João Victor Ribeiro Rocha, Rafael Freire Krause, Carlos Eduardo Ribeiro, Nathália Corrêa de Almeida Oliveira, Lucas Ribeiro de Sousa, Juracy Leandro Santos, Samuel de Melo Castro, Marize Campos Valadares, Mauro Cunha Xavier Pinto, Marcilia Viana Pavam, Eliana Martins Lima, Sebastião Antônio Mendanha, Andris Figueiroa Bakuzis
{"title":"用于核磁共振成像引导热疗的近红外仿生混合磁性纳米载体","authors":"João Victor Ribeiro Rocha, Rafael Freire Krause, Carlos Eduardo Ribeiro, Nathália Corrêa de Almeida Oliveira, Lucas Ribeiro de Sousa, Juracy Leandro Santos, Samuel de Melo Castro, Marize Campos Valadares, Mauro Cunha Xavier Pinto, Marcilia Viana Pavam, Eliana Martins Lima, Sebastião Antônio Mendanha, Andris Figueiroa Bakuzis","doi":"10.1021/acsami.4c03434","DOIUrl":null,"url":null,"abstract":"<p><p>Cell-membrane hybrid nanoparticles (NPs) are designed to improve drug delivery, thermal therapy, and immunotherapy for several diseases. Here, we report the development of distinct biomimetic magnetic nanocarriers containing magnetic nanoparticles encapsulated in vesicles and IR780 near-infrared dyes incorporated in the membranes. Distinct cell membranes are investigated, red blood cell (RBC), melanoma (B16F10), and glioblastoma (GL261). Hybrid nanocarriers containing synthetic lipids and a cell membrane are designed. The biomedical applications of several systems are compared. The inorganic nanoparticle consisted of Mn-ferrite nanoparticles with a core diameter of 15 ± 4 nm. TEM images show many multicore nanostructures (∼40 nm), which correlate with the hydrodynamic size. Ultrahigh transverse relaxivity values are reported for the magnetic NPs, 746 mM<sup>-1</sup>s<sup>-1</sup>, decreasing respectively to 445 mM<sup>-1</sup>s<sup>-1</sup> and 278 mM<sup>-1</sup>s<sup>-1</sup> for the B16F10 and GL261 hybrid vesicles. The ratio of relaxivities <i>r</i><sub>2</sub>/<i>r</i><sub>1</sub> decreased with the higher encapsulation of NPs and increased for the biomimetic liposomes. Therapeutic temperatures are achieved by both, magnetic nanoparticle hyperthermia and photothermal therapy. Photothermal conversion efficiency ∼25-30% are reported. Cell culture revealed lower wrapping times for the biomimetic vesicles. <i>In vivo</i> experiments with distinct routes of nanoparticle administration were investigated. Intratumoral injection proved the nanoparticle-mediated PTT efficiency. MRI and near-infrared images showed that the nanoparticles accumulate in the tumor after intravenous or intraperitoneal administration. Both routes benefit from MRI-guided PTT and demonstrate the multimodal theranostic applications for cancer therapy.</p>","PeriodicalId":5,"journal":{"name":"ACS Applied Materials & Interfaces","volume":" ","pages":"13094-13110"},"PeriodicalIF":8.3000,"publicationDate":"2025-03-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Near Infrared Biomimetic Hybrid Magnetic Nanocarrier for MRI-Guided Thermal Therapy.\",\"authors\":\"João Victor Ribeiro Rocha, Rafael Freire Krause, Carlos Eduardo Ribeiro, Nathália Corrêa de Almeida Oliveira, Lucas Ribeiro de Sousa, Juracy Leandro Santos, Samuel de Melo Castro, Marize Campos Valadares, Mauro Cunha Xavier Pinto, Marcilia Viana Pavam, Eliana Martins Lima, Sebastião Antônio Mendanha, Andris Figueiroa Bakuzis\",\"doi\":\"10.1021/acsami.4c03434\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Cell-membrane hybrid nanoparticles (NPs) are designed to improve drug delivery, thermal therapy, and immunotherapy for several diseases. Here, we report the development of distinct biomimetic magnetic nanocarriers containing magnetic nanoparticles encapsulated in vesicles and IR780 near-infrared dyes incorporated in the membranes. Distinct cell membranes are investigated, red blood cell (RBC), melanoma (B16F10), and glioblastoma (GL261). Hybrid nanocarriers containing synthetic lipids and a cell membrane are designed. The biomedical applications of several systems are compared. The inorganic nanoparticle consisted of Mn-ferrite nanoparticles with a core diameter of 15 ± 4 nm. TEM images show many multicore nanostructures (∼40 nm), which correlate with the hydrodynamic size. Ultrahigh transverse relaxivity values are reported for the magnetic NPs, 746 mM<sup>-1</sup>s<sup>-1</sup>, decreasing respectively to 445 mM<sup>-1</sup>s<sup>-1</sup> and 278 mM<sup>-1</sup>s<sup>-1</sup> for the B16F10 and GL261 hybrid vesicles. The ratio of relaxivities <i>r</i><sub>2</sub>/<i>r</i><sub>1</sub> decreased with the higher encapsulation of NPs and increased for the biomimetic liposomes. Therapeutic temperatures are achieved by both, magnetic nanoparticle hyperthermia and photothermal therapy. Photothermal conversion efficiency ∼25-30% are reported. Cell culture revealed lower wrapping times for the biomimetic vesicles. <i>In vivo</i> experiments with distinct routes of nanoparticle administration were investigated. Intratumoral injection proved the nanoparticle-mediated PTT efficiency. MRI and near-infrared images showed that the nanoparticles accumulate in the tumor after intravenous or intraperitoneal administration. 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Near Infrared Biomimetic Hybrid Magnetic Nanocarrier for MRI-Guided Thermal Therapy.
Cell-membrane hybrid nanoparticles (NPs) are designed to improve drug delivery, thermal therapy, and immunotherapy for several diseases. Here, we report the development of distinct biomimetic magnetic nanocarriers containing magnetic nanoparticles encapsulated in vesicles and IR780 near-infrared dyes incorporated in the membranes. Distinct cell membranes are investigated, red blood cell (RBC), melanoma (B16F10), and glioblastoma (GL261). Hybrid nanocarriers containing synthetic lipids and a cell membrane are designed. The biomedical applications of several systems are compared. The inorganic nanoparticle consisted of Mn-ferrite nanoparticles with a core diameter of 15 ± 4 nm. TEM images show many multicore nanostructures (∼40 nm), which correlate with the hydrodynamic size. Ultrahigh transverse relaxivity values are reported for the magnetic NPs, 746 mM-1s-1, decreasing respectively to 445 mM-1s-1 and 278 mM-1s-1 for the B16F10 and GL261 hybrid vesicles. The ratio of relaxivities r2/r1 decreased with the higher encapsulation of NPs and increased for the biomimetic liposomes. Therapeutic temperatures are achieved by both, magnetic nanoparticle hyperthermia and photothermal therapy. Photothermal conversion efficiency ∼25-30% are reported. Cell culture revealed lower wrapping times for the biomimetic vesicles. In vivo experiments with distinct routes of nanoparticle administration were investigated. Intratumoral injection proved the nanoparticle-mediated PTT efficiency. MRI and near-infrared images showed that the nanoparticles accumulate in the tumor after intravenous or intraperitoneal administration. Both routes benefit from MRI-guided PTT and demonstrate the multimodal theranostic applications for cancer therapy.
期刊介绍:
ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.