Issue 8, 2017, Issue in Progress

Dynamic formation of nanostructured particles from vesicles via invertase hydrolysis for on-demand delivery

Abstract

The unique multicompartmental nanostructure of lipid-based mesophases can be triggered, on-demand, in order to control the release of encapsulated drugs. In this study, these nanostructured matrices have been designed to respond to a specific enzyme, invertase, an enzyme which catalyses the hydrolysis of sucrose. The effect of two sugar esters upon the phase behaviour of two different lipids which form cubic phases, phytantriol and monolinolein, was investigated. Factors affecting the hydrolysis of the sucrose headgroup are discussed in terms of the molecular structure of the sugar surfactant and also its ability to incorporate into the lipid bilayer. By hydrolysing the incorporated sugar esters, a dynamic change in mesophase nanostructure from vesicles to a cubic phase was observed. This phase change resulted in the triggered release of an encapsulated model drug, fluorescein. This investigation demonstrates, for the first time, that changes on a molecular level by subtly controlling the hydrophilic and hydrophobic features of an amphiphilic additive at the interface by enzymatic hydrolysis can result in a global change in the system and so paves the way towards the design and development of lipid-based matrices which are responsive to specific enzymes for the controlled delivery of pharmaceutically active molecules or functional foods.

Graphical abstract: Dynamic formation of nanostructured particles from vesicles via invertase hydrolysis for on-demand delivery

Supplementary files

Article information

Article type
Paper
Submitted
12 Nov 2016
Accepted
11 Dec 2016
First published
16 Jan 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 4368-4377

Dynamic formation of nanostructured particles from vesicles via invertase hydrolysis for on-demand delivery

W. Fong, A. Sánchez-Ferrer, F. G. Ortelli, W. Sun, B. J. Boyd and R. Mezzenga, RSC Adv., 2017, 7, 4368 DOI: 10.1039/C6RA26688F

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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