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Temperature-feedback two-photon-responsive metal-organic frameworks for efficient photothermal therapy
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作者 Xianshun Sun Xin Lu +4 位作者 Wenyao Duan Bo Li Yupeng Tian Dandan Li Hongping Zhou 《中国科学技术大学学报》 CAS CSCD 北大核心 2024年第6期53-59,I0011,共8页
The realization of real-time thermal feedback for monitoring photothermal therapy(PTT)under near-infrared(NIR)light irradiation is of great interest and challenge for antitumor therapy.Herein,by assembling highly effi... The realization of real-time thermal feedback for monitoring photothermal therapy(PTT)under near-infrared(NIR)light irradiation is of great interest and challenge for antitumor therapy.Herein,by assembling highly efficient photothermal conversion gold nanorods and a temperature-responsive probe((E)-4-(4-(diethylamino)styryl)-1-methylpyridin-1-ium,PyS)within MOF-199,an intelligent nanoplatform(AMPP)was fabricated for simultaneous chemodynamic therapy and NIR light-induced temperature-feedback PTT.The fluorescence intensity and temperature of the PyS probe are linearly related due to the restriction of the rotation of the characteristic monomethine bridge.Moreover,the copper ions resulting from the degradation of MOF-199 in an acidic microenvironment can convert H_(2)O_(2)into•OH,resulting in tumor ablation through a Fenton-like reaction,and this process can be accelerated by increasing the temperature.This study establishes a feasible platform for fabricating highly sensitive temperature sensors for efficient temperature-feedback PTT. 展开更多
关键词 metal-organic framework TWO-PHOTON temperature feedback photothermal therapy chemodynamic therapy
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基于透明质酸的靶向纳米探针的构建及体外抗肿瘤活性 被引量:1
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作者 戚筱羽 叶雨霏 +5 位作者 陈雪梅 朱晓南 张雨婷 尹健 王晓丽 周楠迪 《中国药科大学学报》 CAS CSCD 北大核心 2022年第5期542-553,共12页
以透明质酸(hyaluronic acid,HA)为药物递送载体,依次连接阿霉素(doxorubicin,DOX)、天然吲哚花青素染料IR808和过氧化氢酶(catalase,CAT),最后通过自组装得到具有抗肿瘤和荧光成像作用的纳米探针CAT@HA-DOX-IR808NPs。利用紫外可见光... 以透明质酸(hyaluronic acid,HA)为药物递送载体,依次连接阿霉素(doxorubicin,DOX)、天然吲哚花青素染料IR808和过氧化氢酶(catalase,CAT),最后通过自组装得到具有抗肿瘤和荧光成像作用的纳米探针CAT@HA-DOX-IR808NPs。利用紫外可见光分光度计、荧光分光光度计以及透射电子显微镜等对其进行表征,然后在溶液和细胞水平开展其荧光成像和抗肿瘤活性研究。实验结果表明:构建的纳米探针CAT@HA-DOX-IR808为均匀的近球形,尺寸约为75 nm。在pH 5.0和透明质酸酶环境中,DOX在前10 h的释放率达到80%以上。激光共聚焦结果显示,在CD44阳性细胞中,该纳米探针组展现出比游离药物组以及阴性细胞组更显著的荧光信号。细胞毒实验中,在CAT@HA-DOX-IR808 NPs+NIR组,只有大约40%的MDA-MB-231细胞在最高浓度的CAT@HA-DOX-IR808 NPs下存活。因此,纳米探针CAT@HA-DOX-IR808具有显著增强的抗肿瘤功效,在乳腺癌的体外成像和治疗中具有广阔的应用前景。 展开更多
关键词 透明质酸 阿霉素 IR808 纳米探针 乳腺癌 近红外成像 化疗-动力协同治疗
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Catalase-like nanosystem for interlocking trimodal cancer therapy with hypoxia relief 被引量:1
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作者 Liyao Luo Lei Li +3 位作者 Cong Cong Yaqian He Zining Hao Dawei Gao 《Science China Materials》 SCIE EI CAS CSCD 2021年第4期1021-1034,共14页
Hypoxia is a hallmark of solid tumors,and it significantly impairs the overall anticancer efficacy,particularly photodynamic therapy(PDT).Herein,a catalase-like nanovesicle with near-infrared light-responsiveness,that... Hypoxia is a hallmark of solid tumors,and it significantly impairs the overall anticancer efficacy,particularly photodynamic therapy(PDT).Herein,a catalase-like nanovesicle with near-infrared light-responsiveness,that is,platinum/gold nanoshell encapsulated chlorin e6(Ce6)/resveratrol(Res)liposome(Pt@Au-Ce6/Res-Lip),was developed to surmount this intractable issue.The Pt@Au-Ce6/Res-Lip can decompose overexpressed H_(2)O_(2)in tumor microenvironment to produce vast amounts of O_(2)for further enhancement of the PDT.Under the 808 nm laser irradiation,the Au nanoshells induced hyperthermia at the lesion site to ablate tumor cells,simultaneously inducing the controlled release of photosensitizer Ce6 and chemotherapeutic agent Res.Moreover,stimulated by 660 nm laser,numerous reactive oxygen species were formed to induce apoptosis and necrosis of tumor cells.With the cascade of trimodal therapeutic modality options(chemotherapy,photothermal therapy,and PDT),the Pt@Au-Ce6/Res-Lip showed ultrahigh tumor inhabitation rate in in vitro and in vivo studies,signifying that the Pt@AuCe6/Res-Lip nanovesicle is a promising candidate for effective cancer therapy. 展开更多
关键词 HYPOXIA enhanced photodynamic therapy catalaselike HYPERTHERMIA trimodal therapeutic modality
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包载吲哚菁绿和阿霉素胶束的制备与体外抗肿瘤效果评价 被引量:3
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作者 张米娅 陈亮 +1 位作者 庞海燕 杨红 《中国新药杂志》 CAS CSCD 北大核心 2021年第13期1220-1226,共7页
目的:本研究旨在联合光治疗和化疗作用,制备共包载吲哚菁绿(ICG)和阿霉素(DOX)的胶束(ID-M),对制备得到的胶束进行表征并在细胞水平考察其体外抗肿瘤效果。方法:采用超声透析法制备ID-M,制备单包载ICG的胶束(I-M)和单包载DOX的胶束(D-M... 目的:本研究旨在联合光治疗和化疗作用,制备共包载吲哚菁绿(ICG)和阿霉素(DOX)的胶束(ID-M),对制备得到的胶束进行表征并在细胞水平考察其体外抗肿瘤效果。方法:采用超声透析法制备ID-M,制备单包载ICG的胶束(I-M)和单包载DOX的胶束(D-M)作为对照。对胶束的粒径、Zeta电位、包封率及释放行为等进行测定,并通过ID-M对4T1细胞的作用,考察其抗肿瘤效果和作用机制。结果:制得的ID-M平均水合粒径为80.4 nm且带负电,多分散系数为0.252(<0.3),ICG和DOX的包封率分别为92.5%和96.8%;ID-M的升温实验结果达到(36.5±1.1)℃。体外释放实验表明ID-M具有明显的缓释效果。细胞实验证明:4T1细胞对ID-M的摄取量较游离药物均提升了近2倍量。ID-M在光照后抑制4T1细胞生长的IC50为0.72μg·mL-1,较游离ICG/DOX下降了3.6倍。光照前ID-M中的DOX主要定位在溶酶体中,光照后ID-M中的ICG使细胞内的ROS水平提高,溶酶体膜破坏,DOX进入细胞核中发挥化疗作用。结论:本研究成功制备了ID-M,有效结合光治疗和化疗发挥协同抗肿瘤作用。 展开更多
关键词 阿霉素 吲哚菁绿 胶束 光治疗-化疗 协同抗肿瘤作用
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