SN Applied Sciences
·
2020
·Vol. 2
·期 5
·1-8
·
IF 0
Gong Sheng,He Tianhao,Huang Qizhang,Shu Xugang,Zhou Xinhua
A thermo-responsive polymer, poly(N-isopropylacrylamide) (PNIPAM), was anchored on the surface of low-cost natural clay nanorods, attapulgite (ATP), through the interactions including hydrogen bonding and coordination. Premixing the monomers of NIPAM with ATP before polymerization caused that the obtained PNIPAM could distribute among the pore voids of ATP and function as a surface affinity conditioner in response to temperature change. The PNIPAM/ATP composite was then applied in temperature-triggered adsorption and desorption of a hydrophobic drug (typically, an agricultural pesticide: acetamiprid). The results indicated a satisfactory adsorption capacity and reusability with the strong combination of PNIPAM and ATP. Furthermore, the adsorption mechanism was discussed, and the Sips model was employed to explain the adsorption behavior. It was proved to be beneficial for hydrophobic drug loading as well as its delivery, which may also have a potential to extend to other natural products and responsive polymers.
研究领域:
材料科学
·
药物递送
·
高分子化学
✓ 已验证
DOI
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
·
2022
·
IF 4.326
Manting Wang,Rongrong Fan,Jian Zhang,Lingyan Li,Jie-Xin Wang,Yuan Le
Poly(N-isopropylacrylamide) (PNIPAM) microgels have a number of potential biomedical applications, especially being considered as next-generation drug delivery systems. So far, nm-sized PNIPAM microgels have been commonly prepared in lab-scale experiments. In this work, nm-size controllable and monodisperse PNIPAM-based microgels were synthesized for the first time by surfactant-free precipitation polymerization using a high-gravity rotating packed bed reactor (RPB). The microgel size could be synergistically controlled by adjusting the amount of cross-linker and initiator in an RPB. Compared with the conventional stirred tank reactor, the RPB synthesis procedure could obtain a higher yield within 2 h of the reaction time. The higee level exhibited significant influence on the microgel size. Depending on the variation of the higee level, the particle size was tailored from 129 to 325 nm, and the hydrodynamic diameter was tailored from 217.7 to 805.4 nm without the usage of surfactants. In addition, different comonomers were introduced to regulate the lower critical solution temperature (LCST), achieve multiresponsiveness, and control microgel size. The in vitro DOX-loaded release demonstrated that PNIPAM-based microgels dramatically contributed to the sustained release of drugs.
研究领域:
材料科学
·
化学工程
·
药学
·
生物医学工程
✓ 已验证
DOI
高影响因子
RARE METALS
·
2026
·Vol. 45
·期 5
·e70300
·
IF 12.1
Hui Liu,Hongli Jia,Xiaojin Yan,Rouling Chen,Yingying Wang,Kun Chen
en This link goes to a English section zh This link goes to a Chinese section Thermo-responsive hydrogels based on poly(N-isopropylacrylamide) (PNIPAM) are promising candidates for soft actuation, yet their practical applications are often constrained by sluggish thermo-responsive kinetics and insufficient mechanical robustness. Herein, phosphotungstic acid (PTA), a tungsten-containing polyoxometalate, was incorporated to regulate the phase transition behavior and modulate a PNIPAM/P(AA- co -AM) bilayer hydrogel, in which the thermo-responsive PNIPAM layer serves as the actuator whereas the non-thermo-responsive P(AA- co -AM) layer provides mechanical support. By increasing the PTA content up to 4 wt%, the thermally induced deformation time of the PNIPAM layer was prolonged from 30 to 120 s, whereas the recovery time at low temperature was shortened from 120 to 60 min, thereby enabling programmable thermo-responsive kinetics. The thermal transition of the PTA-PNIPAM layer was effectively regulated by PTA, with the lower critical solution temperature (LCST) gradually increasing and tunable up to 42°C, accompanied by an improved thermal stability manifested by reduced mass loss at 150°C. Mechanical characterization demonstrated that the P(AA- co -AM) layer modulated the tensile properties of hydrogel networks, and the bilayer configuration significantly outperformed the pristine PNIPAM hydrogel. Benefiting from the synergistic effects of kinetic regulation and mechanical modulation, the bilayer hydrogel further exhibited multi-substrate adhesion and reversible deformation, enabling an underwater gripping demonstration. This work highlights a polyoxometalate-enabled strategy for simultaneously controlling thermo-responsive kinetics and toughening PNIPAM-based hydrogels, thereby advancing functional soft materials for actuation-related applications. 摘要 en This link goes to a English section zh This link goes to a Chinese section 聚(N-异丙基丙烯酰胺)(PNIPAM)的温敏水凝胶是软体动力领域的有力候选材料,但其迟缓的热响应动力学和有限的机械鲁棒性往往限制了其实际应用。在此,我们在PNIPAM/P(AA- co -AM)双层水凝胶中引入了磷钨酸(PTA),以调控其相变行为并增强材料性能。在该双层结构中,温敏性PNIPAM层作为动力层,而非温敏性P(AA- co -AM)层则提供机械支撑。通过将PTA的含量提高至4 wt%,PNIPAM层的热诱导变形时间从30秒延长至120秒,而在低温下的恢复时间则从120分钟缩短至60分钟,从而实现了可编程的热响应动力学。PTA有效调控了PTA-PNIPAM层的热转变行为,使其低临界溶解温度(LCST)逐渐升高且最高可调至42°C。同时,材料的热稳定性也得到提升,150°C时的质量损失明显减少。力学表征表明,P(AA- co -AM)层调节了水凝胶网络的拉伸性能,且该双层结构的性能显著优于原始PNIPAM水凝胶。得益于动力学调控与机械增韧的协同效应,该双层水凝胶进一步展现出多基底黏附性和可逆变形能力,并成功实现了水下抓取演示。本工作提出了一种基于多金属氧酸盐的水凝胶改性策略,可同时控制PNIPAM基水凝胶的热响应动力学并增强其韧性,从而推动了功能性软材料在相关应用中的发展。
✓ 已验证
DOI
高影响因子
COLLOIDS AND SURFACES B-BIOINTERFACES
·
2026
·
IF 5.9
Hailiang Pei,Tao Xu,Yu Cao,Zhimei Wang,Sidi Zhao,Jiapu Wang,Xuan Wang,Longfei Wang,Ziwei Liang,Di Huang
Chitosan anchors the PNIPAM/Alg/GO/TH double-network hydrogel to wet wound tissue. • NIR-driven LCST transition contracts the hydrogel, pulling wound edges together mechanically. • Photothermal effect triggers on-demand tetracycline release, killing 98.5% S. aureus and 99.25% E. coli. • In infected diabetic mice, the hydrogel reduces inflammation, promotes angiogenesis, and achieves 94.75% closure by day 10. Diabetic wound healing is severely impaired by four core pathological barriers—persistent hyperglycemia, excessive inflammation, bacterial infection, and deficient wound contraction. Herein, we developed a near-infrared (NIR)-responsive antibacterial hydrogel composed of poly(N-isopropylacrylamide), sodium alginate, graphene oxide, and tetracycline hydrochloride (PNIPAM/Alg/GO/TH), in which chitosan serves as an interfacial bridging component that covalently and electrostatically anchors the hydrogel to tissue rather than acting as a bulk matrix constituent. As a natural polysaccharide, sodium alginate serves as the essential hydrogel matrix, endowing the system with high water retention, biocompatibility, and a porous network favorable for exudate absorption and tissue regeneration, while also forming a mechanically robust double-network structure with PNIPAM. Through chitosan-mediated interfacial bioadhesion, the hydrogel firmly adheres to wound tissues, enabling transfer of the contraction force to the wound edges. Under NIR irradiation, the hydrogel exhibited potent broad-spectrum antibacterial activity, with bactericidal rates of 98.5 ± 0.53% against Staphylococcus aureus and 99.25 ± 0.75% against Escherichia coli. Meanwhile, NIR stimulation induced a phase transition and active mechanical contraction, promoting centripetal wound closure, while the photothermal effect triggered sustained tetracycline release for prolonged antimicrobial protection. In vivo, in a Staphylococcus aureus-infected diabetic mouse wound model, the hydrogel significantly downregulated inflammatory markers and promoted neovascularization and collagen deposition, achieving a wound healing rate of 94.75 ± 2.09% on day 10. This study presents a sodium alginate-based interfacial hydrogel strategy that integrates interfacial adhesion, active mechanical contraction, and on-demand drug delivery for rapid diabetic wound healing.
✓ 已验证
DOI
高影响因子
AICHE JOURNAL
·
2014
·Vol. 61
·期 1
·35-45
·
IF 2.581
Feng Xu,Jing-Wen Xu,Bi-Xia Zhang,Luo Yan-Ling
Novel tri-armed star polystyrene-block-poly(N-isopropylacrylamide) block copolymers with trimesic acid as central molecules were synthesized by successive two-step atom transfer radical polymerization, and confirmed by Fourier-transform infrared spectra, 1 H nuclear magnetic resonance, and laser light scattering gel chromatography system. The copolymers could self-assemble into spherical core-shell micelles in aqueous media independent on drug loading. Physicochemical properties of the blank and drug-loaded micelles were examined by surface tension, fluorescence spectroscopy, UV-vis, transmission electron microscope, and dynamic light scattering measurements. The copolymer micelles exhibited thermo-triggered phase transition, with low critical solution temperature of 33.7 and 34.6°C, varying with copolymer compositions. The critical aggregate concentrations were 11.62 and 47.61 mg L −1 , and hydrodynamic diameters from 200 to 220 nm. Water-insoluble 10-hydroxycamptothecine was encapsulated into the micelle aggregates to investigate the change in the resulting physicochemical parameters, thermo-triggered in vitro drug release, and the applicability as drug targeting release carriers. MTT assays were carried out to uncover cytotoxicity of the newly developed micelle-based drug formulations. © 2014 American Institute of Chemical Engineers AIChE J , 61: 35–45, 2015
研究领域:
材料科学
·
药学
·
肿瘤学
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF INORGANIC BIOCHEMISTRY
·
2020
·
IF 3.212
Na Huang,Jun Wang,Xiaoyan Cheng,Yafei Xu,Wuke Li
A luminescent and dual-stimuli-responsive nanocomposite based on mesoporous silica , poly (N-isopropylacrylamide)-chitosan and decatungstoeuropate was prepared. To fabricate the nanocomposite, the mesoporous silica nanoparticles were coated with thermo/pH dual-responsive poly (N-isopropylacrylamide)-chitosan and the luminescent decatungstoeuropate particles were grafted onto copolymers . The designed nanocarrier could show exhibit good red luminescence as well as obvious thermo/pH stimuli-responsive properties, which could be employed as a drug storage reservoir for the loading and release of anticancer drug doxorubicin (DOX). The research indicated that the releases of DOX were thermo/pH dependent and high temperatures/acidic conditions were favorable for the fast release of drug. In vitro cytotoxicity tests revealed that the drug delivery carrier displayed excellent biocompatible and the composites loaded with DOX showed significant suppression effect on HeLa cells. Luminescence spectra showed that the composite containing decatungstoeuropate displayed fine red luminescence at various temperatures and pH values, which could be utilized as a potential labeling material in field of medicine.
研究领域:
材料科学
·
生物医学工程
·
药学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF MEMBRANE SCIENCE
·
2023
·
IF 9.5
Fan Yang,Su Li,Hongyan Qi,Weibo Sun,Jinbao Li,Mei Zhang,Zheng Chen,Jinhui Pang,Zhenhua Jiang
Although poly (ether ether ketone) (PEEK) exhibits excellent solvent resistance , it could not be prepared directly by non-solvent induced phase separation (NIPS) method due to its poor solubility. Herein, PEEK porous membranes were successfully fabricated by combining NIPS and acid hydrolysis. The superhydrophilic thermo-responsive poly (N-isopropylacrylamide) (PNIPAm) polymer was in-situ grafted on the PEEK membrane surface via the UV grafting polymerization and improved the membrane interface hydrophilicity, making the membrane water contact angle changed from 89.5° to 0° at 25 °C. After heating the membrane surface to 40 °C, the membrane exhibited hydrophobicity (100°), realizing the thermo-responsiveness via switching the temperature. Furthermore, due to the transferred membrane wettability at different temperatures, PEEK-g-PNIPAm could separate different types of oil-bearing systems with high rejection above 99.0 %. What’s more, the PNIPAm layer also enhanced the membrane anti-fouling capacity. Benefiting from the extraordinary solvent resistance of the PEEK matrix, PEEK-g-PNIPAm maintains its intact morphology after 6 h immersion in various organic solvents , addressing the commonly reported problem of polymer membranes having certain solubility in solvents. The PEEK-based membranes with excellent solvent resistance could be useful in the oil-bearing separation.
研究领域:
材料科学
·
化学工程
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
·
2015
·Vol. 53
·期 16
·1872-1879
·
IF 3.113
Jianwen Tian,Dazhuang Xu,Meiying Liu,Fengjie Deng,Qing Wan,Zhen Li,Ke Wang,Xiaohui He,Xiaoyong Zhang,Yen Wei
Surface functionalization of carbon nanotubes (CNTs) with a thermo responsive polymer was achieved via combination of mussel inspired chemistry and surface initiated single electron transfer living radical polymerization (SET-LRP). In this procedure, CNTs were first coated with polydopamine (PDA) through self polymerization under a rather mild condition. And then PDA functionalized CNTs bearing with amino and hydroxyl groups were further reacted with bromo isobutyryl bromide. Finally, a thermo responsive polymer poly(N-isopropylacrylamide) (PNIPAM) was introduced on the CNTs via SET-LRP. The successful surface modification of CNT-PDA-PNIPAM was evidenced by a series of characterization techniques. The resulting CNT-PDA-PNIPAM showed significant enhancement of dispersibility in both aqueous and organic solvents. More importantly, these CNT-polymer nanocomposites showed obvious thermo responsive behavior due to the surface coating CNTs with PNIPAM. As compared with previous methods, this method is not required oxidation of CNTs to introduce funcitonal groups for immobilization of the polymerization initiators. More importantly, this method could also be utilized for fabricating many other polymer nanocomposites because of the strong and universal adhesive of PDA to various materials. It is therefore, the novel strategy via marrying mussel inspired chemistry with SET-LRP should be a simple, general and effective method for surface functionalization. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015 , 53 , 1872–1879
研究领域:
材料科学
·
聚合物化学
·
纳米技术
✓ 已验证
DOI
高影响因子
ENVIRONMENTAL TECHNOLOGY
·
2020
·
IF 2.213
Yi-xin Liu,Hui Zhong,Xiao-rong Li,Zhuan-li Bao,Zhi-peng Cheng,Yu-jie Zhang,Chun-xiang Li
In this work, attapulgite (ATP)-based dual sensitive poly (N-isopropylacrylamide-co-acrylic acid) composite hydrogel, P(NIPAM-co-AA)/ATP, was prepared by free radical polymerization. The prepared composite hydrogel was characterized via methods of scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), zeta potential analysis and Brunauer, Emmett, and Teller (BET) etc. The composite hydrogel showed pH and temperature sensitive behaviour, with lower critical solution temperature (LCST) of 35°C and highest swelling occurred at pH 8.0. The adsorption of methyl violet (MV) can be controlled by the hydrogel responsiveness, and 95.78% of MV can be removed at pH 8.0 and 35°C. The addition of a small amount of ATP (3 Wt%) can improve the swelling ratio and adsorption capacity. Kinetic analysis demonstrated that the experimental data were best fitted to the pseudo-second order model. Isotherm analysis showed that the equilibrium data followed Langmuir model with the adsorption capacity of 168.35 mg g−1. In addition, the composite hydrogel has high adsorption selectivity for cationic dyes, and MV-loaded hydrogel is easy to regenerate, which can be used for successive adsorption cycles. These results demonstrate that the composite hydrogel has potential application in dye wastewater treatment.
研究领域:
环境科学
·
材料科学
·
化学工程
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Journal of Materials Chemistry A
·
2026
·
IF 9.5
Xin Li,Xianglei Bu,Jie Huang,Ying Li,Likui Wang,Hongyan Miao,Gang Shi
Poly(N-isopropylacrylamide) (PNIPAM)-based hydrogel thermochromic smart windows exhibit advantages in near-room-temperature phase transition and strong solar modulation. However, their poor water retention performance limits the phase transition cycle stability. Here, PNIPAM microgels as thermochromic components, gelatin, poly(acrylamide-acrylic cacid) (PAM-AA) and AlCl3 were combined to form a PNIPAM/gelatin/PAM-AA/Al3+ hydrogel by copolymerization and cross-linking. This composite hydrogel was then sandwiched between two pieces of glass to form a smart window. The multiple interpenetrating polymer networks can improve the mechanical properties of the hydrogel, and the hydrophilic groups of PAM-AA and gelatin can enhance the water retention capacity of the hydrogel, ensuring the phase transition cycle stability of the smart window. The elongation at break, Young's modulus and toughness of the hydrogel reach up to 460%, 65 kPa and 0.52 MJ/m3, respectively. The smart window exhibits excellent visible light transmittance (Tlum=85.6%) and visible light modulation (ΔTlum=51.8%). During 150 phase transition cycles, the visible light modulation capability of the smart window remained highly stable. In comparison with an air sandwich window, the smart window equipped on a simulated chamber can achieve a maximum temperature reduction of ~ 7 °C in a 7-day outdoor experiment.
✓ 已验证
产品关联
DOI
高影响因子
ACS Applied Materials & Interfaces
·
2011
·
IF 2.925
Jiucun Chen,Mingzhu Liu,Chen Chen,Honghong Gong,Chunmei Gao
Covalent functionalization of azide-modified SiO2 with well-defined, alkyne-terminated poly(N-isopropylacrylamide) was accomplished by the Cu(I)-catalyzed [3 + 2] Huisgen cycloaddition. The alkyne-terminated RAFT chain transfer agent was first synthesized, and then the alkyne-terminated thermoresponsive poly(N-isopropylacrylamide) (PNIPAM) with different molecular weights were synthesized by the RAFT of NIPAM monomer. The polymerization kinetics and the evolution of number-average molecular weights (Mn), and polydispersities (Mw/Mn), with monomer conversions were investigated. A copper(I)-catalyzed azide–alkyne cycloaddition (CuAAC) “grafting to” method was used to attach thermoresponsive polymers onto the exterior surface of SiO2 nanoparticles which produced relatively high grafting density. The as-synthesized hybrid nanoparticles showed thermoresponsive behavior and were characterized by FTIR, XPS, TGA, DLS, and TEM, etc.
研究领域:
高分子化学
·
纳米材料
·
表面改性
·
智能材料
·
胶体与界面科学
✓ 已验证
DOI
高影响因子
PHARMACEUTICAL RESEARCH
·
2013
·Vol. 31
·期 2
·291-304
·
IF 4.742
Yang Xiao-Li,Luo Yan-Ling,Xu Feng,Chen Ya-Shao
Purpose Block copolymer micelles are extensively used as drug controlled release carriers, showing promising application prospects. The comb or brush copolymers are especially of great interest, whose densely-grafted side chains may be important for tuning the physicochemical properties and conformation in selective solvents, even in vitro drug release. The purpose of this work was to synthesize novel block copolymer combs via atom transfer radical polymerization, to evaluate its physicochemical features in solution, to improve drug release behavior and to enhance the bioavailablity, and to decrease cytotoxicity. Methods The physicochemical properties of the copolymer micelles were examined by modulating the composition and the molecular weights of the building blocks. A dialysis method was used to load hydrophobic camptothecin (CPT), and the CPT release and stability were detected by UV–vis spectroscopy and high-performance liquid chromatography, and the cytotoxicity was evaluated by MTT assays. Results The copolymers could self-assemble into well-defined spherical core-shell micelle aggregates in aqueous solution, and showed thermo-induced micellization behavior, and the critical micelle concentration was 2.96–27.64 mg L −1 . The micelles were narrow-size-distribution, with hydrodynamic diameters about 128–193 nm, depending on the chain length of methoxy polyethylene glycol (mPEG) blocks and poly(N-isopropylacrylamide) (PNIPAM) graft chains or/and compositional ratios of mPEG to PNIPAM. The copolymer micelles could stably and effectively load CPT but avoid toxicity and side-effects, and exhibited thermo-dependent controlled and targeted drug release behavior. Conclusions The copolymer micelles were safe, stable and effective, and could potentially be employed as CPT controlled release carriers.
研究领域:
材料科学
·
药学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）