4.8 Article

A peptide for targeted, systemic delivery of imaging and therapeutic compounds into acute brain injuries

期刊

NATURE COMMUNICATIONS
卷 7, 期 -, 页码 -

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/ncomms11980

关键词

-

资金

  1. Defense Advanced Research Projects Agency (DARPA) [HR0011-13-2-0017]
  2. European Research Council [291910]
  3. Wellcome Trust [WT095077MA]
  4. National Multiple Sclerosis Grant [RG-4666-A-2]
  5. NSF SBIR Phase I grant [1548490]
  6. NINDS [NS047101]
  7. Directorate For Engineering
  8. Div Of Industrial Innovation & Partnersh [1548490] Funding Source: National Science Foundation

向作者/读者索取更多资源

Traumatic brain injury (TBI) is a major health and socio-economic problem, but no pharmacological agent is currently approved for the treatment of acute TBI. Thus, there is a great need for advances in this field. Here, we describe a short peptide (sequence CAQK) identified by in vivo phage display screening in mice with acute brain injury. The CAQK peptide selectively binds to injured mouse and human brain, and systemically injected CAQK specifically homes to sites of brain injury in mouse models. The CAQK target is a proteoglycan complex upregulated in brain injuries. Coupling to CAQK increased injury site accumulation of systemically administered molecules ranging from a drug-sized molecule to nanoparticles. CAQK-coated nanoparticles containing silencing oligonucleotides provided the first evidence of gene silencing in injured brain parenchyma by systemically administered siRNA. These findings present an effective targeting strategy for the delivery of therapeutics in clinical management of acute brain injuries.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据