IPC분류정보
국가/구분 |
United States(US) Patent
등록
|
국제특허분류(IPC7판) |
|
출원번호 |
US-0722256
(2003-11-25)
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등록번호 |
US-8172395
(2012-05-08)
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발명자
/ 주소 |
- Carney, Fiona Patricia
- Gabriel, Manal M.
- Morris, Carol Ann
- Lally, John Martin
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출원인 / 주소 |
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대리인 / 주소 |
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인용정보 |
피인용 횟수 :
0 인용 특허 :
4 |
초록
▼
The present invention provides a medical device, preferably a contact lens, which comprises an antimicrobial LbL coating containing one or more antimicrobial pepetides. The antimicrobial coating of the invention can impart to the medical an increased surface hydrophilicity and a relatively high anti
The present invention provides a medical device, preferably a contact lens, which comprises an antimicrobial LbL coating containing one or more antimicrobial pepetides. The antimicrobial coating of the invention can impart to the medical an increased surface hydrophilicity and a relatively high antimicrobial activity coupled with low cytotoxicity. The antimicrobial coating of the invention has a minimal adverse effects on the desirable bulk properties of a contact lens, such as oxygen permeability, ion permeability, and optical properties. An antimicrobial coating of the present invention may find particular use in extended-wear contact lenses. In addition, the invention provides a method for making a medical device, preferably a contact lens, having an antimicrobial LbL coating thereon.
대표청구항
▼
1. A contact lens comprising a core material which is a silicone-containing hydrogel material and an antimicrobial LbL coating that is not covalently attached to the core material, wherein the antimicrobial LbL coating includes: (a) a polyelectrolyte LbL coating and an peptide layer of one or more a
1. A contact lens comprising a core material which is a silicone-containing hydrogel material and an antimicrobial LbL coating that is not covalently attached to the core material, wherein the antimicrobial LbL coating includes: (a) a polyelectrolyte LbL coating and an peptide layer of one or more antimicrobial peptides, wherein the polyelectrolyte LbL coating is composed of (i) at least one layer of a first polyionic material, or(ii) at least one layer of the first polyionic material and at least one layer of a second polyionic material having charges opposite of the charges of the first polyionic material,wherein said first and second polyionic materials, independently of each other, have functional groups which provide reactive sites, and wherein the peptide layer of one or more antimicrobial peptides are covalently attached to the LbL coating through the reactive sites(b) wherein the antimicrobial LbL coating imparts to the core material an increased surface hydrophilicity. 2. A contact lens of claim 1, wherein said one or more antimicrobial peptides are selected from the group consisting of Cecropin A melittin hybrid, indolicidin, lactoferricin, Defensin 1, Bactenecin (bovin), Magainin 2, mutacin 1140, functionally equivalent or suprior analogs thereof, and mixtures thereof. 3. A contact lens of claim 1, wherein said one or more antimicrobial peptides are selected from the group consisting of Cecropin A melittin hybrid and indolicidin. 4. A contact lens of claim 2, wherein the medical device comprises a polyelectrolyte LbL coating and an peptide layer of one or more antimicrobial peptide, wherein the polyelectrolyte LbL coating is composed of (i) at least one layer of a first polyionic material or (ii) at least one layer of the first polyionic material and at least one layer of a second polyionic material having charges opposite of the charges of the first polyionic material, wherein said first and second polyionic materials, independently of each other, have functional groups which provide reactive sites, and wherein the peptide layer of one or more antimicrobial peptides are covalently attached to the LbL coating through the reactive sites. 5. A contact lens of claim 4, wherein one of the first and second polyionic materials is a polyanionic material and the other is a polycationic material, wherein the polyanionic material is selected from the group consisting of polyacrylic acid, polymethacrylic acid, poly(thiophen-3-acetic acid), poly(4-styrenesulfonic acid), PAMAM dendrimers, PAAm-co-PAA, PVP-co-PAA, hyaluronic acid, glycosaminoglycanes, fucoidan, poly-aspartic acid, poly-glutamic acid, carboxymethyl cellulose, carboxymethyl dextrans, alginates, pectins, gellan, carboxyalkyl chitins, carboxymethyl chitosans, sulfated polysaccharides, derivatives thereof and mixtures thereof, wherein the polycationic material is selected from the group consisting of poly(allylamine hydrochloride), poly(ethyleneimine), poly(vynylbenzyltriamethylamine), polyaniline, polypyrrole, poly(pyridinium acetylene), polyquat, polyaminoamide, poly-ε-lysine, albumin or collagen, aminoalkylated polysaccharides, derivatives thereof and mixtures thereof.
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