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Biotechnology 2004, 12th International Symposium

Santiago, Chile, 17-22 October 2004
Messel Bursar Tarit Mukhopadhyay reports

Santiago skylineChile isn't the first place you would think of to hold the 12th symposium on biotechnology. But though there was time for a wine tasting session, several cultural events and a conference dinner, one impression was clear. Chile places a great deal of importance on biotechnology, and its president, Ricardo Lagos Escobar, opened the conference.

In his address President Lagos declared the importance of biotechnology in his country and the noteworthy impact it has on many developing nations, not just through foreign investment but through the vaccines and drug discoveries which benefit many people around the world.

Over 40 nations were represented at this conference, which is held once every four years and is widely regarded as a tour de force by those in the industry. It was a very intensive five days with two keynote speeches delivered each morning and concurrent sessions running thereafter. The subject matter was wide and varied ranging from molecular and genomic tools to cultivation technology and downstream processing.

One of the highlights of the conference was a key note speech delivered by Barry Buckland of Merck Inc. He talked about the development and production of virus like particles for the treatment of human papilloma virus (HPV), which is known to cause cervical cancer.

Worldwide, cervical cancer is the second leading cause of cancer-related deaths in women. Merck's Phase III study targets four different HPV subtypes: HPV 6, 11, 16 and 18, the latter two being associated with a majority of cervical cancer deaths. Mr Buckland showed data collected over the past two years that indicated the vaccine candidate reduced the incidence of infection in 100 percent of women who had not been previously infected with HPV 16, offering a very promising future.

One of the more salient features brought up in his talk discusses the problems of aggregation of virus-like particles which causes total product loss if this occurs before chromatography. With further discussions with him after the talk it became apparent that aggregation is a common problem in the final formulation of many vaccine products, including my own area of interest, meningococcal protein vaccines. He proved to be very helpful and we discussed possible options

My own presentation was met with curiosity and amiably received as I explained the application and limitations of micro-scale devices and methodologies; in particular understanding growth in microwell plates. The assumption that bacterial growth in microwells is a function of oxygen transfer forms the basis of most research in this field. This explains why the greatest focus has been placed into formulating new ways to accurately measure and predict the oxygen mass transfer co-efficient, (kLa). However, calculating this value is notoriously difficult because of the small volumes involved, coupled with the limitation of functional probes. Hence my presentation set to highlight a new approach that uses dimensionless modelling which no longer requires calculating kLa values and allows the prediction of growth in other larger systems. The presentation motivated much feedback and debate which I found very useful and thought provoking.

This conference was one of firsts. It was my first experience of peer review; it was my first experience of presenting at conference. In fact, it was the first conference I had ever attended and indeed my first time in South America. There is little doubt that I have benefited from the SCI's generosity, both academically and personally, for which I am most grateful. Thank you SCI!