4.7 Article

Novel, Biocompatible, and Disease Modifying VIP Nanomedicine for Rheumatoid Arthritis

期刊

MOLECULAR PHARMACEUTICS
卷 10, 期 2, 页码 728-738

出版社

AMER CHEMICAL SOC
DOI: 10.1021/mp300539f

关键词

inflammation; autoimmune disorders; phospholipids; micelles; nanomedicine; vasoactive intestinal peptide

资金

  1. NIH [AG024026, HL72343, CA121797]
  2. VA Merit Review
  3. National Center for Research Resources, NIH [C06RR15482]

向作者/读者索取更多资源

Despite advances in rheumatoid arthritis (RA) treatment, efficacious and safe disease-modifying therapy still represents an unmet medical need. Here, we describe an innovative strategy to treat RA by targeting low doses of vasoactive intestinal peptide (VIP) self-associated with sterically stabilized micelles (SSMs). This spontaneous interaction of VIP with SSM protects the peptide from degradation or inactivation in biological fluids and prolongs circulation half-life. Treatment with targeted low doses of nanosized SSM-VIP but not free VIP in buffer significantly reduced the incidence and severity of arthritis in an experimental model, completely abrogating joint swelling and destruction of cartilage and bone. In addition, SSM associated VIP, unlike free VIP, had no side-effects on the systemic functions due to selective targeting to inflamed joints. Finally, low doses of VIP in SSM successfully downregulated both inflammatory and autoimmune components of RA. Collectively, our data clearly indicate that VIP-SSM should be developed to be used as a novel nanomedicine for the treatment of RA.

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

4.7
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