WO2009120881A1 - Methods for improving lid margin and tear film function and treatment of lid margin desease using tetracycline family antibiotics - Google Patents
Methods for improving lid margin and tear film function and treatment of lid margin desease using tetracycline family antibiotics Download PDFInfo
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- WO2009120881A1 WO2009120881A1 PCT/US2009/038428 US2009038428W WO2009120881A1 WO 2009120881 A1 WO2009120881 A1 WO 2009120881A1 US 2009038428 W US2009038428 W US 2009038428W WO 2009120881 A1 WO2009120881 A1 WO 2009120881A1
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- blepharitis
- eyelid
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- lid margin
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/65—Tetracyclines
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/32—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. carbomers, poly(meth)acrylates, or polyvinyl pyrrolidone
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0048—Eye, e.g. artificial tears
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
Definitions
- the present invention relates generally to novel compositions and methods for the treatment and prevention of lid margin disease. More specifically, the present invention relates a composition comprising an anti-infective/anti-inflammatory agent and a mucoadhesive vehicle for improving lid margin function, thereby treating lid margin and tear film disease and diseases associated therewith, and methods of administering said compositions to a subject in need thereof.
- the lid margin plays a vital role in the production of tear film and maintenance of a healthy ocular surface.
- Lipids which are secreted by the meibomian glands in the eyelids contribute to a mixture along with mucin (secreted by the goblet cells in the conjunctiva, and an aqueous component (secreted by the lacrimal glands) which protects the cornea and serves as the major refracting surface of the eye.
- Lid margin disease is a common, chronic disease with a broad and potentially serious impact.
- the signs and symptoms associated with lid margin disease can affect quality of life, and its sequelae can result in permanent tissue damage and loss of vision.
- Lid margin disease is also an important risk factor for complications and suboptimal outcomes in patients undergoing ocular surgery.
- Lid margin disease is also a common cause, or co-variant in another common ocular surface disease condition, dry eye.
- Lid margin disease can be associated with dry eye and/or can be a cause of dry eye, specifically, evaporative dry eye.
- Lid margin disease is underdiagnosed and commonly misdiagnosed. Little is known about the underlying pathophysiology of lid margin disease and it is difficult to characterize as it frequently co-exists with other ocular conditions. In addition, therapeutic efficacy has been difficult to achieve due to delivery hurdles to the meibomian glands. However, considering its consequences, it is important for ophthalmologists and optometrists to consider lid margin disease so that it will be identified and treated. Presently there is no cure for lid margin disease. Strategies are available to resolve acute flares and maintain disease control, but treatment is challenging because these interventions may be tedious, time-consuming, and must be continued long-term. Educating patients about the chronic nature of lid margin disease and its sequelae is important for increasing compliance that is the basis for effective management. Considering the prevalence of lid margin disease and its burden, there exists a need for an ocular therapeutic and therapeutic regimen for improving lid margin function and treating and preventing diseases related thereto. The present invention meets this need and other needs.
- the present invention provides topical ophthalmic formulations suitable for improving lid margin function which comprise a combination of ingredients capable of acting synergistically to normalize meibomian gland secretion (i.e., decrease meibomian secretion viscosity, increase secretions transparency and decrease the time between gland secretions) and relieve ocular discomfort, thereby treating and/or preventing at least one sign or symptom of lid margin disease.
- the formulations described herein comprise a broad spectrum antibiotic having both anti-infective and anti-inflammatory properties in a mucoadhesive vehicle suitable for intermittent and/or repeated long term use for the treatment and/or prevention of lid margin disease and diseases associated therewith (e.g., dry eye disease, chronic conjunctitivits, chalazia and keratitis).
- lid margin disease and diseases associated therewith e.g., dry eye disease, chronic conjunctitivits, chalazia and keratitis.
- lid margin disease e.g., anterior and posterior blepharitis, meibomianitis, meibomian gland dysfunction
- diseases associated therewith e.g. , dry eye disease
- administering to the eyelid margin, to the front of the eye, under the upper eyelid, on the lower eyelid, to the lacrimal gland or the cul-de-sac of said subject an effective amount of a topical ophthalmic formulation of the invention.
- the ophthalmic formulation is administered at least once a day (e.g., once or twice a day or more) for up to at least three months (i.e., up to three months or longer).
- the medication may be discontinued after three months of therapy and then re-instituted as needed for prolonged periods of time.
- the medication may be used continuously, as determined by the patient's clinical response.
- the ophthalmic formulation is gently massaged into the eyelid of the subject following topical administration to the eyelid margin, to the front of the eye, under the upper eyelid, on the lower eyelid, to the lacrimal gland or the cul-de-sac.
- the topical ophthalmic formulation of the invention is administered in conjunction with a palliative therapeutic, such as lid hyperthermia, eyelid hygiene, and/or nutritional supplements (e.g., omega-3, fish oil, flaxseed oil).
- the broad-spectrum anti-infective agent includes but is not limited to a tetracycline family antibiotic (e.g., tetracycline, doxycycline, minocycline or any derivative thereof).
- the anti-infective agent is doxycycline or a derivative thereof.
- the anti-infective agent is tetracycline or minocycline, or any derivatives thereof.
- mucoadhesive vehicles suitable for use in the methods or formulations of the invention include but are not limited to aqueous polymeric suspensions comprising one or more polymeric suspending agents including without limitation dextrans, polyethylene glycol, polyvinylpyrolidone, polysaccharide gels, Gelrite®, cellulosic polymers, and carboxy-containing polymer systems.
- the polymeric suspending agent comprises a crosslinked carboxy-containing polymer (e.g., polycarbophil).
- cross-linked carboxy-containing polymer systems suitable for use in the topical ophthalmic formulations of the invention include but are not limited to Noveon AA-I, Carbopol®, and/or DuraSite®.
- Also provided by the present invention are methods for delivery a therapeutic agent to the meibomian gland orifice of a subject comprising: (a) formulating the therapeutic agent in a mucoadhesive vehicle comprising a polymeric suspending agent, including without limitation dextrans, polyethylene glycol, polyvinylpyrolidone, polysaccharide gel,Gelrite®, cellulosic polymers, carboxy-containing polymer systems, and any combination thereof; (b) administering the formulation of step (a) to the eyelid margin, to the front of the eye, under the upper eyelid, on the lower eyelid, to the lacrimal gland, or the cul-de-sac of said subject; and (c) massaging the formulation of step (a) into the eyelid of said subject after the application step (b).
- a mucoadhesive vehicle comprising a polymeric suspending agent, including without limitation dextrans, polyethylene glycol, polyvinylpyrolidone, polysaccharide gel,Gel
- the nonaqueous component provides acute protection of the meibomian gland orifice, optimizes efficacy of supporting the tear film of the ocular surface, and increases the dwell time of the active agent to the meibomian gland orifice thereby increasing therapeutic efficacy of the active agent, while the administration to the eyelid margin, to the front of the eye, under the upper eyelid, on the lower eyelid, to the lacrimal gland or the cul-de-sac of said subject and the massaging of the formulation into the eyelid increases the delivery of the active agent to the meibomian gland orifice.
- abnormal meibomian gland secretion refers to a meibomian gland secretion with increased viscosity, decreased secretion, higher melting temperature, increased inflammatory composition, inspissation of the meibomian glands, opacity, color and/or an increased time (refractory period) between gland secretions.
- blepharitis refers to a disorder comprising inflammation of the lid margin associated with abnormal meibomian gland secretions (known as meibum) in which meibomian gland secretions accumulate and obstruct the meibomian gland duct, causing inflammation of the gland and bacterial colonization. Lid keratinization, lid margin rounding, obscuration of the grey line, increased lid margin transparency, and increased vascularity are often observed.
- meibum abnormal meibomian gland secretions
- blepharitis includes anterior and posterior blepharitis, and bacterial, parasitic, seborrheic, eczematoid, and neoplastic forms of blepharitis.
- dry eye disease refers to inadequate tear production, abnormal tear composition and/or abnormalities of the lipid tear layer, encompassing the terms, but not limited to: qualitative dry eye, evaporative dry eye.
- an effective amount is an art-recognized term, and refers to an amount of an agent that, when incorporated into a pharmaceutical composition of the present invention, produces some desired effect at a reasonable benefit/risk ratio applicable to any medical treatment.
- the term refers to that amount necessary or sufficient to eliminate, reduce or maintain (e.g., prevent the spread of) a symptom of lid margin irritation, or prevent or treat lid margin disease.
- the effective amount may vary depending on such factors as the disease or condition being treated, the particular composition being administered, or the severity of the disease or condition. One of skill in the art may empirically determine the effective amount of a particular agent without necessitating undue experimentation.
- mucoadhesive vehicle refers to a polymer which provides prolonged residence time of dosage forms as well as enhanced drug bioavailability by mucoadhesion.
- Mucoadhesion refers to interfacial force interactions between synthetic or natural polymeric materials serving as a dosage form and a mucus layer that covers a mucosal tissue.
- compositions, polymers and other materials and/or salts thereof and/or dosage forms which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of human beings and animals without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit/risk ratio.
- pharmaceutically acceptable carrier refers to, for example, pharmaceutically acceptable materials, compositions or vehicles, such as a liquid (aqueous or non-aqueous) or solid filler, diluent, excipient, solvent or encapsulating material, involved in carrying or transporting any supplement or composition, or component thereof, from one organ, or portion of the body, to another organ, or portion of the body, or to deliver an agent to the surface of the eye.
- a pharmaceutically acceptable carrier is non-pyrogenic.
- pharmaceutically acceptable salts refers to relatively non-toxic, inorganic and organic acid addition salts of compositions of the present invention or any components thereof, including without limitation, therapeutic agents, excipients, other materials and the like.
- pharmaceutically acceptable salts include those derived from mineral acids, such as hydrochloric acid and sulfuric acid, and those derived from organic acids, such as ethanesulfonic acid, benzenesulfonic acid, p-toluenesulfonic acid, and the like.
- suitable inorganic bases for the formation of salts include the hydroxides, carbonates, and bicarbonates of ammonia, sodium, lithium, potassium, calcium, magnesium, aluminum, zinc and the like.
- Salts may also be formed with suitable organic bases, including those that are non-toxic and strong enough to form such salts.
- the class of such organic bases may include mono-, di-, and trialkylamines, such as methylamine, dimethylamine, and triethylamine; mono-, di- or trihydroxyalkylamines such as mono-, di-, and triethanolamine; amino acids, such as arginine and lysine; guanidine; N-methylglucosamine; N-methylglucamine; L-glutamine; N-methylpiperazine; morpholine; ethylenediamine; N-benzylphenethylamine; (trihydroxymethyl)aminoethane; and the like. See, for example, J. Pharm. ScL, 66:1-19 (1977).
- preventing when used in relation to a condition, such as abnormal meibomian gland secretions, is art-recognized, and refers to administration of a composition which reduces the frequency of, or delays the onset of, signs and/or symptoms of a medical condition in a subject relative to a subject which does not receive the composition.
- tetracycline family antibiotics refers to a subclass of polyketides having an octahydrotetracene-2-carboxamide skeleton, and includes but is not limited to tetracycline, chlortetracycline, oxytetracycline, demeclocycline, doxycycline, lymecycline, meclocycline, methacycline, minocycline, and olitetracycline.
- treating is an art-recognized term which refers to curing as well as ameliorating at least one symptom of any condition or disease.
- Lid margin disease can be defined as any abnormality of the lids and associated adnexal structures, including the accessory glands of the eyelid margin, the mucocutaneous junction, and the meibomian glands (Foulks).
- Blepharitis is a general term often used interchangeably with lid margin disease. It describes a spectrum of conditions characterized by inflammation of the eyelids and includes dermatologic diseases, allergic reactions, and infections.
- Anterior blepharitis is defined as disease affecting predominantly the lid region at the base of the eyelashes. It encompasses both staphylococcal blepharitis and seborrheic blepharitis, although a mixed presentation with both types of blepharitis is common.
- Posterior blepharitis involves the lid margin posterior to the eyelashes. It usually results from disorders of the meibomian glands and is also referred to as meibomian gland dysfunction (MGD) or meibomianitis.
- MMD meibomian gland dysfunction
- the meibomian glands are enlarged sebaceous glands that produce meibum, a lipid secretion that is an important component of the normal tear film.
- Posterior blepharitis may involve either obstruction of the meibomian glands with stagnation of meibomian gland secretions and inspissation of the duct orifices (meibomianitis) or overproduction of meibomian gland secretions (meibomian seborrhea).
- Coagulase negative staphylococci, Corynebacterium spp, Staphylococcus epidermidis, and Propionibacterium acnes comprise the most frequently isolated microflora (Driver). Colonization by Staphylococcus aureus is less prevalent, although this organism appears to be more common in patients with staphylococcal blepharitis than in normal individuals (McCulley). Both S. aureus and S. epidermidis are thought to play an etiologic role in staphylococcal blepharitis. The exact mechanisms are yet to be fully defined, but may involve direct infection, reactions to bacterial exotoxins, or an antigen-related immunologic reaction (AAO, Smith).
- Epithelial hyperkeratinization leading to narrowing of the meibomian gland duct is considered important in the pathogenesis of posterior blepharitis.
- biochemical composition of the meibomian secretions is altered in patients with posterior blepharitis compared to normal controls.
- the altered lipid secretions stagnate within the gland where they may provide a medium for bacterial growth and promote tissue inflammation.
- the underlying cause for the qualitative changes in the meibomian secretions is unproven, but may be mediated through the action of bacterial lipases (Smith).
- S. epidermidis eyelid colonization is similar in patients with MGD and controls, there may be differences between these populations in strain type relating to differences in bacterial lipase activity (Dougherty).
- Staphylococcal blepharitis presents with scaling (collarettes), eyelid crusting, and debris formation along the base of the lashes.
- Affected patients may complain of burning, itching, light sensitivity, and foreign body sensation. These symptoms and eyelid crusting are usually worst in the morning.
- Other clinical signs include lid margin thickening and hyperemia.
- Chronic inflammation from long-standing disease can lead to eyelid scarring and lash changes, including lash loss, breakage, and/or misdirection. Ulceration affecting the base of the lash follicles is rare but can develop during a severe, acute exacerbation.
- Corneal complications can occur and include inferior or diffuse punctate epithelial erosions, marginal infiltrates, scarring, neovascularization, pannus, thinning and perforation, phlyctenules, and Salzmann's nodules.
- Conjunctival findings include mild to moderate hyperemia associated with chronic papillary conjunctivitis.
- Other sequelae associated with staphylococcal blepharitis include pustules, recurrent chalazia, external and internal hordeola, and tear film instability.
- Patients with staphylococcal blepharitis generally do not have associated dermatologic disease, although atopy may be present (AAO).
- Seborrheic blepharitis is also manifested by lid erythema, scaling, and lash abnormalities, although the scales have a greasy appearance, the lashes tend to be stuck together, and the anterior lid margin may have a shiny appearance. Inflammation is less severe in seborrheic blepharitis compared with staphylococcal blepharitis, and patients may be more likely to present with a longer duration of symptoms without exacerbations. Conjunctivitis or keratitis have been reported in a minority of patients with seborrheic blepharitis (AAO). When present, the keratitis generally involves the inferior third of the cornea and is manifested by punctate epithelial erosions. Seborrheic dermatitis is a common comorbidity.
- Dry eye disease has been reported as present in 56% of patients with blepharitis, 48% of patients with obstructive MGD, and 79% of patients with seborrheic MGD (Mathers).
- the frequent association between posterior blepharitis and dry eye disease is not surprising considering that the lipids secreted by the meibomian glands are necessary for normal tear film stability and function.
- dry eye disease may arise through alternative mechanisms. It has been theorized that the altered meibomian gland secretions in patients with posterior blepharitis may have a direct, irritant effect on the ocular surface tissues (Smith).
- the bacterial flora associated with blepharitis may also induce tear film abnormalities and ocular surface inflammation through multiple pathways, including release of exotoxins, induction of pro- inflammatory cytokines and other chemical mediators, and provocation of hypersensitivity reactions (Foulks).
- An important consideration in patients with blepharitis is its potential to impact the outcomes of ocular surgery.
- An already compromised tear film in patients with blepharitis may be further degraded by a variety of surgery-related factors, including severing of corneal nerves by surgical incisions or a LASIK flap, surgically-induced inflammation, and irritation caused by topically instilled medications.
- patients may be more debilitated by symptoms of dry eye and achieve a poorer functional result considering that an optimal precorneal tear film is requisite for quality vision.
- Patients with uncontrolled blepharitis undergoing LASIK are also at risk for trapping of meibomian debris beneath the LASIK flap.
- Diagnosis is the first step in the effective management of lid margin disease.
- Blepharitis may be the most common ophthalmologic disease. It is a frequent underlying cause of other common disorders, including dry eye disease and recurrent conjunctivitis, as well as an important risk factor for suboptimal outcomes after ocular surgery. Therefore, ophthalmologists must remember that all patients deserve a thorough lid and ocular surface examination to identify chronic blepharitis and its sequelae.
- blepharitis The diagnosis of blepharitis is often overlooked because its symptoms tend to be nonspecific or interpreted as related to dry eye disease. Certainly, dry eye disease is a common comorbidity in patients with blepharitis, and it is appropriate that the office evaluation include assessment of the tear film and ocular surface. However, blepharitis may be the underlying cause of any identified abnormalities. Other entities to consider in the differential diagnosis of patients who present with eyelid inflammation include entropion, ectropion, floppy eyelid syndrome, lid imbrication syndrome, mucous fishing syndrome, previous lid surgery or trauma, and allergic eye disease. Acute infections of bacterial, viral, or parasitic origin may present as blepharitis, albeit rarely.
- neoplasms may also masquerade as blepharitis.
- the diagnosis of a tumor may be suspected when the lid disease involves only one eye rather than being bilateral and also if the condition persists after conventional treatment. Early diagnosis is important because of the serious and even life -threatening nature of these neoplasms. Eyelid inflammation may also be medication-induced, with oral isotretinoin being one of the most important culprits (Fraunfelder).
- Diagnosis of blepharitis is often made by a combination of patient history, clinical evaluation and ocular surface examination.
- Risk factors for blepharitis that are often assessed when taking a patient's history include but are not limited to the duration and nature of patient's symptoms, exacerbation by any environmental or other extrinsic factors (eg., low humidity, smoke, allergens, contact lens wear), a history of ocular surgery or trauma, exposure to scabies or other infections that may affect the external eye, medication use, and presence of dermato logic diseases associated with blepharitis (rosacea, atopy, seborrhea).
- Clinical evaluation for blepharitis includes but is not limited to gross examination of the lid margin for inflammation and evidence of foreign matter or debris ⁇ e.g., using a slit-lamp to examine the lid margins s for pustules, lash loss, or other abnormalities); eversion of the lids for examination of the meibomian gland orifices and the nature of the secretions.
- Patients with primary meibomitis exhibit discolored meibomian secretions, inspissation and inflammation near the gland orifices, and ductile dilation. Telangiectasia, hyperemia, and thickening can be seen as signs of chronic inflammation of the lid margin, and there may be secondary anterior lid margin involvement.
- the conjunctival staining in patients with blepharitis overlap with those associated with aqueous deficiency dry eye disease.
- the corneal staining in patients with anterior or posterior blepharitis is often localized to the inferior region where the staphylococcus fall into the tear film and are absorbed into the tear lake.
- the diagnostic workup for any patient who complains of foreign body sensation and ocular irritation should also include a Schirmers test to diagnose aqueous deficiency dry eye.
- An abnormal Schirmers test result does not rule out comorbid MGD, but the finding of normal aqueous production should prompt further evaluation for blepharitis as an underlying etiology for the symptomatic complaints. Since patients with dry eye disease associated with MGD have poor quality tears, they also tend to have a shortened fluorescein tear breakup time even in the presence of normal aqueous production (Pflugfelder).
- Biopsy to diagnose malignancy and cultures for microbiologic testing may be considered on a case-by-case basis depending on the individual features of the patient, including response to treatment.
- Blepharitis is a chronic, incurable disorder requiring ongoing care where the goal is to achieve disease control in order to alleviate associated signs and symptoms, improve quality of life, and prevent complications that can result in permanent tissue damage and even vision loss. Addressing blepharitis preoperatively is also important to reduce complications and optimize the functional outcome for their surgical patients.
- Lid hyperthermia involving application of warm compresses to the eyelids, is a mainstay of therapy for both anterior and posterior blepharitis.
- anterior blepharitis the heat acts to loosen adherent plaques while in posterior blepharitis it induces melting of the meibomian gland secretions and helps to relieve blockage of the gland orifices.
- Patients with posterior blepharitis may be advised to gently massage the lids following lid hyperthermia to express secretions from the meibomian glands.
- Eyelid hygiene is also a fundamental component of treatment for blepharitis. It is particularly important in patients with anterior blepharitis where it is helpful for removing deposits from the lid margin and reducing bacterial colonization of the eyelids. However, it also plays a role in patients with posterior blepharitis as it can clean the lids of free fatty acids and bacteria that have been implicated in the pathogenesis of the disorder and associated dry eye disease. Cleansing should be directed to the lid margin and base of the lashes, not just the eyelid skin, and is preferably performed after lid hyperthermia.
- Anti- inflammatory treatment with topical corticosteroids has a limited role in the treatment of chronic blepharitis. It may be prescribed to gain faster control of more severe inflammation, such as in a patient with an active chalazia/hordeolum, marginal infiltrative keratitis, or conjunctival or corneal phlyctenules.
- risks of corticosteroid treatment include lid atrophy, glaucoma, cataract, and severe opportunistic infections. Therefore, selection of a lower potency corticosteroid, or other site-specific agent should be considered, and the duration of treatment should be limited (McCulley, Dougherty).
- Topical cyclosporine offers an alternative agent for treating acute inflammation.
- antibiotics with antistaphylococcal activity may be appropriate treatment for any of these patients.
- ointment preparations particularly bacitracin and erythromycin, have been most widely used for the treatment of acute anterior blepharitis.
- antibiotic ointments are not generally effective for treating posterior blepharitis because the active ingredients in these petrolatum based- vehicles do not penetrate significantly into the eyelid margins and cause blurring of vision that is disturbing to patients.
- Antibiotics formulated in conventional ophthalmic drops penetrate into the conjunctiva and tear film, but bioavailability to the lid margin and penetration into the eyelid tissue is still poor.
- Oral tetracycline family antibiotics have been prescribed for patients with posterior blepharitis when their disease is not adequately controlled by eyelid hygiene and lid hyperthermia, and it may be particularly considered for patients with co-morbid rosacea.
- tetracyclines provide anti-inflammatory activity (Perry) separate and distinct from their antibiotic effects and have been reported to reduce bacterial lipase and collagenase production. (Frucht-Perry).
- Perry anti-inflammatory activity
- Oral tetracycline treatment is also accompanied by the potential for systemic side effects, including sun sensitivity, vaginal yeast infections, GI disturbances, and possibly the risk of breast cancer.
- these agents are contraindicated for use in women who are pregnant or nursing, and may interact with oral contraceptives and warfarin. They should also not be used in young children because of risks to bone and teeth.
- the invention features topical pharmaceutical compositions comprising an anti- infective/anti-inflammatory agent (e.g., a tetracycline family antibioitic) and a mucoadhesive vehicle useful for treating lid margin disease.
- an effective amount of the formulations of the invention may be used to improve lid margin function, thereby treating diseases associated therewith (e.g., blepharitis, meibomianitis, meibomian gland dysfunction, and dry eye).
- lid margin function includes but are not limited to increased meibomian secretion viscosity, decreased secretion, higher melting temperature, increased inflammatory composition, inspissation of the meibomian glands, opacity, color, as well as an increase in the time (refractory period) between gland secretions
- Signs and symptoms of diseases associated with lid margin disease include but are not limited to dry eye, burning, fluctuating vision, redness of the eyes, itching and/or irritation of the eyelid margins and edema, foreign body sensation, and matting of the lashes.
- the anti- infective agent has both broad spectrum anti-infective activity and anti-inflammatory properties, as well as high tissue penetration.
- the efficacy of the formulations described herein is attributed, in part, to the synergistic effect of the combination of ingredients in them.
- the anti-infective/anti-inflammatory agent relieves, inhibits, prevents, or otherwise decreases the signs and symptoms associated with meibomian gland disease by improving lid margin function.
- the mucoadhesive vehicle provides increased contact time and adhesion of the anti-infective agent to the lid margin, and thereby increased penetration of the anti-infective agent into the eyelid tissue and meibomian glands.
- the pharmaceutical compositions of the invention has enhanced therapeutic efficacy and duration of action over other formulations of anti-infective agents that are not combined with such mucoadhesive vehicles as described herein and do not have an anti-inflammatory effect.
- the enhanced therapeutic efficacy of the compositions of the invention allow for less frequent dosing than anti-infective agents combined with conventional vehicles while achieving therapeutic anti-microbial and anti-inflammatory levels.
- anti-infective agents include, but are not limited to tetracycline family antibiotics (e.g., tetracycline, doxycycline, minocycline) or derivatives or analogs thereof, aminoglycoside antibiotics, bacitracin, erythromycin, neomycin, trimethoprim, sulfa drugs, fluoroquinolones, and chlorophenicol.
- the anti-infective agent is doxycycline.
- the anti-infective agent is a tetracycline family antibiotic (e.g., tetracycline, minocycline, doxycycline, or any combination thereof or derivative thereof).
- Pharmaceutical ophthalmic formulations typically contain an effective amount, e.g. , about 0.1% to about 1% w/v, preferably about 0.15% to about 0.85% w/v, more preferably about 0.25% to about .75% w/v, even more preferably about 0.3% to about 6% w/v of an anti- infective agent suitable treating and/or preventing meibomian gland disease.
- concentration within the ocular tissue is desired to be at least 0.25 ⁇ g/g which is the MIC for many antibiotics, however higher concentrations are preferable (e.g., at least 1 ⁇ g/g, more preferably at least 10 ⁇ g/g) to eradicate resistant organisms and to provided more rapid resolution of an infectious process.
- the amount of anti-infective agent actually supplied to the external eye surface will almost always be much higher than the tissue concentration. This reflects the penetration hold up of the anti-infective agent by the outer tissue layers of the eye and that penetration is to some extent concentration driven. Thus, supplying greater amounts to the exterior will drive more anti-infective agent into the tissues.
- compositions of the invention described above may additionally comprise or be administered in conjunction with (simultaneously or sequentially) one or more additional active ingredients, including, but not limited to, an anti- infective agents (e.g., antibiotics, antivirals, antifungals), anti-inflammatory agents (including steroidal and nonsteroidal antiinflammatories), vasoconstrictors, antiallergenic agents, anesthetics, analgesics, and dry eye agents (e.g. secretagogues, mucomimetics, polymers, lipids, antioxidants).
- an anti- infective agents e.g., antibiotics, antivirals, antifungals
- anti-inflammatory agents including steroidal and nonsteroidal antiinflammatories
- vasoconstrictors e.g., antiallergenic agents, anesthetics, analgesics
- dry eye agents e.g. secretagogues, mucomimetics, polymers, lipids, antioxidants.
- compositions of the invention may be formulated as an aqueous suspension or solution.
- other dosage forms for topical administration to the external eye surface may be used (e.g., ointments, suspensions, viscous or semi-viscous gels, or other types of solid or semi-solid compositions).
- any of a variety of pharmaceutically acceptable carriers or vehicles that are compatible with the eye may be used in the formulations of the present invention.
- materials which may serve as pharmaceutically acceptable carriers include: (1) sugars, such as lactose, glucose and sucrose; (2) starches, such as corn starch and potato starch; (3) cellulose, and its derivatives, such as sodium carboxymethyl cellulose, ethyl cellulose and cellulose acetate; (4) powdered tragacanth; (5) malt; (6) gelatin; (7) talc; (8) excipients, such as cocoa butter and suppository waxes; (9) oils such as castor oil, olive oil, peanut oil, macadamia nut oil, walnut oil, almond oil, pumpkinseed oil, cottonseed oil, sesame oil, corn oil, soybean oil, avocado oil, palm oil, coconut oil, sunflower oil, safflower oil, flaxseed oil, grapeseed oil, canola oil, low viscosity silicone oil, light mineral oil, or any combination
- the carrier is capable of increasing the therapeutic efficacy of the anti-infective agent by extending the residence time of the active agent to the meibomian gland orifice.
- the carrier is a mucoadhesive.
- the compositions of the invention are formulated as an aqueous polymeric suspension.
- the anti-infective agent is in suspension although it is possible for the anti-infective agent to be in solution (water soluble) or both in solution and in suspension.
- the polymeric suspending agent is preferably a suspension (i.e. water insoluble and/or water swe liable), although water soluble suspending agents may also be used.
- the suspending agent serves to provide stability to the suspension and to increase the residence time of the dosage form on the eye. It can also enhance the sustained release of the anti-infective agent in terms of both longer release times and a more uniform release curve.
- polymeric suspending agents examples include dextrans, polyethylene glycols, polyvinylpyrolidone, polysaccharide gels, Gelrite®, cellulosic polymers like hydroxypropyl methylcellulose, and carboxy-containing polymers such as polymers or copolymers of acrylic acid, as well as other polymeric demulcents.
- a preferred polymeric suspending agent is a water swellable, water insoluble polymer, especially a crosslinked carboxy-containing polymer.
- Crosslinked carboxy-containing polymers used in practicing this invention are, in general, well known in the art.
- such polymers may be prepared from at least about 90% and preferably from about 95% to about 99.9% by weight, based on the total weight of monomers present, of one or more carboxy-containing monoethylenically unsaturated monomers (also occasionally referred to herein as carboxy-vinyl polymers).
- Acrylic acid is the preferred carboxy-containing monoethylenically unsaturated monomer, but other unsaturated, polymerizable carboxy-containing monomers, such as methacrylic acid, ethacrylic acid, ⁇ - methylacrylic acid (crotonic acid), cis- ⁇ -methylcro tonic acid (angelic acid), trans- ⁇ - methylcrotonic acid (tiglic acid), ⁇ -butylcrotonic acid, ⁇ -phenylacrylic acid, ⁇ -benzylacrylic acid, ⁇ -cyclohexylacrylic acid, ⁇ -phenylacrylic acid (cinnamic acid), coumaric acid (o- hydroxycinnamic acid), umbellic acid (p-hydroxycoumaric acid), and the like can be used in addition to or instead of acrylic acid.
- carboxy-containing monoethylenically unsaturated monomer but other unsaturated, polymerizable carboxy-containing monomers, such as methacrylic acid, e
- Such polymers may be crosslinked by a polyfunctional crosslinking agent, preferably a difunctional crosslinking agent.
- the amount of crosslinking should be sufficient to form insoluble polymer particles, but not so great as to unduly interfere with sustained release of the anti-infective agent.
- the polymers are only lightly crosslinked.
- the crosslinking agent is contained in an amount of from about 0.01% to about 5%, preferably from about 0.1% to about 5.0%, and more preferably from about 0.2% to about 1%, based on the total weight of monomers present.
- crosslinking agents include non-polyalkenyl polyether difunctional crosslinking monomers such as divinyl glycol; 2,3-dihydroxyhexa-l,5- diene; 2,5-dimethyl-l,5- hexadiene; divinylbenzene; N,N-diallylacrylamide; N ,N- diallymethacrylamide and the like.
- alkenyl halide such as allyl bromide or the like, e.g., polyallyl sucrose, polyallyl pentaerythritol, or the like; see, e.g., Brown U.S. Pat. No. 2,798,053, the entire contents of which are incorporated herein by reference.
- Diolefinic non-hydrophilic macromeric crosslinking agents having molecular weights of from about 400 to about 8,000, such as insoluble di-acrylates and polyacrylates and methacrylates of diols and polyols, diisocyanate-hydroxyalkyl acrylate or methacrylate reaction products of isocyanate terminated prepolymers derived from polyester diols, polyether diols or polysiloxane diols with hydroxyalkylmethacrylates, and the like, can also be used as the crosslinking agents; see, e.g., Mueller et al. U.S. Pat. Nos. 4,192,827 and 4,136,250, the entire contents of each Patent being incorporated herein by reference.
- the crosslinked carboxy-vinyl polymers may be made from a carboxy- vinyl monomer or monomers as the sole monoethylenically unsaturated monomer present, together with a crosslinking agent or agents.
- the polymers are ones in which up to about 40%, and preferably from about 0% to about 20% by weight, of the carboxy-containing monoethylenically unsaturated monomer or monomers has been replaced by one or more non-carboxyl-containing monoethylenically unsaturated monomer or monomers containing only physiologically and ophthalmically innocuous substituents, including acrylic and methacrylic acid esters such as methyl methacrylate, ethyl acrylate, butyl acrylate, 2-ethylhexylacrylate, octyl methacrylate, 2- hydroxyethyl-methacrylate, 3- hydroxypropylacrylate, and the like, vinyl acetate, N- vinylpyrrolidone, and the like; see Mueller
- Particularly preferred polymers are lightly crosslinked acrylic acid polymers wherein the crosslinking monomer is 2,3-dihydroxyhexa-l,5-diene or 2,3-dimethylhexa-l,5-diene.
- Preferred commercially available polymers include polycarbophil (Noveon AA-I) and Carbopol®.
- the crosslinked carboxy-vinyl polymers used in practicing this invention are preferably prepared by suspension or emulsion polymerizing the monomers, using conventional free radical polymerization catalysts, to a dry particle size of not more than about 50 ⁇ m in equivalent spherical diameter; e.g., to provide dry polymer particles ranging in size from about 1 to about 30 gm, and preferably from about 3 to about 20 gm, in equivalent spherical diameter.
- polymer particles that were obtained by mechanically milling larger polymer particles to this size is preferably avoided.
- such polymers will have a molecular weight which has been variously reported as being from about 250,000 to about 4,000,000, and from 3,000,000,000 to 4,000,000,000.
- the particles of crosslinked carboxy- vinyl polymer are monodisperse, meaning that they have a particle size distribution such that at least 80% of the particles fall within a 10 ⁇ m band of major particle size distribution. More preferably, at least 90% and most preferably at least 95%, of the particles fall within a 10 ⁇ m band of major particle size distribution.
- a monodisperse particle size means that there is no more than 20%, preferably no more than 10%, and most preferably no more than 5% particles of a size below 1 ⁇ m.
- the use of a monodispersion of particles will give maximum viscosity and an increased eye residence time of the ophthalmic medicament delivery system for a given particle size.
- Monodisperse particles having a particle size of 30 ⁇ m and below are most preferred. Good particle packing is aided by a narrow particle size distribution.
- the aqueous polymeric suspension normally contains 0.05 to 1%, preferably 0.1 to 0.5%, more preferably 0.1 to 0.5%, of the anti-infective agent and 0.1 to 10%, preferably 0.5 to 6.5% of a polymeric suspending agent.
- a more preferred amount of the polymeric suspending agent is an amount ranging from 0.5 to 2.0%, preferably from 0.5% to about 1.2%, and in certain embodiments from 0.6 to 0.9%, based on the weight of the composition.
- the composition contains 0.6 to 0.8 % of a polycarbophil such as NOVEON AA-I.
- the amount of insoluble lightly crosslinked carboxy-vinyl polymer particles, the pH, and the osmotic pressure can be correlated with each other and with the degree of crosslinking to give a composition having a viscosity in the range of from about 500 to about 100,000 centipoise, and preferably from about 1,000 to about 30,000 or about 1,000 to about 10,000 centipoise, as measured at room temperature (about 25° C) using a Brookfield Digital LVT Viscometer equipped with a number 25 spindle and a 13R small sample adapter at 12 rpm.
- the viscosity is within the range of 500 to 3000 centipoise, it may be determined by a Brookfield Model DV-11+, choosing a number cp-52 spindle at 6 rpm.
- the viscosity will typically be about 10 to about 400 centipoise, more typically about 10 to about 200 centipoises or about 10 to about 25 centipoise.
- Aqueous polymeric suspensions of the present invention may be formulated so that they retain the same or substantially the same viscosity in the eye that they had prior to administration to the eye. Alternatively, they may be formulated so that there is increased gelation upon contact with tear fluid. For instance, when a formulation containing DuraSite® or other similar polyacrylic acid-type polymer is administered to the eye at a pH of less than about 6.7, the polymer will swell upon contact with tear fluid since it has a higher pH (around 7). This gelation or increase in gelation leads to entrapment of the suspended anti-infective agent, thereby extending the residence time of the composition in the eye. The anti-infective agent is released slowly as the suspended particles dissolve over time. All these events eventually lead to increased patient comfort and increased contact time of the anti-infective agent with the eye tissues, thereby increasing the extent of drug absorption and duration of action of the formulation in the eye.
- the viscous gels that result from fluid eye drops typically have residence times in the eye ranging from about 2 to about 12 hours, e.g., from about 3 to about 6 hours.
- the agents contained in these drug delivery systems will be released from the gels at rates that depend on such factors as the drag itself and its physical form, the extent of drag loading and the pH of the system, as well as on any drag delivery adjuvants, such as ion exchange resins compatible with the ocular surface, which may also be present.
- compositions used to topically deliver the anti-infective agent of the present invention can be prepared from known or readily available materials through the application of known techniques by workers of ordinary skill in the art without undue experimentation.
- the anti-infective agent is a tetracycline family antibiotic, it may be commercially available or readily obtained by a worker skilled in the art through known reactions techniques.
- the anti-infective-containing composition is topically applied to an eye of a human or non-human animal, the latter including cows, sheep, horses, pigs, goats, rabbits, dogs, cats, and other mammals.
- the composition can be applied as a liquid drop, ointment, a viscous solution or gel, a ribbon or as a solid.
- the composition can be topically applied, without limitation, to the eyelid margin, to the front of the eye, under the upper eyelid, on the lower eyelid, to the lacrimal gland and/or in the cul-de-sac.
- the composition is massaged into the eyelid immediately after topical application.
- the application can be as a treatment of lid margin disease and diseases associated therewith (e.g., dry eye disesase) or as a preventive such as prior to surgery.
- the active agents of the pharmaceutical compositions may be in the form of a pharmaceutically acceptable salt.
- a pharmaceutically acceptable salt for example, where the preferred anti-infective agent is poorly soluble in water, solubility is improved if converted to a salt form.
- Ointments and solid dosage forms can also be used as delivery compositions as are well known in the art.
- concentration of anti-infective agent present in the ophthalmic composition depends upon the dosage form, the release rate, the dosing regimen, and the location and type of infection. Generally speaking, the concentration is from about 0.01 to 2%, more typically 0.1 to 1%, for fluid compositions and 0.5 to 50% for solid dosage forms, however, the compositions are not limited thereto.
- the pharmaceutical ophthalmic compositions of the present invention include both ointments and suspensions, have a viscosity that is suited for the selected route of administration.
- a viscosity in the range of from about 1 ,000 to 30,000 centipoise is useful for a drop.
- About 30,000 to about 100,000 centipoise is an advantageous viscosity range for ophthalmic administration in ribbon form.
- the viscosity can be controlled in many ways known to the worker skilled in the art.
- viscosity enhancing agents include, but are not limited to: polysaccharides, such as hyaluronic acid and its salts, chondroitin sulfate and its salts, dextrans, various polymers of the cellulose family; vinyl polymers; and acrylic acid polymers.
- Additional ingredients that may be included in the formulations of the invention include tonicity enhancers, preservatives, solubilizers, non-toxic excipients, demulcents, sequestering agents, pH adjusting agents, and co-solvents.
- the pH may be adjusted by adding any physiologically and ophthalmically acceptable pH adjusting acids, bases or buffers to within the range of about 5.0 to 8.5.
- acids include acetic, boric, citric, lactic, phosphoric, hydrochloric, and the like
- bases include sodium hydroxide, sodium phosphate, sodium borate, sodium citrate, sodium acetate, sodium lactate, tromethamine, THAM (trishydroxymethylamino-methane), and the like.
- Salts and buffers include boric acid, sodium borate, potassium citrate, citric acid, sodium bicarbonate, TRIS, and various mixed phosphate buffers (including combinations of Na 2 HPC ⁇ , NaH 2 PC ⁇ and KH2PO4) and mixtures thereof.
- Tonicity is adjusted if needed typically by tonicity enhancing agents.
- agents may, for example be of ionic and/or non-ionic type.
- the osmotic pressure ( ⁇ ) of the aqueous ophthalmic composition is generally from about 10 milliosmolar (mOsM) to about 400 mOsM, more preferably from 260 to 340 mOsM. If necessary, the osmotic pressure can be adjusted by using appropriate amounts of physiologically and ophthalmically acceptable salts or excipients.
- Sodium chloride is preferred to approximate physiologic fluid, and amounts of sodium chloride ranging from about 0.01% to about 1% by weight, and preferably from about 0.05% to about 0.45% by weight, based on the total weight of the composition, are typically used.
- Equivalent amounts of one or more salts made up of cations such as potassium, ammonium and the like and anions such as chloride, citrate, ascorbate, borate, phosphate, bicarbonate, sulfate, thiosulfate, bisulfate, sodium bisulfate, ammonium sulfate, and the like can also be used in addition to or instead of sodium chloride to achieve osmolalities within the above-stated range.
- a sugar such as mannitol, dextrose, sorbitol, glucose and the like can also be used to adjust osmolality.
- the topical formulations additionally comprise a preservative.
- a preservative may typically be selected from a quaternary ammonium compound such as benzalkonium chloride, benzoxonium chloride or the like. Benzalkonium chloride is better described as: N-benzyl-N-(Cs -C 18 alkyl)-N,N-dimethylammonium chloride.
- preservatives different from quaternary ammonium salts are alkyl-mercury salts of thiosalicylic acid, such as, for example, thiomersal, phenylmercuric nitrate, phenyhnercuric acetate or phenylmercuric borate, sodium perborate, sodium chlorite, parabens, such as, for example, methylparaben or propylparaben, alcohols, such as, for example, chlorobutanol, benzyl alcohol or phenyl ethanol, guanidine derivatives, such as, for example, chlorohexidine or polyhexamethylene biguanide, sodium perborate, Germal II or sorbic acid.
- alkyl-mercury salts of thiosalicylic acid such as, for example, thiomersal, phenylmercuric nitrate, phenyhnercuric acetate or phenylmercuric borate, sodium perbor
- Preferred preservatives are quaternary ammonium compounds, in particular benzalkonium chloride or its derivative such as Polyquad (see U.S. Patent Number 4,407,791), alkyl-mercury salts and parabens. Where appropriate, a sufficient amount of preservative is added to the ophthalmic composition to ensure protection against secondary contaminations during use caused by bacteria and fungi.
- topical formulations of this invention do not include a preservative.
- Such formulations would be useful for patients who wear contact lenses, or those who use several topical ophthalmic drops and/or those with an already compromised ocular surface (e.g. dry eye) wherein limiting exposure to a preservative may be more desirable.
- the topical formulation may additionally require the presence of a solubilizer, in particular if the active or the inactive ingredients tends to form a suspension or an emulsion.
- a solubilizer suitable for an above concerned composition is for example selected from the group consisting of tyloxapol, fatty acid glycerol polyethylene glycol esters, fatty acid polyethylene glycol esters, polyethylene glycols, glycerol ethers, a cyclodextrin (for example alpha-, beta- or gamma-cyclodextrin, e.g.
- a specific example of an especially preferred solubilizer is a reaction product of castor oil and ethylene oxide, for example the commercial products Cremophor EL ® or Cremophor RH40 ® .
- solubilizers that are tolerated extremely well by the eye.
- Another preferred solubilizer is selected from tyloxapol and from a cyclodextrin.
- concentration used depends especially on the concentration of the active ingredient.
- the amount added is typically sufficient to solubilize the active ingredient.
- the concentration of the solubilizer is from 0.1 to 5000 times the concentration of the active ingredient.
- the formulations may comprise further non-toxic excipients, such as, for example, emulsifiers, wetting agents or fillers, such as, for example, the polyethylene glycols designated
- the amount and type of excipient added is in accordance with the particular requirements and is generally in the range of from approximately 0.0001 to approximately 90% by weight.
- a method of treating lid margin disease may comprise administering to the eyelid margin, to the front of the eye, under the upper eyelid, on the lower eyelid, to the lacrimal gland and/or the cul-de-sac of a subject in need thereof a formulation comprising an effective amount of an anti-effective agent (e.g., a tetracycline family antibiotic) in a mucoadhseive vehicle, and gently massaging the formulation into the eyelid immediately after topical application for 5-7 days or greater, up to and including a month's duration.
- an anti-effective agent e.g., a tetracycline family antibiotic
- this process may be repeated indefinitely as needed.
- patients may be treated on and off (i.e., one month on, one month off) for several months or continuously for several months, before discontinuing the medication for a one month trial.
- the compositions may improve lid margin function by normalizing meibomian gland function, (i.e., decreasing the meibomian secretion viscosity, reducing meibomian gland inflammation, stabilizing the tear film, increasing secretions transparency to a colorless state and decreasing the time (refractory period) between gland secretions).
- compositions of the invention may treat dry eye disease by penetrating into the meibomian gland and improving meibomian gland function, thereby optimizing the efficacy of supporting the tear film of the ocular surface.
- compositions of the invention may treat or prevent dry eye disease by penetrating into the lacrimal glands and improving aqueous tear quality and quantity.
- the formulations of the invention i.e., a mucoadhesive broad spectrum antibiotic with strong tissue penetration
- the therapeutic dosing regimen is administered in conjunction with (simultaneously or sequentially) with one or more palliative and/or therapeutic measures including but not limited to lid hyperthermia, eyelid hygiene, nutritional supplements, another anti-infective agent, an anti-inflammatory agent, or any combination thereof.
- Such administration may reduce at least one symptom of lid margin disease in a subject and may operate by improving lid margin function in the subject.
- an effective amount of the ophthalmic formulation of the invention e.g., a tetracycline family antibiotic in a mucoadhesive vehicle (e.g., Durasite ® )
- a tetracycline family antibiotic in a mucoadhesive vehicle e.g., Durasite ®
- a mucoadhesive vehicle e.g., Durasite ®
- an effective amount of the ophthalmic formulation of the invention e.g., a tetracycline family antibiotic in a mucoadhesive vehicle (e.g., Durasite ® )
- a tetracycline family antibiotic in a mucoadhesive vehicle e.g., Durasite ®
- topical administration of the formulations of the invention is discontinued for a period of time while other treatments are continued (e.g., lid hyperthermia, eyelid hygiene, treatment and anti-infective or anti-inflammatory agent, nutritional supplements, or a combination thereof.
- other treatments e.g., lid hyperthermia, eyelid hygiene, treatment and anti-infective or anti-inflammatory agent, nutritional supplements, or a combination thereof.
- an effective amount of the ophthalmic formulation of the invention e.g., a tetracycline family antibiotic in a mucoadhesive vehicle (e.g., Durasite ® )
- a tetracycline family antibiotic in a mucoadhesive vehicle e.g., Durasite ®
- a palliative regimen including lid hygiene, lid hyperthermia, nutritional supplements (e.g., omega-3, fish oil, flaxseed oil), or any combination thereof.
- topical administration of the formulation of the invention may be stopped or continued with an effective amount of an identical oral tetracycline family antibiotic, anti-inflammatory corticosteroids and/or cyclosporine. In other certain embodiments, topical administration of the formulations of the invention is reinstated every other month as needed.
- the effective amount of active agent to include in a given formulation, and the efficacy of a formulation for improving lid margin function may be assessed by one or more of the following: slit lamp evaluation, fluorescein staining, tear film breakup time, and evaluating meibomian gland secretions quality (by evaluating one or more of secretion viscosity, secretion color, gland alignment, vascularity pattern, vascularity redness, hyperkeratinization, posterior lid edge, lash, mucocutaneous junction, perigland redness, gland geometry and gland height).
- the effective amount of active agent(s) in the formulation will depend on absorption, inactivation, and excretion rates of the drug as well as the delivery rate of the active agent(s) from the formulation. It is to be noted that dosage values may also vary with the severity of the condition to be alleviated. It is to be further understood that for any particular subject, specific dosage regimens should be adjusted over time according to the individual need and the professional judgment of the person administering or supervising the administration of the compositions. Typically, dosing will be determined using techniques known to one skilled in the art.
- any compound of the present invention may vary depending on the symptoms, age and other physical characteristics of the patient, the nature and severity of the disorder to be treated or prevented, the degree of comfort desired, the route of administration, and the form of the supplement. Any of the subject formulations may be administered in a single dose or in divided doses. Dosages for the formulations of the present invention may be readily determined by techniques known to those of skill in the art or as taught herein.
- an effective dose or amount, and any possible effects on the timing of administration of the formulation may need to be identified for any particular formulation of the present invention. This may be accomplished by routine experiment as described herein.
- the effectiveness of any formulation and method of treatment or prevention may be assessed by administering the formulation and assessing the effect of the administration by measuring one or more indices associated with the efficacy of the composition and with the degree of comfort to the patient, as described herein, and comparing the post-treatment values of these indices to the values of the same indices prior to treatment or by comparing the post-treatment values of these indices to the values of the same indices using a different formulation.
- the precise time of administration and amount of any particular formulation that will yield the most effective treatment in a given patient will depend upon the activity, pharmacokinetics, and bioavailability of a particular compound, physiological condition of the patient (including age, sex, disease type and stage, general physical condition, responsiveness to a given dosage and type of medication), route of administration, and the like.
- the guidelines presented herein may be used to optimize the treatment, e.g. , determining the optimum time and/or amount of administration, which will require no more than routine experimentation consisting of monitoring the subject and adjusting the dosage and/or timing.
- compositions of the present invention may reduce the required dosage for any individual component because the onset and duration of effect of the different components may be complimentary.
- the different active agents may be delivered together or separately, and simultaneously or at different times within the day.
- Dysfunctional tear syndrome a Delphi approach to treatment recommendations. Cornea 2006;25:900-7.
- Boerner CF Dry eye successfully treated with oral flaxseed oil. Ocular Surgery News. 2000;10:147-8.
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Abstract
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Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
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EP09724064A EP2285346A1 (en) | 2008-03-26 | 2009-03-26 | Methods for improving lid margin and tear film function and treatment of lid margin desease using tetracycline family antibiotics |
AU2009228205A AU2009228205A1 (en) | 2008-03-26 | 2009-03-26 | Methods for improving lid margin and tear film function and treatment of lid margin disease using tetracycline family antibiotics |
JP2011502063A JP2011515494A (en) | 2008-03-26 | 2009-03-26 | Methods for improving lid and tear film function and treating lid margin disease using tetracycline family antibiotics |
CA2719453A CA2719453A1 (en) | 2008-03-26 | 2009-03-26 | Methods for improving lid margin and tear film function and treatment of lid margin disease using tetracycline family antibiotics |
US12/934,308 US20110059925A1 (en) | 2008-03-26 | 2009-03-26 | Methods for improving lid margin and tear film function and treatment of lid margin disease using tetracycline family antibiotics |
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US7085008P | 2008-03-26 | 2008-03-26 | |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3199163A4 (en) * | 2014-09-23 | 2018-06-20 | Agencia Pública Empresarial Sanitaria Hospital Alto Guadalquivir | Composition of doxycycline in liposomes for the prevention, improvement and/or treatment of ocular pathologies |
US11419886B2 (en) | 2020-11-23 | 2022-08-23 | Sight Sciences, Inc. | Formulations and methods for treating conditions of the eye |
Families Citing this family (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7981145B2 (en) | 2005-07-18 | 2011-07-19 | Tearscience Inc. | Treatment of meibomian glands |
US7981146B2 (en) | 2006-05-15 | 2011-07-19 | Tearscience Inc. | Inner eyelid treatment for treating meibomian gland dysfunction |
US8083787B2 (en) | 2005-07-18 | 2011-12-27 | Tearscience, Inc. | Method and apparatus for treating meibomian gland dysfunction |
US7981095B2 (en) * | 2005-07-18 | 2011-07-19 | Tearscience, Inc. | Methods for treating meibomian gland dysfunction employing fluid jet |
WO2013003594A2 (en) | 2011-06-28 | 2013-01-03 | Tearscience, Inc. | Methods and systems for treating meibomian gland dysfunction using radio-frequency energy |
US20070060988A1 (en) | 2005-07-18 | 2007-03-15 | Grenon Stephen M | Melting meibomian gland obstructions |
US20080114423A1 (en) | 2006-05-15 | 2008-05-15 | Grenon Stephen M | Apparatus for inner eyelid treatment of meibomian gland dysfunction |
US20090043365A1 (en) | 2005-07-18 | 2009-02-12 | Kolis Scientific, Inc. | Methods, apparatuses, and systems for reducing intraocular pressure as a means of preventing or treating open-angle glaucoma |
US8950405B2 (en) | 2006-05-15 | 2015-02-10 | Tearscience, Inc. | Treatment of obstructive disorders of the eye or eyelid |
US8137390B2 (en) | 2006-05-15 | 2012-03-20 | Tearscience, Inc. | System for providing heat treatment and heat loss reduction for treating meibomian gland dysfunction |
US8128673B2 (en) | 2006-05-15 | 2012-03-06 | Tearscience, Inc. | System for inner eyelid heat and pressure treatment for treating meibomian gland dysfunction |
US8128674B2 (en) | 2006-05-15 | 2012-03-06 | Tearscience, Inc. | System for outer eyelid heat and pressure treatment for treating meibomian gland dysfunction |
US7976573B2 (en) | 2006-05-15 | 2011-07-12 | Tearscience, Inc. | Inner eyelid heat and pressure treatment for treating meibomian gland dysfunction |
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US9314369B2 (en) | 2006-05-15 | 2016-04-19 | Tearscience, Inc. | System for inner eyelid treatment of meibomian gland dysfunction |
US20130177599A1 (en) * | 2012-01-06 | 2013-07-11 | Insite Vision Incorporated | Methods and kits for extending contact lens use |
US10842670B2 (en) | 2012-08-22 | 2020-11-24 | Johnson & Johnson Vision Care, Inc. | Apparatuses and methods for diagnosing and/or treating lipid transport deficiency in ocular tear films, and related components and devices |
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WO2014179356A1 (en) | 2013-04-30 | 2014-11-06 | Tear Film Innovations Llc | Systems and methods for the treatment of eye conditions |
US20170232024A1 (en) * | 2014-08-04 | 2017-08-17 | Jerry Tan Eye Surgery Pte Ltd | Pharmaceutical compositions for demodex related blepharitis and eyelid crusting |
US9463201B2 (en) | 2014-10-19 | 2016-10-11 | M.G. Therapeutics Ltd | Compositions and methods for the treatment of meibomian gland dysfunction |
TW201637648A (en) * | 2015-04-03 | 2016-11-01 | 參天製藥股份有限公司 | Drug delivery system targeting lacrimal gland |
US10688122B2 (en) | 2015-09-28 | 2020-06-23 | Azura Ophthalmics Ltd. | Thiol and disulfide-containing agents for increasing meibomian gland lipid secretion |
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US10974063B2 (en) | 2016-06-30 | 2021-04-13 | Alcon Inc. | Light therapy for eyelash growth |
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EP3741367A1 (en) * | 2019-05-21 | 2020-11-25 | Premark Pharma GmbH | Treatment of ocular disease |
EP4087655A4 (en) | 2020-01-10 | 2024-02-21 | Azura Ophthalmics Ltd | Instructions for composition and sensitivity |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6455583B1 (en) * | 1998-05-08 | 2002-09-24 | The University Of Miami | Method for treating meibomian gland disease |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7056893B2 (en) * | 1999-03-31 | 2006-06-06 | Insite Vision, Inc. | Topical treatment for prevention of ocular infections |
IT1313610B1 (en) * | 1999-08-09 | 2002-09-09 | S I F I Societa Ind Farmaceuti | PROCESS FOR THE PREPARATION OF AQUEOUS FORMULATIONS FOR OPHTHALMIC USE |
US7069084B2 (en) * | 2002-06-14 | 2006-06-27 | Seefit Incorporated | Method and apparatus for preventing and treating eyelid problems |
-
2009
- 2009-03-26 CA CA2719453A patent/CA2719453A1/en not_active Abandoned
- 2009-03-26 JP JP2011502063A patent/JP2011515494A/en active Pending
- 2009-03-26 WO PCT/US2009/038428 patent/WO2009120881A1/en active Application Filing
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Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6455583B1 (en) * | 1998-05-08 | 2002-09-24 | The University Of Miami | Method for treating meibomian gland disease |
Non-Patent Citations (3)
Title |
---|
ANONYMOUS: "Rote Liste 2004", 2004, ROTE LIISTE SERVICE GMBH, XP002535973 * |
CHETONI P ET AL: "Silicone rubber/hydrogel composite ophthalmic inserts: Preparation and preliminary in vitro/in vivo evaluation", EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS 199807 NL, vol. 46, no. 1, July 1998 (1998-07-01), pages 125 - 132, XP004256997, ISSN: 0939-6411 * |
KOCH J M ET AL: "THERAPIE VON BENETZUNGSSTOERUNGEN", KLINISCHE MONATSBLAETTER FUER AUGENHEILKUNDE, FERDINAND ENKE VERLAG, STUTTGART, DE, vol. 204, no. 3, 1 March 1994 (1994-03-01), pages 162 - 168, XP000866287, ISSN: 0023-2165 * |
Cited By (4)
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---|---|---|---|---|
EP3199163A4 (en) * | 2014-09-23 | 2018-06-20 | Agencia Pública Empresarial Sanitaria Hospital Alto Guadalquivir | Composition of doxycycline in liposomes for the prevention, improvement and/or treatment of ocular pathologies |
US11419886B2 (en) | 2020-11-23 | 2022-08-23 | Sight Sciences, Inc. | Formulations and methods for treating conditions of the eye |
US11554134B2 (en) | 2020-11-23 | 2023-01-17 | Sight Sciences, Inc. | Formulations and methods for treating conditions of the eye |
US11925657B2 (en) | 2020-11-23 | 2024-03-12 | Sight Sciences, Inc. | Formulations and methods for treating conditions of the eye |
Also Published As
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JP2011515494A (en) | 2011-05-19 |
CA2719453A1 (en) | 2009-10-01 |
AU2009228205A1 (en) | 2009-10-01 |
US20110059925A1 (en) | 2011-03-10 |
EP2285346A1 (en) | 2011-02-23 |
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