitors of fusion with host cells, antisense oligonucleotides, and nucleoside analogues.
In one embodiment, the present formulations may be provided in any form suitable for intranasal administration. In another alternative embodiment, the formulations of the present invention are in solution or suspension form suitable for intranasal administration.
In an embodiment, the formulation of the present invention may comprise a preservative, suspending agent, wetting agent, tonicity agent andlor diluent.
In one embodiment, the formulations provided herein may comprise from about 0.01 % to about 95%, or about 0.01 % to about 50%, or about 0.01 % to about 25%, or about 0.01 % to about 10%, or about 0.01% to about 5% of one or more pharmacologically suitable suspending fluids which is physiologically acceptable upon administration.
Pharmacologically suitable fluids for use herein include, but are not limited to, polar solvents, including, but not limited to, compounds that contain hydroxyl groups or other polar groups. Solvents include, but are not limited to,. water or alcohols, such as ethanol, isopropanol, and glycols including propylene glycol, polyethylene glycol, polypropylene glycol, glycol ether, glycerol and polyoxyethylene alcohols. Polar solvents also include protic solvents, including, but not limited to, water, aqueous saline solutions with one or more pharmaceutically acceptable salt(s), alcohols, glycols or a mixture there of. In one alternative embodiment, the water for use in the present formulations should meet or exceed the applicable regulatory requirements for use in drugs.
In certain embodiments herein, the formulations of the present invention have a pH of about 2.0 to about 9Ø Optionally, the formulations of the present invention may contain a pH buffer. For example, a buffer may comprise any known pharmacologically suitable buffexs which are physiologically acceptable upon administration intranasally.
The buffer may be added to maintain the pH of the formulation between about 3.0 and about 7.0, for example.
Sterility or adequate antimicrobial preservation may be provided as part of the present formulations. Since certain formulations of the present invention are intended to be administered intranasally, it is preferred that they be free of pathogenic organisms. 'A
benefit of a sterile liquid suspension is that it reduces the possibility of introducing contaminants into the individual when the suspension formulation is administered intranasally, thereby reducing the chance of an opportunistic infection.
Processes which may be considered for achieving sterility may include any appropriate sterilization steps known in the art.
In one embodiment, the formulation of the present invention is produced under sterile conditions, and the micronization of the steroidal anti-inflammatory is performed in a sterile environment, and the mixing and packaging is conducted under sterile .
conditions. In one alternative embodiment, one or more ingredients in the present formulation may be sterilized by steam, gamma radiation or prepared using or mixing sterile steroidal powder and other sterile ingredients where appropriate.
Also, the formulations may be prepared and handled under sterile conditions, or may be sterilized before or after packaging.
In addition to or in lieu of sterilization, the formulations of the present invention may contain a pharmaceutically acceptable preservative to minimize the possibility of microbial contamination. Additionally, a pharmaceutically-acceptable preservative may be used in the present formulations to increase the stability of the formulations. It should be noted, however, that any preservative must be chosen for safety, as the treated tissues may be sensitive to irntants. Preservatives suitable for use herein include, but are not limited to, those that protect the solution from contamination with pathogenic particles, including phenylethyl alcohol, benzalkonium chloride, benzoic acid, or benzoates such as sodium benzoate. Preferably, the preservative for use in the present formulations is benzalkonium chloride or phenylethyl alcohol: In certain embodiments, the formulations herein comprise from about 0.01% and about 1.0% w/w of benzalkonium chloride, or from about 0.01% and about 1% v/w phenylethyl alcohol. Preserving agents may also be present in an amount from about 0.01% to about 1%, preferably about 0.002% to about 0.02% by total weight or volume of the formulation.
The formulations provided herein may also comprise from about 0.01 % to about 90%, or about 0.01% to about 50%, or about 0.01% to about 25%, or about 0.01%
to about 10%, or about 0.01 % to about 1 % w/w of one or more emulsifying agent, wetting agent or suspending agent. Such agents for use.herein include, but are not limited to, polyoxyethylene sorbitan fatty esters or polysorbates, including, but not limited to, polyethylene sorbitan monooleate (Polysorbate 80), polysorbate 20 (polyoxyethylene (20) sorbitan monolaurate), polysorbate 65 (polyoxyethylene (20) sorbitan tristearate), polyoxyethylene (20) sorbitan mono-oleate, polyoxyethylene (20) sorbitan monopalmitate, polyoxyethylene (20) sorbitan monostearate; lecithins; algiiiic acid;
sodium alginate; potassium alginate; ammonium alginate; calcium alginate;
propane-1,2-diol alginate; agar; carrageenan; locust bean gum; guar gum; tragacanth;
acacia; xanthan gum; karaya gum; pectin; amidated pectin; ammonium phosphatides;
microcrystalline cellulose; methylcellulose; hydroxypropylcellulose;
hydroxypropylmethylcellulose;
ethylmethylcellulose; carboxymethylcellulose; sodium, potassium and calcium salts of fatty acids; mono-and di-glycerides of fatty acids; acetic acid esters of mono-and di-glycerides of fatty acids; lactic acid esters of mono-and di-glycerides of fatty acids; citric acid esters of mono-and di-glycerides of fatty acids; tartaric acid esters of mono-and di-glycerides of fatty acids; mono-and diacetyltartaric acid esters of mono-and di-glycerides of fatty acids; mixed acetic and tartaric acid esters of mono-and di-glycerides of fatty acids; sucrose esters of fatty acids; sucroglycerides; polyglycerol esters of fatty acids;
polyglycerol esters of polycondensed fatty acids of castor oil; propane-1,2-diol esters of fatty acids; sodium stearoyl-2lactylate; calcium stearoyl-2-lactylate;
stearoyl tartrate;
sorbitan monostearate; sorbitan tristearate; sorbitan monolaurate; sorbitan monooleate;
sorbitan monopalinitate; extract of quillaia; polyglycerol esters of dimerised fatty acids of Soya bean oil; oxidatively polymerised soya bean oil; and pectin extract. Tn certain embodiments herein, the present formulations comprise polysorbate 80, microcrystalline cellulose, carboxymethylcellulose sodium and/or dextrose.
The present formulations may further comprise from about 0.01% to about 90%, or about 0.01% to about 50%, or about 0.01% to about 25%, or about 0.01% to about 10%, or about 0.01% to about 1% wlw of one or more excipients and additives which are pharmacologically suitable. Excipients and additives generally have no pharmacological activity, or at least no undesirable pharmacological activity. The concentration of these may vary with the selected agent, although the presence or absence of these agents, or their concentration is not an essential feature of the invention. The excipients and additives may include, but are not limited to, surfactants, moisturizers, stabilizers, complexing agents, antioxidants, or other additives known in the art.
Complexing agents include, but are not limited to, ethylenediaminetetraacetic acid (EDTA) or a salt thereof, such as the disodium salt, citric acid, nitrilotriacetic acid and the'salts thereof. In another embodiment, particularly in the suspension formulations provided herein, the cornplexing agent is sodium edetate. In one embodiment, the compositions contain sodium edetate at a concentration of about 0.05 mg/mL to about 0.5 mg/mL, or about 0.1 mg/mL to about 0.2 mg/mL. Also, for example, the formulations of the present invention may comprise from about 0.001% to about 5% by weight of a humectant to inhibit drying of the mucous membrane and to prevent irntation. Any of a variety of pharmaceutically acceptable humectants can be employed, including sorbitol, propylene glycol, polyethylene glycol, glycerol or mixtures thereof, far example.
The formulations provided herein also may comprise about 0.01% to about 90%, or about 0.01% to about 50%, or about 0.01% to about 25%, or about 0.01% to about 10%, or about 0.01 % to about 10% w/w of one or more solvents or co-solvents to increase the solubility of any of the components of the present formulations.
Solvents or co-solvents for use herein include, but are not limited to, hydroxylated solvents or other pharmaceutically- acceptable polar solvents, such as alcohols including isopropyl alcohol, glycols such as propylene glycol, polyethylene glycol, polypropylene glycol, glycol ether, glycerol, and polyoxyethylene alcohols. In another embodiment, the formulations of the present invention may comprise one or more conventional diluents known in the art. The preferred diluent is purified water.
Tonicity agents may include, but are not limited to, sodium chloride, potassium chloride, zinc chloride, calcium chloride and mixtures thereof. Other osmotic.adjusting agents may also include, but are not limited to, mannitol, glycerol, and dextrose or mixtures thereof. In an alternative embodiment, the present formulation may comprise about 0.01% to about 10% w/w, or about 1% to about 8% w/w, or 1% to about 6%
w/w, preferably about 5.0% wlw. The preferred tonicity agent is anhydrous dextrose.
In one alternative embodiment, the formulations of the present invention are stable. As used herein, the stability of formulations provided herein refers to the length of time at a given temperature that greater than 80%, 85%, 90% or 95% of the initial amount of the active ingredients is present in the formulation. For example, the formulations provided herein may be stored between about 15°C and about 30°C, and remain stable for at least 1, 2, 12,18, 24 or 36 months. Also, the formulations may be suitable for administration to a subject in need thereof after storage for more than 1, 2, 12,18, 24 or 36 months at 25°. Also, in another alternative embodiment, using Arrhenius Kinetics, more than 80%, or more than 85%, or more than 90%, or more than 95%
of the initial amount of active ingredients remains after storage of the formulations for more than 1, 2,12, 18, 24 or 36 months between about 15°C and about 30°C.
The formulations of the present invention may be manufactured in any conventional manner known in the art, or by minor modification of such means.
For example, the formulations may be manufactured by thoroughly mixing the ingredients described herein at ambient or elevated temperatures in order to achieve solubility of ingredients where,appropriate.
The preparation of the steroidal inflammatory of the present invention, e.g., fluticasone propionate and beclomethasone dipropionate, having a specific particle size distribution profile may be obtained by any conventional means lmown in the art, or by minor modification of such means. For example, suspensions of drug particles can rapidly undergo particulate size reduction when subj ected to "j et milling"
(high pressure particle in liquid milling) techniques. Other known methods for reducing particle size into the micrometer range include mechanical milling, the application of ultrasonic energy and other techniques.
In addition, the formulations of the present invention may comprise any of the following components: (r) antihistamine: (ii) non-steroidal anti-flarnmatories; (iii) decongestants; (iv) mucolytics; (v) anticholinergics; or (vi) mass cell stabilizers.
Examples of such components are found in U.S. 2002/0061281 Al, published May 23, 2002., This reference is incorporated herein by reference in its entirety.
In one alternative embodiment, the present~invention is directed to a pharmaceutical composition that may be useful in treating rhinosinusitis caused by Alpha Hemolytic Sreptococci, Beta Hemolytic Streptococci, Branhamella Catarrhalis, Diptheroids, Heaemophilis influenza (beta-lactamase positive and negative), Moraxella species, Psuedomonas aeroguinosa, Pseudomas maltophilia, Serratia marcesns, Staphylococcus aureus, Streptococcus pheumonia, Aspergillosis, Mucor and Candida albicans, Flusarium, Curvularia, crytococcus, coccidiodes, and histoplasma.
Mode of Administration Administration of the present formulations can be any type of administration that places the present formulations in contact with nasal-paranasal mucosa. Direct intranasal administration includes, without. limitation, nasal irrigations, nasal sprays, nasal inhalations, and nasal packs with, for example, saturated gauze provided the administered agent contacts nasal-paranasal mucosa prior to crossing epithelium. In addition, injections into the nasal-paranasal cavities using, for example, a needle or catheter tube is considered a direct intranasal administration provided the administered agent contacts nasal-paranasal mucosa after leaving the needle or catheter tube and prior to crossing epithelium. Any device can be used to directly administer the present formulations intranasally including, without limitation, a syringe, bulb,, inhaler, canister, spray can, nebulizer, and mask.
Indirect administration to the nasal-paranasal anatomies can include, without limitation, oral, intravenous, intradermal, and intraperitoneal administrations provided the administered agent contacts nasal-paranasal mucosa. In addition, any device can be used to indirectly administer an agent to the nasal-paranasal anatomy including, without limitation, a syringe and regulated release capsule.
The present formulations may be packaged in any conventional manner suitable for administration of the present formulations. Spray administration containers for various types of nasal formulations have been known in the past and substantially all will be equally suitable for the present formulations, provided that the container materials is compatible with the formulation. In an embodiment, the formulation of the present invention herein is packaged in a container such that it can be dispersed as a mist to be directed into each nostril. For. example, the container may be made of flexible plastic such that squeezing the bottle's sides impels the spray out through the nozzle into the nasal cavity. Alternatively, a small pump button may pump air into the container and cause the liquid spray to be emitted on the return stroke when pressed.
In an alternative embodiment, the formulations of the present invention are packaged in a container pressurized with a gas which is inert to the user and to the ingredients of the solution. The gas may be dissolved under pressure in the container or may be generated by dissolution or reaction of a solid material which forms the gas as a product of dissolution or as a reaction product. Suitable inert gases which can be used herein include nitrogen, argon, and carbon dioxide. Also, the formulations herein may be administered as a spray or aerosol wherein the formulation is packaged in a pressurized container with a liquid propellant such as dicholorodifluoro methane or chlorotrifluoro ethylene, or other propellant. .
Preferably, the present formulations are packaged in a metered dose spray pump, or metering atomizing pump, such that each actuation of the pump delivers a fixed volume of the formulation (i.e. per spray-unit). For administration in drop or other topical form, the formulations herein may suitably be packaged in~a container provided with a conventional dropperlclosure device, comprising a pipette or the like, preferably delivering a substantially fixed volume of the formulation.

Method of Treatment The present invention is also directed to a method for treating rhinosinusitis, including fungus-induced rhinosinusitis. In one embodiment, the method of treating rhinosinusitis of the present invention comprises the step of administering a therapeutically effective amount of the formulation of the present invention to a mammal in need thereof. The formulation may comprise the steroidal agent of the present invention alone or in combination with an anti-fungal agent, an antibiotic or antiviral agent. The formulation is preferably administered intranasally. In one embodiment, the formulation is administered directly to the nasal-paranasal mucosa. In an alternative embodiment, the formulation is administered intranasally via a metered dose spray.pump.
In general, the course of treatment for any individual with respect to any of the active ingredients described herein can be readily determined by his or her physician.
The method of the present invention may further comprise administering the formulation of the present for a duration or frequency sufficient to treat one or more symptoms of rhinosinusitis, including fungus-induced rhinosinusitis. For example, the formulation may be administered one time to about 10 times a day for about one day.to about 100 days or more, or until such fungus-induced rhinosinusitis is treated. In an embodiment, the method of the present invention comprises administering to a mammal diagnosed with fungus-induced rhinosinusitis a formulation comprising a therapeutically effective amount of an antifungal agent and a steroidal anti-inflammatory intranasally via a metered dose spray pump one to three times a day for up to two weeks. In an alternative embodiment, the administration of the present formulations may comprise 1, 2, 3, 4, 5, 6, 7 or 8 applications of the present fornnulativn to the nasal-paranasal mucosa one, two, three, four or five times a day.
In an alternative embodiment, the formulation of the method of the present invention further comprises an antibiotic. However, when administering antibiotics, physicians must keep in mind the incidence of drug-resistant bacteria in their community and consider the patient's overall health status. Special attention should be given to diseases that could impede normal recovery from infection and/or predispose to complications (e.g., diabetes mellitus, chronic pulmonary disease, asthma, cystic fibrosis and immune deficiencies). Additionally, physicians should consider whether or not the patient is immunocomprimised in selecting an antibiotic. In one embodiment, the antibiotic is administered for a period of 1 day to about 10 weeks. Iwan alternative embodiment, the antibiotic is administered for about .1 day to about 28 days.
Accordingly, the present invention provides a method of treating fungus-induced rhinosiriusitis associated with a bacterial infection in the nasal paranasal region, comprising the steps of administering a formulation comprising an antifungal agent, steroidal anti-inflammatory, and antibiotic until said bacterial infection is cured, and then administering a formulation comprising an antifungal agent and steroidal anti-.
inflammatory.
In an alternative embodiment, the present invention provides a method of treating fungus-induced rhinosinusitis, comprising the steps of administering a formulation comprising a steroidal anti-inflammatory alone or in combination or in conjunction with an antifungal agent, antibiotic or antiviral agent. For example, the steroidal agent may be administered separately from the antif-.ungal agent ox antibiotic, or each ingredient can be administered simultaneously (e.g., in a single formulation) concurrently, subsequently, or in tandem. In another embodiment, each ingredient is administered individually in its own formulation and pursuant to an appropriate dosage regimen for that particular ingredient. Suitable dosage regimens for steroidal agents, fungal agents, antibiotics or antiviral agents are known by those skilled in the art.
V. EXAMPLES
Examples 1-5 herein are prophetic examples provided to illustrate, but riot to limit, the formulations and methods of the present invention. They are presented with the understanding that changes can be and may need to be made to a specific composition in order to obtain or optimize the formulation. Such modifications to the following prophetic examples, if needed, are normal and understandable to those of ordinary skill in the art, and shall not be used to limit the invention.
It is believed that prophetic examples 1-5 would be suitable for administration to the nasal-paranasal mucosa of an individual suffering from fungus-induced rhinosinusitis associated with a bacterial infection. The formulations may be sterile. It is understood that the steroid, antibiotic, antifungal agent or the other ingredients described herein may be administered in the same formulation, or may be administered individually, or in any combination thereof.
Example 1 Am hotericin B 2.0 -100.0 m ml Neom cin Sulfate 5.0 -100.0 m ml Phen leth 1 Alcohol 0.5 -10.0 m .ml Fluticasone Pro innate 0.25 -1.0 m mI

Microc stalline Cellulose S.0 -15.0 m ml ' Pol orbate 80 0.1-1.0 mg/ml Purified Water - q.s.

Example 1 is a prophetic example of a formulation of the present invention, wherein about 10% of the fluticasone propionate particles have a particle size of less than 0.70 microns; about 25% of the fluticasone propionate particles have a particle size of less than 1.30 microns; about 50% of the fluticasone propionate particles have a particle size of less than 2.5 microns; about 75% of the fluticasone propionate particles have a particle size of less than 4.0 microns; about 90% of the fluticasone propionate particles have a particle size of less than 6.0 microns; and greater than 90% or about 100% of the fluticasone propionate particles have a particle size of less than 10 microns. The solution of Example 1 may be made by methods known to those of ordinary skill in the art.
Example 2 Fluconazole _ _ 1.0 - 20.0 m ml Neomycin Sulfate 5.0 -100.0 m ml Phen leth 1 Alcohol 0.5 -10.0 m ml Fluticasone Pro innate 0.25 -1.0 m ml Microcrystalline Cellulose5.0 -15.0 mg/ml Pol sorbate 80 0.1-1.0 m ml Purified Water .s.

Example 2 is a prophetic example of a formulation of the present invention, wherein about 10% of the fluticasone propionate particles have a particle size of less than 0.70 microns; about 25% of the fluticasone propionate particles have a particle size of less than 1.30 microns; about 50% of the fluticasone propionate particles have a particle size of less than 2.5 microns; about 75% of the fluticasone propionate particles have a .
particle size of less than 4.0 microns; about 90% of the fluticasone propionate particles have a particle size of less than 6.0 microns; and greater than 90% or about 100% of the fluticasone propionate particles have a particle size of less than 10 microns.
The solution of Example 2 may be made by methods known to those of ordinary skill in the art.
Example 3 Am hotericin B 2.0 -100.0 m ml Neom cin Sulfate 5.0 -100.0 m ml Benzalkonium Chloride 0.1- 0.5 rn ml Dextrose 20.0 -100.0 Phen ' leth 1 Alcohol 0.5 -10.0 m .ml Beclomethasone Di ro 0.25 -1.0 m ml innate Purified Water .s.

Example 3 is a prophetic example of a formulation of the present invention, wherein about 10% of the beclomethasone dipropionate particles have a particle size less than 0.40 nucrons; about 25% of the beclomethasone dipropionate particles have a .
particle size less than 0.'70 microns; about 50% of the beclomethasone dipropionate particles have a particle size less than 1.3 microns; about 75% of the beclomethasone dipropionate particles have a particle size less than 2.0 microns; about 90%
of the beclomethasone dipropionate particles have a particle size less than 3.0 microns; and greater than 90% or about 100% of the beclomethasone dipropionate particles have a particle size less than 6.0 microns. Example 3 may be made by methods known to those of ordinary skill in the art.
Example 4 Fluconazole 1.0 - 20.0 m ml Neom cin Sulfate 5.0 -100.0 m ml Benzalkonium Chlaride 0.1- 0.5 m ml ' Dextrose '20.0 -100.0 Phen leth 1 Alcohol 0.5 -10.0 m .ml Beclomethasone Di ro 0.25 -1.0 m ml innate Purified Water .s.

Example 4 is a prophetic example of a formulation of the present invention, wherein about 10% of the beclomethasone dipropionate particles have a particle size less than 0.40 microns; about 25% of the beclomethasone dipropionate particles have a particle size less than 0.70 microns; about 50% of the beclomethasone dipropionate particles have a particle size less than 1.3 microns; about 75% of the beclomethasone dipropionate particles have a particle size Iess than 2.0 microns; about 90%
of the beclomethasone dipropionate particles have a particle size less than 3.0 microns; and greater than 90% or about I00% of the beclomethasone dipropionate particles have a particle size less than 6.0 microns. Example 4 may be made by methods known to those of ordinary skill in the art.
Example 5 Fluconazole . 1.0 - 20.0 m /m1 Benzalkonium Chloride 0.1- 0.5 m ml Dextrose 20.0 -100.0 Phen leth 1 Alcohol 0.5 -10.0 m .ml Beclomethasone Di ro 0.25 -1.0 mg/m1 innate Purified Water .s.

Example 5 is a prophetic example of a formulation of the present invention, wherein about 10% of the beclomethasone dipropionate particles have a particle size less than 0.40 microns; about 25% of the beciomethasone dipropionate particles have a particle size less than 0.70 microns; about 50% of the beclomethasone dipropionate particles have a particle size less than 1.3 microns; about 75% of the becloriiethasone dipropionate particles have a particle size less than 2.0 microns; about 90%
of the beclomethasone dipropionate particles have a particle size less than 3.0 microns; and greater than 90% or about 100% of the beclomethasone dipropionate particles have a particle size less than 6.0 microns. Example 5 may be made by methods known to those of ordinary skill in the art.
The Examples herein are presented for illustrative purposes only. They are not intended to limit the scope of the invention. Further, it should be understood that various changes and modifications to the embodiment described herein will be apparent to those skilled in the art. Such changes and modifications can be made without departing from the spirit and scope of the present invention and without diminishing its attendant advantages. It is therefore intended that such changes and modifications be covered by the appended claims. Also, the invention may suitably comprise, consist of or consist essentially of the elements or steps described herein. Further, the invention described herein suitably may comprise or be practiced in the absence of any element or step which is not specifically disclosed herein. Further, one or more step described herein may be performed simultaneously with another step.

Claims

Claims What is claimed is:

1. ~A formulation for the treatment of fungus-induced rhinosinusitis in a mammal, said formulation comprising:
(a) ~about 1 to about 700 mcg of a steroidal anti-inflammatory, wherein the steroidal anti-inflammatory is fluticasone or a pharmaceutically acceptable derivative thereof, said steroidal anti-inflammatory having the following particle size distribution profile:
i. ~about 10% of the steroidal anti-inflammatory particles have a particle size of less than 0.90 microns;
ii. ~about 25% of the steroidal anti-inflammatory particles have a particle size of less than 1.6 microns;
iii. ~about 50% of the steroidal anti-inflammatory particles have a particle size of less than 3.2 microns;
iv. ~about 75% of the steroidal anti-inflammatory particles have a particle size of less than 6.2 microns; and v. ~about 90% of the steroidal anti-inflammatory particles have a particle size of less than 10.0 microns;
wherein said formulation is suitable for administration to the nasal-paranasal mucosa.

2. ~A formulation for the treatment of fungus-induced rhinosinusitis in a mammal, said formulation comprising:

i) ~about 1 to about 700 mcg a steroidal anti-inflammatory, wherein the steroidal anti-inflammatory is beclomethasone or a pharmaceutically acceptable derivative thereof, sand steroidal anti-inflammatory having the following particle size distribution profile:
i. ~about 10% of the steroidal anti-inflammatory particles have a particle size of less than 0.75 microns;
ii. ~about 25% of the steroidal anti-inflammatory particles have a particle size of less than 1.5 microns;
iii, ~about 50% of the steroidal anti-inflammatory particles have a particle size of less than 2.0 microns;
iv. ~about 75% of the steroidal anti-inflammatory particles have a particle size of less than 3.5 microns; and v. ~about 90% of the steroidal anti-inflammatory particles have a particle size of less than 5.0 microns.
wherein said formulation is suitable for administration to the nasal-paranasal mucosa.

3. The formulation of claims 1 or 2, further comprising about 0.5 to about 150 mg of an antifungal agent.

4. The formulation of claim 3, wherein the antifungal agent is amphotericin .beta..

5. The formulation of claim 3, wherein said formulation comprises about 7.5 to about 15 mg of amphotericin .beta..

.beta.

6. The formulation of claim 3, wherein said formulation comprises about 10 mg of amphotericin ~3.

7. The formulation of claim 3, wherein said formulation comprises about 20 to about 70 mg of fluconazole or itraconazole.

The formulation of claim 3, wherein said formulation comprises about 25 to about 50 mg of fluconazole or itraconazole.

9. The formulation of claim 3, wherein said formulation comprises about 30 mg of fluconazole or itraconazole.

10. The formulation of claim 1, comprising about 25 to about 400 mcg of said steroidal anti-inflammatory.

11. The formulation of claim 1, comprising about 75 to about 300 mcg of said steroidal anti-inflanunatory.

12. The formulation of claim 1, comprising about 200 mcg of said steroidal anti-inflammatory.

13. The formulation of claim 10, wherein the steroidal anti-inflammatory has the following particle size distribution profile:
i. about 10% or less of the steroidal anti-inflammatory particles have a particle size of less than 0.90 microns;
ii. about 25% or less of the steroidal anti-inflammatory particles have a particle size of less than 1.6 microns;
iii. about 50% or less of the steroidal anti-inflammatory particles have a particle size of less than 3.2 microns;' iv. ~about 75% or less of the steroidal anti-inflammatory particles have a particle size of less than 6.10 microns; and, v. ~about 90% or less of the steroidal anti-inflammatory particles have a particle size of less than 10 microns.

14. ~The formulation of claim 1, wherein the steroidal anti-inflammatory is fluticasone propionate having the following particle size distribution profile:
i. ~about 10% of the steroidal anti-inflammatory particles have a particle size of less than 0.70 microns;
ii. ~about 25% of the steroidal anti-inflammatory particles have a particle size of less than 1.30 microns;
iii. ~about 50% of the steroidal anti-inflammatory particles have a particle size of less than 2.5 microns;
iv. ~about 75% of the steroidal anti-inflammatory particles have a particle size of less than 4.0 microns;
v. ~about 90% of the steroid particles have a particle size of less than 6.0 microns; and, vi. ~greater than 90% or about 100% of the steroidal anti-inflammatory particles have a particle size of less than 10 microns.

15. ~The formulation of claim 1, wherein the steroidal anti-inflammatory is fluticasone propionate having the following particle size distribution profile:
i. ~about 10% of the steroidal anti-inflammatory particles have a particle size less than 0.50 microns;

ii, ~about 25% of the steroidal anti-inflammatory particles have a particle size less than 0.90 microns;

iii. ~about 50% of the steroidal anti-inflammatory particles have a~
particle size less than 1.7 microns;

iv. ~about 75% of the steroidal anti-inflammatory particles have a particle size less than 3.5 microns; and, v, ~about 90% of the steroidal anti-inflammatory particles have a particle size less than 5.5 microns.

16. ~The formulation of claim 2, comprising about 0.2 to about 3 mg of said steroidal anti-inflammatory.

17. ~The formulation of claim 2, comprising about 0.2 to about 2 mg of said steroidal anti-inflammatory.

18. ~The formulation of claim 2, comprising about 0.8 mg of said steroidal anti-inflammatory.

19. ~The formulation of claim 16, wherein the steroidal anti-inflammatory has the following particle size distribution profile:
i. ~about 10% of the steroidal anti-inflammatory particles have a particle size of less than 0.35 microns;
ii. ~about 25% of the steroidal anti-inflammatory particles have a particle size of less than 0.70 microns;
iii. ~about 50% of the steroidal anti-inflammatory particles have a particle size of less than 1.25 microns;

iv. ~about 75% of the steroidal anti-inflammatory particles have a particle size of less than 2.0 microns;
v. ~about 90% of the steroidal anti-inflammatory particles have a particle size of less than 3.0 microns; and, vi. ~greater than 90% or about 100% of the steroidal anti-inflammatory particles have a particle size of less than 6.5 microns.

20. ~The formulation of claim 16, wherein the steroidal anti-inflammatory has the following particle size distribution profile:
i. ~about 10% of the steroidal anti-inflammatory particles have a particle size less than 0.40 microns;
ii. ~about 25% of the steroidal anti-inflammatory particles have a particle size less than 0.70 microns;
iii. ~about 50% of the steroidal anti-inflammatory particles have a particle size less than 1.3 microns;
iv. ~about 75% of the steroidal anti-inflammatory particles have a particle size less than 2.0 microns;
v, ~about 90% of the steroidal anti-inflammatory particles have a particle size less than 3.0 microns; and, vi. ~greater than 90% or about 100% of the steroidal anti-inflammatory particles have a particle size less than 6.0 microns.

21. ~The formulation of claim 16, wherein the steroidal anti-inflammatory is beclomethasone dipropionate having the following particle size distribution profile:

i. ~about 10% of the steroidal anti-inflammatory particles have a particle size less than 0.60 microns;
ii. ~25% of the steroidal anti-inflammatory particles have a particle size less than 0.90 microns;
iii. ~about 50% of the steroidal anti-inflammatory particles have a particle size less than 1.5 microns;
iv. ~about 75% of the steroidal anti-inflammatory particles have a particle size less than 2.5 microns;
v. ~about 90% of the steroidal anti-inflammatory particles have a particle size less than 3.5 microns; and, vi. ~greater than 90% or about 100% of the steroidal anti-inflammatory particles have a particle size less than 6.0 microns.

22. ~The formulation of claim 1, wherein the formulation is sterile.

23. ~The formulation of claim 1, wherein the formulation further comprises a preservative.

24. ~The formulation of claim 23, wherein the preservative is benzalkonium chloride.

25. ~The formulation of claim 1, wherein the formulation is stable.

26. ~The formulation of claim 1, wherein the formulation is an aqueous suspension or aqueous solution.

27. ~The formulation of claim 26, wherein.the formulation is in a metered-dose spray pump bottle.

28. ~The formulation of claim 26, further comprising about 0.01% to about 90% by weight on a dried weight basis of one or more of the following compounds:
(a) microcrystalline cellulose;
(b) carboxymethyl cellulose sodium;
(c) dextrose;
(d) benzalkonium chloride;
(e) polysorbate 80; and (g) phenylethyl alcohol.

29. ~The formulation of claim 1, further comprising an antibiotic.

30. ~The formulation of claim 29, wherein the antibiotic is one or more selected from the group consisting of Amikacin, Azithromycin, Aztreonan, Cefazolin, Cefepine, Cefonicid, Cefaperazone, Cefotaxime, Cefotetan, Cefoxitin, Ceftazidime, Ceftizoxime, Ceftriaxone, Cefuroxime, Cephapirin, Ciprofloxacin, Clindamycin, Doxycycline, Erythromycin Lactobionate, Gentamicin, Kanamycin, Linezolid, Mezlocillin, Mupirocin, Nafcillin, Netihnicin, Neomycin, Oxacillin, Paromomycin, Piperacillin, Streptomycin, Ticarcillin, Tobramycin, and Vancomycin.

31. ~The formulation of claim 29, wherein the formulation comprises about 1 to about 800 mg of neomycin sulfate.

32. ~The formulation of claim 29, wherein the formulation comprises about 5 to about 500 mg of neomycin sulfate.

33. ~The formulation of claim 29, wherein the formulation comprises about 50 to about 300 mg of neomycin sulfate.

34. ~The formulation of claim 29, wherein the formulation comprises about 150 mg of neomycin sulfate.

35. ~A formulation for the treatment of fungus-induced rhinosinusitis, said formulation comprising:
(a) ~about 7.5 to about 15 mg of amphotericin .beta.;
(b) ~about 75 to about 300 mcg of the steroidal anti-inflammatory fluticasone propionate having the following particle size distribution profile:
ii. ~about 10% of the steroidal anti-inflammatory particles have a particle size of less than 0.70 microns;
iii, ~about 25% of the steroidal anti-inflammatory particles have a particle size of less than 1.30 microns;
iv. ~about 50% of the steroidal anti-inflammatory particles have a particle size of less than 2.5 microns;
v. ~about 75% of the steroidal anti-inflammatory particles have a particle size of less than 4.0 microns;
vi. ~about 90% of the steroid particles have a particle size of less than 6.0 microns; and, vii, ~greater than 90% or about 100% of the steroidal anti-inflammatory particles have a particle size of less than 10 microns.
wherein said formulation is suitable for administration to the nasal-paranasal mucosa.

36. ~A formulation for the treatment of fungus-induced rhinosinusitis, said formulation comprising:
(a) ~about 7.5 to about 15 mg of amphotericin .beta.;

(b) about 0.2 to about 2 mg of the steroidal anti-inflammatory beclomethasone dipropionate having the following particle size distribution range;
ii. about 10% of the steroidal anti-inflammatory particles have a particle size less than 0.40 microns iii. about 25% of the steroidal anti-inflammatory particles have a particle size less than 0.70 microns;
iv. about 50% of the steroidal anti-inflammatory particles have a particle size less than 1.3 microns;
v. about 75% of the steroidal anti-inflammatory particles have a particle size less than 2.0 microns;
vi. about 90% of the steroidal anti-inflammatory particles have a particle size less than 3.0 microns; and, vii. greater than 90% or about 100% of the steroidal anti-inflammatory particles have a particle size less than 6.0 microns;
wherein said formulation is suitable for administration to the nasal-paranasal mucosa.

37. The formulation of claim 35 or 36, further comprising about 50 to about 250 mg of the antibiotic neomycin sulfate.

38. The formulation of claim 37, wherein said formulation is a sterile aqueous solution or aqueous suspension suitable for administration to the nasal-paranasal mucosa via a metered-dose spray pump bottle.

39. The formulation of claim 38, further comprising about 0.01% to about 90% by weight on a dried weight basis of one or more of the following compounds:
(a) microcrystalline cellulose;
(b) carboxymethyl cellulose sodium;

(c) dextrose;
(d) benzalkonium chloride;
(e) polysarbate 80; and (g) phenylethyl alcohol.

40. A formulation for the treatment of fungus-induced rhinosiriusitis, said formulation comprising:
(a) about 25 to about 45 mg of fluconazole or itraconazole;
(b) about 75 to about 300 mcg of the steroidal anti-inflammatory fluticasone propionate having the following particle size distribution profile:
ii. about 10% of the steroidal anti-inflammatory particles have a particle size of less than 0.70 microns;
iii. about 25% of the steroidal anti-inflammatory particles have a particle size of less than 1.30 microns;
iv. about 50% of the steroidal anti-inflammatory particles have a particle size of less than 2.5 microns;
v. about 75% of the steroidal anti-inflammatory particles have a particle size of less than 4.0 microns;
vi. about 90% of the steroid particles have a particle size of less than 6.0 microns; and, vii. greater than 90% or about 100% of the steroidal anti-inflammatory particles have a particle size of less than 10 microns.

wherein said formulation is suitable for administration to the nasal-paranasal mucosa.

41. A formulation for the treatment of fungus-induced rhinosinusitis, said formulation comprising:
(a) about 25 to about 45 mg of fluconazole or itraconazole;
(b) about 0.2 to about 2 mg of the steroidal anti-inflammatory beclomethasone dipropionate having the following particle size distribution range;
ii. about 10% of the steroidal anti-inflammatory particles have a particle size less than 0.40 microns iii. about 25% of the steroidal anti-inflammatory particles have a particle size less than 0.70 microns;
iv. about 50% of the steroidal anti-inflammatory particles have a particle size less than L3 microns;
v. about 75% of the steroidal anti-inflammatory particles have a particle size less than 2.0 microns;
vi. about 90% of the steroidal anti-inflammatory particles have a particle size less than 3.0 microns; and, vii. greater than 90% or about 100% of the steroidal anti-inflammatory particles have a particle size less than 6.0 microns;
wherein said formulation is suitable for administration to the nasal-paranasal mucosa.

42. The formulation of claim 40 or 41, further comprising about 50 to about 250 mg of the antibiotic neomycin sulfate.

43. The formulation of claim 42, wherein said formulation is a sterile aqueous solution or aqueous suspension suitable for administration to the nasal-paranasal mucosa via a metered-dose spray pump bottle.

44. The formulation of claim 43, further comprising about 0.01 % to about 90% by weight on a dried weight basis of one or more of the following compounds:
(a) microcrystalline cellulose;
(b) carboxymethyl cellulose sodium;
(c) dextrose;
(d) benzalkonium chloride;
(e) polysarbate 80; and (g) phenylethyl alcohol.

45. A method of treating fungus-induced rhinosinusitis in a mammal, said method comprising the steps of applying to the mammal's nasal-paranasal mucosa a formulation comprising:
(a) about 1 to about 700 mcg of a steroidal anti-inflammatory, wherein the steroidal anti-inflammatory is fluticasone or a pharmaceutically acceptable derivative thereof, said steroidal anti-inflammatory having the following particle size distribution profile:
i. about 10% of the steroidal anti-inflammatory particles have a particle size of less than 0.90 microns;
ii. about 25% of the steroidal anti-inflammatory particles have a particle size of less than 1.6 microns;

iii. about 50% of the steroidal anti-inflammatory particles have a particle size of less than 3.2 microns;
iv. about 75% of the steroidal anti-inflammatory particles have a particle size of less than 6.2 microns; and v. about 90% of the steroidal anti-inflammatory particles have a particle size of less than 10.0 microns.

46. A method of treating fungus-induced rhinosinusitis in a mammal, said method comprising the steps of applying to the mammal's nasal-paranasal mucosa a formulation comprising:
(a) about 1 to about 700 mcg a steroidal anti-inflammatory, wherein the steroidal anti-inflammatory is beclomethasone or a pharmaceutically acceptable derivative thereof, said steroidal anti-inflammatory having the following particle size distribution profile:
i. about 10% of the steroidal anti-inflammatory particles have a particle size of less than 0.75 microns;
ii. about 25% of the steroidal anti-inflammatory particles have a particle size of less than 1.5 microns;
iii. about 50% of the steroidal anti-inflammatory particles have a particle size of less than 2.0 microns;
iv. about 75% of the steroidal anti-inflammatory particles have a particle size of less than 3.5 microns; and v. about 90% of the steroidal anti-inflammatory particles have a particle size of less than 5.0 microns.
wherein said formulation is suitable for administration to the nasal-paranasal mucosa.

47. The method of claims 45 or 46, further comprising the step of treating the mammal with an antifungal agent selected from the group consisting of amphotericin .beta., fluconazole, and itraconazole.

48. The method of claim 47, wherein said formulation comprises about 4 mg to about 30 mg of amphotericin .beta..

49. The method of claim 47, wherein said formulation comprises about 10 mg of amphotericin .beta..

50. The method of claim 47, wherein said formulation comprises about 20 to about 70 mg of fluconazole or itraconazole.

51. The method of claim 47, wherein said formulation comprises about 30 mg of fluconazole or itraconazole.

52. The method of claim 45, wherein said formulation comprises about 25 to about 400 mcg of said steroidal anti-inflammatory.

53. The method of claim 52, wherein the steroidal anti-inflammatory has the following particle size distribution profile:
i. about 10% or less of the steroidal anti-inflammatory particles have a particle size of less than 0.90 microns;
ii. about 25% or less of the steroidal anti-inflammatory particles have a particle size of less than 1.6 microns;

iii. about 50% or less of the steroidal anti-inflammatory particles have a particle size of less than 3.2 microns;
iv. about 75% or less of the steroidal anti-inflammatory particles have a particle size of less than 6.10 microns; and, v. about 90% or less of the steroidal anti-inflammatory particles have a particle size of less than 10 microns.

54. The method of claim 52, wherein the steroidal anti-inflammatory is fluticasone propionate having the following particle size distribution profile:
i. about 10% of the steroidal anti-inflammatory particles have a particle size less than 0.50 microns;
ii. about 25% of the steroidal anti-inflammatory particles have a particle size less than 0.90 microns;
iii. about 50% of the steroidal anti-inflammatory particles have a particle size less than 1.7 microns;
iv. about 75% of the steroidal anti-inflammatory particles have a particle size less than. 3.5 microns; and, v. about 90% of the steroidal anti-inflammatory particles have a particle size less than 5.5 microns.

55. The method of claim 46, wherein said formulation comprises about 0.2 to about 3 mg of said steroidal anti-inflammatory.

56. The method of claim 46, wherein said formulation comprises about 0.8 mg of said steroidal anti-inflammatory.

57. The method of claim 55, wherein the steroidal anti-inflammatory has the following particle size distribution profile:
i. about 10% of the steroidal anti-inflammatory particles have a particle size of less than 0.35 microns;
ii. about 25% of the steroidal anti-inflammatory particles have a particle size of less than 0.70 microns;
iii. about 50% of the steroidal anti-inflammatory particles have a particle size of less than 1.25 microns;
iv. about 75% of the steroidal anti-inflammatory particles have a particle size of less than 2.0 microns;
v. about 90% of the steroidal anti-inflammatory particles have a particle size of less than 3.0 microns; and, vi. greater than 90% or about 100% of the steroidal anti-inflammatory particles have a particle size of less than 6.5 microns.

58. The method of claim. 55, wherein the steroidal anti-inflammatory is beclomethasone dipropionate having the following particle size distribution profile:
i. about 10% of the steroidal anti-inflammatory particles have a particle size less than 0.60 microns;
ii. 25% of the steroidal anti-inflammatory particles have a particle size less than 0.90 microns;
iii. about 50% of the steroidal anti-inflammatory particles have a particle size less than 1.5 microns;

iv. about 75% of the steroidal anti-inflammatory particles have a particle size less than 2.5 microns;
v. about 90% of the steroidal anti-inflammatory particles have a particle size less than 3.5 microns; and, vi. greater than 90% or about 100% of the steroidal anti-inflammatory particles have a particle size less than 6.0 microns.

59. The method of claim 45 or 46, wherein the formulation is a sterile aqueous suspension or aqueous solution.

60. The method of claim 59, wherein the formulation is in a metered-dose spray pump bottle.

61. The method of claim 60, wherein the formulation is administered to said mammal as one spray in each nostril from 1 to about 10 times per day.

62. The method of claim 45 or 46wherein said formulation is administered topically to the nasal-paranasal mucosa of said mammal from 1 to about 10 times per day.

63. The method of claim 45 or 46, further comprising the step of administering an antibiotic to said mammal, wherein said mammal is diagnosed with a bacterial infection of the nasal-paranasal mucosa.

64. The method of claim 63, wherein the antibiotic is administered orally.

65. The method of claim 63, wherein the antibiotic is administered intranasally.

66. The method of claim 65, wherein the antibiotic is neomycin sulfate.

67. The method of claim 45 or 46, wherein said formulation further comprises an antibiotic.

68. The method of claim 67, wherein the formulation comprises about 1 to about 800 mg of neomycin sulfate.

69. The formulation of claim 67, wherein the formulation comprises about 50 to about 300 mg of neomycin sulfate.

70. The method of claim 67, wherein the formulation is a sterile aqueous suspension or aqueous solution in a metered-dose spray pump bottle, and wherein the formulation is administered to said mammal as one spray in each nostril from 1 to about times per day.