ES2584858T3 - Composiciones farmacéuticas acuosas que contienen complejos de borato-poliol - Google Patents
Composiciones farmacéuticas acuosas que contienen complejos de borato-poliol Download PDFInfo
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- ES2584858T3 ES2584858T3 ES14150805.1T ES14150805T ES2584858T3 ES 2584858 T3 ES2584858 T3 ES 2584858T3 ES 14150805 T ES14150805 T ES 14150805T ES 2584858 T3 ES2584858 T3 ES 2584858T3
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- 229920005862 polyol Polymers 0.000 title abstract description 10
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 239000000203 mixture Substances 0.000 abstract description 17
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 abstract description 15
- 150000003077 polyols Chemical class 0.000 abstract description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 5
- 229930195725 Mannitol Natural products 0.000 abstract description 4
- HCRKCZRJWPKOAR-JTQLQIEISA-N brinzolamide Chemical compound CCN[C@H]1CN(CCCOC)S(=O)(=O)C2=C1C=C(S(N)(=O)=O)S2 HCRKCZRJWPKOAR-JTQLQIEISA-N 0.000 abstract description 4
- 229960000722 brinzolamide Drugs 0.000 abstract description 4
- 239000003814 drug Substances 0.000 abstract description 4
- 239000000594 mannitol Substances 0.000 abstract description 4
- 235000010355 mannitol Nutrition 0.000 abstract description 4
- XYLJNLCSTIOKRM-UHFFFAOYSA-N Alphagan Chemical compound C1=CC2=NC=CN=C2C(Br)=C1NC1=NCCN1 XYLJNLCSTIOKRM-UHFFFAOYSA-N 0.000 abstract description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 abstract description 2
- 229960003679 brimonidine Drugs 0.000 abstract description 2
- 239000000600 sorbitol Substances 0.000 abstract description 2
- 229940124597 therapeutic agent Drugs 0.000 abstract description 2
- -1 mannitol polyol Chemical class 0.000 abstract 2
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 abstract 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 abstract 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 1
- 230000000845 anti-microbial effect Effects 0.000 abstract 1
- 239000004599 antimicrobial Substances 0.000 abstract 1
- 235000011187 glycerol Nutrition 0.000 abstract 1
- 239000003755 preservative agent Substances 0.000 abstract 1
- 230000002335 preservative effect Effects 0.000 abstract 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 10
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 7
- 239000004327 boric acid Substances 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
- 239000011780 sodium chloride Substances 0.000 description 5
- 241000228245 Aspergillus niger Species 0.000 description 4
- 241000222122 Candida albicans Species 0.000 description 4
- 229960000686 benzalkonium chloride Drugs 0.000 description 4
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 description 4
- 239000008213 purified water Substances 0.000 description 4
- BTIHMVBBUGXLCJ-OAHLLOKOSA-N seliciclib Chemical compound C=12N=CN(C(C)C)C2=NC(N[C@@H](CO)CC)=NC=1NCC1=CC=CC=C1 BTIHMVBBUGXLCJ-OAHLLOKOSA-N 0.000 description 4
- 208000004998 Abdominal Pain Diseases 0.000 description 3
- 208000002881 Colic Diseases 0.000 description 3
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- MDYZKJNTKZIUSK-UHFFFAOYSA-N tyloxapol Chemical compound O=C.C1CO1.CC(C)(C)CC(C)(C)C1=CC=C(O)C=C1 MDYZKJNTKZIUSK-UHFFFAOYSA-N 0.000 description 3
- 229960004224 tyloxapol Drugs 0.000 description 3
- 229920001664 tyloxapol Polymers 0.000 description 3
- 241000588724 Escherichia coli Species 0.000 description 2
- 229940031663 carbomer-974p Drugs 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 238000010606 normalization Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- WLAMNBDJUVNPJU-UHFFFAOYSA-N 2-methylbutyric acid Chemical compound CCC(C)C(O)=O WLAMNBDJUVNPJU-UHFFFAOYSA-N 0.000 description 1
- KAKYNGJFPXFCDD-PPHPATTJSA-N 5-bromo-n-(4,5-dihydro-1h-imidazol-2-yl)quinoxalin-6-amine;(4r)-4-(ethylamino)-2-(3-methoxypropyl)-1,1-dioxo-3,4-dihydrothieno[3,2-e]thiazine-6-sulfonamide Chemical compound C1=CC2=NC=CN=C2C(Br)=C1NC1=NCCN1.CCN[C@H]1CN(CCCOC)S(=O)(=O)C2=C1C=C(S(N)(=O)=O)S2 KAKYNGJFPXFCDD-PPHPATTJSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- YUWPMEXLKGOSBF-GACAOOTBSA-N Anecortave acetate Chemical compound O=C1CC[C@]2(C)C3=CC[C@]4(C)[C@](C(=O)COC(=O)C)(O)CC[C@H]4[C@@H]3CCC2=C1 YUWPMEXLKGOSBF-GACAOOTBSA-N 0.000 description 1
- 101800004538 Bradykinin Proteins 0.000 description 1
- ZGTMUACCHSMWAC-UHFFFAOYSA-L EDTA disodium salt (anhydrous) Chemical compound [Na+].[Na+].OC(=O)CN(CC([O-])=O)CCN(CC(O)=O)CC([O-])=O ZGTMUACCHSMWAC-UHFFFAOYSA-L 0.000 description 1
- QXZGBUJJYSLZLT-UHFFFAOYSA-N H-Arg-Pro-Pro-Gly-Phe-Ser-Pro-Phe-Arg-OH Natural products NC(N)=NCCCC(N)C(=O)N1CCCC1C(=O)N1C(C(=O)NCC(=O)NC(CC=2C=CC=CC=2)C(=O)NC(CO)C(=O)N2C(CCC2)C(=O)NC(CC=2C=CC=CC=2)C(=O)NC(CCCN=C(N)N)C(O)=O)CCC1 QXZGBUJJYSLZLT-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 102100035792 Kininogen-1 Human genes 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229960001232 anecortave Drugs 0.000 description 1
- QXZGBUJJYSLZLT-FDISYFBBSA-N bradykinin Chemical compound NC(=N)NCCC[C@H](N)C(=O)N1CCC[C@H]1C(=O)N1[C@H](C(=O)NCC(=O)N[C@@H](CC=2C=CC=CC=2)C(=O)N[C@@H](CO)C(=O)N2[C@@H](CCC2)C(=O)N[C@@H](CC=2C=CC=CC=2)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O)CCC1 QXZGBUJJYSLZLT-FDISYFBBSA-N 0.000 description 1
- 229960001631 carbomer Drugs 0.000 description 1
- UREBDLICKHMUKA-CXSFZGCWSA-N dexamethasone Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@@H](C)[C@@](C(=O)CO)(O)[C@@]1(C)C[C@@H]2O UREBDLICKHMUKA-CXSFZGCWSA-N 0.000 description 1
- 229960003957 dexamethasone Drugs 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- QEFAQIPZVLVERP-UHFFFAOYSA-N nepafenac Chemical compound NC(=O)CC1=CC=CC(C(=O)C=2C=CC=CC=2)=C1N QEFAQIPZVLVERP-UHFFFAOYSA-N 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- CEIJFEGBUDEYSX-FZDBZEDMSA-N tandospirone Chemical compound O=C([C@@H]1[C@H]2CC[C@H](C2)[C@@H]1C1=O)N1CCCCN(CC1)CCN1C1=NC=CC=N1 CEIJFEGBUDEYSX-FZDBZEDMSA-N 0.000 description 1
- 229950000505 tandospirone Drugs 0.000 description 1
Classifications
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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
- A61K47/02—Inorganic compounds
-
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
-
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/498—Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
-
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
- A61K31/542—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame ortho- or peri-condensed with heterocyclic ring systems
-
- 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
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/10—Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
-
- 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
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/16—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing nitrogen, e.g. nitro-, nitroso-, azo-compounds, nitriles, cyanates
- A61K47/18—Amines; Amides; Ureas; Quaternary ammonium compounds; Amino acids; Oligopeptides having up to five amino acids
- A61K47/186—Quaternary ammonium compounds, e.g. benzalkonium chloride or cetrimide
-
- 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
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/26—Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharides; Derivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin
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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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- 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
- A61K47/36—Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
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- A61K9/00—Medicinal preparations characterised by special physical form
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- A61K9/0048—Eye, e.g. artificial tears
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- A61K2121/00—Preparations for use in therapy
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- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
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- Biochemistry (AREA)
- Medicinal Preparation (AREA)
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- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Composición oftálmica de múltiples dosis que comprende: brinzolamida, brimonidina o una combinación de las mismas como agente terapéutico; un primer poliol, seleccionándose el primer poliol de manitol, sorbitol o una combinación de los mismos, siendo la concentración del primer poliol de al menos el 0,01% en p/v pero no mayor del 0,5% en p/v; un segundo poliol, seleccionándose el segundo poliol de propilenglicol, glicerina o una combinación de los mismos, siendo la concentración del segundo poliol de al menos el 0,1% en p/v pero menor del 5% en p/v de la composición; una cantidad eficaz de borato, siendo la cantidad eficaz de al menos el 0,05% en p/v y menor del 0,5% en p/v de la composición global; BAC como conservante antimicrobiano, siendo la concentración de BAC en la composición mayor del 0,00001% en p/v pero menor del 0,0035% en p/v; y agua.
Description
pueden usarse para suspensiones oftálmicas de fármacos tales como brinzolamida, roscovitina, amfenac amida, dexametasona, inhibidor de bradicinina, acetato de anecortavo, tandospirona, combinaciones de los mismos y sus combinaciones con otros fármacos.
Tabla C: ejemplos A a C con el 0,002% de BAC
- Composición
- A COMPARATIVO B COMPARATIVO C
- Carbómero 974 P
- 0,45 0,45 0,45
- Tiloxapol
- 0,025 0,025 0,025
- Ácido bórico
- 0,3 0,6 0,3
- Manitol
- 0,3 2,0 2
- Propilenglicol
- 0,75 1 0,75
- Cloruro de sodio
- 0,3 Ninguno Ninguno
- Cloruro de benzalconio
- 0,002 0,002 0,002
- Edetato de disodio
- Ninguno Ninguno Ninguno
- Hidróxido de sodio/HCl
- pH 7,0 pH 7,0 pH 7,0
- Agua purificada
- CS CS CS
- Osmolalidad
- 279 324 259
- Viscosidad (cps) a 120 s-1
- 49,6 68,2 127,9
- Viscosidad (cps) a 12 s-1
- 144,4 210,4 480,7
- Microorganismos, tiempo
- Criterios de la Ph. Eur. A Criterios de la Ph. Eur. B Reducciones log
- S. aureus 6 horas 24 horas 7 días 14 días 28 días
- 2,0 3,0 NRa -1,0 3,0 NIb 4,6 4,9 4,9 4,9 4,9 4,9 4,9 4,9 4,9 4,9 2,5 4,9 4,9 4,9 4,9
- P. aeruginosa 6 horas 24 horas 7 días 14 días 28 días
- 2,0 3,0 NR -1,0 3,0 NI 5,0 5,0 5,0 5,0 5,0 5,0 5,0 5,0 5,0 5,0 4,8 4,8 4,8 4,8 4,8
- E. colic 6 horas 24 horas 7 días 14 días 28 días
- NAd NA 5,0 5,0 5,0 5,0 5,0 5,0 5,0 5,0 5,0 5,0 3,0 5,0 5,0 5,0 5,0
- C. albicans 7 días 14 días 28 días
- 2,0 NI NI -1,0 NI 4,7 4,7 4,7 4,7 4,7 4,7 4,8 4,8 4,8
- A. niger 7 días 14 días 28 días
- 2,0 NI NI -1,0 NI 3,1 3,6 5,2 3,1 4,2 5,2 3,7 4,3 5,1
- aNR = Sin recuperación bNI = Sin aumento cLa Ph. Eur. No tiene requisito para E. Coli dNA = No aplicable
Ejemplo D
El ejemplo D presentado en la tabla 3 es una composición con el 0,002% de BAC, ácido bórico y dos polioles diferentes y se proyecta para cumplir con los criterios de PET de la Ph. Eur B y A.
Tabla D: Ejemplo D con el 0,002% de BAC
- Composición
- D
- Ácido bórico
- 0,3
- Sorbitol
- 0,25
- Propilenglicol
- 1,6
10
- Cada una de las composiciones H-J, entre otros usos, puede usarse como vehículos de suspensión para suspender agentes terapéuticos.
- Composición
- H I J
- Cloruro de sodio
- 0,15 0,3 Ninguno
- Cloruro de benzalconio
- 0,001 0,001 0,001
- Hidróxido de sodio/HCl
- pH 7,0 pH 7,0 pH 7,0
- Agua purificada
- CS CS CS
- Osmolalidad
- 278 274 278
- Viscosidad (cps) a 120 s-1
- 63,1 53,8 59,1
- Viscosidad (cps) a 12 s-1
- 169 149 172
- S. aureus 6 horas 24 horas 7 días 14 días 28 días
- 0,2 2,6 5,0 5,0 5,0 0,0 1,4 5,0 5,0 5,0 0,2 3,0 5,0 5,0 5,0
- P. aeruginosa 6 horas 24 horas 7 días 14 días 28 días
- 4,9 4,9 4,9 4,9 4,9 4,9 4,9 4,9 4,9 4,9 4,9 4,9 4,9 4,9 4,9
- E. coli 6 horas 24 horas 7 días 14 días 28 días
- 1,4 3,1 5,0 5,0 5,0 1,4 3,4 5,0 5,0 5,0 3,1 5,0 5,0 5,0 5,0
- C. albicans 7 días 14 días 28 días
- 3,0 4,3 4,8 3,5 4,8 4,8 4,8 4,8 4,8
- A. niger 7 días 14 días 28 días
- 3,2 3,7 3,6 3,5 3,4 3,0 3,6 3,5 3,4
Tabla G: Formulaciones de roscovitina con baja cantidad de BAC, ácido bórico y dos polioles
- Composición
- K
- Roscovitina (AL-39256)
- 1
- Carbómero 974P
- 0,45
- Tiloxapol
- 0,025
- Ácido bórico
- 0,3
- Manitol
- 0,3
- Propilenglicol
- 0,75
- Cloruro de sodio
- 0,28
- Cloruro de benzalconio
- 0,003
- Hidróxido de sodio/HCl
- pH 7,2
- Agua purificada
- CS
- Osmolalidad (mOsm/kg)
- 271
- Viscosidad (cps) a 12 s-1
- 198,1
- Viscosidad (cps) a 120 s-1
- 66,5
- S. aureus
- 6 horas 24 horas 7 días 14 días 28 días 5,1 5,1 5,1 5,1 5,1
- P. aeruginosa
- 6 horas 24 horas 7 días 14 días 28 días 4,9 4,9 4,9 4,9 4,9
- E. colic
- 6 horas 4,9
12
- Composición
- K
- 24 horas
- 4,9
- 7 días
- 4,9
- 14 días
- 4,9
- 28 días
- 4,9
- C. albicans
- 7 días 4,8
- 14 días
- 4,8
- 28 días
- 4,8
- A. niger
- 7 días 5,1
- 14 días
- 5,1
- 28 días
- 5,1
La composición K presenta una resistencia a la normalización de lágrimas de aproximadamente 4,4.
Tabla H: Formulaciones de brinzolamida y brinzolamida/brimonidina con baja cantidad de BAC, ácido bórico y dos polioles
- Composición
- M N
- Brinzolamida
- 1,0 1,0
- Brimonidina
- 0,15 0,15
- Carbopol 974P
- 0,4 0,4
- Tiloxapol
- 0,025 0,025
- Ácido bórico
- 0,3 0,3
- Manitol
- 0,3 0,3
- Propilenglicol
- 0,75 0,75
- Cloruro de sodio
- 0,23 0,23
- Cloruro de benzalconio
- 0,003 0,003
- Hidróxido de sodio y/o ácido clorhídrico
- CS para pH 6,5 ± 0,2 CS para pH 6,5 ± 0,2
- Agua purificada
- CS hasta el 100% CS hasta el 100%
- S. aureus 6 horas 24 horas 7 días 14 días 28 días
- 5,0 5,0 5,0 5,0 5,0 5,0 5,0 5,0 5,0 5,0
- P. aeruginosa 6 horas 24 horas 7 días 14 días 28 días
- 5,0 5,0 5,0 5,0 5,0 5,0 5,0 5,0 5,0 5,0
- E. colic 6 horas 24 horas 7 días 14 días 28 días
- 5,0 5,0 5,0 5,0 5,0 5,0 5,0 5,0 5,0 5,0
- C. albicans 7 días 14 días 28 días
- 4,8 4,8 4,8 4,8 4,8 4,8
- A. niger 7 días 14 días 28 días
- 4,3 4,1 4,2 4,4 4,3 4,1
Tabla I: Ejemplo O a V
Las composiciones M y N presentan una resistencia a la normalización de lágrimas de aproximadamente 18.
Los ejemplos O a V muestran que tanto la osmolalidad como la viscosidad de formulaciones que contienen carbómero pueden obtenerse en el intervalo deseado usando cloruro de sodio al tiempo que se mantiene la concentración de sodio inferior al 0,4%.
13
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- 2016-07-27 SM SM201600249T patent/SMT201600249B/it unknown
- 2016-07-27 HR HRP20160953TT patent/HRP20160953T1/hr unknown
- 2016-07-27 JP JP2016146972A patent/JP2016183198A/ja active Pending
-
2020
- 2020-06-19 HR HRP20200979TT patent/HRP20200979T1/hr unknown
- 2020-07-10 CY CY20201100637T patent/CY1123120T1/el unknown
-
2021
- 2021-05-05 AR ARP210101228A patent/AR122017A2/es unknown
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