FOOD CHEMISTRY
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2024
·
IF 8.5
Kai Wang,Hui Li,Wenya Liu,Pan Liu,Chuang Jiang,Wanqi Jiang,Yaqing Xiao,Yingnan Liu
Based on the previously developed Al 3+ /CuNCs probe, the matrix effect (ME) derived from protein was investigated in the fluorescence determination of fluoroquinolones (FQs) residues in eggs, and a sample pretreatment method was established to rapidly reduce the ME. Molecular docking results indicated that the three main egg proteins and FQs were bound by hydrogen bond, van der Waals force, and alkyl groups, leading to the loss of FQs response signal, and then produced ME. After trichloroacetic acid treatment, the mean particle size of egg matrix decreased, the protein secondary structure changed, and the crystal structure was destroyed. The corresponding ME of the supernatant obtained by centrifugation was only 0.7 %. The standard addition experiment confirmed that the proposed pretreatment method improved the accuracy and reliability of the fluorescence probe. This work is helpful to promote the practical application of fluorescence analysis in the rapid monitoring of food safety hazard factors.
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Research
·
2024
·
IF 8.5
Hao Liu,Ke Huang,Hao Zhang,Xiaohui Liu,Hui Jiang,Xuemei Wang
Achieving antitumor immunotherapy based on hybridization of multiple types of inactivated cells has attracted a lot of attention. However, the hybridized cells of disordered structure could result in the shedding of antigens and their transfer to immune cells, which suppresses tumor immunity through trogocytosis. Here, we report a strategy for in situ solidification of tumor whole cell by biomineralization for sustained stimulation of antitumor immunity. The near-infrared light was used to accelerate the breaking of Au=P bonds in auranofin, and the exposed Au atoms biomineralize at the secondary structure (β-corner) of the protein to form Au nanocrystals with in situ protein coronas in tumor cells. Au nanocrystals are anchored to the tumor cells through protein coronas, which fixes the morphology and antigens of whole tumor cells, rendering them physiologically inactive. Interestingly, this solidified tumor cell prevents immune cells from undergoing trogocytosis, which inhibits proximal and distal tumor growth. Thus, this study presents the strategy of solidified cells and its potential application in tumor immunotherapy.
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ACS Nano
·
2024
·
IF 15.8
Guiqi Ma,Xinyu Zhang,Kunlong Zhao,Shuxuan Zhang,Ke Ren,Mengyao Mu,Chenyu Wang,Ximing Wang,Hui Liu,Jian Dong,Xiao Sun
Rational structure design benefits the development of efficient nanoplatforms for tumor theranostic application. In this work, a multifunctional polydopamine (PDA)-coated manganese sulfide (MnS) nanocluster was prepared. The polyhydroxy structure of PDA enhanced the water interaction with pH-responsive MnS nanoclusters via hydrogen bonds. At pH 5.5 conditions, the spin–lattice relaxation rate of MnS nanoclusters dramatically increased from 5.76 to 19.33 mM–1·s–1 after the PDA coating, which can be beneficial for efficient tumor magnetic resonance imaging. In addition, PDA endowed MnS nanoclusters with excellent biocompatibility and good photothermal conversion efficiency, which can be used for efficient tumor photothermal therapy (PTT). Furthermore, MnS nanoclusters possess the ability to release H2S in the acidic tumor microenvironment, effectively inhibiting mitochondrial respiration and adenosine triphosphate production. As a result, the expression of heat shock protein was obviously reduced, which can reduce the resistance of tumor cells to photothermal stimulation and enhance the efficacy of PTT. The released Mn2+ also displayed efficient peroxidase and glutathione oxidase-like activity, effectively inducing tumor cell ferroptosis and apoptosis at the same time. Therefore, this nanoplatform could be a potential nanotheranostic for magnetic resonance contrast enhancement and synergistic ferroptosis–PTT of tumors.
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Pharmaceutics
·
2024
·Vol. 16
·期 4
·512
·
IF 4.9
Junhong Ling,Yingying Cai,Haozhan Feng,Zhen Liu,Xiao-kun Ouyang
Disulfiram (DSF) degrades to diethyldithiocarbamate (DTC) in vivo and coordinates with copper ions to form CuET, which has higher antitumor activity. In this study, DSF@CuMSN-PDA nanoparticles were prepared using mesoporous silica with copper ions, DSF as a carrier, and polydopamine (PDA) as a gate system. The nanoparticles selectively released CuET into tumor tissue by taking advantage of the tumor microenvironment, where PDA could be degraded. The release ratio reached 79.17% at pH 5.0, indicating pH-responsive drug release from the nanoparticles. The PDA-gated system provided the nanoparticles with unique photothermal conversion performance and significantly improved antitumor efficiency. In vivo, antitumor experiments showed that the designed DSF@CuMSN-PDA nanoparticles combined with near-infrared light (808 nm, 1 W/cm2) irradiation effectively inhibited tumor growth in HCT116 cells by harnessing the combined potential of chemotherapy and photothermal therapy; a synergistic effect was achieved. Taken together, these results suggest that the designed DSF@CuMSN-PDA construct can be employed as a promising candidate for combined chemo-photothermal therapy.
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Food Bioscience
·
2024
·
IF 4.8
Lian Xia,Jia Zheng,Jian Su,Hongli Yang,Zhengmin Xie,Yue Tang,Yuangen Wu
Ethyl carbamate (EC) is a small compound produced and stored during fermentation processes from ethanol, urea, citrulline, and carbamoyl phosphate. EC is commonly found in fermented foods and alcoholic beverages. Prolonged exposure to EC can cause nervous system diseases and liver damage in human beings. EC lacks stable physicochemical properties, and the presence of numerous interfering substances in alcoholic beverages poses challenges for its detection. Herein, it is found that EC1-34 aptamer bound to EC can enhance the laccase-like activity of cubic Ag 2 O nanoparticles (NPs). Subsequently, Ag 2 O NPs are wrapped with EC1-34 aptamer to prepare recognition probes, which are immobilized on a carrier membrane. Thus, a portable paper-based sheet for EC detection in Chinese Baijiu is designed. The visual detection limit of the developed paper-based sheet for EC is 10 μg⋅L −1 , and shows an outstanding linear relationship within the range of 10–200 μg⋅L −1 . Moreover, this colorimetric paper-based sheet has a good practicality in various Chinese Baijiu samples. It is believed that such paper-based sheet can facilitate portable inspection for EC in Baijiu, and may also become a beneficial tool for monitoring EC molecules in other fermented foods.
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INTERNATIONAL BIODETERIORATION & BIODEGRADATION
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2024
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IF 4.1
Liwen Zhang,Luyao Xi,Shuyu He,Huizi Wen,Shanyi Tan,Shaohua Chen
Bioremediation has garnered considerable interest due to its advantages of economy and no secondary pollution. However, the direct electron transfer rate between microorganisms and Cr(VI) is low. The bioreduction of Cr(VI) by Shewanella oneidensis MR-1 ( S. oneidensis ) in the presence of formylmethylflavin (FMF) was conducted to understand how FMF mediated the extracellular electron transfer process to improve Cr(VI) removal. In this study, FMF was firstly synthesized by modifing RF to increase its solubility and redox activity. The findings indicate that S. oneidensis /FMF exhibited better Cr(VI) removal performance compared to that of S. oneidensis . Under optimum conditions, 40 mg/L Cr(VI) could be completely removed by S. oneidensis /FMF within 120 h, while only 48.6% of Cr(VI) was removed by S. oneidensis , and the first order rate constant (k) for the Cr(VI) elimination by S. oneidensis /FMF (0.033 h −1 ) was about 4.1-fold greater than that of S. oneidensis (0.008 h −1 ). Moreover, the removal of Cr(VI) by S. oneidensis /FMF were dominated by reduction, and supplemented by adsorption and complexation. FMF enhance the extracellular electron transfer rate (EETR) was confirmed by electrochemical cyclic voltammetry (CV) and linear scanning voltammetry (LSV) experiments. This study emphasizes the potential important role of FMF in environmental bioremediation.
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MICROCHIMICA ACTA
·
2024
·Vol. 192
·期 1
·1-12
·
IF 5.3
Huang Yuanding,Chen Ping,Niu Meng,Peng Weng Kung
Clinical and immunological assays of white blood cells (WBCs) in human peripheral blood are of significance for disease diagnosis and immunological studies. However, separating WBCs from blood with high recovery and high purity remains challenging. In this study, by incorporating a pair of linearly tapered filter arrays, a crossflow filtration-based microfluidic chip was designed and fabricated for separation of WBCs from blood. The implementation of the linearly tapered filter arrays not only ensures a minimal and consistent flow through each sieve, but also achieves a high filtration ratio (~ 19). The validity and robustness of this straightforward design were substantiated through theoretical analysis, simulations, and model microparticle tests. The microfluidic chip achieved an almost perfect (> 99.2%) recovery and a ~ 20-fold enrichment of the targeted 8 μ m particles (as surrogates for WBCs) from undesired 2 μ m particles (as substitutes for red blood cells, RBCs) at flow rates ranging from 50 to 200 μ L/min, irrespective of the filter array length and particle concentration. When applied to a twenty times diluted blood sample, the chip achieved a 96.6% recovery and 19.7-fold enrichment of WBCs, as well as a 95.0% removal of RBCs, at the optimal flow rate of 100 μ L/min. With its simple design, cost-effectiveness, high recovery, substantial enrichment ratio, and considerable throughput, this chip offers an alternative solution that is potentially applicable to scenarios involving the separation of WBCs as well as other particles/cells. Graphical abstract
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MICROCHEMICAL JOURNAL
·
2025
·
IF 5.1
Ruiwen Li,Guoqing Qian,Hao Shen,Shaoning Yu
The accurate, timely, and convenient detection of multidrug-resistant bacteria (MDRB) is of enormous value in clinical treatment and food safety. Traditional methods include plate culture and polymerase chain reaction, but these strategies are time-consuming, costly, or cumbersome to operate, making it difficult to meet the increasingly severe demands. Here, we describe the synthesis of a metal–organic framework (MOF) heterostructure hybrid (MOF@MOF) self-cascade nanozyme that promotes signal amplification for colorimetric MDRB aptasensing. The MOF@MOF was composed of copper-functionalized MOF-808 with catechol oxidase-mimicking activity and an iron porphyrin MOF with peroxidase-mimicking activity; MOF-808 with open copper sites hydrolyzed the substrate 3,5-ditert-butylcatechol, producing H 2 O 2 in situ , and the iron porphyrin MOF catalyzed H 2 O 2 to further oxidize 3,3′,5,5′-tetramethylbenzidine into a colored product. Benefitting from the nanoproximity effect and confinement effect, the biocatalytic ability of the biomimetic cascade was significantly facilitated, generating a strengthened colorimetric signal. Taking methicillin-resistant Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa (PA) as examples, the MOF@MOF nanozyme coordinated with aptamers to construct a colorimetric aptasensing platform for ultrasensitive detection of MDRB. Compared to frequently used probes containing H 2 O 2 , the inactive substrate did not oxidize TMB to induce a color change, resulting in low background signal. The limit of detection was 5 CFU/mL for MRSA and 2 CFU/mL for PA, with a wide linear range for both (10–10 8 CFU/mL). The proposed aptasensing platform was used to analyze MDRB in biological samples, indicating excellent practicability. The self-cascade MOF@MOF may offer valuable insights into the rational construction of biomimetic sensors based on nanozymes.
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OPTICAL MATERIALS
·
2024
·
IF 3.8
Zhuoyuan Li,Yulin Wang,Jinting Chen,Li Zhang,Yongbiao Hua,Donglan Huang,Huishi Guo,Xiuzhen Qiu
Tetracycline (TC) is a typical emerging pharmaceuticals and personal care products (PPCPs) pollutants in the environment. However, TC residues cause severe effects on human health. It is crucial to exploit simple, rapid and sensitive methods to detect TC in water samples. A ratiometric fluorescent probes (CDs-Eu 3+ ) is constructed using carbon dots (CDs) and europium ions (Eu 3+ ) for the visual detection of tetracycline (TC). Under 390 nm excitation, CDs-Eu 3+ shows a strong yellow fluorescence at 545 nm and a weak red fluorescence at 619 nm, respectively. In the presence of TC, the fluorescence intensity at 545 nm decreased while the fluorescence intensity at 619 nm increased, which attributed to the internal filtering effect (IFE) and “antenna effect”, respectively. Sensing performance of CDs-Eu 3+ probes is further evaluated with respect to various conditions, including salt concentration, Eu 3+ concentration, pH, and reaction time. Results reveal that the proposed ratiometric fluorescent probes exhibits a specific recognition ability toward TC. An excellent linear relationship is observed between the fluorescence intensity ratio (F 619 /F 545 ) and TC concentrations (1⁓100 μM), with a low detection limit (LOD) of 31 nM. The solution (CDs-Eu 3+ -TC) color gradually changes from yellow to red after adding TC. The probes are successfully applied to determine TC in water with recoveries of 85.43⁓97.53%. Finally, a fluorescent test strip is prepared and used for rapid visual semi-quantitative TC detection.
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Advanced Science
·
2024
·Vol. 11
·期 46
·2309053
·
IF 14.3
Lan Chen,Qiqi Yin,Handan Zhang,Jie Zhang,Guizhu Yang,Lin Weng,Tao Liu,Chenghui Xu,Pengxin Xue,Jinchao Zhao,Han Zhang,Yanli Yao,Xin Chen,Shuyang Sun
Oral squamous cell carcinoma (OSCC) often recurs aggressively and metastasizes despite surgery and adjuvant therapy, driven by postoperative residual cancer cells near the primary tumor site. An implantable in situ vaccine hydrogel was designed to target residual OSCC cells post-tumor removal. This hydrogel serves as a reservoir for the sustained localized release of δ-aminolevulinic acid (δ-ALA), enhancing protoporphyrin IX-mediated photodynamic therapy (PDT), and a polydopamine-hyaluronic acid composite for photothermal therapy (PTT). Additionally, immune adjuvants, including anti-CD47 antibodies (aCD47) and CaCO 3 nanoparticles, are directly released into the resected tumor bed. This approach induces apoptosis of residual OSCC cells through sequential near-infrared irradiation, promoting calcium interference therapy (CIT). The hydrogel further stimulates immunogenic cell death (ICD), facilitating the polarization of tumor-associated macrophages from the M2 to the M1 phenotype. This facilitates phagocytosis, dendritic cell activation, robust antigen presentation, and cytotoxic T lymphocyte-mediated cytotoxicity. In murine OSCC models, the in situ vaccine effectively prevents local recurrence, inhibits orthotopic OSCC growth and pulmonary metastases, and provides long-term protective immunity against tumor rechalle nge. These findings support postoperative in situ vaccination with a biocompatible hydrogel implant as a promising strategy to minimize residual tumor burden and reduce recurrence risk after OSCC resection.
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EUROPEAN JOURNAL OF PHARMACOLOGY
·
2024
·
IF 4.2
Yongmei Li,Fengxin Zheng,Shiqi Zhong,Kunlu Zhao,Hui Liao,Jiacheng Liang,Qiang Zheng,Huicong Wu,Shifan Zhang,Ying Cao,Ting Wu,Jianxin Pang
Hyperuricemic nephropathy (HN) is characterized by renal fibrosis and tubular necrosis caused by elevated uric acid levels. Ferroptosis, an iron-dependent type of cell death, has been implicated in the pathogenesis of kidney diseases. The objective of this study was to explore the role of ferroptosis in HN and the impact of a ferroptosis inhibitor, ferrostatin-1 (Fer-1). The study combined adenine and potassium oxonate administration to establish a HN model in mice and treated HK-2 cells with uric acid to simulate HN conditions. The effects of Fer-1 on the renal function, fibrosis, and ferroptosis-associated molecules were investigated in HN mice and HK-2 cells treated with uric acid. The HN mice presented with renal dysfunction characterized by elevated tissue iron levels and diminished antioxidant capacity. There was a significant decrease in the mRNA and protein expression levels of SLC7A11, GPX4, FTL-1 and FTH-1 in HN mice. Conversely, treatment with Fer-1 reduced serum uric acid, serum creatinine, and blood urea nitrogen, while increasing uric acid levels in urine. Fer-1 administration also ameliorated renal tubule dilatation and reduced renal collagen deposition. Additionally, Fer-1 also upregulated the expression levels of SLC7A11, GPX4, FTL-1, and FTH-1, decreased malondialdehyde and iron levels, and enhanced glutathione in vivo and in vitro . Furthermore, we first found that Fer-1 exhibited a dose-dependent inhibition of URAT1, with the IC 50 value of 7.37 ± 0.66 μM. Collectively, the current study demonstrated that Fer-1 effectively mitigated HN by suppressing ferroptosis, highlighting the potential of targeting ferroptosis as a therapeutic strategy for HN.
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Food Bioscience
·
2024
·
IF 4.8
Xin-Yu Zu,Ya-Nan Zhao,Yan Liang,Ying-Qiu Li,Chen-Ying Wang,Xiang-Zhong Zhao,Hua Wang
The rapid screening of angiotensin I-converting enzyme (ACE) inhibitory peptides (ACEIPs) from protein hydrolysates remains a challenge in current researches. The current study presents the development of an efficient affinity medium (AOPAN–ACE) consisting of ACE immobilized on the surface of electrostatically spun polyacrylonitrile nanofibrous membranes for the efficient screening of ACEIPs. The application of this affinity medium followed by liquid chromatography–tandem mass spectrometry analysis resulted in the successful screening and identification of 60 potential ACEIPs from protein hydrolysates of tuna dark muscle. Notably, the application of PeptideRanker, pLM4ACE, and molecular docking approaches resulted in the screening and identification of a novel ACEIP FPPDVA. Furthermore, the peptide FPPDVA was synthesized using the solid-phase method, and its IC 50 value on ACE was determined to be 87.11 ± 1.02 μM. Molecular docking analysis suggested that the ACEIP of the peptide FPPDVA is attributable to the formation of hydrogen bonds with the S1 active site (Ala354 and Tyr523) of ACE and metal–ligand bonds with Zn 2+ . In addition, molecular dynamics simulations revealed that the peptide FPPDVA formed a stable complex with ACE and was consistently localized within the active pocket of ACE over a simulation duration of 100 ns without being displaced from the active site. Lineweaver–Burk analysis further confirmed that the peptide FPPDVA exhibited mixed mode of inhibition against ACE. Overall, the affinity medium developed in the current study is potentially useful for highly efficient screening of ACEIPs, and the novel ACEIP FPPDVA identified herein is a promising functional food ingredient for antihypertensive application.
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