Cameron Alexander

Cameron Alexander


Research Focus & Metrics

Academic Career Length

36Years (1991-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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8 February 2005 in Chemical Society Reviews
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CACarolina de Las Heras Alarcón
Carolina de Las Heras Alarcón
SPSivanand Pennadam
Sivanand Pennadam
CACameron Alexander
Cameron Alexander
Polymers that can respond to external stimuli are of great interest in medicine, especially as controlled drug release vehicles. In this critical review, we consider the types of stimulus response used in therapeutic applications and the main classes of responsive materials developed to date. Particular emphasis is placed on the wide-ranging possibilities for the biomedical use of these polymers, ranging from drug delivery systems and cell adhesion mediators to controllers of enzyme function and gene expression (134 references).

1 March 2006 in Journal of Molecular Recognition
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Journal Article
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CACameron Alexander
Cameron Alexander
HAHåkan S Andersson
Håkan S Andersson
LALars I. Andersson
Lars I. Andersson
RARichard J. Ansell
Richard J. Ansell
NKNicole Kirsch
Nicole Kirsch
MWMichael J. Whitcombe
Michael J. Whitcombe


24 July 2008 in Journal of the American Chemical Society
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Journal Article
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JMJohannes Pall Magnusson
Johannes Pall Magnusson
AKAdnan Khan
Adnan Khan
GPGeorge Pasparakis
George Pasparakis
ASAram Omer Saeed
Aram Omer Saeed
Wenxin WangWenxin Wang
Wenxin Wang
CACameron Alexander
Cameron Alexander

13 August 2014 in PLOS ONE
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Journal Article
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DIDelyan P Ivanov
Delyan P Ivanov
TPTerry L Parker
Terry L Parker
DWDavid A Walker
David A Walker
CACameron Alexander
Cameron Alexander
MAMarianne B Ashford
Marianne B Ashford
MGMartin C. Garnett
Martin C. Garnett
Three-dimensional cell culture has many advantages over monolayer cultures, and spheroids have been hailed as the best current representation of small avascular tumours in vitro. However their adoption in regular screening programs has been hindered by uneven culture growth, poor reproducibility and lack of high-throughput analysis methods for 3D. The objective of this study was to develop a method for a quick and reliable anticancer drug screen in 3D for tumour and human foetal brain tissue in order to investigate drug effectiveness and selective cytotoxic effects. Commercially available ultra-low attachment 96-well round-bottom plates were employed to culture spheroids in a rapid, reproducible manner amenable to automation. A set of three mechanistically different methods for spheroid health assessment (Spheroid volume, metabolic activity and acid phosphatase enzyme activity) were validated against cell numbers in healthy and drug-treated spheroids. An automated open-source ImageJ macro was developed to enable high-throughput volume measurements. Although spheroid volume determination was superior to the other assays, multiplexing it with resazurin reduction and phosphatase activity produced a richer picture of spheroid condition. The ability to distinguish between effects on malignant and the proliferating component of normal brain was tested using etoposide on UW228-3 medulloblastoma cell line and human neural stem cells. At levels below 10 µM etoposide exhibited higher toxicity towards proliferating stem cells, whereas at concentrations above 10 µM the tumour spheroids were affected to a greater extent. The high-throughput assay procedures use ready-made plates, open-source software and are compatible with standard plate readers, therefore offering high predictive power with substantial savings in time and money.

1 March 2003 in Tetrahedron
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Journal Article
Closed access
CACameron Alexander
Cameron Alexander
LDLouise Davidson
Louise Davidson
WHWayne Hayes
Wayne Hayes