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首页> 外文期刊>Analytical and bioanalytical chemistry >Development of uncoated near-spherical gold nanoparticles for the label-free quantification of Lactobacillus rhamnosus GG by surface-enhanced Raman spectroscopy
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Development of uncoated near-spherical gold nanoparticles for the label-free quantification of Lactobacillus rhamnosus GG by surface-enhanced Raman spectroscopy

机译:通过表面增强拉曼光谱法通过表面增强拉曼光谱法开发未涂覆的近球形金纳米粒子的无乳酸rhamosusus Gg的无标记定量

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摘要

The Surface-enhanced Raman spectroscopy (SERS) method based on gold nanoparticles as SERS substrate was investigated for the label-free detection and quantification of probiotic bacteria that are widely used in various pharmaceutical formulations. Indeed, the development of a simple and fast SERS method dedicated to the quantification of bacteria should be very useful for the characterization of such formulations in a more convenient way than the usually performed tedious and time-consuming conventional counting method. For this purpose, uncoated near-spherical gold nanoparticles were developed at room temperature by acidic treatment of star-like gold nanoparticle precursors. In this study, we first investigated the influence of acidic treatment conditions on both the nanoparticle physicochemical properties and SERS efficiency using Rhodamine 6G (R6G) as "model" analyte. Results highlighted that an effective R6G Raman signal enhancement was obtained by promoting chemical effect through R6G-anion interactions and by obtaining a suitable aggregation state of the nanoparticles. Depending on the nanoparticle synthesis conditions, R6G SERS signals were up to 10(2)-10(3)-fold greater than those obtained with star-like gold nanoparticles. The synthesized spherical gold nanoparticles were then successfully applied for the detection and quantification of Lactobacillus rhamnosus GG (LGG). In that case, the signal enhancement was especially due to the combination of anion-induced chemical enhancement and nanoparticle aggregation on LGG cell wall consecutive to non-specific interactions. Both the simplicity and speed of the procedure, achieved under 30 min, including nanoparticle synthesis, sample preparation, and acquisition of SERS spectra, appeared as very relevant for the characterization of pharmaceutical formulations incorporating probiotics.
机译:研究了基于金纳米颗粒的表面增强拉曼光谱(SERS)方法,用于碱基底座的无标菌细菌的无标签检测和定量,这些药物制剂广泛用于各种药物制剂中。实际上,专用于细菌的量化的简单和快速SERS方法的发展对于以比通常进行繁琐且耗时的传统计数方法的更方便的方式表征这种配方的表征应该非常有用。为此目的,通过酸性处理星状金纳米粒子前体,在室温下开发未涂覆的近球形金纳米颗粒。在这项研究中,首先使用罗丹明6G(R6G)作为“模型”分析物,研究了酸性处理条件对纳米粒子物理化学性质和SERS效率的影响。结果突出显示通过促进通过R6G-阴离子相互作用的化学效果和获得纳米颗粒的合适聚集状态来获得有效的R6G拉曼信号增强。取决于纳米颗粒合成条件,R6G SERS信号高达10(2)-10(3) - 比用星状金纳米颗粒获得的那些。然后成功地应用了合成的球形金纳米颗粒用于乳酸杆菌的检测和定量乳杆菌(LGG)。在这种情况下,信号增强尤其是由于阴离子诱导的化学增强和纳米颗粒聚集在LGG细胞壁上连续的非特异性相互作用的组合。在30分钟内实现的过程的简单性和速度,包括纳米粒子合成,样品制备和阶SERS光谱的采集出现非常重要,所述药物制剂的表征具有掺入益生菌的药物制剂。

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