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design of sonochemical assisted synthesis of Zr-MOF/g-C3N4-modified electrode for ultrasensitive detection of antipsychotic drug chlorpromazine from biological samples

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Microchimica Acta 2024年第4期191卷 182-182页

作者： Ashkar, M.A. Kutti Rani, S. Vasimalai, N. Kuo, Chih-Yu Yusuf, Kareem Govindasamy, Mani Department of Chemistry B.S. Abdur Rahman Crescent Institute of Science and Technology Vandalur Chennai600 048 India Department of Chemical Engineering & amp Biotechnology National Taipei University of Technology Taipei10608 Taiwan International Ph.D. Program in Innovative Technology of Biomedical Engineering and Medical Devices Ming Chi University of Technology New Taipei City243303 Taiwan Department of Chemistry College of Science King Saud University Riyadh11451 Saudi Arabia Department of Research and Innovation Saveetha School of Engineering SIMATS Chennai6021055 India Research Center for Intelligence Medical Devices Ming Chi University of Technology New Taipei City243303 Taiwan

The rapid fabrication is described of binary electrocatalyst based on a highly porous metal–organic framework with zirconium metal core (Zr-MOF) decorated over the graph.tic carbon nitride (g-C3N4) nanosheets via facile ultrasonication method. It is used for the robust determination of antipsychotic drug chlorpromazine (CLP) from environmental samples. The electrochemical behaviour of 2d Zr-MOF@g-C3N4 was characterized by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) studies. The crystalline and porous nature of the composite was characterized by XRd and SEM analysis. The functional groups and surface characteristics were investigated by FT-IR, Raman and XPS. The major electrochemical properties of the Zr-MOF@g-C3N4 composite towards CLP detection were analyzed by CV, chronocoulometric (CC), chronoamperometric (CA) and differential pulse voltammetry (dPV) techniques. The composite exhibits a low detection limit (LOd) of 2.45 nM with a linear range of 0.02 to 2.99 µM and attractive sensitivity for CLP. The sensor system shows higher selectivity towards the possible interferences of CLP drug and exhibits better repeatability and stability. Finally, the fabricated sensor system shows a high recovery range varying from 96.2 to 98.9% towards the real samples. The proposed electrochemical probe might be a promising alternative to the prevailing diagnostic tools for the detection of CLP. Graph.cal Abstract: (Figure presented.) © The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature 2024.

关键词： Cyclic voltammetry

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Combinatorial Engineered Immuno-Fragments Targeting SARS-CoV-2 Nucleocapsid Protein for Epitope Complementarity

SSRN

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SSRN 2024年

作者： dlamini, Nhlanhla Benedict Lee, Chi-Hsin Wang, Wei-Chu Huang, Peng-Nien Leu, Sy-Jye Tseng, Sung-Nien Shih, Shin-Ru Chiang, Liao-Chun Mao, Yan-Chiao Tsai, Bor-Yu Yang, Yi-Yuan Ph.D. Program in Medical Biotechnology College of Medical Science and Technology Taipei Medical University Taipei110301 Taiwan School of Medical Laboratory Science and Biotechnology College of Medical Science and Technology Taipei Medical University Taipei110301 Taiwan Research Center for Emerging Viral Infections Chang Gung University Taoyuan333423 Taiwan Division of Infectious Diseases Department of Pediatrics Linkou Chang Gung Memorial Hospital Taoyuan333423 Taiwan Graduate Institute of Medical Sciences College of Medicine Taipei Medical University Taipei110301 Taiwan Department of Microbiology and Immunology School of Medicine College of Medicine Taipei Medical University Taipei110301 Taiwan Department of Laboratory Medicine Linkou Chang Gung Memorial Hospital Taoyuan333423 Taiwan College of Life Sciences National Tsing Hua University Hsinchu300040 Taiwan Division of Clinical Toxicology Department of Emergency Medicine Taichung Veterans General Hospital Taichung407219 Taiwan Navi Bio-Therapeutics Inc. Taipei10351 Taiwan Core Laboratory of Antibody Generation and Research Taipei Medical University Taipei110301 Taiwan

Recombinant avian ph.ge display immunoglobulin Y derivative single chain variable fragment (IgY-scFv) antibodies have evolved as robust single-chain antigen recognizing IgY analogues due to the advent of immuno-nanotechnology and other immunomolecular biotechnology applications. This academic study reports on the engineering and characterization of severe acute respiratory syndrome coronavirus 2 nucleocapsid (SARS-CoV-2 N) monoaffinity recombinant chicken IgY derivative single chain variable fragment (IgY-scFv) antibody fragments as versatile tools for surrogate immunological identification of the SARS-CoV-2 virus nuclear biomarker. To improve the immunopanning selection for specific binders, layer hens were immunised with the SARS-CoV-2 nucleocapsid protein to pre-enrich higher affinity B cell gene repertoires prior to library construction. Pre-enrichment humoral egg yolk polyclonal IgY antibodies were isolated following the PEG-8000 precipitation protocol. An experimental based modelling approach was applied in order to create IgY derivative N protein single chain variable fragments (IgY-scFv N) M13KO7 ph.ge antibody libraries, an immune ph.ge display library constructed system that supported the generation of functional anti-SARS-CoV-2 N protein IgY-scFv affinity monospecific fragment immunomolecules. After the immunopanning enrichment selection process three distinct positive sequence family IgY-scFv fragments obtained demonstrated epitope specific affinity (micromolar range kinetics) towards the targeted recombinant SARS-CoV-2 N protein and also positively identified native SARS-CoV-2 (COVId-19) N protein in formalin-fixed paraffin-embedded (FFPE) 293T cell pellets. © 2024, The Authors. All rights reserved.

关键词： Coronavirus

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diterpenoids and Their Glycosides from the Stems ofTinospora crispawith Beta-Cell Protective Activity

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Journal of Natural Products 2023年第6期86卷 1437-1448页

作者： Sio-Hong Lam Hui-Kang Liu Shih-Yuan Chung Jia-Ling Chang Mao-Xuan Hong Sheng-Chu Kuo Chih-Chuang Liaw School of Pharmacy College of Medicine National Cheng Kung University Tainan 70101 Taiwan Division of Basic Chinese Medicine National Research Institute of Chinese Medicine Ministry of Health and Welfare Taipei 112 Taiwan Ph.D. Program in the Clinical Drug Development of Herbal Medicine Taipei Medical University Taipei 11031 Taiwan Graduate Institute of Pharmaceutical Chemistry China Medical University Taichung 404 Taiwan Department of Marine Biotechnology and Resource National Sun Yat-sen University Kaohsiung 80424 Taiwan Department of Science Application and Dissemination National Taichung University of Education Taichung 403 Taiwan Graduate Institute of Natural Products Kaohsiung Medical University Kaohsiung 807 Taiwan Graduate Institute of Pharmacognosy Taipei Medical University Taipei 11031 Taiwan

Seven previously undescribed diterpenoids, tinocrisposides A–d (1–4) and borapetic acids A (5), B (6), and C (7), together with 16 known compounds, were isolated from the stem ofTinospora crispa(Menispermaceae). The structures of the new isolates were elucidated by spectroscopic and chemical methods. The β-cell protective effect of the tested compounds was examined on insulin-secreting BRIN-Bd11 cells under dexamethasone treatment. diterpene glycosides12,14–16, and18presented a substantial protective effect on BRIN-Bd11 cells treated with dexamethasone in a dose-dependent manner. Compounds4and17with two sugar moieties exhibited clear protective effects on β-cells.

关键词： Alkyls Carbohydrates Carbon Chemical structure Nuclear magnetic resonance spectroscopy

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16-Hydroxybriaranes from the octocoral Briareum stechei

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ph.tochemistry Letters 2023年第1期57卷 92-95页

作者： Liu, Chia-Jung Wang, Chien-Chiao Chang, Chun-Feng Zhang, Mingzi M. Tsou, Lun Kelvin Wen, Zhi-Hong Hwang, Tsong-Long Chen, You-Ying Sung, Ping-Jyun Department of Marine Biotechnology and Resources National Sun Yat-sen University Kaohsiung 804201 Taiwan National Museum of Marine Biology and Aquarium Pingtung 944401 Taiwan Graduate Institute of Natural Products College of Medicine Chang Gung University Taoyuan 333323 Taiwan Graduate Institute of Biomedical Sciences College of Medicine Chang Gung University Taoyuan 333323 Taiwan Division of Urology Department of Surgery Kaohsiung Armed Forces General Hospital Kaohsiung 802301 Taiwan Institute of Molecular and Genomic Medicine National Health Research Institutes Miaoli Zhunan 350401 Taiwan Institute of Biotechnology and Pharmaceutical Research National Health Research Institutes Miaoli Zhunan 350401 Taiwan Department of Anesthesiology Chang Gung Memorial Hospital Taoyuan 333008 Taiwan Research Center for Chinese Herbal Medicine Graduate Institute of Healthy Industry Technology College of Human Ecology Chang Gung University of Science and Technology Taoyuan 333324 Taiwan Department of Chemical Engineering Ming Chi University of Technology New Taipei 243303 Taiwan Chinese Medicine Research and Development Center China Medical University Hospital Taichung 404394 Taiwan Graduate Institute of Natural Products Kaohsiung Medical University Kaohsiung 807378 Taiwan Ph.D. Program in Pharmaceutical Biotechnology Fu Jen Catholic University New Taipei City 242062 Taiwan

Two new 16-hydroxybriaranes, 11-dehydroxybriavioid B (1) and 12-epi-briastecholide L (2), have been isolated from an algal-containing octocoral identified as Briareum stechei. The structures of metabolites 1 and 2 were corroborated by extensive 2d-NMR studies and comparison with literature data. Briarane 2 was found to reduce the release of inducible nitric oxide synthase (iNOS) to 87.92 %, at a concentration of 10 μM. © 2023 ph.tochemical Society of Europe

关键词： Briarane Briareum stechei Briastecholide Briavioid iNOS

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A dual nociceptin and mu opioid receptor agonist exhibited robust antinociceptive effect with decreased side effects

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European Journal of Medicinal Chemistry 2023年第1期258卷 115608页

作者： Hsu, Ying-Ting Chen, Shen-Ren Chang, Yung-Chiao Chang, Hsiao-Fu Yeh, Teng-Kuang Chuang, Jian-Ying Loh, Horace H. Hsieh, Hsing-Pang Ueng, Shau-Hua Yeh, Shiu-Hwa Institute of Biotechnology and Pharmaceutical Research National Health Research Institutes Miaoli County 35053 Taiwan School of Pharmacy College of Medicine National Cheng Kung University Tainan 701 Taiwan The Ph.D. Program in Medical Neuroscience College of Medical Science and Technology Taipei Medical University and National Health Research Institutes Taipei 110 Taiwan Bioland Laboratory (Guangzhou Regenerative Medicine and Health Guangdong Laboratory) Guangzhou 10005 China Department of Pharmacology Medical School University of Minnesota Minneapolis 55455-0217 MN United States

The compelling demand of a consummate analgesic medication without addiction is rising due to the clinical mistreatment. Additionally, the series of severe untoward effects usually deterred the utilization while coping with serious pain. As a possible turning point, we revealed that compound 14 is a dual agonist of mu opioid receptor (MOR) and nociceptin-orph.nin FQ opioid peptide (NOP) receptor in this study. More importantly, compound 14 achieves pain relieving at very small doses, meanwhile, reduces several unwanted side effects such as constipation, reward, tolerance and withdrawal effects. Here, we evaluated the antinociception and side effects of this novel compound from wild type and humanized mice to further develop a safer prescription analgesic drug. © 2023 Elsevier Masson SAS

关键词： Addiction Antinociception Antinociceptive tolerance Constipation Mu-opioid receptor Reward effect

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The mitochondrial stress signaling tunes immunity from a view of systemic tumor microenvironment and ecosystem

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iScience 2024年第9期27卷

作者： Kuo, Cheng-Liang Lin, Ying-Chen Lo, Yu Kang Lu, Yu-Zhi Babuharisankar, Ananth Ponneri Lien, Hui-Wen Chou, Han-Yu Lee, Alan Yueh-Luen National Institute of Cancer Research National Health Research Institutes Miaoli Zhunan 35053 Taiwan Department of Life Sciences College of Health Sciences & Technology National Central University Taoyuan Zhongli 32001 Taiwan Ph.D. Program in Tissue Engineering and Regenerative Medicine College of Medicine National Chung Hsing University Taichung 40402 Taiwan Graduate Institute of Biomedical Sciences China Medical University Taichung 40402 Taiwan Department of Biotechnology College of Life Science Kaohsiung Medical University Kaohsiung 80708 Taiwan

Mitochondria play important roles in cell fate, calcium signaling, mitoph.gy, and the signaling through reactive oxygen species (ROS). Recently, mitochondria are considered as a signaling organelle in the cell and communicate with other organelles to constitute the mitochondrial information processing system (MIPS) that transduce input-to-output biological information. The success in immunotherapy, a concept of systemic therapy, has been proved to be dependent on paracrine interactions within the tumor microenvironment (TME) and distant organs including microbiota and immune components. We will adopt a broader view from the concept of TME to tumor micro- and macroenvironment (TM²E) or tumor-organ ecosystem (TOE). In this review, we will discuss the role of mitochondrial signaling by mitochondrial ROS, calcium flux, metabolites, mtdNA, vesicle transportation, and mitochondria-derived peptide in the TME and TOE, in particular immune regulation and effective cancer immunotherapy. © 2024 The Author(s)

关键词： Cancer Immune response Microenvironment

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Astrocytic Cebpd Regulates Pentraxin 3 Expression to Promote Fibrotic Scar Formation After Spinal Cord Injury

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Molecular neurobiology 2023年第4期60卷 2200-2208页

作者： Shao-Ming Wang Jung-Yu C Hsu Chiung-Yuan Ko Hsiang-En Wu Yu-Wei Hsiao Ju-Ming Wang Graduate Institute of Biomedical Sciences China Medical University Taichung 404333 Taiwan. wangs@mail.cmu.edu.tw. Neuroscience and Brain Disease Center China Medical University Taichung Taiwan. wangs@mail.cmu.edu.tw. Department of Neurology China Medical University Hospital Taichung Taiwan. wangs@mail.cmu.edu.tw. Department of Cell Biology and Anatomy College of Medicine National Cheng Kung University Tainan Taiwan. Ph.D. Program in Medical Neuroscience College of Medical Science and Technology Taipei Medical University Taipei Taiwan. TMU Research Center of Neuroscience Taipei Medical University Taipei Taiwan. TMU Research Center of Cancer Translational Medicine Taipei Taiwan. Cellular Pathobiology Section Integrative Neuroscience Research Branch Intramural Research Program National Institute on Drug Abuse NIH/DHHS Suite 3512 333 Cassell Drive Baltimore MD 21224 USA. Department of Biotechnology and Bioindustry Sciences College of Bioscience and Biotechnology National Cheng Kung University Tainan Taiwan. Department of Biotechnology and Bioindustry Sciences College of Bioscience and Biotechnology National Cheng Kung University Tainan Taiwan. yumingw@mail.ncku.edu.tw. Graduate Institute of Medical Sciences College of Medicine Taipei Medical University Taipei Taiwan. yumingw@mail.ncku.edu.tw. International Research Center for Wound Repair and Regeneration National Cheng Kung University Tainan Taiwan. yumingw@mail.ncku.edu.tw. Graduate Institute of Medicine College of Medicine Kaohsiung Medical University Kaohsiung Taiwan. yumingw@mail.ncku.edu.tw. Institute of Bioinformatics and Biosignal Transduction College of Bioscience and Biotechnology National Cheng Kung University Tainan 701 Taiwan. yumingw@mail.ncku.edu.tw.

Astroglial-fibrotic scars resulted from spinal cord injury affect motor and sensory function, leading to paralysis. In particular, the fibrotic scar is a main barrier that disrupts neuronal regeneration after spinal cord injury. However, the association between astrocytes and fibrotic scar formation is not yet understood. We have previously demonstrated that the transcriptional factor Cebpd contributes to astrogliosis, which promotes glial scar formation after spinal cord injury. Herein, we show that fibrotic scar formation was decreased in the epicenter region in Cebpd mice after contusive spinal cord injury and astrocytic Cebpd promoted fibroblast migration through secretion of Ptx3. Furthermore, the expression of Mmp3 was increased under recombinant protein Ptx3 treatment in fibroblasts by observing microarray data, resulting in fibroblast migration. In addition, regulation of Mmp3 occurs through the NFκB signaling pathway by using an irreversible inhibitor of IκBα ph.sph.rylation in pretreated fibroblasts. Of note, we used the synthetic peptide RI37, which blocks fibroblast migration and decreases fibroblast Mmp3 expression in IL-1β-treated astrocyte conditioned media. Collectively, our data suggest that fibroblast migration can be affected by astrocytic Cebpd through the Ptx3/NFκB/Mmp3 axis pathway and that the RI37 peptide may act as a therapeutic medicine to inhibit fibrotic scar formation after spinal cord injury.

关键词： Astrocyte Cebpd Fibrotic scar Ptx3 Spinal cord injury

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driverdBv4:ã multi-omics integration database for cancer driv er g ene resear c h

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Nucleic Acids Research 2024年第D1期52卷 D1246-D1252页

作者： Liu, Chia-Hsin Lai, Yo-Liang Shen, Pei-Chun Liu, Hsiu-Cheng Tsai, Meng-Hsin Wang, Yu-de Lin, Wen-Jen Chen, Fang-Hsin Li, Chia-Yang Wang, Shu-Chi Hung, Mien-Chie Cheng, Wei-Chung Cancer Biologyãnd Precision Therapeutics Center China Medical University Taichung 404328 Taiwan Department of Radiation Oncology China Medical University Taichung 404328 Taiwan Graduate Institute of Biomedical Sciences China Medical University Taichung 404328 Taiwan Department of Urology China Medical University Taichung 404328 Taiwan School of Medicine China Medical University Taichung 404328 Taiwan Institute of Nuclear Engineeringãnd Science National Tsing Hua University Hsinchu 300044 Taiwan Graduate Institute of Medicine College of Medicine Kaohsiung Medical University Kaohsiung 80708 Taiwan Department of Medical Laboratory Scienceãnd Biotechnology Kaohsiung Medical University Kaohsiung 80708 Taiwan Institute of Biochemistryãnd Molecular Biology China Medical University Taichung 404328 Taiwan Molecular Medicine Center China Medical University Hospital China Medical University Taichung 404328 Taiwan Department of Biotechnology Asia University Taichung 413305 Taiwan The Ph.D. program for Cancer Biologyãnd Drug Discovery China Medical Universityãnd Academia Sinica Taichung 404328 Taiwan

A dvãncements in high-throughput technology offer researchersãn e xtensiv e range of multi-omics data that provide deep insights into the complex landscape of cancer biology . However , traditional statistical modelsãnd databasesãre inadequate to interpret these high-dimensional data withinã multi-omics frame w ork. Toãddress this limitation, we introduce driverdBv4,ãn updated iteration of the driverdB cancer driver gene database ( http://driv *** ***/). T his updated v ersion offers se v eral significant enhancements: (i)ãn increase in the number of cohorts from 33 to 70, encompassingãpproximately 24 0 0 0 samples;(ii) inclusion of proteomics data,ãugmenting the existing types of omics dataãnd thus expanding theãnalytical scope;(iii) implementation of multiple multi-omicsãlgorithms for identification of cancer drivers;(iv) new visualization features designed to succinctly summarize high-context dataãnd redesigned existing sections toãccommodate the increased volume of datasetsãnd (v) two new functions in Customized Analysis, specifically designed for multi-omics driver identificationãnd subgroup e xpressionãnaly sis. driv erdBv4 fãcilitates comprehensiv e interpretãtion of multi-omics datããcross diverse cancer types, thereby enriching the understanding of cancer heterogeneityãndãiding in the de v elopment of personalized clinicalãpproaches. The database is designed to fosterã more nuanced understanding of the multi-faceted nature of cancer. © The Author(s) 2023.

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Biological Evaluation of Sulfonate and Sulfate Analogues of Lithocholic Acid: A Bioisosterism-Guided Approach Towards the discovery of Potential Sialyltransferase Inhibitors for Antimetastatic Study

SSRN

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SSRN 2023年

作者： Perez, Ser John Lynon P. Chen, Chia-Ling Chang, Tzu-Ting Li, Wen-Shan Institute of Chemistry Academia Sinica Taipei115 Taiwan Department of Applied Chemistry National Yang Ming Chiao Tung University Hsinchu300 Taiwan Sustainable Chemical Science and Technology Taiwan International Graduate Program Academia Sinica Taipei115 Taiwan Biomedical Translation Research Center Academia Sinica Taipei115 Taiwan Department of Medicinal and Applied Chemistry College of Life Science Kaohsiung Medical University Kaohsiung807 Taiwan Ph.D. Program in Drug Discovery and Development Industry College of Pharmacy Taipei Medical University Taiwan Doctoral Degree Program in Marine Biotechnology National Sun Yat-Sen University Kaohsiung804 Taiwan Department of Chemistry College of Science Tamkang University New Taipei City251 Taiwan

The naturally occurring bile acid lithocholic acid (LCA) has been a crucial core structure for many non-sugar-containing sialyltranferase (ST) inhibitors documented in literature. With the aim of elucidating the impact of the terminal carboxyl acid substituent of LCA on its ST inhibition, in this present study, we report the (bio)isosteric replacement-based design and synthesis of sulfonate and sulfate analogues of LCA. Among these compounds, the sulfate analogue SPP-002 was found to selectively inhibit N-glycan sialylation by at least an order of magnitude, indicating a substantial improvement in both potency and selectivity when compared to the unmodified parent bile acid. Molecular docking analysis supported the stronger binding of the synthetic analogue in the enzyme active site. Treatment with SPP-002 also hampered the migration, adhesion, and invasion of MdA-MB-231 cells in vitro by suppressing the expression of signaling proteins involved in the cancer metastasis-associated FAK/paxillin pathway. In totality, these findings offer not only a novel structural scaffold but also valuable insights for the future development of more potent and selective ST inhibitors with potential therapeutic effects against tumor cancer metastasis. © 2023, The Authors. All rights reserved.

关键词： Sulfur compounds

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Boron carbide decorated tungsten disulfide nanosheet composite for determination of chloramph.nicol in food and ph.rmaceutical samples

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Microchemical Journal 2024年 203卷

作者： Senthilkumar, dhayanithi Kuo, Chih-Yu Aldossari, Samar A. Govindasamy, Mani Department of Chemical Engineering and Biotechnology National Taipei University of Technology Taipei 10608 Taiwan Department of Chemistry P. O. Box 2455 College of Science King Saud University Riyadh 11451 Saudi Arabia Centre for Applied Research Saveetha School of Engineering Saveetha Institute of Medical and Technical Sciences (SIMATS) Tamil Nadu Chennai 602105 India International Ph.D. Program in Innovative Technology of Biomedical Engineering and Medical Devices Ming Chi University of Technology New Taipei City 243303 Taiwan Research Center for Intelligence Medical Devices Ming Chi University of Technology New Taipei City 243303 Taiwan

Making the nanocomposites of metal oxides or metal sulfides with carbon source materials has a huge impact on the electrochemical determination of toxic chemicals. To determine the adverse side effects of the antibiotics, electrochemical sensors have been used as they can peek into the sensitivity of the drug sample. This work has done the sensitive amperometric evaluation of a chloramph.nicol antibiotic by modifying the electrode of tungsten disulfide decorated boron carbide. Here, tungsten disulfide (WS₂) nanosheets and boron carbide (B₄C) materials were synthesized by conventional methods which give a good amount of yield. The composite was prepared by the green and cost-effective sonochemical approach with good morph.logy. The conductivity of the nanocomposite and the response to chloramph.nicol were determined by cyclic voltammetry. The sensitivity, limit of detection (LOd), and the linear range were observed by the highly sensitive amperometric technique. From the amperometric analysis, the prepared nanocomposite shows nominal LOd as a 17.4 nM, a broad linear range (0.025–1134.6 µM), and good sensitivity of 1.52 µA µM⁻¹ cm⁻². Practicability of the modified sensor was studied in food and ph.rmaceutical samples with adequate recovery performances. Moreover, the modified electrode shows good stability, repeatability, reproducibility, and anti-interfering properties against the array of food and biological interferences. © 2024 Elsevier B.V.

关键词： Amperometric technique Antibiotic detection Boron carbide Food quality test Health analysis Tungsten disulfide

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