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1.
Converting polyethylene terephthalate (PET) wastes to its monomer and valuable chemicals via eco-friendly chemical method is still a challenge task. Previously, phase transfer catalysts used for alkaline hydrolysis were soluble in reaction media and hardly separated after reaction. Here, we reported several pH-responsive catalysts combined alkyl quaternary ammonium units with heteropolyacid anion for achieving stepwise product/catalyst separation and catalyst recycling. The properties of homogeneous/heterogeneous transfer behavior allow catalyst to be easily separated from reaction media by adjusting of pH value. Among them, [C16H33N(CH3)3]3PW12O40 (abbreviated as [CTA]3PW) exhibits the highest activity and the most suitable pH responsive values. Such a pH triggered switchable catalytic system not only shows good performance for depolymerization of pure PET, but also some real PET wastes such as coloured trays and PE/PET complex films could be completely degraded into terephthalic acid. Additionally, the reaction kinetics and activation energy of PET alkaline hydrolysis also studied with and without pH-responsive [CTA]3PW.  相似文献   
2.
以金刚烷为核设计合成了一种具有pH响应功能的四臂星状聚合物金刚烷-[聚(乳酸-共-羟基乙酸)-聚甲基丙烯酸二乙氨基乙酯-聚(乙二醇)单甲醚]4(4sAd-PLGA-D-P), 制备了4sAd-PLGA-D-P自组装胶束, 考察了该胶束对抗癌药物阿霉素(Doxorubicin,DOX)的控释性能。结果表明: 改变聚甲基丙烯酸二乙氨基乙酯(PDEAEMA)的链段长度可实现对聚合物胶束性能的调控。PDEAEMA链段越长, 聚合物胶束的粒径越大, 载药量越高, 药物累计释放量越高。聚合物胶束具有良好的稳定性(临界胶束浓度(Critical Micelle Concentration,CMC)为0.0031 mg/mL)、pH响应性能和载药能力(载药量高达24.8%)。载DOX胶束在肿瘤微环境pH值(pH=5.0)的累计释放量(85.2%)明显高于正常组织pH=7.4条件下的累计释放量(20.9%), 可实现抗癌药物的可控释放。因此, pH响应型聚合物胶束4sAd-PLGA-D-P在抗癌药物递送领域具有潜在的应用前景。  相似文献   
3.
Softwood kraft lignin (SKL) pH-responsive hydrogels were prepared through controlled aggregation using poly[2-(dimethylamino)ethyl methacrylate] (PDMAEMA) and poly(2-(dimethylamino)ethyl methacrylate)-block-poly(ethylene oxide)-block-poly(2-(dimethylamino) ethyl methacrylate) triblock copolymer (PDMAEMA-co-PEO-co-PDMAEMA). At low SKL concentrations, the SKL/polymer (PDMAEMA and PDMAEMA-co-PEO-co-PDMAEMA) aqueous solutions exhibited pH-dependent aggregation arising from the formation of strong intermolecular hydrogen bonds. Decreasing the SKL/polymer weight ratio resulted in the pH-reversible soluble-insoluble (S-I) transition to become a soluble-insoluble-soluble (S-I-S) transition, which upon increasing the SKL concentration resulted in hydrogel formation. Under neutral conditions relatively strong hydrogels were formed, which upon either increasing or decreasing solution pH resulted in the hydrogels collapsing to liquid solutions, but were readily reformed upon neutralization. The effects of polymer structure, concentration, and intermolecular interactions on solution behavior and gelation are thoroughly discussed.  相似文献   
4.
In this work, hollow manganese dioxide/gold nanoparticle (MnO2/GNPs) hybrid drug nanocarriers were prepared by coupling the gold nanoparticles (GNPs) with hollow structure manganese dioxide (MnO2). Among them, GNPs have been used as near-infrared (NIR)-responsive element for photothermal effect under NIR laser irradiation. The glutathione (GSH)-responsive and pH-responsive performances of drug release were derived from hollow MnO2. Particularly, Doxorubicin hydrochloride (DOX) can be loaded into hollow MnO2/GNPs with the drug loading efficiency up to 82.0%. Moreover, the photothermal effect and GSH-/pH-responsive properties of hollow MnO2/GNPs were investigated. The hollow MnO2/GNPs possessed satisfactory drug release efficiency (ca. 87.4% of loaded drug released in 12 h) and have high photothermal conversion efficiency, multiresponsive properties, and degradability. Finally, the kinetics of drug release was discussed in detail. Thus, our finding highlights that the multiresponsive nanocarriers are of great potential in the field of drug controlled release.  相似文献   
5.
A multiresponsive system that consists on pH-responsive polymer microspheres with encapsulated iron oxide magnetic nanoparticles that rendered the core magnetic to enable externally controlled actuation under magnetic induction has been developed. The inorganic nanoparticles were first prepared and, then, further encapsulated in a pH-sensitive poly(4-vinylpyridine). These spheres have been obtained by a modification of the simple, rapid and high-reproducible nanoprecipitation method. Magnetic measurements showed that the iron oxide nanoparticles are superparamagnetic and, therefore, able to undergo a local increase of the temperature when an oscillating magnetic field is applied. Magnetically triggered heating and pH sensitivity can be useful for biomedical applications.  相似文献   
6.
A simple strategy for generating stimuli-responsive peptide-based hydrogels via charge-conversion of a self-assembling peptide (SAP) is described. These materials are formulated as soluble, polyanionic peptides, containing maleic acid, citraconic acid, or dimethylmaleic acid amide masking groups on each lysine residue, which do not form assemblies, but instead flow easily through high gauge needles and catheters. Acid-induced mask hydrolysis renews the zwitterionic nature of the peptides with concomitant and rapid self-assembly via β-sheet formation into rehealable hydrogels. The use of different masks enables one to tune pH responsiveness and assembly kinetics. In anticipation of their potential for in vivo hydrogel delivery and use, progelators exhibit hemocompatibility in whole human blood, and their peptide components are shown to be noncytotoxic. Finally, demonstration of stimuli-induced self-assembly for dye sequestration suggests a simple, non-covalent strategy for small molecule encapsulation in a degradable scaffold. In summary, this simple, scalable masking strategy allows for preparation of responsive, dynamic self-assembling biomaterials. This work sets the stage for implementing biodegradable therapeutic hydrogels that assemble in response to physiological, disease-relevant states of acidosis.  相似文献   
7.
Silica nanoparticles (SiO2) were grafted with the precursor random copolymer of 1′-(2-acryloxyethyl)-3′,3′-dimethyl-6-nitrospiro-(2H-1-benzopyran-2,2′-indoline) (SPMA) and tert-butyl methacrylate (tBMA) by surface-initiated atom transfer radical polymerization (SI-ATRP), and SiO2-g-P(SPMA-co-methacrylic acid (MAA)) was obtained via chemical hydrolysis of the resulting precursor random copolymer in acidic conditions. From transmission electron microscopy, we observed the spherical morphology of monodispersed silica nanoparticles and core-shell structure of SiO2-g-P(SPMA-co-MAA). Energy dispersive spectroscopy, Fourier transform infrared spectra, X-ray photoelectron spectroscopy, and the thermogravimetric analysis indicated that the polymer had been successfully grafted onto the surface of silica nanoparticles. The dual-responsive properties were characterized by means of ultraviolet-visible spectrophotometer and dynamic light scattering. The average hydrodynamic diameter of SiO2-g-P(SPMA-co-MAA) increased from 185.7 to 212.7 nm under ultraviolet light irradiation for 5 min. Also, the particle size of SiO2-g-P(SPMA-co-MAA) increased with the rising pH value of surrounding condition.  相似文献   
8.
We report on the fabrication of polyelectrolyte multilayer-coated hollow silicon dioxide micropillars as pH-responsive drug delivery systems. Silicon dioxide micropillars are based on macroporous silicon formed by electrochemical etching. Due to their hollow core capable of being loaded with chemically active agents, silicon dioxide micropillars provide additional function such as drug delivery system. The polyelectrolyte multilayer was assembled by the layer-by-layer technique based on the alternative deposition of cationic and anionic polyelectrolytes. The polyelectrolyte pair poly(allylamine hydrochloride) and sodium poly(styrene sulfonate) exhibited pH-responsive properties for the loading and release of a positively charged drug doxorubicin. The drug release rate was observed to be higher at pH 5.2 compared to that at pH 7.4. Furthermore, we assessed the effect of the number of polyelectrolyte bilayers on the drug release loading and release rate. Thus, this hybrid composite could be potentially applicable as a pH-controlled system for localized drug release.  相似文献   
9.
A novel 4-arm poly(ethylene glycol)-b-poly(disulfide histamine) copolymer was synthesized by Michael addition reaction of poly(ethylene glycol) (PEG) vinyl sulfone and amine-capped poly(disulfide histamine) oligomer, being denoted as 4-arm PEG-SSPHIS. This copolymer was able to condense DNA into nanoscale polyplexes (<200 nm in average diameter) with almost neutral surface charge (+(5–10) mV). Besides, these polyplexes were colloidal stable within 4 h in HEPES buffer saline at pH 7.4 (physiological environment), but rapidly dissociated to liberate DNA in the presence of 10 mM glutathione (intracellular reducing environment). The polyplexes also revealed pH-responsive surface charges which markedly increased with reducing pH values from 7.4–6.3 (tumor microenvironment). In vitro transfection experiments showed that polyplexes of 4-arm PEG-SSPHIS were capable of exerting enhanced transfection efficacy in MCF-7 and HepG2 cancer cells under acidic conditions (pH 6.3–7.0). Moreover, intravenous administration of the polyplexes to nude mice bearing HepG2-tumor yielded high transgene expression largely in tumor rather other normal organs. Importantly, this copolymer and its polyplexes had low cytotoxicity against the cells in vitro and caused no death of the mice. The results of this study indicate that 4-arm PEG-SSPHIS has high potential as a dual responsive gene delivery vector for cancer gene therapy.  相似文献   
10.
The purpose of this study was to prepare modified-release dosage of indomethacin (IND) in the form of micromatrices based on a superabsorbent hydrogel (SAH), poly(acrylic acid), partly sodium salt-g-poly(ethylene oxide) (PAAc-Na-g-PEO). A soaking procedure was used for the preparation of drug-loaded hydrogel micromatrices. The amount of IND, volume of drug-loading solution, and amount of PAAc-Na-g-PEO granules used for preparing micromatrices were the independent factors. The dependent factors were the measured responses from micromatrices, that is, percent recovery, percent entrapment efficiency, and the time at which 63.2% of the drug was released (Td, minutes). A three-factor, three-level full factorial design (33) was created to optimize formulations. Nonlinear regression analysis indicated a good correlation between the measured responses and the independent factors. Optimum responses were obtained from medium levels of IND and SAH and low level of drug-loading solution. Differential scanning calorimetry, X-ray diffraction analysis, and scanning electron micrography indicated that IND crystals are physically adsorbed into the pores and irregular spaces of the hydrogel.  相似文献   
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