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JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY · 2025 · IF 14.3

Tunable pH-responsive HMSNs-g-PDEAEMA as integrated corrosion inhibition and emulsification multi-functional nanocontainer

Huiling Su,Zhikun Wang,Jianqiang Zhang,Nannan Cui,Fengting Li,Miantuo Li,Wentao Qu,Xupeng Li,Jiaqi Feng,Songqing Hu

Responsive nanocontainers have dual functions in targeted delivery of corrosion inhibitors and emulsion development of shale oil in oil and gas fields, exhibiting potential for simultaneously achieving metal protection and efficient oil and gas development from a material perspective. Here, we propose the preparation of a pH-responsive nanocontainer, HMSNs- g -PDEAEMA (poly [2-(N, N-diethyl amino)-ethyl-methacrylate] (PDEAEMA) grafted onto hollow mesoporous spherical silica (HMSNs)), to integrate the delivery of 2-mercaptobenzothiazole (MBT)) for targeted corrosion inhibition and the emulsification of oil as Pickering emulsifiers. Under acidic conditions (reduced pH value caused by localized corrosion or high concentration acidic gases), PDEAEMA chains are protonated and extended by electrostatic repulsion, exposing pores on HMSNs surface and allowing the controlled release of loaded MBT molecules. Once transforming into a neutral or alkaline environment, the responsive release of the MBT process is inhibited. After the fluid passes through the wellbore and enters the shale layer, the HMSNs- g -PDEAEMA nanocontainers act as Pickering emulsifiers to achieve emulsification. The emulsified oil can be extracted onto the ground more efficiently, and a following pH-responsive demulsification process can be achieved. Overall, through a pH-responsive nanocontainer material, the dual function of corrosion inhibition and emulsification in oil and gas development is possible to be simultaneously achieved.

研究领域: 材料科学 · 化学工程
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CHEMICAL ENGINEERING JOURNAL · 2025 · IF 13.2

Tailoring of a specific pH-induced self-enhanced photothermal cellulose hydrogel for antibiotic-resistant bacteria-infected wound treatment

Rimei Chen,Yonghui He,Lingli Tian,Yu Meng,Zhiping Chen,Nianfang Ma,Chunfang Wang,Hui He

Implementing differentiated photothermal temperatures in the infected area of the wound and adjacent normal tissue areas can achieve photothermal antibacterial effects while protecting adjacent healthy tissues from potential overheating damage associated with photothermal therapy. Here, a specific pH-induced photothermal temperature self-enhancing cellulose hydrogel was tailored using photothermal-responsive cellulose nanocrystals modified with polyaniline and pH-responsive cellulose nanocrystals loaded with taurine as the staggered network skeletons. The hydrogel possesses exceptional in-situ adaptability and tissue adhesion characteristics, enabling it to adhere to the irregular wound bed. Interestingly, polyaniline on cellulose nanocrystals can be converted from the form of adamantane base to the form of adamantane salt under acidic conditions, exhibiting enhanced photothermal effects. Consequently, the specific acidic microenvironment (pH 5.5–6.8) of infected wounds can elevate the photothermal temperature of hydrogel to 45–48 °C, significantly higher than that (42 °C) of adjacent healthy tissue with pH values of 6.8–7.4. Similarly, taurine grafted onto cellulose nanocrystals via dynamic imine bonding gets gradually released from the hydrogel into infected wounds under specific acidic conditions, thus providing an anti-inflammatory effect. This differential temperature regulation on the infected wound achieves effective photothermal antibacterial treatment while preventing overheating damage to normal tissue.

CAS / MDL: 25233-30-1 2564-83-2
研究领域: 生物材料学 · 医学工程 · 药剂学
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INDUSTRIAL CROPS AND PRODUCTS · 2021 · IF 5.645

Preparation of magnesium, nitrogen-codoped carbon quantum dots from lignin with bright green fluorescence and sensitive pH response

Xiaoxu Yang,Shiyao Hou,Tingting Chu,Jiazhi Han,Runsen Li,Yanzhu Guo,Yumei Gong,Haiming Li,Zhiwei Wan

Eco-friendly, renewable and green biomass materials are considered as the superior carbon precursors for producing carbon quantum dots (CQDs) in large scale. A major challenge is the limited contents of fluorophores in biomass, which then results in low quantum yields (QYs) and inferior fluorescence emission ability of the obtained CQDs. Herein, lignin with amounts of unsaturated aromatic and carbonyl fluorophores was employed as the carbon precursors to prepare CQDs through a green, facile approach. The magnesium and nitrogen elements were successfully introduced into CQDs with the aim of enhancing their QYs and extending their emission wavelengths. The prepared magnesium, nitrogen-doped CQDs (Mg, N-CQDs) could emit green fluorescence with a quantum yield (QYs) up to 46.38 %. The mechanism of their fluorescence ability was discussed extensively. More interestingly, the Mg, N-CQDs displayed a fluorescence transition between green and yellow color at pH value of 5.4, indicating their potential application as a probe to detect pH values of complicated environments. The findings in this paper would provide a viable strategy to converse lignin biomass waste into high-quality fluorescence nanomaterials.

研究领域: 材料科学 · 环境科学
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BIOMATERIALS · 2011 · IF 7.883

pH-responsive drug delivery system based on luminescent CaF2:Ce3+/Tb3+-poly(acrylic acid) hybrid microspheres

Yunlu Dai,Cuimiao Zhang,Ziyong Cheng,Ping’an Ma,Chunxia Li,Xiaojiao Kang,Dongmei Yang,Jun Lin

In this study, we design a controlled release system based on CaF 2 :Ce 3+ /Tb 3+ -poly(acrylic acid) (PAA) composite microspheres , which were fabricated by filling the pH-responsive PAA inside CaF 2 :Ce 3+ /Tb 3+ hollow spheres via photopolymerization route. The CaF 2 :Ce 3+ /Tb 3+ hollow spheres prepared by hydrothermal route possess mesoporous structure and show strong green fluorescence from Tb 3+ under UV excitation. Doxorubicin hydrochloride (DOX), a widely used anti-cancer drug, was used as a model drug to evaluate the loading and controlled release behaviors of the composite microspheres due to the good biocompatibility of the samples using MTT assay . The composite carriers provide a strongly pH-dependent drug release behavior owing to the intrinsic property of PAA and its interactions with DOX. The endocytosis process of drug-loaded microspheres was observed using confocal laser scanning microscopy (CLSM) and the in vitro cytotoxic effect against SKOV3 ovarian cancer cells of the DOX-loaded carriers was investigated. In addition, the extent of drug release could be monitored by the altering of photoluminescence (PL) intensity of CaF 2 :Ce 3+ /Tb 3+ . Considering the good biocompatibility, high drug loading content and pH-dependent drug release of the materials, these hybrid luminescent microspheres have potential applications in drug controlled release and disease therapy.

研究领域: 生物材料学 · 药理学 · 肿瘤学
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ACS Sustainable Chemistry & Engineering · 2016 · IF 5.267

One-Pot Assembly of Microfibrillated Cellulose Reinforced PVA–Borax Hydrogels with Self-Healing and pH-Responsive Properties

Beili Lu,Fengcai Lin,Xin Jiang,Jiajia Cheng,Qilin Lu,Jianbin Song,Chong Chen,Biao Huang

A facile, environmentally benign approach has been developed for the preparation of dynamic, multiresponsive, and self-healing hydrogels from inexpensive bamboo pulp, poly(vinyl alcohol) (PVA), and borax. The microfibrillated cellulose (MFC) reinforced PVA–borax hydrogels were produced through a one-pot route in conjunction with ball milling and physical blending in tandem in aqueous medium. In this way, MFC particles could be efficiently generated and well-dispersed in a polymer matrix, and they have been verified by scanning electron microscopy. The rheology analysis indicated a close relationship between the mechanical strength and the MFC loading and ball milling time. Due to the dynamic equilibrium of the didiol–borax linkages and the reinforcement of MFC fibers, the hydrogels showed enhanced self-healing behavior and mechanical stiffness, which was also supported by rheology analyses. In addition, the hydrogels were found to be sensitive to the pH value. The hydrogels present a solvent or gel state with the change of pH value, and this sol–gel transfer can be repeated while maintaining the shape, further demonstrating the dynamic reversible behavior of the hydrogels.

CAS / MDL: 1303-96-4
研究领域: 材料科学 · 生物材料
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Scientific Reports · 2017 ·Vol. 7 ·期 1 ·1-10 · IF 4.259

A smart thermo- and pH-responsive microfiltration membrane based on three-dimensional inverse colloidal crystals

Yu Bing,Song Qianqian,Cong Hailin,Xu Xiaodan,Han Dongwei,Geng Zhongmin,Zhang Xiaoyan,Usman Muhammad

In this paper, a thermo- and pH-responsive microfiltration membrane was prepared based on three-dimensional (3D) inverse colloidal crystals (ICC). To manufacture the smart ICC membrane, the typical thermo-responsive N-isopropylacrylamide (NIPAM) and pH-responsive methacrylic acid (MAA) were polymerized inside silica colloidal crystals. The smart ICC membranes were characterized by SEM, IR and contact angle measurements. Moreover, the permeability of smart microfiltration membrane was carried out by the KCl diffusion tests. The result showed that effective diameter of the polymer ICC membrane can be reversible tuned by temperature and pH. Besides, the functional ICC membrane showed outstanding temperature- and pH-responsive gating property, which was applied to separate particles of different sizes. The savvy environment-responsive gating membranes have potential uses in filtration, separation, purification, sensor and other applications.

研究领域: 材料科学 · 化学工程
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Biomaterials Science · 2019 ·Vol. 7 ·期 4 ·1643-1651 · IF 5.251

pH-Responsive polymeric nanocarriers for efficient killing of cariogenic bacteria in biofilms

Zhouxiang Zhao,Chunmei Ding,Yaqin Wang,Hong Tan,Jianshu Li

Traditional antibacterial treatments, such as chlorhexidine (CHX), destroy cariogenic biofilms. However, they exert negative effects in clinical applications, for example, teeth staining, taste disturbance and harm to oral tissue after a long-term exposure. Therefore, biocompatible strategies for efficient antibacterial drug delivery are in high demand. In this study, aimed at dental caries therapy enhancement, we designed a pH-responsive nanocarrier system, capable of releasing CHX in an acidic environment within cariogenic biofilms. Cationic poly(ethylene glycol)-block-poly(2-(((2-aminoethyl)carbamoyl)oxy)ethyl methacrylate) (PEG-b-PAECOEMA) was synthesized first. Modification of PAECOEMA by citraconic anhydride (CA) forms negatively charged PEG-b-PAECOEMA/CA, which could assemble into core–shell polyionic complex micelles (PICMs) when mixed with cationic CHX via electrostatic interactions. PICMs are stable in healthy neutral oral microenvironments with CHX encapsulated in the core and PEG shell exposed. Once in acidic milieu within caries-producing biofilms, they rapidly disassemble and release CHX cargo owing to degradation of citraconic amide groups. Molecular structures of the above copolymers were confirmed using 1H NMR and gel permeation chromatography (GPC) analysis. The pH-dependent degradation rates of citraconic amide in PEG-b-PAECOEMA/CA copolymer were measured by fluorescamine method. Atomic force microscopy (AFM) studies confirmed successful assembly of well-defined spherical PICMs in aqueous solution. The disassembly of PICMs in acidic microenvironment was observed using dynamic light scattering (DLS). PICMs showed an obvious pH-dependent drug release profile when the pH changed from 7.4 to 5.5. More importantly, the micellar system could reduce drug toxicity of CHX and exhibited outstanding antibacterial capability in the biofilm of Streptococcus mutans. Micelles constructed from pH-sensitive PEG-b-PAECOEMA/CA are highly promising for dental caries therapy and provide guidelines for drug-delivery system design in other acidic pathologic systems.

CAS / MDL: 38183-12-9 121-44-8
研究领域: 牙科学 · 材料科学 · 药剂学
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APPLIED SURFACE SCIENCE · 2020 · IF 6.182

Exploration of pH-responsive carbon dots for detecting nitrite and ascorbic acid

Lanlan Gan,Qian Su,Zhangbao Chen,Xiaoming Yang

Detections of carcinogen and vitamins are generally recognized to be meaningful, especially for nitrites (NO 2 − ) and ascorbic acid (AA). Here blue-fluorescence carbon dots (CDs) with the quantum yield of 11.83% were successfully synthesized by using folic acid and nicotinic acid, and their surfaces were identified to be abundant in the functional groups of amide, carboxyl and hydroxyl. Importantly, the amide on the surfaces of CDs showed the interactions with the nitrites and formed the complex, thus resulting in their quenched fluorescence. To be specific, the fluorescence intensity of CDs proportionally decreased by adding the increased amounts of NO 2 − from 8 to 800 μM, and achieved the detection of NO 2 − at a detection limit of 21.2 µM. Moreover, further introducing ascorbic acid could prevent CDs with NO 2 − to form the complex and recover their fluorescence, and thus providing the new avenue of assaying AA with the generally favorable linear range of 0.1–800 μM, while its related detection limit was 50 µM. In addition, the synthesized CDs exhibited the satisfactory sensitivity toward different pH values, demonstrating their potential of sensing pH. Consequently, the proposed CDs here may provide a new way of monitoring NO 2 − and AA in the target samples.

研究领域: 分析化学 · 生物医学
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Journal of Materials Chemistry C · 2020 ·Vol. 8 ·期 33 ·11563-11571 · IF 7.059

pH-Responsive carbon dots with red emission for real-time and visual detection of amines

Xiaoqin Zhang,Chongyuan Chen,Dongping Peng,Yizi Zhou,Jianle Zhuang,Xuejie Zhang,Bingfu Lei,Yingliang Liu,Chaofan Hu

Biogenic amines (BAs) from rotten food cause serious harm to sensitive people. Therefore, the development of a smart label that can intuitively monitor the degree of food decay in real-time is of great significance in food safety. Herein, we report the synthesis of pH-responsive carbon dots with red emission (R-CDs) by the solvothermal treatment of citric acid and urea. The fluorescence intensity of R-CDs gradually increased as the pH of the solution increased from 1 to 12. We studied the mechanisms of pH response and found that H-aggregation occurred when R-CDs were in acidic solution and caused quenching; when they were distributed in alkaline solution, the Fermi level shift caused reduced self-absorption and enhanced red fluorescence emission. The intense red emission of R-CDs is beneficial for the visual detection of alkaline organic amines and BAs derived from rotten shrimp to achieve food safety detection. Moreover, the R-CDs can be used as a promising pH-sensitive fluorescent ink, which has broad prospects and significance in anticounterfeiting and information encryption.

CAS / MDL: 77-92-9 5949-29-1
研究领域: 食品科学 · 化学 · 材料科学
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Wood Material Science & Engineering · 2024 · IF 2.2

Optimizing the boron-loaded pH/temperature dual responsive polymer for controlled release of boron from wood

Li Jin,Xin Ren,Fei Wang,Zhiwei Fan,Shuaibo Han,Yan Zhang,Hui Wang,Xinxing Wu,Fangli Sun

Disodium octoborate tetrahydrate (DOT) is a well-received and eco-friendly preservative. However, it is prone to leaching from wood in humid conditions or rainy seasons, causing problems such as decreased efficiency in resisting fungi and poor surface performance in surface finishing. To obtain enhanced leaching resistance and simultaneously achieve controlled release of DOT, a pH and temperature dual responsive poly (2-hydroxyethyl methacrylate/2-(Dimethylamino) ethyl methacrylate) (PDH) was prepared and optimized for in situ construction of DOT-loaded PDH (PDHD) in wood. Results showed that PDH displayed obvious pH and temperature-responsive swelling, and when loaded with DOT, the PDHD consequently released DOT in a pH and temperature-responsive way. Fourier transform infrared spectroscopy, Solid-13C NMR analysis and Dynamic mechanical analysis confirmed the copolymerization of 2-Hydroxyethyl methacrylate (HEMA) and 2-(Dimethylamino) ethyl methacrylate (DMAEMA), as well as the presence of crosslinked structure formed from hydrogen bond between the hydroxyl group of HEMA and the N,N-dimethylamino groups of DMAEMA. After that, the PDHD was in situ constructed in wood for controlled release of boron. During the water leaching test, the modified wood exhibited a boron fixation rate of 49.05% compared with 0.72% of the neat DOT-treated wood. Besides, it presented controlled release activity in response to pH and temperature. This work provides new approaches to the fixation of boron preservatives and notably realizes responsive releasing of boron compounds for long-term wood preservation.

CAS / MDL: 110-26-9 7727-21-1
研究领域: 材料科学 · 林学
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MOLECULES · 2024 ·Vol. 29 ·期 22 ·5330 · IF 4.2

pH-Responsive Metal–Organic Framework for Targeted Delivery of Fungicide, Release Behavior, and Sustainable Plant Protection

Shuzhen Yang,Fulin Lü,Li Wang,Sinan Liu,Zhisai Wu,Yanqin Cheng,Fan Liu

A smart and environmentally friendly pesticide system was developed that could respond to environmental stimuli while mitigating environmental risks. In this study, thiabendazole (Thi), an effective fungicide, was loaded onto zeolitic imidazolate framework-8 (ZIF-8) using the impregnation method to fabricate a pH-responsive nano hybrid delivery system (Thi@ZIF-8). The results demonstrated that Thi@ZIF-8 had a rhombic dodecahedral morphology and a loading capacity of approximately 25%. Notably, the amount of Thi released from Thi@ZIF-8 at a pH of 5.0 reached 79.54%, which was higher than that at pH 7.0 and 9.0, for 251 h. Such pH-responsive release characteristics of Thi@ZIF-8 were probably related to the pH-dependent structure stability of ZIF-8. The release mechanism of Thi@ZIF-8 conformed to non-Fickian diffusion. Additionally, Thi@ZIF-8 showed a higher control efficacy againstB. cinereacompared with Thi alone. Importantly, the ZIF-8 carrier could effectively reduce the leaching loss of Thi in soil and showed no negative effects on the three varieties of tomato seedlings, implying good biocompatibility. This work provides a novel and eco-friendly approach to control B. cinerea effectively that has great potential in modern sustainable agriculture.

研究领域: 农业科学 · 材料科学 · 环境科学
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JOURNAL OF SEPARATION SCIENCE · 2025 ·Vol. 48 ·期 1 ·e70082 · IF 2.8

Switchable Deep Eutectic Solvents for the Green Extraction of Tea Saponins From Camellia Oleifera Seed Meal

Bincheng Gong,Lingqi Shen,Yu Wang,Zuguang Li,Guohua Zhu

Tea saponin has garnered tremendous interest for its potential use in surfactant and drug synthesis. This research was designed to develop a technique based on pH-responsive switchable deep eutectic solvents (SDESs) for extracting tea saponins from Camellia oleifera seed meal. SDES synthesized from hexanoic acid and triethanolamine (1:1 molar ratio) offered the optimum extractive performance and the optimal conditions were obtained through single-factor experiments: 30 wt% water content in SDES, solid-liquid ratio of 1:30 g/mL, 60°C extraction temperature, 30 min extraction time, and acid volume of 1500 µL. The extraction yield was 162.14 mg/g after optimization, which increased by 15.65% and 9.47% compared to water and ethanol extraction methods, respectively. After pH adjustment, 98.95% of the tea saponins were recovered in the bottom phase. After precipitation and freeze-drying procedures, the purity of the tea saponin solid was 62.9%.

研究领域: 食品科学 · 环境科学 · 植物化学
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