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Ligand-Targeted Drug Delivery

Srinivasarao, Madduri, Low, Philip S.·2017·Chemical Reviews

Abstract

Safety and efficacy constitute the major criteria governing regulatory approval of any new drug. The best method to maximize safety and efficacy is to deliver a proven therapeutic agent with a targeting ligand that exhibits little affinity for healthy cells but high affinity for pathologic cells. The probability of regulatory approval can conceivably be further enhanced by exploiting the same targeting ligand, conjugated to an imaging agent, to select patients whose diseased tissues display sufficient targeted receptors for therapeutic efficacy. The focus of this Review is to summarize criteria that must be met during design of ligand-targeted drugs (LTDs) to achieve the required therapeutic potency with minimal toxicity. Because most LTDs are composed of a targeting ligand (e.g., organic molecule, aptamer, protein scaffold, or antibody), spacer, cleavable linker, and therapeutic warhead, criteria for successful design of each component will be described. Moreover, because obstacles to successful drug design can differ among human pathologies, limitations to drug delivery imposed by the unique characteristics of different diseases will be considered. With the explosion of genomic and transcriptomic data providing an ever-expanding selection of disease-specific targets, and with tools for high-throughput chemistry offering an escalating diversity of warheads, opportunities for innovating safe and effective LTDs has never been greater.

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Metadata

Authors
Srinivasarao, M., & Low, P. S.
Venue
Chemical Reviews
Published
2017-09-12
Volume
117
Issue
19
Pages
12133-12164
ISSN
  • 0009-2665 (ISSN-L)
  • 1520-6890
OpenAlex
W2754938970
Cited by
605
References
20
FWCI
3.01
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Ligand-Targeted Drug Delivery. https://app.cochat.ai/papers/10.1021/acs.chemrev.7b00013
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Srinivasarao, M., & Low, P. S. (2017). Ligand-Targeted Drug Delivery. Chemical Reviews. https://doi.org/10.1021/acs.chemrev.7b00013

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