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NEW JOURNAL OF CHEMISTRY · 2024 · IF 2.7

Metal–organic framework-based pH/NIR dual-responsive nanoparticles for combined photothermal/photodynamic therapy and chemotherapy of cancer

Lihua Huang,Ying Luo,Yiyang Cong,Jia Liu,Caiyan Xu,Zhaoxiang Zeng,Yihua Yin,Hao Hong,Wenjin Xu

Metal–organic frameworks (MOFs) are unique coordination polymers that have emerged as important candidates for drug delivery in recent years. Herein, we designed a drug delivery system for multi-modal combination therapy (IR-820/DOX@MIL-101-PDA-PEG-F3, simplified as ID@MIL-PPF3). In this study, pH-sensitive nanocarriers MIL-101(Fe) were prepared and loaded with the effective chemotherapy agent doxorubicin (DOX) and the phototherapeutic reagent new indocyanine green (IR-820) using a physical adsorption method. Dopamine was spontaneously polymerized in alkaline solutions to form a hybrid coating on MIL-101(Fe) (denoted as ID@MIL-101-PDA). The surface of ID@MIL-101-PDA was functionalized by the synthesized polymer NH2-PEG-OCH3/F3 to obtain ID@MIL-PPF3. Characterization results show that ID@MIL-PPF3 has a good drug loading rate (27.7%) and photothermal conversion efficiency (28.89%). In addition, Fe3+ released from MIL-101(Fe) can engage in a Fenton-like reaction to generate hydroxyl radicals (˙OH) to realize chemodynamic therapy (CDT). ID@MIL-PPF3 not only demonstrates the ability to intelligently release drugs, but also realizes chemotherapy combined with PDT/PTT/CDT therapy for tumor cells, which was proved by in vitro evaluation. In conclusion, ID@MIL-PPF3 provides a new idea and method for building a multi-modal combination therapy targeted drug delivery platform.

CAS / MDL: 62-31-7
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2024 · IF 4.9

Novel graphene oxide modified LDH@CEO antibacterial materials capable of NIR stimuli-responsive control release for food preservation

Xu Ma,Xinhe Zhao,Ning Zhang,XiaoYu Liu,JiYue Ding,Qingyang Xu,Ke Cui,Yi Wang,Qian Zhang,Hailin Cong

The development of antimicrobial packaging materials serves as an effective means to enhance food preservation and mitigate food waste. This study had developed a near-infrared (NIR)-controlled smart responsive system for the release of antibacterial cinnamon essential oils (CEO), which involves immobilizing CEO within the interlayer of layered double hydroxides (LDHs) and decorating it with graphene oxide (GO), designated as LDH@CEO-GO. LDH@CEO-GO was prepared by co-precipitation method. The release kinetics of CEO at various temperatures was investigated, revealing that the release dynamics conform to the Fickian diffusion mechanism. Under NIR light serves as an intelligent switch that can regulate temperature, thereby facilitating the release of CEO. Antibacterial tests demonstrated that LDH@CEO-GO exhibited good antibacterial properties, achieving inhibition rates of 77.5 % and 68.3 % against E. coli and S. aureus, respectively. NIR irradiation, the inhibition rates increased to 98.3 % and 97.2 %. Through practical exploration of strawberry preservation, it was found that under NIR light stimulation, LDH@CEO-GO can effectively enhance the preservation of strawberries.

CAS / MDL: 7784-27-2 7447-40-7
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ACS Applied Materials & Interfaces · 2024 · IF 8.3

NIR-Mediated Pyroelectric Catalysis for Sustained ROS/RNS Generation and Advanced Cancer Therapy In Vivo via Injectable Hydrogel

Yandai Lin,Yanxi Yang,Xueli Ren,Zhe Liu

Exogenous electrical stimulation has attracted considerable attention due to the advantages of microelectric induction and subsequent biological effects such as actin reorganization and reactive oxygen species (ROS) generation. Herein, an injectable hydrogel of BPR-ARG@Gel (BAG) with pyroelectric BPR nanoparticle loading and l-arginine (ARG) introduction was fabricated for advanced cancer therapy in vivo. Due to the photothermal effect, the holes and electrons in BPR nanoparticles were separated to produce an open-circuit voltage and consequently catalyze water H2O to generate toxic superoxide (•O2–) and hydroxyl radicals (•OH). These ROS substances further oxidize ARG to produce NO for synergistic tumor treatments. The mice experiments indicated that the employment of BAG hydrogel incorporation with a near-infrared laser downregulated the heat shock protein and recruited immune cells with 5-fold-enhanced expression of proinflammatory cytokines of interferon-γ. It was also noteworthy that the injectable hydrogel of BAG substantially induced the generation of reactive oxygen/nitrogen species (ROS/RNS) with reliable biosafety and strong tumor inhibition. Overall, these findings have provided potentially new inspirations and a feasible strategy to translate this multifunctional hydrogel toward tumor therapy in a pyroelectric stimulation manner.

CAS / MDL: 74-79-3 1401-55-4
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JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY · 2024 · IF 11.2

NIR-light-induced plasmonic liquid metal/ionic liquid/MXene polyurethane films with excellent antifouling and self-healing capabilities

Peng Wang,Haohang Yuan,Baoluo He,Ruisheng Guo,Shujuan Liu,Qian Ye,Feng Zhou,Weimin Liu

The potential of organic coatings in antifouling applications has been well-documented. Beyond their exceptional antifouling effects, these coatings should also possess good mechanical strength and self-healing capabilities. Herein, a novel vinyl-based ionic liquid [VEMIM + ] [Cl – ] (IL) was in situ polymerized and then assembled onto the surface of liquid metal (GLM) nanodroplets to prepare GLM-IL. Subsequently, Ti 3 C 2 T x (MXene) was modified with GLM-IL nanodroplets to obtain GLM-IL/MXene composite, which acts as an efficient photon captor and photothermal converters and can be further composited with PU film (GLM-IL/MXene/PU). Notably, the composite film significantly increases by ∼117°C after exposure to 200 mW/cm 2 light irradiation. This increase is attributed to the high photothermal conversion efficiency of MXene and the excellent plasma effect of GLM-IL. Compared with pure PU, the GLM-IL/MXene/PU film shows a 50% improvement in tensile strength and above 85.8% healing efficiency with a local temperature increase. Additionally, the as-prepared GLM-IL/MXene/PU film reveals satisfactory antifouling properties, achieving a 99.7% reduction in bacterial presence and an 80.3% reduction in microalgae. This work introduces a novel coating with antifouling and self-healing properties, offering a wide range of applications in the fields of marine antifouling and biomedicine.

CAS / MDL: 79-41-4
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Materials Today Bio · 2025 · IF 10.2

NIR-triggered and glucose-powered hollow mesoporous Mo-based single-atom nanozymes for cascade chemodynamic diabetic infection therapy

Jingwei Wang,Yin Yu,Lingzhi Chen,Jiaqi Yu,Xiaoying Jin,Runmin Zeng,Xiaomin Luo,Yanguang Cong,Guangxian Xu,Jianglin Zhang,Xueqin Huang,Jiang Pi

Diabetic infections/wounds remain to be a threatening challenge as it seriously leads to lower limb amputation with endless pains and subsequent high economic/psychosocial costs. The exceptional peroxidase-like activity of single-atom nanozymes (SAzymes) holds great promise for chemodynamic therapy (CDT) of diabetic infection, but is extremely restricted by the near-neutral pH and insufficient H 2 O 2 levels in physiological conditions. Herein, we innovated a hollow mesoporous molybdenum single-atom nanozyme (HMMo-zyme) featured with catalytic activity, photothermal performance and drug delivery properties for more effective antibacterial therapeutic in diabetic conditions. The glucose oxidase (GOx) was encapsulated into HMMo-zyme with phase-change material (PCM) to form HMMo/GOx@P system, which could be controllably disassembled by near-infrared ray (NIR) to trigger cascade CDT toward bacterial infections. The results revealed that the release of GOx accelerated by NIR could facilitate the continuous conversion of glucose (Glu) into gluconic acid, accompanied by a sharply decrease in pH to establish a low-pH environment that notably enhanced the catalytic activity of HMMo-zyme, which subsequently drives the conversion of generated H 2 O 2 into toxic hydroxyl radicals ( · OH) for amplified anti-bacterial treatment. As a proof of the concept, this NIR-assisted HMMo/GOx@P strategy could efficiently inhibit/kill bacteria and suppress tissue inflammations, thereby accelerating the wound healing processes both in in vitro and in vivo diabetic infection models. This study provides a novel strategy that may serve as a promising alternative for antibiotic therapeutics against diabetic infection, thus holding promise for more effective diabetic infection treatment manipulating Mo-based SAzymes.

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POWDER TECHNOLOGY · 2025 · IF 4.6

MoS2@AuNRs nanoparticles equipped with MnO2 nanosheets as an efficient NIR/pH/GSH triple-responsive drug delivery carrier

Menglu An,Weiying Wang,Jingguo Li,Shaokui Cao,Yingliang Liu,Jun Shi

MnO 2 nanosheets have attracted extensive attention in the field of photothermal therapy due to their excellent pH/glutathione (GSH) responsiveness. In this study, MoS 2 @gold nanorods (AuNRs)/polydopamine (PDA)@MnO 2 (400–500 nm) nanocomposites with controllable drug release property were prepared by covering MnO 2 nanosheets around near-infrared (NIR) responsive MoS 2 @AuNRs (100–200 nm) via in-situ redox reaction. The large surface area and strong negative charge of MnO 2 nanosheets ensured that MoS 2 @AuNRs/PDA@MnO 2 had a high loading efficiency of 92.44 % for doxorubicin hydrochloride (DOX). MoS 2 @AuNRs/PDA@MnO 2 revealed significant NIR/pH/GSH triple-responsive drug release properties owing to the synergistically enhanced NIR photothermal-response of MoS 2 @AuNRs (61.10 % of photothermal conversion efficiency) and the reaction between MnO 2 and GSH in weakly acidic media. In addition, in vitro cell viability results confirmed that MoS 2 @AuNRs/PDA@MnO 2 could efficiently kill tumor cells under the dual action of acidic media and NIR laser. This study develops a novel nanocarrier with NIR/pH/GSH triple-responsive drug delivery capability, which has broad applications in photothermal therapy and intelligent drug delivery.

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Journal of Materials Chemistry B · 2018 ·Vol. 6 ·期 12 ·1791-1798 · IF 4.776

A NIR rhodamine fluorescent chemodosimeter specific for glutathione: Knoevenagel condensation, detection of intracellular glutathione and living cell imaging

Lulu Tong,Ying Qian

A new near-infrared probe for detecting glutathione based on conjugate addition and intramolecular amino induced spirolactam opening named RhAN was designed and synthesized. Firstly, rhodamine was reacted with 2-(1,3,3-trimethylindolin-2-ylidene) acetaldehyde by a Knoevenagel condensation, and the conjugate chain was extended, obtaining M2. Then, M2 was connected with hydrazide to get M3. Finally, the target molecule RhAN was synthesized via the combination of M3 and acryloyl chloride. In the presence of GSH, RhAN exhibits high selectivity, which specifically identifies GSH over Cys and Hcy, the color change from yellow to green together with the fluorescence appeared within 5 s, and there was no interference from the presence of other biological thiols and amino acids. The absorption and emission wavelength of the probe RhAN reached 717 nm and 739 nm, the molar extinction coefficient is 4.36 × 104 M−1 cm−1 and quantum yield is 0.26. Its absorption and emission intensity were enhanced by more than 117-fold and 90-fold upon addition of GSH, respectively. In addition, it also has high sensitivity with a low detection limit of 0.1 μM, which is lower than most previously reported GSH probes. The probe works excellently within a wide pH range of 2–10. Moreover, RhAN was employed for endogenous and exogenous imaging in MCF-7 cells for GSH. MCF-7 cells incubated with RhAN with GSH or blank RhAN all showed significant fluorescence in the red channel, which indicated that the probe could not only detect exogenous GSH, but it also permeated into the cells and reacted with the intracellular GSH. This is an excellent design for a fluorescence sensor, RhAN, as a quick and effective method for detecting excess GSH in living cells, for maintaining the balance of amino acids in the body and ensuring normal life activities.

CAS / MDL: 108-24-7
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ACS Applied Materials & Interfaces · 2024 · IF 8.3

CeO2 In Situ Growth on Red Blood Cell Membranes: CQD Coating and Multipathway Alzheimer’s Disease Therapy under NIR

Mingyuan Chi,Jichun Liu,Lianxin Li,Yuewen Zhang,Meng Xie

Alzheimer’s disease (AD) has a complex etiology and diverse pathological processes. The therapeutic effect of single-target drugs is limited, so simultaneous intervention of multiple targets is gradually becoming a new research trend. Critical stages in AD progression involve amyloid-β (Aβ) self-aggregation, metal-ion-triggered fibril formation, and elevated reactive oxygen species (ROS). Herein, red blood cell membranes (RBC) are used as templates for the in situ growth of cerium oxide (CeO2) nanocrystals. Then, carbon quantum dots (CQDs) are encapsulated to form nanocomposites (CQD-Ce-RBC). This strategy is combined with photothermal therapy (PTT) for AD therapy. The application of RBC enhances the materials’ biocompatibility and improves immune evasion. RBC-grown CeO2, the first application in the field of AD, demonstrates outstanding antioxidant properties. CQD acts as a chelating agent for copper ions, which prevents the aggregation of Aβ. In addition, the thermal effect induced by near-infrared laser-induced CQD can break down Aβ fibers and improve the permeability of the blood–brain barrier. In vivo experiments on APP/PS1 mice demonstrate that CQD-Ce-RBC combined with PTT effectively clears cerebral amyloid deposits and significantly enhances learning and cognitive abilities, thereby retarding disease progression. This innovative multipathway approach under light-induced conditions holds promise for AD treatment.

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CHEMICAL ENGINEERING JOURNAL · 2024 · IF 13.3

Acid-etched layered double hydroxides armed with dual “Doorkeepers” for Immunomodulatory-NIR III photodynamic therapy of hepatocellular carcinoma

Yuan-Fei Lu,Qiao-Mei Zhou,Xiao-Yan Yang,Jia-Ping Zhou,Xiao-Jie Wang,Jie-Ni Yu,Jin-Guo Zhang,Yong-Zhong Du,Ri-Sheng Yu

Immune checkpoint blockade (ICB) therapy for hepatocellular carcinoma (HCC) is limited due to its immunosuppressive tumor microenvironment (TME). Proinflammatory pyroptosis as a new schedule can induce immunogenic cell death (ICD), thereby reversing immunosuppressive TME and improving ICB efficiency. Herein, we report an acid-etched layered double hydroxides nanosheets (E-LDH)-based smart nanoplatforms armed with H 2 O 2 /pH dual “doorkeepers” (denoted as CTEP) targeting HCC to realize membrane-anchored photodynamic therapy (PDT) and evoke potent pyroptosis to effectively improve anti-tumor immunity. The hybrid Hepa1-6 cancer cell membrane (CM) and thylakoid (TK) membrane is cloaked on the surface of pH-(low)-insertion peptide (pHLIP) modified E-LDH to obtain CTEP. Once CTEP nanoplatforms arrive at tumor regions, the dual “doorkeepers” will orderly open to perform PDT precisely. Given the fact that TK membranes have the catalase mimetic function, CTEP is able to respond to high concentrations of H 2 O 2 in TME and rupture the hybrid CM-TK membrane to expose pH-sensitive peptide pHLIP. Membrane-localized PDT can induce gasdermin-D (GSDMD) mediated pyroptosis, effectively stimulating tumor immunogenicity. Pyroptotic cell death releases damage-associated molecular patterns (DAMPs) and consequently robust IaCB ability. CTEP-evoked pyroptosis together with anti-PD-L1 blockade therapy activates adaptive immunity in HCC, successfully inhibiting the progression of primary and distant HCC tumors with mitigation of the side effects. This research has demonstrated that CTEP with excellent biocompatibility and homologous targeting ability can act as a potent pyroptosis inducer to improve immune efficacy. The combination of PDT and immunotherapy via a photo-pyroptosis pathway can be a smart strategy for HCC treatment.

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ACS Applied Materials & Interfaces · 2024 · IF 8.3

Boosting the UV–vis–NIR Photodetection Performance of MoS2 through the Cavity Enhancement Effect and Bulk Heterojunction Strategy

Xiaolong Li,Jundi Wan,Yulu Tang,Chenyu Wang,Yahui Zhang,Dongjun Lv,Mingyuan Guo,Yongning Ma,Yuhao Yang

Navigating more effective methods to enhance the photon utilization of photodetectors poses a significant challenge. This study initially investigates the impact of morphological alterations in 2H-MoS2 on photodetector (PD) performance. The results reveal that compared to layered MoS2 (MoS2 NLs), MoS2 nanotubes (MoS2 NTs) impart a cavity enhancement effect through multiple light reflections. This structural feature significantly enhances the photodetection performance of the MoS2-based PDs. We further employ the heterojunction strategy to construct Y-TiOPc NPs:MoS2 NTs, utilizing Y-TiOPc NPs (Y-type titanylphthalocyanine) as the vis–NIR photosensitizer and MoS2 NTs as the photon absorption enhancer. This approach not only addresses the weak absorption of MoS2 NTs in the near-infrared region but also enhances carrier generation, separation, and transport efficiency. Additionally, the band bending phenomenon induced by trapped-electrons at the interface between ITO and the photoactive layer significantly enhances the hole tunneling injection capability from the external circuit. By leveraging the synergistic effects of the aforementioned strategies, the PD based on Y-TiOPc NPs:MoS2 NTs (Y:MT-PD) exhibits superior photodetection performance in the wavelength range of 365–940 nm compared to MoS2 NLs-based PD and MoS2 NTs-based PD. Particularly noteworthy are the peak values of key metrics for Y:MT-PD, such as EQE, R, and D* that are 4947.6%, 20588 mA/W, and 1.94 × 1012 Jones, respectively. The multiperiod time-resolved photocurrent response curves of Y:MT-PD also surpass those of the other two PDs, displaying rapid, stable, and reproducible responses across all wavelengths. This study provides valuable insights for the further development of photoactive materials with a high photon utilization efficiency.

CAS / MDL: 20441-06-9
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Materials Today Bio · 2024 · IF 8.7

“Three Birds, One Stone” Strategy of NIR-Responsive CO/H2S Dual-Gas Nanogenerator for Efficient Treatment of Osteoporosis

Guoyu Yang,Jing Ye,Jingcheng Wang,Huijie Liu,Yanli Long,Junkai Jiang,Xinxin Miao,Jianjian Deng,Tianlong Wu,Tao Li,Xigao Cheng,Xiaolei Wang

ABSTRACT Osteoporosis (OP), the most prevalent bone degenerative disease, has become a significant public health challenge globally. Current therapies primarily target inhibiting osteoclast activity or stimulating osteoblast activation, but their effectiveness remains suboptimal. This paper introduced a “three birds, one stone” therapeutic approach for osteoporosis, employing upconversion nanoparticles (UCNPs) to create a dual-gas storage nanoplatform (UZPA-CP) targeting bone tissues, capable of concurrently generating carbon monoxide (CO) and hydrogen sulfide (H 2 S). Through the precise modulation of 808 nm near-infrared (NIR) light, the platform could effectively control the release of CO and H 2 S in the OP microenvironment, and realize the effective combination of promoting osteogenesis, inhibiting osteoclast activity, and improving the immune microenvironment to achieve the therapeutic effect of OP. High-throughput sequencing results further confirmed the remarkable effectiveness of the nanoplatform in inhibiting apoptosis, modulating inflammatory response, inhibiting osteoclast differentiation and regulating multiple immune signaling pathways. The gas storage nanoplatform not only optimized the OP microenvironment with the assistance of NIR, but also restored the balance between osteoblasts and osteoclasts. This comprehensive therapeutic strategy focused on improving the bone microenvironment, promoting osteogenesis and inhibiting osteoclast activity provides an ideal new solution for the treatment of metabolic bone diseases.

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Materials Advances · 2024 ·Vol. 5 ·期 11 ·4902-4912 · IF 5.2

A self-assembled Ru nanozyme with H2O2-activated oxygenation for NIR-II photoacoustic imaging-guided photothermal/photodynamic therapy

Guang Liu,Zhilang Li,Zirong Lv,Qiuping Zheng,Cunji Gao,Jianniao Tian,Xing-Can Shen

The characteristic hypoxia of solid tumors seriously reduced the treatment efficacy of oxygen-dependent photodynamic therapy (PDT). Herein, an oxygen nanogenerator, comprising Ru-based nanomaterials, CS–DA@Ru nanoparticles (NPs), has been constructed to relieve tumor hypoxia along with photodynamic/photothermal therapy for efficient tumor eradication. CS–DA@Ru NPs possess targeting ability and act as catalase-mimic nanozymes to decompose endogenous hydrogen peroxide in the tumor to produce O2. The broad absorbance of CS–DA@Ru NPs in the second near-infrared (NIR-II) region enabled them to possess good photothermal properties and photoacoustic (PA) imaging ability. CS–DA@Ru NPs could generate enough hyperthermia and enormous amounts of 1O2 under NIR-II laser irradiation. Specifically, CS–DA@Ru NPs exhibit catalase-like activity as well as a significantly augmented antitumor efficacy through synergistic PTT/PDT guided by NIR-II PA imaging in both cells and in vivo experiments. This work will advance the development of noble metal nanozymes in enhancing the efficacy of O2-dependent antitumor modalities.

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