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Reactions of cisplatin and oxaliplatin with penicillin G: implications for drug inactivation and biological activity

Determination of the toxicity of compounds toward cancer cells is a frequent procedure in drug discovery. For metal complexes, which are often reactive prodrugs, care has to be taken to consider reactions with components of the cell culture medium that might change the speciation of the metal comple...

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Autores principales: Wang, Fang-Xin, Prokes, Ivan, Song, Lijiang, Shi, Huayun, Sadler, Peter J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9653338/
https://www.ncbi.nlm.nih.gov/pubmed/36153767
http://dx.doi.org/10.1007/s00775-022-01958-z
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author Wang, Fang-Xin
Prokes, Ivan
Song, Lijiang
Shi, Huayun
Sadler, Peter J.
author_facet Wang, Fang-Xin
Prokes, Ivan
Song, Lijiang
Shi, Huayun
Sadler, Peter J.
author_sort Wang, Fang-Xin
collection PubMed
description Determination of the toxicity of compounds toward cancer cells is a frequent procedure in drug discovery. For metal complexes, which are often reactive prodrugs, care has to be taken to consider reactions with components of the cell culture medium that might change the speciation of the metal complex before it is taken up by the cells. Here, we consider possible reactions between the clinical platinum drugs cisplatin and oxaliplatin with penicillin G, an antibiotic added routinely to cell culture media to prevent bacterial contamination. Platinum has a high affinity for ligands with sulfur donors. Penicillin G is an unstable thioether that degrades in a range of pathways. Nuclear magnetic resonance (NMR) and UV–Vis absorption spectroscopic studies show that reactions with cisplatin can occur within minutes to hours at 310 K, but more slowly with oxaliplatin. The identities of the Pt- adducts were investigated by mass spectrometry. The marked effect on cytotoxicity of co-incubation of cisplatin with penicillin G was demonstrated for the HeLa human cervical cancer cell line. These studies highlight the possibility that reactions with penicillin G might influence the cytotoxic activity of metal complexes determined in culture media. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00775-022-01958-z.
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spelling pubmed-96533382022-11-15 Reactions of cisplatin and oxaliplatin with penicillin G: implications for drug inactivation and biological activity Wang, Fang-Xin Prokes, Ivan Song, Lijiang Shi, Huayun Sadler, Peter J. J Biol Inorg Chem Original Paper Determination of the toxicity of compounds toward cancer cells is a frequent procedure in drug discovery. For metal complexes, which are often reactive prodrugs, care has to be taken to consider reactions with components of the cell culture medium that might change the speciation of the metal complex before it is taken up by the cells. Here, we consider possible reactions between the clinical platinum drugs cisplatin and oxaliplatin with penicillin G, an antibiotic added routinely to cell culture media to prevent bacterial contamination. Platinum has a high affinity for ligands with sulfur donors. Penicillin G is an unstable thioether that degrades in a range of pathways. Nuclear magnetic resonance (NMR) and UV–Vis absorption spectroscopic studies show that reactions with cisplatin can occur within minutes to hours at 310 K, but more slowly with oxaliplatin. The identities of the Pt- adducts were investigated by mass spectrometry. The marked effect on cytotoxicity of co-incubation of cisplatin with penicillin G was demonstrated for the HeLa human cervical cancer cell line. These studies highlight the possibility that reactions with penicillin G might influence the cytotoxic activity of metal complexes determined in culture media. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00775-022-01958-z. Springer International Publishing 2022-09-25 2022 /pmc/articles/PMC9653338/ /pubmed/36153767 http://dx.doi.org/10.1007/s00775-022-01958-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Paper
Wang, Fang-Xin
Prokes, Ivan
Song, Lijiang
Shi, Huayun
Sadler, Peter J.
Reactions of cisplatin and oxaliplatin with penicillin G: implications for drug inactivation and biological activity
title Reactions of cisplatin and oxaliplatin with penicillin G: implications for drug inactivation and biological activity
title_full Reactions of cisplatin and oxaliplatin with penicillin G: implications for drug inactivation and biological activity
title_fullStr Reactions of cisplatin and oxaliplatin with penicillin G: implications for drug inactivation and biological activity
title_full_unstemmed Reactions of cisplatin and oxaliplatin with penicillin G: implications for drug inactivation and biological activity
title_short Reactions of cisplatin and oxaliplatin with penicillin G: implications for drug inactivation and biological activity
title_sort reactions of cisplatin and oxaliplatin with penicillin g: implications for drug inactivation and biological activity
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9653338/
https://www.ncbi.nlm.nih.gov/pubmed/36153767
http://dx.doi.org/10.1007/s00775-022-01958-z
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