• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

通过内源性 HS 刺激和荧光同时开启进行细胞特异性吉西他滨激活及跟踪。

Cell-specific activation of gemcitabine by endogenous HS stimulation and tracking through simultaneous fluorescence turn-on.

机构信息

Department of Science, School of Engineering, Amrita Vishwa Vidyapeetham, Coimbatore, 641112, India.

Department of Chemistry, Sookmyung Women's University, Seoul 04310, Korea.

出版信息

Chem Commun (Camb). 2021 Sep 21;57(75):9614-9617. doi: 10.1039/d1cc00118c.

DOI:10.1039/d1cc00118c
PMID:34486009
Abstract

The endogenous HS-driven theranostic H2S-Gem has been invented. The theranostic prodrug H2S-Gem is selectively activated in cancer cells, releasing active gemcitabine with a simultaneous fluorescence turn-on. H2S-Gem selectively inhibited cancer cell growth compared to the mother chemotherapeutic gemcitabine. Overall, it is a unique protocol for tracking and transporting chemotherapeutic agents to tumor areas without the guidance of tumor-directive ligands.

摘要

内源性 HS 驱动的治疗性 H2S-Gem 已被发明。治疗性前药 H2S-Gem 可在癌细胞中选择性激活,同时释放具有荧光开启的活性吉西他滨。与母体化疗药物吉西他滨相比,H2S-Gem 选择性抑制癌细胞生长。总体而言,这是一种独特的方案,可在没有肿瘤导向配体指导的情况下跟踪和输送化疗药物到肿瘤区域。

相似文献

1
Cell-specific activation of gemcitabine by endogenous HS stimulation and tracking through simultaneous fluorescence turn-on.通过内源性 HS 刺激和荧光同时开启进行细胞特异性吉西他滨激活及跟踪。
Chem Commun (Camb). 2021 Sep 21;57(75):9614-9617. doi: 10.1039/d1cc00118c.
2
Synthesis and biological activity of a gemcitabine phosphoramidate prodrug.吉西他滨氨基磷酸酯前药的合成与生物活性
J Med Chem. 2007 Jul 26;50(15):3743-6. doi: 10.1021/jm070269u. Epub 2007 Jun 29.
3
Revealing the impact of modified modules flexibility on gemcitabine prodrug nanoassemblies for effective cancer therapy.揭示修饰模块的灵活性对用于有效癌症治疗的吉西他滨前药纳米组装体的影响。
J Colloid Interface Sci. 2025 Jan;677(Pt A):941-952. doi: 10.1016/j.jcis.2024.08.026. Epub 2024 Aug 5.
4
Enhanced Antitumor Activity of Monophosphate Ester Prodrugs of Gemcitabine: In Vitro and In Vivo Evaluation.吉西他滨单磷酸酯前药增强的抗肿瘤活性:体内外评价
J Pharm Sci. 2016 Sep;105(9):2966-2973. doi: 10.1016/j.xphs.2016.02.006. Epub 2016 Mar 17.
5
Theranostic nanoparticles enabling the release of phosphorylated gemcitabine for advanced pancreatic cancer therapy.载药纳米粒实现磷酸化吉西他滨的释放,用于晚期胰腺癌治疗。
J Mater Chem B. 2020 Mar 25;8(12):2410-2417. doi: 10.1039/d0tb00017e.
6
Stereocomplex Prodrugs of Oligo(lactic acid) -Gemcitabine in Poly(ethylene glycol)- block-poly(d,l-lactic acid) Micelles for Improved Physical Stability and Enhanced Antitumor Efficacy.聚乙二醇-嵌段-聚(丙交酯-乙交酯)胶束中的寡聚(乳酸)-吉西他滨立体复合物前药,提高物理稳定性和增强抗肿瘤疗效。
ACS Nano. 2018 Jul 24;12(7):7406-7414. doi: 10.1021/acsnano.8b04205. Epub 2018 Jul 6.
7
Multi-stimuli responsive polymeric prodrug micelles for combined chemotherapy and photodynamic therapy.载多刺激响应性聚合物前药胶束用于联合化疗和光动力疗法。
J Mater Chem B. 2020 Jun 24;8(24):5267-5279. doi: 10.1039/d0tb00539h.
8
pH and singlet oxygen dual-responsive GEM prodrug micelles for efficient combination therapy of chemotherapy and photodynamic therapy.pH 和单线态氧双重响应 GEM 前药胶束用于化疗和光动力疗法的高效联合治疗。
J Mater Chem B. 2020 Jul 14;8(26):5645-5654. doi: 10.1039/d0tb00622j. Epub 2020 Jun 15.
9
Gemcitabine-based therapy for pancreatic cancer using the squalenoyl nucleoside monophosphate nanoassemblies.基于鲨烯酰核苷单磷酸纳米组装物的胰腺癌吉西他滨治疗。
Int J Pharm. 2015 Mar 30;482(1-2):38-46. doi: 10.1016/j.ijpharm.2014.11.009. Epub 2014 Nov 6.
10
Selective Activation of a Prodrug by Thioredoxin Reductase Providing a Strategy to Target Cancer Cells.硫氧还蛋白还原酶选择性激活前药为靶向癌细胞提供策略。
Angew Chem Int Ed Engl. 2018 May 22;57(21):6141-6145. doi: 10.1002/anie.201801058. Epub 2018 Apr 26.

引用本文的文献

1
Stimuli-Responsive Prodrug Linkers That Simultaneously Release Cargo and Neutralize In Situ Generated (Aza)Quinone Methides.可同时释放药物并中和原位生成的(氮杂)醌甲基化物的刺激响应型前药连接子。
Chemistry. 2025 Jun 3;31(31):e202501278. doi: 10.1002/chem.202501278. Epub 2025 Apr 28.