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Photochemically controlled drug dosing from a polymeric scaffold

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Photochemically controlled drug dosing from a polymeric scaffold. / Donnelly, Louise; Hardy, John George; Gorman, Sean P. et al.
In: Pharmaceutical Research, Vol. 34, No. 7, 07.2017, p. 1469-1476.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Donnelly, L, Hardy, JG, Gorman, SP, Jones, DS, Irwin, NJ & McCoy, CP 2017, 'Photochemically controlled drug dosing from a polymeric scaffold', Pharmaceutical Research, vol. 34, no. 7, pp. 1469-1476. https://doi.org/10.1007/s11095-017-2164-9

APA

Donnelly, L., Hardy, J. G., Gorman, S. P., Jones, D. S., Irwin, N. J., & McCoy, C. P. (2017). Photochemically controlled drug dosing from a polymeric scaffold. Pharmaceutical Research, 34(7), 1469-1476. https://doi.org/10.1007/s11095-017-2164-9

Vancouver

Donnelly L, Hardy JG, Gorman SP, Jones DS, Irwin NJ, McCoy CP. Photochemically controlled drug dosing from a polymeric scaffold. Pharmaceutical Research. 2017 Jul;34(7):1469-1476. Epub 2017 May 15. doi: 10.1007/s11095-017-2164-9

Author

Donnelly, Louise ; Hardy, John George ; Gorman, Sean P. et al. / Photochemically controlled drug dosing from a polymeric scaffold. In: Pharmaceutical Research. 2017 ; Vol. 34, No. 7. pp. 1469-1476.

Bibtex

@article{c8668340eb90438fa910924ee0307913,
title = "Photochemically controlled drug dosing from a polymeric scaffold",
abstract = "PurposeTo develop the first photoactive biomaterial coating capable of controlled drug dosing via inclusion of synthesised drug-3,5-dimethoxybenzoin (DMB) conjugates in a poly(2-methyoxyethyl acrylate) (pMEA) scaffold.MethodsFlurbiprofen- and naproxen-DMB conjugates were prepared via esterification and characterised via NMR spectroscopy and mass spectrometry following chromatographic purification. Conjugate photolysis was investigated in acetonitrile solution and within the pMEA matrix following exposure to low-power 365 nm irradiation. Photo-liberation of drug from pMEA into phosphate buffered saline was monitored using UV-vis spectroscopy.ResultsThe synthetic procedures yielded the desired drug conjugates with full supporting characterisation. Drug regeneration through photolysis of the synthesised conjugates was successful in both acetonitrile solution and within the pMEA scaffold upon UV irradiation. Conjugates were retained within the pMEA scaffold with exclusive drug liberation following irradiation and increased drug dose with increasing exposure. Multi-dosing capacity was demonstrated though the ability of successive irradiation periods to generate further bursts of drug.ConclusionThis study demonstrates the first application of photochemically controlled drug release from a biomaterial coating and the feasibility of using pMEA as a scaffold for housing the photoactive drug-DMB conjugates.",
keywords = "drug delivery, polymers, chemical engineering, pharmacy, Pharmaceutical science, chemistry, materials science, Biomedical Engineering",
author = "Louise Donnelly and Hardy, {John George} and Gorman, {Sean P.} and Jones, {David S.} and Irwin, {Nicola J.} and McCoy, {Colin P.}",
year = "2017",
month = jul,
doi = "10.1007/s11095-017-2164-9",
language = "English",
volume = "34",
pages = "1469--1476",
journal = "Pharmaceutical Research",
issn = "0724-8741",
publisher = "Springer New York",
number = "7",

}

RIS

TY - JOUR

T1 - Photochemically controlled drug dosing from a polymeric scaffold

AU - Donnelly, Louise

AU - Hardy, John George

AU - Gorman, Sean P.

AU - Jones, David S.

AU - Irwin, Nicola J.

AU - McCoy, Colin P.

PY - 2017/7

Y1 - 2017/7

N2 - PurposeTo develop the first photoactive biomaterial coating capable of controlled drug dosing via inclusion of synthesised drug-3,5-dimethoxybenzoin (DMB) conjugates in a poly(2-methyoxyethyl acrylate) (pMEA) scaffold.MethodsFlurbiprofen- and naproxen-DMB conjugates were prepared via esterification and characterised via NMR spectroscopy and mass spectrometry following chromatographic purification. Conjugate photolysis was investigated in acetonitrile solution and within the pMEA matrix following exposure to low-power 365 nm irradiation. Photo-liberation of drug from pMEA into phosphate buffered saline was monitored using UV-vis spectroscopy.ResultsThe synthetic procedures yielded the desired drug conjugates with full supporting characterisation. Drug regeneration through photolysis of the synthesised conjugates was successful in both acetonitrile solution and within the pMEA scaffold upon UV irradiation. Conjugates were retained within the pMEA scaffold with exclusive drug liberation following irradiation and increased drug dose with increasing exposure. Multi-dosing capacity was demonstrated though the ability of successive irradiation periods to generate further bursts of drug.ConclusionThis study demonstrates the first application of photochemically controlled drug release from a biomaterial coating and the feasibility of using pMEA as a scaffold for housing the photoactive drug-DMB conjugates.

AB - PurposeTo develop the first photoactive biomaterial coating capable of controlled drug dosing via inclusion of synthesised drug-3,5-dimethoxybenzoin (DMB) conjugates in a poly(2-methyoxyethyl acrylate) (pMEA) scaffold.MethodsFlurbiprofen- and naproxen-DMB conjugates were prepared via esterification and characterised via NMR spectroscopy and mass spectrometry following chromatographic purification. Conjugate photolysis was investigated in acetonitrile solution and within the pMEA matrix following exposure to low-power 365 nm irradiation. Photo-liberation of drug from pMEA into phosphate buffered saline was monitored using UV-vis spectroscopy.ResultsThe synthetic procedures yielded the desired drug conjugates with full supporting characterisation. Drug regeneration through photolysis of the synthesised conjugates was successful in both acetonitrile solution and within the pMEA scaffold upon UV irradiation. Conjugates were retained within the pMEA scaffold with exclusive drug liberation following irradiation and increased drug dose with increasing exposure. Multi-dosing capacity was demonstrated though the ability of successive irradiation periods to generate further bursts of drug.ConclusionThis study demonstrates the first application of photochemically controlled drug release from a biomaterial coating and the feasibility of using pMEA as a scaffold for housing the photoactive drug-DMB conjugates.

KW - drug delivery

KW - polymers

KW - chemical engineering

KW - pharmacy

KW - Pharmaceutical science

KW - chemistry

KW - materials science

KW - Biomedical Engineering

U2 - 10.1007/s11095-017-2164-9

DO - 10.1007/s11095-017-2164-9

M3 - Journal article

VL - 34

SP - 1469

EP - 1476

JO - Pharmaceutical Research

JF - Pharmaceutical Research

SN - 0724-8741

IS - 7

ER -