Yongdong Jin’s research while affiliated with State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry and other places

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Publications (134)


Label-Free Exosomal SERS Detection Assisted by Machine Learning for Accurately Discriminating Cell Cycle Stages and Revealing the Molecular Mechanisms during the Mitotic Process
  • Article

February 2025

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14 Reads

Analytical Chemistry

Xingkang Diao

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Xinli Li

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Yongdong Jin


Smart and Noninvasive SERS Immunosensors for Monitoring Dynamic Expression of Cytokines during Cell Pyroptosis

January 2025

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4 Reads

Analytical Chemistry

Accompanying with the occurrence of inflammatory reaction to release cytokine, pyroptosis can activate immune response for resistance against cancer. Consequently, elevated levels of cytokine released by cancer cells are highly correlated with the effectiveness of cancer treatment. Herein, a non-invasive surface-enhanced Raman spectroscopy (SERS) immunosensor was developed to sensitively and specifically measure the tumor necrosis factor-α (TNF-α), a proinflammatory cytokine, during cell pyroptosis process. The sandwiched structure of the sensor is functionalized with TNF-α binding antibody for detecting TNF-α at concentrations as low as 1 pg/mL. Importantly, electrical stimulation (ES) can fleetly trigger cancer cell pyroptosis to induce overexpression of receptor interacting protein 3 (RIP3), which is a significant protein that regulates the inflammatory response. The overexpression RIP3 can activate caspase-1 to promote the up-regulation of cytokine levels. Notably, the cytokine levels of TNF-α released from cancer cells (MCF-7 cells) were apparently higher than normal cell (MCF-10A cells) during pyroptosis detected by the SERS immunosensors. Due to its obvious superiorities of simple fabrication and fast readout without sample pretreatment, the developed SERS platform has the potential application value for diagnosis and treatment of cancer.



(a) The approximate equivalent circuit proposed for the explanation of the nanofluidic unijunction transistor, CE1 and CE2 are the double-layer capacitors of the electrodes inside and outside the orifice of nanopipette, respectively; ZE1 and ZE2 are the corresponding Faraday impedances; RS1 and RS2 are the corresponding resistances of the electrolyte solution, and UJT represents the unijunction transistor. (b) SEM image of the orifice of the bare glass nanopipette. (c) Current–voltage curves of the bare glass nanopipette and PDA-coated glass nanopipette, recorded in 0.1 M KCl solution (pH = 7.5). (d) SEM image of the PDA-coated glass nanopipette. (e) Current–voltage curves of the tested nanopipettes, curve (i): modified with PDA but without Cu²⁺ ions; curve (ii): modified with PDA but without Cu²⁺ ions, and with 0.1 M Cu²⁺ ions during the test; curve (iii): modified with PDA but without Cu²⁺ ions, and with 1 M Cu²⁺ ions during the test; curve (iv): modified with PDA and Cu²⁺ ions for 1 day (all tested in 0.1 M KCl solution, pH = 7.5). (f) A flashing rachet model proposed for the explanation of the unijunction transistor with NDR and ICO phenomena. The spheres represent charge carriers and “on” and “off” represent the state of the potential profile.
(a) Time-evoluted ionic current recording of the P-nanopipette. Test condition: 0.1 M KCl solution (pH = 7.5). (b) Statistics of the ionic current oscillation recorded in (a). (c) Time-evoluted ionic current recordings of the nanopipette in the absence of Cu²⁺ ions (i), and with added 0.1 M (ii) and 1 M (iii) Cu²⁺ ions inside the nanopipettes. The units in the ordinate represent the current (pA). Test condition: 0.1 M KCl solution (pH = 7.5). (d) Time-evoluted ionic current recording of nanopipettes doped with 1 M Fe³⁺ ions (i) and La³⁺ ions (ii), the ionic current of the P-nanopipette under the electrolyte at pH = 3.30 condition (iii), and without ethanol treatment (iv). The units in the ordinate represent the current (pA). For curves (i), (ii), and (iv), the test condition: 0.1 M KCl solution (pH = 7.5). (e) The ionic current of the P-nanopipette under the electrolyte condition at pH = 9.27. (f) Corresponding PSD of the bare glass nanopipette (black) and P-nanopipette (red). Test condition: 0.1 M KCl solution (pH = 7.5).
(a) The constructed geometric model for the time-dependent simulation, note that the annular curve around the tip was the grid auxiliary line to improve the mesh quality so that the results would be converged, the unit of length: μm. The legend on the right represents potential (V). (b)–(d) Simulated I−V curves of the P-nanopipette with different electrolyte solutions of 0.01 M (b), 0.1 M (c), and 1 M (d) KCl. (e) Simulated I−V curves of the P-nanopipette with different PDA filling thicknesses. (f) Simulated I−V curves of the P-nanopipette with three different volume charge densities of the surface coating.
(a) Simulated distribution of K⁺ ions in the nanopipette channel with different applied voltages of (i) –0.5 V, (ii) 0 V, (iii) 0.3 V, and (iv) 0.5 V. The legend on the right represents concentration (mM). (b) Simulated distribution of Cl– ions in the nanopipette channel with a different applied voltage of (i) –0.5 V, (ii) 0 V,(iii) 0.3 V, and (iv) 0.5 V. The legend on the right represents concentration (mM). (c) and (d) Experimental and simulated results of the current fluctuation of the nanopore nanofluidic device over time.
Schematic illustration of PDA deposition onto the outer surface of the glass nanopipette (up) and the chemical formation process of the PDA doped with copper ions (down) consisting of (1) the auto-oxidation of dopamine, (2) cyclization, (3) oxidation, (4) isomerization, and (5) self-assembly and complexation with copper ions through phenol hydroxyl groups.
Bioinspired polydopamine coated nanopore nanofluidic unijunction transistor exhibiting negative differential resistance and ion current oscillation
  • Article
  • Full-text available

November 2024

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20 Reads

Nanofluidic devices have turned out to be exemplary systems for investigating fluidic transport properties in a highly restricted area, where the electrostatic interactions or chemical reactions between nanochannel and flowing species strongly dominate the ions and flow transport. Numerous nanofluidic devices have recently been explored to manipulate ion currents and construct electronic devices. Enlightened by electronic field effect transistors, utilizing the electric field effect of nanopore nanochannels has also been adopted to develop versatile nanofluidic devices. Here, we report a nanopore-based nanofluidic unijunction transistor composed of a conical glass nanopipette with the biomaterial polydopamine (PDA) coated at its outer surface. The as-fabricated nanofluidic device exhibited negative differential resistance (NDR) and ion current oscillation (ICO) in ionic transport. The pre-doped copper ions in the PDA moved toward the tip as increasing the potential, having a robust shielding effect on the charge of the tip, thus affecting the surface charge density of the nanopore in the working zone. Finite element simulation based on a continuum model coupled with Stokes–Brinkman and Poisson–Nernst–Planck (PNP) equations revealed that the fluctuations in charge density remarkably affect the transport of ionic current in the nanofluidic device. The as-prepared nanofluidic semiconductor device was a ready-to-use equipment that required no additional external conditions. Our work provides a versatile and convenient way to construct nanofluidic electronic components; we believe by taking advantage of advanced surface modification methods, the oscillation frequency of the unijunction transistors could be controlled on demand, and more nanofluidic devices with resourceful functions would be exploited.

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Electrostimulation Evokes Caspase-3-Activated Fast Cancer Cell Pyroptosis and Its Nuclear Stress Response Pathways

August 2024

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20 Reads

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4 Citations

Analytical Chemistry

Pyroptosis of programmed cell death has been recognized as a more effective way to inhibit the occurrence and development of tumors than the better-studied apoptosis. However, it is still challenging to quickly and effectively trigger pyroptosis of cancer cells for high-efficacy cancer treatment. Here, we report on the first use of mild constant-potential electrostimulation (cp-ES) to quickly trigger cancer-cell pyroptosis with a probability up to 11 ∼91.4% and significantly shortened time (within 1 h), ∼3−6 times faster than typical drug stimulation to induce pyroptosis. We find that the ES-induced cancer-cell pyroptosis is through the activated caspase-3 (pathway) cleavage of gasdermin E (GSDME) to form an N-terminal fragment (GSDME-N) and observe nuclear shrinkage and reduction of the number of nucleoli as well as down-/up regulated expression of two important nucleoproteins of nucleolin and nucleophosmin (NPM1). The study enriches the basic understanding of pyroptosis and provides a new avenue for potential effective treatment of cancer.





Ionic gel based eT-patch for subcutaneous tumor therapy
Schematic illustration of the biological eT-patch prepared from ionic gel doped with MXene and their application for skin tumor therapy under synergistic photothermal and electrical stimulation.
Characterizations of photothermal agents MXene and ionic gels
TEM image (a), SEM image (b), and AFM image and line-scan height analysis (c) of the Ti3C2Tx, respectively. d X-ray diffraction of the Ti3AlC2 and Ti3C2TX. e High-resolution X-ray photoelectron spectroscopy spectra of the Ti 2p region of Ti3C2Tx nanoflakes. f UV-Vis absorbance spectrum of the liquid exfoliated Ti3C2Tx nanoflakes dispersion solution. g SEM image of the MXene doped ionic gels. h Energy-dispersive spectroscopy of the ionic gels. i SEM elemental mapping analyses of the eT-patch. The experiments were repeated for three times with similar results obtained.
ET-patch performance measurement
a Photograph of an ionic gel patch during stretching. Typical stress-strain curves (b) and toughness (c) of the patch doped with different concentrations of MXene (n = 3). d Cycling temperature profile for the eT-patch doped with 0.8 mg/mL MXene under 808 nm laser irradiation at 0.5 W/cm². Thermal images (e) and temperature versus time curves (f) for the eT-patch and pure ionic gel patches without MXene doping under Laser, ES, Laser and ES simultaneous stimulation, respectively. Current-voltage curves (g) and the corresponding current values (h) at 5 V of ionic gel patches doped with MXene of different concentrations (n = 5). i Current-time curves for the eT-patches and pure ionic gel patches under the off/on of 808 nm laser irradiation. Data are presented as mean ± SD.
Mechanism study of PES for inducing cell death
a Live/dead staining fluorescence images of B16F10 cells after the different treatments (Control, Laser, MXene, PTT, ES, and PES). The scale bar is 100 μm. b Cell viability of B16F10 cells after the different treatments. P values were calculated by two-tailed t-tests. (n = 3). c, RT-PCR analyses of Caspase-3, GSDME, IL-1β, Bax, c-Jun, Cyt-c expression within B16F10 cells before and after the PES treatments t (n = 4). d The lactate dehydrogenase (LDH) release levels from B16F10 cells after the treatments under different conditions. P values were calculated by two-tailed t-tests. (n = 3). e ATP content change within B16F10 cells under the same cell number after different treatments tested using the ATP assay kit. P values were calculated by two-tailed t-tests. (n = 3). f Bio-TEM images of B16F10 cells before and after the PES treatments. “M” represents mitochondria, “N” represents cell nucleus. g Fluorescence images of ROS within B16F10 cells detected using the DCFH-DA probe after the different treatments. The scale bar is 50 μm. h The fluorescence images of the JC-1 monomer and aggregate, and their merged images within B16F10 cells stained by JC-1 after the different treatments. The scale bar is 50 μm. i Fluorescence images of DNA double-strand breaks within B16F10 cells after the different treatments (corresponding to red fluorescence of γ-H2AX) followed by DAPI staining (corresponding to blue fluorescence). The scale bar is 50 μm. The experiments were repeated for three times with similar results obtained. Data are presented as mean ± SD.
In vivo treatment with melanoma model
a Schematic diagram of B16F10 tumor-bearing mice model establishment and therapeutic procedures. b Thermal images of tumor-bearing mice under different treatments during different time. c Representative photographs of the tumor-bearing mice during the various treatment procedures under different days (5th, 10th, and 15th days). The red circle represents melanoma. d Photographs of tumors dissected from mice at 15th day of each treatment (Control, Laser, PTT, ES, and PES). e, f Tumor weights and relative volume of tumors dissected from each group after therapy for 15 days. P values were calculated by two-tailed t-tests. (n = 3). g The body weight curves of tumor-bearing mice in different groups. (n = 3). h H&E, Tunel, Ki-67, GSDME and caspase-3 staining of tumor tissues collected from the corresponding mice at 15th day of each treatment. The scale bar is 100 μm. The experiments were repeated for three times with similar results obtained. The experiments were repeated for three times with similar results obtained. Data are presented as mean ± SD.
A wearable electrostimulation-augmented ionic-gel photothermal patch doped with MXene for skin tumor treatment

January 2024

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78 Reads

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31 Citations

A wearable biological patch capable of producing multiple responses to light and electricity without interfering with daily activities is highly desired for skin cancer treatment, but remains a key challenge. Herein, the skin-mountable electrostimulation-augmented photothermal patch (eT-patch) comprising transparent ionic gel with MXene (Ti3C2Tx) doping is developed and applied for the treatment of melanoma under photostimulation at 0.5 W/cm². The eT-patch designed has superior photothermal and electrical characteristics owing to ionic gels doped with MXene which provides high photothermal conversion efficiency and electrical conductivity as a medium. Simultaneously, the ionic gel-based eT-patch having excellent optical transparency actualizes real-time observation of skin response and melanoma treatment process under photothermal and electrical stimulation (PES) co-therapy. Systematical cellular study on anti-tumor mechanism of the eT-patch under PES treatment revealed that eT-patch under PES treatment can synergically trigger cancer cell apoptosis and pyroptosis, which together lead to the death of melanoma cells. Due to the obvious advantages of relatively safe and less side effects in healthy organs, the developed eT-patch provides a promising cost-effective therapeutic strategy for skin tumors and will open a new avenue for biomedical applications of ionic gels.


Citations (82)


... When exosomal miRNAs of cancer cells and normal cells were analyzed, exosomes derived from cancer cells were richer in miRNAs. In addition, exosomal miRNA levels were found to increase when cells were subjected to electrical stimulation [81]. miRNA-seq was performed on urinary exosomes from renal-cell carcinoma patients and healthy controls, and an increased expression of miR-542-5p and decreased expression of miR-320a were observed in cancer patients [82]. ...

Reference:

Recent Exploration of Solid Cancer Biomarkers Hidden Within Urine or Blood Exosomes That Provide Fundamental Information for Future Cancer Diagnostics
Electroactivated SERS Nanoplatform for Rapid and Sensitive Detection and Identification of Tumor-Derived Exosome miRNA
  • Citing Article
  • November 2024

Analytical Chemistry

... Additionally, MX's large surface area and tunable chemistry allow for facile functionalization and loading of therapeutic agents [ 21 ] as a platform for dual-mode cancer therapy [ 22 , 23 ]. For examples, MX was used for the photothermal and electrical stimulation co-therapy [ 24 ], PTT and enzymatic dynamic therapy accompanied by photoacoustic imaging [ 25 ], and synergistic sonodynamic/chemo dynamic therapy [ 26 ]. However, the direct use of MX in cancer therapy has been limited by challenges such as the aggregation in the physiological environment, the reduced stability, and the difficulty in combining its photothermal properties with long termcontrolled drug delivery [ 27 ]. ...

A wearable electrostimulation-augmented ionic-gel photothermal patch doped with MXene for skin tumor treatment

... Traditional studies of this kind mostly focused on the modification of the inner channel wall of the nanopores, since they come into contact with the transported ions directly and are easily manipulated to regulate the transmission behaviors. Although the deposition of a layer of metal such as gold on the outer surface of solid-state nanopores followed by grafting nucleic acids or metal-organic framework on the metal layer has been implemented in some studies to improve detection sensitivity [36−38], the contribution of the elements on the outer surface of glass nanopipette was always ignored [39] and has not been exploited for the design of potential new nanofluidic devices. So far, most nanofluidic devices with complex functions and modification steps were concentrated on polyethylene terephthalate (PET) nanopores or carbon nanotubes, while for the glass nanopipettes, they function only by simply changing the solution conditions [17]. ...

Dual-signal readout sensing of ATP content in single dental pulp stem cells during differentiation via functionalized glass nanopipettes
  • Citing Article
  • March 2024

Analytica Chimica Acta

... There was an urgent need to develop new candidate drugs for the treatment of esophageal cancer. NCL was a multifunctional nuclear protein that was overexpressed in the cell membrane, cytoplasm, and nucleus of cancer cells and played an important role in regulating the physiological activities of cells [26]. Considering the key role of NCL in cancer development, some studies have studied NCL as a key receptor for therapeutic agents and imaging probes. ...

“Light-On” Fluorescent Nanoprobes for Monitoring Dynamic Distribution of Cellular Nucleolin During Pyroptosis
  • Citing Article
  • December 2023

Analytical Chemistry

... 75 Concerning the combination of NIR and ES, a Ti 3 C 2 T x acid acrylic ionic gel enhanced skin wound healing due to combined NIR antibacterial effects on E. coli and S. aureus and increased cell migration due to ES in infected mice. 74 In this study, while the inflammation and necrotic tissue were evident in the wounds in the control, only the combined ES and PTT, decreased the margins of the wound with enhanced collagen deposition, lower expression of TNF-α and upregulation of FGF-2. ...

Photoelectric-driven conductive composite ionogel patch for effective wound healing
  • Citing Article
  • December 2023

eScience

... [37,38] Previous studies have shown that the concentration of miRNA-21 is rising during the apoptosis process of tumor cells. [39] Therefore, we designed DNA probe (MB-21) with miRNA-21 dectection ability to verify the capability of USD to induce apoptosis ( Figure S22 and S23), and the results were validated using standard RT-qPCR test (Figure S24). The results confirmed a significant upregulation of miRNA content in HeLa cells treated with USD plus NIR, demonstrating the ability of USD to promote apoptosis. ...

Glass Nanopipette-Based Plasmonic SERS Platform for Single-Cell MicroRNA-21 Sensing during Apoptosis
  • Citing Article
  • October 2023

Analytical Chemistry

... Metal-organic frameworks (MOFs) offer significant advantages over other nanocarriers used for cancer treatment. They possess a highly porous structure, allowing for high drug loading capacity and controlled release, which is crucial for targeted therapy [14]. Our platform utilizes the photodynamic and photothermal properties of this composite MOFs, which then enhanced by copper doping and gold nanoparticle decoration [15,16]. ...

Atomically Fe‐anchored MOF‐on‐MOF nanozyme with differential signal amplification for ultrasensitive cathodic electrochemiluminescence immunoassay

... Monitoring the dynamic changes of active components within a biological system is crucial in drug development. SERS technology, with its high temporal resolution, is particularly suited for real-time monitoring of molecular dynamics [71,72]. This includes processes such as absorption, distribution, metabolism, and excretion (ADME) of drugs [73]. ...

Machine Learning-Based Label-Free SERS Profiling of Exosomes for Accurate Fuzzy Diagnosis of Cancer and Dynamic Monitoring of Drug Therapeutic Processes
  • Citing Article
  • May 2023

Analytical Chemistry

... Table S1 (in Supplementary Materials) summarizes the comparison between Trolox detection performance using different methods [12,19,[52][53][54]. The LOD obtained using the fabricated sensor is lower than that obtained by differential pulse voltammetry (DPV) detection using a copper-neocuproine complex ([Cu(Nc) 2 ] 2+ ) probe [52], or a square-wave voltammetry (SWV) detection using a 2,2-diphenyl-1-picrylhydrazyl (DPPH) probe [19], or electrochemiluminescence (ECL) detection based on luminol emitter [53,54], or colorimetric detection using Fe(III)(phen) 3 probe [12]. Thus, the fabricated sensor also has advantages of convenient fabrication, simple detection, and high sensitivity, demonstrating great potential for TAC determination. to measure the electrochemical oxidation current of Fe(II)(phen)3 using chronoamperometry. ...

Integration of High-Entropy Oxide with Nitrogen-Doped Graphene for the Ultrasensitive Electrochemiluminescence Detection of Trolox and Dopamine
  • Citing Article
  • March 2023

ACS Applied Nano Materials

... Based on the literature, it has been observed that tumor cells exhibit a comparatively higher susceptibility to external stimulation than normal cells, particularly with regards to their cytoskeletal structure [197]. For instance, Jin's group from State Key Laboratory of Electroanalytical Chemistry of Chinese Academy of Sciences [198] demonstrated that electrostimulation (ES) significantly inhibits glucose and energy metabolism in cancer cells, resulting in rapid cell death (Figure 8A-C). From a mechanical perspective, ES leads to cytoskeletal disruption (Figure 8D), which reduces the Young's modulus of MCF-7 cell membranes ( Figure 8E) due to the depolymerization of F-actin and the down regulation and irregular distribution of glucose transporter 1 (GLUT1) (Figure 8F). ...

Molecular/Nanomechanical Insights into Electrostimulation-Inhibited Energy Metabolism Mechanisms and Cytoskeleton Damage of Cancer Cells