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10 results about "Mucoadhesive polymers" patented technology

Solid mucoadhesive composition

A solid mucoadhesive composition comprising or consisting of (a) at least one active agent, preferably at least one perfume or fragrance molecule; (b) at least one carrier; and (c) at least one mucoadhesive polymer, wherein the carrier is selected from the group comprising silicon dioxide, silica and silicates.
Owner:SYMRISE GMBH & CO KG

Reinforcement of mucus barrier properties

A composition or a contraceptive composition comprising a mucoadhesive polymer in a physiologically acceptable carrier, wherein the mucoadhesive polymer consists of 4 to 20 monomers units linked to each other via ether, ester or amide bonds, which monomer units are selected from the list consisting of amino functionalised C6 sugars, C6 sugars, amino functionalised C5 sugars, C5 sugars, amino acids, fatty acid derivatised C6 sugars and fatty acid derivatised C5 sugars and its uses thereof.
Owner:CIRQLE BIOMEDICAL CONTRACEPTION IVS

Stable ophthalmic emulsion

The present invention is directed to an ophthalmic emulsion. The emulsion has a unique combination of ingredients that promotes the thermal stability of small oil droplets within the emulsion. The emulsion also includes a mucoadhesive polymer that aid in delivering a lipid to the ocular surface.
Owner:ALCON INC

Stable ophthalmic emulsion

The present invention is directed to an ophthalmic emulsion. The emulsion has a unique combination of ingredients that promotes the thermal stability of small oil droplets within the emulsion. The emulsion also includes a mucoadhesive polymer that aid in delivering a lipid to the ocular surface.
Owner:ALCON INC

Mucus membrane formulations and uses thereof

The invention features a mucosal coating composition including: (i) water: (ii) at least one mucoadhesive polymer / polysaccharide (e.g., a concentration between 0.1-20% w / v); and (iii) at least one surfactant (e.g., a concentration between 0.005-5% w / v). Exhibit long-lasting residence times on mucosal tissues and prophylactic protection against transmucosal pathogens.
Owner:THE BRIGHAM & WOMEN S HOSPITAL INC

Adhesive oral discs for sustained cannabinoid release

PendingJP2026522980ACannabinoidOral ulcers
The present invention relates to an adhesive intraoral disc for sustained release of cannabinoids. The disc comprises one or more cannabinoids and consists of a mucosal contact layer having a mucosal contact surface usable to be fixed to the gingiva of a person requiring relief or treatment of a medical condition, comprising one or more mucosal adhesive polymers that enable the adhesive intraoral disc to adhere to the gingiva for an extended period. Furthermore, the disc comprises a non-mucosal adhesive module fused with the mucosal contact layer, comprising a solid tablet composition that enables the non-mucosal adhesive module to dissolve for an extended period when the adhesive intraoral disc adheres to the gingiva. The present invention is particularly useful for the relief or treatment of ulcers.
Owner:FERTIN PHARMA AS

Dissolvable medical device for drugs delivery

A dissolvable medical device for placing on the outer exposed surface of the eye to deliver a drug to the eye comprises: a polymeric film has sufficient dimensions to cover a cornea when applied to an eye and the polymeric film comprising one or more mucoadhesive polymers. The polymeric film dissolves between 15 minutes to 120 minutes to release the mucoadhesive and the pharmaceutically active agents after applying the polymeric film to the eye. The dissolved polymeric film is not impeding visualization of ocular tissue while maintaining a protective film on outer surface of the eye.
Owner:ALCON INC

Mucosal adhesive polymeric drug delivery compositions and methods

The present invention provides compositions for controlled local deposition of one or more drugs within an individual. More specifically, described herein are compositions comprising a) a polyethylene glycol (PEG) composition having a first low molecular weight PEG (Mw of 200-500 Da) and a second low molecular weight PEG (Mw of 500-2000 Da) and b) a mucoadhesive polymer. Alternatively, the compositions can comprise a) a polyethylene glycol (PEG) composition having a first low molecular weight PEG (Mw of 200-500 Da) and a second low molecular weight PEG (Mw of 500-2000 Da), b) a water insoluble polymer and c) a mucoadhesive polymer. In addition, the compositions can further comprise one or more drugs. Also provided are methods of making and administering the compositions described herein, which are used as biodegradable, injectable, mucoadhesive, low viscosity pastes.
Owner:THE UNIV OF BRITISH COLUMBIA

Oral articles and methods of use

Articles that include from 20 wt-% to 45 wt-% of one or more plant based oils based on the total weight of the article; from 50 wt-% to 70 wt-% of one or more polymer film formers based on the total weight of the article; and from 5 wt-% to 15 wt-% of one or more humectants based on the total weight of the article. Further articles comprises this combination of oil, film former and humectant as a first layer adjacent to which a second layer comprises a mucoadhesive polymer. The articles may be used to prevent formation or maintenance of biofilm in an oral tissue, affect hydration loss in an oral tissue, affect lubricity or lubriciousness in an oral tissue or treat xerostomia or dry mouth. Preferred polymer film formers include pullulan, xanthan gum, HP guar, ethyl cellulose and carrageenan.
Owner:SOLVENTUM INTELLECTUAL PROPERTIES CO

A mucoadhesive polymer microcarrier loaded with tetrasodium clavuloxate, its preparation method and application

The application discloses a mucous membrane-adhesive polymeric microcarrier loaded with disodium cladribine tetrasodium and a preparation method and application thereof. Sodium alginate is modified by phenylboronic acid to obtain a PBA-Alg polymer; disodium cladribine tetrasodium is mixed with the polymer to obtain a precursor solution; microdroplets are formed by a microfluidic electrospray technology and sprayed into a calcium ion crosslinking solution to be solidified to obtain the microcarrier. In the microcarrier, the phenylboronic acid groups form reversible borate ester bonds with cis-diol groups in the disodium cladribine tetrasodium molecules, so that stable anchoring and continuous release of the drug are realized. The phenylboronic acid groups on the surface of the microcarrier can form dynamic covalent bonds with sialic acid residues in ocular surface mucin, so that long-acting adhesion on the ocular surface is realized; meanwhile, the borate ester bonds are oxidatively cleaved in the presence of excess active oxygen on the ocular surface, so that the active oxygen is consumed and inflammation is inhibited. The microcarrier has a highly uniform size and shear thinning characteristics, and can be safely, comfortably, efficiently and low-frequency used for the treatment of ocular surface diseases such as dry eye.
Owner:NANJING DRUM TOWER HOSPITAL