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pmid:35858906

Comprehensive and systematic characterization of multi-functionalized cisplatin nano-conjugate: from the chemistry and proteomic biocompatibility to the animal model.

Ángela-Patricia Hernández · Ania Micaelo · Rafael Piñol · Marina L García-Vaquero · José J Aramayona · Julio J Criado · Emilio Rodriguez · José Ignacio Sánchez-Gallego · Alicia Landeira-Viñuela · Pablo Juanes-Velasco · Paula Díez · Rafael Góngora · Ricardo Jara-Acevedo · Alberto Orfao · Javier Miana-Mena · María Jesús Muñoz · Sergio Villanueva · Ángel Millán · Manuel Fuentes

Journal of nanobiotechnology · 2022 doi:10.1186/s12951-022-01546-y

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Comprehensive and systematic characterization of multi-functionalized cisplatin nano-conjugate: from the chemistry and proteomic biocompatibility to the animal model.
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Ángela-Patricia Hernández
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Ania Micaelo
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Rafael Piñol
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Marina L García-Vaquero
[4]
José J Aramayona
[5]
Julio J Criado
[6]
Emilio Rodriguez
[7]
José Ignacio Sánchez-Gallego
[8]
Alicia Landeira-Viñuela
[9]
Pablo Juanes-Velasco
[10]
Paula Díez
[11]
Rafael Góngora
[12]
Ricardo Jara-Acevedo
[13]
Alberto Orfao
[14]
Javier Miana-Mena
[15]
María Jesús Muñoz
[16]
Sergio Villanueva
[17]
Ángel Millán
[18]
Manuel Fuentes
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Journal of nanobiotechnology
year
2022
abstract
BACKGROUND: Nowadays, nanoparticles (NPs) have evolved as multifunctional systems combining different custom anchorages which opens a wide range of applications in biomedical research. Thus, their pharmacological involvements require more comprehensive analysis and novel nanodrugs should be characterized by both chemically and biological point of view. Within the wide variety of biocompatible nanosystems, iron oxide nanoparticles (IONPs) present mostly of the required features which make them suitable for multifunctional NPs with many biopharmaceutical applications. RESULTS: Cisplatin-IONPs and different functionalization stages have been broadly evaluated. The potential application of these nanodrugs in onco-therapies has been assessed by studying in vitro biocompatibility (interactions with environment) by proteomics characterization the determination of protein corona in different proximal fluids (human plasma, rabbit plasma and fetal bovine serum),. Moreover, protein labeling and LC-MS/MS analysis provided more than 4000 proteins de novo synthetized as consequence of the nanodrugs presence defending cell signaling in different tumor cell types (data available via ProteomeXchanges with identified PXD026615). Further in vivo studies have provided a more integrative view of the biopharmaceutical perspectives of IONPs. CONCLUSIONS: Pharmacological proteomic profile different behavior between species and different affinity of protein coating layers (soft and hard corona). Also, intracellular signaling exposed differences between tumor cell lines studied. First approaches in animal model reveal the potential of theses NPs as drug delivery vehicles and confirm cisplatin compounds as strengthened antitumoral agents.
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Comprehensive and systematic characterization of novel nanodrug conjugate based on multi-functionalized magnetic iron-nanoparticles conjugated with cisplatin derivative: From the chemistry to the animal model
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CONCLUSIONS: Pharmacological proteomic profile different behavior between species a", "lementary tables. The full mass spectrometry proteomics data reported in this paper has been deposit"], "order_basis": "paper_text_order:74", "id": "assay:1"}, {"role": "data_generation", "definition_id": "animal_model", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.99, "evidence": ["Xchanges with identified PXD026615). Further in vivo studies have provided a more integrative vie", "NPs synthesized in this report were tested “in vivo” in New Zealand rabbits in Animal Experiment"], "order_basis": "paper_text_order:1361", "id": "assay:2"}]}