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ISSN 2457-9459 (Online)
ISSN-L 0576-9787 (Print)


2023

Journal Citation Reports
Impact factor 2023: 1.3
5-Year Impact Factor: 1.2
Article Influence® Score: 0.140
Ranked 9 out of 23
MATERIALS SCIENCE, PAPER & WOOD (Q2)

Scopus
CiteScore 2023: 2.3
SNIP: 0.405

SCImago
SJR: 0.264
H-Index: 42
Ranked Q3

 

Title
Development and optimization of a QBD-guided RPHPLC method for the quantitative determination of rutin in bulk and lipid-polymer hybrid nanocarriers
Authors
SWATI DEVENDRA RAYSING and ASHISH PRAKASH GORLE

Received August 28, 2025
Published Volume 59 Issue 9-10 October-December
Keywords Quality by Design, rutin, RPHPLC, LPHN, Box Behnken design

Abstract
Quality by Design (QbD) is a structured, scientifically driven methodology aimed at ensuring product quality through well-defined objectives and proactive risk management. In the present work, a reverse-phase high-performance liquid chromatography (RPHPLC) method was developed and optimized following QbD principles for the precise quantification of rutin in its bulk form, as well as in lipid–polymer hybrid nanoparticle (LPHN) formulations. Optimization was guided by Box Behnken design using Design Expert® software, which enabled systematic evaluation of three critical analytical parameters. The developed method demonstrated linearity within a concentration range of 10 50 μg/mL. System suitability testing showed a theoretical plate count of 7033 and a tailing factor of 1.12, both within acceptable analytical limits. High precision was confirmed by relative standard deviation (%RSD) values below 1%, while robustness was maintained with variability restricted to under 2%. The quantitative analysis yielded a rutin recovery rate of 98.78 ± 0.61%, with no interference from nearby eluting peaks. Validation of the method adhered strictly to ITH Q2(R1) guidelines, confirming the method’s suitability across key parameters, such as accuracy, linearity, precision, robustness, and specificity. This QbD-driven development approach provided a clear insight into variable interactions and enabled the creation of a dependable, reproducible, and accurate analytical method well-suited for application in pharmaceutical formulation development and quality control processes.


Link https://doi.org/10.35812/CelluloseChemTechnol.2025.59.90

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