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国家重点基础研究发展计划(2012CB932500)

作品数:3 被引量:31H指数:2
相关作者:郑晓鹏田甘谷战军更多>>
相关机构:中国科学院大学中国科学院四川大学更多>>
发文基金:国家重点基础研究发展计划更多>>
相关领域:生物学化学工程医药卫生农业科学更多>>

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3 条 记 录,以下是 1-6
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Lipid Enveloped Hollow Mesoporous Silica Nanoparticles for Hydrophilic and Hydrophobic Immunogenic Peptide Co-delivery
<正>Cancer is one of the deadliest killers to human lives,and both the incidence and mortality of cancers are c...
Chaohua YangJintao ZhuZhiping Zhang
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聚合物凝胶颗粒稳定的纳米Pickering乳液的制备及性能
<正>Pickering乳液,即由纳米颗粒作为稳定剂在油水界面组装形成的乳液。由于具有很好的热力学稳定性、可调的界面渗透性和可控的药物释放等特性,pickering乳液已被广泛应用于化学工业、材料科学和生物技
胡龙王芹朱锦涛
关键词:稳定性
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A novel nitric oxide donor for enhancing anti-tumor activity of doxorubicin
<正>Nitric oxide(NO) is a kind of low molecular weight endogenous signaling molecule which was well-known as "M...
Qingle SongSongwei TanYuanyuan GuoXiangting ZhuangYuling BaoYupei WuZhiping Zhang
关键词:DOXORUBICINANTI-TUMOR
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荧光上转换纳米材料在光动力学治疗癌症中的应用被引量:7
2014年
作为微创的光疗方法,光动力学治疗有着重要的临床价值。近年来,荧光上转换纳米粒子(UCNPs)在光动力治疗领域脱颖而出。在组织穿透能力强的近红外(NIR)光激发下,UCNPs可以发射高能量的可见光,通过能量共振转移激活周围的光敏剂(PS)分子产生单线态氧杀死癌细胞,达到治疗的效果。基于UCNPs的光动力学疗法可以克服传统光动力疗法中光敏剂难输运,难靶向和难以治疗深层组织的缺点。此外,UCNPs可以和其它诊疗分子相结合,达到协同治疗和诊疗一体化的目的。本文综述了上转换纳米材料在癌症光动力学中的应用以及研究进展。
郑晓鹏田甘谷战军
关键词:癌症光动力学治疗
Novel redox-responsive paclitaxel produg with P-gp inhibiting activity
<正>A simple Paclitaxel(PTX) prodrug based on TPGS and disulfide bond(TPGS-S-S-PTX) was synthesized by a two st...
Yuanyuan GuoXiangting ZhuangYuling BaoSongwei TanZhiping Zhang
关键词:PACLITAXELPRODRUG
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Microparticles released by Listeria monocytogenes-infected macrophages are required for dendritic cell-elicited protective immunity被引量:1
2012年
Interplay between macrophages and dendritic cells in the processing and presentation of bacterial antigens for T-cell immune responses remains poorly understood. Using a Listeria monocytogenes (Lm) infection model, we demonstrate that dendritic cells (DCs) require the support of macrophages to elicit protective immunity against Lm infection. DCs themselves were inefficient at taking up Lm but capable of taking up microparticles (MPs) released by Lm-infected macrophages. These MPs transferred Lm antigens to DCs, allowing DCs to present Lm antigen to effector T cells. MP-mediated Lm antigen transfer required M HC class I participation, since M HC class I deficiency in macrophages resulted in a significant reduction of T-cell activation. Moreover, the vaccination of mice with MPs from Lm-infected macrophages produced strong protective immunity against Lm infection. We here identify an intrinsic antigen transfer program between macrophages and DCs during Lm infection, and emphasize that macrophages also play an essential role in DC-elicited Lm-specific T-cell responses.
Yi ZhangRuihua ZhangHuafeng ZhangJing LiuZhuoshun YangPingwei XuWenqian CaiGeming LuMiao CuiReto A SchwendenerHuang-Zhong ShiHuabao XiongBo Huang
关键词:MICROPARTICLESMACROPHAGE
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