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21.
22.
Simultaneous estimation of levodopa,carbidopa and 3‐oxymethyldopa in rat plasma using HPLC‐ECD
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Prashant P. Raut Shrikant Y. Charde Pradeep Bishnoi 《Biomedical chromatography : BMC》2016,30(10):1696-1700
The aim of study was to develop a suitable analytical method for simultaneous estimation of levodopa, carbidopa and 3‐O‐methyl dopa in rat plasma. Chromatographic separation of plasma samples was achieved using a reverse‐phase C18 column. The mobile phase used consisted of a mixture of methanol and phosphate buffer (10 mM , pH 3.50) in the ratio of 90:10 v/v. All analytes were estimated by electrochemical detection at +800 mV. The developed method has been validated as per the standard guidelines. Precision study results were found to be satisfactory, with percentage relative standard deviation for repeatability and intermediate precision <3.96 and 6.56%, respectively, for all analytes detected in rat plasma. The developed method in rat plasma was found to be simple, rapid, accurate, precise and specific. The proposed method has been successfully applied for analysis of rat plasma samples obtained during an oral pharmacokinetic study of sustained release pellets of levodopa and carbidopa in rats. Copyright © 2016 John Wiley & Sons, Ltd. 相似文献
23.
Shrinivas S. Kottawar Shaphi A. Siddiqui Shrikant S. Pendalwar Wamanrao N. Jadhav Sudhakar R. Bhusare 《Research on Chemical Intermediates》2014,40(8):2929-2934
The molecular iodine-catalyzed direct coupling of indoles with 1,3-dicarbonyl compounds is described. This new method for C–C bond formation allows high functional group tolerance, regioselectivity, and scope under mild conditions. 相似文献
24.
The aqueous polymerization of methyl methacrylate initiated by the redox system K2S2O8-ascorbic acid has been studied at 35°C under the influence of oxygen. The rate of polymerization increases with increasing ascorbic acid concentration at low activator concentration, remains constant within the range 4.375 × 10?3 to 11.25 × 10?3 mole/liter, and at higher ascorbic acid concentration again decreases. The rate varies linearly with monomer concentration. The initial rate and the limiting conversion increase with increasing polymerization temperature. Organic solvents (water-miscible only) and small amounts of neutral salts like KC1 and Na2SO4 depress the initial rate and the maximum conversion. The addition of small amounts of salts like Cu2+ and Mn2+ increases the initial rate, but no appreciable increase in the limiting conversion is observed. 相似文献
25.
Soni A. Singh Shilpi Kabiraj Reena P. Khandare Shrikant P. Nalawade Kiran B. Upar 《合成通讯》2013,43(1):74-80
Amberlyst-15 (H+) resin catalyzes efficient cationic endo-cyclization of γ- and δ-unsaturated alcohols to yield tetrahydro-(2 H)-pyrans and oxepanes. The merits of the present protocol are good yield of the products under mild conditions, simple workup, and reusability of the resin. 相似文献
26.
Shrikant B. Kulkarni Richard M. Rodebaugh Norman H. Cromwell 《Journal of heterocyclic chemistry》1976,13(2):329-332
A number of 1-alkyl-2-carbomethoxyazetidines have been prepared from the reaction of primary amines with α,γ-dibromoearbonyl compounds. A series of base catalyzed reactions performed on selected cis, trans-1-alkyl-2-carbomethoxy-4-alkyl(aryl)azetidines reveal the cis isomer to be of greater thermodynamic stability. Furthermore, base catalyzed deuterium exchange studies suggest this to be the case. 相似文献
27.
Miniaturized electrochemiluminescence (ECL) systems are widely recognized as a highly detection, user-friendly, and turnkey strategy to develop point-of-care-testing devices. The ECL sensing approach provides numerous advantages over other methods, including high signal-to-noise ratio and measurement with minimal or no background signal. The ECL signal can be easily controlled by a small external potential while providing high sensitivity and decreased electrode fouling, resulting in the use of ECL-based miniaturized systems for detection and monitoring of different analytes, including DNA and bacteria. In this work, different types of miniaturized ECL systems with various fabrication techniques are reviewed and their application in point-of-care-testing is thoroughly discussed. Furthermore, such ECL platforms have been summarized based on the type of the ECL mechanism, electrodes, range of detection, and limit of detection. Finally, some of the upcoming technological interventions to make such a miniaturized ECL platform amenable for portable and on-field analysis have been discussed. 相似文献
28.
Shrikant A. Mohitkar 《Journal of solid state chemistry》2011,184(4):735-740
Nine new A2Mo4Sb2O18 (A=Ce, Pr, Eu, Tb, Ho, Er, Tm, Yb, Lu) compounds have been synthesized by solid-state reactions. They are isostructural with six reported analogues of yttrium and other lanthanides and the monoclinic unit cell parameters of all fifteen of them vary linearly with the size of A3+ ion. Single crystal X-ray structures of eight A2Mo4Sb2O18 (A=Ce, Pr, Eu, Gd, Tb, Ho, Er, Tm) compounds have been determined. Neat A2Mo4Sb2O18 (A=Pr, Sm, Eu, Tb, Dy, Ho, Er, Tm) compounds exhibit characteristic rare earth metal photoluminescence. 相似文献
29.
Shrikant B. Kanawade Shivaraj P. Patil Prashant S. Nikam Sachin A. Gangurde Madhukar N. Jachak Raghunath B. Toche 《Journal of heterocyclic chemistry》2012,49(2):363-369
o‐Aminothiophene dicarbonitrile 1 on neat reaction with cyclic ketones in anhydrous ZnCl2 yielded mixture of fused aminopyridine 3 and iminospirooxazine 4 derivatives. Similarly, pyrimidine derivatives 5 and 8 were obtained by the reaction of this intermediate 1 with formic acid and DMF‐DMA followed by hydrazine hydrate, respectively. The reaction of o‐amino‐thiophene dicarboxamide 2 at ambient temperature with cyclic ketones yielded spiropyrimidine 10 as a sole product in quantitative yield. The regioselective anellated pyrimidine 9 , 11 , and dihydropyrimidine 12 derivatives were also obtained by the reaction with aromatic aldehydes in presence of piperidine and iodine respectively. J. Heterocyclic Chem., (2012). 相似文献