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A V R Reddy

Publications and source records attributed to A V R Reddy.

9 recordsLinked to original sources
PubMed2006

Development and applications of the k0-based internal mono standard INAA method.

The k0-based internal monostandard instrumental neutron activation analysis (IM-INAA) method, developed and standardized in our laboratory, is capable of analyzing both small and large samples of different sizes and shapes. Use of in-situ relative efficiency makes the method geometry independent. In this paper, we present the development of this methodology and applications to two types of alloys namely, stainless steel and brass. A stainless steel certified reference material, BCS 466 was also analyzed to evaluate the accuracy of the method. Absolute concentrations in these alloys were arrived by a standard-less method. The method has also been applied for the analysis of large-size wheat samples (0.45-1 kg) and the results were compared with the data obtained for selected elements in sub-samples (50-1000 mg).

Journal Article↗
PubMed2006

Evaluation of the antioxidant activity of wheatgrass (Triticum aestivum L.) as a function of growth under different conditions.

The antioxidant activity of wheatgrass, which is consumed as a dietary supplement, was estimated at different levels. The methods employed include FRAP (ferric reducing antioxidant power), ABTS (2,2'-azobis-3-ethylbenzthiazoline-6-sulfonic acid) and DPPH (1,1'-diphenyl-2-picrylhydrazyl) assays. Aqueous and ethanol extracts of wheatgrass grown under different conditions over a period of 6, 7, 8, 10 and 15 days were used. Lipid peroxidation and oxygen radical absorbance capacity (ORAC) were determined and utilized to check the potency of a few selected extracts. Different conditions used for growth were (1) tap water, (2) tap water with nutrients, (3) soil and tap water, and (4) soil with nutrients. For comparison, a commercially available wheatgrass tablet was analysed. To explain the reasons behind the observed differences, the total phenolic and flavonoid contents of the extracts were measured. These contents increased with growth under all the conditions. The ethanol extracts were found to have a higher phenolic and flavonoid content than the aqueous extracts. The highest FRAP values occurred on day 15 of growth under condition 4, the values being 0.463 and 0.573 mmol of ascorbic acid and Trolox equivalents/100 g fresh wheatgrass for aqueous and ethanol extracts, respectively. In the aqueous extracts no specific trend was observed with the DPPH assay for the different conditions nor for the growth period. In the case of ethanol extracts, however, it increased with the growth period and the wheatgrass grown in condition 4 was found to be the most effective. These extracts were also found to inhibit significantly ascorbate-Fe2+ induced lipid peroxidation in rat liver mitochondria. The ORAC values of aqueous and ethanol extracts of day 10 with condition 4 were found to be 39.9 and 48.2, respectively, being higher than those reported for many natural extracts or vegetables.

Animals↗
PubMed2006

Bhasmas: unique ayurvedic metallic-herbal preparations, chemical characterization.

Bhasmas are unique Ayurvedic metallic preparations with herbal juices/fruits, known in the Indian subcontinent since the seventh century BC and widely recommended for treatment of a variety of chronic ailments. Twenty bhasmas based on calcium, iron, zinc, mercury, silver, potassium, arsenic, copper, tin, and gemstones were analyzed for up to 18 elements by instrumental neutron activation analysis, including their C, H, N, and S contents. In addition to the major constituent element found at % level, several other essential elements such as Na, K, Ca, Mg, V, Mn, Fe, Cu, and Zn have also been found in microg/g amounts and ultratrace (ng/g) amounts of Au and Co. These seem to remain chelated with organic ligands derived from medicinal herbs. The bhasmas are biologically produced nanoparticles and are taken along with milk, butter, honey, or ghee (a preparation from milk); thus, this makes these elements easily assimilable, eliminating their harmful effects and enhancing their biocompatibility. Siddha Makaradhwaja, a mercury preparation is found to be stoichiometrically HgS without any traces of any other element. Similarly, Swet Parpati is stoichiometrically KNO3 but is found to have Mn, Cu, Zn, Na, P, and Cl as well. An attempt has been made to correlate the metallic contents with their medicinal importance. Na and K, the two electrolytic elements, seem to be well correlated, although K/Na varies in a wide range from 0.06 to 95, with specifically low values for Ca-, Fe-, and Zn-based bhasmas. K/P also varies in a wide range from 0.23 to 12, although for most bhasmas (n = 12), it is 2.3 +/- 1.2. Further, Fe/Mn is linearly correlated (r = 0.96) with Fe in nine noniron bhasmas.

Calcium↗
PubMed2004

Analysis of essential elements in Pragya-peya--a herbal drink and its constituents by neutron activation.

Ayurvedic herbal formulations are a good source of several nutrient elements essential for metabolic processes. Pragya-peya, a herbal drink and its 12 herbal constituents have been analyzed for 7 minor (Al, Ca, Cl, Mg, Na, K, P) and 15 trace (Ba, Br, Co, Cr, Cs, Fe, Hg, La, Mn, Rb, Sc, Se, Th, V, Zn) elements by instrumental neutron activation analysis (INAA). The method involves thermal neutron irradiation in a reactor followed by counting at several intervals. Also Cd, Cu, Ni and Pb contents were determined by atomic absorption spectrometry (AAS). Elemental data were validated by simultaneously analysing reference materials (RMs) such as mixed Polish herbs (INCT-MPH-2) and peach leaves (SRM-1547). Sample homogeneity was tested by analysing samples from three different batches collected at different intervals. Pragya-peya has been found to be especially rich in several nutrient elements such as Ca, K, V, Fe, Mn, Se and Zn whereas no single constituent is enriched in all the nutrient elements. Concentrations of elements are discussed vis-a-vis their medicinal/therapeutic uses. Several elements such as Na, K, P, Ca, Fe, Co, and Zn seem to be well correlated in 12 constituent herbs.

Beverages↗
PubMed2003

Development of an internal monostandard instrumental neutron activation analysis method based on in situ detection efficiency for analysis of large and nonstandard geometry samples.

A k0-based internal monostandard instrumental neutron activation analysis method for determination of relative elemental concentration in samples of large size and irregular geometry has been developed. In this method, one of the elements present in the sample is used as comparator. A priori knowledge of the concentration of one of the constituents is required to convert the relative concentration into absolute values. The problems of gamma-ray self-attenuation and geometrical effects that arise in the assay of large and nonstandard geometry samples were overcome by an in situ relative detection efficiency calibration procedure, which requires one or more activation products emitting gamma-rays over a wide range of the spectrum. To minimize the problem of neutron flux perturbations that may arise in large samples, irradiations were carried out using a thermal column with thermal neutron component of more than 99.9%. The method has been standardized with samples of silica (approximately 0.5 kg) and water (0.5 L) spiked with known amounts of different elements and has been advantageously applied to some alloy and metal samples of irregular geometry, where complete compositional characterization was carried out using mass balance. This approach is highly valuable for analysis of large, irregularly shaped samples if not too high demands are set to the degree of accuracy.

Journal Article↗
PubMed2002

Selective preconcentration and determination of chromium(VI) using a flat sheet polymer inclusion sorbent: potential application for Cr(VI) determination in real samples.

A method for sorption preconcentration of Cr(VI) from aqueous samples was developed using a polymer inclusion sorbent (PIS). The PIS used in this method was prepared by physical inclusion of Aliquat-336 in the matrix formed by cellulose triacetate and 2-nitrophenyl octyl ether. This sorbent was found to be stable, cost-effective, efficient for preconcentration of Cr(VI) present in the aqueous samples, and amenable to direct quantitative analysis of Cr(VI) held in it by neutron activation analysis and spectrophotometry. The quantifying of Cr(VI) in PIS by spectrophotometry was carried out by developing color directly on the PIS after reacting it with 1,5-diphenylcarbazide. The distinct color developed on the PIS even at very low concentrations of Cr(VI) suggests its possible use for field determination of Cr(VI). The composition of PIS was optimized to obtain maximum uptake of Cr(VI) without sacrificing uniformity in terms of thickness and distribution of ion-exchange sites, stability, and time required for quantitative sorption of Cr(VI) from aqueous samples. The Cr(VI) species held in the PIS, mainly HCrO4- and CrO4(2-), were found to vary as a function of pH of the aqueous samples from which Cr(VI) was preconcentrated. A close agreement was found in the abundances of Cr(VI) species held in the PIS with those reported in the literature for aqueous solutions at different pH. The variation of Cr(VI) species as a function of pH was found to have a significant impact on the tolerance to anions on the uptake of Cr(VI) in the PIS. The high selectivity of PIS toward Cr(VI) from aqueous solution at pH = 2 was explained on the basis of hydration of anions. The uptake of Cr(VI) was found to be fairly constant (88 +/- 3%) up to nearly complete exchange of counterions present in the PIS. The method developed in the present work was successfully used for the preconcentration of Cr(VI) from tap water and seawater samples containing low levels of Cr(VI).

Anion Exchange Resins↗
PubMed2002

Validation of a neutron activation analysis method using k0-standardization.

A neutron activation analysis method using k0-standardization has been adopted for multielement analysis using our research reactors. Gold has been used as the comparator. The input parameters, used for calculation of elemental concentration, such as subcadmium to epithermal neutron flux ratio (f), the epithermal neutron flux shape factor (alpha), and the absolute efficiency of the detector (epsilon) have been determined. The values of k0-factors and Q0 (the ratio of resonance integral to thermal neutron cross section) have been taken from the literature. The validity of applying this method in our laboratory is evaluated by analyzing the elemental concentrations with respect to the certified values in eight reference materials of different origin obtained from USGS, IAEA and NIST. The percent deviation of the measured elemental concentrations are found to be within +/- 15% to that of the certified values whereas the percent relative standard deviation ranged from 2% to 10% for most of the elements analyzed.

Journal Article↗
PubMed2002

Heavy metal concentration and distribution in a dated sediment core of Nainital Lake in the Himalayan region.

The concentrations and distribution of the elements, including heavy metals such as As, Ba, Br, Co, Cr, Cs, Fe, Ga, K, Mn, Na, Rb, Sc, Sr, Th and Zn, were investigated in dated sediment cores of Nainital Lake located in the Himalayan region, in Uttar Pradesh state of India, which is considered as a remote background area. The concentrations of the elements were measured by instrumental neutron activation analysis using the k0 method. The International Atomic Energy Agency certified reference material SL-3 was used to evaluate the accuracy of the method. The normalized data for a series of elements were used to understand the source of loading. Elements like Br, Co, Cr, Fe, K, Mn and Zn show a negative correlation with increasing depth whereas elements like As, Ba, Cs, Na and Rb show a positive correlation with increasing depth. By considering the concentration for the bottom segments of the core as close to the baseline concentration, recent flux values for different elements were calculated. An increase in the flux value was observed for Br, Cr, Fe, K, Mn and Zn, which can be attributed to anthropogenic contribution in recent years.

Environmental Monitoring↗