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通过一种新型的有机物辅助开孔空心球组装法合成大孔磁性Fe₃O₄微粒

Synthesis of Macroporous Magnetic Fe₃O₄ Microparticles Via a Novel Organic Matter Assisted Open-Cell Hollow Sphere Assembly Method.

作者信息

Wang Huixia, Pu Ximing, Zhou Yaquan, Chen Xianchun, Liao Xiaoming, Huang Zhongbing, Yin Guangfu

机构信息

College of Materials Science and Engineering, Sichuan University, Chengdu 610065, China.

出版信息

Materials (Basel). 2018 Aug 23;11(9):1508. doi: 10.3390/ma11091508.

Abstract

Macroporous magnetic Fe₃O₄ microparticles, which might act as both drug carriers and magnetocaloric media, were expected to have broad application prospects on magnetocaloric-responsively controlled drug release systems. A kind of macroporous magnetic Fe₃O₄ microparticle was prepared by an organic matter assisted open-cell hollow sphere (hollow sphere with holes on shell) assembly method in this study. 1-vinyl-2-pyrrolidinone (NVP) and 2-acrylamido-2-methyl propane sulfonic acid (AMPS) were selected as the template and the binder, respectively. Ferrous ions were specifically bound to carbonyl groups on NVP and were then reduced by NaBH₄. The reduced irons underwent heterogeneous nucleation and grain growth to form Fe⁰/Fe₃O₄ microspheres consisting of a lot of nano-Fe⁰ grains, and were then assembled into Fe⁰/Fe₃O₄ microparticles wrapped by AMPS. Results indicate that NVP binding with ferrous ions can promote a self-polymerization process and the formation of Fe⁰/Fe₃O₄ microspheres, while AMPS enwrapping around the resultant microspheres can facilitate their assembly into larger aggregates. As a result, macroporous Fe₃O₄ microparticles composed of several open-cell hollow Fe₃O₄ microspheres can be obtained under a Kirkendall-controlled oxidation. Moreover, these as-prepared macroporous Fe₃O₄ microparticles possess a narrow particle size distribution and exhibit ferromagnetism (Ms = 66.14 emu/g, Mr = 6.33 emu/g, and Hc = 105.32 Oe). Our work, described here, would open up a novel synthesis method to assemble macroporous magnetic Fe₃O₄ microparticles for potential application in magnetocaloric-responsively controlled drug release systems.

摘要

大孔磁性Fe₃O₄微粒有望在磁热响应控制药物释放系统中具有广阔的应用前景,它既可以作为药物载体,又可以作为磁热介质。本研究采用有机物辅助开孔空心球(壳上有孔的空心球)组装法制备了一种大孔磁性Fe₃O₄微粒。分别选用1-乙烯基-2-吡咯烷酮(NVP)和2-丙烯酰胺基-2-甲基丙磺酸(AMPS)作为模板和粘结剂。亚铁离子特异性结合到NVP上的羰基上,然后被NaBH₄还原。还原后的铁发生异质形核和晶粒生长,形成由许多纳米Fe⁰晶粒组成的Fe⁰/Fe₃O₄微球,然后组装成被AMPS包裹的Fe⁰/Fe₃O₄微粒。结果表明,NVP与亚铁离子的结合可以促进自聚合过程和Fe⁰/Fe₃O₄微球的形成,而AMPS包裹在所得微球周围可以促进它们组装成更大的聚集体。因此,在柯肯达尔控制氧化条件下,可以得到由几个开孔空心Fe₃O₄微球组成的大孔Fe₃O₄微粒。此外,这些制备的大孔Fe₃O₄微粒具有窄的粒径分布,并表现出铁磁性(Ms = 66.14 emu/g,Mr = 6.33 emu/g,Hc = 105.32 Oe)。我们在此描述的工作将开辟一种新颖的合成方法来组装大孔磁性Fe₃O₄微粒,用于磁热响应控制药物释放系统的潜在应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d224/6164256/ec7953f0d74c/materials-11-01508-g001.jpg

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