Institute of Materials Research and Engineering (IMRE) Agency for Science, Technology and Research (A*STAR) , 2 Fusionopolis Way , Singapore 138634 , Singapore.
Division of Chemical and Biological Chemistry, School of Physical and Mathematical Sciences , Nanyang Technological University , 21 Nanyang Link , Singapore 637371 , Singapore.
ACS Appl Mater Interfaces. 2019 Jul 31;11(30):27233-27242. doi: 10.1021/acsami.9b08708. Epub 2019 Jul 18.
Hybrid nanoparticles (NPs) have emerged as an important class of nanomaterials owing to their integrated enhanced properties and functionality. In this study, we have developed an effective nanodot templating strategy for the in situ formation of surfactant-free nanohybrids with unique plasmonic-fluorescent properties. A bright photoluminescent biodot synthesized from serine and histamine biomolecular precursors (Ser-Hist dot) was first engineered to have rich functional groups on the nanosurface capable of anchoring Ag ions via electrostatic interaction. Upon UV irradiation, free electrons could transfer from the photoexcited Ser-Hist dot to the Ag ions, facilitating the in situ growth of AgNPs. The resulting nanohybrid system (Bio@AgNPs) exhibits distinct characteristic surface plasmon resonance absorbance and highly quenched PL intensity due to the inner filter effect. Furthermore, the Bio@AgNP nanohybrid retains its redox capability, enabling hydrogen peroxide sensing via AgNP etching, which in turn empowers a dual colorimetric and fluorescent detection of glucose and cholesterol in complex biological samples (i.e., synthetic urine and human plasma) with high selectivity and sensitivity. This finding reveals a new effective and facile method for the preparation of highly functional hybrid nanomaterials for dual-mode detection of hydrogen peroxide-producing species and/or reactions.
杂化纳米粒子 (NPs) 因其综合增强的性质和功能而成为一类重要的纳米材料。在这项研究中,我们开发了一种有效的纳米点模板策略,用于原位形成具有独特等离子体-荧光性质的无表面活性剂纳米杂化物。首先,设计了一种由丝氨酸和组氨酸生物分子前体合成的具有丰富纳米表面功能基团的亮荧光电生物点(Ser-Hist dot),这些功能基团能够通过静电相互作用锚定 Ag 离子。在紫外光照射下,来自 Ser-Hist dot 的光激发电子可以转移到 Ag 离子上,从而促进 AgNPs 的原位生长。所得的纳米杂化体系(Bio@AgNPs)由于内滤效应表现出独特的特征表面等离子体共振吸收和高度猝灭的 PL 强度。此外,Bio@AgNP 纳米杂化物保留其氧化还原能力,通过 AgNP 刻蚀实现对过氧化氢的传感,从而能够在复杂生物样品(即合成尿液和人血浆)中高选择性和灵敏度地进行双比色和荧光检测葡萄糖和胆固醇。这项发现揭示了一种新的有效且简便的方法,用于制备用于双模式检测产过氧化氢物种和/或反应的高功能杂化纳米材料。