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Preparation and performance of a pH-sensitive cisplatin-loaded magnetic nanomedicine that targets tumor cells via folate receptor mediation

The present study aimed to prepare cisplatin (CDDP)-loaded magnetic nanoparticles (MNPs), which target folate receptors via a pH-sensitive release system (FA-PEG-NH-N=MNPs-CDDP). This is of interest for the development of intelligent drug delivery systems that target tumors of the head and neck. The...

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Autores principales: CHEN, SHUAI-JUN, ZHANG, HONG-ZHENG, WAN, LIANG-CAI, JIANG, SHAN-SHAN, XU, YI-MING, LIU, FANG, ZHANG, TAO, MA, DONG, XIE, MIN-QIANG
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4878549/
https://www.ncbi.nlm.nih.gov/pubmed/27109546
http://dx.doi.org/10.3892/mmr.2016.5154
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author CHEN, SHUAI-JUN
ZHANG, HONG-ZHENG
WAN, LIANG-CAI
JIANG, SHAN-SHAN
XU, YI-MING
LIU, FANG
ZHANG, TAO
MA, DONG
XIE, MIN-QIANG
author_facet CHEN, SHUAI-JUN
ZHANG, HONG-ZHENG
WAN, LIANG-CAI
JIANG, SHAN-SHAN
XU, YI-MING
LIU, FANG
ZHANG, TAO
MA, DONG
XIE, MIN-QIANG
author_sort CHEN, SHUAI-JUN
collection PubMed
description The present study aimed to prepare cisplatin (CDDP)-loaded magnetic nanoparticles (MNPs), which target folate receptors via a pH-sensitive release system (FA-PEG-NH-N=MNPs-CDDP). This is of interest for the development of intelligent drug delivery systems that target tumors of the head and neck. The chemical coprecipitation method was used to prepare ferroferric oxide MNPs. These were modified with aldehyde sodium alginate complexed with the chemotherapeutic agent, CDDP on the surface of the nanoparticles. Double hydrazine-poly(ethylene glycol; PEG) was also prepared by attaching the carboxyl group of hydrazine-folate on one side of the double hydrazine-PEG, obtaining folate-hydrazine-PEG-diazenyl. This binds the aldehyde group of sodium alginic acid on the MNP to enclose CDDP, in order that it is sequestered within the carrier. This method obtained a pH-sensitive, FA-modified CDDP-loaded MNP (FA-PEG-NH-N=MNPs-CDDP), which acts as an intelligent tumor targeting drug delivery system. The mean size of the MNPs was ~10.2±1.5 nm, the mean hydrodynamic diameter detected by laser particle sizing instruments was 176.6±1.1 nm, and the ζ-potential was −20.91±1.76 mV. The CDDP content was 0.773 mg/ml, the iron content was ~1.908 mg/ml and the maximum saturation magnetization was 16.3±0.2 emu/g. The current study produced a pH-sensitive FA-modified CDDP-loaded MNP that is stable and exhibits magnetic responsiveness, which releases CDDP in a low pH environment.
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spelling pubmed-48785492016-05-25 Preparation and performance of a pH-sensitive cisplatin-loaded magnetic nanomedicine that targets tumor cells via folate receptor mediation CHEN, SHUAI-JUN ZHANG, HONG-ZHENG WAN, LIANG-CAI JIANG, SHAN-SHAN XU, YI-MING LIU, FANG ZHANG, TAO MA, DONG XIE, MIN-QIANG Mol Med Rep Articles The present study aimed to prepare cisplatin (CDDP)-loaded magnetic nanoparticles (MNPs), which target folate receptors via a pH-sensitive release system (FA-PEG-NH-N=MNPs-CDDP). This is of interest for the development of intelligent drug delivery systems that target tumors of the head and neck. The chemical coprecipitation method was used to prepare ferroferric oxide MNPs. These were modified with aldehyde sodium alginate complexed with the chemotherapeutic agent, CDDP on the surface of the nanoparticles. Double hydrazine-poly(ethylene glycol; PEG) was also prepared by attaching the carboxyl group of hydrazine-folate on one side of the double hydrazine-PEG, obtaining folate-hydrazine-PEG-diazenyl. This binds the aldehyde group of sodium alginic acid on the MNP to enclose CDDP, in order that it is sequestered within the carrier. This method obtained a pH-sensitive, FA-modified CDDP-loaded MNP (FA-PEG-NH-N=MNPs-CDDP), which acts as an intelligent tumor targeting drug delivery system. The mean size of the MNPs was ~10.2±1.5 nm, the mean hydrodynamic diameter detected by laser particle sizing instruments was 176.6±1.1 nm, and the ζ-potential was −20.91±1.76 mV. The CDDP content was 0.773 mg/ml, the iron content was ~1.908 mg/ml and the maximum saturation magnetization was 16.3±0.2 emu/g. The current study produced a pH-sensitive FA-modified CDDP-loaded MNP that is stable and exhibits magnetic responsiveness, which releases CDDP in a low pH environment. D.A. Spandidos 2016-06 2016-04-21 /pmc/articles/PMC4878549/ /pubmed/27109546 http://dx.doi.org/10.3892/mmr.2016.5154 Text en Copyright: © Chen et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
CHEN, SHUAI-JUN
ZHANG, HONG-ZHENG
WAN, LIANG-CAI
JIANG, SHAN-SHAN
XU, YI-MING
LIU, FANG
ZHANG, TAO
MA, DONG
XIE, MIN-QIANG
Preparation and performance of a pH-sensitive cisplatin-loaded magnetic nanomedicine that targets tumor cells via folate receptor mediation
title Preparation and performance of a pH-sensitive cisplatin-loaded magnetic nanomedicine that targets tumor cells via folate receptor mediation
title_full Preparation and performance of a pH-sensitive cisplatin-loaded magnetic nanomedicine that targets tumor cells via folate receptor mediation
title_fullStr Preparation and performance of a pH-sensitive cisplatin-loaded magnetic nanomedicine that targets tumor cells via folate receptor mediation
title_full_unstemmed Preparation and performance of a pH-sensitive cisplatin-loaded magnetic nanomedicine that targets tumor cells via folate receptor mediation
title_short Preparation and performance of a pH-sensitive cisplatin-loaded magnetic nanomedicine that targets tumor cells via folate receptor mediation
title_sort preparation and performance of a ph-sensitive cisplatin-loaded magnetic nanomedicine that targets tumor cells via folate receptor mediation
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4878549/
https://www.ncbi.nlm.nih.gov/pubmed/27109546
http://dx.doi.org/10.3892/mmr.2016.5154
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