Comparative assessment of extraction methods and quantitative estimation of luteolin in the leaves of Vitex negundo Linn. by HPLC

AbstractObjectiveTo find out the ideal organic solvent and extraction technique for the isolation of luteolin from the leaves of Vitex negundo Linn. (V. negundo) by quantitative estimation of luteolin through high performance liquid chromatography (HPLC) method.MethodsThe leaves of V. negundo were identified by a botanist, cleaned, dried under shade and powdered. Maceration, reflux, Soxhlet and ultrasound assisted extraction techniques were used for the extraction of luteolin from the leaves by using four different solvents of varying polarity such as methanol, ethanol, chloroform, and dichloromethane. A simple HPLC method was used to determine the quantity of luteolin in each sample extract.ResultsThe calibration plot of standard luteolin showed a linear relationship in the concentration range of 100-500 μg/mL with a correlation coefficient, r2 of 0.998. The methanolic extract was found to contain highest amount of luteolin and among various techniques employed for extraction and isolation of luteolin, reflux technique was observed to be the most efficient.ConclusionBased on the HPLC results, it can be concluded that reflux technique using methanol is better than the other extraction techniques and should be preferred for the extraction and isolation of luteolin from V. negundo leaves extract in research labs or industries

Microwave-assisted green synthesis and antimicrobial activity of silver nanoparticles derived from a supercritical carbon dioxide extract of the fresh aerial parts of Phyllanthus niruri L

Purpose: To synthesize and evaluate the antimicrobial activity of silver nanoparticles (AgNPs) derived from a supercritical carbon dioxide extract of the fresh aerial parts of Phyllanthus niruri. Methods: The synthesis of AgNPs of a P. niruri extract was carried out in a microwave oven. The extraction was carried out using a supercritical fluid extractor. The AgNPs were characterized by the Ultraviolet-visible (UV-vis) spectral analysis, Dynamic Light Scattering (DLS) zetasizer analysis, Transmission electron microscopy (TEM), X-ray diffraction (XRD) analysis and Fourier transform infrared (FT-IR) spectroscopy. The antimicrobial assays of AgNPs were carried out against different bacterial and fungal strains. Results: Results of various analytical techniques confirmed the synthesis of AgNPs of a P. niruri extract. The UV–vis spectroscopy showed an intense silver surface plasmon resonance band at 415 NM. The AgNPs had a mean size of 110 nm in the Zetasizer analysis. TEM images illustrated spherical AgNPs having a mean particle size of 110 nm. The X-ray diffractograms showed peaks at 38.17°, 44.28°, and 64.52°. The average crystallite size of Ag-NPs was found to be 110 nm. FT-IR spectra confirmed the stability of the AgNPs. The AgNPs demonstrated good antimicrobial effects against several tested pathogenic microbes. Conclusion: An efficiently synthesized AgNPs of P. niruri (SC-CO2) extract has been prepared by a simple, eco-friendly, cost-effective, rapid green chemistry methodology. The AgNPs of P. niruri extract possesses significant antimicrobial properties against the tested bacterial and fungal strains. Keywords: Nanoparticles, Phyllanthus niruri, Supercritical fluid extraction, Microwave, Antimicrobial activit

Quantitative Analysis of Total Phenolic, Flavonoid Contents and HPTLC Fingerprinting for Standardization of Glycyrrhiza glabra Linn. Roots

The Glycyrrhiza glabra Linn is an important medicinal plant and its roots are commonly used in various indigenous system of medicine to cure many acute and chronic diseases. The current study was designed to quantify total phenolic, flavonoid contents in G. glabra Linn roots to evaluate the antioxidant potential and to carry out the pharmacognostical investigations along with HPTLC fingerprinting in order to develop the quality control parameters for the standardization of this important medicinal plant. A variety of pharmacognostical investigations e.g., extractive values, total ash, water soluble ash, and acid insoluble ash, moisture content, loss on drying, pH and phytochemical screening of G. glabra Linn roots were analyzed as per the standard methods. The content of total phenolics, flavonoids, pesticide residues, aflatoxin and heavy metals were also determined as per the reported methods. The HPTLC fingerprinting of methanolic extract of the G. glabra roots was also carried out using CAMAG-HPTLC system. The results of phytochemicals investigations revealed the presence of carbohydrates, phenolic compounds, flavonoids, alkaloids, proteins, saponins, lipids, sterols and tannins in various solvent extracts. Total phenolic and flavonoid contents in methanolic extract were found to be 7.47 mg/gm and 2.25 µg/gm, respectively. Heavy metals concentrations were found to be under the standard limits. Aflatoxins and pesticides residues were not detected in the extract. The standard parameters established through this study may prove important tools for authentication, identification, purification and standardization of G. glabra Linn roots in herbal pharmaceutical industries

Quantification of rutin in rats brain by UHPLC/ESI-Q-TOF-MS/MS after intranasal administration of rutin loaded chitosan nanoparticles

Rutin (RT), an antioxidant drug, has been utilized to treat cerebral ischemia hence a sensitive quantification method for estimation of RT in brain homogenate is necessary to develop. This study aims to prepare RT loaded Chitosan Nanoparticles (RT-CS-NPs) develop and validate ultra-high performance liquid chromatography-electrospray ionization-synapt mass spectrometric method Synapt Mass Spectrometry (Synapt MS) (UHPLC/ESI-QTOF-MS/MS) for quantification of RT in brain homogenate from Wistar rat. The process of chromatographic separation was carried out on Waters ACQUITY UPLC™ with the components of separation in detail as; column: BEH C-18 with dimension as 2.1 mm×100 mm and particle size 1.7 µm, mobile phase: acetonitrile (85 % v/v/v): 2 mM ammonium formate (15 % v/v/v): formic acid (0.1 % v/v/v) and flow rate: 0.25 mL/min. Liquid-liquid extraction method (LLE), in mixture, i.e. ethyl acetate:acetonitrile, was considered to optimize the recovery of analyte from the brain homogenate of Wistar rat. Over a total run time of 5 minutes, the elution time for RT and internal standard (IS), i.e. Tolbutamide, observed was 2.67 and 2.82 min respectively whereas the transition observed for RT and IS was at m/z 611.1023/303.1071 and 271.1263/155.1073, respectively. Results, regarding various processes and parameters studied for RT as summarized, established a linear dynamic range over a concentration range of 1.00 ng/mL - 1000.0 ng/mL with r2; 0.9991±0.0010. Accuracy for intra and inter-assay in terms of % CV revealed a range of 0.45- 2.11 whereas lower limit of detection (LOD) and quantitation (LOQ) observed was 0.09 ng/mL and 0.142 ng/mL, respectively. The analyte stability as well as method specificity and accuracy, i.e. recovery > 86 %, supports the idea for application of current developed method in order to quantify and evaluate the RT-loaded-CS-NPs for RT determination in brain homogenate after intranasal drug delivery

Effects of Nigella sativa and Lepidium sativum on Cyclosporine Pharmacokinetics

The present study was conducted to investigate the effects of Nigella sativa and Lepidium sativum on the pharmacokinetics of cyclosporine in rabbits. Two groups of animals were treated separately with Nigella sativa (200 mg/kg p.o.) or Lepidium sativum (150 mg/kg p.o.) for eight consecutive days. On the 8th day, cyclosporine (30 mg/kg p.o.) was administered to each group one hour after herbal treatment. Blood samples were withdrawn at different time intervals (0.0, 0.5, 1.0, 1.5, 2.0, 3.0, 4.0, 6.0, 8.0, 12, and 24 hrs) from marginal ear vein. Cyclosporine was analyzed using UPLC/MS method. The coadministration of Nigella sativa significantly decreased the max and AUC 0−∞ of cyclosporine; the change was observed by 35.5% and 55.9%, respectively ( ≤ 0.05). Lepidium sativum did not produce any significant change in max of cyclosporine, although its absorption was significantly delayed compared with control group. A remarkable change was observed in max and AUC 0− of Lepidium sativum treated group. Our findings suggest that concurrent consumption of Nigella sativa and Lepidium sativum could alter the pharmacokinetics of cyclosporine at various levels

Effect of Garden Cress Seeds Powder and Its Alcoholic Extract on the Metabolic Activity of CYP2D6 and CYP3A4

The powder and alcoholic extract of dried seeds of garden cress were investigated for their effect on metabolic activity of CYP2D6 and CYP3A4 enzymes. In vitro and clinical studies were conducted on human liver microsomes and healthy human subjects, respectively. Dextromethorphan was used as a common marker for measuring metabolic activity of CYP2D6 and CYP3A4 enzymes. In in vitro studies, microsomes were incubated with NADPH in presence and absence of different concentrations of seeds extract. Clinical investigations were performed in two phases. In phase I, six healthy female volunteers were administered a single dose of dextromethorphan and in phase II volunteers were treated with seeds powder for seven days and dextromethorphan was administered with last dose. The O-demethylated and N-demethylated metabolites of dextromethorphan were measured as dextrorphan (DOR) and 3-methoxymorphinan (3-MM), respectively. Observations suggested that garden cress inhibits the formation of DOR and 3-MM metabolites. This inhibition of metabolite level was attributed to the inhibition of CYP2D6 and CYP3A4 activity. Garden cress decreases the level of DOR and 3-MM in urine and significantly increases the urinary metabolic ratio of DEX/DOR and DEX/3-MM. The findings suggested that garden cress seeds powder and ethanolic extract have the potential to interact with CYP2D6 and CYP3A4 substrates

Study of Ground Water Behaviour in the Tons Pump Canal Command Area of Karchhana Tehsil, Prayagaraj

The study of groundwater behaviour in the Tons Pump canal command area of Karchhana Tehsil was carried out by utilizing ground water table data from 1997 to 2021 (25 years). During the study period, the pre-monsoon water table depth ranged from 3.25 m to 19.55 m, whereas the post-monsoon depth ranged from 1.71 m to 17.70 m. The water table trend in the study area during the pre-monsoon season revealed that at 83.55% of the locations having falling trend, while the remaining 16.45% experienced neither rising nor falling trend in the water table. During post-monsoon season, the water table was falling at 89.99% locations, with the rest 10.10% having neither rising nor falling trend. Therefore, the study found that the majority of the study area was experiencing water table fall due to over-exploitation of ground water in the both pre and post-monsoon season. Development stages of the groundwater utilization study from 1997 to 2021 showed that during the year 1997, all block of the study area was found under safe category.The overall utilisation of groundwater development stage was determined to be 44.93%. In 2021, the overall development stage of groundwater utilization was found to be 64.11% and the entire study area comes under safe category of groundwater utilization. It was found that groundwater levels in the study area were progressively rising. Therefore, it was necessary to enhance the surface water supply through canal systems to reduce the draft of groundwater as well as artificial groundwater recharge is necessary to arrest the groundwater at the desired level in the study area

Sustainable Development: A Cosmetics or a Substance to India

 This Paper will investigate about the India’s perspective on sustainable development is it a Cosmetic development that is only going on social media’s, banners, and speeches or is it a real substance that changes life of people around in INDIA. Paper will also investigate what impact sustainable development did from past 20 years by Different schemes of Government did the policy, schemes really bring change in the life of not economically well section in INDIA and how much Government is spending on these schemes ? This question will be the key for this paper.  </p