Quantification of rutin in rats brain by UHPLC/ESI-Q-TOF-MS/MS after intranasal administration of rutin loaded chitosan nanoparticles
dc.contributor.author | Ahmad, Niyaz | |
dc.contributor.author | Ahmad, Rizwan | |
dc.contributor.author | Naqvi, Atta Abbas | |
dc.contributor.author | Alam, Md Aftab | |
dc.contributor.author | Samim, Mohd | |
dc.contributor.author | Iqbal, Zeenat | |
dc.contributor.author | Ahmad, Farhan Jalees | |
dc.date.accessioned | 2016-11-24T15:24:47Z | |
dc.date.available | 2016-11-24T15:24:47Z | |
dc.date.issued | 2016-08-17 | |
dc.description.abstract | 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. | en |
dc.identifier.doi | 10.17179/excli2016-361 | |
dc.identifier.issn | 1611-2156 | |
dc.identifier.uri | http://hdl.handle.net/2003/35624 | |
dc.identifier.uri | http://dx.doi.org/10.17877/DE290R-17665 | |
dc.language.iso | en | |
dc.relation.ispartofseries | EXCLI Journal;Vol. 15, 2016 | en |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | |
dc.subject | Rutin | en |
dc.subject | UHPLC-MS/MS-ESI-Q-TOF | en |
dc.subject | method development and validation | en |
dc.subject | chitosan nanoparticles | en |
dc.subject | brain pharmacokinetic | en |
dc.subject.ddc | 610 | |
dc.title | Quantification of rutin in rats brain by UHPLC/ESI-Q-TOF-MS/MS after intranasal administration of rutin loaded chitosan nanoparticles | en |
dc.type | Text | |
dc.type.publicationtype | article | |
dcterms.accessRights | open access | |
eldorado.dnb.zdberstkatid | 2132560-1 |