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Current Developments in Pt(IV) Prodrugs Conjugated with Bioactive Ligands

To overcome the side effects of and resistance to cisplatin, a variety of Pt(IV) prodrugs were designed and synthesized via different modifications including combination with lipid chains to increase hydrophobicity, conjugation with short peptide chains or nanoparticles to improve drug delivery, or...

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Detalles Bibliográficos
Autores principales: Li, Xuejiao, Liu, Yahong, Tian, Hongqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6191961/
https://www.ncbi.nlm.nih.gov/pubmed/30402082
http://dx.doi.org/10.1155/2018/8276139
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author Li, Xuejiao
Liu, Yahong
Tian, Hongqi
author_facet Li, Xuejiao
Liu, Yahong
Tian, Hongqi
author_sort Li, Xuejiao
collection PubMed
description To overcome the side effects of and resistance to cisplatin, a variety of Pt(IV) prodrugs were designed and synthesized via different modifications including combination with lipid chains to increase hydrophobicity, conjugation with short peptide chains or nanoparticles to improve drug delivery, or addition of bioactive ligands to the axial positions of Pt(IV) complexes to exert dual-function effects. This review summarizes the recent progress in the development of Pt(IV) prodrugs conjugated with bioactive-targeting ligands, including histone deacetylase inhibitors, p53 agonists, alkylating agents, and nonsteroidal anti-inflammatory agents. Although Pt(IV) complexes that conjugated with bioactive ligands show satisfactory anticancer effects, none has been approved for clinical use. Therefore, we hope that this review will contribute to further study and development of Pt(IV) complexes conjugated with bioactive and other ligands.
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spelling pubmed-61919612018-11-06 Current Developments in Pt(IV) Prodrugs Conjugated with Bioactive Ligands Li, Xuejiao Liu, Yahong Tian, Hongqi Bioinorg Chem Appl Review Article To overcome the side effects of and resistance to cisplatin, a variety of Pt(IV) prodrugs were designed and synthesized via different modifications including combination with lipid chains to increase hydrophobicity, conjugation with short peptide chains or nanoparticles to improve drug delivery, or addition of bioactive ligands to the axial positions of Pt(IV) complexes to exert dual-function effects. This review summarizes the recent progress in the development of Pt(IV) prodrugs conjugated with bioactive-targeting ligands, including histone deacetylase inhibitors, p53 agonists, alkylating agents, and nonsteroidal anti-inflammatory agents. Although Pt(IV) complexes that conjugated with bioactive ligands show satisfactory anticancer effects, none has been approved for clinical use. Therefore, we hope that this review will contribute to further study and development of Pt(IV) complexes conjugated with bioactive and other ligands. Hindawi 2018-10-01 /pmc/articles/PMC6191961/ /pubmed/30402082 http://dx.doi.org/10.1155/2018/8276139 Text en Copyright © 2018 Xuejiao Li et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Li, Xuejiao
Liu, Yahong
Tian, Hongqi
Current Developments in Pt(IV) Prodrugs Conjugated with Bioactive Ligands
title Current Developments in Pt(IV) Prodrugs Conjugated with Bioactive Ligands
title_full Current Developments in Pt(IV) Prodrugs Conjugated with Bioactive Ligands
title_fullStr Current Developments in Pt(IV) Prodrugs Conjugated with Bioactive Ligands
title_full_unstemmed Current Developments in Pt(IV) Prodrugs Conjugated with Bioactive Ligands
title_short Current Developments in Pt(IV) Prodrugs Conjugated with Bioactive Ligands
title_sort current developments in pt(iv) prodrugs conjugated with bioactive ligands
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6191961/
https://www.ncbi.nlm.nih.gov/pubmed/30402082
http://dx.doi.org/10.1155/2018/8276139
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