Self-assembling peptide nanofibers containing phenylalanine for the controlled release of 5-fluorouracil

Abstract

The study shows that RADA-F6 peptide with pH-responsive self-assembling nature can be effectively used as a drug delivery system for the sustained release of a potent anticancer drug 5-fluorouracil (5-FU) at basic pH. As 5-FU contains the aromatic pyrimidine ring, RADA-F6 system is suitable for entrapping an aromatic drug due to effective π–π stacking with phenylalanine and be able to show better controlled release behavior. The stability and controlled release nature of RADA-F6 in different conditions followed by 5-FU entrapment at in silico conditions was confirmed by molecular dynamics simulation taking RADA-16 as control. Cytotoxicity of the drug-loaded RADA-F6 was measured by MTT assay and cellular uptake by confocal microscopy. Physicochemical characterization and further Western blot analysis and flow cytometric studies confirm that RADA-F6 can be successfully used as an efficient vector for pH-sensitive, controlled 5-FU delivery system.

Keywords:

• scaffold
• drug delivery
• nanofibrous
• aromatic

Acknowledgments

The authors are thankful to the Department of Biotechnology, New Delhi for providing the financial assistance for the research and the Council for Scientific and Industrial Research (CSIR), New Delhi for the Junior Research Fellowship to N Ashwanikumar.

Disclosure

The authors report no conflicts of interest in this work.