Philip Welsby

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Associate Head PG/CPD Medical Education, Programme Lead Masters in Medicine (MMed)

Edge Hill University
Country flagUnited Kingdom

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About

Philip Welsby is the Associate Head of PG/CPD Medical Education and Programme Lead for the Masters in Medicine (MMed) at Edge Hill University, UK. His research primarily focuses on multidisciplinary approaches in medicinal chemistry, specifically involving glycogen phosphorylase inhibitors, lipid-based nanoparticles for gene delivery, and structure-based drug design targeting Glycogen Synthase Kinase-3β. Recent publications highlight his contributions to understanding the potential of baicalein against glioblastoma and improving transfection efficiencies for mRNA and DNA therapies.

Recent Grants

Grant: Close

Guava EasyCyte™ HT Sampling Flow Cytometer – a state of the art benchtop flow cytometer

Open Date: 2014-03-01

Close Date:

Grant: Close

Live and fixed cell fluorescent imaging system to support research projects

Open Date: 2012-11-01

Close Date:

Grant: Close

IRCSET Embark

Open Date: 2008-10-01

Close Date: 2011-09-01

Grant: Close

Millenium Fund

Open Date: 2007-10-01

Close Date: 2008-09-01

Articles (3)

Lipid‐based nanoparticles have recently shown great promise, establishing themselves as the gold standard in delivering novel RNA therapeutics. However, research on the effects of storage on their efficacy, safety, and stability is still lacking. Herein, the impact of storage temperature on two types of lipid‐based nanocarriers, lipid nanoparticles (LNPs) and receptor‐targeted nanoparticles (RTNs), loaded with either DNA or messenger RNA (mRNA), is explored and the effects of different cryoprotectants on the stability and efficacy of the formulations are investigated. The medium‐term stability of the nanoparticles was evaluated by monitoring their physicochemical characteristics, entrapment and transfection efficiency, every two weeks over one month. It is demonstrated, that the use of cryoprotectants protects nanoparticles against loss of function and degradation in all storage conditions. Moreover, it is shown that the addition of sucrose enables all nanoparticles to remain stable and maintain their efficacy for up to a month when stored at −80 °C, regardless of cargo or type of nanoparticle. DNA‐loaded nanoparticles also remain stable in a wider variety of storage conditions than mRNA‐loaded ones. Importantly, these novel LNPs show increased GFP expression that can signify their future use in gene therapies, beyond the established role of LNPs in RNA therapeutics.

Year:

2023

Year:

2023

Year:

2021

Collaborators (4)

Jane Elizabeth Alder

Deputy Head of School

University of Central Lancashire

UNITED KINGDOM
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Aristides D. Tagalakis

-

UNITED KINGDOM
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Anna-Maria G. Psarra

University of Thessaly

GREECE
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Joseph M Hayes

Lecturer in Synthetic Biology

University of Central Lancashire

UNITED KINGDOM
View details
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