Ma et al., 2018 - Google Patents
Core Cross-linked micelles made of glycopolymers bearing dopamine and cholic acid pendantsMa et al., 2018
- Document ID
- 877894543229224510
- Author
- Ma Z
- Zhu X
- Publication year
- Publication venue
- Molecular Pharmaceutics
External Links
Snippet
A series of block glycopolymers bearing galactose, dopamine, and cholic acid (CA) pendants have been synthesized by RAFT polymerization. These copolymers can self- assemble into micelles in water. The dopamine moieties, located near the interface of the …
- 239000000693 micelle 0 title abstract description 346
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
- A61K9/51—Nanocapsules; Nanoparticles
- A61K9/5107—Excipients; Inactive ingredients
- A61K9/513—Organic macromolecular compounds; Dendrimers
- A61K9/5146—Organic macromolecular compounds; Dendrimers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, polyamines, polyanhydrides
- A61K9/5153—Polyesters, e.g. poly(lactide-co-glycolide)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives
- A61K47/48—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives the non-active ingredient being chemically bound to the active ingredient, e.g. polymer drug conjugates
- A61K47/48769—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives the non-active ingredient being chemically bound to the active ingredient, e.g. polymer drug conjugates the conjugate being characterized by a special physical or galenical form
- A61K47/48853—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives the non-active ingredient being chemically bound to the active ingredient, e.g. polymer drug conjugates the conjugate being characterized by a special physical or galenical form the form being a particulate, powder, adsorbate, bead, sphere
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives
- A61K47/48—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives the non-active ingredient being chemically bound to the active ingredient, e.g. polymer drug conjugates
- A61K47/48169—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives the non-active ingredient being chemically bound to the active ingredient, e.g. polymer drug conjugates the modifying agent being an organic macromolecular compound, i.e. an oligomeric, polymeric, dendrimeric molecule
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G83/00—Macromolecular compounds not provided for in groups C08G2/00 - C08G81/00
- C08G83/002—Dendritic macromolecules
- C08G83/003—Dendrimers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives
- A61K47/30—Macromolecular compounds
-
- 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
- C08F293/00—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule
- C08F293/005—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule using free radical "living" or "controlled" polymerisation, e.g. using a complexing agent
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K49/00—Preparations for testing in vivo
- A61K49/06—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Fan et al. | Recent development of unimolecular micelles as functional materials and applications | |
| Calderón et al. | Dendritic polyglycerols for biomedical applications | |
| Lin et al. | Development of zwitterionic polypeptide nanoformulation with high doxorubicin loading content for targeted drug delivery | |
| Aiertza et al. | Single-chain polymer nanoparticles | |
| Lei et al. | Chitosan/sodium alginate modificated graphene oxide-based nanocomposite as a carrier for drug delivery | |
| Zhou et al. | Endosomal pH-activatable poly (ethylene oxide)-graft-doxorubicin prodrugs: synthesis, drug release, and biodistribution in tumor-bearing mice | |
| Panja et al. | Tailor-made temperature-sensitive micelle for targeted and on-demand release of anticancer drugs | |
| Wei et al. | Thermo-sensitive polymeric micelles based on poly (N-isopropylacrylamide) as drug carriers | |
| Utama et al. | Biocompatible glycopolymer nanocapsules via inverse miniemulsion periphery RAFT polymerization for the delivery of gemcitabine | |
| Yang et al. | Synthesis and physicochemical characterization of amphiphilic triblock copolymer brush containing pH-sensitive linkage for oral drug delivery | |
| Jia et al. | Unimolecular micelles of amphiphilic cyclodextrin-core star-like copolymers with covalent pH-responsive linkage of anticancer prodrugs | |
| Seidi et al. | Functional materials generated by allying cyclodextrin-based supramolecular chemistry with living polymerization | |
| Chen et al. | Bio-inspired amphoteric polymer for triggered-release drug delivery on breast cancer cells based on metal coordination | |
| Huang et al. | Zwitterionic nanoparticles constructed with well-defined reduction-responsive shell and pH-sensitive core for “spatiotemporally pinpointed” drug delivery | |
| Jiang et al. | A pH-sensitive nano drug delivery system of doxorubicin-conjugated amphiphilic polyrotaxane-based block copolymers | |
| Ma et al. | Glycopolymers bearing galactose and betulin: Synthesis, encapsulation, and lectin recognition | |
| Wang et al. | Synthesis of zwitterionic diblock copolymers with cleavable biotin groups at the junction points and fabrication of bioconjugates by biotin–streptavidin coupling | |
| Zhang et al. | “Bitter-sweet” polymeric micelles formed by block copolymers from glucosamine and cholic acid | |
| Ma et al. | Core Cross-linked micelles made of glycopolymers bearing dopamine and cholic acid pendants | |
| Manna et al. | Amino acid inspired alginate-based ph sensitive polymeric micelles via reversible addition–fragmentation chain transfer polymerization | |
| Lu et al. | Development of core–shell nanostructures by in situ assembly of pyridine-grafted diblock copolymer and transferrin for drug delivery applications | |
| Jia et al. | Thermo-and pH-responsive copolymers bearing cholic acid and oligo (ethylene glycol) pendants: Self-assembly and pH-controlled release | |
| Asadi et al. | Dual responsive nanogels for intracellular doxorubicin delivery | |
| Rezaei et al. | pH-triggered prodrug micelles for cisplatin delivery: preparation and in vitro/vivo evaluation | |
| Holm et al. | Impact of branching on the solution behavior and serum stability of starlike block copolymers |