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shivani R pandya
    Magnetic nanoparticle accumulated dendrimers (MADs) have been prepared using a 1 : 1 ratio of MNPs and trimesoyl 1,3,5-trimethyl malonate ester (TTDMM), a 1st tier dendrimer, in ethanolic medium at 100 °C on refluxing for 24 h. The MADs... more
    Magnetic nanoparticle accumulated dendrimers (MADs) have been prepared using a 1 : 1 ratio of MNPs and trimesoyl 1,3,5-trimethyl malonate ester (TTDMM), a 1st tier dendrimer, in ethanolic medium at 100 °C on refluxing for 24 h. The MADs formed were characterized for their structural, functional and morphological properties using XRD, VSM, FTIR, SEM-EDX, TEM and DLS techniques. The MNPs show superparamagnetic character which moderates the structural ability of TTDMM to bind silibinin (SB) and methotrexate (MTX) anticancer drugs for their potential use in drug delivery systems. In this context, the MADs have shown higher silibinin and methotrexate binding activities compared to those of the dendrimer only, which are confirmed through FTIR, DLS and SEM-EDX. An UV-Vis spectrophotometry study shows 32.65% and 53.03% in vitro release of SB and MTX respectively at 10 h, in PBS with a 10% DMSO (PD) medium at 37 °C. Furthermore, chemosensitivity testing of MAD was carried out on a human lung...
    Correction for ‘Physicochemical interaction of cerium oxide nanoparticles with simulated biofluids, hemoglobin, insulin, and ds-DNA at 310.15 K’ by Rajlakshmi Chetty et al., New J. Chem., 2020, 44, 1825–1845, DOI: 10.1039/C9NJ04155A.
    Abstract Nowadays smart and multifunctional materials with unique optical and several other physicochemical properties have pooled up potential to contribute with various applications in science and technological development. We have... more
    Abstract Nowadays smart and multifunctional materials with unique optical and several other physicochemical properties have pooled up potential to contribute with various applications in science and technological development. We have initiated a new innovative research work for synthesis of lanthanide nanocomposite by developing certain stoichiometric functional combinations of proteins and lanthanides as per energy distribution and Boltzmann partition functions which are based on capping, binding or occupying surface areas by adsorption on generating suitable Vander Waals and London dispersive forces as functional materials matrix. This work aims to synthesize a novel Albumen-CeO2 Biofunctional nanocomposite (BFNC) and further study its potential antioxidant properties. In our work, 25µM to 150 µM CeO2NP with 150µM Albumen Physicochemical interaction was carried out to understand the optical behavior and aggregation. The result shows maximum interaction with 1:1 150µM CeO2NP: Albumen confirmed through UV-Vis spectrophotometer. The CeO2-Albumen BFNC was synthesized by facile eco-friendly ex-situ methodology with hydrodynamic diameter of 110.6 nm confirmed by Dynamic light scattering (DLS). The BFNC were characterized by UV-Vis spectrophotometer, FT-IR and DLS. The bare CeO2 NP and synthesized BFNC were tested for Antioxidant property by using 2, 2-Diphenyl-1-picrylhydrazyl (DPPH•). Thus BFNC shows 48.92% scavenging activity compared to that of 22.71% scavenging activity of bare CeO2NP. Thus the present research work shows that the design of such lanthanide based BFNC which exhibit unusual optical and surface functionalized biological properties could induce suitable biomedical properties for the host matrix, which can be used for the development of new inorganic or organic hybrid matrix systems.
    Interaction study in cerium oxide nanoparticles with biofluids and biomolecules via physicochemical, spectroscopic and in silico analytical approaches, showing conformational change.
    Abstract Biofunctionalized magnetic nanoparticles (FMNPs) were synthesized through in situ coprecipitations of Fe (II) and Fe (III) salts under air followed by the addition of amino acids (AA): serine (Ser), alanine (Ala), cysteine (Cys),... more
    Abstract Biofunctionalized magnetic nanoparticles (FMNPs) were synthesized through in situ coprecipitations of Fe (II) and Fe (III) salts under air followed by the addition of amino acids (AA): serine (Ser), alanine (Ala), cysteine (Cys), histidine (His), and methionine (Met) via bottom-up approach without following any sophisticated route. However, the effect of amino acid side chain on the formation of γ-Fe2O3 (maghemite) and Fe3O4 (magnetite) was attained through XRD, HR-TEM, SEM, VSM, FTIR, DLS and Mercury Porosimeter (MP). Surprisingly, our study depicts that except His; Ser, Ala, Cys and Met produced more than 50% of magnetite phase and inhibited the oxidation of Fe3O4 in the presence of air. Furthermore, AA@MNPs were used for in vitro biological assessment such as salmon testes DNA (ST-DNA) binding efficiency, DPPH scavenging activity, antimicrobial and anticancer properties using UV–visible spectrophotometry and colorimeter respectively. The ST-DNA binding efficiency was observed at λmax 259 nm and quantitative interaction was determined using 15–125 µM AA@MNPs and 500 µg/ml DNA at physiological temperature, shows stacking interaction. The Cys@MNPs have exhibited highest DPPH scavenging activity with SC50 2.5 µg/mL at λmax 525 nm. Antimicrobial property of AA@MNPs was studied on gram-positive (B. subtilis), gram-negative (E. coli) bacteria and fungi (C. albicans) using disc diffusion assay by measuring zone of inhibition (ZOI) in mm, mentioned as a diameter. Alongside, minimum inhibition concentration (MIC) was estimated by the dilution method for those strains sensitive against AA@MNPs. Although, AA@MNPs showed ∼100% control growth of human lung cancer cell line (A549) with LC50, TGI and GI50 >80 µg/ml shown cells compatibility. These significant results revealed the impact of AA side chain with different surface activities of FMNPs.
    Synthesis of Magnetic nanoparticles were made using coprecipitation method on mixing Fe+3 and Fe+2 in 2:1 ratio with aqueous 8M NaOH which on heating at 90°C for 2 h has yielded 85% magnetic (Fe3O4) nanoparticles (MNPs), characterized by... more
    Synthesis of Magnetic nanoparticles were made using coprecipitation method on mixing Fe+3 and Fe+2 in 2:1 ratio with aqueous 8M NaOH which on heating at 90°C for 2 h has yielded 85% magnetic (Fe3O4) nanoparticles (MNPs), characterized by XRD, VSM, SEM, and HR-TEM. The formic acid (FA), oxalic acid (OA) and citric acid (CA), the series of aliphatic organic acids along with Trimesoyl 1, 3, 5 tridimethyl malonate (TTDMM), trimesoyl 1, 3, 5 tridiethyl malonate (TTDEM), trimesoyl 1, 3, 5 tridipropyl malonate (TTDPM), trimesoyl 1, 3, 5 tridibutyl malonate (TTDBM) and trimesoyl 1, 3, 5 tridihexyl malonate (TTDHM) 1st tier dendrimers were used separately for preparing nanomagnetic fluid. From 25 to 150 µM MNPs at an interval of 25 µM were dispersed in 150 µM of acids and dendrimers separately with DMSO. UV-VIS spectrophotometry showed a maximum MNPs dispersion with TTDMM against others and found to be most stable nanomagnetic fluid on account of capping type mechanism of acids.
    Developing new smart materials and tracking their structural potential have been in focus for curing disease and other applications such as catalyzing biomolecules like proteins and selective bioremediation of toxic metals, dyes,... more
    Developing new smart materials and tracking their structural potential have been in focus for curing disease and other
    applications such as catalyzing biomolecules like proteins and selective bioremediation of toxic metals, dyes, pesticides have
    been thrust areas of research in the field of materials and biomaterials sciences. Since materials are most important need of the
    society which develops somewhere food, drug, fuel, protective cover, defense materials, fire resistant and acoustic mechanism,
    UV sensitive, UV absorbing, solar radiation trapping activities. In this context, the dendrimers have been considered as ideal
    and smart materials to be applied for wider applications and directly, indirectly or catalyze modulator and many others. Thus,
    the dendrimers act as smart materials and the synthesis of such architectural and potential molecules is being considered as a
    new thrust area for multitasking materials with better activities to catalyze chemical and biochemical processes. The
    multifunctional materials of multipurpose uses with several dendrimeric branching, having innumerable binding sites and are in
    high demands for their drug binding, loading potential and bio coatings.
    Research Interests:
    Magnetic nanoparticle accumulated dendrimers (MADs) have been prepared using a 1 : 1 ratio of MNPs and trimesoyl 1,3,5-trimethyl malonate ester (TTDMM), a 1 st tier dendrimer, in ethanolic medium at 100 C on refluxing for 24 h. The MADs... more
    Magnetic nanoparticle accumulated dendrimers (MADs) have been prepared using a 1 : 1 ratio of MNPs and trimesoyl 1,3,5-trimethyl malonate ester (TTDMM), a 1 st tier dendrimer, in ethanolic medium at 100 C on refluxing for 24 h. The MADs formed were characterized for their structural, functional and morphological properties using XRD, VSM, FTIR, SEM-EDX, TEM and DLS techniques. The MNPs show superparamagnetic character which moderates the structural ability of TTDMM to bind silibinin (SB) and methotrexate (MTX) anticancer drugs for their potential use in drug delivery systems. In this context, the MADs have shown higher silibinin and methotrexate binding activities compared to those of the dendrimer only, which are confirmed through FTIR, DLS and SEM-EDX. An UV-Vis spectrophotometry study shows 32.65% and 53.03% in vitro release of SB and MTX respectively at 10 h, in PBS with a 10% DMSO (PD) medium at 37 C. Furthermore, chemosensitivity testing of MAD was carried out on a human lung cancer cell line (A549) using a sulforhodamine B (SRB) assay. The test showed that the newly developed drug delivery system for SB and MTX inhibits the growth of A549 human lung cancer cells by 13.9% and 44.3% respectively with 80 mg mL À1 of the total complex. The results of our study have provided new insight for developing MADs as a potential carrier for anticancer drugs with a controlled and sustained release tendency.
    Research Interests:
    Overexposure of TiO2 NPs has raised concerns over safety. This study focuses on stability and DNA binding activity of TiO2 NPs in water and cell culture growth media RPMI-1640 at physiological temperature. Borosil Mansingh Survismeter was... more
    Overexposure of TiO2 NPs has raised concerns over safety. This study focuses on stability and DNA binding activity of TiO2 NPs in water and cell culture growth media RPMI-1640 at physiological temperature. Borosil Mansingh Survismeter was used to assess dispersion and physicochemical properties. Values of density, viscosity, surface tension, particle size, friccohesity and activation energy were calculated for a range of TiO2 NP concentrations (25 μM/L to 125 μM/L). The results demonstrate higher limiting density and viscosity in culture media than water, suggesting a stronger association of TiO2 NPs in growth media. Interaction of TiO2 NPs with human genomic DNA was analyzed by UV–visible spectroscopy and fluorescence spectroscopy. UV–visible spectroscopy showed hyperchromic effect due to strong stacking interactions between human genomic DNA and TiO2 NPs. Fluorescence spectral characteristics revealed that with increasing concentrations of TiO2 NPs bound to DNA, there was a marked decrease in fluorescence spectra which indicates interaction of TiO2 NP with human genomic DNA. Understanding structural and physicochemical properties of TiO2 NPs and their interaction with human genomic DNA will be important for in vitro genotoxicity studies as stability of nano form in media is a major concern.
    Research Interests:
    Coprecipitation of Fe + (III) and Fe + (II) out of FeCl 3 and FeSO 4 ·7H O sources in 2:1 ratio with aqueous 8 MNaOH on heating at 90 °C for 2 h has yielded 85% magnetic (Fe 3 O 4 2 ) nanoparticles (MNPs), and has been characterized by... more
    Coprecipitation of Fe
    +
    (III) and Fe
    +
    (II) out of FeCl
    3
    and FeSO
    4
    ·7H
    O sources in 2:1 ratio with aqueous 8 MNaOH
    on heating at 90 °C for 2 h has yielded 85% magnetic (Fe
    3
    O
    4
    2
    ) nanoparticles (MNPs), and has been characterized
    by XRD, FTIR and SEM. Their surface area and pore size distribution are found 0.075 m
    2
    /g and 3588.82 nmrespectively determined with a Mercury Porosimeter. Formic acid (FA), oxalic acid (OA) and citric acid (CA), the serieof aliphatic organic acids along with trimesoyl 1,3,5-tridimethyl malonate (TTDMM), trimesoyl 1,3,5-tridiethyl
    malonate (TTDEM), trimesoyl 1,3,5-tridipropyl malonate (TTDPM), trimesoyl 1,3,5-tridibutyl malonate
    (TTDBM) and trimesoyl 1,3,5-tridihexyl malonate (TTDHM) 1st tier dendrimers separately were used for MNdispersion. From 25 to 150 μMMNPsatanintervalof25μM were dispersed in 150 μM of acids and dendrimerseparately with DMSO. UV–vis spectrophotometry showed a maximum MNP dispersion with TTDMM thaothers. The acids had resulted a lower absorbance with lower MNP dispersion in DMSO.
    Research Interests: