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Liposomes, Exosomes, and Virosomes: From Modeling Complex

Membrane Processes to Medical Diagnostics and Drug Delivery

Poster Abstracts

84

32-POS

Board 16

Feedback-Controlled pH-Switching Within Vesicle Nanoreactors

Stephen J. Jones

1

, Paul A. Beales

1

, Annette F. Taylor

2

.

1

University of Leeds, Leeds, West Yorkshire, United Kingdom,

2

University of Sheffield,

Sheffield, South Yorkshire, United Kingdom.

Within the field of bottom-up synthetic biology, vesicular nanoreactors can be utilised in the

compartmentalisation of a variety of different entities. Such entities, depending on their

biological or chemical function, can be used to define these systems within a specific field of

technological advancement, e.g., therapeutics, biosensing, protocell technology, etc. A

significant challenge for the therapeutic application of vesicle technology is to improve the

communication between a vesicle and its environment, allowing for smart, regulated release of

active compounds in response to a variety of complex biological cues. The primary challenge in

designing an effective and efficient drug delivery system, capable of self-mediating its own

permeability and eliciting a controlled drug-release profile, is the incorporation of self-

regulation. Undoubtedly, to achieve this, some form of feedback control is required. One option,

which complies with the biocompatibility of these therapeutic systems, is enzymatic feedback.

Towards this goal, we will demonstrate a urea-urease base-catalysed feedback-controlled pH-

switch within vesicular confinement. By varying initial reaction conditions, membrane

physicochemical properties, and vesicle sizes (ranging from the nano- to the microscale), we will

demonstrate tuneable temporal and spatial control of the pH-switching behaviour. By

understanding feedback-controlled reactions within self-assembled vesicle compartments, our

long term aim is to engineer systems that can regulate a desired drug release profile, in response

to changing environmental signals.