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基于改性多糖的新型磁性纳米复合材料的制备。

Obtaining of new magnetic nanocomposites based on modified polysaccharide.

机构信息

Petru Poni Institute of Macromolecular Chemistry, Gr. Ghica Voda Alley, 41A, 700487 Iasi, Romania.

出版信息

Carbohydr Polym. 2013 Oct 15;98(1):451-9. doi: 10.1016/j.carbpol.2013.05.080. Epub 2013 Jun 4.

Abstract

The study presents the preparation of some composite materials with magnetic properties by two different encapsulation methods of magnetite (Fe3O4) in a polymer matrix based on carboxymethyl starch-g-polylactic acid (CMS-g-PLA). The copolymer matrix used to obtain the magnetic nanocomposites was synthesized by grafting reaction of carboxymethyl starch (CMS) with D,L-lactic acid (DLLA), in the presence of Sn octanoate [Sn(Oct)2] as catalyst. Magnetite was obtained by co-precipitation from aqueous salt solutions FeCl2/FeCl3 (molar ratio 1/2). The magnetic composites were prepared by precipitation method in acetone (non-solvent) of the DMSO solutions of magnetite and copolymer, and synthesis in situ of the nanocomposites. In the first case, the particle size measured by DLS-technique was 168 nm, and the magnetization was 46.82 emu/g, while after in situ synthesis, the composite materials showed smaller size (141 nm), but the magnetization was reduced (3.04 emu/g). The higher magnetization in the first case is due to the great degree of encapsulation of the magnetite, which was about 43.4 wt.%, compared to 4.37 wt.% for the in situ synthesis (determined by thermogravimetry). The CMS-g-PLA copolymer, magnetite, and the nanocomposites were characterized by infrared spectroscopy (FTIR), near infrared chemical imagistic (NIR-CI), dynamic light scattering (DLS) technique, X-ray diffraction (WAXD), scanning electron microscopy (SEM), vibrating sample magnetometer (VSM) and thermal analyses. Since the polymer matrix and magnetite are biodegradable and biocompatible, the magnetic nanocomposites can be used for conjugation of some drugs. The polymer matrix CMS-g-PLA acts as a shell, and vehicle for the active component, whereas magnetite is the component which makes targeting possible by external magnetic field manipulation.

摘要

本研究通过两种不同的方法制备了一些具有磁性的复合材料,即将磁铁矿(Fe3O4)包封在基于羧甲基淀粉-g-聚乳酸(CMS-g-PLA)的聚合物基质中。用于获得磁性纳米复合材料的共聚物基质是通过羧甲基淀粉(CMS)与 D,L-乳酸(DLLA)的接枝反应,在辛酸亚锡[Sn(Oct)2]作为催化剂的存在下合成的。通过共沉淀从 FeCl2/FeCl3(摩尔比 1/2)的水溶液中获得磁铁矿。通过在二甲基亚砜(DMSO)溶液中沉淀法在丙酮(非溶剂)中制备磁性复合材料和共聚物,并在原位合成纳米复合材料。在第一种情况下,通过 DLS 技术测量的粒径为 168nm,磁化强度为 46.82emu/g,而在原位合成后,复合材料的粒径较小(141nm),但磁化强度降低(3.04emu/g)。在第一种情况下,较高的磁化强度是由于磁铁矿的封装程度很高,约为 43.4wt.%,而原位合成的为 4.37wt.%(通过热重分析确定)。CMS-g-PLA 共聚物、磁铁矿和纳米复合材料通过红外光谱(FTIR)、近红外化学成像(NIR-CI)、动态光散射(DLS)技术、X 射线衍射(WAXD)、扫描电子显微镜(SEM)、振动样品磁强计(VSM)和热分析进行了表征。由于聚合物基质和磁铁矿是可生物降解和生物相容的,因此磁性纳米复合材料可用于某些药物的偶联。聚合物基质 CMS-g-PLA 作为外壳和活性成分的载体,而磁铁矿是通过外部磁场操纵实现靶向的成分。

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