Size Of Spherical Particles Research Articles

Advanced hybrid nanomaterials based on carboxymethyl-modified biopolymer: Green synthesis and application in sustainable antimicrobial products

The utilization of agricultural by-products for the synthesis of hybrid nanomaterials represents an environmentally sustainable approach. This research aims to comprehensively investigate high-performance silver and copper nanoparticles hybrid materials based on carboxymethyl-modified cellulose / lignin derived from rice husks (CMC / CML-AgNPs and CMC / CML-CuONPs) and apply them for antimicrobial activities. CMC / CML was used to reduce Ag / Cu cations to the atomic level and then efficiently stabilize Ag / CuO nanoparticles, an eco-friendly method and sustainable development. The hybrid nanomaterials were successfully synthesized with spherical shapes and particle sizes ranging from 4 to 16 nm. The diffraction peaks at 38.46°, 46.57°, 64.93°, and 77.55° were ascribed to the face-centered cubic crystal lattice (111), (200), (220), and (311) of silver nanoparticles in the CMC / CML-AgNPs. The peaks were 32.26°, 46.06°, 52.16°, 61.71°, 63.80°, and 71.23° associating with the (110,20−2), (112), (11−3), (310), and (221) plane orientations of CuO nanoparticles. The proposed materials demonstrated highly efficient antimicrobial performances. Particularly, CMC-AgNPs and CML-CuONPs exhibited an inhibitory capability of up to 100 % against E. coli and S. aureus within 72 h. Simultaneously, the antifungal results showed that hybrid nanomaterials have a better ability to inhibit the A. niger than A. flavus fungus. When experimenting on peanut seeds, hybrid nanomaterials showed an inhibitory capability of up to 99.0 % against A. niger. IC50 values of the hybrid nanomaterials range from 0.872 mg/mL to 1.188 mg/mL, confirming that these materials are non-cytotoxic. These materials exhibit significant stability and enduring antimicrobial efficacy, making them ideal for sustainable development of various antibacterial and antifungal blocks for the near future.

Synthesis and Characterization of Self-Dispersion Monodisperse Silica-Based Functional Nanoparticles for Enhanced Oil Recovery (EOR) in Low-Permeability Reservoirs

A controllable particle size mono-dispersing nanofluid system has been developed to address the challenges of low porosity and low-permeability in low to ultra-low-permeability reservoirs. This system combines high dispersion stability with enhanced oil recovery performance, and its effectiveness in improving recovery rates in low-permeability reservoirs, where conventional chemical flooding is ineffective, has been well demonstrated. Using the in situ method to prepare monodispersed nano-silica particles, the effects of the water concentration, ammonia concentration, and silica precursor concentration on the morphology, particle size, and formation time of the silica spherical particles were analyzed. Building on this foundation, a partially hydrophobic modified nano-silica oil displacement fluid was synthesized in situ. The system’s dispersion stability, ability to reduce oil-water interfacial tension, and capacity to alter rock wettability were evaluated. Core physical models were used to evaluate the oil displacement efficiency and the permeability applicability limits of the self-dispersing nano-silica oil displacement system. The experiments confirmed that the particle size distribution of the self-dispersing nano-silica oil displacement system can be controlled within a range of 10 nm to 300 nm. The nanofluids exhibited excellent stability, effectively altering the rock wettability from oil-wet to water-wet and reducing the oil-water interfacial tension to approximately 10−1 mN/m. The nano-displacement system increased the recovery rate of the low permeability reservoirs by more than 17%. The in situ modification method used to prepare these self-dispersing nanoparticles provides valuable insights for synergistic enhancement of recovery when combined with other systems, such as surfactants and CO2. This approach also opens up new possibilities and drives further development in the field of nano-enhanced oil recovery chemistry.

Green Synthesis of Zinc Oxide Nanoparticles Using Dillenia Indica and Mikania Micrantha Leaf Extracts: Applications in Photocatalysis and Antibacterial Activity.

Researchers are keenly interested in developing metal-based nanoparticles using plant sources as they are eco-friendly, less expensive and simpler. Zinc oxide nanoparticles, symbolized as D-ZnONPs and M-ZnONPs were synthesized in this study utilizing the leaves of D. indica and M. micrantha, respectively, and studied their impact on the growth inhibition of various bacterial strains and on the photocatalysis. By displaying the distinctive surface plasmon resonance (SPR) band at 373 nm in UV-Vis and bands at 450-480 cm-1 corresponding to Zn-O stretching FTIR spectroscopy imparted the formation of ZnONPs which was further supported by X-ray diffraction analysis by showing the polycrystalline nature and a hexagonal wurtzite structure. The spherical form and average particle size of 30 nm of the produced ZnONPs, as confirmed by electron microscopy, are also confirmed to be crystalline. Under natural sunlight, both ZnONPs demonstrate excellent degradation efficacy about 96-99 % within 100 min towards methylene blue (MB). Furthermore, it is noteworthy that both the synthesized ZnONPs exhibited 55-60 % efficacy with respect to antibiotics in inhibiting the growth of various pathogenic bacterial strains. Overall, ZnONPs can be produced on a large-scale using plant sources and employed them in environmental remediation and cosmetic industries as prominent components.

The cruciality of particle size and shape on fracture mechanism of aluminum matrix composites

Metal matrix composites are generally believed to achieve better performance with spherical reinforcements than irregular ones. In this work, through experiments and computational simulations, we have demonstrated that spherical reinforcements do not necessarily enhance the tensile ductility of composites. There exists a critical size for spherical particles. Using an Al2O3-Al2024 composite as an example, we found that when the size of spherical Al2O3 particles is less than 3 µm, they are not fractured during deformation, resulting in enhanced ductility. We elucidated the competitive mechanism between particle and matrix fracture under various reinforcement sizes and volume fractions, and constructed a deformation map that can be utilized to determine fracture mechanisms. This work clarifies the micro-mechanical mechanisms of reinforcements on material fracture behavior, providing guidance for the design and fabrication of strong and ductile metal matrix composites.

An Experimental Study of Zinc Evaporation from Bottom Zinc Dross at Atmospheric Pressure and in Inert Atmosphere with Integrated CFD Modelling.

In the present study, the recycling process of bottom zinc dross was performed by evaporation and subsequent condensation at 800 °C for 30 min with an observed argon flow rate of 100-400 mL/min to ensure an inert atmosphere, to observe the evaporation rate and final form of the product. Under the set conditions of over 98% zinc purity, products in the form of nanofibres (thickness 500 nm), powder (size of spherical particles 2-5 μm), dendrites, and metallic forms were obtained. The employed mathematical modelling (via Ansys 2023R1 software) predicted the behaviour of the argon flow current in the quartz tube, as well as the temperature gradient in the quartz tube and in the close vicinity of the zinc sample. Via Inventor 2014 software, the rate of zinc sample heating was calculated. All the simulations were compared with the physical measurements and correlation was proven.

Efficient Delivery of Gold Nanoparticles and miRNA-33a Via Cationic PEGylated Niosomal Formulation to MCF-7 Breast Cancer Cells

To overcome the challenges associated with the co-delivery of AuNPs (gold nanoparticles) and miRNA as an anti-breast cancer combination therapy, niosomal systems were developed using Span 60, cholesterol, and a cationic lipid (CTAB), and the formulations were optimized using Box-Behnken experimental design. The niosomal formulations with the smallest size were selected for further optimization of size, surface charge, entrapment efficiency, and stability. To achieve this, AuNPs and DSPE-PEG2000 (2-distearoyl-sn-glycero-3-phosphoethanolamine-N-[amino(polyethylene glycol)-2000)were added to the formulation. The optimized niosomal formulation could effectively encapsulate AuNPs with an entrapment efficiency of 34.49% ± 0.84 and a spherical particle size of 153.6 ± 4.62 nm. The incorporation of PEG and CTAB led to notable enhancements in the overall characteristics of the delivery system. To evaluate the effectiveness of the combination therapy, various assessments such as cytotoxicity, apoptosis, and gene expression properties were conducted. The results demonstrated that the combination delivery using the new C-PEG-Nio-AuNPs (cationic pegylated niosomal gold nanoparticles) system and miRNA had the lowest IC50, the highest apoptosis rate, and the most significant upregulation of miRNA and BAX/BCL2 expression in MCF-7 cell growth. In conclusion, this innovative co-delivery approach represents a promising breakthrough in the development of therapeutic agents for breast cancer treatment. By combining multiple therapeutic agents within a single delivery system, this method has the potential to enhance treatment efficacy, reduce side effects, and improve patient outcomes.Graphical

Synthesis and multifunctional application of two novel carbon quantum dots as corrosion inhibitors

N, S- and N-doped carbon quantum dots (CDs) were synthesized by calcination in the presence of L-cysteine and 2-aminobutyric acid by using P-phenylenediamine as the raw material. The CDs were characterized by Fourier transform infrared spectroscopy, transmission electron microscopy, and fluorescence spectroscopy. Results show that both kinds of CDs have spherical structures and particle sizes. The CDs were dispersed in 3.5 wt% NaCl solution and doped into the epoxy coating to prepare the composite coating. The two kinds of CDs have good corrosion inhibition effects in both applications.

Preparation of micron-sized benzamidine-modified magnetic agarose beads for trypsin purification from fish viscera

The effective method for trypsin purification should be established because trypsin has important economic value. In this work, a novel and simple strategy was proposed for fabricating micron-sized magnetic Fe3O4@agarose-benzamidine beads (MABB) with benzamidine as a ligand, which can efficiently and selectively capture trypsin. The micro-sized MABB, with clear spherical core-shell structure and average particle size of 6.6 μm, showed excellent suspension ability and magnetic responsiveness in aqueous solution. The adsorption capacity and selectivity of MABB towards target trypsin were significantly better than those of non-target lysozyme. According to the Langmuir equation, the maximum adsorption capacity of MABB for trypsin was 1946 mg g−1 at 25 °C, and the adsorption should be a physical sorption process. Furthermore, the initial adsorption rate and half equilibrium time of MABB toward trypsin were 787.4 mg g−1 min−1 and 0.71 min, respectively. To prove the practicability, MABB-based magnetic solid-phase extraction (MSPE) was proposed, and the related parameters were optimized in detail to improve the purification efficiency. With Tris-HCl buffer (50 mM, 10 mM CaCl2, pH 8.0) as extraction buffer, Tris-HCl buffer (50 mM, 100 mM CaCl2, pH 8.0) as rinsing buffer, acidic eluent (0.01 M HCl, 0.5 M NaCl, pH 2.0) as eluent buffer and alkaline buffer (1 M Tris-HCl buffer, pH 10.0) as neutralization solution, the MABB-based MSPE was successfully used for trypsin purification from the viscera of grass carp (Ctenopharyngodon idella). The molecular weight of purified trypsin was determined as approximate 23 kDa through sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). The purified trypsin was highly active from 30 °C to 60 °C, with an optimum temperature of 50 °C, and was tolerant to pH variation, exhibiting 85 % of maximum enzyme activity from pH 7.0 to 10.0. The results demonstrated that the proposed MABB-based MSPE could effectively purify trypsin and ensure the biological activity of purified trypsin. Therefore, we believe that the novel MABB could be applicable for efficient purification of trypsin from complex biological systems.

Evolution of self-assembled amphiphilic colloidal particles in strong-flavor Chinese baijiu

This study proposed the evolution of self-assembled amphiphilic colloidal particles in Strong-Flavor (SF) Baijiu based on Ostwald ripening for the first time. The evolution process occurs in two stages: disordered amphiphilic molecules self-assemble into small colloidal particles and subsequently undergo Oswald ripening to form larger hydrophobic particles. Microscopic observations revealed the average size of oil-like spherical colloidal particles in Baijiu increased from 1.86 μm to 2.96 μm while the number of particles decreased by 39.50% during the 16-year cellaring process of SF Baijiu, consistent with the particle size trend observed via laser scattering. During fusion process, the charge-to-mass ratio of positively charged colloidal particles decreased, leading ζ-potential decreased from 23.7 mV to 4.66 mV within 16 years of storage. The electrochemical impedance spectroscopy approach tracked the unidirectional variation in the dielectric constant during evolution of SF Baijiu, reflecting the gradual expansion of colloidal particles, which aligns with the evolution trend observed in molecular dynamics simulations. By integrating direct microscopic observations of amphiphilic colloidal particles with electrochemical techniques, the evolution of Baijiu samples is capable to be evaluated in-situ, laying the foundation for intelligent Baijiu aging monitoring technology.

Unveiling the impact of stabilization pretreatment on sodium storage performance in hard carbon

Stabilization pretreatment coupled with molecular cross-linking is commonly used to modify starch, aiming to obtain starch-based hard carbon materials with appropriate spherical particle sizes. Nevertheless, the impact of the intermediate stabilization process on its sodium storage performance remains unclear. Herein, a hard carbon material with no surface open pores, low specific surface area and abundant internal closed pores with thinner pore walls is successfully synthesized and exhibits significantly improved initial Coulombic efficiency and plateau capacity through a simple low-temperature pretreatment strategy, using renewable and cost-effective soluble starch as the raw material. Additionally, research indicates that an appropriate degree of disorder or defectiveness is conducive to forming a larger quantity of closed pores with thinner pore walls. Both excessively low and high defect levels are detrimental to the formation of closed pores. This work will encourage researchers to further focus on the impact of defectiveness on closed pores, which will promote the development of high-energy practical sodium-ion batteries.

Ruxolitinib-loaded poly-ɛ-caprolactone (PCL) nanoparticles inhibit JAK2/STAT5 signaling in BT474 breast cancer cells by downregulating Bcl-2 and Mcl-1.

JAK/STAT signaling plays an important role in regulating cell proliferation. Reducing proliferation and inducing cell death with gene-specific inhibitors such as ruxolitinib, Receptor tyrosine kinases (RTK) inhibitor targeting JAK1/2, are therapeutic approaches. The use of nanoparticles can reduce the toxicity and side effects of drugs, as they act directly on cancer cells and can selectively increase drug accumulation in tumor cells. Poly-ɛ-caprolactone (PCL) is a polymer that is frequently used in drug development. In this study, Rux-PCL-NPs were synthesized to increase the effectiveness of ruxolitinib. In addition, this study aimed to determine the effect of Rux-PCL-NPs on JAK/STAT signaling and apoptotic cell death. Rux-PCL-NPs were synthesized by nanoprecipitation. The Rux-PCL-NPs had a spherical and mean particle size of 219 ± 88.66nm and a zeta potential of 0.471 ± 0.453 mV. In vitro cytotoxicity and antiproliferative effects were determined by MTT and soft agar colony formation assays, respectively. The effects of ruxolitinib, PCL-NPs, and Rux-PCL-NPs on apoptosis and the JAK/STAT pathway in cells were examined by western blot analysis. PCL-NPs did not have a toxic effect on the cells. The IC50 value of Rux-PCL-NPs was decreased 50-fold compared to that of ruxolitinib. Rux-PCL-NPs promoted cell death by downregulating JAK2 and STAT5, thereby inhibiting the JAK/STAT pathway. Our results revealed that Rux-PCL-NPs, which increased the efficacy of ruxolitinib, regulated apoptosis and the JAK2/STAT5 pathway.

Non-Destructive Analysis of Subvisible Particles with Mie-Scattering-Based Light Sheet Technology: System Development

The characteristics of subvisible particles (SbVPs) are critical quality attributes of injectable and ophthalmic solutions in pharmaceutical manufacturing. However, current compendial SbVP testing methods, namely the light obstruction method and the microscopic particle count method, are destructive and wasteful of target samples. In this study, we present the development of a non-destructive SbVP analyzer aiming to analyze SbVPs directly in drug product (DP) containers while keeping the samples intact. Custom sample housings are developed and incorporated into the analyzer to reduce optical aberrations introduced by the curvature of typical pharmaceutical DP sample containers. The analyzer integrates a light-sheet microscope structure and models the side scattering event from a particle with Mie scattering theory with refractive indices as prior information. Equivalent spherical particle size under assigned refractive index values is estimated, and the particle concentration is determined based on the number of scattering events and the volume sampled by the light sheet. The resulting analyzer's capability and performance to non-destructively analyze SbVPs in DP containers were evaluated using a series of polystyrene bead suspensions in ISO 2R and 6R vials. Our results and analysis show the particle analyzer is capable of directly detecting SbVPs from intact DP containers, sorting SbVPs into commonly used size bins (e.g. ≥ 2 µm, ≥ 5 µm, ≥ 10 µm, and ≥ 25 µm), and reliably quantifying SbVPs in the concentration range of 4.6e2 to 5.0e5 particle/mL with a margin of ± 15 % error based on a 90 % confidence interval.

Particle Tracking of Orientation and Velocity Of Arbitrary Shape

Dispersions or particulate systems are prevalent in numerous natural and practical applications. Characterisation of such multiphase systems usually involves measuring size, spatial location, velocity and number density, which is usually non-trivial. The 'Depth from Defocus' (DFD) technique provides an imaging-based volumetric approach for estimating the size and position of dispersed spherical particles using the blurring information from a shadowgraph image. The two-image DFD approach involves two cameras to capture simultaneous images at different degrees of blur, which, although simpler, requires a mandatory calibration procedure. This study proposes a single-image DFD technique that provides a calibration-free size estimation using theoretical functions while evaluating position requires a simple calibration. The efficacy of this technique is demonstrated for various sparse spherical dispersions, including target dots, dispersed glass beads, liquid droplets in sprays and surface bubble rupture, and pollen grains. The method further enables precise determination of the measurement volume, which is crucial, allowing for bias-free estimates of the size distribution and volume concentration. The simple optical configuration and semi-automatic calibration procedure make this method easily deployable and accessible for diverse applications. The pixelation effect on the limiting value of the degree of blur is also estimated theoretically and compared with experiments. This effect is of interest concerning any typical discrete sensor imaging system in general.

Effect of Spherical Silver Particles Size of the Catalyst Bed on Hydrogen Peroxide Monopropellant Thruster Performance

Effect of Spherical Silver Particles Size of the Catalyst Bed on Hydrogen Peroxide Monopropellant Thruster Performance

Comparing novel small-angle x-ray scattering approaches for absolute size and number concentration measurements of spherical SiO2 particles to established methods

Biomedical analytical applications, as well as the industrial production of high-quality nano- and sub-micrometre particles, require accurate methods to quantify the absolute number concentration of particles. In this context, small-angle x-ray scattering (SAXS) is a powerful tool to determine the particle size and concentration traceable to the Système international d’unités (SI). Therefore, absolute measurements of the scattering cross-section must be performed, which require precise knowledge of all experimental parameters, such as the electron density of solvent and particles, whereas the latter is often unknown. Within the present study, novel SAXS-based approaches to determine the size distribution, density and number concentrations of sub-micron spherical silica particles with narrow size distributions and mean diameters between 160 nm and 430 nm are presented. For the first-time traceable density and number concentration measurements of silica particles are presented and current challenges in SAXS measurements such as beam-smearing, poorly known electron densities and moderately polydisperse samples are addressed. In addition, and for comparison purpose, atomic force microscopy has been used for traceable measurements of the size distribution and single particle inductively coupled plasma mass spectrometry with the dynamic mass flow approach for the accurate quantification of the number concentrations of silica particles. The possibilities and limitations of the current approaches are critically discussed in this study.

Nanoencapsulation-mediated curcumin and its incorporation in nutraceutical cookies: Cell viability, bioavailability, and anti-inflammatory activity studies

The anti-inflammatory activity of curcumin, Curcuma longa, is known, however, its low bioavailability is a limiting factor. The nanoencapsulated curcumin was developed and its spherical particle size ∼20 nm was confirmed using TEM. An in vitro study was performed to determine the cytotoxicity of standard and nanoencapsulated curcumin, and their effect on lipopolysaccharide-induced nitric oxide, and IL-6 production in RAW 264.7 cells. The plasma bioavailability of nanoencapsulated curcumin was 12 times higher compared to native curcumin in Swiss albino mice. The anti-inflammatory activity of native curcumin and nanoencapsulated curcumin was compared in the carrageenan-induced paw edema model. A paw thickness reduction of 33.7 % and 46 % was observed with the treatment of native curcumin and nanoencapsulated curcumin, respectively and the histology studies validated the results. Further, the in vitro COX-1 inhibition of cookies incorporated with nanoencapsulated curcumin was 20 and 24 % higher than native curcumin and control cookies, respectively indicating their nutraceutical application.

Influence of minor Mg/Ca/Nb/Ag addition on the morphology and microstructure of Fe-rich phase in powder metallurgy Cu[sbnd]10Fe alloy

The effect of Mg/Ca/Nb/Ag alloying on the morphology and microstructure of powder metallurgy Cu10Fe alloy was investigated systemically in this work. Alloying of Ca reduces the size of Fe-rich particles, while alloying of Mg/Nb/Ag increases the Fe-rich particles. This is attributed to the different roles of various alloying elements on the liquid-phase separation behaviors as well as diffusion of Fe atoms during the solidification. Coarse size spherical Fe-rich particles with a face centered cubic structure are observed in CuFe alloys bearing Mg/Ag/Nb, whilst the alloying of Ca favors the formation of fine spherical Fe-rich particles with a body centered cubic structure. The factor governing the morphology is found to be interfacial energy for CuFe alloys containing Mg/Ag/Nb and elastic energy for Cu-Fe-Ca alloy, respectively. Coarse size Fe-rich particles are hard to deform during subsequent rolling, but the fine Fe-rich particles can co-deform with Cu matrix. This study could provide a detailed picture regarding the influence of various alloying element types on the size, morphology, and lattice structure of Fe phase of CuFe alloy.

CuO−La2O3 Nanocomposite as a Recyclable and Eco‐Friendly, Heterogeneous Catalyst for the One‐Pot Synthesis of Pyrano [2, 3‐c] Pyrazoles

AbstractIn this work, the unique performance of binary acid‐base CuO/La2O3 nanocomposite as a highly efficient heterogeneous catalyst was successfully examined for the one‐pot multicomponent synthesis of pyrano [2, 3‐c] pyrazole derivatives. The strong interactions between La and Cu had a profound effect on the catalytic activity of nanocatalysts. In addition, high selectivity, easy recovery, reusability, a very reasonable price, simple preparation and eco‐friendliness are other important advantages of this nanocatalyst. The characterized nanocomposite demonstrated excellent structural and morphological properties, leading to high catalytic efficiency. Characterization using Fourier Transform Infrared Spectroscopy (FT‐IR), X‐ray Powder Diffraction (XRD) confirmed crystallographic structure, and Field Emission Scanning Electron Microscopy (FE‐SEM) showed a spherical particle size of approximately 43 nm. Energy‐Dispersive X‐ray (EDX) analysis confirmed the composition of La, O, and Cu elements in the nanocomposite as 86.4 %, 13.5 %, and 0.2 %, respectively. The optimal condition for the synthesis resulted in a 98 % yield of pyrano [2, 3‐c] pyrazole derivatives under reflux with 0.02 g of CuO/La2O3 catalyst in a 10‐minute reaction time.

Flow and clogging behavior of a mixture of particles in a silo

We investigated the clogging behavior observed during the flow of aspherical particles from a silo in the presence of spherical particles of different sizes and proportions using flow visualization experiments and discrete element method simulations. The size of the avalanche, essentially the tendency of clogging, exhibits non-monotonic dependence on the spherical particle volume fraction. For small enough content of spherical particles, the clogging tendency intensifies, whereas it reduces rapidly for high enough spherical particle fractions, with a minimum in between. The non-monotonic behavior is observed to persist over for different spherical particle sizes. The overall behavior is shown to arise due to competing effects between the localized total particle fraction influencing avalanche strength and mean size of the particles exiting the silo, influencing the probability of arch formation.

Development of cancer-targeted nano gold functionalized ruthenium(III)-doxorubicin complex: Synthesis, characterization and evaluation of DNA cleavage, anticancer and bioimaging activity

Metal-based drugs have attracted greater attention for cancer diseases because of biological relevance. However, some drawbacks are present in the metal complexes such as low stability and low bioavailability. Nanomaterials functionalized metal complexes can protect the stability and enhanced the bioavailability. In the present study, Nano gold functionalized ruthenium(III) complex from doxorubicin have been synthesized from ruthenium(III) complex and characterized using various spectrochemical techniques such as IR, UV, and NMR. In the metal complex, Doxorubicin (DOX) acts as a monobasic bidentate ligand and is coordinated through the carbonyl oxygen and phenolate oxygen of the anthracene ring. Based on spectral evidences, the complex [Ru(DOX)(PPh3)2Cl2] has an octahedral geometry. The Nano Au-Ru(III) DOX is analysed for their size, and morphology using XRD, SEM and HRTEM. X-ray diffraction pattern revealed that the complex has nanocrystalline in nature. The Nano Au-Ru(III) DOX is spherical shape and particle size is less than 15 nm. The DNA cleavage activity of [Ru(DOX)(PPh3)2Cl2] and Nano Au-Ru(III) DOX has been evaluated using pUC18 plasmid DNA and the results showed significant cleavage. The [Ru(DOX)(PPh3)2Cl2] and Nano Au-Ru(III) DOX have been tested against human breast cancer (MCF-7) and leukemia cancer cell lines (K-562) in vitro for its antitumor effects. The tumour activity of the Nano Au-Ru(III) DOX showed more promising activity than the [Ru(DOX)(PPh3)2Cl2]. The cell imaging of the Nano Au-Ru(III) DOX was examined against epithelial human breast cancer cell line (MDA-MB-231) using fluorescent microscopy. The fluorescence images showed high scattering light in tumour tissue at 100 µg/mL Hence, Nano Au-Ru(III) DOX can serve as a promising drug for cancer therapy and cellular imaging.