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肿瘤微环境调节型细胞器靶向递药系统的研究进展 被引量:1

Research progress of tumor microenvironmentally regulating organelle targeted drug delivery system
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摘要 近年来,利用机体免疫系统进行抗肿瘤的免疫疗法受到了广泛关注。然而抑制性肿瘤微环境限制了免疫治疗的效果,因此克服肿瘤微环境及其中的免疫抑制性细胞的作用成为肿瘤免疫疗法的一大热点。纳米制剂具有重新编程免疫抑制性微环境的巨大潜力,为免疫治疗提供了有效策略。随着主动靶向性纳米载体技术的不断发展和对药物作用位点研究的不断深入,具有更精准主动靶向功能的亚细胞器靶向性纳米载体材料也受到越来越多的关注。本文简要介绍了各亚细胞器与肿瘤的关系,概述了基于酸碱性调节、活性氧含量、免疫原性及免疫抑制细胞的肿瘤微环境特点的纳米药物靶向递送系统的设计策略与研究进展,为亚细胞器途径靶向递药系统的构建及其在肿瘤免疫治疗方面的应用提供借鉴和参考。 In recent years,the use of the body’s immune system for anti-tumor immunotherapy has received extensive attention.However,the immunosuppressive tumor microenvironment(TME)limits the effect of immunotherapy.Therefore,overcoming the limitations of TME and immunosuppressive cells plays an important role in tumor immunotherapy.Nano agents have great potential to reprogram the immunosuppressive microenvironment and provide an effective strategy for immunotherapy.With the continuous development of active targeting nano carrier technology and the deepening of the research on drug action sites,subcellular organ targeting nano carrier materials with more accurate active targeting function have also attracted more and more attention.This review will briefly introduce the relationship between subcellular organelles and tumor,summarize the design strategy and research progress of targeted nano drug delivery system based on the characteristics of acidity,reactive oxygen species(ROS)activity,immunogenicity,and TME of immunosuppressive cells,to provide reference for the construction of subcellular pathway targeted drug delivery system in tumor immunotherapy.
作者 吴诗洋 常爽 陈晴 史梦浩 赵明 胡海洋 陈大为 WU Shi-yang;CHANG Shuang;CHEN Qing;SHI Meng-hao;ZHAO Ming;HU Hai-yang;CHEN Da-wei(Department of Pharmaceutics,Shenyang Pharmaceutical University,Shenyang 110016,China;Department of Pharmacology,Iowa University,Iowa City 50011,USA)
出处 《药学学报》 CAS CSCD 北大核心 2022年第6期1771-1780,共10页 Acta Pharmaceutica Sinica
基金 国家自然科学基金资助项目(81872820)。
关键词 药物递送系统 肿瘤微环境 细胞器 靶向 酸碱度 活性氧 免疫原性 免疫抑制 drug delivery system tumor microenvironment organelle targeting hydrogen-ion concentration reactive oxygen species immunogenicity immunosuppression
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