ABSTRACT
Bauhinia foveolata Dalzell is an endemic tree, native to Southwest India (the Western Ghats). 13-Docosenamide wasisolated from ethyl acetate fraction, and quercetin (1), isorhamnetin (2), and odoratin-7-glucoside (3) were isolatedfrom butanol fraction of leaves. A spectroscopic analysis, including mass spectra and Nuclear Magnetic Resonance(NMR), and also comparison with reported data were used to elucidate the chemical structures of isolated compounds.Furthermore, all the isolated compounds were analyzed for 3-(4, 5-dimethylthiazol-2-yl)-5-diphenyltetrazoliumbromide -based cytotoxicity studies on human colon cancer cell lines, HT-29 and HCT-15; among all the testedcompounds, quercetin and odoratin-7-glucoside have shown a good cytotoxicity toward the selected cell lines.
ABSTRACT
The development of resistance by pathogenic microorganisms to synthetic antibiotics encouraged researchers to find novel drugs for the treatment of infectious diseases. This opened new avenues to investigate the antimicrobial efficacy of active extracts/constituents from plant endophytes. In the present study, we have isolated endophytic bacteria (ULB-I, II and III) from green algae Ulva lactuca Linn. and the same bacteria were used for fermentation and extraction. Chloroform and ethyl acetate fractions of ULB-I, II and III were prepared and screened for in-vitro antimicrobial activities and also against Kleibesella pnumoniae infected mice in-vivo. In-vitro anti-microbial activities of ULB-I, II and III were performed against pathogenic bacteria, fungi and Mycobacterium tuberculosis H37 RV strain. From the phylogenetic analysis, the isolated endophytic organisms were identified as Bacillus subtilis JCM strain (ULB-I) and Enterobacter cloacae NBRC strain (ULB-II and III). ULB–I was found to be active against Staphylococcus aureus (1.6µg/ml) and Enterococcus feacalis (0.2µg/ml). The MIC against Staphylococcus aureus and Kleibesella pnumoniae was found to be 0.4µg/ml for ULB-II. A significant anti-fungal activity was observed against Aspergillus flavus (0.2-3.2µg/ml) and Aspergillus niger (0.2-0.4µg/ml). Further, Chloroform fraction of ULB-II and ethyl acetate fraction of ULB-III have shown significant anti-tubercular activity against the tested organism with MIC of 6.25µg/ml. This was supported by in-vivo antimicrobial activity against K. pneumoniae infection in mice and least hemolytic activity against erythrocytes was observed. HPTLC analysis of above fractions further confirmed the presence of polyvalent secondary metabolites.
ABSTRACT
The objective of the present work to prepare Rutin-phospholipid complex (RPC), a phytoformulation and characterization, evaluation for its antidiabetic activity in streptozotocin induced diabetic model. Prepared RPC was characterized and screened for antidiabetic activity by OGTT in normoglycemic and diabetic rats for RT and RPC at different time intervals. Effect of RT and RPC (50 and 100 mg/kg b.w. p.o. respectively) in STZ induced diabetic rats for one day and fifteen days was studied. This is followed by estimation of Estimation of SG, and lipid parameters. Histopathology studies of pancreatic tissue and bioavailability studies of RT & RPC were also carried out. SEM data showed that RPC has irregular size vesicles consisting of phosphatidylcholine. RPC showed a single endothermal peak at 147.68°C in DSC studies. OH group has shifted to lower frequency in phytosome compared to rutin phospholipid in FTIR spectra. Treatment with RPC (50 and 100 mg/kg b.w. p.o.) significantly reduced the blood glucose levels and restored the altered lipid parameters as compared to RT. Histopathological studies revealed that RPC also restored back the size of pancreatic islets and maintained the normal β-cells. A higher serum concentration of RT (13.20 μg/mL) in RPC treated group was observed in bioavailability studies as compared to RT. RPC maintained effective concentration of rutin for a longer period in rat serum.