Nano Research
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2020
·Vol. 14
·期 3
·879-886
·
IF 8.183
Zhao Shen Fei,Hu Fang Xin,Shi Zhuan Zhuan,Fu Jing Jing,Chen Yue,Dai Fang Yin,Guo Chun Xian,Li Chang Ming
It is critical for fabricating flexible biosensors with both high sensitivity and good selectivity to realize real-time monitoring superoxide anion (O 2 •− ), a specific reactive oxygen species that plays critical roles in various biological processes. This work delicately designs a Mn 3 (PO 4 ) 2 /MXene heterostructured biomimetic enzyme by assembling two-dimensional (2-D) Mn 3 (PO 4 ) 2 nanosheets with biomimetic activity and 2-D MXene nanosheets with high conductivity and abundant functional groups. The 2-D nature of the two components with strong interfacial interaction synergistically enables the heterostructure an excellent flexibility with retained 100% of the response when to reach a bending angle up to 180°, and 96% of the response after 100 bending/relaxing cycles. It is found that the surface charge state of the heterostructure promotes the adsorption of O 2 •− , while the high-energy active site improves electrochemical oxidation of O 2 •− . The Mn 3 (PO 4 ) 2 /MXene as a sensing platform towards O 2 •− achieves a high sensitivity of 64.93 µA·µM −1 ·cm −2 , a wide detection range of 5.75 nM to 25.93 µM, and a low detection limit of 1.63 nM. Finally, the flexible heterostructured sensing platform realizes real-time monitoring of O 2 •− in live cell assays, offering a promising flexible biosensor towards exploring various biological processes.
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HIGH PERFORMANCE POLYMERS
·
2020
·
IF 1.568
Hai-Hui Liu,Meng-Qi Zhang,Zi-Han Tian,Peng-Fei Liu,Yan-Xin Liu,Xing-Xiang Zhang
Freestanding poly(3,4-ethylenedioxythiophene) (PEDOT) nanowires (NWs) were synthesized using a facile, self-assembled, micellar soft-template method. Thermoelectric properties of the PEDOT NWs under different reaction conditions were measured, and optimal experimental conditions were confirmed. To obtain preferential thermoelectric performance, PEDOT NWs/graphene composite films with various graphene mass fractions were fabricated. The maximum power factor of the hybrids was observed to reach 42.0 μWm−1K−2 with 3 wt% graphene loading, corresponding to a 200% improvement compared with pure PEDOT NWs. The thermoelectric devices were investigated using the PEDOT NWs/graphene hybrids as a p-type leg and PEDOT NWs/nitrogen-doped graphene as an n-type leg. The device, in series, shows a preferable cooling effect with an approximate temperature decrease of 0.5°C after energization. Our work provides a novel means of fabricating n-type PEDOT hybrids and promotes their practical applications as thermoelectric coolers. These findings indicate a new means of developing high-performance, flexible, organic thermoelectric materials and devices.
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2020
·
IF 3.99
Yunran Zhang,Haiping Zhou,Zhe Zhang,Yijun Zhu,Tao Wang,Liguo Yu,Hongrui Song
Betulinic acid (BA) is a new class of anticancer drug , but its relatively short half-life and poor water solubility limit its therapeutic effect and clinical application. Herein, to tackle the dilemma, BA prodrugs were prepared by conjugating BA onto the polyethylene glycol (PEG) polymer via cleavable disulfide bonds. The prodrugs exhibited high water solubility (270-fold of free BA) and a relatively high drug-loading efficiency of 14.2 %. To further endow the BA prodrugs with a photothermal therapeutic effect, the near-infrared (NIR) agent Cypate was grafted on the Pluronic triblock copolymer . The different PEG polymers and different Pluronic polymers were chosen to obtain the optimal drug loading efficiency and the photothermal generation effect. The P-SS-BA/F68-Cy prodrug micelles integrate the redox-responsive BA prodrugs and the NIR-responsive amphiphilic triblock polymer into one single nanocomposite . The release of BA was less than 20 % in pH 7.4 PBS in the absence of glutathione (GSH), whereas the release of BA was obviously accelerated in pH 5.0 PBS with 10 mM GSH. In addition, the release of BA was further accelerated under the NIR irradiation. The P-SS-BA/F68-Cy micelles showed an excellent photothermal heating effect under NIR irradiation. The prepared P-SS-BA/F68-Cy micelles showed the synergistic thermochemotherapeutic effect on tumors both in vitro and in vivo . Therefore, the present study shows the great potential of dual-triggered drug delivery and thermochemotherapy for combination therapy.
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MICROCHIMICA ACTA
·
2020
·Vol. 187
·期 8
·1-11
·
IF 6.232
Qu Fei,Wang Bingjie,Li Kexin,You Jinmao,Han Wenli
The aggregates of glutathione-capped CuNCs induced by Al 3+ (named CuNCs@Al 3+ complexes) show a stable aggregation-induced emission (AIE) for about 1 month. Their fluorescence maintains a high level in the pH range 4.0 to 7.0, while it quenches as pH increases from 7.0 to 7.7 or decreases from 4.0 to 3.0. Under urease-catalyzed hydrolysis, urea produces ammonia, which can be further hydrolyzed to yield OH − . This leads to a pH increase of the immediate environment. Hence, the CuNCs@Al 3+ complexes are a suitable probe to determine urea. The fluorescence of CuNCs@Al 3+ complexes quenches linearly at 585 nm with the excitation wavelength at 340 nm when the concentration of urea increases from 20 to 150 μM. The limit of detection (LOD) of urea is 5.86 μM. This sensitivity is superior to other reported works due to the narrow pH response range of CuNCs@Al 3+ complexes. This method has been successfully applied for measuring urea in human urine samples with satisfactory recoveries.
Schematic representation of urea determination based on pH-responsive property of copper nanoclusters@Al 3+ complexes. Ammonia is produced in the hydrolysis of urea by urease, and it is further hydrolyzed to yield OH − , leading to increasing pH of the environment.
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ACS Applied Materials & Interfaces
·
2020
·
IF 8.758
Chenglong Ma,Wei Sun,Waqas Qamar Zaman,Zhenhua Zhou,Hao Zhang,Qicheng Shen,Limei Cao,Ji Yang
Research has been focused on regulating the amorphous surface of Ir-based materials to achieve a higher oxygen evolution reaction (OER) activity. The IrOx amorphous layer is generally considered to be substantial enough to break the limitation created by the conventional adsorbate evolution mechanism (AEM) in acidic media. In this work, we used lanthanides to regulate IrOx amorphization–crystallization through inhibiting the crystallization of iridium atoms in the calcination process. The chosen route created abundant crystalline–amorphous (c-a) interfaces, which greatly enhanced the charge transfer kinetics and the stability of the materials. The mass activity of iridium in the synthesized IrO2@LuIr1–nOx(OH)y structure reached 128.3 A/gIr, which is 14.6-fold that of the benchmark IrO2. All the IrO2@LnIr1–nOx(OH)y (Ln = La–Lu) structures reflected 290–300 mV of overpotential at 10 mA/cmgeo2. We demonstrate that a highly active c-a interface possesses an efficient charge transfer capability and is conducive to the stability of the activated oxygen species. The surface-activated oxygen species and the tensile strain [IrO6] octahedron regulated by lanthanides are synergistically beneficial for increasing the intrinsic OER activity. Our research findings introduce c-a interface generation by the regulation of lanthanides as a new method for the rational design of robust OER catalysts.
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CHEMOSPHERE
·
2020
·
IF 5.778
Xiaoqi Li,Xiaofan Liu,Zhenzhen Jia,Tian Wang,Hongyan Zhang
Vitellogenin (VTG) is typically produced by females but when present in males can indicate contamination with estrogenic endocrine-disrupting chemicals (EDCs). Here we used primary hepatocytes isolated from male crucian carp uncontaminated with estrogenic EDCs as a culture model. Nine EDCs were used for validation, and an enzyme-linked immunosorbent assay (ELISA) was used to quantify VTG production by primary hepatocytes. The lower limit of detection of 17β-E2, DES, and HES using the method was 10 −12 M. Fresh pork was roasted, and non-hydrolytic acetonitrile-vortexing was used to extract potential estrogenic EDCs. The extracted substances were separated by thin-layer chromatography (TLC), and dimethyl terephthalate present in roast pork was found to induce high VTG concentrations. Therefore, the detection of VTG by ELISA provides a sensitive and reliable method for detecting known and unknown estrogenic EDCs in food products.
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高影响因子
ELECTROANALYSIS
·
2021
·Vol. 34
·期 2
·415-422
·
IF 3.223
Lanjie Lei,Chao Zhao,Xiaofei Zhu,Shuai Yuan,Xing Dong,Yinxiu Zuo,Hong Liu
We report on a nonenzymatic electrochemical sensor for wearable glucose monitoring in interstitial fluid. The sensor exhibited acceptable selectivity and reliability for continuous glucose detection for up to 30 days. The sensor tip is coated with polyurethane, and the biocompatibility of the tip is investigated by tissue staining. A fully integrated wearable glucose monitoring system is developed with a wireless connection with a smartphone. The test results are in agreement with reference methods. So, we believe the sensor is promising for the development of a continuous glucose monitoring system and diabetes management.
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ACS Applied Materials & Interfaces
·
2020
·
IF 8.758
Yuhao Weng,Qiaoyu Zhu,Zhen-Zhong Huang,Hongliang Tan
In this work, we proposed a new strategy of fabricating time-resolved fluorescent nanoprobes by using an enzyme-integrated lanthanide coordination polymer (CP) composite for the detection of superoxide anions (O2•–). This CP composite was constructed with terbium ions (Tb3+) as a metal node, adenosine triphosphate (ATP) as a bridge ligand, and carboxyphenylboronic acid (CPBA) as a sensitizer in which superoxide dismutase (SOD) was encapsulated by a self-adaptive inclusion process. The as-prepared SOD@ATP/Tb-CPBA displays both catalytic and fluorescence properties. Benefiting from the shielding effect of ATP/Tb CP, greatly enhanced catalytic activity and stability against harsh environments can be obtained in the loaded SOD. Meanwhile, the loaded SOD can remove the water molecules on the coordination sphere of Tb3+, leading to a significant increase in the fluorescence intensity and lifetime of SOD@ATP/Tb-CPBA. However, upon the addition of O2•–, the fluorescence of SOD@ATP/Tb-CPBA was quenched significantly. This is because SOD can convert O2•– into H2O2 to induce the deboronation of CPBA, resulting in an intramolecular charge transfer process. On this basis, by taking advantage of Tb3+ in long lifetime emission, a time-resolved fluorescence method was developed for the detection of O2•–, and satisfactory results have been achieved in both buffered aqueous solutions and serum samples. We believe that the presented study will open up a new avenue to develop enzyme-involved fluorescent nanoprobes.
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Analytical Methods
·
2020
·Vol. 12
·期 27
·3462-3469
·
IF 2.596
Xiaoyan He,Huimin Han,Wenyu Shi,Jiandi Dong,Xiong Lu,Wu Yang,Xiaoquan Lu
It is urgent to develop a more simple and sensitive method to detect antibiotic residues considering the harm of antibiotic residues in food to the human body. Herein we designed a label-free electrochemical DNA biosensor for the sensitive detection of kanamycin (KAN) based on diblock DNA with a 15-mer of poly-cytosine (poly-C). The diblock DNA can be immobilized on graphene oxide (GO) due to strong physical adsorption between the 15-mer of poly-C and GO. The aptamer of KAN acted as the other block for rapidly binding the target. It can specifically capture the target, which leads to the change of electrochemical signal. Consequently, the DNA biosensor exhibited high sensitivity and specificity towards KAN, the linear range was from 0.05 pM to 100 nM with a detection limit of 0.0476 pM. The developed DNA biosensor was constructed easily and showed promising applications for the detection of antibiotic residues for food safety.
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ACS Applied Materials & Interfaces
·
2020
·
IF 8.758
Yang Zhu,Hongdong Shi,Tuanwei Li,Jianing Yu,Zhengxi Guo,Junjie Cheng,Yangzhong Liu
The combination of photodynamic therapy (PDT) and enzyme therapy is a highly desirable approach in malignant tumor therapies as it takes advantage of the spatial-controlled PDT and the effective enzyme-catalyzed bioreactions. However, it is a challenge to co-encapsulate hydrophilic enzymes and hydrophobic photosensitizers, and these two agents often interfere with each other. In this work, a protocell-like nanoreactor (GOx-MSN@MnPc-LP) has been designed for synergistic starvation therapy and PDT. In this nanoreactor, the hydrophilic glucose oxidase (GOx) is loaded in the pore of mesoporous silica nanoparticles (MSNs), while the hydrophobic manganese phthaleincyanide (MnPc) is loaded in the membrane layer of liposome. This spatial separation of two payloads protects GOx and MnPc from the cellular environment and avoids interference with each other. GOx catalyzes the oxidation of glucose, which generates hydrogen peroxide and gluconic acid, leading to the starvation therapy via glucose consumption in cancer cells, as well as the disruption of cellular redox balance. MnPc produces cytotoxic singlet oxygen under 730 nm laser irradiation, achieving PDT. The antitumor effects of the nanoreactor have been verified on tumor cells and tumor-bearing mice models. GOx-MSN@MnPc-LP efficiently inhibits tumor growth in vivo with a single treatment, indicating the robust synergy of starvation therapy and PDT treatment. This work also offers a versatile strategy for delivering hydrophilic enzymes and hydrophobic photosensitizers using a protocell-like nanoreactor for effective cancer treatment.
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BIOCHEMICAL PHARMACOLOGY
·
2020
·
IF 4.96
Shuai Guo,Liang Qiu,Yafei Chen,Xuzhao Wang,Biao Ma,Chang Qu,Jianmin Cui,Hailin Zhang,Chengfen Xing,Yong Zhan,Hailong An
To overcome the adverse effects of conventional chemotherapy for cancers, various nanoparticles based drug delivery systems have been developed. However, nanoparticles delivering drugs directly to kill tumor cells still faced with challenges, because tumors possessed adopt complex mechanism to resist damages, which compromised the therapeutic efficacy. TMEM16A/CaCCs (Calcium activates chloride channels) has been identified to be overexpressed in lung adenocarcinoma which can serve as a novel tumor specific drug target in our previous work. Here, we developed a novel dual-targeted antitumor strategy via designing a novel nano-assembled, pH-sensitive drug-delivery system loading with specific inhibitors of TMEM16A against lung adenocarcinoma. For validation, we assayed the novel dual-targeting therapy on xenograft mouse model which exhibited significant antitumor activity and not affect mouse body weight. The dual targeting therapy accomplished in this study will shed light on the development of advanced antitumor strategy.
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SENSORS AND ACTUATORS B-CHEMICAL
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2020
·
IF 7.1
Hai-Bo Wang,Zi-Tao Zhong,Ting Zhang,Yuan-Di Zhao
Hepatitis B virus (HBV) can cause liver cancer, thus the detection of HBV-DNA is of great significance for liver cancer prevention. Since the concentration of HBV-DNA is often low, it is important to establish a highly sensitive detection method. In this study, microplate amplification and hybridization chain reaction (HCR) were used to improve the sensitive detection of HBV-DNA on dual strip biosensors. For the microplate-based amplification strategy on RS strip, the dual-DNA-AuNP probe could be immobilized on SA-Biotin-Anti-HBV-DNA-1 covered microplate through HBV-DNA. By adding dithiothreitol (DTT), a large amount of HS-RS-DNA on the dual-DNA-AuNP probe was dissociated. The indirect detection of HS-RS-DNA on RS strip could achieve the signal amplification of HBV-DNA. For the HCR-based strategy on HCR strip, HBV-DNA triggered the cascade reaction of H1-AuNP probe and H2-Biotin, a large amount of HCR product (AuNP-H1-H2-Biotin-AuNP-H1…) was produced. Thus, a lot of AuNP was fixed on the test zone of HCR strip to improve the HBV-DNA detection sensitivity. The detection limits by HCR strategy on HCR strip and microplate strategy on RS strip could reach to 5 pM and 0.1 nM, respectively, which were 200 and 10-fold higher than that of unamplified strategy, respectively. The recovery of HBV-DNA ranged from 97.2 to 102 % in the spiked human serum, presented a good accuracy for HBV-DNA detection in actual samples.
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