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European Biopharmaceutical Review

Targeted Nanoparticles

The mainstreams of conventional cancer treatment remain chemotherapy and radiotherapy. These traditional therapeutic approaches are plagued by poor tissue targeting, inducing destruction of healthy tissue, which results in toxic side-effects, as well as suboptimal dosing of the targeted area.

In addition to traditional small molecule chemotherapeutic agents, a plethora of biological agents have the potential to be used in the treatment of cancer. Many substances have demonstrated useful efficacies in vitro, but have failed in their ability to alleviate the disease in vivo due to a wide range of issues including poor dosing of target area, low bioavailability and inability to internalise to the tumour cells.

Thus, once administered into the circulatory system, biologics such as proteins and peptides are subjected to various immune mechanisms, such as opsonisation and receptor endocytosis. Those mechanisms, in addition to renal filtration induce rapid degradation of most therapeutic proteins, limiting their usefulness.

In recent years, drug delivery research has examined the formulation of a full spectrum of nanoparticles that can suit various drugs types, with different parameters, such as size, entrapment efficiency or release profile, studied in depth. Additionally, delivery of poor water soluble chemotherapy drugs, such as Docetaxel or Paclitaxel, have been improved through their encapsulation inside nanoparticle carriers, demonstrating increased in vivo efficiency compared with naked administration.

Furthermore, in an attempt to produce specific targeted delivery carriers, a range of molecules have been grafted on the surface of the nanoparticles to induce interaction with cells and active internalisation of the particles inside the tumours. The main classes of nanoparticle and antibody mediated targeting strategies are briefly discussed in this article.

CLASSES OF NANOPARTICLE

Liposomes
Lipososmes are among the first and most intensely studied and evaluated nanoparticles. The development of liposomal vesicular carriers has been pursued based on the concept of mimicking natural lipid bilayers and micelle formation.

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Francois Fay graduated in Biotechnology in 2006 from the Bordeaux II University Institute of Biotechnology (Bordeaux, France). Francois is currently completing his PhD at the School of Pharmacy, Queen’s University Belfast, where he is developing polymeric nanoparticles formulations for cell cytosolic delivery of bioactive proteins and nucleic acids.

Dr Richard Buick is the Technical Director of Fusion Antibodies Ltd and has ten years industrial experience in the recombinant antibody field. His PhD from Queen’s University, Belfast was in engineering antibody therapeutics for cancer. At Fusion Antibodies, he manages client projects and in-house recombinant antibody research projects.

Dr Shane Olwill is R&D Director of Fusion Antibodies Ltd. He joined the Company in 2003 as a Senior Scientist after receiving his PhD in molecular haematology from the University of Ulster, where he studied chemotherapy induced regulation of proteins. Shane is responsible for the Company’s drug discovery programme which focuses on of the development of novel antibody based therapeutics.

Dr Christopher Scott obtained his PhD in Biochemistry at Queen’s University Belfast in 2000, then undertaking a postdoctoral fellowship. Chris then moved to Fusion Antibodies Ltd, developing their protein engineering platforms before being appointed lecturer in the School of Pharmacy at Queen’s University. His current research programmes involve the application of antibodies and antibody conjugates for the treatment of cancer.

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Francois Fay
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Dr Richard Buick
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Dr Shane Olwill
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Dr Christopher Scott
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6th European Forum for Qualified Person for Pharmacovigilance (QPPV)

24-26 April 2012, London, UK

This event is for European qualified persons for pharmacovigilance; deputy qualified persons; senior pharmacovigilance regulators and inspectors; CROs and consultants providing QPPV services; and national responsible persons for pharmacovigilance.
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The new DASGIP Product Catalogue is now available online. The catalogue offers a user-friendly update on our technology. You will find a comprehensive overview on our portfolio including information on recently launched products such as our Bioprocess Software Suite DASware and the Minibioreactor System DASbox.
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