WO2018131835A1 - 설글리코타이드 또는 이의 약학적으로 허용가능한 염을 포함하는 안구건조증의 예방 또는 치료용 약학 조성물 - Google Patents
설글리코타이드 또는 이의 약학적으로 허용가능한 염을 포함하는 안구건조증의 예방 또는 치료용 약학 조성물 Download PDFInfo
- Publication number
- WO2018131835A1 WO2018131835A1 PCT/KR2018/000149 KR2018000149W WO2018131835A1 WO 2018131835 A1 WO2018131835 A1 WO 2018131835A1 KR 2018000149 W KR2018000149 W KR 2018000149W WO 2018131835 A1 WO2018131835 A1 WO 2018131835A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- pharmaceutical composition
- group
- dry eye
- sos
- pharmaceutically acceptable
- Prior art date
Links
Images
Classifications
-
- 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
- A61P27/04—Artificial tears; Irrigation solutions
-
- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/715—Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
- A61K31/726—Glycosaminoglycans, i.e. mucopolysaccharides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/1703—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- A61K38/1709—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
-
- 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
-
- 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
- A61K9/08—Solutions
-
- 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 to a pharmaceutical composition for the prophylaxis or treatment of dry eye syndrome comprising a sulglicote or a pharmaceutically acceptable salt thereof.
- Dry eye syndrom is an ophthalmic disorder called keratoconjunctivitis sicca, which occurs in 5.5-15% of adults worldwide. Dry eye is understood to be a multifunctional disorder of the tear film and the ocular surface, which causes eye surface damage due to discomfort, visual impairment and even tear film instability.
- the main physiological function of the tear film is the lubrication of the ocular surface and the inner eyelid.
- the tear film also provides nutrients to the ocular surface, provides a smooth and even optical surface for the eye, and protects the ocular surface.
- the tear film is composed of a mucous component, an aqueous component, and a lipid component. Problems with lacrimal gland secretion can cause dry eye syndrome.
- Dry eye syndrome causes eyeball discomfort and tear layer instability due to tears and inflammation of the ocular surface (cornea and conjunctiva), causing damage to the ocular surface, resulting in ocular pain, irregular corneal surface, corneal ulcer, It leads to poor vision.
- the altered corneal permeability in chronic dry eye causes inflammation and increases the cytokines that mediate inflammation in tears.
- patients often develop reversible squameous metaphase and punctate erosions of the ocular epithelium.
- Secondary diseases that can be triggered by dry eye include filamentous keratitis, microbial keratitis, corneal angiogenesis, and ocular surface keratinization.
- a common approach is to supplement and stabilize the tear layer of the eye using buffered isotonic saline solutions or artificial tears containing water soluble polymers.
- Artificial tears are, for example, carboxymethylcellulose and its sodium salt (CMC, carmellose), polyvinyl alcohol, hydroxypropyl methylcellulose (HPMC, hypromellose), hyaluronic acid and its sodium salt, and hydroxy Profile guar gum and the like.
- Another approach involves having a lubricating material instead of artificial tears.
- US Pat. No. 4,818,537 discloses the use of lubricated liposome-based compositions
- US Pat. No. 5,800,807 discloses a composition for treating dry eye, containing glycerin and propylene glycol.
- the present inventors conducted various studies to develop a therapeutic agent that can effectively prevent or treat dry eye syndrome.
- sulglycotide which is used as a therapeutic agent for gastric ulcers and reflux esophagitis
- it significantly increases tear production, improves corneal surface irregularities, and improves the density of conjunctival goblet cells. It has been found that it can be usefully applied to the treatment of dry eye by increasing inflammatory cytokines in the ocular surface and tear glands.
- an object of the present invention is to provide a pharmaceutical composition for the prevention or treatment of dry eye syndrome comprising a sulglicote or a pharmaceutically acceptable salt thereof as an active ingredient.
- a pharmaceutical composition for the prevention or treatment of dry eye syndrome comprising a sulglicote or a pharmaceutically acceptable salt thereof as an active ingredient.
- the sulfiglitide or a pharmaceutically acceptable salt thereof may be present at a concentration ranging from 0.01 w / v% to 30 w / v%.
- the pharmaceutical composition of the present invention may have a formulation of an eye drop, which may be in the form of an aqueous solution or an aqueous suspension.
- the pharmaceutical composition of the present invention is a carrier selected from the group consisting of a buffer, a viscosity modifier, an isotonic agent, an antioxidant, a chelating agent and a pH adjusting agent in an aqueous medium, in addition to a sulfoglycotide or a pharmaceutically acceptable salt thereof. Or additives.
- the viscosity modifier is selected from the group consisting of polyvinyl alcohol, polyvinylpyrrolidone, methyl cellulose, hydroxypropyl methylcellulose, hydroxyethyl cellulose, carboxymethyl cellulose, and hydroxypropyl cellulose And preferably polyvinylpyrrolidone or hydroxypropyl methylcellulose.
- the pharmaceutical composition according to the present invention can be usefully applied for the prevention or treatment of dry eye syndrome.
- FIG. 1 shows the effect of sulfoglitide-containing eye drops on tear production in dry eye model (DED).
- FIG. 2 shows the effect of sulglucotide-containing eye drops on corneal surface irregularities in dry eye model (DED).
- FIG. 3 shows the effect of sulfoglitide-containing eye drops on corneal fluorescence staining in dry eye model (DED).
- FIG. 4 shows the effect of sulfoglitide-containing eye drops on the isolation of corneal epithelial cells in dry eye animal model (DED).
- FIG. 5 shows the effect of sulfoglitide-containing eye drops on conjunctival goblet cell density in dry eye model (DED).
- FIG. 6 shows the effect of sulfoglitide-containing eye drops on inflammation in dry eye animal models (DED).
- the present invention provides a pharmaceutical composition for the prevention or treatment of dry eye syndrome comprising a sulglicote or a pharmaceutically acceptable salt thereof as an active ingredient.
- Sulglycotide is a known substance known as a sulfur polyester of glycopeptide extracted from the mucosa of the stomach or duodenum of pigs. Sulglycotide is used for the protection of the stomach, duodenum, prevention and treatment of ulcers. It is rarely absorbed by the gastro-intestinal tract and is effective only in the lumen. It is usually administered as a gastroprotective agent to individuals whose stomach wall is attacked by drugs such as aspirin and taurocholic acid or by nonsteroidal anti-inflammatory (NSAID) drugs.
- NSAID nonsteroidal anti-inflammatory
- sulfoglycotide when sulfoglycotide is administered to dry eye animal models, tear production is significantly increased, corneal surface irregularities are improved, conjunctival goblet cells are increased, and also inflammatory in the ocular surface and lacrimal glands. It has been newly found to reduce cytokines.
- the sulfiglitide may be used in a non-salt form.
- the sulfoglycotide may also be used in the form of a pharmaceutically acceptable salt thereof, which may be appropriately prepared by those skilled in the art.
- the sulfiglitide or a pharmaceutically acceptable salt thereof may be dosed according to the age, weight, sex, dosage form, health condition and degree of disease of the patient. For example, based on an adult patient weighing 70 kg, the dosage ranges from 0.1 to 300 mg / day, preferably 0.5 to 100 mg / day, more preferably 1 to 60 mg / day. It may be, and may be divided once to several times a day at regular intervals according to the judgment of the doctor or pharmacist.
- the sulfoglycotide or pharmaceutically acceptable salt thereof is at a concentration ranging from 0.01 w / v% to 30 w / v%, preferably at a concentration ranging from 0.1 w / v% to 10 w / v%. It may be present, but is not limited thereto.
- the pharmaceutical composition of the present invention may preferably have a formulation of an eye drop, which may be in the form of an aqueous solution or an aqueous suspension.
- the pharmaceutical composition of the present invention may include a carrier or additive commonly used in the eye drop field.
- the pharmaceutical composition of the present invention may be selected from the group consisting of buffers, viscosity modifiers, tonicity agents, antioxidants, chelating agents and pH adjusting agents in an aqueous medium, in addition to sulfoglitide or a pharmaceutically acceptable salt thereof. It may comprise a carrier or additive selected from more than one species.
- buffers commonly used in the field of eye drops, for example phosphoric acid or salts thereof, boric acid or salts thereof, carbonic acid or salts thereof, citric acid or salts thereof, acetic acid or salts thereof, maleic acid or salts thereof, succinic acid Or salts thereof, tartaric acid or salts thereof, and the like.
- the buffer may also be used in the form of a buffer solution such as, for example, phosphate / phosphate buffer solution, boric acid / borate buffer solution.
- Examples of the viscosity modifier may be selected from the group consisting of polyvinyl alcohol, polyvinylpyrrolidone, methyl cellulose, hydroxypropyl methyl cellulose, hydroxyethyl cellulose, carboxymethyl cellulose, and hydroxypropyl cellulose. .
- the viscosity modifier may preferably be polyvinylpyrrolidone or hydroxypropyl methylcellulose, more preferably hydroxypropyl methylcellulose.
- tonicity agents examples include sodium chloride, potassium chloride, calcium chloride, sorbitol, mannitol, and the like.
- antioxidants examples include ascorbic acid and its esters, sodium bisulphite, butylated hydroxytoluene, butylated hydroxyanisole, tocopherol and the like.
- chelating agents examples include ethylenediaminetetraacetic acid (EDTA), ethylenediamine, and the like.
- pH adjusting agent examples include hydrochloric acid, amino acids, alkali metal hydroxides, alkaline earth metal hydroxides, and the like.
- the pharmaceutical compositions of the present invention may include wetting agents, sweetening agents, flavoring agents, emulsifying agents, suspending agents, preservatives, and the like, which are commonly used in the eye drop field.
- the pharmaceutical compositions of the present invention in the form of eye drops may, for example, be dissolved in a solution with sulglucotide or a pharmaceutically acceptable salt thereof in an aqueous solution (eg, water or buffer) under agitation and dissolved in the above-mentioned carrier or additive. Or by suspending.
- the resulting solution or suspension can be prepared in the form of eye drops, typically by aseptic filtration.
- Purified water 400 mL was stirred at 50 rpm while dissolving phosphoric acid (0.0425 g), sodium dihydrogen phosphate (4.43 g), and potassium dihydrogen phosphate (0.29 g), followed by dissolving sulglucotide (5 g) I was. Sodium chloride (2.6 g) was dissolved in the solution. Purified water was added to the obtained solution to adjust the final volume to 500 ml, and then aseptically filtered with a 0.22 um PVDF syringe filter to prepare 1 w / v% of eye drops.
- Purified water 400 mL was stirred at 50 rpm while dissolving phosphoric acid (0.0425 g), sodium dihydrogen phosphate (4.43 g), and potassium dihydrogen phosphate (0.29 g), followed by dissolving sulglucotide (10 g) I was. Sodium chloride (2.4 g) was dissolved in the solution. Purified water was added to the obtained solution, the final volume was adjusted to 500 ml, and then aseptically filtered with a 0.22 um PVDF syringe filter to prepare an eye drop of 2 w / v%.
- Purified water 400 mL was stirred at 50 rpm while dissolving phosphoric acid (0.0425 g), sodium dihydrogen phosphate (4.43 g), and potassium dihydrogen phosphate (0.29 g), followed by dissolving sulglucotide (15 g) I was.
- Sodium chloride 2.2 g was dissolved in the solution.
- Purified water was added to the obtained solution, the final volume was adjusted to 500 ml, and then aseptically filtered with a 0.22 um PVDF syringe filter to prepare 3 w / v% of eye drops.
- Purified water 400 mL was stirred at 50 rpm while dissolving phosphoric acid (0.0425 g), sodium dihydrogen phosphate (4.43 g), and potassium dihydrogen phosphate (0.29 g), followed by dissolving sulglucotide (20 g) I was.
- Sodium chloride 2.0 g was dissolved in the solution.
- Purified water was added to the obtained solution, the final volume was adjusted to 500 ml, and then aseptically filtered with a 0.22 um PVDF syringe filter to prepare 4 w / v% of eye drops.
- Purified water 400 mL was stirred at 50 rpm while dissolving phosphoric acid (0.0425 g), sodium dihydrogen phosphate (4.43 g), and potassium dihydrogen phosphate (0.29 g), followed by dissolving sulglucotide (10 g) I was. Hydroxypropyl methylcellulose (1 g) and sodium chloride (2.4 g) were dissolved in the solution. Purified water was added to the obtained solution, the final volume was adjusted to 500 ml, and then aseptically filtered with a 0.22 um PVDF syringe filter to prepare an eye drop of 2 w / v%.
- Eyedrops were prepared according to the ingredients and contents of Tables 1 and 2 below. Purified water (800 mL) was stirred at 50 rpm while the buffer was dissolved, followed by dissolving the sulfoglycotide. The buffer, viscosity modifiers (Examples 9 and 14), and antioxidants (Examples 10 and 15) were dissolved in the solution, and then adjusted to about pH 7 by addition of a pH adjuster. Purified water was added to the resulting solution to adjust the final volume to 1000 ml, followed by aseptic filtration with a 0.22 um PVDF syringe filter to prepare an eye drop.
- NOD.B10.H2 b mice were purchased from Jackson Laboratory (Bar Harbor, ME, USA). Male NOD.B10.H2 b mice, 12-16 weeks of age, are subjected to desiccation stress by exposure to air draft from a fan at 30-40% humidity for 18 hours / 1 day for 10 days. 0.5mg / 0.2ml scopolamine hydrobromide (Sigma-Aldrich, St. Johns) four times a day (8am, 11am, 2pm, 5pm) in alternating hindquarters. Louis, MO), 0.2 mL subcutaneous injection to cause dry eyes. Animal behavior and food and water intake were not limited during the experiment. After dry eye induction, the scopolamine injection was discontinued and the dry stress was removed by placing the mouse in an environment with normal humidity and temperature.
- the eye drop administration group of the SOS 1 to SOS 5 group each used the eye drops of Examples 1 to 5 5 ⁇ L / 4 times a day (8 AM, 11 PM, 2 PM, 5 PM) for 10 days after dry stress relief. Both eyes were instilled at a dose of eye.
- Tear yield was measured using a phenol-red impregnated cotton thread, according to previously reported methods (Oh HN, Kim CE, Lee JH, Yang JW.Effects of Quercetin in a Mouse Model of Experimental Dry Eye.Cornea. 2015; 34: 1130-6).
- Phenol-red impregnated cotton yarn (Zone-quick, Oasis, Glendora, Calif.) was grasped by the jeweler's forceps and contacted with the lateral canthus for 20 seconds. Tear volumes were expressed in millimeters of the length of the wet thread turned red by tears, measured under a microscope (SZX7, Olympus Corporation, Tokyo, Japan).
- Tear fluid uptake is measured in millimeters and the known uptake volumes of a known stock basic solution (1500 mL of 0.9% saline and 5 mL of 5N NaOH) over 20 seconds. Standard curves prepared from cotton yarns were used and compared to standard curves within the range expected for mouse tears (Villareal AL, Farley W, Pflugfelder SC. Effect of topical ophthalmic epinastine and olopatadine on tear volume in mice.Eye Contact Lens. 2006 32: 272-6; Chen Z, Li Z, Basti S, Farley WJ, Pflugfelder SC.Altered morphology and function of the lacrimal functional unit in protein kinase C alpha knockout mice.Invest Ophthalmol Vis Sci. 2010; 51: 5592- 600). Tear production was measured in both eyes and the mean value of both eyes was analyzed.
- the reflected image of the white ring of the fiber optic ring illuminator of the stereoscopic zoom microscope was measured.
- the distortion of the white ring as a reflection off from the corneal epithelium in the digital image was evaluated by grading by two blinded observers (De Paiva CS, Corrales RM, Villarreal AL, Farley W, Li DQ, Stern ME, Pflugfelder SC.Apical corneal barrier disruption in experimental murine dry eye is abrogated by methylprednisolone and doxycycline.Invest Ophthalmol Vis Sci. 2006; 47: 2847-56).
- the corneal irregularity severity score was calculated using the 5-point scale based on the number of distorted quadrants in the reflected ring. Scored as follows: 0, no distortion; distortion in 1 quadrant of the ring; distortion in 2 quadrants; distortion in third and third quarters ( distortion in 3 quadrants; 4, distortion in all 4 quadrants; and 5, severe distortion, in which no ring could be recognized.
- mice The eyes and adnexa of each group of mice were surgically excised, fixed in 10% formalin, capped with paraffin and cut into 6 ⁇ m fragments. The obtained fragments were stained with H & E (hematoxylin & eosin) and PAS (periodic-Schiff), respectively.
- H & E hematoxylin & eosin
- PAS periodic-Schiff
- the conjunctiva was subjected to H & E staining to calculate the epithelial cell detachment in the 0.1 mm 2 area.
- the conjunctival tissue was subjected to PAS staining to evaluate the number of goblet cells in the conjunctival inferior fornix in the area of 0.1 mm 2 .
- the number of isolated corneal epithelial cells and the number of conjunctival goblet cells were averaged from three non-consecutive cross-section slides for each mouse and 3 or 4 mice per group. It was measured by. Sections of each group were examined and imaged using a virtual microscope (NanoZoomer 2.0 RS, Hamamatsu, Japan).
- Eyes and adnexa were surgically excised, embedded in paraffin and flash frozen in liquid nitrogen. 6 ⁇ m fragments were cut with cryostat. Fragments were fixed for 5 minutes using pre-cooled acetone and primary antibodies against TNF- ⁇ (Abcam Inc., Cambridge, MA), primary antibodies against MMP-2 (Abcam Inc., Cambridge, MA) , Primary antibody against MMP-9 (Lifespan Biosciences Inc., Seattle, WA), primary antibody against ICAM-1 (Bioss Inc., Woburn, MA), and primary antibody against VCAM-1 (Bioss Inc , Woburn, MA) was added and incubated for 1 hour at room temperature. After washing, each fragment was incubated with secondary antibody (DAKO Corp, Glostrup, Denmark) for 30 minutes.
- TNF- ⁇ Abcam Inc., Cambridge, MA
- MMP-2 Abcam Inc., Cambridge, MA
- MMP-9 Lifespan Biosciences Inc., Seattle, WA
- ICAM-1 Bioss Inc., Woburn, MA
- VCAM-1 Bioss
- the SOS 1 group showed a 6.7-fold increase (0.165 ⁇ 0.027 ⁇ L) compared to the DS 10D group (0.025 ⁇ 0.008 ⁇ L) ( P ⁇ 0.05);
- the SOS 2 group showed a 7.6-fold increase (0.157 ⁇ 0.027 ⁇ L) compared to the DS 10D group (0.021 ⁇ 0.009 ⁇ L) ( P ⁇ 0.05);
- the SOS 3 group showed an 8.5-fold increase (0.176 ⁇ 0.030 ⁇ L) compared to the DS 10D group (0.021 ⁇ 0.009 ⁇ L) (P ⁇ 0.05);
- the SOS 4 group showed a 14.6-fold increase (0.246 ⁇ 0.022 ⁇ L) compared to the DS 10D group (0.017 ⁇ 0.008 ⁇ L) ( P ⁇ 0.05);
- the SOS 5 group showed a 15.5-fold increase (0.262 ⁇ 0.018 ⁇
- the corneal irregularity (3.375 ⁇ 0.479 score) of the DS 10D group increased by 13.5 times compared to the control group (0.250 ⁇ 0.289 score), and the decrease observed in the SOS 1 group was 7.4% (3.125) at 10 days. ⁇ 0.250 score, P ⁇ 0.05).
- corneal irregularities observed in the SOS 2 and SOS 3 groups were 8% (2.875 ⁇ 0.250 score, P ⁇ 0.05) and 20.7% (2.875 ⁇ 0.250 score, P ⁇ 0.05) at 10 days, respectively, compared to the DS 10D group. Decreased.
- the irregularities in the SOS 4 and SOS 5 groups decreased to 83.3% (0.625 ⁇ 0.479 score, P ⁇ 0.05) and 87.9% (0.500 ⁇ 0.408 score, P ⁇ 0.05) at 10 days, respectively, compared to the DS 10D group. Especially. The distortion of the white ring in the SOS 4 and 5 groups improved near the control at day 10.
- the control cornea showed no uptatke of fluorescent staining, indicating an intact epithelial barrier.
- the DS 10D cornea showed a patchy staining pattern, indicating a damaged corneal epithelial barrier.
- Corneal fluorescence (9.333 ⁇ 1.155 score) in the DS 10D group showed a 28-fold increase compared to the control (0.333 ⁇ 0.577 score) and did not decrease in the SOS 1 group on day 10 (9.333 ⁇ 0.577 score, P ⁇ 0.05).
- corneal fluorescence observed in the SOS 2 and SOS 3 groups decreased to 3.4% (9.333 ⁇ 0.577, P ⁇ 0.05) and 10% (9.0 ⁇ 0 score, P ⁇ 0.05) at 10 days, respectively, compared to the DS 10D group.
- corneal fluorescence in the SOS 4 and SOS 5 groups decreased to 72.4% (2.667 ⁇ 0.577, P ⁇ 0.05) and 83.3% (1.667 ⁇ 0.577, P ⁇ 0.05) at 10 days, respectively, compared to the DS 10D group.
- damage to the corneal epithelial membrane was improved near the control at day 10.
- the number of isolated corneal epithelial cells increased 8.5-fold in the DS 10D group compared to the control group (0.190 ⁇ 0.165 cells / 0.1 mm 2 ) (1.619 ⁇ 0.165 cells / 0.1 mm 2 , P ⁇ 0.05) .
- the number of isolated corneal epithelial cells increased 1.1-fold (1.810 ⁇ 0.165 cells / 0.1 mm 2 ) in the SOS 1 group compared to the DS 10D group.
- the number of isolated corneal epithelial cells (1.238 ⁇ 0.165 and 1.238 ⁇ 0.165 cells / 0.1 mm 2 ) observed in the SOS 2 and SOS 3 groups decreased by 23.5% and 23.5%, respectively, compared to the DS 10D group ( P ⁇ 0.05).
- the number of isolated corneal epithelial cells was 70.6% (0.476 ⁇ 0.165 / 0.1 mm 2 , P ⁇ 0.05) and 76.5% (0.381 ⁇ 0.165 cells / 0.1 mm 2 in the SOS 4 and SOS 5 groups, respectively, compared to the DS 10D group. , P ⁇ 0.05).
- the number of conjunctival goblet cells decreased by 57.7% (7.333 ⁇ 1.288 cells / 0.1 mm 2 ) in the DS 10D group compared to the control group (17.333 ⁇ 0.873 cells / 0.1 mm 2 ), but in the SOS 1 group, DS Compared to the 10D group, it was increased 1.1 times (8.095 ⁇ 0.165 cells / 0.1 mm 2 , P ⁇ 0.05).
- the number of conjunctival goblet cells was 1.2 times (8.762 ⁇ 0.825 cells / 0.1 mm 2 , P ⁇ 0.05) and 1.4 times (10.381 ⁇ 0.436 cells / 0.1 mm 2 , P ⁇ in the SOS 2 and SOS 3 groups, respectively, compared to the DS 10D group. 0.05) increased.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Ophthalmology & Optometry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Immunology (AREA)
- Gastroenterology & Hepatology (AREA)
- Zoology (AREA)
- Marine Sciences & Fisheries (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Molecular Biology (AREA)
- Dermatology (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Description
건성안군(DS 10D, n=3) | 점안제 투여군(n=3) | |
SOS 1 | 건성안-유발 마우스 | 실시예 1의 점안제를 투여한 마우스 |
SOS 2 | 건성안-유발 마우스 | 실시예 2의 점안제를 투여한 마우스 |
SOS 3 | 건성안-유발 마우스 | 실시예 3의 점안제를 투여한 마우스 |
SOS 4 | 건성안-유발 마우스 | 실시예 4의 점안제를 투여한 마우스 |
SOS 5 | 건성안-유발 마우스 | 실시예 5의 점안제를 투여한 마우스 |
Claims (7)
- 설글리코타이드 또는 이의 약학적으로 허용가능한 염을 유효성분으로 포함하는 안구 건조증의 예방 또는 치료용 약학 조성물.
- 제1항에 있어서, 설글리코타이드 또는 이의 약학적으로 허용가능한 염이 0.01 w/v% 내지 30 w/v% 범위의 농도로 존재하는 것을 특징으로 하는 약학 조성물.
- 제1항에 있어서, 점안제의 제형을 갖는 것을 특징으로 하는 약학 조성물.
- 제3항에 있어서, 상기 점안제가 수성 용액 또는 수성 현탁액 형태인 것을 특징으로 하는 약학 조성물.
- 제3항 또는 제4항에 있어서, 수성 매질 중에, 설글리코타이드 또는 이의 약학적으로 허용가능한 염에 추가하여, 완충제, 점도 조절제, 등장화제, 항산화제, 킬레이트화제 및 pH 조절제로 이루어진 군으로부터 1종 이상 선택된 담체 또는 첨가제를 포함하는 약학 조성물.
- 제5항에 있어서, 상기 점도 조절제가 폴리비닐 알코올, 폴리비닐피롤리돈, 메틸 셀룰로오스, 히드록시프로필 메틸셀룰로오스, 히드록시에틸 셀룰로오스, 카르복시메틸 셀룰로오스, 및 히드록시프로필 셀룰로오스로 이루어진 군으로부터 1종 이상 선택되는 것을 특징으로 하는 약학 조성물.
- 제6항에 있어서, 상기 점도 조절제가 폴리비닐피롤리돈 또는 히드록시프로필 메틸셀룰로오스인 것을 특징으로 하는 약학 조성물.
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
MX2019008338A MX2019008338A (es) | 2017-01-13 | 2018-01-04 | Composicion farmaceutica que contiene sulglicotido o una sal farmaceuticamente aceptable del mismo para la prevencion o tratamiento del ojo seco. |
EP18738486.2A EP3569242B1 (en) | 2017-01-13 | 2018-01-04 | Pharmaceutical composition containing sulglycotide or pharmaceutically acceptable salt thereof for preventing or treating dry eye |
CN201880006936.1A CN110430891B (zh) | 2017-01-13 | 2018-01-04 | 包含硫糖肽或其药学上可接受的盐的用于预防或治疗干眼症的药学组合物 |
RU2019124179A RU2722485C1 (ru) | 2017-01-13 | 2018-01-04 | Фармацевтическая композиция, содержащая сульгликотид или фармацевтически приемлемую соль, для профилактики или лечения сухости глаз |
AU2018208549A AU2018208549A1 (en) | 2017-01-13 | 2018-01-04 | Pharmaceutical composition containing sulglycotide or pharmaceutically acceptable salt thereof for preventing or treating dry eye |
CA3049515A CA3049515A1 (en) | 2017-01-13 | 2018-01-04 | Pharmaceutical composition containing sulglycotide or pharmaceutically acceptable salt thereof for preventing or treating dry eye |
JP2019559244A JP6982634B2 (ja) | 2017-01-13 | 2018-01-04 | スルグリコチドまたはその薬学的に許容可能な塩を含む眼球乾燥症候群の予防用または治療用の医薬組成物 |
US16/477,711 US10806752B2 (en) | 2017-01-13 | 2018-01-04 | Pharmaceutical composition containing sulglycotide or pharmaceutically acceptable salt thereof for preventing or treating dry eye |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR10-2017-0006118 | 2017-01-13 | ||
KR1020170006118A KR101819709B1 (ko) | 2017-01-13 | 2017-01-13 | 설글리코타이드 또는 이의 약학적으로 허용가능한 염을 포함하는 안구건조증의 예방 또는 치료용 약학 조성물 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2018131835A1 true WO2018131835A1 (ko) | 2018-07-19 |
Family
ID=61025756
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/KR2018/000149 WO2018131835A1 (ko) | 2017-01-13 | 2018-01-04 | 설글리코타이드 또는 이의 약학적으로 허용가능한 염을 포함하는 안구건조증의 예방 또는 치료용 약학 조성물 |
Country Status (11)
Country | Link |
---|---|
US (1) | US10806752B2 (ko) |
EP (1) | EP3569242B1 (ko) |
JP (1) | JP6982634B2 (ko) |
KR (1) | KR101819709B1 (ko) |
CN (1) | CN110430891B (ko) |
AU (1) | AU2018208549A1 (ko) |
CA (1) | CA3049515A1 (ko) |
MX (1) | MX2019008338A (ko) |
RU (1) | RU2722485C1 (ko) |
TW (1) | TWI770106B (ko) |
WO (1) | WO2018131835A1 (ko) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR102270073B1 (ko) * | 2019-10-24 | 2021-06-28 | 삼일제약주식회사 | 설글리코타이드를 유효성분으로 포함하는 염증성 장질환의 예방 또는 치료용 조성물 |
CN114588250B (zh) * | 2022-03-18 | 2024-01-09 | 宁夏杞肽科技有限公司 | 枸杞糖肽在制备预防或治疗干眼症的药物中的用途 |
CN117186202B (zh) * | 2023-11-08 | 2024-02-02 | 北京大学第三医院(北京大学第三临床医学院) | 一种新细胞因子csbf及其在干眼治疗中的应用 |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4818537A (en) | 1986-10-21 | 1989-04-04 | Liposome Technology, Inc. | Liposome composition for treating dry eye |
US5800807A (en) | 1997-01-29 | 1998-09-01 | Bausch & Lomb Incorporated | Ophthalmic compositions including glycerin and propylene glycol |
US20020013345A1 (en) * | 1998-10-09 | 2002-01-31 | Charles L. Berman | Treatment of diseases of the eye characterized by the formation of metalloproteinase |
KR20070031933A (ko) * | 2004-05-18 | 2007-03-20 | 젠티엄 에스피에이 | 점막염 치료를 위한 설글리코타이드의 용도 |
KR20090053892A (ko) * | 2006-07-25 | 2009-05-28 | 오스모티카 코프. | 점안액 |
KR20120020534A (ko) * | 2010-08-30 | 2012-03-08 | 강동원 | 안구 건조증의 예방 또는 치료용 조성물 |
KR20120094253A (ko) * | 2011-02-16 | 2012-08-24 | 삼일제약주식회사 | 안정성이 개선된 설글리코타이드 및 h2 수용체 길항제 함유 다층 정제 및 이의 제조방법 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IT1050366B (it) * | 1972-10-18 | 1981-03-10 | Chinos Ind Farmacobilologica S | Sali di amminoacidi con esteri polisolforici di glicopeptidi naturali e loro preparazione |
IT1061352B (it) * | 1973-03-27 | 1983-02-28 | Crinos Industria Farmaco | Sali misti di esteri polisolforici di glicopeptidi naturali con metalli e con basi organiche e procedimento per la loro preparazione |
IT1215332B (it) * | 1987-01-12 | 1990-02-08 | Crinos Industria Farmaco | Composizione farmaceutica contenente sulglicotide per la terapia dell'ulcera gastrica |
US7029712B1 (en) * | 2002-07-17 | 2006-04-18 | Biosyntrx Inc | Treatment for dry eye syndrome |
ITMI20040989A1 (it) * | 2004-05-18 | 2004-08-18 | Gentium Spa | Uso del sulglicotide per iul trattamento delle mucositi |
CN102321151B (zh) * | 2011-08-10 | 2013-06-26 | 山东众山生物科技有限公司 | 一种硫糖肽的纯化工艺 |
KR101373246B1 (ko) * | 2011-12-29 | 2014-03-12 | 연세대학교 산학협력단 | Pge2 합성 억제제를 포함하는 안구 통증 치료용 약학 조성물 |
-
2017
- 2017-01-13 KR KR1020170006118A patent/KR101819709B1/ko active IP Right Grant
-
2018
- 2018-01-04 MX MX2019008338A patent/MX2019008338A/es unknown
- 2018-01-04 AU AU2018208549A patent/AU2018208549A1/en not_active Abandoned
- 2018-01-04 CA CA3049515A patent/CA3049515A1/en not_active Abandoned
- 2018-01-04 RU RU2019124179A patent/RU2722485C1/ru active
- 2018-01-04 US US16/477,711 patent/US10806752B2/en active Active
- 2018-01-04 WO PCT/KR2018/000149 patent/WO2018131835A1/ko unknown
- 2018-01-04 EP EP18738486.2A patent/EP3569242B1/en active Active
- 2018-01-04 CN CN201880006936.1A patent/CN110430891B/zh active Active
- 2018-01-04 JP JP2019559244A patent/JP6982634B2/ja active Active
- 2018-01-12 TW TW107101328A patent/TWI770106B/zh active
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4818537A (en) | 1986-10-21 | 1989-04-04 | Liposome Technology, Inc. | Liposome composition for treating dry eye |
US5800807A (en) | 1997-01-29 | 1998-09-01 | Bausch & Lomb Incorporated | Ophthalmic compositions including glycerin and propylene glycol |
US20020013345A1 (en) * | 1998-10-09 | 2002-01-31 | Charles L. Berman | Treatment of diseases of the eye characterized by the formation of metalloproteinase |
KR20070031933A (ko) * | 2004-05-18 | 2007-03-20 | 젠티엄 에스피에이 | 점막염 치료를 위한 설글리코타이드의 용도 |
KR20090053892A (ko) * | 2006-07-25 | 2009-05-28 | 오스모티카 코프. | 점안액 |
KR20120020534A (ko) * | 2010-08-30 | 2012-03-08 | 강동원 | 안구 건조증의 예방 또는 치료용 조성물 |
KR20120094253A (ko) * | 2011-02-16 | 2012-08-24 | 삼일제약주식회사 | 안정성이 개선된 설글리코타이드 및 h2 수용체 길항제 함유 다층 정제 및 이의 제조방법 |
Non-Patent Citations (7)
Title |
---|
CHEN ZLI ZBASTI SFARLEY WJPFLUGFELDER SC: "Altered morphology and function of the lacrimal functional unit in protein kinase C alpha knockout mice", INVEST OPHTHALMOL VIS SCI., vol. 51, 2010, pages 5592 - 600 |
DE PAIVA CSCORRALES RMVILLARREAL ALFARLEY WLI DQSTERN MEPFLUGFELDER SC: "Apical corneal barrier disruption in experimental murine dry eye is abrogated by methylprednisolone and doxycycline", INVEST OPHTHALMOL VIS SCI., vol. 47, 2006, pages 2847 - 56 |
LEMP MA: "Report of the National Eye Institute/Industry Workshop on Clinical Trials in Dry Eyes", CLAO J., vol. 21, 1995, pages 221 - 32, XP000933694 |
OH HNKIM CELEE JHYANG JW: "Effects of Quercetin in a Mouse Model of Experimental Dry Eye", CORNEA, vol. 34, 2015, pages 1130 - 6 |
RASHID SJIN YECOIFFIER TBARABINO SSCHAUMBERG DADANA MR: "Topical omega-3 and omega-6 fatty acids for treatment of dry eye", ARCH OPHTHALMOL., vol. 126, 2008, pages 219 - 25, XP002669468, DOI: doi:10.1001/archophthalmol.2007.61 |
See also references of EP3569242A4 |
VILLAREAL ALFARLEY WPFLUGFELDER SC: "Effect of topical ophthalmic epinastine and olopatadine on tear volume in mice", EYE CONTACT LENS, vol. 32, 2006, pages 272 - 6 |
Also Published As
Publication number | Publication date |
---|---|
CA3049515A1 (en) | 2018-07-19 |
EP3569242A4 (en) | 2020-08-19 |
CN110430891B (zh) | 2023-08-04 |
TWI770106B (zh) | 2022-07-11 |
JP6982634B2 (ja) | 2021-12-17 |
RU2722485C1 (ru) | 2020-06-01 |
AU2018208549A1 (en) | 2019-07-25 |
US10806752B2 (en) | 2020-10-20 |
CN110430891A (zh) | 2019-11-08 |
KR101819709B1 (ko) | 2018-01-17 |
US20190358255A1 (en) | 2019-11-28 |
EP3569242A1 (en) | 2019-11-20 |
EP3569242B1 (en) | 2022-11-09 |
TW201828954A (zh) | 2018-08-16 |
MX2019008338A (es) | 2019-11-11 |
JP2020505450A (ja) | 2020-02-20 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2018131835A1 (ko) | 설글리코타이드 또는 이의 약학적으로 허용가능한 염을 포함하는 안구건조증의 예방 또는 치료용 약학 조성물 | |
WO2016104964A1 (ko) | 안구 표면 질환 예방 또는 치료용 약학조성물 | |
EP0774254B1 (en) | Ophthalmic composition for preventing or treating dry eye or disease caused thereby comprising 12-sulfodehydroabietic acid | |
CN112516080B (zh) | 一种眼用药物组合物及其制备方法和应用 | |
KR20140125230A (ko) | 레바미피드 또는 이의 전구체를 포함하는 안구건조증의 예방 또는 치료를 위한 경구용 약제학적 조성물 | |
WO2023014113A1 (ko) | 안구건조증 치료를 위한 레코플라본 함유 점안 조성물 | |
WO2018155773A1 (ko) | 폴리에틸렌 글리콜 및 플라보노이드 나노복합체를 유효성분으로 함유하는 안구 건조증 예방 또는 치료용 조성물 | |
JP6820658B2 (ja) | ジピリダモールを用いる眼疾患の治療において使用するための組成物 | |
Robin et al. | The effect of collagen shields on rabbit corneal reepithelialization after chemical debridement. | |
KR102093643B1 (ko) | 세비메린 또는 이의 약학적으로 허용가능한 염을 포함하는 안구건조증의 예방 또는 치료용 점안제 | |
JPH0748262A (ja) | 外眼部投与用組成物 | |
JP6779599B2 (ja) | 角結膜障害治療剤 | |
CN101347619A (zh) | 一种药物组合物及其在制备治疗眼部炎症的药物中的应用 | |
US11426346B2 (en) | Lutein-containing ophthalmic composition | |
KR102675216B1 (ko) | 눈 염증의 예방 및 치료를 위한 아미노포스핀 유도체 | |
RU2669768C1 (ru) | Гелеобразные капли для лечения воспалительных заболеваний глаз, включая инфекционные, устойчивые к антибиотикам | |
JP5605072B2 (ja) | 角結膜疾患の予防又は治療剤 | |
JP2020075918A (ja) | 角膜上皮創傷治癒促進用の眼科用組成物 | |
WO2023014117A1 (ko) | 안구건조증 치료를 위한 레코플라본 함유 점안 조성물 및 이의 제조방법 | |
Kumar et al. | PART III Differential Diagnosis of Selected Problems in Cornea and External Eye Disease | |
JP2023527082A (ja) | ペプスタチンおよびアルギン酸またはそれらの塩を含む組成物、並びにその使用 | |
CN108261541A (zh) | 含纤连蛋白及环孢素的复方滴眼液及其制备方法和应用 | |
WO2023048174A1 (ja) | 角膜疾患治療剤 | |
CN116474105A (zh) | 一种预防、缓解或治疗眼部疾病的药物组合物、制备方法及其应用 | |
Edmonds | Keratoconus: A keratographic study of corneal destabilization during acute hydrops |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 18738486 Country of ref document: EP Kind code of ref document: A1 |
|
ENP | Entry into the national phase |
Ref document number: 3049515 Country of ref document: CA |
|
ENP | Entry into the national phase |
Ref document number: 2019559244 Country of ref document: JP Kind code of ref document: A |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
ENP | Entry into the national phase |
Ref document number: 2018208549 Country of ref document: AU Date of ref document: 20180104 Kind code of ref document: A |
|
ENP | Entry into the national phase |
Ref document number: 2018738486 Country of ref document: EP Effective date: 20190813 |