Literature DB >> 26338226

An additional fluorenylmethoxycarbonyl (Fmoc) moiety in di-Fmoc-functionalized L-lysine induces pH-controlled ambidextrous gelation with significant advantages.

Samala Murali Mohan Reddy1, Ganesh Shanmugam, Natarajan Duraipandy, Manikantan Syamala Kiran, Asit Baran Mandal.   

Abstract

In recent years, several fluorenylmethoxycarbonyl (Fmoc)-functionalized amino acids and peptides have been used to construct hydrogels, which find a wide range of applications. Although several hydrogels have been prepared from mono Fmoc-functionalized amino acids, herein, we demonstrate the importance of an additional Fmoc-moiety in the hydrogelation of double Fmoc-functionalized L-lysine [Fmoc(Nα)-L-lysine(NεFmoc)-OH, (Fmoc-K(Fmoc))] as a low molecular weight gelator (LMWG). Unlike other Fmoc-functionalized amino acid gelators, Fmoc-K(Fmoc) exhibits pH-controlled ambidextrous gelation (hydrogelation at different pH values as well as organogelation), which is significant among the gelators. Distinct fibrous morphologies were observed for Fmoc-K(Fmoc) hydrogels formed at different pH values, which are different from organogels in which Fmoc-K(Fmoc) showed bundles of long fibers. In both hydrogels and organogels, the self-assembly of Fmoc-K(Fmoc) was driven by aromatic π-π stacking and hydrogen bonding interactions, as evidenced from spectroscopic analyses. Characterization of Fmoc-K(Fmoc) gels using several biophysical methods indicates that Fmoc-K(Fmoc) has several advantages and significant importance as a LMWG. The advantages of Fmoc-K(Fmoc) include pH-controlled ambidextrous gelation, pH stimulus response, high thermal stability (∼100 °C) even at low minimum hydrogelation concentration (0.1 wt%), thixotropic property, high kinetic and mechanical stability, dye removal properties, cell viability to the selected cell type, and as a drug carrier. While single Fmoc-functionalized L-lysine amino acids failed to exhibit gelation under similar experimental conditions, the pH-controlled ambidextrous gelation of Fmoc-K(Fmoc) demonstrates the benefit of a second Fmoc moiety in inducing gelation in a LMWG. We thus strongly believe that the current findings provide a lead to construct or design various new synthetic Fmoc-based LMW organic gelators for several potential applications.

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Year:  2015        PMID: 26338226     DOI: 10.1039/c5sm01767j

Source DB:  PubMed          Journal:  Soft Matter        ISSN: 1744-683X            Impact factor:   3.679


  5 in total

1.  Simple Tyrosine Derivatives Act as Low Molecular Weight Organogelators.

Authors:  Güzide Aykent; Cansu Zeytun; Antoine Marion; Salih Özçubukçu
Journal:  Sci Rep       Date:  2019-03-20       Impact factor: 4.379

2.  Cyclohexamer [-(d-Phe-azaPhe-Ala)2-]: good candidate to formulate supramolecular organogels.

Authors:  Mohamed I A Ibrahim; Guillaume Pickaert; Loïc Stefan; Brigitte Jamart-Grégoire; Jacques Bodiguel; Marie-Christine Averlant-Petit
Journal:  RSC Adv       Date:  2020-12-07       Impact factor: 4.036

Review 3.  Short Peptide-Based Smart Thixotropic Hydrogels.

Authors:  Bapan Pramanik
Journal:  Gels       Date:  2022-09-07

4.  New Fmoc-Amino Acids/Peptides-Based Supramolecular Gels Obtained through Co-Assembly Process: Preparation and Characterization.

Authors:  Alexandra Croitoriu; Loredana Elena Nita; Alina Gabriela Rusu; Alina Ghilan; Maria Bercea; Aurica P Chiriac
Journal:  Polymers (Basel)       Date:  2022-08-17       Impact factor: 4.967

5.  Stable Formulations of Peptide-Based Nanogels.

Authors:  Elisabetta Rosa; Carlo Diaferia; Enrico Gallo; Giancarlo Morelli; Antonella Accardo
Journal:  Molecules       Date:  2020-07-29       Impact factor: 4.411

  5 in total

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