Luo Yang, Zhang Wei, Liao Zhengfang, Yang Shengnan, Yang Shengtao, Li Xinhua, Zuo Fang, Luo Jianbin
College of Chemistry & Environment Protection Engineering, Southwest Minzu University, Chengdu 610041, China.
Nanomaterials (Basel). 2018 Jun 26;8(7):466. doi: 10.3390/nano8070466.
Core-shell (C/S) structured upconversion coated Fe₃O₄ nanoparticles (NPs) are of great interest due to their potential as magnetic resonance imaging (MRI) and upconversion luminescent (UCL) imaging agents, as well as near-infrared activated photodynamic therapy (PDT) platforms. When C/S structured Fe₃O₄@Mn-doped NaYF₄:Yb/Er NPs were prepared previously, well-defined C/S-NPs could not be formed without the doping of Mn during synthesis. Here, the role of Mn doping on the synthesis of core-shell structured magnetic-upconversion nanoparticles (MUCNPs) is investigated in detail. Core-shell-shell nanoparticles (C/S/S-MUCNPs) with Fe₃O₄ as the core, an inert layer of Mn-doped NaYF₄ and an outer shell consisting of Mn-doped NaYF₄:Yb/Er were prepared. To further develop C/S/S-MUCNPs applications in the biological field, amphiphilic poly(maleic anhydride-alt-1-octadecene) (CPMH) modified with amine functionalized methoxy poly(ethylene glycol) (CPMH-mPEG) was used as a capping ligand to modify the surface of C/S/S-MUCNPs to improve biocompatibility. UCL imaging, T₁-weighted MRI ascribed to the Mn ions and T₂-weighted MRI ascribed to the Fe₃O₄ core of C/S/S-MUCNPs were then evaluated. Finally, chlorine e6 (Ce6) was loaded on the C/S/S-MUCNPs and the PDT performance of these NPs was explored. Mn doping is an effective method to control the formation of core-shell structured MUCNPs, which would be potential candidate as multifunctional nanoprobes for future T₁/T₂-weighted MR/UCL imaging and PDT platforms.
核壳(C/S)结构的上转换包覆Fe₃O₄纳米颗粒(NPs)因其作为磁共振成像(MRI)和上转换发光(UCL)成像剂以及近红外激活光动力疗法(PDT)平台的潜力而备受关注。先前制备C/S结构的Fe₃O₄@Mn掺杂NaYF₄:Yb/Er NPs时,合成过程中若不掺杂Mn则无法形成明确的C/S-NPs。在此,详细研究了Mn掺杂在核壳结构磁性上转换纳米颗粒(MUCNPs)合成中的作用。制备了以Fe₃O₄为核、Mn掺杂NaYF₄的惰性层以及由Mn掺杂NaYF₄:Yb/Er组成的外壳的核壳壳纳米颗粒(C/S/S-MUCNPs)。为进一步拓展C/S/S-MUCNPs在生物领域的应用,用胺官能化甲氧基聚(乙二醇)修饰的两亲性聚(马来酸酐-alt-1-十八碳烯)(CPMH-mPEG)作为封端配体修饰C/S/S-MUCNPs的表面以提高生物相容性。然后评估了C/S/S-MUCNPs的UCL成像、归因于Mn离子的T₁加权MRI以及归因于Fe₃O₄核的T₂加权MRI。最后,将氯e6(Ce6)负载到C/S/S-MUCNPs上并探究了这些纳米颗粒的PDT性能。Mn掺杂是控制核壳结构MUCNPs形成的有效方法,其有望成为未来T₁/T₂加权MR/UCL成像和PDT平台的多功能纳米探针。