Drug delivery systems: anticancer prodrugs and their polymeric conjugates
- 1 June 1997
- journal article
- Published by Informa Healthcare in Expert Opinion on Therapeutic Patents
- Vol. 7 (6) , 601-609
- https://doi.org/10.1517/13543776.7.6.601
Abstract
Prodrugs and their polymeric conjugates (transport forms) offer many promising modalities for new cancer chemotherapies. They present unique opportunities to increase the therapeutic index of a particular drug by exploiting the properties associated with the disease in a predictable fashion. Drugs can be chemically modified with a promoiety to achieve an exclusive selectivity by utilising specific enzymes, fenestrated vasculatures, more acidic environments and other unique properties of the tumour. Additionally, by incorporating a promoiety into existing immunoconjugates, greater efficacy can be achieved.Keywords
This publication has 27 references indexed in Scilit:
- Characterization of novel anthracycline prodrugs activated by human β-glucuronidase for use in antibody-directed enzyme prodrug therapyBiochemical Pharmacology, 1996
- Design, Synthesis, and Pharmacokinetic Evaluation of a Chemical Delivery System for Drug Targeting to Lung TissueJournal of Pharmaceutical Sciences, 1996
- Design, Synthesis, and Evaluation of Latent Alkylating Agents Activated by Glutathione S-TransferaseJournal of Medicinal Chemistry, 1996
- Improved Characteristics of a Human β-Glucuronidase−Antibody Conjugate after Deglycosylation for Use in Antibody-Directed Enzyme Prodrug TherapyBioconjugate Chemistry, 1996
- β-Glucuronyl carbamate based pro-moieties designed for prodrugs in ADEPTTetrahedron Letters, 1995
- A monoclonal antibody-β-glucuronidase conjugate as activator of the prodrug epirubicin-glucuronide for specific treatment of cancerBritish Journal of Cancer, 1992
- Enediyne Compounds Equipped with Acid‐, Base‐ and Photo‐Sensitive Triggering Devices. Chemical Simulation of the Dynemicin A Reaction CascadeAngewandte Chemie International Edition in English, 1991
- Development of a drug-release strategy based on the reductive fragmentation of benzyl carbamate disulfidesThe Journal of Organic Chemistry, 1990
- A novel connector linkage applicable in prodrug designJournal of Medicinal Chemistry, 1981
- Increased selectivity of drugs by linking to carriersPublished by Elsevier ,1978