Self-assembly of a 5-fluorouracil-dipeptide hydrogel

Chem Commun (Camb). 2016 Apr 18;52(30):5254-7. doi: 10.1039/c6cc01195k. Epub 2016 Mar 21.

Abstract

The self-assembly of 5-fluorouracil dilysine conjugates into self-supporting hydrogels, comprised of entangled nanofibers or rigid nanotubes with diameters of 10 and 16 nm, respectively, is reported. The rate of release of 5-Fu from the conjugates was highly dependent on concentration in solution, whereas, release from the fully formed hydrogels was significantly slower. The 5-Fu conjugate also exhibited promising in vitro cytotoxicity against human tumor cell lines A549, H460 and H23.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Antimetabolites, Antineoplastic / administration & dosage*
  • Antimetabolites, Antineoplastic / chemistry
  • Antimetabolites, Antineoplastic / pharmacology
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Delayed-Action Preparations / chemistry*
  • Dipeptides / chemistry*
  • Fluorouracil / administration & dosage*
  • Fluorouracil / chemistry
  • Fluorouracil / pharmacology
  • Humans
  • Hydrogels / chemistry*
  • Neoplasms / drug therapy

Substances

  • Antimetabolites, Antineoplastic
  • Delayed-Action Preparations
  • Dipeptides
  • Hydrogels
  • lysyllysine
  • Fluorouracil