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Drug Targeting Organ-Specific Strategies

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304 11 Development of Proteinaceous <strong>Drug</strong> <strong>Targeting</strong> Constructs<br />

11.10 Concluding Remarks<br />

This chapter has presented many approaches to the preparation of drug targeting constructs.<br />

In these constructs, a protein or part of it may function as a carrier for attached drug molecules,<br />

as a specific targeting moiety, or as a therapeutically active substance. Two entirely different<br />

approaches have been followed in the preparation of proteinaceous drug targeting<br />

constructs. First, chemical derivatization of existing proteins with site-directing ligands<br />

and/or drug molecules, and second, the engineering and expression of recombinant DNA<br />

constructs. Depending on the type of construct required, each approach has its own unique<br />

advantages. For instance, the engineering of protein backbone structures is most accurately<br />

performed by recombinant techniques. On the other hand, chemical approaches can be used<br />

for the attachment of small organic drug molecules, offering numerous opportunities for<br />

therapeutic intervention which cannot be matched by proteinaceous drug substances. Therefore,<br />

with reference to the title of this chapter, proteinaceous drug targeting constructs<br />

should preferably be prepared by chemical and recombinant DNA techniques, rather than by<br />

the exclusive use of either one.<br />

Acknowledgements<br />

R. J. Kok and S. A. Ásgeirsdóttir are members of UNYPHAR, a network collaboration between<br />

the universities of Groningen, Leiden and Utrecht and the pharmaceutical company<br />

Yamanouchi.<br />

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