Quality by design (Qbd) approach to develop stability indicating HPLC method for estimation of rutin in chitosan-sodium alginate nanoparticles

Rutin is a flavonoid glycoside, mainly consists of phenolic compounds, responsible for many biological activities. The objective of the present study was to develop and validate a precise, simple, robust, rapid and reliable reverse phase high -performance liquid chromatography (RP-HPLC) technique by...

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Main Authors: Surendran Vijayaraj (Author), Narahari N Palei (Author), Devalapalli Archana (Author), Kuppam Lathasri (Author), Ponnusamy Rajavel (Author)
Format: Book
Published: Universidade de São Paulo, 2021-04-01T00:00:00Z.
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100 1 0 |a Surendran Vijayaraj  |e author 
700 1 0 |a Narahari N Palei  |e author 
700 1 0 |a Devalapalli Archana  |e author 
700 1 0 |a Kuppam Lathasri  |e author 
700 1 0 |a Ponnusamy Rajavel  |e author 
245 0 0 |a Quality by design (Qbd) approach to develop stability indicating HPLC method for estimation of rutin in chitosan-sodium alginate nanoparticles 
260 |b Universidade de São Paulo,   |c 2021-04-01T00:00:00Z. 
500 |a 2175-9790 
500 |a 10.1590/s2175-97902020000318793 
520 |a Rutin is a flavonoid glycoside, mainly consists of phenolic compounds, responsible for many biological activities. The objective of the present study was to develop and validate a precise, simple, robust, rapid and reliable reverse phase high -performance liquid chromatography (RP-HPLC) technique by using Qbd approach for evaluating the rutin in nanoparticles. Central composite design (CCD) was employed for optimizing the experimental conditions of RP-HPLC method. Buffer pH, methanol content in the mobile phase composition, flow rate, and wavelength were selected as independent variables whereas retention time, peak area, and asymmetry factor was selected as dependent variables. The retention time, peak area and asymmetric factor of rutin by using optimized independent variables were found to be 3.75 min, 1014.79 mV, and 1.26 respectively. The limit of detection and limit of quantitation values were found to be 0.005 µg/mL and 0.15 µg/mL respectively. For confirming linearity, accuracy, precision, and robustness, the optimized assay condition was validated as per ICH guidelines. The proposed method, which was optimized by QbD approach was found to be a suitable method for analyzing the rutin in chitosan-sodium alginate nanoparticles. 
546 |a EN 
690 |a Rutin 
690 |a Chitosan 
690 |a sodium aliginate 
690 |a nanoparticles 
690 |a RP-HPLC 
690 |a central composite design 
690 |a QbD 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Brazilian Journal of Pharmaceutical Sciences, Vol 56 (2021) 
787 0 |n http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1984-82502020000100632&tlng=en 
787 0 |n https://doaj.org/toc/2175-9790 
856 4 1 |u https://doaj.org/article/cc67cb9dc47b4a48a2717dd3c37e7ded  |z Connect to this object online.