Jiangsu Key Laboratory of Advanced Functional Polymer Design and Application, Department of Polymer Science and Engineering, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, China.
Langmuir. 2011 Oct 18;27(20):12684-92. doi: 10.1021/la202749v. Epub 2011 Sep 15.
Fluorescent/magnetic nanoparticles are of interest in many applications in biotechnology and nanomedicine for its living detection. In this study, a novel method of surface modification of nanoparticles was first used to modify a fluorescent monomer on the surfaces of magnetic nanoparticles directly. This was achieved via iron(III)-mediated atom-transfer radical polymerization with activators generated by electron transfer (AGET ATRP). Fluorescent monomer 9-(4-vinylbenzyl)-9H-carbazole (VBK) was synthesized and was grafted from magnetic nanoparticles (ferroferric oxide) via AGET ATRP using FeCl(3)·6H(2)O as the catalyst, tris(3,6-dioxaheptyl)amine (TDA-1) as the ligand, and ascorbic acid (AsAc) as the reducing agent. The initiator for ATRP was modified on magnetic nanoparticles with the reported method: ligand exchange with 3-aminopropyltriethoxysilane (APTES) and then esterification with 2-bromoisobutyryl bromide. After polymerization, a well-defined nanocomposite (Fe(3)O(4)@PVBK) was yielded with a magnetic core and a fluorescent shell (PVBK). Subsequently, well-dispersed bifunctional nanoparticles (Fe(3)O(4)@PVBK-b-P(PEGMA)) in water were obtained via consecutive AGET ATRP of hydrophilic monomer poly(ethylene glycol) methyl ether methacrylate (PEGMA). The chemical composition of the magnetic nanoparticles' surface at different surface modification stages was investigated with Fourier transform infrared (FT-IR) spectra. The magnetic and fluorescent properties were validated with a vibrating sample magnetometer (VSM) and a fluorophotometer. The Fe(3)O(4)@PVBK-b-P(PEGMA) nanoparticles showed an effective imaging ability in enhancing the negative contrast in magnetic resonance imaging (MRI).
荧光/磁性纳米粒子因其在生物技术和纳米医学中的活体检测而受到广泛关注。在本研究中,首次使用一种新型的纳米粒子表面修饰方法,直接将荧光单体修饰在磁性纳米粒子的表面上。这是通过铁(III)介导的原子转移自由基聚合(ARGET ATRP),用电子转移生成的引发剂(AGET ATRP)来实现的。荧光单体 9-(4-乙烯基苄基)-9H-咔唑(VBK)被合成,并通过 AGET ATRP 从磁性纳米粒子(四氧化三铁)上接枝,使用三氯化铁(III)六水合物(FeCl3·6H2O)作为催化剂,三(3,6-二氧杂庚基)胺(TDA-1)作为配体,抗坏血酸(AsAc)作为还原剂。ATRP 的引发剂通过报道的方法修饰在磁性纳米粒子上:与 3-氨丙基三乙氧基硅烷(APTES)进行配体交换,然后与 2-溴异丁酰溴进行酯化反应。聚合后,得到了具有磁性核和荧光壳(PVBK)的定义明确的纳米复合材料(Fe3O4@PVBK)。随后,通过连续的亲水性单体聚乙二醇甲醚甲基丙烯酸酯(PEGMA)的 AGET ATRP,在水中得到了分散良好的双功能纳米粒子(Fe3O4@PVBK-b-P(PEGMA))。通过傅里叶变换红外(FT-IR)光谱研究了不同表面修饰阶段的磁性纳米粒子表面的化学组成。通过振动样品磁强计(VSM)和荧光光度计验证了磁性和荧光性质。Fe3O4@PVBK-b-P(PEGMA)纳米粒子在磁共振成像(MRI)中具有增强负对比的有效成像能力。