4.8 Article

Antibody fragment-conjugated polymeric micelles incorporating platinum drugs for targeted therapy of pancreatic cancer

Journal

BIOMATERIALS
Volume 39, Issue -, Pages 23-30

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2014.10.069

Keywords

Drug delivery; Platinum; Micelle; Nanoparticle; Chemotherapy

Funding

  1. Japan Society for the Promotion of Science (JSPS)
  2. Japanese Ministry of Health, Labor, and Welfare (MHLW)
  3. Ministry of Education, Culture, Sports, Science and Technology (MEXT)
  4. Challenging Exploratory Research [24659584]
  5. Initiative for Accelerating Regulatory Science in Innovative Drug, Medical Device, and Regenerative Medicine
  6. National Cancer Center Research and Development Fund
  7. Health and Labour Sciences Research Grants (Clinical Trial on Development of New Drugs and Medical Devices)
  8. [23700526]
  9. [25750172]
  10. [24689051]
  11. Grants-in-Aid for Scientific Research [24659584, 25670010, 24689051, 23390009, 25750172] Funding Source: KAKEN

Ask authors/readers for more resources

Antibody-mediated therapies including antibody-drug conjugates (ADCs) have shown much potential in cancer treatment by tumor-targeted delivery of cytotoxic drugs. However, there is a limitation of pay-loads that can be delivered by ADCs. Integration of antibodies to drug-loaded nanocarriers broadens the applicability of antibodies to a wide range of therapeutics. Herein, we developed antibody fragment-installed polymeric micelles via maleimide-thiol conjugation for selectively delivering platinum drugs to pancreatic tumors. By tailoring the surface density of maleimide on the micelles, one tissue factor (TF)-targeting Fab' was conjugated to each carrier. Fab'-installed platinum-loaded micelles exhibited more than 15-fold increased cellular binding within 1 h and rapid cellular internalization compared to non-targeted micelles, leading to superior in vitro cytotoxicity. In vivo, Fab'-installed micelles significantly suppressed the growth of pancreatic tumor xenografts for more than 40 days, outperforming non-targeted micelles and free drugs. These results indicate the potential of Fab'-installed polymeric micelles for efficient drug delivery to solid tumors. (C) 2014 Elsevier Ltd. All rights reserved.

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