pH响应两亲嵌段锌酞菁聚合物光敏剂的制备及光活性

将氨基锌酞菁（ZnTAPc）与甲基丙烯酰氯反应制备出含有不饱和双键的取代锌酞菁衍生物（MeZnAPc）,采用ATRP法将聚乙二醇单甲醚大分子引发剂（mPEG110-Br）与甲基丙烯酸（2-异丙胺基）乙酯（DPA）和MeZnAPc共聚,制得一种新型pH响应两亲嵌段锌酞菁聚合物光敏剂（PEG110-b-P（DPAn-co-MeZnAPcm））.用1HNMR,FTIR对MeZnAPc和聚合物光敏剂进行表征.UV-vis测试表明该聚合物光敏剂在pH6.0～6.5具有较好的pH响应性.以1,3-二苯基苯并呋喃（DPBF）为底物研究了该聚合物光敏剂的光催化氧化效率,结果表明其具有较高光活性.利用该聚合物光敏剂在不同pH的水溶液中对L-色氨酸进行光催化氧化实验,结果发现在pH5.5不存在胶束时,锌酞菁可以较好地分散在溶液中,并能维持较高光活性,而在pH7.4形成胶束时可以将锌酞菁很好地包裹在其内部,使其光活性大大降低.因此,这种pH响应两亲嵌段锌酞菁聚合物作为一种新型光敏剂,在光动力学治疗领域有较好的应用前景.     

Synthesis of self-assemble pH-responsive cyclodextrin block copolymer for sustained anticancer drug delivery

Well-defined p H-responsive poly(ε-caprolactone)-graft-β-cyclodextrin-graft-poly(2-(dimethylamino)ethylmethacrylate)-co-poly(ethylene glycol) methacrylate amphiphilic copolymers(PCL-g-β-CD-g-P(DMAEMA-co-PEGMA)) were synthesized using a combination of atom transfer radical polymerization(ATRP),ring opening polymerization(ROP) and "click" chemistry.Successful synthesis of polymers was confirmed by Fourier transform infrared spectroscopy(FTIR),proton nuclear magnetic resonance(1H-NMR),and gel permeation chromatography(GPC).Then,the polymers could selfassemble into micelles in aqueous solution,which was demonstrated by dynamic light scattering(DLS) and transmission electron microscopy(TEM).The p H-responsive self-assembly behavior of these copolymers in water was investigated at different p H values of 7.4 and 5.0 for controlled doxorubicin(DOX) release,and these results revealed that the release rate of DOX could be effectively controlled by altering the p H,and the release of drug loading efficiency(DLE) was up to 88%(W/W).CCK-8 assays showed that the copolymers had low toxicity and possessed good biodegradability and biocompatibility,whereas the DOX-loaded micelles remained with high cytotoxicity for He La cells.Moreover,confocal laser scanning microscopy(CLSM) images revealed that polymeric micelles could actively target the tumor site and the efficient intracellular DOX release from polymeric micelles toward the tumor cells further confirmed the anti-tumor effect.The DOX-loaded micelles could easily enter the cells and produce the desired pharmacological action and minimize the side effect of free DOX.These results successfully indicated that p H-responsive polymeric micelles could be potential hydrophobic drug delivery carriers for cancer targeting therapy with sustained release.     

聚乙二醇-聚谷氨酸-聚丙氨酸三嵌段共聚物的合成及其胶束的pH-响应性药物控制释放

通过大分子引发剂ω-胺基-α-甲氧基聚乙二醇引发N-羧基-α-氨基环内酸酐开环聚合和酸性水解制备了一种具有pH-响应性的三嵌段共聚物聚乙二醇-聚谷氨酸-聚丙氨酸(mPEG-PLGA-PLAA).通过核磁共振、ζ-电势、动态光散射、电子显微镜等手段表征了此类三嵌段共聚物的自组装过程及所形成胶束的pH-响应性.使用圆二色谱和红外光谱,分析了胶束结构随环境pH值转变过程中聚氨基酸链段二级结构的变化.以阿霉素作为模型药物,研究了三嵌段共聚物的载药能力和在不同pH条件下的药物释放能力.在碱性条件下,PLGA链段去质子化,链段从疏水性变为亲水性,胶束中间层由于水合作用变得松散,药物释放速率增加;在酸性条件下,PLGA链段质子化,不带电荷,与阿霉素药物分子间的静电相互作用消失.同时,PLGA链段α-螺旋含量增加,形成由链内氢键维持的刚性棒状结构,将链段周围包埋的药物分子"挤出",加速了药物的释放.     

Investigation of pH-responsive properties of polymeric micelles with a core-forming block having pendant cyclic ketal groups

In this study, three kinds of amphiphilic block copolymers, termed MPEG-block-PDMMA, MPEG-block-PCPMA, and MPEG-block-PMPMA, which were composed of one hydrophilic monomethoxy poly(ethylene glycol) (MPEG) block and one hydrophobic polyacrylate block bearing pendant six-member cyclic ketal groups, were synthesized by atom transfer radical polymerization (ATRP). These polymers can disperse in aqueous media to self-assemble into micellar aggregates with a spherical core-shell structure with mean diameter below 300 nm. The stimuli-responsiveness of polymeric micelles from MPEG-block-PDMMA was detected by fluorescence-probe technique at pH 3.5 and 37 °C. The effect of chemical architecture and composition of the polymers on the pH-responsive properties of polymeric micelles was also studied. A combination of pH and temperature to trigger release behavior of these polymeric micelles was discussed by comparing the encapsulated molecule release ability under various pH and temperature conditions and analyzing chemical structural changes of the polymer before and after the triggering.     

RAFT聚合法制备聚合物胶束及其应用前景

聚合物胶束由于具有优良的组织渗透性、增容效果好、结构多样性和热稳定性等特点,成为国内外研究的热点之一。本文综述了近几年发展起来的一些具有特殊结构和特殊性能的双亲性嵌段聚合物胶束的研究进展,详细阐述了RAFT聚合法合成聚合物胶束的机理和优势,表明了RAFT聚合法可直接在水溶液中方便快捷地制备出温度和pH双响应性聚合物胶束。然而,当聚合物胶束的浓度低于其临界胶束浓度时,胶束的稀释效应大大影响了其实际应用,为提高聚合物胶束的稳定性,文章归纳总结了一系列有关壳交联聚合物胶束的制备方法及研究进展。最后,文章展望了聚合物胶束在药物可控释放、靶向、生物成像、催化剂负载及其他领域的应用前景。     

Electrospun Polyacrylic Acid Polymer Fibers Functionalized with Metallophthalocyanines for Photosensitizing and Gas Sensing Applications

The photophysical and photochemical properties of tetraaminophthalocyanine complexes of lutetium and zinc covalently linked to polyacrylic acid were studied alongside those of unsubstituted zinc phthalocyanine within the same polymeric fiber matrix. All three phthalocyanines within the solid fiber matrices showed photoactivity by the generation of singlet oxygen as was observed in solution. The fluorescence behaviors of the composite fibers equally parallel those in solution. For the unsubstituted zinc phthalocyanine composite, the fiber showed fluorescence quenching on interaction with gaseous nitrogen dioxide similar to that in DMF and, thus could be a promising nanofabric material in developing optoelectronic devices that are responsive to the gas.     

Synthesis,self-assembly,and pH-responsive drug release of PHMEMA-PEG-PHMEMA ABA triblock copolymers

Abstract

A series of tertiary amine containing PHMEMA-PEG-PHMEMA ABA triblock copolymers were synthesized by atom transfer radical polymerization (ATRP) using bromine-capped poly(ethylene glycol) (Br-PEG-Br) and 2-(hexamethyleneimino)ethyl methacrylate (HMEMA) as macro-initiator and monomers, respectively. The chemical structures and molecular weights of triblock copolymers were characterized by ¹H NMR and gel permeation chromatography (GPC). The self-assembly behaviors of copolymers in different pH conditions were studied by dynamic light scattering (DLS) and transmission electron microscopy (TEM). Triblock copolymers self-assembled into micelles in water (pH 7.4) and the micelles disassembled at acidic pH (pH 5.0). Anticancer drug doxorubicin (DOX) was used as a drug model and physically encapsulated into polymeric micelles. The drug release of DOX-loaded polymeric micelles was pH-responsive; the drug-loaded micelles that had higher contents of tertiary amine in polymer pendant groups showed faster release speed. In addition, the drug-loaded micelles showed excellent inhibition efficacy against HeLa cells in vitro.     

Local detection of pH-induced disaggregation of biocompatible micelles by fluorescence switch ON

Fluorogenic nanoparticles (NPs) able to sense different physiological environments and respond with disaggregation and fluorescence switching OFF/ON are powerful tools in nanomedicine as they can combine diagnostics with therapeutic action. pH-responsive NPs are particularly interesting as they can differentiate cancer tissues from healthy ones, they can drive selective intracellular drug release and they can act as pH biosensors. Controlled polymerization techniques are the basis of such materials as they provide solid routes towards the synthesis of pH-responsive block copolymers that are able to assemble/disassemble following protonation/deprotonation. Ring opening metathesis polymerization (ROMP), in particular, has been recently exploited for the development of experimental nanomedicines owing to the efficient direct polymerization of both natural and synthetic functionalities. Here, we capitalize on these features and provide synthetic routes for the design of pH-responsive fluorogenic micelles via the assembly of ROMP block-copolymers. While detailed photophysical characterization validates the pH response, a proof of concept experiment in a model cancer cell line confirmed the activity of the biocompatible micelles in relevant biological environments, therefore pointing out the potential of this approach in the development of novel nano-theranostic agents.

pH-responsive micelles disassembly, upon acidification during lysosomal uptake, leads to fluorescence switch ON. These nanoparticles are promising candidates for the design of novel stimuli-responsive drug delivery systems.     

Engineering polyzwitterion with acylsulfonamide-based betaine structure for protonated switch of surface chemistry at tumoral pH and reductive responsive drug release of polymeric micelles

The surface chemistry of stimulus-responsive nanoparticles plays an important role in mediating nano-bio interactions in cancer nanomedicine by targeting the unique features of the tumor microenvironment, such as low extracellular pH. To develop therapeutic nanoparticles with high sensitivity and instant response to slight pH differences in the systemic circulation, we produced a novel polyzwitterion with acylsulfonamide-based betaine structure by one-step modification of polycarboxybetaine (PCB) with benzene sulfonamide. The zwitterionic micellar shells show high antifouling in the blood circulation and acutely convert into positive charge via acylsulfonamide protonation, thereby improving cell affinity at tumor sites. Moreover, a disulfide bond between the shell and poly-ε-caprolactone (PCL) core allows for reductive-responsive release of doxorubicin (DOX) after internalization of the polymeric micelles. Finally, in vitro and in vivo competition assays demonstrated that dual responsive drug-loaded micelles have better anticancer efficiency than free DOX or micelles without zwitterionic pH-responsive properties. Thus, we have developed a simple and valuable strategy to enhance pH sensitivity of micellar carriers for cancer treatment.     

pH敏感型mPEG-Hz-PLA聚合物纳米载药胶束的制备

以合成的含有腙键的聚乙二醇大分子(mPEG-Hz-OH)为引发剂,以丙交酯为单体引发开环聚合反应,并通过调整投料比,制备出3种不同分子量的含腙键的生物可降解嵌段聚合物(mPEG-Hz-PLA).将腙键引入到聚合物的骨架中,以此构建聚合物胶束并作为pH敏感型纳米药物载体.制备的pH敏感型胶束的CMC值等于或低于5.46×10-4 mg/m L,DLS和TEM显示粒径均小于100 nm,且粒径分布均匀.非pH敏感型胶束在不同pH下的粒径变化不明显,而pH敏感型胶束在酸性环境下(pH=4.0和pH=5.0)胶束粒径出现了明显变化.以阿霉素为模型药物制备了pH敏感型载药胶束,其粒径比空白胶束大(100~200 nm),且粒径分布均匀.药物释放实验表明pH敏感型载药胶束随着释放介质pH降低累积释药量增高.MTT实验表明空白胶束对HeLa细胞和RAW264.7细胞几乎没有抑制作用,而载阿霉素的胶束对2种细胞的抑制作用都随着剂量的增大和时间的延长而增强.     

Morphological transformation of [60]fullerene-containing poly(acrylic acid) induced by the binding of surfactant

Water-soluble pH-responsive [60]fullerene end-capped poly(acrylic acid) (PAA85-b-C60) was synthesized using atom-transfer radical polymerization (ATRP) technique. The unusual morphological transformation of the polymer induced by the binding of nonionic surfactant Triton X-100 (TX100) at different degrees of neutralization (alpha) was investigated using isothermal titration calorimetry (ITC), UV-vis spectroscopy, dynamic light scattering (DLS), and transmission electron microscopy (TEM). For the 5 mM (monomer concentration) polymer solution at pH < 4, approximately 1.3 mM TX100 binds specifically to C60 domains of the polymeric micelles driven by hydrophobic interaction, which induces a structural transformation of the polymer from a large compound micelle with a radius of 110 nm to a dense precipitated spherical polymer/surfactant complex (PSC) with a radius of 500 nm. The precipitates are resolubilized by a wetting layer of TX100 in excess surfactant (> 1.7 mM in the polymer solution). The binding is significantly weakened and the complexation is disrupted with increasing pH, where the interaction completely ceased at pH > 6.     

Characterization of novel pH-sensitive polymeric micelles prepared by the self-assembly of amphiphilic block copolymer with poly-4-vinylpyridine block synthesized by mechanochemical solid-state polymerization

We fabricated novel pH-sensitive polymeric micelles consisting of amphiphilic block copolymer containing pyridyl groups as side chains in the hydrophobic block. The number average particle diameter of the polymeric micelles at pH 7 was approximately 200 nm. A decrease in pH resulted in deformation of the polymeric micelles over a very narrow pH range (between pH 5.7 and 5.6). Interestingly, micellization and demicellization occurred reversibly in this narrow pH range. Polymeric micelles incorporating 5-fluorouracil (5FU) were also prepared. Decreasing the pH of this polymeric micelle solution from 7 to 5.5 resulted in the rapid release of 5FU at pH 5.6; the drug was completely released within 30 min. These results suggest that deformation of the polymeric micelles caused the rapid release of 5FU.     

Preparation and photoactivity of thermosensitive polymer supported metallophthalocyanine

A novel reactive metallophthalocyanine derivative,zinc tetra(2,4-dichloro-1,3,5-triazine)aminophthalo-cyanine(Zn-TDTAPc),was prepared and immobilized on poly(N-isopropylacrylamide)(PNIPAAm) by covalent bonding to obtain a thermosensitive polymer(Zn-TDTAPc-g-PNIPAAm).Compared with zinc tetraaminophthalocyanine(Zn-TAPc),Zn-TDTAPc-g-PNIPAAm exhibits excellent solubility in water and in most organic solvents.Furthermore,it has a special thermosensitive property in water and the lower critical solution temperature(LCST) is 34.1℃.It was found that both dissolved and precipitated Zn-TDTAPc-g-PNIPAAm present high photoactivity evidenced by the experiment of photocatalytic degra-dation of 1,3-diphenylisobenzofuran(DPBF) in the presence of Zn-TDTAPc-g-PNIPAAm.These proper-ties suggest that it can be used potentially in photodynamic therapy(PDT).     

pH-responsive self-assembly of carboxyl-terminated hyperbranched polymers

This work has presented a typical example to reveal the great influence of the terminal groups on the self-assembly of hyperbranched polymers. The hyperbranched polymers with hydroxyl terminal groups (HBPO-OH) were hydrophobic and precipitated in water, however, they displayed a pH-responsive self-assembly behavior when the terminal groups were replaced by carboxyl groups. The obtained carboxyl-terminated hyperbranched polymers (HBPO-COOH) existed as unimolecular micelles at high pH (12.21) due to the ionization of carboxyl groups, while the polymers aggregated into multimolecular micelles from 10 to 500 nm with the decrease of pH as a result of the partial protonation of the carboxyl groups. The size of the obtained micelles depended strongly on the solution pH - the lower the pH, the bigger the micelles. TEM, DLS, ATR-FT-IR, (1)H NMR and AFM measurements substantiated that the multimolecular micelles were formed by the secondary aggregation of unimolecular micelles driven by the hydrogen bonding interaction depending on the solution pH.     

Preparation and characterization of monolithic column by grafting pH-responsive polymer

A novel modified monolithic column with pH-responsive polymer chains was prepared by grafting methacrylic acid onto the poly(glycidyl methacrylate-co-ethylene dimethacrylate) monolith. The grafting polymerization was achieved in an in situ manner which was performed by pumping methacrylic acid directly through an acidic hydrolysis monolithic column using potassium peroxydisulfate initiated free-radical polymerization. The grafted monolithic column was demonstrated to be the pH-responsive to the pore structure and the chromatographic characterization. The permeability of the column and the retention factors of five benzene homologues decreased due to the conformational changes of the polymer chains when the pH of mobile phase increased from 4.5 to 7.5. Furthermore, the modified monolithic column was used as the pH-responsive stationary phase and exhibited an excellent separation of four basic proteins.     

Photocatalytic oxidation of phenol in aqueous solutions with oxygen catalyzed by supported metallophthalocyanine catalyst

In this paper, zinc tetraaminophthalocyanine (Zn-APc) was immobilized on cellulosic fiber by covalent bond to obtain a novel cellulosic fiber supported metallophthalocyanine, named Zn-TDTAPc-F. At pH 11, upon visible light irradiation for 6 h in the presence of O2, Zn-TDTAPc-F was found to be highly effective for the degradation of phenol in aqueous solution, and the degradation rate of phenol was more than 95%. HPLC was used to confirm formic acid, fumaric acid and maleic acid as its main degradation products.     

Temperature- and pH-responsive unimolecular micelles with a hydrophobic hyperbranched core

The dendritic unimolecular polymeric micelles with a hydrophobic dendritic polyester (Boltorn H40) as the core and the grafted biocompatible poly(N, N-diethylacrylamide)-b-poly(2-(dimethylamino)ethyl methacrylate) (PDEAAM-b-PDMAEMA) as the shell were synthesized by successive reversible addition–fragmentation transfer (RAFT) polymerization of N, N-diethylacrylamide (DEAAM) and 2-(dimethylamino)ethyl methacrylate (DMAEMA) monomers. Laser light scattering studies indicated that the resulting unimolecular polymeric micelles H40–PDEAAM–PDMAEMA with double stimuli-responsive shells exhibited a reversible two-stage phase transition behavior. The effect of varying the block length of PDMAEMA on the thermosensitivity of unimolecular polymeric micelles was studied. With an increase in the outer corona length of PDMAEMA, the temperature range of phase transition for the inner shell PDEAAM would become broad. As pH decreased to 2, the high hydrophilic PDMAEMA blocks with high protonation were independent of temperature, and the size of unimolecular polymeric micelles increased due to the extended-chain conformation of outer layer. The internal core cavities of the unimolecular polymeric micelles exhibited a great potential of loading guest molecules according to the analysis of pyrene probe fluorescence spectra.     

Loading and in vitro controlled release of indomethacin using amphiphilic cholesteryl-bearing carboxymethylcellulose derivatives

Amphiphilic CCMCs were synthesized under mild conditions and their chemical structures were characterized by FT-IR and 1H NMR spectroscopy. Fluorescence analysis showed that CCMCs could self-associate to form polymeric micelles in aqueous solution. IND was encapsulated during the formation of CCMC micelles and its in vitro release properties were investigated. The loading capacity was more than 50% and the loaded IND was slowly and steadily released into the medium over a period of 8 h. The CCMC micelles showed pH-responsive behavior during the drug-loading and release processes. CCMC is promising as a potential delivery system for the controlled release of IND with a pH-responsive property.     

Core‐stabilized polymeric micelle as potential drug carrier: increased solubilization of taxol

Poly(ethylene glycol‐b‐lactide) possessing a methoxy group at the poly(ethylene glycol) (PEG) chain end and a polymerizable methacryloyl group at the poly(lactic acid) (PLA) chain end (MeO–PEG/PLA–methacryloyl) was prepared by an anionic ring‐opening polymerization of ethylene oxide and DL ‐lactide in tandem manner initiated with a potassium 2‐methoxyethanolate, followed by end‐capping with an excess of methacrylic anhydride. The molecular weight of the obtained polymer was controlled by the initial monomer/initiator ratio, which was confirmed by the combination of gel permeation chromatography and nuclear magnetic resonance analyses. The functionality of the methacryloyl–PLA end was almost quantitative. The MeO–PEG/PLA–methacryloyl (38/35; these numbers in parentheses denote the molecular weights of PEG and PLA segments divided by 100, respectively) formed a core–shell type spherical micelle in aqueous media obtained by a dialysis technique, the cumulant diameter of which was ca. 30 nm with very low polydispersity factor. The methacryloyl group adjacent to the PLA was polymerized in the PLA core of the micelle. The polymerization proceeded thermally with radical initiator and photochemically with photo‐initiator to produce core‐polymerized nanoparticles, which was found by spectroscopic and light‐scattering techniques. Taxol‐incorporated micelles were prepared to entrap Taxol into MeO–PEG/PLA–methyacryloyl block copolymer micelles by the oil/water emulsion method. Copyright © 1999 John Wiley & Sons, Ltd.     

A novel macroinimer of polyethylene oxide: synthesis of hyper branched networks by photoinduced H-abstraction process

A novel poly(ethylene oxide) macroinimer (PEO-macronimer) possesing methacryloyl and tertiary amino end groups was prepared by ring-opening polymerization of ethylene oxide initiated by potassium 2-methylaminoethoxide and termination of living ends of PEO with methacryloyl chloride. NMR analysis showed that the macronimer contains equal amount of amino and methacrolyl groups indicating efficient initiation and termination processes. The dimethylamine end group in conjunction with benzophenone under UV irradiation produced ternary amine methylene radicals via H-abstraction mechanism which initiates the polymerization. Photopolymerization in solutions at high macroinimer concentration or in films resulted in the formation of insoluble networks. The crosslinked polymers exhibit high swelling capacity in organic solvents and water due to the hyperbranched nature.