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Pharmacokinetics and toxicity considerations for antibody–drug conjugates: an overview

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dc.contributor.author Taliyan, Rajeev
dc.date.accessioned 2023-12-14T04:13:56Z
dc.date.available 2023-12-14T04:13:56Z
dc.date.issued 2023-09
dc.identifier.uri https://www.future-science.com/doi/full/10.4155/bio-2023-0104
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/13415
dc.description.abstract Antibody–drug conjugates (ADCs) is one of the fastest-growing drug-delivery systems. It involves a monoclonal antibody conjugated with payload via a ligand that directly targets the expressive protein of diseased cell. Hence, it reduces systemic exposure and provides site-specific delivery along with reduced toxicity. Because of this advantage, researchers have gained interest in this novel system. ADCs have displayed great promise in drug delivery and biomedical applications. However, a lack of understanding exists on their mechanisms of biodistribution, metabolism and side effects. To gain a better understanding of the therapeutics, careful consideration of the pharmacokinetics and toxicity needs to be undertaken. In this review, different pharmacokinetics parameters including distribution, bioanalysis and heterogeneity are discussed for developing novel therapeutics. en_US
dc.language.iso en en_US
dc.publisher Future Science Group en_US
dc.subject Pharmacy en_US
dc.subject Antibody–drug conjugate en_US
dc.subject Toxicity en_US
dc.subject LBA-LC–MS assays en_US
dc.subject Pharmacokinetics en_US
dc.title Pharmacokinetics and toxicity considerations for antibody–drug conjugates: an overview en_US
dc.type Article en_US


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