Ellipsoidal Morphology Research Articles

Microfluidics assisted generation of innovative polysaccharide hydrogel microparticles.

Capillary flow-based approach such as microfluidic devices offer a number of advantages over conventional flow control technology because they ensure highly versatile geometry and can be used to produce monodisperse spherical and non-spherical polymeric microparticles. Based on the principle of a flow-focusing device to emulsify the coflow of aqueous solutions in an organic phase, we were able to produce the following innovative polysaccharide hydrogel microparticles: - Janus hydrogel microparticles made of pectin–pectin (homo Janus) and pectin–alginate (hetero Janus) were produced. The efficiency of separation of the two hemispheres was investigated by confocal scanning laser microscopy (CSLM) of previously labelled biopolymers. The Janus structure was confirmed by subjecting each microparticle hemisphere to specific enzymatic degradation. As a proof of concept, free BSA or BSA grafted with dextran, were encapsulated in each hemisphere of the hetero Janus hydrogel microparticles. While BSA, free or grafted with dextran, was always confined in the alginate hemisphere, a fraction of BSA diffused from the pectin to the alginate hemisphere. Methoxy groups along the pectin chain will be responsible of the decrease of the number of attractive electrostatic interactions occurring between amino groups of BSA and carboxylic groups of pectin. - Pectin hydrogel microparticles of complex shapes were successfully produced by combining on-chip the phenomenon of gelation and water diffusion induced self-assembly, using dimethyl carbonate as continuous phase, or by deformation of the pre-gelled droplets off-chip at a fluid–fluid interface. Sphere, oblate ellipsoid, torus or mushroom-type morphologies were thus obtained. Moreover, it was established that after crossing the interface during their collect, mushroom-type microparticles did not migrate in the calcium or DMC phase but stayed at the liquid–liquid interface. These new and original hydrogel microparticles will open up opportunities for studying relationships between combined enzymatic hydrolysis and active release for Janus particles and relationships between shape and swelling behaviour for anisotropic pectin microparticles.

Contact mechanics studies of an ellipsoidal contact bearing surface of metal-on-metal hip prostheses under micro-lateralization

The morphology of the contact bearing surfaces plays an important role in the contact mechanics and potential wear of metal-on-metal (MOM) hip prostheses. An ellipsoidal bearing surface was proposed for MOM hip implants and the corresponding contact mechanics were studied by using the finite element method (FEM) under both standard and micro-lateralization conditions. When under micro-lateralization, the maximum contact pressure decreased from 927.3MPa to 203.0MPa, with increased ellipticity ratio medial-laterally. And the contact region was found to shift from the rim of the cup to the inner region compared to the spherical design. Under standard conditions, an increasing trend of the maximum contact pressure for the acetabular component was predicted as the major radius of the ellipsoidal bearing surface was increased. Nevertheless, the maximum contact pressure reached an asymptotic value when the ellipticity ratio was increased to 1.04. Therefore it is critical to optimize the ellipticity ratio in order to reduce the contact pressure under micro-lateralization condition and yet not to cause a markedly increased contact pressure under normal condition. Additionally, the maximum contact pressure in the ellipsoidal bearing surface remained relatively constant with the increased micro-lateralization. It is concluded that an ellipsoidal bearing surface morphology may be a promising alternative by offering better contact mechanisms when micro-lateralization should occur and attributing to minimized wear.

Synthesis and application of a targeting diagnosis system via quantum dots coated by amphiphilic polymer for the detection of liver cancer cells

Water-soluble quantum dots (QDs) for liver cancer diagnosis were prepared using QDs with oleylamine ligand coated with poly(aspartate)-graft-poly(ethylene glycol)-dodecylamine (PASP-Na-g-PEG-DDA). Dynamic light scattering and transmission electron microscopy imaging showed that the novel QDs have an ellipsoidal morphology with a size of ~ 45 nm which could be used for biomedical application. Furthermore, the PASP-Na-g-PEG-DDA was then modified with anti-(vascular endothelial growth factor) (VEGF antibody), and a 1-(4,5-dimethylthiazol-2-yl)-3,5-diphenylformazan (MTT) assay showed that the novel anti-VEGF-targeting QDs in vitro had low toxicity. Confocal laser scanning microscopy observations revealed an intracellular (HepG2) distribution of the novel anti-VEGF-targeting QDs and the targeting efficiency of anti-VEGF. These novel QDs could be used as a probe for liver cancer cell imaging because of anti-VEGF targeting.

Hydrothermal formation and characteristics of rare-earth niobate phosphors and solid solutions between YNbO4 and TbNbO4

Monoclinic fergusonite-type niobate, YNbO4:Tb3+ and complete solid solutions with luminescent properties in the YNbO4–TbNbO4 system were directly formed as nanocrystals from the precursor solutions of NbCl5, TbCl3, and YCl3 under hydrothermal conditions at 240 °C. The niobate nanocrystals possessed distinguishing feature of ellipsoidal morphology. The optical band gap of the as-prepared samples, Y1−xTbxNbO4, x = 0–1.0, decreased from 3.7 to 2.9 eV as the terbium concentration increased from x = 0 to 1.0. The photoluminescence spectra of the as-prepared nanocrystals containing terbium are responsible for the characteristic blue (490 nm) and green (545 nm) luminescence, associated with 5D4 → 7F6 and 5D4 → 7F5 transitions, respectively. The strongest emission bands in the green spectral domain corresponding to 5D4 → 7F5 transition of Tb3+ are located at 545 and 550 nm under excitation at 240 nm Xe lamp. By heat treatment at 1300 °C, the luminescence intensity of the as-prepared solid solution x = 0.10 that presented the highest photoluminescence intensity increased more than 8 times as high as that before heat treatment.

Synthesis of luminescent nanocrystals and solid solutions in the YNbO4–EuNbO4 system via hydrothermal route

Luminescent nanocrystals having distinctive ellipsoidal morphology and the complete solid solution of monoclinic phase in the YNbO4–EuNbO4 system were hydrothermally formed under weakly basic conditions at 180–240°C for 5h. The excitation spectra of the Y1−xEuxNbO4 nanocrystals, which consisted of the charge transfer (CT) band around 240–270nm due to [NbO4]3−–Eu3+ interaction and several sharp bands corresponding to the f–f transitions of Eu3+, e.g. the most intense absorption band at 395nm (7F0→5L6), showed that the compounds could be excited by both ultraviolet and visible light. A dominant red emission at 610nm and a weak orange emission at 590nm assigned to 5D0→7F2 and 5D0→7F1 transitions of Eu3+, respectively were observed in the as-prepared nanocrystals containing europium under excitation at 395nm. The heat treatment at temperatures more than 1000°C in air was effective for the improvement in the photoluminescence intensity of the as-prepared solid solutions. By the enhancement in the crystallinity and crystallite growth of the monoclinic phase through heat treatment at 1300°C in air, the luminescence intensity of the as-prepared solid solution, Y0.75Eu0.25NbO4 (x=0.25), which showed the most significant photoluminescence, became more than 5 times as strong as that before the heat treatment.

Direct Formation and Luminescence Properties of Yttrium Niobate YNbO4 Nanocrystals via Hydrothermal Method

Yttrium niobate YNbO4 nanocrystals with ellipsoidal morphology were directly formed from the precursor solution mixtures of YCl3 and NbCl5 under weakly basic conditions in the presence of aqueous ammonia by hydrothermal method. The hydrothermal treatment at 180°C for 5 h was necessary to obtain nanocrystals (18 nm) with sufficient crystallinity. The optical band gap of the as‐prepared samples was 3.6 eV. The as‐prepared YNbO4 nanocrystals showed UV‐blue and broadband emission centered at 405 nm under excitation at 235 nm, which was due to the blue recombination luminescence, associated with charge‐transfer transitions involving the tetrahedral NbO4 group. The emission intensity increased with increased hydrothermal treatment temperature. The photoluminescence intensity of the YNbO4 was extremely improved via heating above 1000°C in air, which was accompanied by the increase in the optical band gap from 3.6 to 4.0 eV. By heat treatment at 1300°C, the intensity of the UV‐blue and broadband emission (with maximum at 400 nm) for the YNbO4 became more than 22.5 times as strong as that before heat treatment.

An automatic method for robust and fast cell detection in bright field images from high-throughput microscopy

BackgroundIn recent years, high-throughput microscopy has emerged as a powerful tool to analyze cellular dynamics in an unprecedentedly high resolved manner. The amount of data that is generated, for example in long-term time-lapse microscopy experiments, requires automated methods for processing and analysis. Available software frameworks are well suited for high-throughput processing of fluorescence images, but they often do not perform well on bright field image data that varies considerably between laboratories, setups, and even single experiments.ResultsIn this contribution, we present a fully automated image processing pipeline that is able to robustly segment and analyze cells with ellipsoid morphology from bright field microscopy in a high-throughput, yet time efficient manner. The pipeline comprises two steps: (i) Image acquisition is adjusted to obtain optimal bright field image quality for automatic processing. (ii) A concatenation of fast performing image processing algorithms robustly identifies single cells in each image. We applied the method to a time-lapse movie consisting of ∼315,000 images of differentiating hematopoietic stem cells over 6 days. We evaluated the accuracy of our method by comparing the number of identified cells with manual counts. Our method is able to segment images with varying cell density and different cell types without parameter adjustment and clearly outperforms a standard approach. By computing population doubling times, we were able to identify three growth phases in the stem cell population throughout the whole movie, and validated our result with cell cycle times from single cell tracking.ConclusionsOur method allows fully automated processing and analysis of high-throughput bright field microscopy data. The robustness of cell detection and fast computation time will support the analysis of high-content screening experiments, on-line analysis of time-lapse experiments as well as development of methods to automatically track single-cell genealogies.

Structure of glycoproteins from Acacia gum: An assembly of ring-like glycoproteins modules

The glycoprotein (GP) molecular fraction structure of the gum exudate of Acacia senegal (gum Arabic) isolated from hydrophobic interaction chromatography was investigated using high-performance size exclusion chromatography–multi angle laser light scattering (HPSEC–MALLS), small angle X-ray scattering (SAXS), synchrotron radiation circular dichroism (SRCD) and transmission electron microscopy (TEM) observations. In solution, GP would be a mixture of spheroidal monomers and more anisotropic oligomers as suggested by the two exponent values found in the Rg vs. Mw relationship and TEM observations. The GP conformation probed by SAXS was ascribed to a thin object with a triaxial ellipsoid morphology, certainly attributed to GP oligomers. A 9nm diameter particle was also identified by SAXS in agreement with the dimensions identified by TEM on single isolated ring-like structures. The GP oligomerization process, as probed by TEM, would be the result of ring-like subunits self-association. This self-association would lead to more linear or, sometimes, cyclised assembly. At the molecular level, GP fraction was found to have secondary structures mainly made of β-sheets and turns (64%) but also, to a lesser extent, made of polyproline II (PPII) and α-helices (19%). These features were characteristic of hydroxyprolin-rich glycoproteins with arabinosylated and arabinogalactan polysaccharide side chains grafted to the polypeptide backbone. The GP molecular fraction structure from Acacia gum would be an assembly of ring-like glycoproteins modules. These ring-like structures were certainly due to hydroxyproline (Hyp)–arabinogalactan (AG) subunits.

One-step synthesis of hydrophobic mesoporous silica ellipsoidal particles with a bimodal mesopore system

Highly CH3-functionalized mesoporous silica ellipsoidal particles with bimodal mesopore structure were prepared via a one-step route using polymethylhydrosiloxane (PMHS) and tetraethoxysilane (TEOS) with triblock copolymer P123 as template under acidic conditions. N2 adsorption–desorption, XRD, HRTEM, SEM and 29Si MAS NMR were used to characterize the obtained material. The introduction of PMHS into the synthetic system led to the formation of a bimodal mesopore system consisting of framework mesopores of ∼7.2nm and textural mesopores of ∼29.4nm. The two scale pores were directly observed in HRTEM images and indirectly proved by the two-step increase in N2 adsorption–desorption isotherm. Also, PMHS played an important role in morphology controlling and organic functionalization, ensuring monodisperse ellipsoidal particle morphology and high CH3 functionalization degree of the mesoporous silica product. Subjected to removing highly diluted nonylphenol from aqueous solution, the hydrophobic bimodal mesoporous silica ellipsoidal particles showed high adsorption performance.

Microstructure evolution of nanoprecipitates in half-Heusler TiNiSn alloys

The microstructures of thermoelectric TiNiSn half-Heusler alloys have been studied in detail. For concentration ratios that are slightly rich in Ni, a high density of Heusler-phase nanosized precipitates tended to precipitate within a half-Heusler matrix. The morphology and average size of the Heusler nanoprecipitates were very sensitive to the Ni concentration ratio in the half-Heusler matrix of the alloys. Smaller Heusler nanoprecipitates with coherent ellipsoidal (<5nm) and disc (<10nm wide) morphologies tended to precipitate within the matrices of alloys with slightly elevated Ni concentration ratios (Ti:Ni:Sn=1.0:1.1:1.0). However, much larger coherent discs (<45nm wide and <5nm thick), semicoherent platelets (up to 1μm long and <30nm thick) and spheres (up to 1μm wide) were observed in the matrices of the alloys with larger Ni concentration ratios (Ti:Ni:Sn=1.0:1.2:1.0). Tetragonal structures were observed in the coherent Heusler nanoprecipitates. The formation of such structures was closely associated with the size, morphology and interface coherency of the nanoprecipitates. Moreover, most of the coherent Heusler nanoprecipitates were preferentially oriented parallel to the cubic {001}HH orientations. Interfacial defects between the Heusler and half-Heusler phases, as well as lattice point defects, Ni antisites and vacancies, were found to be closely related to the formation of the Heusler nanoprecipitates. A mechanism has been proposed in this study to describe the coarsening of the Heusler nanoprecipitates via the formation of lattice point defects and interfacial defects.

Rapid preparation of pH-sensitive polymeric nanoparticle with high loading capacity using electrospray for oral drug delivery

Drug loading capacity is an important property for an ideal drug delivery system. However, the drug loading capacity of prepared pH-sensitive polymeric nanoparticles is usually low. To overcome this drawback, the electrospray method was used to prepare Eudragit L 100-55 nanoparticles with high drug loading capacity in one step. Omeprazole was selected as the model drug. The maximum loading capacity of nanoparticles was 43.21% by changing the mass ratio of drug to polymer, and the entrapment efficiency was nearly 100%. The prepared nanoparticle showed spherical or ellipsoidal morphology and the average diameter was about 300nm. The pH-sensitive nanoparticle displayed pH-dependent release in vitro. In addition, a slight cytotoxicity was detected in the cytotoxicity study. The results indicated that electrospray is an easy, rapid and efficient technique for the preparation of high-loading pH-sensitive polymeric nanoparticles, and the pH-sensitive nanoparticle is a promising carrier for oral drug delivery.

Characterisation of precipitates in a Mg–7Gd–5Y–1Nd–0.5Zr alloy aged to peak-ageing plateau

The precipitates in a Mg–7Gd–5Y–1Nd–0.5Zr alloy aged to peak-ageing plateau (aged at 210°C from 18h to 180h) were studied using transmission electron microscopy (TEM), high-resolution TEM (HRTEM) and high-angle annular detector dark-field scanning transmission electron microscopy (HAADF-STEM). Precipitation at the peak-ageing plateau involves the formation of the β′ phase and a new type of plate-shaped phase precipitated along the (0001)α habit plane. The ellipsoid morphology of β′ was illustrated according to [0001]α and [101¯0]α zone axes observations. The orientation relationship between the β′ precipitates and matrix satisfies [001]β′//[0001]α and (100)β′//(112¯0)α, respectively. The TEM and HRTEM results indicate that the β′ precipitates have a base-centred orthorhombic structure with lattice parameters a=0.64nm, b=2.22nm and c=0.52nm. Further, atomic-scaled HAADF-STEM observations suggest a Mg7RE-type and not a Mg15RE-type structure for the β′ phase. The positive thermal stability of the alloy at 210°C ageing is attributed to the coherent relationship with the matrix and the formation of an interlaced network of the β′ precipitates. Aside from the β′ phase, a large amount of precipitate particles were observed to form on the (0001)α habit plane in the peak-aged samples. The new type of precipitates have a plate shape, of approximately 5nm wide along the [101¯0]α direction of the matrix and approximately 5nm long along the [2¯110]α direction. A completely coherent relationship with the matrix can also be observed.

Effect of preparation parameters on the morphologically induced photocatalytic activities of hierarchical zinc oxide nanostructures

Abstract Hierarchical zinc oxide nanostructures were successfully synthesized by facile hydrothermal and sonochemical routes using citrate and PEG as structure directing agents. The effect of precursor concentration and preparation methods on the formation of typical morphology was systematically studied under hydrothermal and sonochemical conditions. Different concentrations of zinc acetate, sodium citrate and NaOH under hydrothermal and sonochemical methods generate different hierarchical structures such as flower-like, cabbage-like, and ellipsoidal ball-like morphologies, depending on the preparation conditions. The as-prepared ZnO samples were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), transmission election microscopy (TEM), photoluminescence (PL) spectroscopy, Fourier transform infrared spectroscopy (FTIR) and particle size distribution (PSD) analysis. Catalytic activities of the as-prepared samples were studied by photodegradation of Methylene blue.

Ethanol assisted reduction and nucleation of ferromagnetic Co and Ni nanocrystalline particles

In this report, we demonstrate the ability of ethanol to act as a solvent and reducing agent to nucleate nanocrystalline Co and Ni particles. Under solvothermal conditions, Co and Ni particles can be produced at 200 °C. The Ni and Co particles crystallized into FCC and a mixture of FCC and HCP crystal phases, respectively. Ni particles possessed a spherical morphology with diameters in the range of 200 nm to 300 nm. Co particles took on an ellipsoidal morphology, with diameters greater than 500 nm. Magnetizations for the Ni and Co particles were commensurate with bulk values, showing their high crystallinity and the presence of little oxide impurity. By finding inexpensive solvents with a lowered environmental impact, steps towards a “greener” synthetic process for ferromagnetic nanoparticles can be established.

The role of surface chemistry-induced cell characteristics on nonviral gene delivery to mouse fibroblasts

BackgroundGene delivery approaches serve as a platform to modify gene expression of a cell population with applications including functional genomics, tissue engineering, and gene therapy. The delivery of exogenous genetic material via nonviral vectors has proven to be less toxic and to cause less of an immune response in comparison to viral vectors, but with decreased efficiency of gene transfer. Attempts have been made to improve nonviral gene transfer efficiency by modifying physicochemical properties of gene delivery vectors as well as developing new delivery techniques. In order to further improve and understand nonviral gene delivery, our approach focuses on the cell-material interface, since materials are known to modulate cell behavior, potentially rendering cells more responsive to nonviral gene transfer. In this study, self-assembled monolayers of alkanethiols on gold were employed as model biomaterial interfaces with varying surface chemistries. NIH/3T3 mouse fibroblasts were seeded on the modified surfaces and transfected using either lipid- or polymer- based complexing agents.ResultsTransfection was increased in cells on charged hydrophilic surfaces presenting carboxylic acid terminal functional groups, while cells on uncharged hydrophobic surfaces presenting methyl terminations demonstrated reduced transfection for both complexing agents. Surface–induced cellular characteristics that were hypothesized to affect nonviral gene transfer were subsequently investigated. Cells on charged hydrophilic surfaces presented higher cell densities, more cell spreading, more cells with ellipsoid morphologies, and increased quantities of focal adhesions and cytoskeleton features within cells, in contrast to cell on uncharged hydrophobic surfaces, and these cell behaviors were subsequently correlated to transfection characteristics.ConclusionsExtracellular influences on nonviral gene delivery were investigated by evaluating the upregulation and downregulation of transgene expression as a function of the cell behaviors induced by changes in the cells’ microenvronments. This study demonstrates that simple surface modifications can lead to changes in the efficiency of nonviral gene delivery. In addition, statistically significant differences in various surface-induced cell characteristics were statistically correlated to transfection trends in fibroblasts using both lipid and polymer mediated DNA delivery approaches. The correlations between the evaluated complexing agents and cell behaviors (cell density, spreading, shape, cytoskeleton, focal adhesions, and viability) suggest that polymer-mediated transfection is correlated to cell morphological traits while lipid-mediated transfection correlates to proliferative characteristics.

A Stepwise “Micellization–Crystallization” Route to Oblate Ellipsoidal, Cylindrical, and Bilayer Micelles with Polyethylene Cores in Water

Micellar polymorphism from block copolymers has been well documented, but most attention has focused on noncrystalline hydrophobic systems. We have investigated the micellization in water of model diblock copolymers with semicrystalline polyethylene (PE) as the core-forming component. Poly(N,N-dimethylacrylamide)–polyethylene (AE) diblock copolymers were synthesized by a combination of anionic and RAFT polymerizations. The bulk nanostructures were probed by small-angle X-ray scattering (SAXS) and AE diblock copolymers were found to be moderately segregated at 140 °C. Dispersions of AE amphiphiles in water were prepared by direct dissolution at 120 °C (i.e., above the melting transition of PE) followed by cooling to 25 °C. By manipulating the composition of AE diblock copolymers, discrete structures with oblate ellipsoidal, cylindrical, and bilayer morphologies were produced, as evidenced in cryogenic transmission electron microscopy (cryo-TEM). The self-assembled aggregates were also studied by small-angle neutron scattering (SANS) and dilute solution rheology. The semicrystalline nature of the nanostructures was further revealed by differential scanning calorimetry (DSC) and wide-angle X-ray scattering (WAXS). A stepwise “micellization–crystallization” process was proposed as the micelle formation mechanism, as supported by the existence of similar nanostructures at 120 °C using SANS. This strategy holds promise for a general protocol toward the production of giant wormlikemore » micelles and vesicles with semicrystalline polymeric cores.« less

Modeling colloid deposition on a protein layer adsorbed to iron-oxide-coated sand

Our recent study reported that conformation change of granule-associated Bovine Serum Albumin (BSA) may influence the role of the protein controlling colloid deposition in porous media (Flynn et al., 2012). The present study conceptualized the observed phenomena with an ellipsoid morphology model, describing BSA as an ellipsoid taking a side-on or end-on conformation on granular surface, and identified the following processes: (1) at low adsorbed concentrations, BSA exhibited a side-on conformation blocking colloid deposition; (2) at high adsorbed concentrations, BSA adapted to an end-on conformation promoted colloid deposition; and (3) colloid deposition on the BSA layer may progressively generate end-on molecules (sites) by conformation change of side-on BSA, resulting in sustained increasing deposition rates. Generally, the protein layer lowered colloid attenuation by the porous medium, suggesting the overall effect of BSA was inhibitory at the experimental time scale. A mathematical model was developed to interpret the ripening curves. Modeling analysis identified the site generation efficiency of colloid as a control on the ripening rate (declining rate in colloid concentrations), and this efficiency was higher for BSA adsorbed from a more dilute BSA solution.

Development of poly(vinyl acetate-methylacrylic acid)/chitosan/Fe3O4 nanoparticles for the diagnosis of non-alcoholic steatohepatitis with magnetic resonance imaging

Non-alcoholic steatohepatitis is a burgeoning health problem. To diagnose NASH with magnetic resonance imaging (MRI), an effective contrast agent, a stable suspension of superparamagnetic Fe(3)O(4) nanoparticles, were newly developed. The negatively charged Fe(3)O(4) nanoparticles were coated with positive chitosan (CS) firstly, and then assembled with poly(vinyl acetate-methylacrylic acid) (P(VAc-MAA)). Transmission electron microscope and dynamic light scattering confirmed that the obtained P(VAc-MAA)/CS/Fe(3)O(4) nanoparticles had a spherical or ellipsoidal morphology with an average diameter in the range of 14-20 nm. The superparamagnetic property and spinel structure of the Fe(3)O(4) nanoparticles were well preserved due to the protection of the P(VAc-MAA)/CS layers on the surface of the Fe(3)O(4) nanoparticles. The in vivo rat experiments confirmed that the P(VAc-MAA)/CS/Fe(3)O(4) nanoparticles were an effective contrast agent for MRI to diagnose NASH.

Macromol. Biosci. 9/2012

Front Cover: Reversible self-assembly of Poly(L-glutamic acid)-b-poly(L-lysine-r-dihydroxyphenyl alanine) at acidic and basic pHs forms an ellipsoidal morphology and vesicles, respectively. Subsequent O2-mediated oxidation of the phenolic groups of the DOPA at pH 12 lead to intermolecular dimerization to stabilize the vesicles via in situ cross-linking. Further details can be found in the article by A. Sulistio, A. Blencowe, J. Wang, G. Bryant, X. Zhang, G. G. Qiao* on page 1220.

Vibrational Investigations of Silver-Doped Hydroxyapatite with Antibacterial Properties

Silver-doped hydroxyapatite (Ag:HAp) was obtained by coprecipitation method. Transmission electron microscopy (TEM), infrared, and Raman analysis confirmed the development of Ag:HAp with good crystal structure. Transmission electron microscopy analysis showed an uniform ellipsoidal morphology with particles from 5 nm to 15 nm. The main vibrational bands characteristic to HAp were identified. The bands assigned to phosphate vibrational group were highlighted in infrared and Raman spectra. The most intense peak Raman spectrum is the narrow band observed at 960 cm−1. In this article Ag:HAp-NPs were also evaluated for their antimicrobial activities againstgram-positive, gram-negative, and fungal strains. The specific antimicrobial activity revealed by the qualitative assay demonstrates that our compounds are interacting differently with the microbial targets.