Functionalized Gold Nanoparticles Research Articles

G-quadruplex fluorescent and lateral flow colorimetric aptasensor for the detection of capsaicin in illicit cooking oil

The safety of cooking oil is a major global concern and capsaicin (CAP) serves as a crucial marker for assessing its quality. To address this issue, we have devised an innovative biosensor using a truncated aptamer, Cap-1–2, as the foundation for a dual-mode aptasensor. The aptasensor employs a combination of Mg2+-dependent DNAzyme (MNAzyme) cleavage and hybridization chain reaction (HCR) to achieve highly sensitive CAP detection. Notably, the fluorescence signal originates from the inherent fluorescence of thioflavin T (ThT) embedded in a G-quadruplex (G4) structure, enabling the detection of CAP in high-throughput oil samples. Additionally, the biosensor employed the MNAzyme to cleave biotinylated DNA (S1-Biotin), which is subsequently ligated to functionalized gold nanoparticles (AuNPs-Poly A-cDNA), generating outstanding colorimetric signals on lateral flow test strips for immediate point-of-care testing (POCT). The linear detection ranges of the established fluorescence and colorimetric aptasensor were 0.15–80 ng mL−1 and 0.2–100 ng mL−1, respectively, and the limits of detection (LOD) were 0.054 ng mL−1 and 0.137 ng mL−1, respectively. These results demonstrate the practicality of the aptasensor for detecting CAP in real-world samples. Moreover, the aptasensor surpasses traditional biosensors in terms of high-throughput, portability, and sensitivity, making it highly promising for rapid detection in the food industry.

Cysteamine functionalized gold nanoparticles exhibit high efficiency delivery of genetic materials in embryonic stem cells majorly via clathrin mediated endocytosis

Efficient and safe gene delivery is vital for genetic manipulation of stem cells for regenerative medicine. Gold nanoparticles have been used for various biomedical applications in the past, and are currently being researched as transfection agents. In this study, we report a simple one-pot synthesis of positively charged gold nanoparticles functionalized with cysteamine. The nanoparticles exhibit no cytotoxicity and can bind to both plasmid DNA (pDNA) as well as small interference RNA (siRNA). We observed that a five fold lower concentration of pDNA was sufficient for achieving comparable overexpression as that of a commercial transfection agent. We also observed that about 70 % transient silencing of the target gene was achieved with only 25 nM siRNA delivered by our nano-vehicle. To better understand the fate of the nanoparticle, we attempted to identify its uptake mechanism. The results indicate that while all the mechanisms contribute to the uptake, the clathrin-dependent pathway plays a major role. This is the first study on understanding the mechanism of uptake of CA-AuNPs conjugated to pDNA by embryonic stem cells. This is also the first study, where a successful transfection using gold based nanoparticles has been achieved in ESCs at a concentration as low as 0.5 µg/ml for pDNA and 25ƞM siRNA.

Diverse Role of Buffer Mediums and Protein Concentrations to Mediate the Multimodal Interaction of Phenylalanine-Functionalized Gold Nanoparticle and Lysozyme Protein at Same Nominal pH.

Recently, buffer molecules have been known to affect intermolecular protein-protein interactions at physiological pH. However, the roles of buffer molecules and different monolayer protein concentrations remain elusive in controlling the interaction of gold nanoparticles (Au NPs) with protein molecules. Herein, for the first time taking phenylalanine functionalized gold nanoparticles (Au-Phe NPs) and lysozyme (Lyz) protein as model systems, we report that buffer molecules of different charges (at a particular pH) play diverse roles in protein-Au NPs interaction, particularly in protein induced Au NPs aggregation. Among different buffers, negatively charged buffer (citrate and phosphate) induces aggregation of both Au-Phe NPs and Lyz protein, whereas zwitterionic and positive buffer (HEPES, MOPS, and Tris) only cause the Au NPs aggregation. Taking the diverse role of buffer into account, we propose multimodal models for stability and protein induced aggregation mechanism of NPs at different monolayer (sub-, near-, and excess) concentrations of Lyz in different medium.

Detection of Non-caloric artificial sweetener saccharine in soft drinks and ice-creams through intermolecular H-bonding by using AuNPs-based fluorescent probe

Artificial sweeteners (ASs) are widely utilized as sugar substitutes in food products. However, excessive consumption of ASs poses potential health risks, necessitating their early detection. In this study, pamoic acid (PA)-functionalized gold nanoparticles (PA@AuNPs) were employed for the detection of ASs using fluorescence spectroscopy. The PA@AuNPs exhibited high selectivity and excellent sensitivity towards saccharine (SAC) (LoD (limit of detection) = 0.14 × 10−6 M and LoQ (limit of quantification) = 0.47 × 10−6 M), compared to other commercially available ASs. The fluorescence emission intensity of PA@AuNPs was significantly quenched (∼3-fold) upon the addition of SAC (0 → 50 × 10−6 M) through the formation of a ground state complex, PA@AuNPs•SAC. This complex formation was corroborated by FTIR analysis. The non-radiative process validated by time-resolved fluorescence analysis. Morphological analysis revealed that the spherical morphology of PA@AuNPs remained unchanged upon SAC interaction. PA@AuNPs effectively detected SAC in soft drinks and ice creams, with recovery ranges from 121 % to 105 %.

A target-triggered colorimetric sensor for ultrasensitive detection of miRNAs based on self-powered three-dimensional DNA walker

MicroRNAs (miRNAs) play an important role in the process of heart failure (HF) and are emerging biomarkers that can be used for the auxiliary diagnosis of HF. However, it is very challenging to accurately analyze the expression levels of trace miRNAs in complex clinical samples. Here, we developed an enzyme-free colorimetric sensor for the ultrasensitive detection of miRNA-423-5p (HF-associated miRNA) based on three-dimensional DNA walkers constructed from functional nucleic acids and gold nanoparticles (AuNPs). DNAzyme with cleavage activity was specifically activated by miRNA-423-5p to sustainably cleave the substrate, thereby releasing the trigger sequence to initiate the subsequent mismatched catalytic hairpin assembly (MCHA) cycle. Then, as the MCHA cycle proceeded to continuously expose the G-quadruplex (GQ) sequence, the sequence bound with hemin to form a large amount of GQ/hemin DNAzyme on the surface of the AuNPs, which rapidly catalyzed the chromogenic oxidation of 3,3′,5,5′-tetramethylbenzidine to yield an amplified colorimetric signal readout. The colorimetric sensor exhibited an ultralow detection limit (32 fM), showed excellent specificity and performed well in serum samples. The sensor was applied to detect miRNA-423-5p in clinical plasma samples from healthy individuals and HF patients, and the results revealed its good clinical application in HF diagnosis. Thus, the developed colorimetric sensor provides a convenient detection tool for early screening and diagnosis of HF, as well as for pathophysiological studies.

Design and optimization of a colorimetric biosensor using functionalized gold nanoparticles and bi-functional linker for agriculture and food industry

This study aims to develop a highly sensitive colorimetric detection system utilizing functionalized gold nanoparticles (f-AuNPs) and bifunctional linkers (BLs) for the detection of pathogens and contaminants in food matrices. The primary objective was to explore and optimize key parameters, including reaction time, system volume and the concentration of bifunctional linkers, in order to enhance the system’s detection capabilities. The core mechanism of the bi-functional linker-based detection system is based on the aggregation of streptavidin-functionalized AuNPs (stAuNPs), which varies in accordance with the concentration of the bifunctional linkers (BLs) and reflects the quantity of effective linkers (EALs) available in the system. The process comprises the binding of the targets and BLs, a reduction in EAL concentration, an increase in the BLs concentration required for the aggregation of the stAuNPs, and a shift in the range exhibiting a visible color change (REVC). In systems without a target, all BLs induce aggregation. In contrast, in systems with a target present, some BLs are bound by the target, reducing EAL concentration and altering the optimal BLs concentration for stAuNP aggregation. The system was shown to be capable of detecting protein in PBS at concentrations as low as 2 nM, as well as Salmonella at 101 CFU/mL. In whole milk, the detection limits were 20 nM for protein and 102 CFU/mL for Salmonella. The principal conclusion is that the BLs-based system provides a robust and adaptable platform for pathogen detection, even in complex food matrices, obviating the need for preprocessing. The findings demonstrate the system’s potential for practical applications in the fields of food safety and agricultural contaminant detection, offering clear visual signals and high sensitivity.

Carboxy-PEG-thiol functionalized gold nanoparticle conjugates for the detection of SARS-CoV-2: Detection tools and analytical method development

Addressing the need for accessible SARS-CoV-2 testing, carboxy-PEG 12-thiol functionalized gold nanoparticles conjugates were developed for rapid point-of-care (POC) detection against SARS-CoV-2 spike protein, pseudo-SARS-CoV-2, and authentic Beta SARS-CoV-2 virus particles. These conjugates leverage gold nanoparticles (AuNPs) as signal transducers, cross-linked to either angiotensin-converting enzyme 2 (ACE2) or SARS-CoV-2 spike protein receptor-binding domain (RBD) antibodies as bioreceptors and showed a distinct color shift from pink to blue. To assess their POC feasibility, the conjugates were integrated into facemasks and breathalyzers, wherein aerosolized SARS-CoV-2 antigens were successfully detected, producing a color change within 10 and 30 minutes for the breathalyzer and facemask prototypes, respectively. Furthermore, we explored quantitative analysis using varying concentrations of SARS-CoV-2 spike protein. Both conjugates demonstrated a linear relationship between blue color intensity and virus concentration, with linear ranges of 0.08–0.6 ng/mL and 0.04–0.5 ng/mL, respectively. Low limits of detection and quantification were also achieved. They exhibited specificity, responding solely to SARS-CoV-2 even in complex matrices containing diverse proteins, including the SARS-CoV-1 spike protein. Precision tests yielded coefficient of variations below 2 %, showcasing their remarkable reproducibility. This work presents a promising approach for rapid, sensitive, and specific POC detection of SARS-CoV-2 paving the way for improved pandemic response and management.

On-line enrichment and separation of glycoprotein by capillary electrophoresis based on pH response coating column

A capillary column coated with 3-aminophenylboronic acid (APBA)-functionalized gold nanoparticles (AuNPs@APBA) was prepared via electrostatic self-assembly. The coated column exhibited anti-nonspecific adsorption of glycoproteins, enabling selective online enrichment during capillary electrophoresis (CE). First, gold nanoparticles (AuNPs) were synthesized using the sodium citrate reduction method. Then, APBA was self-assembled electrostatically on the surface of the AuNPs to obtain AuNPs@APBA. This nanomaterial was bonded to the inner wall of a capillary through ion adsorption to produce a AuNPs@APBA-coated capillary column. Glycoproteins were adsorbed via bond formation with boric acid groups under alkaline conditions (pH 8) to generate borate esters. Under acidic conditions (pH 3), the borate esters dissociated to release the glycoproteins, thereby achieving the selective online enrichment and separation of glycoproteins. The AuNPs and AuNPs@APBA were characterized using Fourier transform infrared spectroscopy, and their sizes and Zeta potentials were determined. In addition, the electroosmotic flow (EOF) of the AuNPs@APBA-coated capillary column was measured. The results showed that the surface of the AuNPs was successfully modified with APBA and that AuNPs@APBA was adsorbed on the inner wall of the capillary. The peak area of ovalbumin (OVA) on the AuNPs@APBA-coated column was 26.46 times higher than that on a bare column via conventional electrophoresis. In contrast, the peak area of bovine serum albumin (BSA) only increased by 8.47 times, indicating that the AuNPs@APBA coated column selectively enriched glycoproteins. Evaluation of the reproducibility and stability of this method revealed that the AuNPs@APBA coated capillary column could be used continually for 33-67 h. The relative standard deviations (RSDs) of the peak areas for intra-day (n=5) and inter-day (n=6) analyses were 2.2% and 3.0%, respectively. The developed method was successfully applied to enrich glycoproteins in a 1×106-fold diluted egg white sample. Glycoproteins were not detected using conventional electrophoresis on the bare column, whereas the AuNPs@APBA-coated capillary column effectively enriched and separated glycoproteins, resulting in a peak area of 10469 mAU·ms. Furthermore, the entire enrichment and separation process was completed within 3 min. This new online enrichment and separation method for glycoproteins has the advantages of low sample consumption, simple operation, and high separation efficiency.

A Route to the Colorimetric Detection of Alpha-Fetoprotein Based on a Smartphone.

Alpha-fetoprotein (AFP) is a key marker for early cancer detection and assessment. However, the current detection methods struggle to balance accuracy with the need for decentralized medical treatment. To address this issue, a new AFP analysis platform utilizing digital image colorimetry has been developed. Functionalized gold nanoparticles act as colorimetric agents, changing from purple-red to light gray-blue when exposed to different AFP concentrations. A smartphone app captures these color changes and calculates the AFP concentration in the sample. To improve detection accuracy, a hardware device ensures uniform illumination. Testing has confirmed that this system can quantitatively analyze AFP using colorimetry. The limit of detection reached 0.083 ng/mL, and the average accuracy reached 90.81%. This innovative method enhances AFP testing by offering portability, precision, and low cost, making it particularly suitable for resource-limited areas.

Dual-mode iodine sensing: Colorimetric and electrochemical detection methods using functionalized gold nanoparticles

Iodine in natural and treated waters exists mainly as iodide, iodate, and molecular iodine (I2). I2 is a highly volatile and reactive species impacting biological and chemical systems. Iodine, a vital micronutrient, is essential for human and animal growth and metabolism. It also plays a crucial role in synthesising artificial adrenaline within the metabolic processes of humans and animals. It is also widely used as an antiseptic, disinfectant, and for emergency water disinfection. Moreover, iodine deficiency can result in various diseases, especially hypothyroidism and goitre. Given its critical functions, it is imperative to have a straightforward, dependable, and efficient method for monitoring iodine levels. This study introduces a simple and innovative I2 detection system based on its reactivity, toxicity, and role as an indicator of oxidative conditions in water. It operates in terms of based on optical and electrochemical signal changes, utilising the anti-aggregation mechanism of gold nanoparticles (AuNPs) and 6-mercaptohexanol (MHA) for sensitive and selective detection under mild conditions. I2 determination is achieved by observing the colour change in AuNPs, which is influenced by competitive interactions between MHA, I2, and AuNPs. The optical detection system, with its low detection limit (LOD=260 nM), is based on the straightforward observation of colour changes. On the other hand, the electrochemical detection method utilises changing redox peaks observed in anodic region, providing selective and sensitive I2 detection (LOD=100 nM). The probe effectively detects the presence of I2 in real water samples as a practical application. Moreover, the proposed method revolutionises I2 detection by incorporating a smartphone for signal reading, eliminating the need for specialised equipment and significantly reducing the detection cost. This cost-effective approach carries the potential to expedite on-site and naked-eye I2 detection, opening up new possibilities for research and application.

Nucleic acid-functionalized gold nanoparticles as intelligent photothermal therapy agents for precise cancer treatment.

We present an intelligent photothermal therapy agents by functionalizing gold nanoparticles with specific nucleic acid sequences. Hairpin nucleic acids are modified to the nanoparticles, forming AuNPs-1 and AuNPs-2. Upon infiltrating cancer cells, these nanoparticles undergo catalytic hairpin assembly in the presence of target miRNA, leading to aggregation and subsequent photothermal conversion. Under near-infrared laser irradiation, aggregated gold nanoparticles exhibit efficient photothermal conversion, selectively damaging cancer cells. This approach offers heightened selectivity, as nanoparticles only aggregate in environments with cancer biomarkers present, sparing normal cells. Cytotoxicity assays confirm minimal toxicity to normal cells. In vivo studies on mice bearing solid tumors validate the system's efficacy in tumor regression. Overall, this study highlights the potential of nucleic acid-functionalized gold nanoparticles in intelligent and selective cancer photothermal therapy, offering insights for targeted diagnosis and treatment development.

A dual-targeted electrochemical aptasensor for neuroblastoma-related microRNAs detection

Neuroblastoma (NB) is a significant pediatric cancer associated with high mortality rates, demanding innovative and appropriate approaches for its accurate detection. This paper described the design of a dual-target electrochemical aptasensor capable of simultaneously detecting neuroblastoma-associated microRNAs (miRNA-181 and miRNA-184) with exceptional sensitivity. Screen-printed carbon electrodes (SPCEs) were utilized with gold nanorods (AuNRs), and aptamers functionalized gold nanoparticles (AuNPs) to improve sensitivity, specificity, and portable detection ability. The detection method employed in this study includes differential pulse voltammetry (DPV) and cyclic voltammetry (CV). Our aptasensor exhibited remarkable limits of detections (LODs) of 5.10 aM for miRNA-181 and 9.39 aM for miRNA-184, respectively, along with a broad linear range spanning from 0.1 fM to 100 pM for both miRNAs. The practical significance of neuroblastoma diagnosis was shown through the validation of serum samples and comparison with quantitative polymerase chain reaction (qPCR). Our electrochemical aptasensor is user-friendly, easy to engineer, and offers a promising approach for accurately and selectively detecting important miRNA biomarkers in cancer screening and diagnosis, showing potential application in various clinical scenarios.

Shape-Specific Gold Nanoparticles for Multiplex Biosensing Applications.

The biosensing field faces a significant challenge in efficiently detecting multiple analytes in a single diagnostic sample in order to compete with other established multiplex molecular diagnostic technologies such as PCR and ELISA. In response, we have developed a colorimetric nanobiosensor based on multiple morphological forms of functionalized gold nanoparticles (AuNPs) for the simultaneous detection of the influenza virus and SARS-CoV-2 virus. Gold nanospheres (GNSp) were modified with oligonucleotides specific for the influenza A virus, while gold nanoshells (GNSh) were modified with oligonucleotides specific for the SARS-CoV-2 virus. In the presence of their respective targets, AuNPs remain stable due to DNA-DNA interactions; conversely, in the absence of targets, AuNPs aggregate. Consequently, the hybrid system exhibits an indigo color with the SARS-CoV-2 target, a blue color with the Influenza A target, and a purple color with both targets, visible to the naked eye. Analytical sensitivity was 100 nM, and no cross-reactivity was observed with potentially confounding pathogens. This approach holds great promise for the simultaneous identification of multiple pathogens in a rapid manner without the need for equipment or trained personnel.

Electrochemical-based amine functionalized gold nanoparticles decorated on nanosheets for normetanephrine detection in plasma and serum

Metals and metal oxide composites are prominent materials for detecting biomolecules in body fluids through electrochemical methods. In this study, iron-cobalt nanosheets (FeCoNS) decorated with glucosamine-functionalized gold nanoparticles (Gln-AuNPs) were synthesized to detect normetanephrine (NMN) in human plasma and serum samples. The morphology and chemical composition of the Gln-AuNPs@FeCoNS were analyzed via high-resolution transmission electron microscopy, field-emission scanning electron microscopy, atomic force microscopy, ultraviolet-visible spectroscopy, Fourier-transform infrared spectroscopy, and X-ray photoelectron spectroscopy. A glassy carbon electrode (GCE) was modified with Gln-AuNPs@FeCoNS, exhibiting high electrochemical activity for determining NMN in phosphate buffer saline (PBS) and in real samples. Importantly, the increase in the oxidation current during the reaction between the GCE modified with Gln-AuNPs@FeCoNS and NMN enabled the detection and quantification of NMN. Cyclic voltammetry, differential pulse voltammetry, and amperometry (i-t) were used to assess the sensing performance of the GCE modified with Gln-AuNPs@FeCoNS. The fabricated sensor was highly sensitive toward NMN, with a limit of detection of 0.066, 0.085, and 0.7 µM in PBS, plasma, and serum samples, respectively. The proposed electrochemical sensor provides a new platform for utilizing active metal-based catalysts to detect various biomolecules.

Rational design of ROS scavenging and fluorescent gold nanoparticles to deliver siRNA to improve plant resistance to Pseudomonas syringae

Bacterial diseases are one of the most common issues that result in crop loss worldwide, and the increasing usage of chemical pesticides has caused the occurrence of resistance in pathogenic bacteria and environmental pollution problems. Nanomaterial mediated gene silencing is starting to display powerful efficiency and environmental friendliness for improving plant disease resistance. However, the internalization of nanomaterials and the physiological mechanisms behind nano-improved plant disease resistance are still rarely understood. We engineered the polyethyleneimine (PEI) functionalized gold nanoparticles (PEI-AuNPs) with fluorescent properties and ROS scavenging activity to act as siRNA delivery platforms. Besides the loading, protection, and delivery of nucleic acid molecules in plant mature leaf cells by PEI-AuNPs, its fluorescent property further enables the traceability of the distribution of the loaded nucleic acid molecules in cells. Additionally, the PEI-AuNPs-based RNAi delivery system successfully mediated the silencing of defense-regulated gene AtWRKY1. Compared to control plants, the silenced plants performed better resistance to Pseudomonas syringae, showing a reduced bacterial number, decreased ROS content, increased antioxidant enzyme activities, and improved chlorophyll fluorescence performance. Our results showed the advantages of AuNP-based RNAi technology in improving plant disease resistance, as well as the potential of plant nanobiotechnology to protect agricultural production.

Photoelectrochemical sensor for hypochlorous acid detection based on the MWNTs doped PEDOT loaded with BP5 functionalized gold nanoparticles

Hypochlorous acid concentration anomaly may cause many serious diseases, so the development method to detect HClO high sensitivity and selectivity is of great significance in clinical diagnosis. Among many methods for detecting HClO, photoelectric chemical sensor has the advantages of high sensitivity and strong anti-interference ability, and has been widely used in the field of detecting HClO. Herein, a simple and specific photoelectrochemical sensor was constructed using A1/B1-type pillar[5]arene functionalized Au NPs and multi-walled carbon nanotube-polythiophene composites for the detection of hypochlorous acid. This approach was based on a sulfhydryl-borate ester modified A1/B1 type pillar[5]arene (BP5) as the main body, hypochlorous acid (HClO) as the guest, multi-walled carbon nanotube (MWNTs) conducting polymers doped with poly(3,4-ethylenedioxythiophene) (PEDOT) as the transport bridge and signal amplifier, as well as spherical gold nanoparticles act as the signal reporter. Specifically, the photoelectrochemical efficiency was further enhanced by the localized surface plasmon resonance effect (LSPR) of gold nanoparticles (Au NPs) and the host-guest complexation between BP5 and HClO. The large specific surface area of MWNTs doped with PEDOT significantly enhanced the electrical conductivity and chemical stability of PEDOT, facilitating accelerated electron transfer and mitigating the recombination of the photogenerated electron-hole pairs. Benefiting from the combination of Au NPs, BP5, MWNTs and PEDOT, the sensor exhibited excellent sensitivity with detection range of 0.5–340 μM and a detection limit of 0.17 μM, and distinguished selectivity against 6 interfering substances. Due to the adsorption and removal effects of pillar[5]arenes on heavy metal ions and pollutants in water, as well as their effective catalytic performance, we anticipate that this composite material also has great potential in photoelectrochemical detection, catalysis, and adsorption.

Enzyme-Assisted Colorimetric Salivary miR-21 Detection by Functional Gold Nanoparticles

miRNA-21 (miR-21) is a potential biomarker for the monitoring of diseases through its expression levels. Simple, portable and sensitive miR-21 detection of is advantageous for health monitoring in Point of Care Testing (POCT). Gold nanoparticles (AuNP) as excellent colorimetric sensors are widely used in the POCT. However, their low sensitivity is a limitation of their clinical use. Herein, we developed an AuNPs-based miR-21 assay with enzyme-assisted amplification reaction to construct the colorimetric platform capable of detecting as low as 0.1[Formula: see text]nM. In this platform, template ssDNA as a signal molecule could hybridize with ssDNA-modified AuNPs to generate the color reaction. The target miR-21 specifically hybridized to the template ssDNA, which was then cleaved by exonuclease III (Exo III) to release the target miR-21. As a trigger, miR-21 catalyzed the degradation of the template ssDNA to amplify the signal by Exo III. By hybridizing miR-21 and template ssDNA in the presence of Exo III, R-21 induced a significant decrease in the level of template ssDNA to reduce the aggregation of AuNPs. There is a clear color difference in the presence/absence of miR-21 in the assay. In this assay, the optimal concentration of templated ssDNA and Exo III were 100[Formula: see text]nM and 0.06[Formula: see text]U/[Formula: see text]L in a 100[Formula: see text][Formula: see text]L detection system. The LoD for UV–Vis spectrum and colorimetric reaction were 0.1[Formula: see text]nM and 0.5[Formula: see text]nM, respectively. The detection system has good selectivity and can be used to detect miR-21 in the simulated saliva. It has great potential for application in biomedical research as well as in clinical diagnostics.

Incorporation strategy for organic dyes into gold nanoparticle supercrystals.

Ordered arrays of plasmonic nanoparticles, supercrystals can lead to the formation of plasmon-polaritons. Coupling light emitters with plasmon polaritons might allow the formation of exciton-plasmon polaritons with properties tuneable by the supercrystal design. To construct such optically active materials, the inclusion of emitters is imperative. The addition of organic dyes without affecting the periodic order of the nanocrystals is difficult, as post-formation protocols might dissolve the supercrystals, and pre-formation addition might affect the self-assembly process. Here, we present an exemplary strategy to functionalize gold nanoparticles prior to self-assembly with a cyanine isothiocyanate dye that was obtained by a straightforward reaction of the amine functionalized dye with carbon disulfide. In the second step, the nanoparticles are functionalized with a thiol-terminated polystyrene, which stabilizes the nanoparticles and governs the self-assembly process. The dye can be integrated in a quantitative fashion, and the nanoparticles can be self-assembled into supercrystals. The strategy should be applicable in general for amine functionalized dyes, which is a common modification.

Gold Nanoparticles: An Emerging Novel Technology for Targeted Delivery System for Site-Specific Diseases

Abstract: Gold Nanoparticles (GNPs) have emerged as a novel technology in the field of targeted delivery systems, offering promising solutions for site-specific disease treatment. These nanoparticles possess unique physicochemical properties, such as controlled size, shape, and surface chemistry, which enable precise manipulation for enhanced therapeutic efficacy. The biocompatibility and ease of functionalization of GNPs facilitate the conjugation with various biomolecules, including drugs, peptides, and nucleic acids, thereby improving their targeted delivery capabilities. Recent advancements in nanotechnology have leveraged GNPs for the treatment of a range of diseases, particularly in oncology, cardiology, and neurology. In cancer therapy, GNPs can be engineered to target tumor cells selectively, minimizing damage to healthy tissues and reducing side effects. This is achieved through the conjugation of GNPs with tumor-specific ligands, antibodies, or aptamers, which direct the nanoparticles to malignant cells, allowing for localized drug release and improved therapeutic outcomes. Moreover, GNPs exhibit remarkable potential in diagnostic imaging and photothermal therapy. Their unique optical properties, such as surface plasmon resonance, enable their use as contrast agents in imaging techniques, providing high-resolution and real-time monitoring of disease progression. In photothermal therapy, GNPs convert light energy into heat, effectively destroying targeted cells with minimal invasiveness. The development of GNP-based delivery systems also addresses significant challenges in drug resistance and bioavailability. By overcoming biological barriers and enhancing cellular uptake, GNPs improve the pharmacokinetics and pharmacodynamics of therapeutic agents. However, despite these advancements, the clinical translation of GNPs faces challenges such as potential toxicity, long-term stability, and regulatory hurdles. In conclusion, gold nanoparticles represent a cutting-edge approach in targeted delivery systems, offering significant potential for site-specific disease treatment. Continued research and innovation are essential to overcome existing challenges and fully realize the clinical applications of GNPs, ultimately revolutionizing precision medicine. Gold nanoparticles exhibit unique physicochemical and optical properties. The gold nanoparticles have advanced techniques to cure different chronic diseases. Today, gold nanoparticles are aided by photodynamic therapy and radiation therapy as drug carriers. Due to this, researchers now focus on medical sciences to treat various diseases and therapeutic applications. This review provides all the aspects of gold-based nanoparticles, methods, and their pharmacological benefits in different fields of medical sciences. We also discuss various preparation methods and their advantages in pharmaceutical formulations.

A ratiometric SERS aptasensor based on catalytic hairpin self-assembly mediated cyclic signal amplification strategy for the reliable determination of E. coli O157:H7.

Aratiometric SERS aptasensor based on catalytic hairpin self-assembly (CHA) mediated cyclic signal amplification strategy was developed for the rapid and reliable determination of Escherichia coli O157:H7. The recognition probe was synthesized by modifying magnetic beads with blocked aptamers, and the SERS probe was constructed by functionalizing gold nanoparticles (Au NPs) with hairpin structured DNA and 4-mercaptobenzonitrile (4-MBN). The recognition probe captured E. coli O157:H7 specifically and released the blocker DNA, which activated the CHA reaction on the SERS probe and turned on the SERS signal of 6-carboxyl-x-rhodamine (ROX). Meanwhile, 4-MBN was used as an internal reference to calibrate the matrix interference. Thus, sensitive and reliable determination and quantification of E. coli O157:H7 was established using the ratio of the SERS signal intensities of ROX to 4-MBN. This aptasensor enableddetection of 2.44 × 102 CFU/mL of E. coli O157:H7 in approximately 3h without pre-culture and DNA extraction. In addition, good reliability and excellent reproducibility were observed for the determination of E. coli O157:H7 in spiked water and milk samples. This study offered a new solution for the design of rapid, sensitive, and reliable SERS aptasensors.