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

Narayanan Ashwanikumar,1 Nisha Asok Kumar,2 Padma S Saneesh Babu,2 Krishnankutty C Sivakumar,3 Mithun Varghese Vadakkan,1 Parvathi Nair,1 Ilamathi Hema Saranya,1 Sivakumari Asha Nair,2 Gopalakrishnapillai S Vinod Kumar1 1Chemical Biology, Nano Drug Delivery Systems, Bio-Innovation Center, 2Cancer R...

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Autores principales: Ashwanikumar N, Kumar NA, Saneesh Babu PS, Sivakumar KC, Vadakkan MV, Nair P, Hema Saranya I, Asha Nair S, Vinod Kumar GS
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Publicado: Dove Medical Press 2016
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spelling oai:doaj.org-article:3db97da7dc4042c68371541f1c3b655e2021-12-02T02:08:25ZSelf-assembling peptide nanofibers containing phenylalanine for the controlled release of 5-fluorouracil1178-2013https://doaj.org/article/3db97da7dc4042c68371541f1c3b655e2016-10-01T00:00:00Zhttps://www.dovepress.com/self-assembling-peptide-nanofibers-containing-phenylalanine-for-the-co-peer-reviewed-article-IJNhttps://doaj.org/toc/1178-2013Narayanan Ashwanikumar,1 Nisha Asok Kumar,2 Padma S Saneesh Babu,2 Krishnankutty C Sivakumar,3 Mithun Varghese Vadakkan,1 Parvathi Nair,1 Ilamathi Hema Saranya,1 Sivakumari Asha Nair,2 Gopalakrishnapillai S Vinod Kumar1 1Chemical Biology, Nano Drug Delivery Systems, Bio-Innovation Center, 2Cancer Research Programme, 3Distributed Information Sub-Centre (Bioinformatics Centre), Rajiv Gandhi Centre for Biotechnology, Poojappura, Thiruvananthapuram, Kerala, India 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, aromaticAshwanikumar NKumar NASaneesh Babu PSSivakumar KCVadakkan MVNair PHema Saranya IAsha Nair SVinod Kumar GSDove Medical Pressarticlescaffolddrug deliverynanofibrousaromaticMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol Volume 11, Pp 5583-5594 (2016)
institution DOAJ
collection DOAJ
language EN
topic scaffold
drug delivery
nanofibrous
aromatic
Medicine (General)
R5-920
spellingShingle scaffold
drug delivery
nanofibrous
aromatic
Medicine (General)
R5-920
Ashwanikumar N
Kumar NA
Saneesh Babu PS
Sivakumar KC
Vadakkan MV
Nair P
Hema Saranya I
Asha Nair S
Vinod Kumar GS
Self-assembling peptide nanofibers containing phenylalanine for the controlled release of 5-fluorouracil
description Narayanan Ashwanikumar,1 Nisha Asok Kumar,2 Padma S Saneesh Babu,2 Krishnankutty C Sivakumar,3 Mithun Varghese Vadakkan,1 Parvathi Nair,1 Ilamathi Hema Saranya,1 Sivakumari Asha Nair,2 Gopalakrishnapillai S Vinod Kumar1 1Chemical Biology, Nano Drug Delivery Systems, Bio-Innovation Center, 2Cancer Research Programme, 3Distributed Information Sub-Centre (Bioinformatics Centre), Rajiv Gandhi Centre for Biotechnology, Poojappura, Thiruvananthapuram, Kerala, India 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
format article
author Ashwanikumar N
Kumar NA
Saneesh Babu PS
Sivakumar KC
Vadakkan MV
Nair P
Hema Saranya I
Asha Nair S
Vinod Kumar GS
author_facet Ashwanikumar N
Kumar NA
Saneesh Babu PS
Sivakumar KC
Vadakkan MV
Nair P
Hema Saranya I
Asha Nair S
Vinod Kumar GS
author_sort Ashwanikumar N
title Self-assembling peptide nanofibers containing phenylalanine for the controlled release of 5-fluorouracil
title_short Self-assembling peptide nanofibers containing phenylalanine for the controlled release of 5-fluorouracil
title_full Self-assembling peptide nanofibers containing phenylalanine for the controlled release of 5-fluorouracil
title_fullStr Self-assembling peptide nanofibers containing phenylalanine for the controlled release of 5-fluorouracil
title_full_unstemmed Self-assembling peptide nanofibers containing phenylalanine for the controlled release of 5-fluorouracil
title_sort self-assembling peptide nanofibers containing phenylalanine for the controlled release of 5-fluorouracil
publisher Dove Medical Press
publishDate 2016
url https://doaj.org/article/3db97da7dc4042c68371541f1c3b655e
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