In vitro evaluation of growth reticence and anticancer potential of 5α,8α-epidioxy-24ᶓ-methylcholesta-6,22-dien-3ß-ol and ergosta-5,7,22-trien-3ß-ol bioactive isolated from an edible mushroom Lentinus tuberregium (fr.).

The focus point of this current work is to evaluate the anticancer and growth inhibitory efficacy of compounds 5α,8α-epidioxy-24ᶓ-methylcholesta-6,22-dien-3ß-ol (LT1), and Ergosta-5,7,22-trien-3ß-ol (LT2) of Lentinus tuberregium (Fr.) on three cell lines such as A673 (Rhabdomyosarcoma), MCF7 (breast cancer), and HCT116 (colorectal carcinoma) by MTT assay. LT1 and LT2 exerted maximal growth inhibition in the order as A673 > HCT116 > MCF7. Comparatively, LT1 was more potent in causing cell growth inhibition than LT2 in the A673 cancer cell line. Based on the MTT assay, A673 cells alone proceeded further as a model to evaluate the anticancer potential of LT1 and LT2 at three different semilogarithmic concentrations (3, 10, 30 µM). The cells exposed with compounds at 24 and 48 h were analyzed by flow cytometry. Exposure of LT1 at 3 and 10 µM concentrations for 24 h caused a G2-M arrest. At 10 µM concentration, cells also accumulated in the G0-G1 phase, indicating a G1 block. These effects were only transient as prolonged exposure (48 h) of LT1 treatment brought back the cell population to normalcy. Both the compounds only at 30 µM concentration have the potential to induce a hypodiploid peak (sub G0), indicating an induction of apoptosis which was explicit by nuclear condensation and fragmentation of nuclei in cells. The dose-dependent and compound-specific apoptotic induction was further confirmed by caspase activity higher in LT1 than LT2. The results highlight the significant growth inhibitory activity and anticancer potential of LT1 and LT2 which are recommended for further in-depth analysis.

Fungal chitosan based nanocomposites sponges-An alternative medicine for wound dressing.

The porous structured and cell proliferative biodegradable fungal chitosan (FCS) based composites with potential antibacterial property was prepared with Aloe vera extract (ALE) and the plant Cuscuta reflexa mediated biosynthesized silver nanoparticles (CUS-AgNPS) were developed for wound dressing applications by freeze drying method. Fungal chitosan was derived from Cunninghamella elegans a species belongs the family of Zygomycetes. The CUS-AgNPS were characterized by the UV-vis spectrum, XRD and SEM. CUS-AgNPS were loaded into the FCS-ALE sponges and were characterized by UV-vis spectrum, FT-IR and SEM. The nanocomposite sponges (FCS-ALE/CUS-AgNPS) showed prominent results against the different pathogenic bacteria and did not affect the cells were tested in vitro cell viability against human dermal fibroblast cell (HDF cells) which revealed significant cell viability. Based on these observations our composite formulation (FCS/ALE/CUS-AgNPS) could be suggested potential for wound dressing applications.

Comparative studies of chitosan and its nanoparticles for the adsorption efficiency of various dyes.

Chitosan has been considered as a chelating agent with the potential for the adsorption of dyes, metal ions and proteins. This study was aimed to prepare and characterize different fungal chitosan nanoparticles (FCI-1 to FCI-6 NPs) by ionic gelation method and to evaluate its efficacy on the sorption of various commercial dyes. Morphological observations showed that the FCI-1 is nearly spherical in shape with particle size ranging from 2 to 30nm, as determined by electron microscopic studies. Electron micrograph revealed that FCI-1 NPs were stable even after eighteen months of storage at 4°C. Adsorption efficiencies of FCI-1 NPs and FCI-1 were estimated against various dyes such as RBB, MO, DR, NBB and CSB using spectrophotometry. Out of the dyes tested, FCI-1 NPs showed better adsorption efficiency for CSB whereas only RBB followed Langmuir isotherm. The adsorption of remaining dyes may probably be through random adsorption. The results indicated that FCI-1 NPs could be used as efficient sorbents in treating industrial dye effluents.

Cytotoxicity and antimicrobial activities of green synthesized silver nanoparticles.

Bio-inspired silver nanoparticles are synthesized using Malus domestica (apple) extract. Polyphenols present in the apple extract act as a reducing and capping agent to produce the silver nanoparticles. UV-Visible analysis shows the surface plasmon resonance (SPR) absorption at 420 nm. The FTIR analysis was used to identify the functional groups responsible for the bio-reduction of silver ion. The XRD and HRTEM images confirm the formation of silver nanoparticles. The minimal inhibitory concentration (MIC) of silver nanoparticles was recorded against most of the bacteria and fungus. Further, MCF-7 human breast adenocarcinoma cancer cell line was employed to observe the efficacy of cancer cell killing.

Electrochemical, catalytic and antimicrobial activity of N-functionalized tetraazamacrocyclic binuclear nickel(II) complexes.

The five binuclear nickel(II) complexes have been synthesized by the Schiff base condensation of 1,8-[bis(3-formyl-2-hydroxy-5-methyl)benzyl]-l,4,8,11-tetraazacyclo-tetradecane (PC) with appropriate aliphatic diamines and nickel(II) perchlorate. All the five complexes were characterized by elemental and spectral analysis. The electronic spectra of the complexes show three d-d transition in the range of 550-1055 nm due to 3A2g→3T2g(F), 3A2g→3T1g(F) and 3A2g→3T1g(P). These spin allowed electronic transitions are characteristic of an octahedral Ni2+ center. Electrochemical studies of the complexes show two irreversible one electron reduction waves at cathodic region. The reduction potential of the complexes shifts towards anodically upon increasing the chain length of the macrocyclic ring. All the nickel(II) complexes show two irreversible one electron oxidation waves at anodic region. The oxidation potential of the complexes shift towards anodically upon increasing the chain length of the macrocyclic ring. The catalytic activities of the complexes were observed to be increase with increase the macrocyclic ring size. The observed rate constant values for the catalytic hydrolysis of 4-nitrophenyl phosphate are in the range of 5.85×10(-3) to 9.14×10(-3) min(-1). All the complexes were screened for antimicrobial activity.