Shanta Raj Bhattarai

Deposition of gold nanoparticles on electrospun MgTiO3 ceramic nanofibers

A nanocomposite photocatalyst consisting of deposited CdS nanoparticles on TiO2 nanosheets was fabricated by a simple one-pot method. The contact between two phases was maximized by making a composite structure of TiO2 nanosheet decorated with CdS nanoparticles. The composite photocatalyst showed higher photoactivity for hydrogen production from aqueous Na2S/Na2SO3 solution and decomposition of methylene blue under visible light irradiation (lamda > or =420 nm) compared with single component CdS nanoparticles or a physical mixture of CdS nanoparticles and TiO2 nanorods. The intentional formation of nanoscale heterojunctions between two phases appears beneficial for inducing an efficient electron-hole separation.

Aqueous solution properties of amphiphilic triblock copolymer poly(p-dioxanone-co-l-lactide)-block-poly(ethylene glycol)

Abstract A poly(ethylene glycol) (PEG)-based new amphiphilic block copolymer bearing the poly(p-dioxanone-co- l -lactide) (PPDO/PLLA) hydrophobic moieties was prepared. Depending on the copolymer composition and molecular weights, solubility of the polymeric samples in water was varied. Its diluted aqueous solution properties were studied by viscometry, dye solubilization, 1H-NMR and dynamic light scattering. 1,6-Diphenyl-1,3,5-hexatriene solubilization and 1H-NMR spectra carried out in CDCl3 and D2O were used to prove the existence of hydrophobic domains as the core of micelle. Average particle size of 60–165 nm with low polydispersity and lower negative zeta (ξ) potential of −3 to −14 mV were observed on the aqueous copolymer dispersion.

Engineered phage-based therapeutic materials inhibit Chlamydia trachomatis intracellular infection.

Developing materials that are effective against sexually transmitted pathogens such as Chlamydia trachomatis (Ct) and HIV-1 is challenging both in terms of material selection and improving bio-membrane and cellular permeability at desired mucosal sites. Here, we engineered the prokaryotic bacterial virus (M13 phage) carrying two functional peptides, integrin binding peptide (RGD) and a segment of the polymorphic membrane protein D (PmpD) from Ct, as a phage-based material that can ameliorate Ct infection. Ct is a globally prevalent human pathogen for which there are no effective vaccines or microbicides. We show that engineered phage stably express both RGD motifs and Ct peptides and traffic intracellularly and into the lumen of the inclusion in which the organism resides within the host cell. Engineered phage were able to significantly reduce Ct infection in both HeLa and primary endocervical cells compared with Ct infection alone. Polyclonal antibodies raised against PmpD and co-incubated with constructs prior to infection did not alter the course of infection, indicating that PmpD is responsible for the observed decrease in Ct infection. Our results suggest that phage-based design approaches to vector delivery that overcome mucosal cellular barriers may be effective in preventing Ct and other sexually transmitted pathogens.

Stabilization of gold nanoparticles by hydrophobically-modified polycations.

Surface-modified gold nanoparticles have pronounced benefits in the biomedical field due to their significant interaction with delivery materials. In the present study we used hydrophobically-modified polycations (i.e., N-acylated chitosan) to stabilize gold nanoparticles. Aliphatic hydrophobic groups, having carbon chains of different lengths, were first grafted onto the backbone of chitosan by N-acylation with fatty-acid chlorides in order to increase its hydrophobicity. Gold nanoparticles stabilized with native chitosan and N-acylated chitosan were prepared by the graft-onto approach. Chemical modification and its quantification were studied by Fourier-transform infrared (FT-IR) spectroscopy. Further, the stabilized gold nanoparticles were characterized by different physico-chemical techniques such as UV-Vis, FT-IR, TEM, TGA and DLS. Spectral studies of gold nanoparticles show the backbone and the side chain functional groups of chitosan were not cleaved during the conjugation process. TEM observations revealed that the modified chitosan gold nanoparticles were well dispersed and spherical in shape with average size around 10–12 nm in triply-distilled water at pH 7.4, whereas the native chitosan gold nanoparticles appeared as clusters with 9.9 nm as average diameter and were dispersed only in dilute HCl. The size of modified chitosan gold nanoparticles varied depending on the length of grafting molecules.

Amphiphilic triblock copolymer poly(p-dioxanone-co-L-lactide)-block-poly(ethylene glycol), enhancement of gene expression and inhibition of lung metastasis by aerosol delivery.

We describe the development of an aerosol system for topical gene delivery to the lungs of C57BL/6 mice. This system is based on the combination of the commercial cationic lipid Lipofectin with a novel amphiphilic triblock copolymer, poly(p-dioxanone-co-L-lactide)-block-poly(ethylene glycol) (PPDO/PLLA-b-PEG, and abbreviated in the text as polymeric micelles). After optimizing conditions for DNA delivery to the lungs of mice using the combination of polymeric micelles with Lipofectin and LacZ DNA, we used the Lipofectin/polymeric micelle system to deliver the tumor suppressor gene PTEN to the lungs of C57BL/6 mice bearing the B16-F10 melanoma. Lipofectin/PTEN/polymeric micelles significantly improved gene expression of PTEN in the lungs of mice with no evidence of cell toxicity or acute inflammation. Importantly, lung metastasis, as measured by lung weight, was significantly reduced (P<0.001), as were total tumor foci in the lungs (P<0.001) and size of individual tumor nodules in animals treated with Lipofectin/PTEN/polymeric micelles compared with control animals. Survival time was also extended. These results suggest that the Lipofectin/polymeric micelle system is appropriate for enhancing gene delivery in vivo and that it can be applied as a non-invasive gene therapy for lung cancer.

Novel polymeric micelles of amphiphilic triblock copolymer poly (p-dioxanone-co-L-lactide)-block-poly (ethylene glycol).

AbstractPurpose. The objective of this study is to characterize the micelles of novel block copolymer of poly (p-Dioxanone-co-L-Lactide)-block-Poly (ethylene glycol) (PPDO/PLLA-b-PEG-) and evaluate its ability to induce gene transfection. Methods. The ability of the block copolymer to self-assemble was determined by viscometery, dye solublization, NMR spectra and dynamic light scattering. The Trypan blue assay for in vitro biocompatibility of the block copolymer was carried out with NIH 3T3, CT-26 and MCF-7 cells, and β-glactosidase assay was applied to measure the transfection efficiency of the block copolymer on MCF-7 breast cancer cell. Results. Depending on the block lengths and molecular weights, solubility of the polymeric samples in water was varied. Diluted aqueous solution properties of the copolymer were studied. 1,6-Diphenyl-1,3,5-hexatriene solubilization and 1H NMR spectra carried out in CDCl3 and D2O, were used to prove the existence of hydrophobic domains as the core of micelle. Average particle size of 60-165 nm with low polydispersity, and lower negative ξ potential of −3 to −14 mV were observed on the aqueous copolymer dispersion. Copolymer was found with almost no cytotoxic effect and was able to promote the transfection efficiency (about 3-fold) in MCF-7 cells.Conclusions. The PPDO/PLLA-b-PEG copolymer has ability to assemble into nanoscopic structures in aqueous environment, which enable to enhance gene transfection.

pH-Responsive PLGA Nanoparticle for Controlled Payload Delivery of Diclofenac Sodium

Poly(lactic-co-glycolic acid) (PLGA) based nanoparticles have gained increasing attention in delivery applications due to their capability for controlled drug release characteristics, biocompatibility, and tunable mechanical, as well as degradation, properties. However, thorough study is always required while evaluating potential toxicity of the particles from dose dumping, inconsistent release and drug-polymer interactions. In this research, we developed PLGA nanoparticles modified by chitosan (CS), a cationic and pH responsive polysaccharide that bears repetitive amine groups in its backbone. We used a model drug, diclofenac sodium (DS), a nonsteroidal anti-inflammatory drug (NSAID), to study the drug loading and release characteristics. PLGA nanoparticles were synthesized by double-emulsion solvent evaporation technique. The nanoparticles were evaluated based on their particle size, surface charge, entrapment efficacy, and effect of pH in drug release profile. About 390–420 nm of average diameters and uniform morphology of the particles were confirmed by scanning electron microscope (SEM) imaging and dynamic light scattering (DLS) measurement. Chitosan coating over PLGA surface was confirmed by FTIR and DLS. Drug entrapment efficacy was up to 52%. Chitosan coated PLGA showed a pH responsive drug release in in vitro. The release was about 45% more at pH 5.5 than at pH 7.4. The results of our study indicated the development of chitosan coating over PLGA nanoparticle for pH dependent controlled release DS drug for therapeutic applications.

Biodegradable and Bioabsorbable Inorganic Particles in Cancer Nanotechnology

Volume 4 • Issue 3 • 1000170 J Nanomed Nanotechol ISSN: 2157-7439 JNMNT, an open access journal Cancer is the second leading cause of death in the United States after heart disease. A total of 1,660,290 new cancer cases and 580,350 deaths from cancer were estimated to occur in the United States in 2013 [1]. Nanomedicine involves the application of nanotechnology to treatment and detection of this disease [2]. In this context, nanotechnology is almost paronymous with nanoparticles. High surface area to volume ratios associated with nanoparticles, in concert with facile surface functionalization chemistries allows the technology for loading large amounts of cargo including toxic chemotherapeutic drugs, plasmid DNA, and siRNA. For cancer disease, nanoparticles between 10 and 100 nm in size preferably accumulate at tumour sites due to the Enhanced Permeability and Retention (EPR) effect [3,4].

Effect of collector temperature and conductivity on the chain conformation of nylon 6 electrospun nanofibers

Electrospinning is a versatile process used to prepare micro- and nano- sized fibers from various polymer solution. Here, we dealt with the variation in the morphology of nylon 6 electrospun nanofibers and their polymorphism depending on the type and physical state of the collectors. SEM study showed that the fiber diameter was increased from 80 to 103 nm while it was collected in water bath. Similarly the fiber diameter and bonding was increased 103 to 115 nm with the temperature whereas it was linearly decreased 103 to 90 nm with the conductivity of the water bath. Spectroscopic analysis (FT-Raman, FT-IR) showed that the polymorphism of nylon 6 depended on the types of collector (aluminum sheet and water bath). Nylon 6 electrospun nanofibers display theγ-phase while collected in aluminum sheet andα-phase while collection in water bath. The extent of transformation fromγ- toα-phase was linearly increased with temperature and conductivity of the water bath.