Cu Nanoparticle-Based Solution and Paper Strips for Colorimetric and Visual Detection of Heavy Metal Ions.

The intrinsic toxicity of heavy metal ions to human health or other species calls for the need to develop an analytical tool for the easy and rapid detection of these ions based on inexpensive and stable nanomaterials. This article describes the potential utility of stable Cu nanoparticles (CuNPs) in the detection of toxic metal ions by solution and paper strip-based methods. For this, first, a dodecyl sulfate ion-stabilized CuNP (DS-CuNP) colloid was synthesized by a chemical reduction method. This was followed by treating the dispersion with heavy metal ions and monitoring the spectral change by spectrophotometric and colorimetric techniques. Among a host of metal ions, Hg2+, Cd2+, and Pb2+ have been found to significantly affect the surface plasmon resonance band of CuNPs by concomitantly altering the color of its solution. Notably, the brownish color of CuNP solution changed readily to milky white in the presence of Hg2+. Furthermore, the fabricated brownish-yellow test paper strips containing DS-CuNPs transformed to a prominent white color in the presence of a few drops of Hg2+ solution. This change in color of the paper strips could be visually detected by the naked eye. The experiments involving the detection of the various ions were carried out by optimizing the experimental conditions qualitatively as well as quantitatively. The limit of detection of the analytes (metal ions) has been found to be 10 µM. Routine analytical techniques like UV-vis spectroscopy, dynamic light scattering, transmission electron microscopy, and Fourier transform infrared spectroscopy formed part of the experiments.

An Anti-inflammatory Fe3 O4 -Porphyrin Nanohybrid Capable of Apoptosis through Upregulation of p21 Kinase Inhibitor Having Immunoprotective Properties under Anticancer PDT Conditions.

We report the influence of Fe3 O4 nanoparticles (NPs) on porphyrins in the development of photosensitizers (PSs) for efficient photodynamic therapy (PDT) and possible post-PDT responses for inflicting cancer cell death. Except for Au, most metal-based nanomaterials are unsuitable for clinical applications. The US Food and Drug Administration and other agencies have approved Feraheme and a few other iron oxide NPs for clinical use, paving the way for novel biocompatible immunoprotective superparamagnetic iron oxide nanohybrids to be developed as nanotherapeutics. A water-soluble nanohybrid, referred to here as E-NP, comprising superparamagnetic Fe3 O4 NPs functionalised with tripyridyl porphyrin PS was introduced through a rigid 4-carboxyphenyl linker. As a PDT agent, the efficacy of E-NP toward the AGS cancer cell line showed enhanced photosensitising ability as determined through in vitro photobiological assays. The cellular uptake of E-NPs by AGS cells led to apoptosis by upregulating ROS through cell-cycle arrest and loss of mitochondrial membrane potential. The subcellular localisation of the PSs in mitochondria stimulated apoptosis through upregulation of p21, a proliferation inhibitor capable of preventing tumour development. Under both PDT and non-PDT conditions, this nanohybrid can act as an anti-inflammatory agent by decreasing the production of NO and superoxide ions in murine macrophages, thus minimising collateral damage to healthy cells.

Zein film functionalized with gold nanoparticles and the factors affecting its mechanical properties.

In this article, we report a simple method to synthesize biodegradable zein films functionalized with gold nanoparticles (AuNPs) with significantly improved mechanical properties, as an environmentally benign substitute to biologically hazardous polymers. Zein-coated AuNPs were synthesized using the zein protein as a reducing agent and characterized with IR, UV, CD, ζ-potential, and TEM measurements. The zein protein interaction with the negatively charged surface of AuNPs provides excellent strength to the zein thin film. For the first time, FT-IR spectral studies suggested the strong interaction between AuNPs and zein protein, which was further supported by the higher binding constant (K b) value. The films were characterized for mechanical properties with spectroscopic and physical experimental investigations. The surface morphology of AuNP-doped zein film was explored by AFM and SEM, which suggested that the AuNPs prevent the buckling of zein film and increase the strength as well as flexibility of the film.

Protein-Based Multifunctional Nanocarriers for Imaging, Photothermal Therapy, and Anticancer Drug Delivery.

We report a simple approach for fabricating plasmonic and magneto-luminescent multifunctional nanocarriers (MFNCs) by assembling gold nanorods, iron oxide nanoparticles, and gold nanoclusters within BSA nanoparticles. The MFNCs showed self-tracking capability through single- and two-photon imaging, and the potential for magnetic targeting in vitro. Appreciable T2-relaxivity exhibited by the MFNCs indicated favorable conditions for magnetic resonance imaging. In addition to successful plasmonic-photothermal therapy of cancer cells (HeLa) in vitro, the MFNCs demonstrated efficient loading and delivery of doxorubicin to HeLa cells leading to significant cell death. The present MFNCs with their multimodal imaging and therapeutic capabilities could be eminent candidates for cancer theranostics.

Nanocrystalline p-hydroxyacetanilide (paracetamol) and gold core-shell structure as a model drug deliverable organic-inorganic hybrid nanostructure.

We report on the generation of core-shell nanoparticles (NPs) having an organic nanocrystal (NC) core coated with an inorganic metallic shell, being dispersed in aqueous medium. First, NCs of p-hydroxyacetanilide (pHA)--known also as paracetamol--were generated in an aqueous medium. Transmission electron microscopy (TEM) and powder X-ray diffraction (XRD) evidenced the formation of pHA NCs and of their crystalline nature. The NCs were then coated with Au to form pHA@Au core-shell NPs, where the thickness of the Au shell was on the order of nanometers. The formation of Au nanoshell--surrounding pHA NC--was confirmed from its surface plasmon resonance (SPR) band in the UV/Vis spectrum and by TEM measurements. Further, on treatment of the core-shell particles with a solution comprising NaCl and HCl (pH < 3), the Au shell could be dissolved, subsequently releasing pHA molecules. The dissolution of Au shell was marked by a gradual diminishing of its SPR band, while the release of pHA molecules in the solution was confirmed from TEM and FTIR studies. The findings suggest that the core-shell NP could be hypothesized to be a model for encapsulating drug molecules, in their crystalline forms, for slow as well as targeted release.

Plasmonic signatures in the composite crystals of gold nanoparticles and p-hydroxyacetanilide (paracetamol).

A new type of inorganic nanoparticle-organic hybrid crystalline material consisting of gold nanoparticles (Au NPs) and p-hydroxyacetanilide (pHA) is reported. The composite crystals were on the order of several millimeters in dimensions. They could be grown from a solution of Au NPs and pHA at 35 °C. The optical properties of the crystals not only reflected the presence of Au NPs but also their degree of association inside the crystals. Single crystal X-ray diffraction data indicated that the crystal motifs were those of pHA. Transmission electron microscopic images indicated Au NPs being dispersed randomly in the crystal with increase in their density when crystallized in the presence of low concentration of pHA. FTIR measurements indicated attachment of -NH group to the NPs. Optical microscopic investigation revealed the presence of Au NP crystals, the color of which represented their density, being red at low concentration of NPs and purple at their high concentration.