Attachment Of Gold Nanoparticles Research Articles

EGaIn-Modified ePADs for Simultaneous Detection of Homocysteine and C-Reactive Protein in Saliva toward Early Diagnosis of Cardiovascular Disease.

Homocysteine (Hcy) and C-reactive protein (CRP) are critical biomarkers for numerous chronic diseases, with cardiovascular disease (CVD) being the most prevalent. The ability to simultaneously detect both biomarkers in point-of-care settings is in high demand for CVD early diagnosis and prevention. Herein, we prepared the eutectic gallium indium (EGaIn) nanoparticles decorated with p-phenylenediamine (PPD) on the surface to facilitate the subsequent attachment of gold nanoparticles (AuNPs) to achieve EGaIn-PPD@Au, which was modified on the screen-printed electrochemical paper-based analytical devices (ePADs). Aptamers that are specific to Hcy and CRP were then immobilized on the EGaIn-PPD@Au surface to achieve the sensing interface on ePADs. The presence of EGaIn-PPD@Au significantly enhanced the electrical conductivity, leading to amplified electrochemical signals. This aptasensor demonstrated high specificity, capable of detecting Hcy in a range of 1-50 μM with a detection limit of 0.22 μM, and the detection range for CRP was 1-100 ng/mL with a detection limit of 0.039 ng/mL. The aptasensor also effectively detected Hcy and CRP in clinical saliva samples, yielding an area under the curve (AUC) of about 0.80 when the individual biomarker was considered and 0.93 when both biomarkers were taken into account. The positive correlation observed between salivary and blood concentrations of Hcy and CRP, coupled with their association with cardiovascular disease (CVD), suggested the potential of this methodology as a noninvasive point-of-care strategy for the early diagnosis of CVD.

Gold Nanoparticle Sensitized Zinc Oxide Nanorods-Based Nitric Oxide Gas Sensors with High Sensitivity, Selectivity and Low Detection Limit

Development of a low-cost hand-held nitric oxide (NO) sensor with high selectivity, sensitivity and low detection limit is attractive for environment and health monitoring applications. NO gas sensor was fabricated using hydrothermally grown ZnO nanorods (ZnO NRs). The sensing performance like sensor response, sensitivity, detection limit has been improved significantly by attaching gold nanoparticles (Au NPs) with ZnO NRs. Au NPs were synthesized by chemical reduction method from gold chloride trihydrate. The attachment of Au NPs on nanorods was done by spin coating method. The maximum sensor response and sensitivity were obtained at [Formula: see text]C operating temperature with [Formula: see text]l gold loading. The interference study of the sensor was carried out with acetone, ammonia, carbon monoxide, hydrogen peroxide and propanol. It demonstrated high selectivity towards the interfering gases and high humid condition. Au-decorated ZnO NRs exhibited very low detection limit [Formula: see text][Formula: see text]ppb, which is attractive for biomedical applications.

(Invited) Ultrafast Charge Transfer Dynamics in WS2–Au Nanohybrid System Fabricated by Pulsed Laser Ablation in Liquid

Nanosheet semiconductor materials have attracted much attention in recent years due to their unique optical, electronic, and chemical properties for various applications such as photodetectors, light emitters, photocatalysts, and biosensors. We have fabricated tungsten disulfide (WS2) nanostructures by pulsed laser ablation in liquid. We applied nanosecond and femtosecond lasers and found the latter to be suitable for nanosheet fabrication [1]. Visible light response was enhanced by attaching gold nanoparticles (AuNPs) onto WS2 nanosheets [2]. The charge transfer dynamics in the WS2-Au nanohybrid system was characterized using femtosecond diffuse reflectance spectroscopy. The nanosheet structure was found to reduce the bulk carrier property. Furthermore, modification with AuNPs was found to enhance the formation of carriers trapped deeply in the WS2 nanosheets. These findings will be useful for the design of future metal-nanosheet semiconductor hybrid systems.Reference Pankaj Koinkar, Kohei Sasaki, Tetsuro Katayama and Akihiro Furube, International Journal of Modern Physics B, 35, 2140007 (2021)Tatsuki Kokufu, Daichi Nakayama, Tetsuro Katayama, Koinkar Pankaj, and Akihiro Furube, The 13th Asia-Pacific Conference on Near-Field Optics, OL30-A13 (2022)

Development and Characterization of a AuNP-Genipin-Viscoelastic Collagen Material.

Lower back pain is one of the leading causes of disability, affecting 11.9% of the population worldwide and studies have shown that intervertebral disc degeneration is a common cause for chronic lower back pain. We have explored the combination of three components, viscoelastic collagen, genipin, and gold nanoparticles to determine its potential to promote regeneration of the intervertebral disc, specifically for nucleus pulposus regeneration. The goal of this study was to develop, fabricate and characterize different formulations of viscoelastic collagen conjugated with gold nanoparticles and genipin to assess the feasibility as a tissue template. Results demonstrated the successful attachment of gold nanoparticles to the viscoelastic collagen utilizing the genipin crosslinker. For each of the viscoelastic collagen compositions examined, cell biocompatibility was achieved. The results also demonstrated an increase in stiffness of the material with different sizes and concentrations of AuNPs. Results from the TEM and STEM also demonstrated that the viscoelastic collagen that was developed did not display the characteristic D banding pattern of polymerized collagen. The findings from this study could lead to the development of a more efficient and cost-effective treatment for patients with chronic back pain caused by IVD degeneration.

A novel electrochemical immunosensor that amplifies Poly(o-phenylenediamine) signal by pH-driven cascade reaction used for alpha-foetoprotein detection

The present protocol develops an electrochemical immunosensor with poly(o-phenylene diamine) attached gold nanoparticles (PPD@Au NPs) as the immune platform, polydopamine-loaded cobalt ions (Co2+-PDA) as the immune probe, and K2S2O8 as the signal amplifying substance with pH-driven cascade reaction. The application of conventional immunosensors often leads to easy leakage of the current signal and increases the impedance due to assembly. However, this new immunosensor offers the following advantages: (1) The signal substance PPD is modified on the electrode surface, effectively reducing the signal loss and leakage of the immunosensor; (2) The pH response reduces the impedance of the immunosensor while destroying the Co2+-PDA secondary antibody label; (3) The pH response releases a small amount of Co2+, leading to SO4−· generation by K2S2O8 through a cascade reaction, further amplifying the PPD response current signal; (4) The pH response generates excess Co2+ and the by-product PDA fragments can consume the SO4−· generated by K2S2O8, so that the final response signal decreases with the increasing antigen concentration. The experimental results showed that the immunosensor exhibited good selectivity, long-term stability, and reproducibility for AFP detection in the range of 1 pg/mL-100 ng/mL, with a detection limit of 0.214 pg/mL. Interestingly, it is expected to be used for detecting AFP in actual blood samples.

Enhanced thermoelectric performance of vertically aligned silicon nanowires through the cold spot effect and charge carrier trapping effect of attached gold nanoparticles

The thermoelectric performance of vertically aligned silicon (Si) nanowires (NWs) with diameters of 100–150 nm fabricated through metal-assisted chemical etching is improved using electroless-deposited gold (Au) nanoparticles (NPs) (ф ≈ 10 nm). After the deposition of metal NPs, the thermal conductivity and Seebeck coefficient of the Si NWs decrease 5.78-fold and increased 2.71-fold, respectively. Despite the 3.23-fold increase in the electric resistivity of Si NWs through the deposition of Au NPs, the figure of merit of the Au NP-deposited Si NWs is enhanced by 1320% (0.444) compared to that of pristine Si NWs (0.0337). The power factor is enhanced 2.28-fold after Au NP deposition (0.175–0.400 mV·K−2m−1). Based on finite-element method simulations of Au NP-deposited Si NW, a cold spot is generated inside the Si NW by the attached Au NP. Moreover, charge carrier trapping at the interface between the Si NW and Au NP is anticipated due to interfacial Fermi-level pinning. Cold spot and charge carrier trapping effects are proposed as important factors for enhancing the thermoelectric performance of Au NP-deposited Si NWs.

Controlling Oriented Attachment of Gold Nanoparticles by Size and Shape

The concept of nanoparticles (NPs) as building blocks offers new possibilities to produce complex and tailored structures from the nano- to the mesoscale. In order to control a “polymerization” of particles, knowledge of the mechanism and kinetics of the reaction are necessary. We show that controlled assembly of cetylpyridinium chloride-stabilized gold NPs utilizing induced dipole–dipole interactions can lead to the formation of defined one-dimensional structures in solution. Three different shaped NPs (cubes, octahedra, and truncated cuboctahedra) were investigated individually. The assembly process is analogous to a step growth polymerization and is quantitatively describable with kinetics of a polyesterification. In situ kinetic studies reveal that there is an ideal particle size and shape for the induced dipole-driven assembly. Even small changes in size have remarkable effects on the assembly behavior. We further demonstrate that the transition from oriented assembly to oriented attachment requires a critical particle size (critical interface area) resulting from a size-dependent energy barrier for the crystallographic fusion. A combination of ideal size, shape, and degree of destabilization enables controlled oriented attachment of gold NPs in solution to chainlike structures under ambient conditions.

Thermosetting supramolecular polymerization of compartmentalized DNA fibers with stereo sequence and length control

Thermosetting supramolecular polymerization of compartmentalized DNA fibers with stereo sequence and length control

Biogenic Synthesis of Gold Nanoparticles on a Green Support as a Reusable Catalyst for the Hydrogenation of Nitroarene and Quinoline.

Direct attachment of gold nanoparticles to a green support without the use of an external reducing agent and using it for removing toxic pollutants from wastewater, i. e., reduction of nitroarene to amine, are described. A novel approach involving the reduction of gold by the jute plant (Corchorus genus) stem-based (JPS) support itself to form nanoparticles (AuNPs) to be used as a catalytic system ('dip-catalyst') and its catalytic activity for the hydrogenation of series of nitroarenes in aqueous media are presented. AuNPs/JPS catalyst was characterized using SEM, UV-Vis, FTIR, TEM, XPS, and ICP-OES. Confined area elemental mapping exhibits uniform and homogeneous distribution of AuNPs on the support surface. TEM shows multi-faceted AuNPs in the range of 20-30 nm. The reactivity of AuNPs/JPS for the transfer hydrogenation of nitroarene as well as hydrogenation of quinoline under molecular H2 pressure was evaluated. Sodium borohydride, when used as the hydrogen source, demonstrates a high catalytic efficiency in the transfer hydrogenation reduction of 4-nitrophenol (4-NP). Quinoline is quantitatively and chemoselectively hydrogenated to 1,2,3,4-tetrahydroquinoline (py-THQ) using molecular hydrogen. Reusability studies show that AuNPs are stable on the support surface and their selectivity is not affected.

Systematically engineered graphene sheets with electrostatic Au-reinforcement to strengthen 2D nanofibrous scaffolds for improved bone regeneration

Here, we report the polycaprolactone (PCL) based 2D nanofibrous scaffold with minimal loading (0.0005–0.002 wt%) of Au-reinforced graphene (RG) sheets for improved bone tissue regeneration. The microsized graphene oxide (GO) sheets (829 nm) were tailored strategically to 282 nm-sized monodispersed nanosheets for uniform electrostatic attachment of gold nanoparticles (GNPs). The GNPs-GO sheets were reduced to GNPs-RG sheets using a visible-light-induced chemical-free green method where the oxygen functional groups of GO have not been removed completely to enhance the functionality of GNPs-RG for bone tissue regeneration. The monodispersibility of GNPs-RG sheets helped to prepare PCL-based nanofibrous scaffolds with uniformly distributed GNPs-RG (0.002 wt%) with higher electrical conductivity (>3.5 times) and greater mechanical strength (>4.5 times). The electrostatic field simulation studies with COMSOL suggested that there was a uniform distribution of the electric field. The GNPs-RG addition creates an apt adhesion site due to their multifunctional and conductive properties for PCL@GNPs-RG nanofibrous scaffold which resulted in enhanced cell adhesion and proliferation of MC3T3-E1 cells. The PCL@GNPs-RG nanofibrous scaffold showed higher alkaline phosphatase activity and improved calcium mineralization after 21 d of incubation. The results indicated that the PCL@GNPs-RG scaffold has a promising capacity and potential for bone tissue regeneration.

Bringing immuno-assemblies to optoelectronics: sandwich assay integration of a nanostructured porous-silicon/gold-nanoparticle phototransistor

The exquisite specificity of biomolecular interactions can be used to integrate photonic and electronic components into nanomaterial-based architectures. In this line, a field-effect phototransistor based on Si/porous silicon (PSi) structures was fabricated by quantitatively attaching Gold nanoparticles (AuNPs) to the PSi surface by an immunoassay. Two antibodies, linked onto PSi and AuNPs, were used against different epitopes of prostate specific antigen, the common conjugating marker for these antibodies. Under white light illumination the photocurrent increases with increasing AuNP surface density. The gate voltage is effective in decoupling electron-hole pairs created at the nanostructured PSi interface. In turn, the main effect of the immune-assembled AuNPs is the optimization of charge transport through the surface. The analysis of the photocurrent shows an outstanding spectral selectivity in the 980 ± 50 nm NIR bandwidth. This report underlines the potential of the insertion of immune-assay protocols for the development of optoelectronic devices.

Transport and coarsening of gold nanoparticles in an orogenic deposit by dissolution\u2013reprecipitation and Ostwald ripening

The role of nanoparticle gold in the formation of gold deposits has long been debated. Evidence in support of this process is generally limited to epithermal-, Carlin- and seafloor massive-sulfide-type deposits where gold nanoparticles are associated with primary fluid related processes. At the Kenty orogenic deposit in Ontario, Canada, gold has been remobilized from early pyrite through secondary coupled dissolution-reprecipitation processes to form high-grade gold external to pyrite. Here we report gold nanoparticles and related textures that help document this gold coarsening process. A combination of focused ion beam technology and transmission electron microscopy provides a rare glimpse of gold coarsening frozen in time, which includes nanoparticles trapped in iron oxides and rutile and non-oriented attachment of gold nanoparticles to bulk gold suggesting coarsening via Ostwald ripening. The processes documented are applicable to orogenic deposits formed through Earth’s history, and may explain the formation of ultra high-grade ore zones.

The rapid diagnosis and effective inhibition of coronavirus using spike antibody attached gold nanoparticles.

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the cause of the coronavirus disease that began in 2019 (COVID-19), has been responsible for 1.4 million deaths worldwide as of 13 November 2020. Because at the time of writing no vaccine is yet available, a rapid diagnostic assay is very urgently needed. Herein, we present the development of anti-spike antibody attached gold nanoparticles for the rapid diagnosis of specific COVID-19 viral antigen or virus via a simple colorimetric change observation within a 5 minute time period. For rapid and highly sensitive identification, surface enhanced Raman spectroscopy (SERS) was employed using 4-aminothiophenol as a reporter molecule, which is attached to the gold nanoparticle via an Au–S bond. In the presence of COVID-19 antigen or virus particles, owing to the antigen–antibody interaction, the gold nanoparticles undergo aggregation, changing color from pink to blue, which allows for the determination of the presence of antigen or virus very rapidly by the naked eye, even at concentrations of 1 nanogram (ng) per mL for COVID-19 antigen and 1000 virus particles per mL for SARS-CoV-2 spike protein pseudotyped baculovirus. Importantly, the aggregated gold nanoparticles form “hot spots” to provide very strong SERS signal enhancement from anti-spike antibody and 4-aminothiophenol attached gold nanoparticles via light–matter interactions. Finite-difference time-domain (FDTD) simulation data indicate a 4-orders-of-magnitude Raman enhancement in “hot spot” positions when gold nanoparticles form aggregates. Using a portable Raman analyzer, our reported data demonstrate that our antibody and 4-aminothiophenol attached gold nanoparticle-based SERS probe has the capability to detect COVID-19 antigen even at a concentration of 4 picograms (pg) per mL and virus at a concentration of 18 virus particles per mL within a 5 minute time period. Using HEK293T cells, which express angiotensin-converting enzyme 2 (ACE2), by which SARS-CoV-2 enters human cells, we show that anti-spike antibody attached gold nanoparticles have the capability to inhibit infection by the virus. Our reported data show that antibody attached gold nanoparticles bind to SARS-CoV-2 spike protein, thereby inhibiting the virus from binding to cell receptors, which stops virus infection and spread. It also has the capability to destroy the lipid membrane of the virus.

Comparison of Gold Nanoparticles Deposition Methods and Their Influence on Electrochemical and Adsorption Properties of Titanium Dioxide Nanotubes.

The increasing interest of attachment of gold nanoparticles (AuNPs) on titanium dioxide nanotubes (TNTs) has been devoted to obtaining tremendous properties suitable for biosensor applications. Achieving precise control of the attachment and shape of AuNPs by methods described in the literature are far from satisfactory. This work shows the comparison of physical adsorption (PA), cyclic voltammetry (CV) and chronoamperometry (CA) methods and the parameters of these methods on TNTs properties. The structural, chemical, phase and electrochemical characterizations of TNTs, Au/TNTs, AuNPs/TNTs are carried out using scanning electron microscopy (SEM), electrochemical impedance spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy. The use of PA methods does not allow the deposition of AuNPs on TNTs. CV allows easily obtaining spherical nanoparticles, for which the diameter increases from 20.3 ± 2.9 nm to 182.3 ± 51.7 nm as a concentration of tetrachloroauric acid solution increase from 0.1 mM to 10 mM. Increasing the AuNPs deposition time in the CA method increases the amount of gold, but the AuNPs diameter does not change (35.0 ± 5 nm). Importantly, the CA method also causes the dissolution of the nanotubes layer from 1000 ± 10.0 nm to 823 ± 15.3 nm. Modification of titanium dioxide nanotubes with gold nanoparticles improved the electron transfer and increased the corrosion resistance, as well as promoted the protein adsorption. Importantly, after the deposition of bovine serum albumin, an almost 5.5-fold (324%) increase in real impedance, compared to TNTs (59%) was observed. We found that the Au nanoparticles—especially those with smaller diameter—promoted the stability of bovine serum albumin binding to the TNTs platform. It confirms that the modification of TNTs with gold nanoparticles allows the development of the best platform for biosensing applications.

Lipid Nanotubes as an Organic Template for an Electrically Conductive Gold Nanostructure Network

We demonstrate an approach to fabricate a gold nanowire network that presents a macroscopic electrical conductivity based on a lipid nanotube (LNT) template with attached gold nanoparticles. The poor electrical conductivity that we have previously faced was overcome by centrifugation and resuspension of gold nanoparticle solution for removing stabilizing agents, which increased the density of gold nanoparticles on the LNTs. An additional electroless metal plating further enhanced their contacts at nanoscale. Thanks to these procedures, the sheet resistance was improved by 11 orders of magnitude. As a proof of principle, transparent conductive films were fabricated with these gold nanowires, which exhibited sheet resistance of maximum 70 Ω/□ and transmittance of 50-75% in visible light.

In Situ Grown Monolithic Au/TiO2 Catalysts on Flexible Ti Mesh for Efficient Low‐Temperature CO Oxidation

AbstractThe development of advanced catalyst integration strategy is of great importance and promising for long‐term and stable gas catalysis in environmental processing. However, conventional catalyst fabrication techniques including spray method and spin coating cannot overcome the key problems of catalyst peeling off from substrate and related severe performance degradation. In this work, an in situ integration strategy of monolithic Au/TiO2 catalysts on Ti mesh for efficient and stable low‐temperature CO oxidation is reported. Plasma electrolytic oxidation technology can create a porous TiO2 seeding layer with strong substrate adherence. Subsequent hydrothermal reaction, ion exchange, and calcination processes can induce the in situ nucleation of sodium titanate nanosheets and their follow‐up conversion to TiO2 nanosheets with huge surface area. The oxygen defects generated in anatase TiO2 nanosheet supports can not only provide sufficient anchoring sites for the deposition and attachment of gold nanoparticles (Au NPs) during deposition–precipitation process, but also absorb and activate oxygen species. Meanwhile, the strong interactions between Au NPs and TiO2 support make the catalysts more chemically active. As a result, the Au/TiO2 monolithic catalysts can eliminate CO completely at low temperature and exhibit considerably high stability, suggesting their potential in practical applications.

Gold nanoparticles-functionalized monolithic column for enantioseparation of eight basic chiral drugs by capillary electrochromatography.

Poly(glycidyl methacrylate)-co-(ethylene dimethacrylate) [poly(GMA-co-EDMA)] monoliths were prepared, and used as a support to attach gold nanoparticles (AuNP) via Au-S bond. Pepsin, acting as a chiral selector, was linked to the surface of the carboxyl-modified AuNP through a hydrochloride/N-hydroxysuccinimide coupling reaction. The material was characterized by scanning electron microscopy, energy dispersive X-ray spectrometry, transmission electron microscopy, thermogravimetric analysis, Fourier transform infrared spectroscopy and N2 adsorption-desorption isotherm. The pepsin@AuNP@poly(GMA-co-EDMA) monolith showed preferable enantioselectivity for hydroxychloroquine (HCQ), chloroquine (CHQ), hydroxyzine (HXY), labetalol (LAB), nefopam (NEF), clenbuterol (CLE), amlodipine (AML) and chlorpheniramine (CHL) in capillary electrochromatography (CEC). These racemic drugs were monitored at the maximum absorption wavelength (220nm for HXQ, CHQ, HXY, LAB, NEF; 240nm for AML; 215nm for CLE, CHL). In comparison with the pepsin@poly(GMA-co-EDMA) monolith loaded with 5nm AuNP, the pepsin@poly(GMA-co-EDMA) monolith loaded with 13nm AuNP shows significantly enhanced enantiomeric resolution (HCQ: 0.62 → 3.45; CHQ: 0.60 → 2.11; HXY: 0.49 → 2.30; LAB: 1.03 → 2.45, 1.45 → 3.46, 0 → 0.67; NEF: 0.53 → 1.29; CLE: 0.42 → 0.56; AML: 0 → 0.83; CHL: 0.24 → 0.55). Pepsin concentration, buffer pH value, buffer concentration and applied voltage were investigated in detailwith (±) HCQ and (±) HXY as model analytes. The reproducibility of intra-day, inter-day and column-to-column were explored, and found to be satisfactory. Graphical abstractSchematic presentation of the preparation of gold nanoparticles (AuNP) modified.

Genipin Attachment of Conjugated Gold Nanoparticles to a Decellularized Tissue Scaffold

Decellularized allograft tissue is used for a wide array of tissue injuries and repair with tenons and ligament repair being among the most common. However, despite their frequent use there is concern over the lengthy inflammatory period and slow healing associated with allografts. One promising solution has been the use of nanoparticles. There is currently no easy, fast method to achieve consistent conjugation of nanoparticles to tissue. The available conjugation methods can be time-consuming and/or may create numerous cytotoxic byproducts. Genipin, a naturally derived crosslinking agent isolated from the fruits of Gardenia jasminoides was investigated as a conjugation agent to achieve fast, consistent crosslinking without cytotoxic byproducts. The rational of utilizing genipin is that is reacts spontaneously with amino-group-containing compounds such as proteins, collagens, and gelatins, and does not require extensive washing after conjugation. Porcine diaphragm tendons were decellularized and then immersed in cysteamine functionalized gold nanoparticles and genipin for various time points. Tissue scaffolds were tested for the degree of crosslinking, gold nanoparticle concentrations, and fibroblast attachment and biocompatibility. Results demonstrated that genipin can successfully and reproducibly attach gold nanoparticles to tissue in as little as 15 min. The genipin had no cytotoxic effects and improved fibroblast attachment and proliferation. Genipin can be used to attach gold nanoparticles to tissue in a fast, cell safe manner.

Gold Nanoparticle-Enhanced Photodynamic Therapy from Photosensitiser-Entrapped Ormosil Nanoparticles.

Herein, we investigate the effect of the surface attachment of gold nanoparticles (AuNPs) on photosensitiser-entrapped organically modified silica (ormosil) nanoparticles for enhanced photodynamic therapy (PDT). Photosensitiser methylene blue (MB)-entrapped ormosil nanoparticles of three different diameters (30/55/80 nm) were synthesised, and AuNPs were attached to their surface. Subsequent light irradiation with a 630 nm laser resulted in the production of singlet oxygen (1O₂), with different amounts depending on the diameter of the ormosil nanoparticle. Enhancement in 1O₂ production was observed upon the AuNP attachment on the ormosil surface. In vitro studies in pancreatic cancer (Panc-1) cells have demonstrated that cellular uptake and photodynamic cytotoxicity are also dependent on the size of ormosil nanoparticles and AuNP attachment. These studies pave the way for designing ormosil nanoparticles with suitable size and surface attachment for PDT applications.

Signal enhancement on gold nanoparticle-based lateral flow tests using cellulose nanofibers

Lateral flow paper-based biosensors merge as powerful tools in point-of-care diagnostics since they are cheap, portable, robust, selective, fast and easy to use. However, the sensitivity of this type of biosensors is not always as high as required, often not permitting a clear quantification. To improve the colorimetric response of standard lateral flow strips (LFs), we have applied a new enhancement strategy that increases the sensitivity of LFs based on the use of cellulose nanofibers (CNF). CNF penetrate inside the pores of LFs nitrocellulose paper, compacting the pore size only in the test line, particularly near the surface of the strip. This modification retains the bioreceptors (antibodies) close to the surface of the strips, and thus further increasing the density of selectively attached gold nanoparticles (AuNPs) in the top part of the membrane, in the test line area, only when the sample is positive. This effect boosts in average a 36.6% the sensitivity of the LFs. The optical measurements of the LFs were carried out with a mobile phone camera whose imaging resolution was improved by attaching microscopic lens on the camera objective. The characterization of CNF into paper and their effect was analyzed using atomic force microscope (AFM) and scanning electron microscope (SEM) imaging techniques.