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Versatile theranostics agents designed by coating ferrite nanoparticles with biocompatible polymers

机译:通过用生物相容性聚合物包覆铁氧体纳米粒子设计的多功能治疗剂

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Three biocompatible polymers, polyethylene glycol (PEG), dextran and chitosan, have been used in this work to control the colloidal stability of magnetic nanoparticles (14 +/- 5 nm in diameter) and to vary the aggregation state in order to study their effect on relaxometric and heating properties. Two different coating strategies have been deeply developed; one based on the formation of an amide bond between citric acid coated nanoparticles (NPs) and amine groups present on the polymer surface and the other based on the NP encapsulation. Relaxometric properties revealed that proton relaxation rates strongly depend on the coating layer hydrophilicity and the aggregation state of the particles due to the presence of magnetic interactions. Thus, while PEG coating reduces particle aggregation by increasing inter-particle spacing leading to reduction of both T-1 and T-2 relaxation, dextran and chitosan lead to an increase mainly in T-2 values due to the aggregation of particles in bigger clusters where they are in close contact. Dextran and chitosan coated NPs have also shown a remarkable heating effect during the application of an alternating magnetic field. They have proved to be potential candidates as theranostic agents for cancer diagnosis and treatment. Finally, cytotoxicity of PEG conjugated NPs, which seem to be ideal for intravenous administration because of their small hydrodynamic size, was investigated resulting in high cell viability even at 0.2 mg Fe ml(-1) after 24 h of incubation. This suspension can be used as drug/biomolecule carrier for in vivo applications.
机译:三种生物相容性聚合物,聚乙二醇(PEG),右旋糖酐和壳聚糖,已用于这项工作中,以控制磁性纳米粒子(直径14 +/- 5 nm)的胶体稳定性并改变聚集状态,以研究其效果。弛豫和加热特性。已经深入开发了两种不同的涂层策略。一种基于在柠檬酸涂覆的纳米颗粒(NP)与聚合物表面上存在的胺基之间形成酰胺键,另一种基于NP包封。弛豫特性表明,由于存在磁性相互作用,质子弛豫速率在很大程度上取决于涂层的亲水性和颗粒的聚集状态。因此,尽管PEG涂层通过增加颗粒间的间隔而导致T-1和T-2弛豫的减小而减少了颗粒的聚集,但是由于较大簇中的颗粒的聚集,葡聚糖和壳聚糖主要导致T-2值的增加。他们密切联系的地方。葡聚糖和壳聚糖包被的纳米颗粒在交变磁场的施加过程中也显示出显着的加热效果。事实证明它们是治疗癌症的治疗手段的潜在候选者。最后,研究了PEG缀合的NPs的细胞毒性,由于其较小的流体动力学尺寸,似乎是静脉内给药的理想选择,即使在孵育24小时后甚至在0.2 mg Fe ml(-1)下也能产生高细胞活力。该悬浮液可用作体内应用的药物/生物分子载体。

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