CHEMICAL ENGINEERING JOURNAL
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2022
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IF 16.744
Shuang Tian,Linzhu Su,Yingli An,Henny C. van der Mei,Yijin Ren,Henk J. Busscher,Linqi Shi
DNase can break down the extracellular matrix that keeps infectious bacterial biofilm together through cleavage of eDNA. Herewith, biofilm bacteria can become dispersed to assist antibiotic eradication but this has hitherto remained an in vitro possibility. In vivo DNase is rapidly broken down in blood, impeding blood-injection of DNase combined with antibiotics to cure bacterial infections. Herein, we report the synthesis of pH-responsive, self-targeting micelles self-assembled from a solution of poly(ethylene glycol)- block -poly(ε-caprolactone) (PEG- b -PCL) and poly(ε-caprolactone)- block -poly(amino ester) (PCL- b -PAE) with DNase conjugated to PAE-blocks. At physiological pH, this conjugation protected DNase inside the micellar shell, while PEG prevented adsorption of blood-borne proteins to the micelles. PAE became positively-charged below pH 6.4 facilitating self-targeting to an infectious biofilm. Simultaneously, PAE became hydrophilic and stretched to expose DNase upon accumulation in an infectious S. aureus biofilm where it degraded the biofilm matrix. PEG/PAE-DNase micelles internally core-loaded with ciprofloxacin significantly better eradicated murine pneumonia after blood-injection than ciprofloxacin-loaded PEG/PAE micelles without conjugated DNase or ciprofloxacin free in solution. Considering that DNase is clinically approved for use in cystic fibrosis patients, this paves the way for clinical translation of ciprofloxacin-loaded, PEG/PAE-DNase micelles for the treatment of pneumonia and other infections that can be reached through self-targeting after blood-injection.
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
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2022
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IF 8.025
Panpan Song,Zhongxia Lu,Tianze Jiang,Wenwei Han,Xiangyan Chen,Xia Zhao
The complex tumor microenvironment (TME) makes it difficult for single chemotherapy to achieve satisfactory therapeutic effects. Here, chitosan-coated hyaluronic acid micelles (R/C/ [email protected] ) that co-delivers doxorubicin (DOX) and programmed death-ligand 1 small interfering RNA (siPD-L1) are developed to enhance anti-tumor effect by combination of immunotherapy and chemotherapy. The pH/reduction dual-responsive co-delivery micelles R/C/ [email protected] are spherical particles about 180 nm, and have good drug loading performance, stability, biocompatibility, and TME-responsive drug release properties. The CD44 receptor targeting HA significantly enhances the cellular uptake of DOX and siPD-L1, and siPD-L1 causes the immune infiltration of CD4 + /CD8 + T cells by silencing PD-L1 expression. In vivo studies show that R/C/ [email protected] exhibits significantly stronger anti-breast cancer effect than that of free DOX and micelles loaded only DOX. Therefore, the dual-stimulus responsive micelles provide a promising strategy for combining chemotherapy and siRNA-based immunotherapy to enhance efficacy.
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CARBOHYDRATE RESEARCH
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2022
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IF 2.975
Jiangqin Lu,Shan Lu,Qinghua Cao,Juncheng Huang,Fei Liu,Haining Na,Jin Zhu,Zhen Jia
An easy and effective way to synthesize dual-functionalized cellulose derivatives with processability and fluorescence functionality by one-pot modification of successive esterification and carbonation under mild condition is established with the use of DMSO/DBU/CO 2 system. Accordingly, four kinds of dual-functionalized cellulose derivatives with rather good fluorescent response are obtained. After blending the synthesized dual-functionalized cellulose derivative with cellulose acetate as functional additive in solution, cast film with the elastic modulus , stress and strain reaches to 2.2 GPa, 34.1 MPa and 5.7% is prepared. Besides, the cast film also exhibits the ability to detect the pH value at 12–14 with detection accuracy of 0.4 through the change of fluorescent color. This research shows a simple but effective way to prepare dual-functionalized cellulose derivatives for the high-quality applications in field of detection.
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
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2022
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IF 8.025
Yunxia He,Lun Lu,Yanyun Lin,Ruyi Li,Yuan Yuan,Xuli Lu,Ying Zou,Wei Zhou,Zhuo Wang,Jihua Li
We aimed to prepare a new pH-sensing film based on the immobilization of purple cabbage anthocyanins (PCA) into Polyvinyl alcohol (PVA) reinforced by cellulose nanocrystals (CNC). FT-IR, XRD and TGA were used to assess the intermolecular interactions and thermo-stability of films. The addition of CNC and PCA resulted in an enhancement in UV–vis barrier, mechanical properties and moisture resistance. Inclusion of PCA imparted intelligent properties to the films. PCA-loaded films displayed strong visually detectable colorimetric responses to pH (2−13) and volatile ammonia. When applied to monitor shrimp freshness at 4 °C, PVA/CNC films containing 0.6 % PCA exhibited conspicuous color fluctuations from purple to gray blue upon deterioration. As a result, PVA/CNC-PCA colorimetric films were considered as intelligent packaging labels with significant mechanical, water vapor barrier properties and pH-sensing qualities for visual quality evaluation of fresh seafood products.
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BIOORGANIC & MEDICINAL CHEMISTRY
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2022
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IF 3.461
Chunyan Yang,Zhongzhen Yang,Siqi Wang,Jinxia Chen,Qijun Liu,Tianle Huang,Li Hai,Runxin Lu,Yong Wu
Chemotherapy is a conventional treatment for glioma, but its efficacy is greatly limited due to low blood–brain barrier (BBB) permeability and lack of specificity. Herein, intelligent and tumor microenvironment (TME)-responsive folic acid (FA) derivatives and mitochondria-targeting berberine (BBR) derivatives co-modified liposome coated with Tween 80 loading paclitaxel (PTX-Tween 80-BBR + FA-Lip) was constructed. Specifically speaking, liposomes modified by FA can be effectively target ed to glioma cells. BBR, due to its delocalized positive electricity and lipophilicity, can be attracted by mitochondrial membrane potential and concentrate on mitochondria to achieve mitochondrial targeting and induce cell apoptosis. By simultaneously modifying the liposome with FA and BBR to deliver drugs, leads to a good therapeutic effect of glioma through FA-based glioma targeting and BBR-based mitochondrial targeting. In addition, the surface of the liposome was coated with Tween 80 to further improve BBB penetration. All results exhibited that PTX-Tween 80-BBR + FA-Lip can observably improve the chemotherapy therapeutic efficacy through the highly specific tumor targeting and mitochondrial targeting, which can provide new ideas and methods for the targeted therapy of glioma.
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FOOD CONTROL
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2022
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IF 6.652
Jie-Qiong Wang,Yan-Qing Fu,Daniel Granato,Peigen Yu,Jun-Feng Yin,Liang Zeng,Yong-Quan Xu
The effects of pH (2.2–8.0) and temperature (25–100 °C) on the instrumental color of a model beverage containing (−)-epigallocatechin-3-gallate (EGCG) were investigated. As the pH and temperature increased, the lightness ( L *) decreased while the redness and yellowness ( a* and b* , respectively) increased. Using spectral scanning, it was possible to verify that color changes might be related to the structural rearrangement of the EGCG aqueous solution in the system under alkaline and heating conditions. There were 6 key substances identified in the EGCG solutions, among which (2R)-2-Hydroxy-3-(2,4,6-trihydroxyphenyl)-1-(3,4,5-trihydroxyphenyl)-1-propanone 2- O -gallate ( m/z 473.0720) and theacitrin C/dehydrotheasinensin AQ ( m/z 911.1340) were identified as key coloring substances. Color changes did not decrease antioxidant activity of the beverage model. These results provide new insights on the mechanism of color change during storage of green tea beverages, and enable the understanding of key contributors to the browning of infusions color in tea beverages for the first time.
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FOOD CHEMISTRY
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2022
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IF 9.231
Hongwei Jiang,Lei Zhou,Yuefang Sun,Kaibo Yu,Wenzhi Yu,Yuqing Tian,Junping Liu,Liqiang Zou,Wei Liu
It is still unclear how pH affects the inhibitory effects of phenolic acids and flavonoids on polyphenol oxidase (PPO). In this study, 4-hydroxycinnamic acid and naringenin were selected to investigate their interactions with PPO from pH 6.8 to 5.0. Results showed that acidic pH could enhance the inhibitory effect of inhibitors and a greater enhancement effect was observed in 4-hydroxycinnamic acid. Fluorescence emission spectra indicated that 4-hydroxycinnamic acid and naringenin interacted with PPO and quenched its intrinsic fluorescence, which was also enhanced by acidic pH. Circular dichroism suggested that 4-hydroxycinnamic acid and naringenin could reversibly bind to PPO molecules and transform α-helix into β-sheet. Molecular docking results revealed that 4-hydroxycinnamic acid and naringenin interacted with PPO through hydrogen bond and hydrophobic interaction, and more interactions were observed near the carboxyl group. These results indicated that acidic pH could significantly enhance the inhibitory effect of phenolic acid on PPO.
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ACS Omega
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2022
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IF 4.132
Jiamei Xiang,Ruixue Li,Xiang Long,Shaogui Wu,Jiayang Wang,Zhuo Wang
In this work, ultrabright fluorescent carbon dots (U-CDs) were synthesized by using a strict twice iterative optimization strategy. Their relative photoluminescence (PL) quantum yield is close to 100%, exceeding most of the reported fluorescent CDs and greatly boosting the practical applications of fluorescent CDs in many fields. Then serving as fluorescent anti-counterfeiting ink was taken as an example to briefly introduce the application of the U-CDs. The PL emission of the U-CDs is quenched at the range of pH < 4 or pH > 11 and restored at the range of pH = 5–10. This pH-sensitive PL feature allows the U-CDs to be used as fluorescent ink for pH and UV dual information encryption. The written or printed information is invisible under daylight but visible under UV light. After acid treatment or alkali treatment, the information is invisible even under a UV lamp but visible after neutralization treatment. This work provides a standardized scheme for optimizing the synthesis conditions of fluorescent CDs and paves the way for large-scale production of high-performance fluorescent CDs.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2022
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IF 9.965
Lijuan Yang,Yujie Zhao,Lijun Zhu,Daohong Xia
Superionic conductors regulated transition metal chalcogenides are the newly emerged electrocatalyst in water electrolysis into clean hydrogen and oxygen. However, there is still much room for the development of structural design, electronic modulation and heterogeneous interface construction to improve the overall water splitting performance in pH-universal solutions, especially in alkaline and neutral mediums. Herein, using β-cyclodextrin (β-CD) and citric acid (CA) organics with abundant hydroxyl (–OH) and carboxyl (–COOH), a special Ag 2 Se nanoparticles-decorated CoSe 2 flower-like nanosheets loaded on porous and conductive nickel foam substrate (Ag 2 Se-CoSe 2 /NF) was successfully constructed by a new method of monometallic cation release of coordinated cobalt. The Ag 2 Se phase exerts the nature characteristics of superionic conductors to modulate the morphological and electronic structures of CoSe 2 as well as improve its conductivity. The generated rich active interfaces and abundant Se vacancy defects facilitate numerous active sites exposure to accelerate the hydrogen ion transport and charge transfer. Compared to the single-phase Ag 2 Se/NF-8 and CoSe 2 /NF, the prepared Ag 2 Se-CoSe 2 /NF-8 with a two-phase synergistic effect achieves an outstanding pH-universal electrocatalytic hydrogen production performance by water electrolysis, as evidenced by a lower overpotential (60 mV, 212 mV and 85 mV vs RHE at 10 mA cm −2 for pH = 0.36, 7.00 and 13.70, respectively). Only a voltage of 1.55 V at 10 mA cm −2 is required to implement the overall water splitting in an alkaline electrolyzer. This work provides significant guidance for the future designation and practical development of transition metal chalcogenides with superionic conductors applied in the electrocatalytic field.
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TALANTA
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2021
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IF 6.057
Jinying Liu,Jiabao Zhang,Yue Zhang,Yan Wang,Mengke Wang,Ziwen Li,Guannan Wang,Xingguang Su
In this paper, we proposed a dual-signal fluorometric and colorimetric system based on silicon quantum dots (SiQDs) and 4-nitrophenol (4-NP) for pH and urease sensing. SiQDs with fluorescence emission of 460 nm were prepared via aqueous-phase synthesis. As the pH of the system gradually increased, the absorption band of 4-NP at 400 nm increased and a color reaction from colorless to yellow occurred. The absorption of 4-NP overlapped quiet well with the fluorescence excitation spectrum of SiQDs, which can effectively quench the fluorescence of SiQDs. Therefore, the change of fluorescence and absorption intensities could be used to quantify pH value. The fluorometric and colorimetric pH-sensing systems both exhibited a linear respond to pH ranging from 6.0 to 7.8 with an interval of 0.2 pH unit. Urease could specifically hydrolyze urea to generate carbon dioxide and ammonia, causing an obvious increase of the pH value. Thus, urease could also be detected quantitatively by the above dual-signal pH sensing system. The linear ranges of the fluorometric and colorimetric methods for urease detection were both 2–40 U L-1. The limits of detection were 1.67 and 1.07 U L-1, respectively. More importantly, this established dual-signal system has been successfully exploited in the detection of urease in real samples with satisfactory recoveries. Compared with other traditional single-signal assay strategies, the results obtained by dual-signal methods are more accurate and reliable.
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Acta Biomaterialia
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2021
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IF 8.947
Ye Yuan,Jia Liu,Xiangnan Yu,Xingxin Liu,Yanni Cheng,Cheng Zhou,Mingyi Li,Lin Shi,Yan Deng,Huan Liu,Guobin Wang,Lin Wang,Zheng Wang
Multidrug resistance (MDR) is a major cause accounting for chemotherapy failure and recurrence of malignant tumors. A prominent mechanism underlying MDR is overexpression of P-glycoprotein (P-gp, a drug efflux pump). Promoting drug delivery efficacy by targeting tumor and concurrently suppressing drug efflux through down-regulating P-gp emerges as an effective strategy to enhance intracellular drug accumulation for combating MDR tumor. General Control Non-repressed 5 (GCN5), a histone acetyltransferase acting as an epigenetic regulator of multidrug resistance protein 1 (MDR1), positively regulates P-gp levels in drug-resistant cancer cells. Herein, a hyaluronic acid-coated, pH/redox dual-responsive nanosystem (HPMSNs) is fabricated for co-delivering doxorubicin (DOX) and GCN5 siRNA (siGCN5). This nanosystem can effectively encapsulate DOX and siRNA preventing premature leakage and releasing these therapeutics intracellularly via its pH/redox dual responsiveness. Through CD44-mediated targeting, DOX/ [email protected] increases drug internalization in CD44-overexpressing cancer cells, and markedly promotes DOX retention by down-regulating P-gp expression in drug-resistant cancers through silencing GCN5. Of note, in an MDR breast tumor model, DOX and siGCN5 co-delivered HPMSNs inhibits MDR tumor growth by 77%, abolishes P-gp-mediated drug resistance, and eliminates DOX's systemic toxicity. Thus, the tumor-targeting, stimuli-responsive nanosystem is an effective carrier for co-delivering anticancer drug and siRNA for combating cancer drug resistance. Statement of significance We designed a tumor-targeting, pH/redox dual-responsive nanosystem (HPMSNs) for chemo-drug and siRNA co-delivery. This nanosystem efficiently co-delivered DOX and siGCN5 into drug-resistant cancer cells and significantly inhibited the tumor growth through: (1) HA shell enhanced the cellular internalization of loaded DOX and siGCN5 via CD44-mediated targeting; (2) the pH/redox dual-responsive nanosystem released the cargos in response to the intracellular environment; (3) the released siGCN5 downregulated P-gp epigenetically. In an MDR breast tumor model (MCF7/ADR), DOX and siGCN5 loaded HPMSNs markedly inhibited tumor growth, almost completely abolished P-gp expression, and minimized systemic toxicity of DOX.
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JOURNAL OF CHROMATOGRAPHY A
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2021
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IF 4.759
Qiqi Wang,Tao Chen,Yunbin Cui,Si Li,Xinhao Jiang,Guodong Zhao,Yulin Li,Denglang Zou
Biosynthesis is a research hot-spot in recent years, however, the purification of its final products is a tough work. Liquid stationary phase and large-scale separation ability of PZRCCC could easily avoid the commonly disadvantages occurred in traditional column chromatography. These characteristics makes PZRCCC particularly applicable for final products separation in biosynthesis. In this study, the glycosylation products of ellagic acid by one-pot glycosylation were successfully purified by PZRCCC to show the applicability of PZRCCC for preparative separation of biosynthesis products. An optimized ethyl acetate/n-buthanol/water (3:3:5, v/v/v) system was applied in this study, where 5 mM trifluoroacetic acid (TFA) as the retainer and 30 mM triethylamine (TEA) as the eluter were added. As a result, four ellagic acid glycosylation products, including 51 mg of ellagic acid-4, 3’-O- β -D-diglucoside ( EG-1 ), 24 mg of ellagic acid-4, 4’-O- β -D-diglucoside ( EG-2 ), 11 mg of ellagic acid-4-O- β -D-glucosyl (1→2)- β -D-glucoside ( EG-3 ) and 64 mg of ellagic acid-4-O- β -D-glucoside ( EG-4 ) were simultaneously separated from 500 mg of glycosylation crude products, with the purity of 93.3%, 91.2%, 89.4% and 95.5%, respectively. Their structures were identified by spectroscopic analysis.
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