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SEMINAR ANNOUNCEMENT

Design and evaluation of Selective adenosine receptors antagonists and Development of FUNctionalized carbon nanotubes as delivery systems

by

Dr Giorgia Pastorin
Institut de Biologie Moleculaire et Cellulaire
France

on

Date: Wednesday, 11 Jan 2006
Time: 10.00am
Venue: Seminar Room (S4-05-16)
Department of Pharmacy

Synopsis:

The selective modulation of Adenosine receptors represents the basis for understanding the pathophysiological role of such unknown receptors. In particular, it has already been reported that some pyrazolotriazolopyrimidines resulted to be highly potent antagonists of the human A3 subtype, whose inhibition seems to be useful in the treatment of inflammation and regulation of cell growth. Starting from that, we decided to synthetize new compounds that allowed us to evaluate the effects of each substituent both from a chemical and a sterical point of view. This study was associated to a molecular modeling evaluation to support the results and to suggest the design of new potent antagonists.

Recently, carbon nanotubes (CNT) have attracted the attention of several scientists, due to their unique and intriguing structure and properties. These nanoobjects hold a lot of promises for application in medicinal chemistry for different reasons: inducible water solubility, high stability of the dispersion, lack of intrinsic immunogenicity and an efficient loading capacity. Functionalization of the surface of CNT has allowed not only a great improvement of their solubility, but also paved the way to new interesting applications, as suggested by their recent use as vectors for internalization into the cell of therapeutic molecules.

In this Communication, I will cover my main research interests. In the first part I will talk about the design, the synthesis and the QSAR profile of some policyclic systems as potent adenosine antagonists. In the second part, I will describe an efficient strategy for the funcionalization of carbon nanotubes and some examples of their potential biological applications in the field of drug delivery, together with a brief evaluation of the important issue concerning their toxicity.

ALL ARE WELCOME

 

 

 

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