ES2550105B2 - Lentes de contacto para conjuntivitis alérgica - Google Patents
Lentes de contacto para conjuntivitis alérgica Download PDFInfo
- Publication number
- ES2550105B2 ES2550105B2 ES201530906A ES201530906A ES2550105B2 ES 2550105 B2 ES2550105 B2 ES 2550105B2 ES 201530906 A ES201530906 A ES 201530906A ES 201530906 A ES201530906 A ES 201530906A ES 2550105 B2 ES2550105 B2 ES 2550105B2
- Authority
- ES
- Spain
- Prior art keywords
- allergic conjunctivitis
- contact lenses
- hydrogels
- olopatadine
- hema
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
Classifications
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
- C08F220/1807—C7-(meth)acrylate, e.g. heptyl (meth)acrylate or benzyl (meth)acrylate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/50—Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
- A61L27/52—Hydrogels or hydrocolloids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/04—Acids; Metal salts or ammonium salts thereof
- C08F220/06—Acrylic acid; Methacrylic acid; Metal salts or ammonium salts thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
- C08L33/08—Homopolymers or copolymers of acrylic acid esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
- C08L33/10—Homopolymers or copolymers of methacrylic acid esters
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/04—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Polymers & Plastics (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Inorganic Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Dermatology (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Transplantation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
Abstract
Lentes de contacto para conjuntivitis alérgica. La presente invención se refiere a hidrogeles, sistemas de liberación y dispositivos ópticos adecuados para el tratamiento o prevención de la conjuntivitis alérgica, en particular, la conjuntivitis alérgica estacional. Los hidrogeles de la invención son útiles en lentes de contacto blandas, y para cargar principios activos antihistamínicos como olopatadina, ketotifeno o azelastina en una cantidad suficiente para provocar una respuesta de eficacia adecuada.
Description
durante 24 horas y finalmente en agua otra semana. Finalmente, los discos se secaron a 70 ºC durante 12 h.
Tabla 1. Composición de los hidrogeles imprinted (hidrogeles con números pares) y no imprinted (hidrogeles con números impares). A todas las mezclas de monómeros se les incorporó 1 mL de DMSO y 0.00821 g de AIBN.
- Hidrogel
- HEMA (mL) Fármaco (g) AAc (µL) BzMA (µL) AAm (g) AMPSA (g) EGDMA (µL)
- 1
- 4 0 0 0 0 0 188.6
- 3
- 4 0 68.6 0 0.072 0 188.6
- 17
- 4 0 68.6 338.9 0 0 188.6
- 23
- 4 0 137.2 0 0.144 0 188.6
- 25
- 4 0 68.6 338.9 0 0.207 188.6
- 29
- 4 0 68.6 338.9 0.072 0.207 377.2
- 2
- 4 0.1869 0 0 0 0 188.6
- 4
- 4
- 0.1869 68.6 0 0.072 0 188.6
- 18
- 4 0.1869 68.6 338.9 0 0 188.6
- 24
- 4 0.1869 137.2 0 0.144 0 188.6
- 26A
- 4 0.1869 68.6 338.9 0 0.207 188.6
- 26B
- 4 0.0935 68.6 338.9 0 0.207 188.6
- 30A
- 4 0.1869 68.6 338.9 0.072 0.207 377.2
- 30B
- 4 0.0935 68.6 338.9 0.072 0.207 377.2
10 2. Caracterización de los hidrogeles A continuación se recogen los métodos empleados en la caracterización de los hidrogeles preparados, y los resultados.
15 Se llevaron a cabo análisis de DSC en un DSC Q-100 (TA Instruments, USA) equipado con un sistema de refrigeración. Fragmentos de discos secos (4-6 mg) se colocaron en cápsulas de aluminio y se sometieron a calefacción hasta 150ºC, se mantuvieron 5
20 días. Los discos preparados con HEMA sin monómeros funcionales (hidrogeles 1 y 2) fueron capaces de incorporar 30 mg/g en los primeros 5 días y hasta 38 mg/g cuando alcanzaron el equilibrio. La cantidad de olopatadina que estos discos de HEMA fueron capaces de alojar en fase acuosa fue de 0.1 mg/g lo que significa que el coeficiente de 5 reparto de olopatadina entre la red polimérica y el agua es de 188 (tabla 3). La cantidad de olopatadina cargada por el hidrogel 1 está en concordancia con los datos publicados para Acuvue (J&J) sumergidas en Patanol (hidrocloruro de olopatadina disolución oftálmica al 0.1%) (N.L. Dassanayake, T. C. Carey, G. R. Owen. A Laboratory Model to Determine the Uptake and Release of Olopatadine by Soft Contact Lenses. Acta
10 Ophthalmol. Scand. 2000: 78: 16–17). Los hidrogeles que combinan AAc, BzMA y AMPSA (hidrogel 25) cargan olopatadina más rápido y en una cantidad dos veces mayor que los hidrogeles preparados solamente con HEMA (figura 3). Tabla 3. Datos de carga de olopatadina y coeficiente de reparto de olopatadina entre la
15 red polimérica y el agua.
- Hidrogel
- Olopatadina incorporada (mg/g) KN/W
- 1
- 38.51 188
- 3
- 39.34 192
- 17
- 52.05 255
- 23
- 52.27 255
- 25
- 79.42 389
- 29
- 87.22 427
- 2
- 37.25 182
- 4
- 46.39 227
- 18
- 41.87 205
- 24
- 50.64 248
- 26A
- 59.51 291
- 26B
- 69.15 339
- 30A
- 56.70 277
- 30B
- 85.64 420
Claims (1)
-
imagen1 imagen2 imagen3
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ES201530906A ES2550105B2 (es) | 2015-06-25 | 2015-06-25 | Lentes de contacto para conjuntivitis alérgica |
PCT/ES2016/070466 WO2016207460A1 (es) | 2015-06-25 | 2016-06-20 | Lentes de contacto para conjuntivitis alérgica |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ES201530906A ES2550105B2 (es) | 2015-06-25 | 2015-06-25 | Lentes de contacto para conjuntivitis alérgica |
Publications (2)
Publication Number | Publication Date |
---|---|
ES2550105A1 ES2550105A1 (es) | 2015-11-04 |
ES2550105B2 true ES2550105B2 (es) | 2016-10-07 |
Family
ID=54353325
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES201530906A Active ES2550105B2 (es) | 2015-06-25 | 2015-06-25 | Lentes de contacto para conjuntivitis alérgica |
Country Status (2)
Country | Link |
---|---|
ES (1) | ES2550105B2 (es) |
WO (1) | WO2016207460A1 (es) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106084116B (zh) * | 2016-06-17 | 2019-02-05 | 宁波国际材料基因工程研究院有限公司 | 水凝胶及其制备方法,水凝胶的应用 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4123407A (en) * | 1976-11-26 | 1978-10-31 | American Optical Corporation | Hydrophilic contact lens |
MX2007009417A (es) * | 2005-02-04 | 2007-08-17 | Univ Auburn | Sistema de suministro de farmaco de contacto. |
US9389336B2 (en) * | 2013-08-02 | 2016-07-12 | Bausch & Lomb Incorporated | Hydrogel monomer mix containing added water |
-
2015
- 2015-06-25 ES ES201530906A patent/ES2550105B2/es active Active
-
2016
- 2016-06-20 WO PCT/ES2016/070466 patent/WO2016207460A1/es active Application Filing
Also Published As
Publication number | Publication date |
---|---|
ES2550105A1 (es) | 2015-11-04 |
WO2016207460A1 (es) | 2016-12-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Elbaum-Garfinkle et al. | The disordered P granule protein LAF-1 drives phase separation into droplets with tunable viscosity and dynamics | |
Liu et al. | Trehalose induces autophagy against inflammation by activating TFEB signaling pathway in human corneal epithelial cells exposed to hyperosmotic stress | |
Rog et al. | The synaptonemal complex has liquid crystalline properties and spatially regulates meiotic recombination factors | |
Knobloch et al. | Dendritic spine loss and synaptic alterations in Alzheimer’s disease | |
Benson et al. | Mathematical optimization of procedures for cryoprotectant equilibration using a toxicity cost function | |
ES2481641T3 (es) | Uso de receptor inmunosupresor | |
Liu et al. | Autophagy activation aggravates neuronal injury in the hippocampus of vascular dementia rats | |
ES2550105B2 (es) | Lentes de contacto para conjuntivitis alérgica | |
ES2688030T3 (es) | Péptidos permeables celulares inhibidores de la ruta de transducción de la señal JNK para su uso en el tratamiento de enfermedades oculares inflamatorias | |
Han et al. | A mouse model of corneal endothelial decompensation using cryoinjury | |
Caldeira-Dias et al. | Resveratrol improves endothelial cell markers impaired by plasma incubation from women who subsequently develop preeclampsia | |
Muraleva et al. | The mitochondria-targeted antioxidant SkQ1 restores α B-crystallin expression and protects against AMD-like retinopathy in OXYS rats | |
Lanzini et al. | In vivo and impression cytology study on the effect of compatible solutes eye drops on the ocular surface epithelial cell quality in dry eye patients | |
Turedi et al. | The diagnostic value of plasma SCUBE1, a novel biomarker of platelet activation, in testicular torsion: A randomized, controlled, experimental study | |
KR20160004288A (ko) | 약학적 조성물 및 이의 용도 | |
Nikoletopoulou et al. | Necrotic cell death in Caenorhabditis elegans | |
Buzgariu et al. | Chapter Twenty‐Six Methods to Investigate Autophagy During Starvation and Regeneration in Hydra | |
Salmon et al. | CXL at the slit lamp: no clinically relevant changes in corneal riboflavin distribution during upright UV irradiation | |
Ktistakis | Monitoring the localization of MAP1LC3B by indirect immunofluorescence | |
Marrari et al. | Analysis of microtubule movement on isolated Xenopus egg cortices provides evidence that the cortical rotation involves dynein as well as Kinesin Related Proteins and is regulated by local microtubule polymerisation | |
Morris | Cytotoxic swelling of sick excitable cells–impaired ion homeostasis and membrane tension homeostasis in muscle and neuron | |
Lee et al. | Spatiotemporal regulation of signaling in and out of dendritic spines: CaMKII and Ras | |
RU2016111957A (ru) | Офтальмическая композиция для цвиттерионных мягких контактных линз | |
Sheng et al. | Cortical localization of α-and γ-tubulin and the assembly of cortical microtubule cytoskeleton in Hypotrichous ciliate Euplotes eurystomus | |
Hipolito et al. | Enhanced and selective translation expands the lysosome size and promotes antigen presentation during phagocyte activation |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG2A | Definitive protection |
Ref document number: 2550105 Country of ref document: ES Kind code of ref document: B2 Effective date: 20161007 |