Advances in surface-enhanced Raman spectroscopy for analysis of pharmaceuticals: A review

Recently, Raman spectroscopy become a popular and potential analytical technique for the analysis of pharmaceuticals as a result of its advancement. The innovation of laser technology, Fourier Transform-Raman spectrometers with charge coupled device (CCD) detectors, ease of sample preparation and handling, mitigation of sub-sampling problems using different geometric laser irradiance patterns and invention of different optical components of Raman spectrometers are contributors of the advancement of Raman spectroscopy. Transmission Raman Spectroscopy is a useful tool in pharmaceutical analysis to address the problems related with sub-sampling in conventional Raman back scattering. More importantly, the development of surface-enhanced Raman scattering (SERS) has been a prominent advancement for Raman spectroscopy to be applied for pharmaceuticals analysis as it avoids the inherent insensitivity and fluorescence problems. As the active pharmaceutical ingredients (APIs) contain aromatic or conjugated domains with strong Raman scattering activity, Raman spectroscopy is an attractive alternative conventional analytical method for pharmaceuticals. Coupling of Raman spectroscopy with separation techniques is also another advancement applied to reduce or avoid possible spectral interferences. Therefore, in this review, transmission Raman spectroscopy, SERS, and SERS coupled with various separation techniques for pharmaceutical analysis are presented.     

表面增强拉曼散射活性基底

表面增强拉曼散射(SERS)是人们将激光拉曼光谱应用到表面科学研究中所发现的异常表面光学现象。它可以将吸附在材料表面的分子的拉曼信号放大106到1014倍,这使其在探测器的应用和单分子检测方面有着巨大的发展潜力。由于分子所吸附的基底表面形态是SERS效应能否发生和SERS信号强弱的重要影响因素,所以分子的承载基体是很关键的,因而SERS活性基底的研究一直是该领域的研究热点之一。本文总结了形态各异的表面增强拉曼散射活性基底,分析了最新发展并对其未来作一展望。     

Surface-enhanced Raman Scattering of Self-assembled Superstructures

Surface-enhanced Raman scattering(SERS) is a molecular specific spectroscopic technique that amplifies the Raman signal of absorbed molecules for up to 10¹⁰times. Over the past decades, SERS substrates experienced rapid growth, resulting in excellent development for SERS analysis. Because the surface plasmonic resonance coupling between individual materials can form a "hotspot" region to maximize the Raman signal, among many substrate construction strategies, self-assembly attracts more attention in constructing superstructures with strong, uniform and stable SERS activity. In addition, a number of plasmon-free nanomaterials with appropriate superstructures samely show enhanced SERS activity, which is primarily attributed to the formation of the optical resonator. This review aims to provide a scientific synopsis on the progress of self-assembled superstructures for SERS and ignite new dis˗ coveries in the SERS platform, as well as SERS applications in various fields.     

Sub-wavelength Raman spectroscopy on isolated silver islands

Surface Enhanced Raman Spectroscopy (SERS) is a valuable analytical tool for the investigation of molecules adsorbed on roughened noble metal surfaces. The shape, size, and surrounding of the metal protrusions play an important role in the Raman scattering enhancement. By combining scanning near-field optical microscopy (SNOM) with Raman spectroscopy the spatial resolution suffices for investigating isolated silver islands on SERS active substrates. We demonstrate an optical resolution below 70 nm for recording spectra on specifically prepared and fully characterized SERS substrates. For a quantitative evaluation of the SERS signal the spatial distribution of Rhodamine 6G (R6G) deposited on the SERS substrate was determined by friction force measurements. By comparing the Raman intensities of the SERS substrates with those of unmetallized support plates absolute SERS enhancement factors at specific locations on top and in the vicinity of the silver islands were determined directly.     

Cantilever tip near-field surface-enhanced Raman imaging of tris(bipyridine)ruthenium(II) on silver nanoparticles-coated substrates

The near-field surface-enhanced Raman scattering (SERS) and surface-enhanced fluorescence (SEF) images of tris(bipyridine)ruthenium(II) adsorbed on a silver nanoparticles-coated substrate were obtained with a scanning near-field optical microscope (SNOM, or near-field scanning optical microscopy, NSOM) using a cantilever tip. In comparison with the most widely used fiber tip for SNOM, the cantilever tip has higher optical throughput and better thermal stability, making it more suitable for detecting the extremely low Raman signal in the near-field spectroscopic investigations. Our preliminary results show that the near-field SERS with the higher spatial resolution can provide richer fingerprint information than the far-field SERS. A comparison of the two types of images shows that there are more SERS than SEF hot spots, and the two types of hot spots do not overlap. More surprisingly, the near-field SERS spectra differ from the far-field SERS spectra obtained on the same sample in the band frequency and relative intensities of some major Raman bands, and some IR-active bands were observed with the near-field mode. These results are explained mainly by the electric field gradient effect and heterogeneous polarization character that operate only in the near-field SERS.     

Surface-enhanced Raman scattering (SERS) based on surface plasmon resonance coupling techniques

Surface plasmon resonance (SPR) can provide a remarkably enhanced electromagetic field around metal surface. It is one of the enhancement models for explaining surface-enhanced Raman scattering (SERS) phonomenon. With the development of SERS theories and techniques, more and more studies referred to the configurations of the optical devices for coupling the excitation and radiation of SERS, including the prism-coupling, waveguide-coupling, and grating-coupling modes. In this review, we will summarize the recent experimental improvements on the surface plasmoncoupled SERS.     

Bioanalytical applications of SERS (surface-enhanced Raman spectroscopy)

Surface-enhanced Raman scattering (SERS) is a powerful technique for analyzing biological samples as it can rapidly and nondestructively provide chemical and, in some cases, structural information about molecules in aqueous environments. In the Raman scattering process, both visible and near-infrared (NIR) wavelengths of light can be used to induce polarization of Raman-active molecules, leading to inelastic light scattering that yields specific molecular vibrational information. The development of surface enhancement has enabled Raman scattering to be an effective tool for qualitative as well as quantitative measurements with high sensitivity and specificity. Recent advances have led to many novel applications of SERS for biological analyses, resulting in new insights for biochemistry and molecular biology, the detection of biological warfare agents, and medical diagnostics for cancer, diabetes, and other diseases. This trend article highlights many of these recent investigations and provides a brief outlook in order to assess possible future directions of SERS as a bioanalytical tool.     

Structural properties and Raman spectroscopy of lipid Langmuir monolayers at the air-water interface

Spectra of octadecylamine (ODA) Langmuir monolayers and egg phosphatidylcholine (PC)/ODA-mixed monolayers at the air-water interface have been acquired. The organization of the monolayers has been characterized by surface pressure-area isotherms. Application of polarized optical microscopy provides further insight in the domain structures and interactions of the film components. Surface-enhanced Raman scattering (SERS) data indicate that enhancement in Raman spectra can be obtained by strong interaction between headgroups of the surfactants and silver particles in subphase. By mixing ODA with phospholipid molecules and spreading the mixture at the air-water interface, we acquired vibrational information of phospholipid molecules with surfactant-aided SERS effect.     

Surface-enhanced Raman scattering: a new optical probe in molecular biophysics and biomedicine

Sensitive and detailed molecular structural information plays an increasing role in molecular biophysics and molecular medicine. Therefore, vibrational spectroscopic techniques, such as Raman scattering, which provide high structural information content are of growing interest in biophysical and biomedical research. Raman spectroscopy can be revolutionized when the inelastic scattering process takes place in the very close vicinity of metal nanostructures. Under these conditions, strongly increased Raman signals can be obtained due to resonances between optical fields and the collective oscillations of the free electrons in the metal. This effect of surface-enhanced Raman scattering (SERS) allows us to push vibrational spectroscopy to new limits in detection sensitivity, lateral resolution, and molecular structural selectivity. This opens up exciting perspectives also in molecular biospectroscopy. This article highlights three directions where SERS can offer interesting new capabilities. This includes SERS as a technique for detecting and tracking a single molecule, a SERS-based nanosensor for probing the chemical composition and the pH value in a live cell, and the effect of so-called surface-enhanced Raman optical activity, which provides information on the chiral organization of molecules on surfaces.     

Application of Dual-Enhanced Surface-Enhanced Raman Scattering Probe Technology in the Diagnosis of Tumor Cells in Vitro

With the development of precision medicine, antigen/antibody-targeted therapy has brought great hope to tumor patients; however, the migration of tumor cells, especially a small number of cells flowing into blood or other tissues, remains a clinical challenge. In particular, it is difficult to use functional gold nanomaterials for targeted clinical tumor diagnosis while simultaneously obtaining stable and highly sensitive Raman signals. Therefore, we developed a detection method for functional Au Nanostars (AuNSs) with dual signal enhancement that can specifically track location and obtain high-intensity surface-enhanced Raman scattering (SERS) signals. First, AuNSs with specific optical properties were synthesized and functionalized. The Raman dye 4-mercapto-hydroxybenzoic acid and polyethylene glycol were coupled with the tumor marker, epidermal growth factor receptor, to obtain the targeted SERS probes. In addition, a detection chip was prepared for Raman detection with physical enhancement, exhibiting a 40-times higher signal intensity than that of quartz glass. This study combines physical enhancement and SERS enhancement technologies to achieve dual enhancement, enabling the detection of a highly sensitive and stable Raman signal; this has potential clinical value for antigen/antibody-targeted tumor diagnosis and treatment.     

Individual nanostructured materials: fabrication and surface-enhanced Raman scattering

The progress of surface-enhanced Raman scattering (SERS) microscopy and spectroscopy on individual nanostructured materials has been reviewed in this feature article. After a brief introduction on individual nanomaterial SERS, we provide a systematic overview on the fabrication and SERS studies of individual nanoparticulates, nano-junctions and hierarchical nano-aggregate. These SERS-active nanomaterials have great potential in designing novel highly sensitive SERS substrates for the development of SERS-based sensing devices with a broad range of applications.     

Surface enhanced Raman with anodized aluminum oxide films

Aluminum is not a platform of choice for surface enhanced Raman scattering (SERS) experiments despite its large negative permittivity value (larger than gold or silver at optical wavelengths). It is also widely believed that an oxide layer on top of any platform substantially impedes SERS signals. Yet, anodized aluminum oxide may be perforated in an organized fashion and we have used it to examine SERS of single walled carbon nanotubes (SWCNTs) at micron length and fullerene (C60) at the nanoscale. The signal-to-noise ratio of the corresponding Raman signals exhibited a large signal enhancement for SWCNTs but not for C60. We attributed the SERS to the formation of standing surface charge waves in this subwavelength environment.     

Polarization-dependent effects in surface-enhanced Raman scattering (SERS)

A few key examples of polarization effects in surface-enhanced Raman scattering (SERS) are highlighted and discussed. It is argued that the polarization of the local field, which is felt by an analyte molecule in a location of high electromagnetic field enhancement (hot-spot), can be very different from that of the incident exciting beam. The polarization dependence of the SERS signal is, therefore, mostly dictated by the coupling of the laser to the plasmons rather than by the symmetry of the Raman tensor of the analyte. This sets serious restrictions for the interpretation of both single-molecule SERS polarization studies and for the use of circularly polarized light in techniques like surface-enhanced Raman optical activity.     

Inherent complexities of trace detection by surface-enhanced Raman scattering.

Surface-enhanced Raman scattering (SERS) and surface-enhanced resonance Raman scattering (SERRS) are powerful optical scattering techniques used in such frontier areas of research as ultrasensitive chemical analysis, the characterization of nanostructures, and the detection of single molecules. However, measuring and, most importantly, interpreting SERS/SERRS spectra can be incredibly challenging. This is the result of modifications to the measured spectra that are due to of a variety of instabilities and contributions. These interferences and modifications arise from the nature of the enhancement itself, as well as the conditions used to attain SERS spectra. The present report is an attempt to collect in one place the analytical interferences that are most commonly found during the collection of SERS/SERRS spectra.     

等离子体金属纳米结构在SERS传感及可穿戴应力传感中的应用

等离子体金属(金、银)纳米结构因其特有的理化性能,被广泛应用于表面增强拉曼散射(Surface-enhanced Raman scattering,SERS)传感及可穿戴应力传感领域.其中,SERS是一种应用贵金属纳米材料增强拉曼散射信号的检测技术,该技术灵敏度高、特异性强,已被广泛用于生物医学、环境监测、食品药品检测...     

SERS-based mercury ion detections: principles,strategies and recent advances

Mercury ion (Hg²⁺), known as one of the highly toxic and soluble heavy metal ions, is causing serious environmental pollution and irreversible damage to the health. It is urgent to develop some rapid and ultrasensitive methods for detecting trace mercury ions in the environment especially drink water. Surface-enhanced Raman scattering (SERS) is considered as a novel and powerful optical analysis technique since it has the significant advantages of ultra-sensitivity and high specificity. In recent years, the SERS technique and its application in the detection of Hg²⁺ have become more prevalent and compelling. This review provides an overall survey of the development of SERS-based Hg²⁺ detections and presents a summary relating to the basic principles, detection strategies, recent advances and current challenges of SERS for Hg²⁺ detections.     

Surface-enhanced Raman scattering substrates fabricated using electroless plating on polymer-templated nanostructures

Surface-enhanced Raman scattering (SERS) has great potential as an analytical technique based on the unique molecular signatures presented even by structurally similar analyte species and the minimal interference of scattering from water when sampling in aqueous environments. Unfortunately, analytical SERS applications have been restricted on the basis of limitations in substrate design. Herein, we present a simple SERS substrate that exploits electroless deposition onto a nanoparticle-seeded polymer scaffold that can be fabricated quickly and without specialized equipment. The polymer-templated nanostructures have stable enhancement factors that are comparable to the traditional silver film over nanospheres (AgFON) substrate, broad localized surface plasmon resonance spectra that allow various Raman excitation wavelengths to be utilized, and tolerance for both aqueous and organic environments, even after 5 day exposure. These polymer-templated nanostructures have an advantage over the AgFON substrate based on the ease of fabrication; specifically, the ability to generate fresh SERS substrates outside the laboratory environment will facilitate the application of SERS to new analytical spectroscopy applications.     

Surface-enhanced Raman spectroscopy: substrate-related issues

After over 30 years of development, surface-enhanced Raman spectroscopy (SERS) is now facing a very important stage in its history. The explosive development of nanoscience and nanotechnology has assisted the rapid development of SERS, especially during the last 5 years. Further development of surface-enhanced Raman spectroscopy is mainly limited by the reproducible preparation of clean and highly surface enhanced Raman scattering (SERS) active substrates. This review deals with some substrate-related issues. Various methods will be introduced for preparing SERS substrates of Ag and Au for analytical purposes, from SERS substrates prepared by electrochemical or vacuum methods, to well-dispersed Au or Ag nanoparticle sols, to nanoparticle thin film substrates, and finally to ordered nanostructured substrates. Emphasis is placed on the analysis of the advantages and weaknesses of different methods in preparing SERS substrates. Closely related to the application of SERS in the analysis of trace sample and unknown systems, the existing cleaning methods for SERS substrates are analyzed and a combined chemical adsorption and electrochemical oxidation method is proposed to eliminate the interference of contaminants. A defocusing method is proposed to deal with the laser-induced sample decomposition problem frequently met in SERS measurement to obtain strong signals. The existing methods to estimate the surface enhancement factor, a criterion to characterize the SERS activity of a substrate, are analyzed and some guidelines are proposed to obtain the correct enhancement factor.     

An integrated portable Raman sensor with nanofabricated gold bowtie array substrates for energetics detection

An integrated field-portable surface enhanced Raman scattering (SERS) sensing system has been developed and evaluated for quantitative analysis of energetics such as perchlorate (ClO(4)(-)) and trinitrotoluene (TNT) at environmentally relevant concentrations and conditions. The detection system consists of a portable Raman spectrometer equipped with an optical fiber probe that is coupled with novel elevated gold bowtie nanostructural arrays as a sensitive and reproducible SERS substrate. Using the standard addition technique, we show that ClO(4)(-) and TNT can be quantified at concentrations as low as 0.66 mg L(-1) (or ~6.6 μM) and 0.20 mg L(-1) (~0.9 μM), respectively, in groundwater samples collected from selected military sites. This research represents the first step toward the development of a field SERS sensor which may permit rapid, in situ screening and analysis for various applications including national security, chemical, biological and environmental detection.