• 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

血管内药物递送的药物载体。

Drug carriers for vascular drug delivery.

机构信息

Department of Pharmaceutical Sciences, Center for Pharmaceutical Biotechnology and Nanomedicine, Northeastern University, Boston, MA 02115, USA.

出版信息

IUBMB Life. 2011 Aug;63(8):586-95. doi: 10.1002/iub.496. Epub 2011 Jul 15.

DOI:10.1002/iub.496
PMID:21766415
Abstract

The currently used drug carriers for vascular drug delivery are reviewed. The human vascular system possesses unique physiological features that can be exploited for enhanced and effective targeted drug delivery. Although the thin layer of endothelial cells (EC) lines the interior surface of blood vessels forming an interface between circulating blood in the lumen and the tissue beyond the vessel wall, it can also function as a target for drugs to EC in different vascular areas. ECs overexpress specific cell-surface molecules under various pathological conditions (tumor neovasculature, inflammation, oxidative stress, and thrombosis), which are absent or barely detectable in established normal blood vessels. By coupling unique endothelial surface markers, such as antibodies, specific peptides, and growth factors to a variety of drug carriers, effective active vascular-targeted drug delivery systems can be achieved. This review focuses on the recent advances and strategies for effective targeted vascular drug delivery using a variety of drug-loaded carriers along with new targeting approaches that can be used in the design and optimization of such carriers.

摘要

目前用于血管药物输送的药物载体得到了回顾。人类的血管系统具有独特的生理特征,可以被利用来增强和实现有效的靶向药物输送。尽管内皮细胞(EC)的薄层排列在血管的内表面,形成管腔中循环血液与血管壁外组织之间的界面,但它也可以作为药物向不同血管区域的 EC 的靶点。在各种病理条件下(肿瘤新生血管、炎症、氧化应激和血栓形成),EC 过度表达特定的细胞表面分子,而在已建立的正常血管中,这些分子几乎不存在或难以检测到。通过将独特的内皮表面标记物(如抗体、特定的肽和生长因子)与各种药物载体偶联,可以实现有效的主动靶向血管药物输送系统。本文综述了近年来使用各种载药载体进行有效靶向血管药物输送的最新进展和策略,以及新的靶向方法,这些方法可用于此类载体的设计和优化。

相似文献

1
Drug carriers for vascular drug delivery.血管内药物递送的药物载体。
IUBMB Life. 2011 Aug;63(8):586-95. doi: 10.1002/iub.496. Epub 2011 Jul 15.
2
Novel platforms for vascular carriers with controlled geometry.具有可控几何形状的新型血管载体平台。
IUBMB Life. 2011 Aug;63(8):596-606. doi: 10.1002/iub.497. Epub 2011 Jun 30.
3
Recent advances in tumor vasculature targeting using liposomal drug delivery systems.近年来,利用脂质体药物递送系统靶向肿瘤血管的研究进展。
Expert Opin Drug Deliv. 2009 Dec;6(12):1297-309. doi: 10.1517/17425240903289928.
4
Passive and active drug targeting: drug delivery to tumors as an example.被动和主动药物靶向:以肿瘤药物递送为例
Handb Exp Pharmacol. 2010(197):3-53. doi: 10.1007/978-3-642-00477-3_1.
5
Advanced drug delivery systems that target the vascular endothelium.靶向血管内皮的先进药物递送系统。
Mol Interv. 2006 Apr;6(2):98-112. doi: 10.1124/mi.6.2.7.
6
Pharmaceutical approaches to colon targeted drug delivery systems.结肠靶向给药系统的药物学方法。
J Pharm Pharm Sci. 2003 Jan-Apr;6(1):33-66.
7
Targeted polymeric micelles for delivery of poorly soluble drugs.用于递送难溶性药物的靶向聚合物胶束。
Cell Mol Life Sci. 2004 Oct;61(19-20):2549-59. doi: 10.1007/s00018-004-4153-5.
8
Improved tumor-targeting drug delivery and therapeutic efficacy by cationic liposome modified with truncated bFGF peptide.经截短 bFGF 肽修饰的阳离子脂质体提高了肿瘤靶向药物递送和治疗效果。
J Control Release. 2010 Jul 1;145(1):17-25. doi: 10.1016/j.jconrel.2010.03.007. Epub 2010 Mar 20.
9
Lymphatic versus blood vascular endothelial growth factors and receptors in humans.人类体内的淋巴管与血管内皮生长因子及受体
Microsc Res Tech. 2001 Oct 15;55(2):108-21. doi: 10.1002/jemt.1162.
10
Active targeting with particulate drug carriers in tumor therapy: fundamentals and recent progress.肿瘤治疗中基于微粒药物载体的主动靶向:基础与最新进展
Drug Discov Today. 2004 Mar 1;9(5):219-28. doi: 10.1016/S1359-6446(03)02988-X.

引用本文的文献

1
Scalable lipid droplet microarray fabrication, validation, and screening.可扩展的脂滴微阵列的制作、验证和筛选。
PLoS One. 2024 Jul 5;19(7):e0304736. doi: 10.1371/journal.pone.0304736. eCollection 2024.
2
Red blood cell-derived materials for cancer therapy: Construction, distribution, and applications.用于癌症治疗的红细胞衍生材料:构建、分布及应用
Mater Today Bio. 2023 Dec 15;24:100913. doi: 10.1016/j.mtbio.2023.100913. eCollection 2024 Feb.
3
Dual Coating of Chitosan and Albumin Negates the Protein Corona-Induced Reduced Vascular Adhesion of Targeted PLGA Microparticles in Human Blood.
壳聚糖和白蛋白的双重包衣消除了蛋白质冠层诱导的靶向聚乳酸-羟基乙酸共聚物微粒在人血液中血管黏附性降低的现象。
Pharmaceutics. 2022 May 9;14(5):1018. doi: 10.3390/pharmaceutics14051018.
4
Low Dose Curcumin Administered in Hyaluronic Acid-Based Nanocapsules Induces Hypotensive Effect in Hypertensive Rats.低剂量姜黄素经透明质酸基纳米胶囊给药可在高血压大鼠中诱导降压作用。
Int J Nanomedicine. 2021 Feb 24;16:1377-1390. doi: 10.2147/IJN.S291945. eCollection 2021.
5
Nanoparticle-Mediated Drug Delivery for the Treatment of Cardiovascular Diseases.纳米颗粒介导的药物递送用于治疗心血管疾病。
Int J Nanomedicine. 2020 May 27;15:3741-3769. doi: 10.2147/IJN.S250872. eCollection 2020.
6
Targeting functionalized nanoparticles to activated endothelial cells under high wall shear stress.在高壁面剪应力作用下将功能化纳米颗粒靶向至活化的内皮细胞。
Bioeng Transl Med. 2019 Dec 13;5(2):e10151. doi: 10.1002/btm2.10151. eCollection 2020 May.
7
Molecularly Engineered Nanobodies for Tunable Pharmacokinetics and Drug Delivery.分子工程纳米抗体用于可调节的药代动力学和药物递送。
Bioconjug Chem. 2020 Apr 15;31(4):1144-1155. doi: 10.1021/acs.bioconjchem.0c00003. Epub 2020 Mar 20.
8
Biodistribution and toxicological evaluation of micron- and nano-sized erythrocyte-derived optical particles in healthy Swiss Webster mice.健康瑞士 Webster 小鼠中微米和纳米级红细胞衍生光学粒子的生物分布和毒理学评价。
Biomater Sci. 2019 Apr 23;7(5):2123-2133. doi: 10.1039/c8bm01448e.
9
Multiscale bioprinting of vascularized models.多尺度生物打印血管化模型。
Biomaterials. 2019 Apr;198:204-216. doi: 10.1016/j.biomaterials.2018.08.006. Epub 2018 Aug 3.
10
Targeting therapeutics to endothelium: are we there yet?靶向内皮细胞的治疗药物:我们成功了吗?
Drug Deliv Transl Res. 2018 Aug;8(4):883-902. doi: 10.1007/s13346-017-0464-6.