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1.
Dong Cui Jiaguo Huang Xu Zhen Jingchao Li Yuyan Jiang Kanyi Pu 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(18):5981-5985
Photodynamic therapy (PDT) holds great promise for cancer therapy; however, its efficacy is often compromised by tumor hypoxia. Herein, we report the synthesis of a semiconducting polymer nanoprodrug (SPNpd) that not only efficiently generates singlet oxygen (1O2) under NIR photoirradiation but also specifically activates its chemotherapeutic action in hypoxic tumor microenvironment. SPNpd is self‐assembled from a amphiphilic polymer brush, which comprises a light‐responsive photodynamic backbone grafted with poly(ethylene glycol) and conjugated with a chemodrug through hypoxia‐cleavable linkers. The well‐defined and compact nanostructure of SPNpd (30 nm) enables accumulation in the tumor of living mice. Owing to these features, SPNpd exerts synergistic photodynamic and chemo‐therapy, and effectively inhibits tumor growth in a xenograft tumor mouse model. This study represents the first hypoxia‐activatable phototherapeutic polymeric prodrug system with a high potential for cancer therapy. 相似文献
2.
Yan Lyu Shasha He Jingchao Li Yuyan Jiang He Sun Yansong Miao Kanyi Pu 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(50):18365-18369
Noninvasive regulation of CRISPR/Cas9 gene editing is conducive to understanding of gene function and development of gene therapy; however, it remains challenging. Herein, a photolabile semiconducting polymer nanotransducer (pSPN) is synthesized to act as the gene vector to deliver CRISPR/Cas9 plasmids into cells and also as the photoregulator to remotely activate gene editing. pSPN comprises a 1O2‐generating backbone grafted with polyethylenimine brushes through 1O2‐cleavable linkers. NIR photoirradiation spontaneously triggers the cleavage of gene vectors from pSPN, resulting in the release of CRISPR/Cas9 plasmids and subsequently initiating gene editing. This system affords 15‐ and 1.8‐fold enhancement in repaired gene expression relative to the nonirradiated controls in living cells and mice, respectively. As this approach does not require any specific modifications on biomolecular components, pSPN represents the first generic nanotransducer for in vivo regulation of CRISPR/Cas9 gene editing. 相似文献
3.
Jianhua Zou Jianwei Zhu Zhen Yang Ling Li Wenpei Fan Liangcan He Wei Tang Liming Deng Jing Mu Yuanyuan Ma Yaya Cheng Wei Huang Xiaochen Dong Xiaoyuan Chen 《Angewandte Chemie (International ed. in English)》2020,59(23):8833-8838
Continuous irradiation during photodynamic therapy (PDT) inevitably induces tumor hypoxia, thereby weakening the PDT effect. In PDT‐induced hypoxia, providing singlet oxygen from stored chemical energy may enhance the cell‐killing effect and boost the therapeutic effect. Herein, we present a phototheranostic (DPPTPE@PEG‐Py NPs) prepared by using a 2‐pyridone‐based diblock polymer (PEG‐Py) to encapsulate a semiconducting, heavy‐atom‐free pyrrolopyrrolidone‐tetraphenylethylene (DPPTPE) with high singlet‐oxygen‐generation ability both in dichloromethane and water. The PEG‐Py can trap the 1O2 generated from DPPTPE under laser irradiation and form a stable intermediate of endoperoxide, which can then release 1O2 in the dark, hypoxic tumor microenvironment. Furthermore, fluorescence‐imaging‐guided phototherapy demonstrates that this phototheranostic could completely inhibit tumor growth with the help of laser irradiation. 相似文献
4.
Yue Yang Mei Chen Bingzhe Wang Peng Wang Yongchun Liu Yan Zhao Kun Li Guosheng Song Xiao‐Bing Zhang Weihong Tan 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(42):15213-15219
Hypoxia, as a characteristic feature of solid tumor, can significantly adversely affect the outcomes of cancer radiotherapy (RT), photodynamic therapy, or chemotherapy. In this study, a strategy is developed to overcome tumor hypoxia‐induced radiotherapy tolerance. Specifically, a novel two‐dimensional Pd@Au bimetallic core–shell nanostructure (TPAN) was employed for the sustainable and robust production of O2 in long‐term via the catalysis of endogenous H2O2. Notably, the catalytic activity of TPAN could be enhanced via surface plasmon resonance (SPR) effect triggered by NIR‐II laser irradiation, to enhance the O2 production and thereby relieve tumor hypoxia. Thus, TPAN could enhance radiotherapy outcomes by three aspects: 1) NIR‐II laser triggered SPR enhanced the catalysis of TPAN to produce O2 for relieving tumor hypoxia; 2) high‐Z element effect arising from Au and Pd to capture X‐ray energy within the tumor; and 3) TPAN affording X‐ray, photoacoustic, and NIR‐II laser derived photothermal imaging, for precisely guiding cancer therapy, so as to reduce the side effects from irradiation. 相似文献
5.
Gongyuan Liu Jiawei Zhu Heng Guo Aihui Sun Peng Chen Lei Xi Wei Huang Xuejiao Song Xiaochen Dong 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(51):18814-18819
To overcome the current limitations of chemodynamic therapy (CDT), a Mo2C‐derived polyoxometalate (POM) is readily synthesized as a new CDT agent. It permits synergistic chemodynamic and photothermal therapy operating in the second near‐infrared (NIR‐II) biological transparent window for deep tissue penetration. POM aggregated in an acidic tumor micro‐environment (TME) whereby enables specific tumor targeting. In addition to the strong ability to produce singlet oxygen (1O2) presumably via Russell mechanism, its excellent photothermal conversion enhances the CDT effect, offers additional tumor ablation modality, and permits NIR‐II photoacoustic imaging. Benefitting from the reversible redox property of molybdenum, the theranostics based on POM can escape from the antioxidant defense system. Moreover, combining the specific responsiveness to TME and localized laser irradiation, side‐effects shall be largely avoided. 相似文献
6.
Zhiyong Liu Tianye Cao Yudong Xue Mengting Li Mengsi Wu Jonathan W. Engle Qianjun He Weibo Cai Minbo Lan Weian Zhang 《Angewandte Chemie (International ed. in English)》2020,59(9):3711-3717
Nanocarriers are employed to deliver photosensitizers for photodynamic therapy (PDT) through the enhanced penetration and retention effect, but disadvantages including the premature leakage and non‐selective release of photosensitizers still exist. Herein, we report a 1O2‐responsive block copolymer (POEGMA‐b‐P(MAA‐co‐VSPpaMA) to enhance PDT via the controllable release of photosensitizers. Once nanoparticles formed by the block copolymer have accumulated in a tumor and have been taken up by cancer cells, pyropheophorbide a (Ppa) could be controllably released by singlet oxygen (1O2) generated by light irradiation, enhancing the photosensitization. This was demonstrated by confocal laser scanning microscopy and in vivo fluorescence imaging. The 1O2‐responsiveness of POEGMA‐b‐P(MAA‐co‐VSPpaMA) block copolymer enabled the realization of self‐amplified photodynamic therapy by the regulation of Ppa release using NIR illumination. This may provide a new insight into the design of precise PDT. 相似文献
7.
Yongmei Wen Qingyan Jia Fuchun Nan Xiuli Zheng Weimin Liu Jiasheng Wu Haohui Ren Jiechao Ge Pengfei Wang 《化学:亚洲杂志》2019,14(12):2162-2168
Carbon dots (CDs), a kind of phototheranostic agent with the capability of simultaneous bioimaging and phototherapy [i.e., photodynamic therapy (PDT) or photothermal therapy (PTT)], have received considerable attention because of their remarkable properties, including flexibility for surface modification, high biocompatibility, low toxicity and photo‐induced activity for malignant tumor cells. Among numerous carbon sources, it has been found that natural biomass are good candidates for the preparation of CD phototheranostic agents. In this study, pheophytin, a type of Mg‐free chlorophyll derivative and also a natural product with low toxicity, was used as a raw carbon source for the synthesis of CDs by using a microwave method. The obtained hydrophobic CDs exhibited a maximum near‐infrared (NIR) emission peak at approximately 680 nm, and high singlet oxygen (1O2) generation with a quantum yield of 0.62. The self‐assembled CDs from the as‐prepared CDs with DSPE‐mPEG2000 retained efficient 1O2 generation. The obtained carbon dot assembly was not only an efficient fluorescence (FL) imaging agent but also a smart PDT agent. Our studies indicated that the obtained hydrophilic CD assembly holds great potential as a new phototheranostic agent for cancer therapy. This work provides a new route for synthesis of CDs and proposes a readily available candidate for tumor treatment. 相似文献
8.
Temperature‐Correlated Afterglow of a Semiconducting Polymer Nanococktail for Imaging‐Guided Photothermal Therapy
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Dr. Xu Zhen Dr. Chen Xie Prof. Kanyi Pu 《Angewandte Chemie (International ed. in English)》2018,57(15):3938-3942
Nanoparticles for photothermal therapy: Real‐time temperature monitoring is critical to reduce the nonspecific damage during photothermal therapy (PTT); however, PTT agents that can emit temperature‐related signals are rare and limited to few inorganic nanoparticles. We herein synthesize a semiconducting polymer nanococktail (SPNCT) that can not only convert photo‐energy to heat but also emit temperature‐correlated luminescence after cessation of light excitation. Such an afterglow luminescence of the SPNCT detects tumors more sensitively than fluorescence as a result of the elimination of tissue autofluorescence, while its temperature‐dependent nature allows tumor temperature to be optically monitored under near‐infrared (NIR) laser irradiation. Thus, SPNCT represents the first organic optical nanosystem that enables optical‐imaging guided PTT without real‐time light excitation. 相似文献
9.
Non‐Aqueous Sol–Gel Synthesis of Ultra Small Persistent Luminescence Nanoparticles for Near‐Infrared In Vivo Imaging
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Dr. Thomas Maldiney Nicole Lièvre Dr. Guillaume Yangshu Wang Prof. Laurence Motte Dr. Cyrille Richard Dr. Yoann Lalatonne 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(20):7350-7354
Ultra‐small ZnGa2O4:Cr3+ nanoparticles (6 nm) that exhibit near‐infrared (NIR) persistent luminescence properties are synthesized by using a non‐aqueous sol–gel method assisted by microwave irradiation. The nanoparticles are pegylated, leading to highly stable dispersions under physiological conditions. Preliminary in vivo studies show the high potential for these ultra‐small ZnGa2O4:Cr3+ nanoparticles to be used as in vivo optical nanotools as they emit without the need for in situ excitation and, thus, avoid the autofluorescence of tissues. 相似文献
10.
Chuang Nie Peng Du Hongwei Zhao Hainan Xie Yuxin Li Li Yao Yuanyuan Shi Lianna Hu Shaoyan Si Maonian Zhang Jianwen Gu Ling Luo Zaicheng Sun 《化学:亚洲杂志》2020,15(1):148-155
Melanoma is a primary reason of death from skin cancer and associated with high lethality. Photothermal therapy (PTT) has been developed into a powerful cancer treatment technique in recent years. Here, we created a low‐cost and high‐performance PTT agent, Ag@TiO2 NPs, which possesses a high photothermal conversion efficiency of ≈65 % and strong near‐infrared (NIR) absorption about 808 nm. Ag NPs were synthesized using a two‐step method and coated with TiO2 to obtain Ag@TiO2 NPs by a facile sol‐gel method. Because of the oxide, Ag@TiO2 NPs exhibit remarkable high photothermal conversion efficiencies and biocompatibility in vivo and in vitro. Cytotoxicity and therapeutic efficiency of photothermal cytotoxicity of Ag@TiO2 NPs were tested in B16‐F10 cells and C57BL/6J mice. Under light irradiation, the elevated temperature causes cell death in Ag NPs‐treated (100 μg mL?1) cells in vitro (both p<0.01). In the case of subcutaneous melanoma tumor model, Ag@TiO2 NPs (100 μg mL?1) were injected into the tumor and irradiated with a 808 nm laser of 2 W cm?2 for 1 minute. As a consequence, the tumor volume gradually decreased by NIR laser irradiation with only a single treatment. The results demonstrate that Ag@TiO2 NPs are biocompatible and an attractive photothermal agent for cutaneous melanoma by local delivery. 相似文献
11.
Jin‐Yue Zeng Xiao‐Shuang Wang Yong‐Dan Qi Yun Yu Xuan Zeng Xian‐Zheng Zhang 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(17):5748-5752
Polycyclic aromatic derivatives can trap 1O2 to form endoperoxides (EPOs) for O2 storage and as sources of reactive oxygen species. However, these materials suffer from structural amorphism, which limit both practical applications and fundamental studies on their structural optimization for O2 capture and release. Metal–organic frameworks (MOFs) offer advantages in O2 binding, such as clear structure–performance relationships and precise controllability. Herein, we report the reversible binding of O2 is realized via the chemical transformation between anthracene‐based and the corresponding EPO‐based MOF. It is shown that anthracene‐based MOF, the framework featuring linkers with polycyclic aromatic structure, can rapidly trap 1O2 to form EPOs and can be restored upon UV irradiation or heating to release O2. Furthermore, we confirm that photosensitizer‐incorporated anthracene‐based MOF are promising candidates for reversible O2 carriers controlled by switching Vis/UV irradiation. 相似文献
12.
Lei Chen Dandan Chen Yifei Jiang Jicheng Zhang Jiangbo Yu Christopher C. DuFort Sunil R. Hingorani Xuanjun Zhang Changfeng Wu Daniel T. Chiu 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(21):7082-7086
Bright long‐wavelength‐excitable semiconducting polymer dots (LWE‐Pdots) are highly desirable for in vivo imaging and multiplexed in vitro bioassays. LWE‐Pdots have been obtained by incorporating a near‐infrared (NIR) emitter into the backbone of a polymer host to develop a binary donor–acceptor (D–A) system. However, they usually suffer from severe concentration quenching and a trade‐off between fluorescence quantum yield (Φf) and absorption cross‐section (σ). Herein, we describe a ternary component (D1/D2–A) strategy to achieve ultrabright, green laser‐excitable Pdots with narrow‐band NIR emission by introducing a BODIPY‐based assistant polymer donor as D1. The D1/D2–A Pdots possess improved Φf and σ compared to corresponding binary D2–A Pdots. Their Φf is as high as 40.2 %, one of the most efficient NIR Pdots reported. The D1/D2–A Pdots show ultrahigh single‐particle brightness, 83‐fold brighter than Qdot 705 when excited by a 532 nm laser. When injected into mice, higher contrast in vivo tumor imaging was achieved using the ternary Pdots versus the binary D–A Pdots. 相似文献
13.
Magnetic Nanohybrids Loaded with Bimetal Core–Shell–Shell Nanorods for Bacteria Capture,Separation, and Near‐Infrared Photothermal Treatment
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Dr. Bo Hu Ning Wang Lu Han Prof. Dr. Ming‐Li Chen Prof. Dr. Jian‐Hua Wang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(17):6582-6589
A novel antimicrobial nanohybrid based on near‐infrared (NIR) photothermal conversion is designed for bacteria capture, separation, and sterilization (killing). Positively charged magnetic reduced graphene oxide with modification by polyethylenimine (rGO–Fe3O4–PEI) is prepared and then loaded with core–shell–shell Au–Ag–Au nanorods to construct the nanohybrid rGO–Fe3O4–Au–Ag–Au. NIR laser irradiation melts the outer Au shell and exposes the inner Ag shell, which facilitates controlled release of the silver shell. The nanohybrids combine physical photothermal sterilization as a result of the outer Au shell with the antibacterial effect of the inner Ag shell. In addition, the nanohybrid exhibits high heat conductivity because of the rGO and rapid magnetic‐separation capability that is attributable to Fe3O4. The nanohybrid provides a significant improvement of bactericidal efficiency with respect to bare Au–Ag–Au nanorods and facilitates the isolation of bacteria from sample matrixes. A concentration of 25 μg mL?1 of nanohybrid causes 100 % capture and separation of Escherichia coli O157:H7 (1×108 cfu mL?1) from an aqueous medium in 10 min. In addition, it causes a 22 °C temperature rise for the surrounding solution under NIR irradiation (785 nm, 50 mW cm?2) for 10 min. With magnetic separation, 30 μg mL?1 of nanohybrid results in a 100 % killing rate for E. coli O157:H7 cells. The facile bacteria separation and photothermal sterilization is potentially feasible for environmental and/or clinical treatment. 相似文献
14.
Jianwu Tian Zitong Liu Wenlin Jiang Dandan Shi Liangliang Chen Xisha Zhang Guanxin Zhang Chong‐an Di Deqing Zhang 《Angewandte Chemie (International ed. in English)》2020,59(33):13844-13851
Optically tunable field‐effect transistors (FETs) with near infra‐red (NIR) light show promising applications in various areas. Now, arylazopyrazole groups are incorporated in the side chains of a semiconducting donor–acceptor (D‐A) polymer. The cis–trans interconversion of the arylazopyrazole can be controlled by 980 nm and 808 nm NIR light irradiation, by utilizing NaYF4:Yb,Tm upconversion nanoparticles and the photothermal effect of conjugated D‐A polymers, respectively. This reversible transformation affects the interchain packing of the polymer thin film, which in turn reversibly tunes the semiconducting properties of the FETs by the successive 980 nm and 808 nm light irradiation. The resultant FETs display fast response to NIR light, good resistance to photofatigue, and stability in storage for up to 120 days. These unique features will be useful in future memory and bioelectronic wearable devices. 相似文献
15.
Chemical and Structural Stability of Zirconium‐based Metal–Organic Frameworks with Large Three‐Dimensional Pores by Linker Engineering
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Dr. Suresh B. Kalidindi Dr. Sanjit Nayak Dr. Michael E. Briggs Dr. Susanna Jansat Dr. Alexandros P. Katsoulidis Dr. Gary J. Miller Dr. John E. Warren Dr. Dmytro Antypov Dr. Furio Corà Dr. Ben Slater Dr. Mark R. Prestly Dr. Carlos Martí‐Gastaldo Prof. Matthew J. Rosseinsky 《Angewandte Chemie (International ed. in English)》2015,54(1):221-226
The synthesis of metal–organic frameworks with large three‐dimensional channels that are permanently porous and chemically stable offers new opportunities in areas such as catalysis and separation. Two linkers (L1=4,4′,4′′,4′′′‐([1,1′‐biphenyl]‐3,3′,5,5′‐tetrayltetrakis(ethyne‐2,1‐diyl)) tetrabenzoic acid, L2=4,4′,4′′,4′′′‐(pyrene‐1,3,6,8‐tetrayltetrakis(ethyne‐2,1‐diyl))tetrabenzoic acid) were used that have equivalent connectivity and dimensions but quite distinct torsional flexibility. With these, a solid solution material, [Zr6O4(OH)4(L1)2.6(L2)0.4]?(solvent)x, was formed that has three‐dimensional crystalline permanent porosity with a surface area of over 4000 m2 g?1 that persists after immersion in water. These properties are not accessible for the isostructural phases made from the separate single linkers. 相似文献
16.
Clément Falaise Dr. Christophe Volkringer Dr. Jean‐François Vigier Dr. Natacha Henry Dr. Arnaud Beaurain Dr. Thierry Loiseau 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(17):5324-5331
Four metal–organic frameworks (MOF) with tetravalent uranium have been solvothermally synthesized by treating UCl4 with rigid dicarboxylate linkers in N,N‐dimethylfomamide (DMF). The use of the ditopic ligands 4,4′‐biphenyldicarboxylate ( 1 ), 2,6‐naphthalenedicarboxylate ( 2 ), terephthalate ( 3 ), and fumarate ( 4 ) resulted in the formation of three‐dimensional networks based on the hexanuclear uranium‐centered motif [U6O4(OH)4(H2O)6]. This motif corresponds to an octahedral configuration of uranium nodes and is also known for thorium in crystalline solids. The atomic arrangement of this specific building unit with organic linkers is similar to that found in the zirconium‐based porous compounds of the UiO‐66/67 series. The structure of [U6O4(OH)4(H2O)6(L)6] ? X (L=dicarboxylate ligand; X=DMF) shows the inorganic hexamers connected in a face‐centered cubic manner through the ditopic linkers to build up a three‐dimensional framework that delimits octahedral (from 5.4 Å for 4 up to 14.0 Å for 1 ) and tetrahedral cavities. The four compounds have been characterized by using single‐crystal X‐ray diffraction analysis (or powder diffraction analysis for 4 ). The tetravalent state of uranium has been examined by using XPS and solid‐state UV/Vis analyses. The measurement of the Brunauer–Emmett–Teller surface area indicated very low values (Langmuir <300 m2 g?1 for 1 , <7 m2 g?1 for 2 – 4 ) and showed that the structures are quite unstable upon removal of the encapsulated DMF solvent. 相似文献
17.
Xiahui Lin Shuya Liu Xuan Zhang Rong Zhu Shan Chen Xiaoyuan Chen Jibin Song Huanghao Yang 《Angewandte Chemie (International ed. in English)》2020,59(4):1682-1688
Sonodynamic therapy (SDT) has the advantages of high penetration, non‐invasiveness, and controllability, and it is suitable for deep‐seated tumors. However, there is still a lack of effective sonosensitizers with high sensitivity, safety, and penetration. Now, ultrasound (US) and glutathione (GSH) dual responsive vesicles of Janus Au‐MnO nanoparticles (JNPs) were coated with PEG and a ROS‐sensitive polymer. Upon US irradiation, the vesicles were disassembled into small Janus Au‐MnO nanoparticles (NPs) with promoted penetration ability. Subsequently, GSH‐triggered MnO degradation simultaneously released smaller Au NPs as numerous cavitation nucleation sites and Mn2+ for chemodynamic therapy (CDT), resulting in enhanced reactive oxygen species (ROS) generation. This also allowed dual‐modality photoacoustic imaging in the second near‐infrared (NIR) window and T1‐MR imaging due to the released Mn2+, and inhibited orthotopic liver tumor growth via synergistic SDT/CDT. 相似文献
18.
Qiuxiang Wen Yejun Zhang Chunyan Li Sisi Ling Xiaohu Yang Guangcun Chen Yang Yang Qiangbin Wang 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(32):11117-11122
Fluorescence‐guided cytoreductive surgery is one of the most promising approaches for facile elimination of tumors in situ, thereby improving prognosis. Reported herein is a simple strategy to construct a novel chainlike NIR‐II nanoprobe (APP‐Ag2S‐RGD) by self‐assembly of an amphiphilic peptide (APP) into a nanochain with subsequent chemical crosslinking of NIR‐II Ag2S QDs and the tumor‐targeting RGD peptide. This probe exhibits higher capability for cancer cell detection compared with that of RGD‐functionalized Ag2S QDs (Ag2S‐RGD) at the same concentration. Upon intraperitoneal injection, superior tumor‐to‐normal tissue signal ratio is achieved and non‐vascularized tiny tumor metastatic foci as small as about 0.2 mm in diameter could be facilely eliminated under NIR‐II fluorescent imaging guidance. These results clearly indicate the potential of this probe for fluorescence‐guided tumor staging, preoperative diagnosis, and intraoperative navigation. 相似文献
19.
Prof. Jingchao Li Ningyue Yu Dr. Dong Cui Dr. Jiaguo Huang Dr. Yu Luo Prof. Kanyi Pu 《Angewandte Chemie (International ed. in English)》2023,62(30):e202305200
Immunotherapy has provided a promising modality for cancer treatment, while it often has the issues of limited response rates and potential off-target side effects in clinical practice. We herein report the construction of semiconducting polymer pro-nanomodulators (SPpMs) with ultrasound (US)-mediated activatable pharmacological actions for deep-tissue sono-immunotherapy of orthotopic pancreatic cancer. Such SPpMs consist of a sonodynamic semiconducting polymer backbone grafted with poly(ethylene glycol) chains linked with two immunomodulators (a programmed death-ligand 1 blocker and an indoleamine 2,3-dioxygenase inhibitor) via a singlet oxygen (1O2)-cleavable segment. In view of the excellent sonodynamic property of the semiconducting polymer core, SPpMs enable effective generation of 1O2 under US treatment, even in a deep-tissue depth up to 12 cm. The generated 1O2 not only ablates tumors via a sonodynamic effect and induces immunogenic cell death, but also destroys the 1O2-cleavable segments to allow in situ release of immunomodulators in tumors. This synergetic action results in boosted antitumor immune response via reversing two tumor immunosuppressive pathways. As such, SPpMs mediate deep-tissue sono-immunotherapy to completely eradicate orthotopic pancreatic cancer and effectively prevent tumor metastasis. Moreover, such an immune activation reduces the possibility of immune-related adverse events. This study thus provides a smart activatable nanoplatform for precise immunotherapy of deep-seated tumors. 相似文献
20.
Ben Shi Ning Ren Luyan Gu Ge Xu Rongchen Wang Tianli Zhu Ying Zhu Chunhai Fan Chunchang Zhao He Tian 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(47):16982-16986
NIR light responsive nanoplatforms hold great promise for on‐demand drug release in precision cancer medicine. However, currently available systems utilize “always‐on” photothermal transducers that lack target specificity, and thus inaccurately differentiate tumors from normal tissues. Developed here is a theranostic nanoplatform featuring H2S‐mediated in situ production of NIR photothermal agents for imaging‐guided and photocontrolled drug release. The system targets H2S‐rich cancers. This nanoplatform shows H2S‐activatable NIR‐II emission and NIR light controllable release of the drug Camptothecin‐11. Upon administering the system to HCT116 tumor‐bearing mice, the tumor is greatly suppressed with minimal side effects, arising from the synergy of the cancer‐specific and NIR light activated therapy. This theranostic nanoplatform thus sheds light on precision medicine with guidance through NIR‐II imaging. 相似文献