Martin, Claire - University of Wolverhampton - Faculty of Science & Engineering

个人简介

Dr. Claire Martin (BSc Hons, PG Dip, FHEA, PhD, MAPS, FRSB, CBiol), is a highly experienced formulation scientist with an established track record of high quality national and international research, income generation, publications, presentations and industrial collaborations. After completing her PhD in pharmaceutical science at The University of London, School of Pharmacy (ULSOP), Dr. Martin developed key research themes of novel homogenisation strategies for biopharmaceutical products during a BBSRC-funded postdoctoral fellowship at ULSOP and University of Cambridge. Currently a Senior Lecturer in Pharmaceutics and Director of the Anti-Infective Delivery Research Group (AIDRG), Dr. Martin leads a collective of 18 scientists based in the UK and Malaysia. Dr. Martin’s research interests and those of the AIDRG centre around the development of responsive controlled release delivery systems for wound management, formulation and assay development of novel antimicrobial agents as well as development of non-parenteral formulations for the delivery of anti-infective agent. Dr. Martin is an active member of the academic pharmaceutical sciences community both nationally and internationally through collaborations, external examining and professional networking. She is author/co-author of over 60 publications, including book chapters, reviews, journal articles and conference proceedings. Dr. Martin is a regular reviewer for sixteen high impact pharmaceutical and analytical science journals, national funding bodies and international conference committees. Her contribution to the biological sciences has been recognised by the Royal Society of Biology with the award of Fellowship (FRSB) and granting of Chartered Biologist status (CBiol).

研究领域

Environmentally responsive, controlled release delivery systems for wound management Formulation and assay development of novel antimicrobial agents In vitro modelling of wound healing Development of platform solid dosage formulation technologies combined with advanced drug delivery systems for the treatment of oropharyngeal and gastrointestinal infections

近期论文

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Mohamad, N., Amin, M.C.I.M., Martin, C. and Buang, F. (2016). Characterization and biocompatibility of bacterial cellulose-based wound dressing hydrogel: The effect of electron beam irradiation doses and concentrations of acrylic acid. Journal of Biomedical Materials Research Part B: Applied Biomaterials. Available at: http://onlinelibrary.wiley.com/doi/10.1002/jbm.b.33776/full. Low, W.L., Kenward, M.A., Britland, S.T., Amin, M.C.I.M. and Martin, C. (2016). Essential oils and metal ions as alternative antimicrobial agents: A focus on tea tree oil and silver. International Wound Journal. In press. Available at http://onlinelibrary.wiley.com/doi/10.1111/iwj.12611/epdf. Gupta, A., Low, W.L., Radecka, I., Britland, S.T., Amin, M.C.I.M., and Martin, C. (2016). Characterisation and in vitro antimicrobial activity of biosynthetic silver-loaded bacterial cellulose hydrogels. Journal of Microencapsulation, 33 (8): 725 – 734. Gupta, A., Britland, S.T., Radecka, I. and Martin, C. (2016). Antimicrobial silver nanoparticle-loaded Bacterial cellulose hydrogels: Wound Management Applications. Chemistry: The Science Around Us Proceedings, 9th September 2016, University of Sheffield, Sheffield, U.K. #13. Wansi, J.D., Alain, T.T., Toze, F.A.A., Nahar, L., Martin, C. and Sarker, S.D. (2016). Cytotoxicity of Acridone and Idoloquinazoline Alkaloids from Zanthoxylum poggei. Phytochemistry Letters, 17: 293-298. Gupta, A., Britland, S.T., Radecka, I., Low, W.L. and Martin, C. (2016). Improved antimicrobial activity of silver nanoparticle-loaded bacterial cellulose hydrogels. UKPharmSci 2016 Conference Proceedings, 5th – 7th September 2016, Technology & Innovation Centre, University of Strathclyde, Glasgow, U.K. Wansi, J.D., Wandji, J., Sewald, N., Nahar, L., Martin, C. and Sarker, S.D. (2016). Phytochemistry and pharmacology of the genus Drypetes: A review. Journal of Ethnopharmacology, 190: 328 – 353.