Amita Pathak

The potential of celecoxib-loaded hydroxyapatite-chitosan nanocomposite for the treatment of colon cancer

Celecoxib has shown potential anticancer activity against most carcinomas, especially in patients with familial adenomatous polyposis and precancerous disease of the colon. However, serious side effects of celecoxib restrict its generalized use for cancer therapy. In order to resolve these issues and develop an alternative strategy/preliminary approach, chitosan modified hydroxyapatite nanocarriers-mediated celecoxib delivery represents a viable strategy. We characterized the nanoparticle for morphology, particle size, zeta potential, crystalinity, functional group analysis, entrapment efficiency, drug release and hemocompatibility. The effects of celecoxib-loaded nanoparticles on colon cancer cell proliferation, morphology, cytoskeleton, cellular uptake and apoptosis were analysed in vitro. Further, we evaluated the antiproliferative, apoptotic and tumor inhibitory efficacy of celecoxib-loaded nanocarriers in a nude mouse human xenograft model. Nanoparticles exhibited small, narrow hydrodynamic size distributions, hemocompatibility, high entrapment efficiencies and sustained release profiles. In vitro studies showed significant antiproliferation, apoptosis and time-dependent cytoplasmic uptake of celecoxib-loaded Hap-Cht nanoparticles in HCT 15 and HT 29 colon cancer cells. Additional in vivo studies demonstrated significantly greater inhibition of tumor growth following treatment with this modified nanoparticle system. The present study indicates a promising, effective and safe means of using celecoxib, and potentially other therapeutic agents for colon cancer therapy.

Synthesis of biocompatible multicolor luminescent carbon dots for bioimaging applications

Abstract Water-soluble carbon dots (C-dots) were prepared through microwave-assisted pyrolysis of an aqueous solution of dextrin in the presence of sulfuric acid. The C-dots produced showed multicolor luminescence in the entire visible range, without adding any surface-passivating agent. X-ray diffraction and Fourier transform infrared spectroscopy studies revealed the graphitic nature of the carbon and the presence of hydrophilic groups on the surface, respectively. The formation of uniformly distributed C-dots and their luminescent properties were, respectively, revealed from transmission electron microscopy and confocal laser scanning microscopy. The biocompatible nature of C-dots was confirmed by a cytotoxicity assay on MDA-MB-468 cells and their cellular uptake was assessed through a localization study.

Photoresponsive coumarin-tethered multifunctional magnetic nanoparticles for release of anticancer drug

Recently, photoresponsive nanoparticles have received significant attention because of their ability to provide spatial and temporal control over the drug release. In the present work, we report for the first time photoresponsive multifunctional magnetic nanoparticles (MNPs) fabricated using coumarin-based phototrigger and Fe/Si MNPs for controlled delivery of anticancer drug chlorambucil. Further, newly fabricated photoresponsive multifunctional MNPs were also explored for cell luminescence imaging. In vitro biological studies revealed that coumarin tethered Fe/Si MNPs of ~9 nm size efficiently delivered the anticancer drug chlorambucil into cancer cells and thereby improving the drug action to kill the cancer cells upon irradiation. Such multifunctional MNPs with strong fluorescence, good biocompatibility and efficient photocontrolled drug release ability will be of great benefit in the construction of light-activated multifunctional nano drug delivery systems.

A new chemical route for the preparation of fine ferrite powders

Precursors to MFe2O4 [spinels ferrites; where M = Ni(II), Co(II) and Zn(II)] have been prepared by the evaporation of polyvinyl alcohol added mixed metal nitratesolution, in presence and absence of urea. Theprecursor materials have low ignition temperature and are spontaneously combustible at low temperatures (250°C to 400°C). The heat liberated through the process is sufficient for the crystallization of the desired ferrite phase. The urea added process resulted in finer, superparamagnetic particles (12–17 nm) compared to the process without urea (particle size 25–30 nm). The ultrafine ferrite powders obtained have been characterized by X-ray powder diffraction (XRD), thermal gravimetry (TG), differential scanning calorimetry (DSC), infrared spectroscopy (IR), transmission electron microscopy (TEM) and room temperature magnetic measurement studies.

Low temperature preparation of nanocrystalline solid solution of strontium barium niobate by chemical process

Abstract Nanocrystalline powders of strontium–barium–niobate (SBN) with the composition Sr x Ba 1− x Nb 2 O 6 (with x =0.4, 0.5 and 0.6) have been prepared using a single step chemical synthesis process starting from a precursor solution constituting of triethanolamine (TEA), niobium–tartarate and EDTA complexes of strontium and barium ions. The complete dehydration of the TEA-soluble metal ion complex precursor solution through heating yield in a fluffy, carbonaceous precursor material, which on heat-treatment at 750 °C/2 h resulted in the single phase SBN powders. The precursor and heat-treated powders have been characterized by thermal analysis and X-ray diffraction (XRD) studies. The crystallite size and average particle size as measured from X-ray broadening and transmission electron microscope were found to be 15 and 20 nm, respectively.

Effect of functionalized magnetic MnFe2O4 nanoparticles on fibrillation of human serum albumin.

Pathogenesis of amyloid-related diseases is related to nonnative folding of proteins with the formation of insoluble deposits in the extracellular space of various tissues. Having the unique properties of small size, large surface area, biodegradability, and relative nontoxicity, magnetic nanoparticles have drawn a lot of attention in biomedical applications. Herein, we demonstrate the effect of bare and differently functionalized magnetic MnFe2O4 nanoparticles on fibrillation of human serum albumin in vitro. The process has been monitored using Thioflavin T fluorescence, Congo red binding assay, circular dichroism, fluorescence microscopy, and transmission electron microscopy. From our experimental results, amine functionalized MnFe2O4 nanoparticles are found to inhibit formation of fibrils more effectively than bare ones, while carboxylated nanoparticles do not have a significant effect on fibrillation. This study has explored the prospects of using specific magnetic nanoparticles with appropriate modification to control self-assembly of proteins and may act as a precursor in therapeutic applications.

Novel ZnO hollow-nanocarriers containing paclitaxel targeting folate-receptors in a malignant pH-microenvironment for effective monitoring and promoting breast tumor regression

Low pH in the tumor micromilieu is a recognized pathological feature of cancer. This attribute of cancerous cells has been targeted herein for the controlled release of chemotherapeutics at the tumour site, while sparing healthy tissues. To this end, pH-sensitive, hollow ZnO-nanocarriers loaded with paclitaxel were synthesized and their efficacy studied in breast cancer in vitro and in vivo. The nanocarriers were surface functionalized with folate using click-chemistry to improve targeted uptake by the malignant cells that over-express folate-receptors. The nanocarriers released ~75% of the paclitaxel payload within six hours in acidic pH, which was accompanied by switching of fluorescence from blue to green and a 10-fold increase in the fluorescence intensity. The fluorescence-switching phenomenon is due to structural collapse of the nanocarriers in the endolysosome. Energy dispersion X-ray mapping and whole animal fluorescent imaging studies were carried out to show that combined pH and folate-receptor targeting reduces off-target accumulation of the nanocarriers. Further, a dual cell-specific and pH-sensitive nanocarrier greatly improved the efficacy of paclitaxel to regress subcutaneous tumors in vivo. These nanocarriers could improve chemotherapy tolerance and increase anti-tumor efficacy, while also providing a novel diagnostic read-out through fluorescent switching that is proportional to drug release in malignant tissues.

A new co-precipitation technique for the preparation of mixed-oxides

Fine ceramic oxide powders of the composition MN2O4 [Spinels; where M = Ni(II), Zn(II), Co(II), Cd(II) and N = Fe(III), Cr(III)], M3Fe5O12 [Garnets; where M = Y, Gd] and RBa2Cu3O7+σ [Ceramic superconductors; where R = rare earths] have been synthesized through a novel coprecipitation technique. The novelty of this route lies in its simplicity and cost effectiveness. The coprecipitation has been done using a mixture of (NH4)2CO3(NH4)HCO3, triethylamine and formaline in presence of soluble polymers, like polyvinyl alcohol (PVA). The final product formation is confirmed and characterized by X-ray diffraction (XRD) and energy dispersive X-ray spectroscopy (EDX).

Shape dependent peroxidase mimetic activity towards oxidation of pyrogallol by H2O2

Truncated octahedron shaped magnetite nanoparticles have been prepared via a chemical method and subsequently their shape dependent peroxidase mimetic activity has been verified using pyrogallol substrate. Their peroxidase mimetic activity has been found to be superior to that of spherical-shaped nanoparticles.

Inhibition of fibrillation of human serum albumin through interaction with chitosan-based biocompatible silver nanoparticles

To understand the pharmacokinetics of administered nanomaterials, it is essential to examine the stability and biological activity of proteins by investigating the physicochemical characteristics of the protein–nanoparticle bioconjugate. In this work, the mechanistic detail of the interaction between human serum albumin (HSA) and silver nanoparticles synthesized using nontoxic and biodegradable chitosan as a reducing and stabilizing agent, have been investigated at the nanobio interface. A combination of spectroscopic, calorimetric, and microscopic techniques have been employed to monitor the interaction process. The results illustrate that the chitosan-mediated silver nanoparticles spontaneously bind to HSA without appreciable conformational changes of the protein. Furthermore the potential of the nanoparticles to inhibit the formation of HSA amyloid-like fibrils, in vitro, has been analyzed using thioflavin T fluorescence, circular dichroism, fluorescence microscopy, and transmission electron microscopy. The experimental observations indicate that interactions between HSA and chitosan-based silver nanoparticles have led to appreciable reduction in amyloid fibril formation. Additionally, cytotoxicity and hemolytic assays are performed to ensure the biocompatibility of the nanoparticles within the application limit.