Claudia Moscheni , Patrizia Sartori , Kaiyue Hu , Silvia Zecchini , Luigi Brambilla , Alessandro Arcari , Alessandra Napoli , Emanuele Mocciaro , Marco Uboldi , Lucia Zema , Cristiana Perrotta , Chiara Castiglioni
{"title":"用于生物医学应用的定制石墨烯纳米颗粒:模型细胞系功能的初步体外表征。","authors":"Claudia Moscheni , Patrizia Sartori , Kaiyue Hu , Silvia Zecchini , Luigi Brambilla , Alessandro Arcari , Alessandra Napoli , Emanuele Mocciaro , Marco Uboldi , Lucia Zema , Cristiana Perrotta , Chiara Castiglioni","doi":"10.1016/j.ijpharm.2024.124914","DOIUrl":null,"url":null,"abstract":"<div><div>Thanks to an environmentally friendly physical treatment of high purity graphite, a good control of the structure of graphene nanoparticles (GNPs) has been obtained with the production of stable and reproducible GNPs water dispersions. The preparation protocol entailed ball-milling of synthetic graphite followed by sonication in water and centrifugation/separation procedures. This way, two different GNPs samples with slightly different structural characteristics were harvested: TOP60, showing an average lateral size of the graphene layers <L> = 70 nm and average number of stacked layers <N> = 4, and BOTTOM60, with <L> = 120 nm and <N> = 6. A detailed structural characterization of GNPs was performed as mandatory pre-requisite to build reliable structure/properties correlations, in terms of both biomedical efficacy and toxicity, aiming at a rationale design of tailored materials for applications in biological environments.</div><div>To this end, in this study GNPs were thoroughly characterized, focusing on cytotoxicity, cellular uptake, and inflammatory response, by testing their effect in different cell lines. BOTTOM60 GNPs in culture medium and in the presence of cells showed a tendency to form big aggregates, phenomenon that was probably responsible for their cytotoxicity at high concentrations. On the other hand, TOP60 GNPs showed a diverse behavior depending on the cell type under investigation. Indeed, the nanoparticles were internalized by cells specialized in endo/phagocytosis, such as astrocytoma cells, but not by carcinoma cells of epithelial origin. Moreover, TOP60 GNPs caused a reduction of proliferation only at high concentration and did not trigger an inflammatory response in THP-1-derived macrophages.</div><div>The evidence here collected paves the way for further investigations towards the development of GNPs-based drug delivery systems.</div></div>","PeriodicalId":14187,"journal":{"name":"International Journal of Pharmaceutics","volume":"667 ","pages":"Article 124914"},"PeriodicalIF":5.3000,"publicationDate":"2024-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Tailored graphene nanoparticles for biomedical application: preliminary in vitro characterization of the functionality in model cell lines\",\"authors\":\"Claudia Moscheni , Patrizia Sartori , Kaiyue Hu , Silvia Zecchini , Luigi Brambilla , Alessandro Arcari , Alessandra Napoli , Emanuele Mocciaro , Marco Uboldi , Lucia Zema , Cristiana Perrotta , Chiara Castiglioni\",\"doi\":\"10.1016/j.ijpharm.2024.124914\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Thanks to an environmentally friendly physical treatment of high purity graphite, a good control of the structure of graphene nanoparticles (GNPs) has been obtained with the production of stable and reproducible GNPs water dispersions. The preparation protocol entailed ball-milling of synthetic graphite followed by sonication in water and centrifugation/separation procedures. This way, two different GNPs samples with slightly different structural characteristics were harvested: TOP60, showing an average lateral size of the graphene layers <L> = 70 nm and average number of stacked layers <N> = 4, and BOTTOM60, with <L> = 120 nm and <N> = 6. A detailed structural characterization of GNPs was performed as mandatory pre-requisite to build reliable structure/properties correlations, in terms of both biomedical efficacy and toxicity, aiming at a rationale design of tailored materials for applications in biological environments.</div><div>To this end, in this study GNPs were thoroughly characterized, focusing on cytotoxicity, cellular uptake, and inflammatory response, by testing their effect in different cell lines. BOTTOM60 GNPs in culture medium and in the presence of cells showed a tendency to form big aggregates, phenomenon that was probably responsible for their cytotoxicity at high concentrations. On the other hand, TOP60 GNPs showed a diverse behavior depending on the cell type under investigation. Indeed, the nanoparticles were internalized by cells specialized in endo/phagocytosis, such as astrocytoma cells, but not by carcinoma cells of epithelial origin. 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Tailored graphene nanoparticles for biomedical application: preliminary in vitro characterization of the functionality in model cell lines
Thanks to an environmentally friendly physical treatment of high purity graphite, a good control of the structure of graphene nanoparticles (GNPs) has been obtained with the production of stable and reproducible GNPs water dispersions. The preparation protocol entailed ball-milling of synthetic graphite followed by sonication in water and centrifugation/separation procedures. This way, two different GNPs samples with slightly different structural characteristics were harvested: TOP60, showing an average lateral size of the graphene layers <L> = 70 nm and average number of stacked layers <N> = 4, and BOTTOM60, with <L> = 120 nm and <N> = 6. A detailed structural characterization of GNPs was performed as mandatory pre-requisite to build reliable structure/properties correlations, in terms of both biomedical efficacy and toxicity, aiming at a rationale design of tailored materials for applications in biological environments.
To this end, in this study GNPs were thoroughly characterized, focusing on cytotoxicity, cellular uptake, and inflammatory response, by testing their effect in different cell lines. BOTTOM60 GNPs in culture medium and in the presence of cells showed a tendency to form big aggregates, phenomenon that was probably responsible for their cytotoxicity at high concentrations. On the other hand, TOP60 GNPs showed a diverse behavior depending on the cell type under investigation. Indeed, the nanoparticles were internalized by cells specialized in endo/phagocytosis, such as astrocytoma cells, but not by carcinoma cells of epithelial origin. Moreover, TOP60 GNPs caused a reduction of proliferation only at high concentration and did not trigger an inflammatory response in THP-1-derived macrophages.
The evidence here collected paves the way for further investigations towards the development of GNPs-based drug delivery systems.
期刊介绍:
The International Journal of Pharmaceutics is the third most cited journal in the "Pharmacy & Pharmacology" category out of 366 journals, being the true home for pharmaceutical scientists concerned with the physical, chemical and biological properties of devices and delivery systems for drugs, vaccines and biologicals, including their design, manufacture and evaluation. This includes evaluation of the properties of drugs, excipients such as surfactants and polymers and novel materials. The journal has special sections on pharmaceutical nanotechnology and personalized medicines, and publishes research papers, reviews, commentaries and letters to the editor as well as special issues.