[go: up one dir, main page]

Ma et al., 2018 - Google Patents

Core Cross-linked micelles made of glycopolymers bearing dopamine and cholic acid pendants

Ma 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 …
Continue reading at pubs.acs.org (other versions)

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/48Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/50Microcapsules 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
    • A61K9/51Nanocapsules; Nanoparticles
    • A61K9/5107Excipients; Inactive ingredients
    • A61K9/513Organic macromolecular compounds; Dendrimers
    • A61K9/5146Organic macromolecular compounds; Dendrimers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, polyamines, polyanhydrides
    • A61K9/5153Polyesters, e.g. poly(lactide-co-glycolide)
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives
    • A61K47/48Medicinal 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
    • A61K47/48769Medicinal 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
    • A61K47/48853Medicinal 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives
    • A61K47/48Medicinal 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
    • A61K47/48169Medicinal 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
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G83/00Macromolecular compounds not provided for in groups C08G2/00 - C08G81/00
    • C08G83/002Dendritic macromolecules
    • C08G83/003Dendrimers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives
    • A61K47/30Macromolecular compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F293/00Macromolecular 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
    • C08F293/005Macromolecular 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
    • A61K49/00Preparations for testing in vivo
    • A61K49/06Nuclear 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