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学者姓名：陈海军
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Abstract ：
Heptamethine indocyanine dyes (HMICDs) have excellent near-infrared (NIR) properties and are capable of converting light energy into heat energy under NIR laser irradiation, enabling their use in photothermal therapy (PTT) of tumors. However, their photostability is poor, and they are easily inactivated by photobleaching after prolonged and repeated exposure to NIR laser. In addition, unmodified HMICDs have poor water solubility and tend to aggregate, limiting their biological applications. Herein, we designed and synthesized HMICDs with hydrophilic side chains and different substituent groups on polymethine chain, and explored the effects of these modifications on the water solubility, photostability and photothermal properties of the dyes. The introduction of tri-ethylene glycol hydrophilic side chains can improve the water solubility of HMICDs, and enhance the photostability and photothermal properties by increasing the spatial hindrance of the dyes. Furthermore, the incorporation of substituents with strong electron-withdrawing ability into the polymethine chain can improve the photostability and photothermal effect of the dyes. Under laser irradiation, the dyes can inhibit the proliferation of tumor cells by enhancing intracellular reactive oxygen species levels, decreasing mitochondrial membrane potential, and inducing cell apoptosis. In two tumor-bearing mouse models, dye 11 can effectively inhibit tumor growth by exerting photothermal effects with good biosafety. This work can provide a research foundation for the subsequent construction of HMICDs-based photothermal therapeutic agents for clinical applications.
Keyword ：
Heptamethine indocyanine dyes Heptamethine indocyanine dyes Photostability Photostability Photothermal therapy Photothermal therapy Water solubility Water solubility
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| GB/T 7714 | Shen, Xinyi , Yu, Jing , Chen, Tingyan et al. Structural modification of heptamethine indocyanine dyes with improved aqueous solubility and stability for photothermal therapy [J]. | EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY , 2025 , 290 . |
| MLA | Shen, Xinyi et al. "Structural modification of heptamethine indocyanine dyes with improved aqueous solubility and stability for photothermal therapy" . | EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY 290 (2025) . |
| APA | Shen, Xinyi , Yu, Jing , Chen, Tingyan , Sun, Xianbin , Long, Haixin , Du, Manyi et al. Structural modification of heptamethine indocyanine dyes with improved aqueous solubility and stability for photothermal therapy . | EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY , 2025 , 290 . |
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The challenging treatment outcomes for nonsmall cell lung cancer (NSCLC) necessitate the development of innovative therapeutic strategies. In this work, we developed a multifunctional nanoplatform by modifying mesoporous silica nanoparticles (MSNs) with an aptamer (Apt) targeting epidermal growth factor (EFGR), and coloading a sonosensitizer, hematoporphyrin (HP), along with the natural nitric oxide (NO) donor, l-arginine (l-Arg). The resulting Apt-modified MSN loaded with l-Arg and HP (designated as AMLH) was designed for the targeted gas-assisted sonodynamic therapy (SDT) of NSCLC. AMLH exhibited an appropriate particle size, good drug loading ability, and ultrasound-responsive drug release. The coloading of HP and l-Arg resulted in higher encapsulation efficiency compared to single-drug loading, and AMLH remained stable when stored at 4 degrees C for 15 days. AMLH was capable of generating reactive oxygen species (ROS) and NO under ultrasound stimulation, leading to the further production of peroxynitrite (ONOO-). AMLH demonstrated specific targeting and recognition of EGFR-positive NSCLC cells, with preincubation of free Apt reducing cellular uptake, confirming the specificity of the Apt-functionalized nanoparticles. Cellular distribution studies revealed that AMLH was primarily localized in lysosomes after internalization. MTT assays and live/dead cell staining confirmed the superior cytotoxicity of AMLH, which effectively inhibits cell proliferation through mitochondrial membrane potential collapse and nuclear damage under ultrasound stimulation. These results highlight the combined efficacy of EGFR targeting, SDT, and NO gas therapy, offering a promising strategy to improve the NSCLC treatment outcomes.
Keyword ：
aptamer aptamer nitricoxide nitricoxide nonsmallcell lung cancer nonsmallcell lung cancer peroxynitrite peroxynitrite sonodynamic therapy sonodynamic therapy
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| GB/T 7714 | Zheng, Fangying , Zhang, Peixia , Zhang, Yinglu et al. Aptamer-Modified Mesoporous Silica Nanoparticle for Nitric Oxide-Enhanced Targeted Sonodynamic Therapy against Lung Cancer [J]. | ACS APPLIED NANO MATERIALS , 2025 , 8 (10) : 5179-5192 . |
| MLA | Zheng, Fangying et al. "Aptamer-Modified Mesoporous Silica Nanoparticle for Nitric Oxide-Enhanced Targeted Sonodynamic Therapy against Lung Cancer" . | ACS APPLIED NANO MATERIALS 8 . 10 (2025) : 5179-5192 . |
| APA | Zheng, Fangying , Zhang, Peixia , Zhang, Yinglu , Long, Haixin , Zhu, Fangyin , Chen, Haijun et al. Aptamer-Modified Mesoporous Silica Nanoparticle for Nitric Oxide-Enhanced Targeted Sonodynamic Therapy against Lung Cancer . | ACS APPLIED NANO MATERIALS , 2025 , 8 (10) , 5179-5192 . |
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The physical and chemical properties of gold nanoparticles can significantly influence their anti-tumor efficacy. Streamlining synthesis methods to modulate these properties and enhance therapeutic effects could facilitate their translation into clinical applications. This study presents a new approach to synthesize small alkynylmodified gold nanoparticles (Alk-GNP) at room temperature using sodium citrate and propiolic acid (PA) to reduce chloroauric acid. The resulting Alk-GNP, approximately 11 nm in size with narrow dispersion, contrasts with larger gold nanoparticles (GNP) synthesized by the classical Turkevich method using boiling water. Subsequently, a round composite (CHAM) was developed using chitosan and hyaluronic acid to co-deliver Alk-GNP and the photosensitizer methylene blue for synergistic treatment. CHAM showed excellent stability and strong CD44-positive tumor targeting capabilities. It significantly boosted photothermal activity and reactive oxygen species generation compared to current GNP-based formulations. In tumor-bearing mouse models, CHAM effectively localized in tumor tissue and exhibited potent photothermal and photodynamic therapeutic effects to inhibit tumor growth while ensuring safety. The robust data presented in this study supports the potential translation of this approach, offering a simplified preparation process and improved tumor treatment efficacy.
Keyword ：
Alkynyl-modified gold nanoparticles Alkynyl-modified gold nanoparticles Chitosan/hyaluronic acid co-carriers Chitosan/hyaluronic acid co-carriers Phototherapy Phototherapy
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| GB/T 7714 | Tan, Ding , Long, Haixin , Du, Manyi et al. Fabrication of a nanoplatform based on chitosan and hyaluronic acid containing alkyne-functionalized gold nanoparticles for tumor targeted synergistic phototherapy [J]. | INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES , 2025 , 309 . |
| MLA | Tan, Ding et al. "Fabrication of a nanoplatform based on chitosan and hyaluronic acid containing alkyne-functionalized gold nanoparticles for tumor targeted synergistic phototherapy" . | INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES 309 (2025) . |
| APA | Tan, Ding , Long, Haixin , Du, Manyi , Yu, Jing , Sun, Xianbin , Wang, Ya et al. Fabrication of a nanoplatform based on chitosan and hyaluronic acid containing alkyne-functionalized gold nanoparticles for tumor targeted synergistic phototherapy . | INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES , 2025 , 309 . |
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Ferrocene, known for its 'sandwich' structure and Fenton catalytic activity for tumor treatment, its twodimensional (2D) self-assembly has not yet been exploited for therapeutic applications. Perfluorocarbons (PFCs) can carry and transport oxygen to alleviate tumor hypoxia. Nevertheless, designing ferrocene derivatives with PFC chains to alleviate tumor hypoxia and improve cancer treatment remains a challenge. Here, we first synthesized ferrocene derivatives with different PFC chains (nF-Fc, n = 5, 9, 13) by conjugating perfluorocarbonic acids with 2-(ferrocenylethynyl)aniline (Fc). These derivatives were able to self-assemble into 2D nanosheets, with hydrated particle size decreasing as the chain length increased. The chain lengths also influenced the oxygen-carrying capacity, iron release capacity, and glutathione consumption capacity, all of which impacted their ability to alleviate tumor hypoxia, produce intracellular reactive oxygen species, and enhance chemodynamic therapeutic efficacy. Notably, PFC incorporation altered the mechanism of induced cell death. By elucidating the effects of ferrocene derivatives with different PFC chains on the hypoxic tumor microenvironment (TME) and their therapeutic efficacy, this research advances the development of ferrocene-based 2D materials for cancer treatment and offers a novel approach to optimize compound structures better regulation of the hypoxic TME, ultimately improving therapeutic outcomes.
Keyword ：
Anti-tumor Anti-tumor Ferrocene derivatives Ferrocene derivatives Perfluorocarbon chains Perfluorocarbon chains Tumor hypoxia Tumor hypoxia Two-dimensional nanosheets Two-dimensional nanosheets
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| GB/T 7714 | Wang, Ya , Tan, Ding , Zheng, Fangying et al. Oxygen self-supplying perfluorocarbon-functionalized ferrocene nanosheets for enhanced cancer chemodynamic therapy [J]. | MATERIALS TODAY CHEMISTRY , 2025 , 45 . |
| MLA | Wang, Ya et al. "Oxygen self-supplying perfluorocarbon-functionalized ferrocene nanosheets for enhanced cancer chemodynamic therapy" . | MATERIALS TODAY CHEMISTRY 45 (2025) . |
| APA | Wang, Ya , Tan, Ding , Zheng, Fangying , Sun, Xianbin , Li, Xudong , Zheng, Yilin et al. Oxygen self-supplying perfluorocarbon-functionalized ferrocene nanosheets for enhanced cancer chemodynamic therapy . | MATERIALS TODAY CHEMISTRY , 2025 , 45 . |
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Despite significant advances in diverse cancer treatment methods, chemotherapy remains the primary approach, and the development of chemoresistance is still a persistent problem during treatment. Here, we developed a derivative of the natural product mangiferin as a carrier for delivering chemotherapeutic drug, aiming to overcome drug resistance through a distinctive four-pronged strategy, including modulation of inflammatory tumor microenvironment (TME), induction of ferroptosis, deep tumor penetration, and the combinatory anticancer effects. After clarifying the promotion effects of the cancer associated fibroblasts (CAFs) in chemoresistance, and leveraging our previous elucidation of the anti-inflammatory and ferroptosis-inducing ability of mangiferin, we synthesized mangiferin amphiphile (MMF) and developed a self-assembled carrier-free nanomedicine, named MP, through the self-assembly of MMF and the representative chemotherapeutic drug paclitaxel (PTX). MP possessed a particle size of approximately 68 nm with compact filamentous nanostructures. MP demonstrated efficient tumor-targeting and deep tumor penetration abilities. Furthermore, MP effectively suppressed glutathione peroxidase 4 (GPX4) expression to induce ferroptosis, mitigated the activation of IL-6/STAT3 pathway to deactivate CAFs within the inflammatory TME, and exhibited robust anti-cancer effects against PTXresistant breast cancer both in vitro and in vivo. This mangiferin derivative represents a promising "all-in-one" nanocarrier for delivering chemotherapeutic drugs, offering a green, safe, and convenient self-assembled carrierfree nanomedicine to effectively overcome drug resistance.
Keyword ：
CAFs CAFs Carrier-free nanomedicine Carrier-free nanomedicine Drug resistance Drug resistance Ferroptosis Ferroptosis Inflammatory tumor microenvironment Inflammatory tumor microenvironment
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| GB/T 7714 | Zheng, Yilin , Xu, Ruofei , Chen, Tingyan et al. Four-pronged reversal of chemotherapy resistance by mangiferin amphiphile [J]. | JOURNAL OF CONTROLLED RELEASE , 2025 , 378 : 776-790 . |
| MLA | Zheng, Yilin et al. "Four-pronged reversal of chemotherapy resistance by mangiferin amphiphile" . | JOURNAL OF CONTROLLED RELEASE 378 (2025) : 776-790 . |
| APA | Zheng, Yilin , Xu, Ruofei , Chen, Tingyan , Wang, Ya , Chen, Xiaoye , Chen, Haijun et al. Four-pronged reversal of chemotherapy resistance by mangiferin amphiphile . | JOURNAL OF CONTROLLED RELEASE , 2025 , 378 , 776-790 . |
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Reactive oxygen species (ROS)-based nanodynamic therapy is emerging as a promising approach for tumor treatment, particularly in eliciting immune responses for tumor immunotherapy. Nevertheless, the complex tumor microenvironment (TME) and the constraints of current sensitizers substantially compromise therapeutic efficacy. To address these challenges, we developed a rationally designed nanoplatform (LP/CuTT) through lipoic acid-modified orchestrated Cu-2(+)-coordinated tetracycline-porphyrin self-assembly, to precisely remodel the immunosuppressive TME while potentiating antitumor immunotherapy via a novel photo-enhanced chemodynamic therapy (CDT) strategy. In vitro studies demonstrated that LP/CuTT-mediated photo-enhanced CDT effectively promoted concurrent apoptosis and cuproptosis in B16-F10 melanoma cells, coupled with robust induction of immunogenic cell death (ICD). Mechanistic investigations revealed that LP/CuTT drives macrophage polarization from tumor-promoting M2 to antitumor M1 phenotypes while promoting dendritic cell (DC) maturation, thereby orchestrating potent antitumor immune responses. In vivo evaluations showed preferential tumor accumulation of LP/CuTT, correlating with substantial ROS generation at tumor sites and remarkable therapeutic outcomes. Quantitative assessments further demonstrated elevated M1 macrophage infiltration in both tumor and splenic tissues, accompanied by enhanced CD8(+) and CD4(+) T cell recruitment. These findings provide key insights into developing orchestrated metal-coordinated nanotherapeutics by repurposing existing therapeutic agents, enabling the design of multifunctional systems that integrate efficient chemodynamic activity, TME remodeling, and immune activation for effective nanodynamic therapy.
Keyword ：
Chemodynamic therapy Chemodynamic therapy Cuproptosis Cuproptosis Immunogenic cell death Immunogenic cell death Orchestrated coordination Orchestrated coordination Tumor microenvironment Tumor microenvironment
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| GB/T 7714 | Sun, Xianbin , Wang, Xinyi , Li, Xudong et al. Orchestrated Cu2+-coordinated tetracycline-porphyrin self-assembly remodels tumor microenvironment for photo-enhanced immuno-chemodynamic therapy [J]. | JOURNAL OF NANOBIOTECHNOLOGY , 2025 , 23 (1) . |
| MLA | Sun, Xianbin et al. "Orchestrated Cu2+-coordinated tetracycline-porphyrin self-assembly remodels tumor microenvironment for photo-enhanced immuno-chemodynamic therapy" . | JOURNAL OF NANOBIOTECHNOLOGY 23 . 1 (2025) . |
| APA | Sun, Xianbin , Wang, Xinyi , Li, Xudong , Wang, Ya , Xu, Ruofei , Shen, Xinyi et al. Orchestrated Cu2+-coordinated tetracycline-porphyrin self-assembly remodels tumor microenvironment for photo-enhanced immuno-chemodynamic therapy . | JOURNAL OF NANOBIOTECHNOLOGY , 2025 , 23 (1) . |
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Photothermal therapy (PTT) is a promising noninvasive cancer treatment with high spatial-temporal selectivity and low systemic toxicity. However, its efficiency is restricted by the poor photostability, low tumor selectivity and inadequate deep tumor penetration of current photothermal agents. This study synthesized oleanolic acid (OA)-modified chitosan (CsO) using click chemistry and developed a nano-photothermal agent (COI) through the self-assembly of CsO and a representative photothermal agent indocyanine green (ICG). COI possessed a particle size of approximately 120 nm, good physical stability, and pH-responsive drug release properties. Under 808 nm laser irradiation, COI exhibited high photothermal conversion efficiency and photostability. The cellular uptake of COI in B16 and 4T1 cancer cells was several-fold higher than that of free ICG, while remaining comparable to ICG in normal 3T3 cells. CsO inhibited cancer-associated fibroblasts proliferation and modulated the tumor microenvironment by reducing alpha-smooth muscle actin expression, enhancing deep penetration of COI in threedimensional multicellular tumor spheres and solid tumors. The promising anti-proliferative effects of COI in vitro and in vivo indicated notable synergistic effects between the chemotherapeutic effect of OA and the photothermal therapeutic effect of ICG. These results suggest that COI could serve as a promising deep tumor-penetrating nanophotothermal agent for enhanced chemo-photothermal anticancer therapy.
Keyword ：
Chitosan Chitosan Deep penetration Deep penetration Oleanolic acid Oleanolic acid Photothermal therapy Photothermal therapy
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| GB/T 7714 | Zheng, Fangying , Tan, Ding , Zheng, Yilin et al. A chitosan-based deep tumor-penetrating nano-photothermal agent for enhanced chemo-photothermal combination therapy [J]. | MATERIALS TODAY CHEMISTRY , 2025 , 45 . |
| MLA | Zheng, Fangying et al. "A chitosan-based deep tumor-penetrating nano-photothermal agent for enhanced chemo-photothermal combination therapy" . | MATERIALS TODAY CHEMISTRY 45 (2025) . |
| APA | Zheng, Fangying , Tan, Ding , Zheng, Yilin , Chen, Haijun , Gao, Yu . A chitosan-based deep tumor-penetrating nano-photothermal agent for enhanced chemo-photothermal combination therapy . | MATERIALS TODAY CHEMISTRY , 2025 , 45 . |
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Non-invasive therapies such as photodynamic therapy (PDT) and chemodynamic therapy (CDT) have received wide attention due to their low toxicity and side effects, but their efficacy is limited by the tumor microenvironment (TME), and monotherapy cannot achieve satisfactory efficacy. In this work, a multifunctional nanoparticle co -assembled from oleanolic acid (OA), chlorin e6 (Ce6) and hemin was developed. The as -constructed nanoparticle named OCH with diameters of around 130 nm possessed good biostability, pH/GSH dual -responsive drug release properties, and remarkable cellular internalization and tumor accumulation capabilities. OCH exhibited prominent catalytic activities to generate center dot OH, deplete GSH, and produce O 2 to overcome the hypoxia TME, thus potentiating the photodynamic and chemodynamic effect. In addition, OCH can induce the occurrence of ferroptosis in both ferroptosis-sensitive and ferroptosis-resistant cancer cells. The multi -pronged effects of OCH including hypoxia alleviation, GSH depletion, ferroptosis induction, CDT and PDT effects jointly facilitate excellent anticancer effects in vitro and in vivo . Hence, this work will advance the development of safe and effective clinically transformable nanomedicine by employing clinically -applied agents to form drug combinations for efficient multi -pronged combination cancer therapy.
Keyword ：
Carrier -free Carrier -free Ferroptosis Ferroptosis Synergistic therapy Synergistic therapy Tri-component Tri-component Tumor microenvironment Tumor microenvironment
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| GB/T 7714 | Shi, Huifang , Zheng, Fangying , Zheng, Yilin et al. A carrier-free tri-component nanoreactor for multi-pronged synergistic cancer therapy [J]. | JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY , 2024 , 253 . |
| MLA | Shi, Huifang et al. "A carrier-free tri-component nanoreactor for multi-pronged synergistic cancer therapy" . | JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY 253 (2024) . |
| APA | Shi, Huifang , Zheng, Fangying , Zheng, Yilin , Sun, Xianbin , Chen, Haijun , Gao, Yu . A carrier-free tri-component nanoreactor for multi-pronged synergistic cancer therapy . | JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY , 2024 , 253 . |
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Photothermal therapy (PTT) has attracted extensive attention in cancer treatment because of its advantages of non-invasive and few side effects. Gold nanoparticles and boron-fluorine-dipyrrole (BODIPY) dye have been used as photothermal agents (PTAs), but they have problems such as easy aggregation, poor water solubility and low photothermal conversion efficiency. In this work, we used conventional liposomes for in situ generation of small gold nanoparticles and sequentially loading BODIPY to overcome the drawbacks of the two PTAs and simultaneously realize enhanced PTT. Gold- and BODIPY-coordinated liposomal nanocomplexes LAB with small gold nanoparticles adsorbed on the surface and BODIPY entrapped inside showed uniform size of about 100 nm with good stability. LAB demonstrated laser-responsive drug release property, good cellular uptake efficiency and tumor accumulation ability. After laser irradiation, LAB can exert enhanced PTT in cancer cell lines by reducing mitochondrial membrane potential and increase intracellular reactive oxygen species level to promote cell apoptosis. In tumor-bearing mice, LAB showed fantastic tumor inhibition effect with good biosafety. This work provides a convenient method to develop PTA combinations for enhanced PTT, which could lay the foundation for the green construction of new PTAs for PTT by employing clinically used formulations and PTAs.
Keyword ：
Anti -tumor Anti -tumor BODIPY BODIPY Gold nanoparticles Gold nanoparticles Lipid nanocomplexes Lipid nanocomplexes Synergistic photothermal therapy Synergistic photothermal therapy
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| GB/T 7714 | Wang, Yuran , Li, Xudong , Wang, Ya et al. Facile construction of gold- and BODIPY-coordinated liposomal nanocomplexes for enhanced photothermal therapy of cancer [J]. | MATERIALS & DESIGN , 2024 , 241 . |
| MLA | Wang, Yuran et al. "Facile construction of gold- and BODIPY-coordinated liposomal nanocomplexes for enhanced photothermal therapy of cancer" . | MATERIALS & DESIGN 241 (2024) . |
| APA | Wang, Yuran , Li, Xudong , Wang, Ya , Chen, Haijun , Gao, Yu , Lin, Yuxiang . Facile construction of gold- and BODIPY-coordinated liposomal nanocomplexes for enhanced photothermal therapy of cancer . | MATERIALS & DESIGN , 2024 , 241 . |
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Photoredox catalysis has become a mainstay in synthetic methodology over the past decade. However, its application in the functionalization of natural products remains to be further explored. Herein, we report an efficient approach to synthesize artemisinin G from artemisinin via photocatalysis in high yield. Photoredox catalysis has become a mainstay in synthetic methodology over the past decade. Herein, an efficient method for the synthesis of artemisinin G from artemisinin by using 0.5 mol % of TBADT as the catalyst was reported. The reaction proceeds smoothly and rapidly (complete within 30 min) at room temperature in high yield. image
Keyword ：
Artemisinin Artemisinin Artemisinin G Artemisinin G Photocatalysis Photocatalysis Practical synthesis Practical synthesis Radical chemistry Radical chemistry
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| GB/T 7714 | Wang, Menghan , Liu, Xiaoling , Zheng, Xiaoshan et al. Synthesis of Artemisinin G from Artemisinin via Photocatalysis [J]. | EUROPEAN JOURNAL OF ORGANIC CHEMISTRY , 2024 , 27 (15) . |
| MLA | Wang, Menghan et al. "Synthesis of Artemisinin G from Artemisinin via Photocatalysis" . | EUROPEAN JOURNAL OF ORGANIC CHEMISTRY 27 . 15 (2024) . |
| APA | Wang, Menghan , Liu, Xiaoling , Zheng, Xiaoshan , Luo, Yining , Gao, Yu , Chen, Haijun . Synthesis of Artemisinin G from Artemisinin via Photocatalysis . | EUROPEAN JOURNAL OF ORGANIC CHEMISTRY , 2024 , 27 (15) . |
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