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A. J. MacRobert
Researcher at University College London
Publications - 82
Citations - 4344
A. J. MacRobert is an academic researcher from University College London. The author has contributed to research in topics: Photodynamic therapy & Protoporphyrin IX. The author has an hindex of 38, co-authored 82 publications receiving 4227 citations. Previous affiliations of A. J. MacRobert include Royal Institution.
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Journal ArticleDOI
Photosensitisation and photodynamic therapy of oesophageal, duodenal, and colorectal tumours using 5 aminolaevulinic acid induced protoporphyrin IX--a pilot study
Jaroslaw Regula,A. J. MacRobert,A Gorchein,G Buonaccorsi,Sally Thorpe,G M Spencer,A R Hatfield,Sg Bown +7 more
TL;DR: Photodynamic therapy with systemically administered ALA may be a promising technique for the treatment of small tumours and areas of dysplasia such as in Barrett's oesophagus.
Journal ArticleDOI
In Vivo Killing of Porphyromonas gingivalis by Toluidine Blue-Mediated Photosensitization in an Animal Model
N Komerik,H. Nakanishi,H. Nakanishi,A. J. MacRobert,Brian Henderson,Paul M. Speight,Michael Wilson +6 more
TL;DR: The results of this study show that toluidine blue-mediated lethal photosensitization of P. gingivalis is possible in vivo and that this results in decreased bone loss, suggesting that photodynamic therapy may be useful as an alternative approach for the antimicrobial treatment of periodontitis.
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Photodynamic therapy of oral cancer: photosensitisation with systemic aminolaevulinic acid
TL;DR: This is the first report of tumour necrosis brought about by photodynamic activation of a temporary endogenous porphyrin accumulation, after an oral dose of the haem precursor, 5-aminolaevulinic acid.
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Fluorescence distribution and photodynamic effect of ALA-induced PP IX in the DMH rat colonic tumour model.
TL;DR: ALA may be superior to conventional sensitiser for tumours that produce haem as the PP IX is synthesised in malignant cells while the other sensitisers mainly localise to the vascular stroma of tumours, raising the possibility of more selective necrosis in tumours.
Journal ArticleDOI
Oral versus intravenous administration of 5-aminolaevulinic acid for photodynamic therapy
TL;DR: The porphyrin sensitisation kinetics profile in the stomach, colon and bladder in normal rats following enterally and parenterally administered ALA was studied using microscopic fluorescence photometric studies of frozen tissue sections and the highest level of fluorescence was achieved in the gastric mucosa and in decreasing levels, colonic and bladder mucosa.