Imperial College London

Dr Nick Brooks

Faculty of Natural SciencesDepartment of Chemistry

Reader in Membrane Biophysics
 
 
 
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Contact

 

+44 (0)20 7594 2677n.brooks Website

 
 
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Location

 

207JMolecular Sciences Research HubWhite City Campus

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Summary

 

Publications

Citation

BibTex format

@article{Strutt:2022:10.1039/d1lc01155c,
author = {Strutt, R and Sheffield, F and Barlow, N and Flemming, AJ and Harling, JD and Law, RV and Brooks, NJ and Barter, LMC and Ces, O},
doi = {10.1039/d1lc01155c},
journal = {Lab on a Chip: miniaturisation for chemistry, physics, biology, materials science and bioengineering},
pages = {972--985},
title = {UV-DIB: label-free permeability determination using droplet interface bilayers},
url = {http://dx.doi.org/10.1039/d1lc01155c},
volume = {22},
year = {2022}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - Simple diffusion of molecular entities through a phospholipid bilayer, is a phenomenon of great importance to the pharmaceutical and agricultural industries. Current model lipid systems to probe this typically only employ fluorescence as a readout, thus limiting the range of assessable chemical matter that can be studied. We report a new technology platform, the UV-DIB, which facilitates label free measurement of small molecule translocation rates. This is based upon the coupling of droplet interface bilayer technology with implemented fiber optics to facilitate analysis via ultraviolet spectroscopy, in custom designed PMMA wells. To improve on current DIB technology, the platform was designed to be reusable, with a high sampling rate and a limit of UV detection in the low μM regime. We demonstrate the use of our system to quantify passive diffusion in a reproducible and rapid manner where the system was validated by investigating multiple permeants of varying physicochemical properties across a range of lipid interfaces, each demonstrating differing kinetics. Our system permits the interrogation of structural dependence on the permeation rate of a given compound. We present this ability from two structural perspectives, that of the membrane, and the permeant. We observed a reduction in permeability between pure DOPC and DPhPC interfaces, concurring with literature and demonstrating our ability to study the effects of lipid composition on permeability. In relation to the effects of permeant structure, our device facilitated the rank ordering of various compounds from the xanthine class of compounds, where the structure of each permeant differed by a single group alteration. We found that DIBs were stable up to 5% DMSO, a molecule often used to aid solubilisation of pharmaceutical and agrochemical compounds. The ability of our device to rank-order compounds with such minor structural differences provides a level of precision that is rarely seen in current, industr
AU - Strutt,R
AU - Sheffield,F
AU - Barlow,N
AU - Flemming,AJ
AU - Harling,JD
AU - Law,RV
AU - Brooks,NJ
AU - Barter,LMC
AU - Ces,O
DO - 10.1039/d1lc01155c
EP - 985
PY - 2022///
SN - 1473-0189
SP - 972
TI - UV-DIB: label-free permeability determination using droplet interface bilayers
T2 - Lab on a Chip: miniaturisation for chemistry, physics, biology, materials science and bioengineering
UR - http://dx.doi.org/10.1039/d1lc01155c
UR - https://pubs.rsc.org/en/content/articlelanding/2022/LC/D1LC01155C
UR - http://hdl.handle.net/10044/1/94273
VL - 22
ER -