Curcumin loaded mesoporous silica nanoparticles: assessment of bioavailability and cardioprotective effect

Abstract

Rhizomes of the plant Curcuma longa has been traditionally used in medicine and culinary practices in India. It possesses various pharmacological effect, namely, antioxidant, hepatoprotective, anti-inflammatory, anti-thrombosis, and anti-apoptotic. The study was undertaken to assess the effect of curcumin and curcumin loaded mesoporous silica nanoparticles (MSNs) against doxorubicin (DOX)-induced myocardial toxicity in rats. Furthermore, the study also included the bioavailability estimation of curcumin delivered alone and delivered via mesoporous technology. Cardiotoxicity was produced by cumulative administration of DOX (2.5?mg/kg for two weeks). Curcumin and curcumin loaded mesoporous nanoparticles (MSNs) each 200?mg/kg, po was administered as pretreatment for two weeks and then for two alternate weeks with DOX. The repeated administration of DOX induced cardiomyopathy associated with an antioxidant deficit and increased level of cardiotoxic biomarkers. Pretreatment with curcumin (alone and via MSNs) significantly protected myocardium from the toxic effects of DOX by significantly decreased the elevated level of malondialdehyde and increased the reduced level of reduced glutathione (GSH), superoxide dismutase (SOD) and catalase (CAT) in cardiac tissue. MSNs based delivery was found superior compared to curcumin delivered alone. Moreover, the results of bioavailability assessment in rats clearly indicated higher C_max and AUC values in rats when curcumin was administered via MSNs indicating superior bioavailability. The bioavailability of curcumin loaded MSNs, biochemical and histopathology reports support the good cardioprotective effect of curcumin which could be attributed to its increased bioavaibility lead to good antioxidant and anti-inflammatory activity.     

Facile synthesis by a covalent binding reaction for pH‐responsive drug release of carboxylated chitosan coated hollow mesoporous silica nanoparticles

In this study, a promising drug nano‐carrier system consisting of mono‐dispersed and pH sensitive carboxylated chitosan‐hollow mesoporous silica nanoparticles (Ccs‐HMSNs) suitable for the treatment of malignant cells was synthesised and investigated. At neutral pH, the Ccs molecules are orderly aggregated state, which could effectively hinder the release of loaded drug molecules. However, in slightly acidic environment, Ccs chains are heavily and flexibly entangled in gel state, which would enhance the subsequent controlled release of the loaded drug. Using doxorubicin hydrochloride (DOX•HCl) as the drug model, their results demonstrated that the system had an excellent loading efficiency (64.74 μg/mg Ccs‐HMSNs) and exhibited a pH‐sensitive release behaviour. Furthermore, confocal laser scanning microscopy revealed that the Ccs‐HMSNs nanocomposite could effectively deliver and release DOX•HCl to the nucleus of HeLa cells, thereby inducing apoptosis. In addition, MTT assay also confirmed that DOX•HCl loaded Ccs‐HMSNs (DOX•HCl@Ccs‐HMSNs) exhibited a good anticancer effect on HeLa cells with a time‐dependent manner. Finally, haemolysis experiment showed Ccs‐HMSNs had no haemolytic activity at all the tested concentrations (5–320 μg/mL). Thus, this biocompatible and effective nano‐carrier system will have potential applications in controllable drug delivery and cancer therapy.Inspec keywords: drug delivery systems, mesoporous materials, silicon compounds, nanoparticles, nanocomposites, nanofabrication, drugs, nanomedicine, biomedical materials, pH, aggregation, gels, optical microscopy, cellular biophysics, cancer, filled polymersOther keywords: facile synthesis, covalent binding reaction, pH‐responsive drug release, carboxylated chitosan coated hollow mesoporous silica nanoparticles, drug nanocarrier system, monodispersed carboxylated chitosan‐hollow mesoporous silica nanoparticles, pH sensitive carboxylated chitosan‐hollow mesoporous silica nanoparticles, malignant cell treatment, neutral pH, orderly aggregated state, loaded drug molecules, acidic environment, gel state, doxorubicin hydrochloride, drug model, confocal laser scanning microscopy, nanocomposite, HeLa cells, apoptosis, MTT assay, anticancer effect, haemolysis experiment, biocompatible nanocarrier system, drug delivery, cancer therapy, SiO₂      

On-chip evaluation of shear stress effect on cytotoxicity of mesoporous silica nanoparticles

In this work, nanotoxicity in the bloodstream was modeled, and the cytotoxicity of sub-50 nm mesoporous silica nanoparticles to human endothelial cells was investigated under microfluidic flow conditions. Compared to traditional in vitro cytotoxicity assays performed under static conditions, unmodified mesoporous silica nanoparticles show higher and shear stress-dependent toxicity to endothelial cells under flow conditions. Interestingly, even under flow conditions, highly organo-modified mesoporous silica nanoparticles show no significant toxicity to endothelial cells. This paper clearly demonstrates that shear stress is an important factor to be considered in in vitro nanotoxicology assessments and provides a simple device for pursuing this consideration.     

水热法合成介孔氧化硅材料的结构及表面特性

以十六烷基三甲基溴化氨 (CTMABr)为模板剂 ,利用碱性水热法制备了介孔氧化硅材料 ,并采用小角度XRD、HRTEM、BET和FT IR等测试手段研究了其孔的结构、表面N2 吸附特性和孔径分布情况。结果表明 :碱性水热法制得的介孔氧化硅材料具有规则的六方结构 ,介孔的最可几半径为 1 9mm ,比表面积为 5 42 8m2 / g ,孔容为 0 4 5 6cm3/ g。     

Position-specific chemical modification and quantitative proteomics disclose protein orientation adsorbed on silica nanoparticles

We describe a method for determining the orientation of cytochrome c, RNase A, and lysozyme on silica nanoparticles (SNPs) using chemical modification combined with proteolysis-mass spectrometry. The proteins interacted with SNPs through preferential adsorption sites, which are dependent on SNP diameter; 4 nm SNPs induce greater structural stabilization than 15 nm particles, presumably due to greater surface curvature of the former. These results suggest that nanoparticle size and protein structure influence protein orientation on SNPs.     

Solvent effect in the synthesis of hydrophobic drug‐loaded polymer nanoparticles

Quercetin is an abundant flavonoid in fruits, vegetables such as onion, tea leaves, cranberry, radish leaves etc. with numerous biological activities and widely used as an effective antioxidant. Its low solubility in water and chemical decomposition in intestinal environment are predicaments in delivery through dietary or oral intake. Noble polymeric nanoparticles are of particular interest today because of their applications in many areas. Polymer nanoparticles have attracted the interest of many research groups and have been utilised in an increasing number of fields such as site targeted drug delivery in cancer research during the last decades. Various techniques can be used to produce polymer nanoparticles, such as solvent evaporation, salting‐out, dialysis, supercritical fluid technology etc. The choice of method depends on a number of factors, such as, particle size, particle size distribution, area of application, etc. In the present study, single emulsion‐solvent evaporation technique has been utilised with two different organic solvents: acetone and chloroform/methanol to prepare quercetin loaded poly(D,L‐lactide‐co‐glycolide) nanoparticles. According to the authors’ observations acetone is a better solvent for encapsulating quercetin in polymer nanoparticles owing to its physical and chemical properties.Inspec keywords: solvent effects, nanofabrication, nanomedicine, nanoparticles, hydrophobicity, cancer, drug delivery systems, emulsions, evaporationOther keywords: particle size, single emulsion‐solvent evaporation technique, acetone, chloroform/methanol, cancer research, drug delivery, antioxidant, flavonoid, quercetin, hydrophobic drug‐loaded polymer nanoparticles, nanoparticle synthesis, solvent effect     

The effect of surface modification on physicochemical properties of precipitated silica

The main goal of this study was to obtain hydrophobic silica whose properties would allow their application as plasto- and elastomer fillers. Thus, hydrated silica was modified by silane and titanate coupling agents. The modification procedure and appropriate modification apparatus were developed. The degree of silica surface modification was evaluated by different methods. As grounds for this evaluation, changes in the physicochemical properties, brought about by the condensation reaction of surface silanol groups with alkoxyl or hydroxyl groups of the molecules of coupling agents, were used. The degree of hydrophobicity of the silica surface was determined on the basis of the heat of immersion of this surface, and silanol groups were identified by the infrared spectroscopy. Moreover, changes in the tendency to form agglomerates and aggregates of molecules were studied by microscopy. It was found that modification with silane and titanate coupling agents leads to an increase in silica activity. Application of these agents results in the change of the hydrophilic character to the hydrophobic one. This revised version was published online in November 2006 with corrections to the Cover Date.     

Cationic silica nanoparticles as gene carriers: synthesis, characterization and transfection efficiency in vitro and in vivo

The potential of cationic SiO2 nanoparticles was investigated for in vivo gene transfer in this study. Cationic SiO2 nanoparticles with surface modification were generated using amino-hexyl-amino-propyltri-methoxysilane (AHAPS). The zeta potential of the nanoparticles at pH = 7.4 varied from -31.4 mV (unmodified particles; 10 nm) to +9.6 mV (modified by AHAPS). Complete immobilization of DNA at the nanoparticle surface was achieved at a particle ratio of 80 (w/w nanoparticle/DNA ratio). The surface modified nanoparticle had a size of 42 nm with a distribution from 10-100 nm. The ability of these particles to transfect pCMVbeta reporter gene was tested in Cos-1 cells, and optimum results were obtained in the presence of FCS and chloroquine at a particle ratio of 80. These nanoparticles were tested for their ability to transfer genes in vivo in the mouse lung, and a two-times increase in the expression levels was found with silica particles in comparison to EGFP alone. Very low or no cell toxicity was observed, suggesting silica nanoparticles as potential alternatives for gene transfection.     

Novel photothermal-responsive sandwich-structured mesoporous silica nanoparticles: synthesis,characterization, and application for controlled drug delivery

Novel thermal nanoparticles [hollow mesoporous silica nanospheres (HMSNs)–poly (N-isopropyl acrylamide-acrylic acid) PNIPAM-AA] were developed with Ag nanoparticles (AgNps) as the core, mesoporous silica nanoparticles as the layer, and thermally responsive polymers PNIPAM-AA as the shell. The AgNps had good photothermal effects, PNIPAM-AA was responsive to temperature, the combination of AgNps and PNIPAM-AA could be used as a photothermal-responsive switch for drug release, and HMSNs greatly increased the drug loading of the carrier. The samples were characterized by means of scanning electron microscopy, transmission electron microscopy, N₂ adsorption–desorption, thermogravimetric analysis, Fourier transform infrared spectroscopy, and UV–Vis absorption spectra. The results showed that Ag@HMSN nanoparticles possessed a uniform diameter (330 nm), high specific surface area (822.45 m²/g), and mesoporous pore size (2.75 nm). Using ibuprofen (IBU) as a model drug, the release process was monitored under in vitro conditions to investigate its release characteristics at different temperatures. The results showed that the nanoparticles had a significant regulatory effect on IBU release.

Graphical abstract

     

Facile microwave‐assisted synthesis of NiO nanoparticles and its effect on soybean (Glycine max)

NiO nanoparticles in high purity, 15 ± 0.5 nm in size, were prepared via solid‐state microwave irradiation. The [Ni(NH₃)₆](NO₃)₂ complex as a novel source was decomposed in the presence of microwave irradiation for a short time (10 min). The present method is facile, safe, and low‐cost. This method exhibits other advantages; there is no need of a solvent, fuel, surfactant, expensive material, or complex instrument. Synthesised NiO nanoparticles were determined by various analyses. Also, for the first time, NiO nanoparticle effects on biochemical factors in soybean were investigated. Seeds of soybean were grown in the Murashige and Skoog agar medium containing different concentrations of NiO nanoparticles (0, 200, and 400 mg/L) for 21 days under growth chamber conditions. Estimates of malondialdehyde, hydrogen peroxide contents, and antioxidant enzymes (catalase and ascorbate peroxidase) under treatment of NiO nanoparticles were assayed. The result showed that by significantly increasing the concentration of NiO nanoparticles, the activity of catalase and ascorbate peroxidase enzymes was enhanced. Malondialdehyde and hydrogen peroxide contents significantly increased in the presence of NiO nanoparticles. In this study, the increasing activity of catalase and ascorbate peroxidase was not enough for radical oxygen species detoxification.Inspec keywords: nickel compounds, molecular biophysics, biotechnology, microorganisms, nanoparticles, biochemistry, microwave materials processing, hydrogen compounds, enzymes, cellular biophysicsOther keywords: solid‐state microwave irradiation, synthesised NiO nanoparticles, soybean, facile microwave‐assisted synthesis, biochemical factors, Murashige, Skoog agar medium, malondialdehyde, hydrogen peroxide contents, antioxidant enzymes, ascorbate peroxidase enzymes, radical oxygen species detoxification, NiO, [Ni(NH₃)₆](NO₃)₂      

Rapid synthesis of ordered hexagonal mesoporous silica and their incorporation with Ag nanoparticles by solution plasma

Rapid synthesis of silica with ordered hexagonal mesopore arrangement was obtained using solution plasma process (SPP) by discharging the mixture of P123 triblock copolymer/TEOS in acid solution. SPP, moreover, was utilized for Ag nanoparticles (AgNPs) incorporation in silica framework as one-batch process using silver nitrate (AgNO₃) solution as precursor. The turbid silicate gel was clearly observed after discharge for 1 min and the white precipitate formed at 3 min. The mesopore with hexagonal arrangement and AgNPs were observed in mesoporous silica. Two regions of X-ray diffraction patterns (2θ < 2° and 2θ = 35–90°) corresponded to the mesoporous silica and Ag nanocrystal characteristics. Comparing with mesoporous silica prepared by a conventional sol–gel route, surface area and pore diameter of mesoporous silica prepared by solution plasma were observed to be larger. In addition, the increase in Ag loading resulted in the decrease in surface area with insignificant variation in the pore diameter of mesoporous silica. SPP could be successfully utilized not only to enhance gelation time but also to increase surface area and pore diameter of mesoporous silica.     

Phyto‐assisted synthesis of bio‐functionalised silver nanoparticles and their potential anti‐oxidant,anti‐microbial and wound healing activities

Bio‐ synthesis of silver nanoparticles (AgNPs) was made by using the aqueous leaf extract of Ardisia solanacea. Rapid formation of AgNPs was observed from silver nitrate upon treatment with the aqueous extract of A. solanacea leaf. The formation and stability of the AgNPs in the colloidal solution were monitored by UV–visible spectrophotometer. The mean particle diameter of AgNPs was calculated from the DLS with an average size ∼4 nm and ∼65 nm. ATR‐FTIR spectroscopy confirmed the presence of alcohols, aldehydes, flavonoids, phenols and nitro compounds in the leaf which act as the stabilizing agent. Antimicrobial activity of the synthesized AgNPs was performed using agar well diffusion and broth dilution method against the Gram‐positive and Gram‐negative bacteria. Further, robust anti‐oxidative potential was evaluated by DPPH assay. The highest antimicrobial activity of synthesized AgNPs was found against Pseudomonas aeruginosa (28.2 ± 0.52 mm) whereas moderate activity was found against Bacillus subtilis (16.1 ± 0.76), Candida kruseii (13.0 ± 1.0), and Trichophyton mentagrophytes (12.6 ± 1.52). Moreover, the potential wound healing activity was observed against the BJ‐5Ta normal fibroblast cell line. Current research revealed that A. solanacea was found to be a suitable source for the green synthesis of silver nanoparticles.Inspec keywords: antibacterial activity, nanoparticles, silver, nanomedicine, wounds, microorganisms, X‐ray diffraction, ultraviolet spectra, visible spectra, Fourier transform infrared spectra, transmission electron microscopyOther keywords: phyto‐assisted synthesis, biofunctionalised silver nanoparticles, antioxidant antimicrobial wound healing activities, silver nanoparticle biosynthesis, aqueous leaf extract, Ardisia solanacea, silver nitrate, UV–visible spectroscopy, dynamic light scattering, Fourier transform infra‐red spectroscopy, X‐ray diffraction, electron microscopy, attenuated total reflection Fourier transform infra‐red spectroscopy, dilution method, Gram‐positive bacteria, Gram‐negative bacteria, radical scavenging method, Pseudomonas aeruginosa, Trichophyton mentagrophytes, Bacillus subtilis, Candida kruseii, BJ‐5Ta normal fibroblast cell line, SEM, alcohols, aldehydes, flavonoids, phenols, nitro compounds, Ag     

Ordered mesoporous silica fibers: effects of synthesis conditions on fiber morphology and length

Ordered mesoporous silica fibers offer potential industrial application in several areas including polymerization catalysis and separation. Understanding the effects of synthesis conditions on these fibers prepared by the interfacial self-assembly growth method is important to their production and application. The focus of this work is to understand the effect of two previously unstudied factors: silica source height (tetrabutylorthosilicate, TBOS) and the humidity, on the formation of ordered mesoporous silica fibers by the interfacial self-assembly method. Here the TBOS content, interface area, height of source, and humidity of the environment were varied to study their effect on fiber growth. The results show that the TBOS content and interface area do not have a significant impact on results of ordered mesoporous silica fibers. Increasing silica source height or environmental humidity, which lowers the water evaporation rate, gives silica fibers with lower length, less ordered inner pore structure and macroscopic morphology, and smaller pore size. Attempts to mix the growth medium eliminate the fiber morphology and yield gyroidal shapes. A mechanism that combines evaporation of water resulting in local concentration and surfactant, self-assembly, and reaction and diffusion of silica source is proposed to describe the formation of ordered mesoporous silica fibers.     

Effect of functional groups on condensation and properties of sol–gel silica nanoparticles prepared by direct synthesis from organoalkoxysilanes

Silsesquioxane nanoparticles were synthesized from organotrialkoxysilanes in ethanol/water medium by a two-step hydrolysis–condensation process. Regular shaped spheres functionalized by vinyl, methyl, ethyl, phenyl, amyl, octyl, 3-aminopropyl groups were obtained, with sizes in the range 100–400 nm. The integrity of the organic functional groups and the condensation degree of the silsesquioxane networks were detected by multinuclear solid state Nuclear Magnetic Resonance (NMR). The nanoparticles thermal behavior was studied by thermogravimetric analyses, and N₂ sorption was used to measure the particles porosity. Coatings were obtained from particles suspensions by spin coating technique and the surface properties were studied by contact angle measurements. The emission of Rhodamine 6G doped nanoparticles was analyzed in the visible light region. The fluorescence experiments highlight the influence of the different matrices on amount of dye retained into the network and fluorescence intensity.     

Nano‐biosensor based on reduced graphene oxide and gold nanoparticles,for detection of phenylketonuria‐associated DNA mutation

Phenylketonuria (PKU)‐associated DNA mutation in newborn children can be harmful to his health and early detection is the best way to inhibit consequences. A novel electrochemical nano‐biosensor was developed for PKU detection, based on signal amplification using nanomaterials, e.g. gold nanoparticles (AuNPs) decorated on the reduced graphene oxide sheet on the screen‐printed carbon electrode. The fabrication steps were checked by field emission scanning electron microscope imaging as well as cyclic voltammetry analysis. The specific alkanethiol single‐stranded DNA probes were attached by self‐assembly methodology on the AuNPs surface and Oracet blue was used as an intercalating electrochemical label. The results showed the detection limit of 21.3 fM and the dynamic range of 80–1200 fM. Moreover, the selectivity results represented a great specificity of the nano‐biosensor for its specific target DNA oligo versus other non‐specific sequences. The real sample simulation was performed successfully with almost no difference than a synthetic buffer solution environment.Inspec keywords: biosensors, nanosensors, nanoparticles, graphene compounds, gold, nanomedicine, DNA, molecular biophysics, biomedical equipment, electrochemical sensors, electrochemical electrodes, field emission scanning electron microscopy, voltammetry (chemical analysis), self‐assembly, biochemistryOther keywords: reduced graphene oxide, gold nanoparticles, phenylketonuria‐associated DNA mutation, newborn children, electrochemical nanobiosensor, signal amplification, nanomaterials, reduced graphene oxide sheet, screen‐printed carbon electrode, field emission scanning electron microscopy imaging, cyclic voltammetry, alkanethiol single‐stranded DNA probes, self‐assembly methodology, Oracet blue, intercalating electrochemical label, Au‐CO     

Effect of chitosan with different molecular weight on the stability,antioxidant and anticancer activities of well‐dispersed selenium nanoparticles

This study was designed to evaluate and compare the stability, antioxidant and anticancer activities of selenium nanoparticles (SeNPs) decorated with different molecular weight (MW) of chitosan (CS) (1500 Da, 48 kDa, 510 kDa). The size range of well‐dispersed SeNPs was effectively controlled by I⁻ first and then coated with CS. The morphology, size and surface charge of generated SeNPs were characterised by several technologies. Fourier transform infrared spectroscopy was used to investigate the relationship between SeNPs and CS. SeNPs decorated with CS (510 kDa) can keep stable for more than 45 days. As observed from the results of a simple photometric system, the antioxidant activities of decorated SeNPs were enhanced compared to undecorated SeNPs. SeNPs coated with higher MW of CS (510 kDa) showed the strongest antioxidant activities. Moreover, the treatments of SeNPs decorated with CS inhibited the growth of HepG2 cells in a time‐ and dose‐dependent manner. The proposed results demonstrated the critical roles of the MW of CS on the stability, antioxidant and anticancer properties of CS‐coated SeNPs, which provided an important design cue for future applications of functional foods and additives.Inspec keywords: selenium, drug delivery systems, cellular biophysics, nanoparticles, molecular biophysics, cancer, biomedical materials, biochemistry, polymers, nanomedicine, Fourier transform infrared spectra, surface charging, surface morphologyOther keywords: chitosan, surface charge, anticancer properties, anticancer activities, antioxidant activities, molecular weight, selenium nanoparticles, CS‐coated SeNP, Fourier transform infrared spectroscopy, photometric system, HepG2 cells, time 45.0 d, Se     

Influence of mesoporous silica and hydroxyapatite nanoparticles on the mechanical and morphological properties of polypropylene

This paper presents the effect of different types of additives on the morphology and mechanical performance of polypropylene (PP). Three different types of nanoparticles, containing mesoporous silica (MCM-41), Hydroxyapatite (HA) and the composite of MCM-41 and HA (MH) were used. Nanocomposites containing PP, 3 wt.% of maleic anhydride grafted polypropylene (PP-g-MA) and 3 wt.% of different nanoparticles were prepared using the melt-compounding technique in a twin-screw extruder. The bulk mechanical response of the nanocomposites such as tensile, flexural and Izod impact properties were studied. The results of mechanical tests show that at the same nanomaterial content, all the nanofillers cause better tensile, flexural and impact strength than neat PP. The MH nanoparticle improves the mechanical properties of PP, better than the other nanoparticles because this nanofiller contains good properties of both MCM-41 and HA nanoparticles in itself. In order to investigate the effect of foam agent on the mechanical properties of neat PP and nanocomposites based on PP, inorganic azodicarboxamide was added to the aforementioned mixtures as chemical blowing agent and the foamed specimens were resulted using the melt-compounding technique. The results reveal that addition of foam agent to mixtures, leads to increase the flexural characteristics of samples, but the tensile properties and impact strength decrease. Scanning electron microscopy (SEM) was used to assess the fracture surface morphology and the dispersion of the nanoparticles. X ray diffractometry (XRD) was used to examine the intercalation effect on the nanocomposites. The observations show that the nanomaterials were well dispersed in the polymer matrix and the enhancement of the interface between the matrix and fillers was obtained by the incorporation of MH, MCM-41 and HA nanoparticles into PP matrix.     

不同偶联剂对白炭黑表面的改性及其表征

采用3种硅烷偶联剂双-[γ-(三乙氧基硅)丙基]四硫化物(Si69)、γ-甲基丙烯酰氧基丙基三甲氧基硅烷(KH570)、乙基三甲氧基硅烷(11-100)对沉淀法白炭黑粉体进行有机湿法改性。借助傅里叶红外光谱、接触角仪、纳米粒度及Zeta电位仪、扫描电镜等检测手段对白炭黑改性前后的结构及性能进行表征,研究考察3种不同偶联剂对沉淀法白炭黑的疏水性及分散性的影响。结果表明:3种不同硅烷偶联剂都已成功接枝到白炭黑表面,其中Si69改性的白炭黑剩余羟基数与未改性白炭黑表面羟基数的比值最小,为34.23%;经偶联剂改性后的白炭黑,团聚现象减弱,粒径分布变窄,分散性得到改善,疏水性大小依次为Si69-Si O_2KH570-Si O_211-100-Si O_2;综合对比3种偶联剂的改性效果,Si69的改性效果最好。     

Cross‐linking gold nanoparticles aggregation method based on localised surface plasmon resonance for quantitative detection of miR‐155

MiR‐155 plays a critical role in the formation of cancers and other diseases. In this study, the authors aimed to design and fabricate a biosensor based on cross‐linking gold nanoparticles (AuNPs) aggregation for the detection and quantification of miR‐155. Also, they intended to compare this method with SYBR Green real‐time polymerase chain reaction (PCR). Primers for real‐time PCR, and two thiolated capture probes for biosensor, complementary with miR‐155, were designed. Citrate capped AuNPs (18.7 ± 3.6 nm) were synthesised and thiolated capture probes immobilised to AuNPs. The various concentrations of synthetic miR‐155 were measured by this biosensor and real‐time PCR method. Colorimetric changes were studied, and the calibration curves were plotted. Results showed the detection limit of 10 nM for the fabricated biosensor and real‐time PCR. Also, eye detection using colour showed the weaker detection limit (1 µM), for this biosensor. MiR‐133b as the non‐complementary target could not cause a change in both colour and UV–visible spectrum. The increase in hydrodynamic diameter and negative zeta potential of AuNPs after the addition of probes verified the biosensor accurately fabricated. This fabricated biosensor could detect miR‐155 simpler and faster than previous methods.Inspec keywords: RNA, molecular biophysics, biochemistry, cancer, nanoparticles, gold, aggregation, surface plasmon resonance, molecular configurations, nanosensors, enzymes, calibration, ultraviolet spectra, visible spectra, eye, hydrodynamics, electrokinetic effects, biosensors, nanofabricationOther keywords: cross‐linking gold nanoparticles aggregation method, localised surface plasmon resonance, quantitative detection, cancers, diseases, biosensor, miR‐155 detection, miR‐155 quantification, SYBR green real‐time polymerase chain reaction, thiolated capture probes, citrate capped AuNPs, synthetic miR‐155, real‐time PCR method, colorimetric changes, calibration curves, eye detection, colour, detection limit, MiR‐133b, noncomplementary target, UV‐visible spectrum, hydrodynamic diameter, negative zeta potential, Au