Detection of chemical and biological agents plays a fundamental role in biomedical, forensic and environmental sciences1–4 as well as in anti bioterrorism applications.5–7 The development of highly sensitive, cost effective, miniature sensors is therefore in high demand which requires advanced technology coupled with fundamental knowledge in chemistry, biology and material sciences.8–13

In general, sensors feature two functional components: a recognition element to provide selective/specific binding with the target analytes and a transducer component for signaling the binding event. An efficient sensor relies heavily on these two essential components for the recognition process in terms of response time, signal to noise (S/N) ratio, selectivity and limits of detection (LOD).14,15 Therefore, designing sensors with higher efficacy depends on the development of novel materials to improve both the recognition and transduction processes. Nanomaterials feature unique physicochemical properties that can be of great utility in creating new recognition and transduction processes for chemical and biological sensors15–27 as well as improving the S/N ratio by miniaturization of the sensor elements.28

Gold nanoparticles (AuNPs) possess distinct physical and chemical attributes that make them excellent scaffolds for the fabrication of novel chemical and biological sensors (Figure 1).29–36 First, AuNPs can be synthesized in a straightforward manner and can be made highly stable. Second, they possess unique optoelectronic properties. Third, they provide high surface-to-volume ratio with excellent biocompatibility using appropriate ligands.30 Fourth, these properties of AuNPs can be readily tuned varying their size, shape and the surrounding chemical environment. For example, the binding event between recognition element and the analyte can alter physicochemical properties of transducer AuNPs, such as plasmon resonance absorption, conductivity, redox behavior, etc. that in turn can generate a detectable response signal. Finally, AuNPs offer a suitable platform for multi-functionalization with a wide range of organic or biological ligands for the selective binding and detection of small molecules and biological targets.30–32,36 Each of these attributes of AuNPs has allowed researchers to develop novel sensing strategies with improved sensitivity, stability and selectivity. In the last decade of research, the advent of AuNP as a sensory element provided us a broad spectrum of innovative approaches for the detection of metal ions, small molecules, proteins, nucleic acids, malignant cells, etc. in a rapid and efficient manner.37



Figure 1

Physical properties of AuNPs and schematic illustration of an AuNP-based detection system.



In this current review, we have highlighted the several synthetic routes and properties of AuNPs that make them excellent probes for different sensing strategies. Furthermore, we will discuss various sensing strategies and major advances in the last two decades of research utilizing AuNPs in the detection of variety of target analytes including metal ions, organic molecules, proteins, nucleic acids, and microorganisms.

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Gold nanoparticles in chemical and biological sensing.

9.2. Protein-Based Hg(II) Detectors 3467 9.3. Oligonucleotide-Based Hg(II) Detector 3467 9.4. DNAzyme-Based Hg(II) Detectors 3469 9.5. Antibody-Based Hg(II) Detector 3469 10. Mercury Detectors Based on Materials 3469 10.1. Soluble and Fluorescent Polymers 3469 10.2. Membranes, Films, and Fibers 3471 10.3. Micelles 3473 10.4. Nanoparticles 3473 11. Perspectives 3474 12. Addendum 3475 12.1. Small Molecules 3475 12.2. Biomolecules 3477 12.3. Materials 3477 13. List of Abbreviations 3477 14. Acknowledgments 3478 15. References 3478

Tools and tactics for the optical detection of mercuric ion.

/pdf/functional-nucleic-acid-sensors-k8tlieshyr.pdf

Functional Nucleic Acid Sensors

Gold nanoparticles (GNPs) with controlled geometrical, optical, and surface chemical properties are the subject of intensive studies and applications in biology and medicine. To date, the ever increasing diversity of published examples has included genomics and biosensorics, immunoassays and clinical chemistry, photothermolysis of cancer cells and tumors, targeted delivery of drugs and antigens, and optical bioimaging of cells and tissues with state-of-the-art nanophotonic detection systems. This critical review is focused on the application of GNP conjugates to biomedical diagnostics and analytics, photothermal and photodynamic therapies, and delivery of target molecules. Distinct from other published reviews, we present a summary of the immunological properties of GNPs. For each of the above topics, the basic principles, recent advances, and current challenges are discussed (508 references).

Gold nanoparticles in biomedical applications: recent advances and perspectives

Coupling nanomaterials with biomolecular recognition events represents a new direction in nanotechnology toward the development of novel molecular diagnostic tools. Here a graphene oxide (GO)-based multicolor fluorescent DNA nanoprobe that allows rapid, sensitive, and selective detection of DNA targets in homogeneous solution by exploiting interactions between GO and DNA molecules is reported. Because of the extraordinarily high quenching efficiency of GO, the fluorescent ssDNA probe exhibits minimal background fluorescence, while strong emission is observed when it forms a double helix with the specific targets, leading to a high signal-to-background ratio. Importantly, the large planar surface of GO allows simultaneous quenching of multiple DNA probes labeled with different dyes, leading to a multicolor sensor for the detection of multiple DNA targets in the same solution. It is also demonstrated that this GO-based sensing platform is suitable for the detection of a range of analytes when complemented with the use of functional DNA structures.

A Graphene Nanoprobe for Rapid, Sensitive, and Multicolor Fluorescent DNA Analysis

A gold nanoparticle-based detection strategy for ATP assays. In the absence of ATP, gold nanoparticles are not stabilized by the rigid duplex, thus they are readily aggregated by salt (solution displaying blue colors); in contrast induces a duplex-to-aptamer structural switching, liberating a random coil-like ssDNA. Gold nanoparticles are stabilized by the liberated ssDNA, showing high resistance to salt-induced aggregation (solution staying in red).

A gold nanoparticle-based aptamer target binding readout for ATP assay

Unmodified gold nanoparticles as a colorimetric probe for potassium DNA aptamers

A conjugated-polymer-based "mix-and-detect" optical sensor for mercury ions is fabricated by using a water-soluble poly[3-(3'-N,N,N-triethylamino-1'-pro-pyloxy)-4-methyl-2,5-thiophene hydrochloride] (PMNT) and a label-free, mercury-specific oligonucleotide (MSO) probe. PMNT binds to the Hg(2+)-free MSO and the Hg(2+)-MSO complex in different ways, and exhibits distinguishable and specific optical responses to the target-induced conformation change.

https://onlinelibrary.wiley.com/doi/pdf/10.1002/adma.200790049

Optical Detection of Mercury(II) in Aqueous Solutions by Using Conjugated Polymers and Label‐Free Oligonucleotides

Herein, a reliable surface-enhanced Raman scattering (SERS)-active substrate has been prepared by synthesizing gold nanoparticles (AuNPs)-decorated MoS2 nanocomposite. The AuNPs grew in situ on the surface of MoS2 nanosheet to form efficient SERS hot spots by a spontaneous redox reaction with tetrachloroauric acid (HAuCl4) without any reducing agent. The morphologies of MoS2 and AuNPs-decorated MoS2 nanosheet were characterized by TEM, HRTEM, and AFM. The formation of hot spots greatly depended on the ratio of MoS2 and HAuCl4. When the concentration of HAuCl4 was 2.4 mM, the as-prepared AuNPs@MoS2-3 nanocomposite exhibited a high-quality SERS activity toward probe molecule due to the generated hot spots. The spot-to-spot SERS signals showed that the relative standard deviation (RSD) in the intensity of the main Raman vibration modes (1362, 1511, and 1652 cm–1) of Rhodamine 6G were about 20%, which displayed good uniformity and reproducibility. The AuNPs@MoS2-based substrate was reliable, sensitive, and re...

Creating SERS Hot Spots on MoS2 Nanosheets with in Situ Grown Gold Nanoparticles

An electrochemical sensor has been developed for simultaneous detection of dopamine (DA), uric acid (UA) and ascorbic acid (AA) based on a gold nanoparticle-decorated MoS2 nanocomposite (AuNPs@MoS2) modified electrode. The AuNPs@MoS2 nanocomposite has been synthesized by electrodeposition of AuNPs on the MoS2 nanosheets, which possesses better properties than pure AuNPs and MoS2. The AuNPs@MoS2 film modified electrode showed excellent electrocatalytic activity toward the oxidation of AA, DA and UA with three well-resolved oxidation peaks. The peak separation of AA–DA, DA–UA and AA–UA is 151 mV, 137 mV and 288 mV, respectively, which permits the modified electrode to individually or simultaneously analyze AA, DA and UA by differential pulse voltammetry (DPV). Under optimum conditions, the AuNPs@MoS2 modified electrode exhibits linear response toward AA, DA and UA in the range of 50–100 000 μM, 0.05–30 μM and 50–40 000 μM, respectively. Moreover, the MoS2-based modified electrode was successfully employed to determine DA in human serum samples with satisfactory results.

/pdf/gold-nanoparticle-decorated-mos2-nanosheets-for-simultaneous-sbpjw4uvrj.pdf

Xingfen Liu

Papers

A gold nanoparticle-based aptamer target binding readout for ATP assay

Unmodified gold nanoparticles as a colorimetric probe for potassium DNA aptamers

Optical Detection of Mercury(II) in Aqueous Solutions by Using Conjugated Polymers and Label‐Free Oligonucleotides

Creating SERS Hot Spots on MoS2 Nanosheets with in Situ Grown Gold Nanoparticles

Gold nanoparticle-decorated MoS2 nanosheets for simultaneous detection of ascorbic acid, dopamine and uric acid