A folate‐conjugated copolymer PEG‐PLA‐PLL/folate was synthesized and mixed with pure PEG‐PLA‐PLL and a fluorescent model drug mFITC to prepare folate‐conjugated micelles. The distribution of micelles was studied on cancer‐cell‐bearing mice via frozen slicing. The r e sults show that mFITC is successfully encapsulated into folate(+) and folate(?)micelles; PEG‐PLA‐PLL micelles the latter can be internalized by both HeLa and CHO cells without selectivity due to their cationic surface charges, while folate(+)micelles exhibit more preferential endocytosis by HeLa cells than by CHO cells. The folate(?)micelles showed retention in both organs and tumors. The folate(+)micelles are a promising active targeting drug delivery system for FR over‐expressing cells and they accumulate in tumor beds.
Summary: The grafting of poly(ethylene oxide) (PEO) onto silica nanoparticles was performed in situ by the ring‐opening polymerization of the oxirane monomer initiated from the mineral surface using aluminium isopropoxide as an initiator/heterogeneous catalyst. Alcohol groups were first introduced onto silica by reacting the surfacic silanols with prehydrolyzed 3‐glycidoxypropyl trimethoxysilane. The alcohol‐grafted silica played the role of a coinitiator/chain‐transfer agent in the polymerization reaction and enabled the formation of irreversibly bonded polymer chains. Silica nanoparticles containing up to 40 wt.‐% of a hairy layer of grafted PEO chains were successfully produced by this technique.
The grafting of poly(ethylene oxide) (PEO) onto silica nanoparticles by in‐situ ring‐opening polymerization of the oxirane monomer. 相似文献
Deposition of hole injection layers including a perfluorinated ionomer has been demonstrated using layer‐by‐layer spin self‐assembly for enhanced device efficiency and lifetime in PLEDs. We show that the LBL spin self‐assembled thin films enable to control work functions of indium‐tin oxide anodes by changing the PFI concentration and that a resulting green‐emitting device has an enhanced luminescence efficiency and 18 times longer half lifetime than a device using a conventional HIL. We also fabricate a gradient of energy levels by the LBL self‐assembly of the PFI that results in a work function of 5.74 eV, which can be used to improve carrier injection even for an emitting layer whose ionization potential is over 5.7 eV.
The Lewis acid B(C6F5)3 in combination with hydrosilanes exhibits remarkable activity in the oligomerization of sulfone‐ and phosphonate‐based monomers. This process opens new routes to high‐tech silicone‐based materials, i.e., thermoplastic elastomers and heat‐resistant polysiloxanes.
We herein develop a facile catalyst‐free method to prepare hyperbranched hydroxyl‐enriched aliphatic polycarbonate according to SCROP strategy. PEG‐attached multiarm hyperbranched copolymer HEHDO‐star‐mPEG was further designed. It was found that HEHDO‐star‐mPEG can self‐assemble into supramolecular multimolecular micelles in water. HEHDO‐star‐mPEG micelle showed excellent stability with respect to micellar size upon dilution, and displayed good cell‐biocompatibility. An anticancer drug of doxorubicin with hydrogen‐bonding functionality was incorporated into obtained micelles to establish a drug delivery system model. A high drug‐loading content as well as sustained release pattern for HEHDO‐star‐mPEG based delivery system was achieved.
Sixteen parallel polymerization reactions of 2‐ethyl‐2‐oxazoline have been performed at different temperatures in an automated synthesizer that allowed individual heating of each reactor. During the reactions samples were taken automatically, which were characterized by means of both online GPC and offline GC, in order to optimize the reaction temperature and to determine the activation energy of the polymerization.
π‐Conjugated microporous networks have been prepared from the tetraarylated diketopyrrolo[3,4‐c]pyrrole unit as a tetrafunctional building block. The reactions are carried out using microwave‐assisted Yamamoto or Sonogashira cross‐coupling. Red insoluble powders are obtained, showing intense fluorescence. The polymer networks exhibit a high gas storage capability, with BET surface areas up to about 500 m2 · g−1.
The nucleophilic living ring‐opening polymerization of N‐substituted glycine N‐carboxyanhydrides using solid‐phase synthesis resins is reported. By variation of experimental parameters, products with near Poisson distributions are obtained. As opposed to reversible deactivation radical polymerization, the living polymerization is demonstrated to be viable to high monomer conversion and through multiple monomer addition steps. Successful preparation of a multiblock copolypeptoid is proof for a highly living and robust character of the solid‐phase peptoid polymerization.
We report syntheses of phenylene‐, biphenylene‐, and terphenylene‐layered polymers with a xanthene scaffold by the modified Suzuki‐Miyaura coupling reaction. Their optical properties were studied in detail. The polymer end‐capped by nitrobenzene units, which act as fluorescence quenchers, exhibited the photo‐excited energy transfer from the layered oligophenylenes to the terminal units.
Summary: Novel hyperbranched poly(amine‐ester) (HPAE) cross‐linked films were prepared by cross‐linking the terminal hydroxyl groups of HPAE using glutaraldehyde (GA). Atom force microscope and scanning electron microscope revealed their smooth surfaces, dense and homogenous matrices. Property characterizations indicated that these cross‐linked films had good hydrophilicity, relative low protein adsorption, and high tensile strength. Also, their swelling behavior varied with the solvent.
Structure of the hyperbranched poly(amine‐ester). 相似文献
Layer‐by‐layer (LBL) films consisting of layers of the azo dye Sunset Yellow alternated with chitosan display spontaneous birefringence, which is attributed to the film anisotropy imparted by the LBL method. This is unusual for azobenzene‐containing materials as they normally form films with randomly oriented molecules, presenting birefringence only due to photoinduced isomerization cycles. Spontaneous birefringence does not appear in cast films, but occurs for LBL films obtained under various experimental conditions.
Chemical structures of (a) Sunset Yellow and (b) chitosan. 相似文献
A series of well‐defined rod‐coil PAA‐b‐DPS block copolymers, containing Fréchet‐type dendronized polystyrene (DPS) with different generation as a rod‐like hydrophobic block and poly(acrylic acid) (PAA) as a hydrophilic coil were synthesized. The procedure included the following steps: the precursor PMA‐b‐DPS copolymer was prepared through ATRP of Fréchet‐type dendritic styrene macromonomer bearing the first to the third generation (G1–G3), respectively, initiated by poly(methyl acrylate) (PMA‐Br). Then, by converting PMA into PAA by subsequent hydrolysis, the targeted amphiphilic copolymers were obtained. Moreover, by using the rod‐coil amphiphiles as building blocks, large compound micelles and vesicles were formed in a binary solvent mixture of DMF/H2O. Morphological changes in self‐assembly showed dependence on the length of the dendronized block.
Au nanoparticles (NPs) and polymer composite particles with phase‐separation structures were prepared based on phase separation structures. Au NPs were successfully synthesized in amphiphilic block‐copolymer micelles, and then composite particles were formed by a simple solvent evaporation process from Au NPs and polymer solution. The phase separated structures (Janus and Core‐shell) were controlled by changing the combination of polymers having differing hydrophobicity.
