Zou et al., 2012 - Google Patents
Well‐defined drug‐conjugated biodegradable nanoparticles by azide–alkyne click crosslinking in miniemulsionZou et al., 2012
- Document ID
- 17890073351463418801
- Author
- Zou J
- Yu Y
- Yu L
- Li Y
- Chen C
- Cheng C
- Publication year
- Publication venue
- Journal of Polymer Science Part A: Polymer Chemistry
External Links
Snippet
A new type of biodegradable polymer–drug nanoconjugate was fabricated via the combination of oil‐in‐water miniemulsion and Huisgen azide–alkyne click chemistry. Diazide‐functionalized paclitaxel (PTXL) were prepared through functional group …
- 239000002105 nanoparticle 0 title abstract description 70
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/02—Making solutions, dispersions or lattices by other methods than by solution, emulsion or suspension polymerisation techniques
- C08J3/03—Making solutions, dispersions or lattices by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media
-
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/91—Polymers modified by chemical after-treatment
-
- 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
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
-
- 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
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/02—Polyamines
-
- 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
-
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/06—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from hydroxycarboxylic acids
-
- 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
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
-
- 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
- C08G79/00—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule
-
- 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
- C08G8/00—Condensation polymers of aldehydes or ketones with phenols only
- C08G8/04—Condensation polymers of aldehydes or ketones with phenols only of aldehydes
-
- 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
- C08F8/00—Chemical modification by after-treatment
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Zou et al. | Well‐defined drug‐conjugated biodegradable nanoparticles by azide–alkyne click crosslinking in miniemulsion | |
Chang et al. | Fabrication of thermosensitive PCL‐PNIPAAm‐PCL triblock copolymeric micelles for drug delivery | |
Dai et al. | Synthesis, self‐assembly and recognition properties of biomimetic star‐shaped poly (ε‐caprolactone)‐b‐glycopolymer block copolymers | |
Zhao et al. | Boronic acid shell‐crosslinked dextran‐b‐PLA micelles for acid‐responsive drug delivery | |
Wang et al. | Single‐chain nanoparticles with well‐defined structure via intramolecular crosslinking of linear polymers with pendant benzoxazine groups | |
Silvers et al. | Functional aliphatic polyesters and nanoparticles prepared by organocatalysis and orthogonal grafting chemistry | |
Hu et al. | Novel bioresorbable hydrogels prepared from chitosan‐graft‐polylactide copolymers | |
Antoniraj et al. | Synthesis and characterization of poly (N-isopropylacrylamide)-g-carboxymethyl chitosan copolymer-based doxorubicin-loaded polymeric nanoparticles for thermoresponsive drug release | |
Liu et al. | Photo‐responsive amphiphilic poly (α‐hydroxy acids) with pendent o‐nitrobenzyl ester constructed via copper‐catalyzed azide‐alkyne cycloaddition reaction | |
Meenarathi et al. | Near infrared dye functionalized MWCNT as an effective initiator for the ring opening polymerization of ε-caprolactone | |
Bahadur et al. | Novel amphiphilic triblock copolymer based on PPDO, PCL, and PEG: Synthesis, characterization, and aqueous dispersion | |
Cao et al. | Synthesis of nanogels of poly (ε-caprolactone)-b-poly (glycidyl methacrylate) by click chemistry in direct preparation | |
Moghadam et al. | Design of a new light curable starch-based hydrogel drug delivery system to improve the release rate of quercetin as a poorly water-soluble drug | |
Guo et al. | Poly (ε‐caprolactone)‐graft‐poly (2‐(dimethylamino) ethyl methacrylate) Amphiphilic Copolymers Prepared via a Combination of ROP and ATRP: Synthesis, Characterization, and Self‐Assembly Behavior | |
Bi et al. | Well‐defined thermoresponsive dendritic polyamide/poly (N‐vinylcaprolactam) block copolymers | |
Hu et al. | Core crosslinking of biodegradable block copolymer micelles based on poly (ester carbonate) | |
Icart et al. | Fluorescent microspheres of poly (ethylene glycol)–poly (lactic acid)–fluorescein copolymers synthesized by Ugi four‐component condensation | |
Chen et al. | Preparation of amphiphilic copolymers for covalent loading of paclitaxel for drug delivery system | |
Sahin et al. | Polyoxazoline‐modified graphene oxides with improved water and epoxy resin dispersibility and stability towards composite applications | |
Lu et al. | Facile synthesis of amphiphilic chitosan‐g‐poly (lactic acid) derivatives and the study of their controlled drug release | |
Kampmann et al. | Formation of Well‐Defined Polymer Particles in the Sub‐100 nm Size Range by Using Amphiphilic Block Copolymer Surfactants and a Microemulsion Approach | |
Dashan et al. | Preparation of single chain nanoparticles via photoinduced double collapse process | |
Dal Poggetto et al. | Nanoparticles decorated with folate based on a site-selective αCD-rotaxanated PEG-b-PCL copolymer for targeted cancer therapy | |
Sanchez-Sanchez et al. | Efficient Synthesis of Single‐Chain Polymer Nanoparticles via Amide Formation | |
Yang et al. | Hyperbranched Poly (ester‐enamine) from Spontaneous Amino‐yne Click Reaction for Stabilization of Gold Nanoparticle Catalysts |