Cargando…

Oxaliplatin–Biomimetic Magnetic Nanoparticle Assemblies for Colon Cancer-Targeted Chemotherapy: An In Vitro Study

Conventional chemotherapy against colorectal cancer (CRC), the third most common cancer in the world, includes oxaliplatin (Oxa) which induces serious unwanted side effects that limit the efficiency of treatment. Therefore, alternative therapeutic approaches are urgently required. In this work, biom...

Descripción completa

Detalles Bibliográficos
Autores principales: Jabalera, Ylenia, Garcia-Pinel, Beatriz, Ortiz, Raul, Iglesias, Guillermo, Cabeza, Laura, Prados, José, Jimenez-Lopez, Concepcion, Melguizo, Consolación
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6723246/
https://www.ncbi.nlm.nih.gov/pubmed/31390773
http://dx.doi.org/10.3390/pharmaceutics11080395
_version_ 1783448723233177600
author Jabalera, Ylenia
Garcia-Pinel, Beatriz
Ortiz, Raul
Iglesias, Guillermo
Cabeza, Laura
Prados, José
Jimenez-Lopez, Concepcion
Melguizo, Consolación
author_facet Jabalera, Ylenia
Garcia-Pinel, Beatriz
Ortiz, Raul
Iglesias, Guillermo
Cabeza, Laura
Prados, José
Jimenez-Lopez, Concepcion
Melguizo, Consolación
author_sort Jabalera, Ylenia
collection PubMed
description Conventional chemotherapy against colorectal cancer (CRC), the third most common cancer in the world, includes oxaliplatin (Oxa) which induces serious unwanted side effects that limit the efficiency of treatment. Therefore, alternative therapeutic approaches are urgently required. In this work, biomimetic magnetic nanoparticles (BMNPs) mediated by MamC were coupled to Oxa to evaluate the potential of the Oxa–BMNP nanoassembly for directed local delivery of the drug as a proof of concept for the future development of targeted chemotherapy against CRC. Electrostatic interactions between Oxa and BMNPs trigger the formation of the nanoassembly and keep it stable at physiological pH. When the BMNPs become neutral at acidic pH values, the Oxa is released, and such a release is greatly potentiated by hyperthermia. The coupling of the drug with the BMNPs improves its toxicity to even higher levels than the soluble drug, probably because of the fast internalization of the nanoassembly by tumor cells through endocytosis. In addition, the BMNPs are cytocompatible and non-hemolytic, providing positive feedback as a proof of concept for the nanoassembly. Our study clearly demonstrates the applicability of Oxa–BMNP in colon cancer and offers a promising nanoassembly for targeted chemotherapy against this type of tumor.
format Online
Article
Text
id pubmed-6723246
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-67232462019-09-10 Oxaliplatin–Biomimetic Magnetic Nanoparticle Assemblies for Colon Cancer-Targeted Chemotherapy: An In Vitro Study Jabalera, Ylenia Garcia-Pinel, Beatriz Ortiz, Raul Iglesias, Guillermo Cabeza, Laura Prados, José Jimenez-Lopez, Concepcion Melguizo, Consolación Pharmaceutics Article Conventional chemotherapy against colorectal cancer (CRC), the third most common cancer in the world, includes oxaliplatin (Oxa) which induces serious unwanted side effects that limit the efficiency of treatment. Therefore, alternative therapeutic approaches are urgently required. In this work, biomimetic magnetic nanoparticles (BMNPs) mediated by MamC were coupled to Oxa to evaluate the potential of the Oxa–BMNP nanoassembly for directed local delivery of the drug as a proof of concept for the future development of targeted chemotherapy against CRC. Electrostatic interactions between Oxa and BMNPs trigger the formation of the nanoassembly and keep it stable at physiological pH. When the BMNPs become neutral at acidic pH values, the Oxa is released, and such a release is greatly potentiated by hyperthermia. The coupling of the drug with the BMNPs improves its toxicity to even higher levels than the soluble drug, probably because of the fast internalization of the nanoassembly by tumor cells through endocytosis. In addition, the BMNPs are cytocompatible and non-hemolytic, providing positive feedback as a proof of concept for the nanoassembly. Our study clearly demonstrates the applicability of Oxa–BMNP in colon cancer and offers a promising nanoassembly for targeted chemotherapy against this type of tumor. MDPI 2019-08-06 /pmc/articles/PMC6723246/ /pubmed/31390773 http://dx.doi.org/10.3390/pharmaceutics11080395 Text en © 2019 by the author. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Jabalera, Ylenia
Garcia-Pinel, Beatriz
Ortiz, Raul
Iglesias, Guillermo
Cabeza, Laura
Prados, José
Jimenez-Lopez, Concepcion
Melguizo, Consolación
Oxaliplatin–Biomimetic Magnetic Nanoparticle Assemblies for Colon Cancer-Targeted Chemotherapy: An In Vitro Study
title Oxaliplatin–Biomimetic Magnetic Nanoparticle Assemblies for Colon Cancer-Targeted Chemotherapy: An In Vitro Study
title_full Oxaliplatin–Biomimetic Magnetic Nanoparticle Assemblies for Colon Cancer-Targeted Chemotherapy: An In Vitro Study
title_fullStr Oxaliplatin–Biomimetic Magnetic Nanoparticle Assemblies for Colon Cancer-Targeted Chemotherapy: An In Vitro Study
title_full_unstemmed Oxaliplatin–Biomimetic Magnetic Nanoparticle Assemblies for Colon Cancer-Targeted Chemotherapy: An In Vitro Study
title_short Oxaliplatin–Biomimetic Magnetic Nanoparticle Assemblies for Colon Cancer-Targeted Chemotherapy: An In Vitro Study
title_sort oxaliplatin–biomimetic magnetic nanoparticle assemblies for colon cancer-targeted chemotherapy: an in vitro study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6723246/
https://www.ncbi.nlm.nih.gov/pubmed/31390773
http://dx.doi.org/10.3390/pharmaceutics11080395
work_keys_str_mv AT jabaleraylenia oxaliplatinbiomimeticmagneticnanoparticleassembliesforcoloncancertargetedchemotherapyaninvitrostudy
AT garciapinelbeatriz oxaliplatinbiomimeticmagneticnanoparticleassembliesforcoloncancertargetedchemotherapyaninvitrostudy
AT ortizraul oxaliplatinbiomimeticmagneticnanoparticleassembliesforcoloncancertargetedchemotherapyaninvitrostudy
AT iglesiasguillermo oxaliplatinbiomimeticmagneticnanoparticleassembliesforcoloncancertargetedchemotherapyaninvitrostudy
AT cabezalaura oxaliplatinbiomimeticmagneticnanoparticleassembliesforcoloncancertargetedchemotherapyaninvitrostudy
AT pradosjose oxaliplatinbiomimeticmagneticnanoparticleassembliesforcoloncancertargetedchemotherapyaninvitrostudy
AT jimenezlopezconcepcion oxaliplatinbiomimeticmagneticnanoparticleassembliesforcoloncancertargetedchemotherapyaninvitrostudy
AT melguizoconsolacion oxaliplatinbiomimeticmagneticnanoparticleassembliesforcoloncancertargetedchemotherapyaninvitrostudy