4.4 Article

HDL Nanoparticles Have Wound Healing and Anti-Inflammatory Properties and Can Topically Deliver miRNAs

期刊

ADVANCED THERAPEUTICS
卷 3, 期 12, 页码 -

出版社

WILEY
DOI: 10.1002/adtp.202000138

关键词

alkali burns; corneal epithelium; diabetic corneas; EphA2; microRNA

资金

  1. National Institute of Arthritis and Musculoskeletal and Skin Diseases Grant [AR075049]
  2. NCI [CCSG P30 CA060553]
  3. NIH [1S10OD021704 -01]
  4. National Institutes of Health [EY06769, EY017539, EY019463]
  5. Dermatology Foundation
  6. Eversight research grant
  7. Northwestern University Post Graduate Program in Cutaneous Biology of the National Institutes of Health [T32AR060710, AR064144, AR071168]
  8. Prostate Cancer Foundation
  9. Center for Regenerative Nanomedicine (CRN)
  10. Nanyang Technological Institute-Northwestern University (NTU-NU) Institute for Nanomedicine

向作者/读者索取更多资源

microRNAs regulate numerous biological processes, making them potential therapeutic agents. Problems with delivery and stability of these molecules have limited their usefulness as treatments. It is demonstrated that synthetic high-density lipoprotein nanoparticles (HDL NPs) topically applied to the intact ocular surface are taken up by epithelial and stromal cells. microRNAs complexed to HDL NPs (miR-HDL NPs) are similarly taken up by cells and tissues and retain biological activity. Topical treatment of diabetic mice with either HDL NPs or miR-HDL NPs significantly improves corneal reepithelialization following wounding compared with controls. Mouse corneas with alkali burn-induced inflammation, topically treated with HDL NPs, display clinical, morphological, and immunological improvement. These results yield a novel HDL NP-based eye drop for patients with compromised wound healing ability (diabetics) and/or corneal inflammatory diseases (e.g., dry eye).

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