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dc.contributor.authorTaliyan, Rajeev-
dc.date.accessioned2023-12-14T04:13:56Z-
dc.date.available2023-12-14T04:13:56Z-
dc.date.issued2023-09-
dc.identifier.urihttps://www.future-science.com/doi/full/10.4155/bio-2023-0104-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/13415-
dc.description.abstractAntibody–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.isoenen_US
dc.publisherFuture Science Groupen_US
dc.subjectPharmacyen_US
dc.subjectAntibody–drug conjugateen_US
dc.subjectToxicityen_US
dc.subjectLBA-LC–MS assaysen_US
dc.subjectPharmacokineticsen_US
dc.titlePharmacokinetics and toxicity considerations for antibody–drug conjugates: an overviewen_US
dc.typeArticleen_US
Appears in Collections:Department of Pharmacy

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