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

被引:2
作者
Vijayaraj, Surendran [1 ]
Palei, Narahari N. [2 ]
Archana, Devalapalli [1 ]
Lathasri, Kuppam [2 ]
Rajavel, Ponnusamy [1 ]
机构
[1] Sree Vidyanikethan Coll Pharm, Dept Pharmaceut Anal, Tirupati, Andhra Pradesh, India
[2] Sree Vidyanikethan Coll Pharm, Dept Pharmaceut, Tirupati, Andhra Pradesh, India
关键词
Rutin; Chitosan; sodium aliginate; nanoparticles; RP-HPLC; central composite design; QbD; OPTIMIZATION; QUERCETIN;
D O I
10.1590/s2175-97902020000318793
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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 mu g/mL and 0.15 mu g/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.
引用
收藏
页数:14
相关论文
共 50 条
  • [41] Development and validation of RP-HPLC method for estimation of brexpiprazole in its bulk and tablet dosage form using Quality by Design approach
    Amol S. Jagdale
    Nilesh S. Pendbhaje
    Rupali V. Nirmal
    Poonam M. Bachhav
    Dayandeo B. Sumbre
    Future Journal of Pharmaceutical Sciences, 7
  • [42] Development and validation of RP-HPLC method for estimation of brexpiprazole in its bulk and tablet dosage form using Quality by Design approach
    Jagdale, Amol S.
    Pendbhaje, Nilesh S.
    Nirmal, Rupali V.
    Bachhav, Poonam M.
    Sumbre, Dayandeo B.
    FUTURE JOURNAL OF PHARMACEUTICAL SCIENCES, 2021, 7 (01)
  • [43] Stability Indicating Assay for the Determination of Bilastine in Bulk Drug and Method Development Validation by RP-HPLC Using Analytical Quality by Design Approaches
    Nayak, Anjali
    Alwin, R. Maria Danish
    Sangeetha, G.
    Sowmya, C. Y.
    Reddy, Yashwanth V.
    Dang, Raman
    INDIAN JOURNAL OF PHARMACEUTICAL EDUCATION AND RESEARCH, 2024, 58 (02) : s582 - s590
  • [44] The Novel Quality by Design Concept in the Development and Validation of a Stability-Indicating RP-HPLC PDA Method for Estimating Terlipressin in an Injectable Dosage Form
    Salva, Charumathi
    Galla, Rajitha
    CHROMATOGRAPHIA, 2024, 87 (09) : 567 - 579
  • [45] Quality by design (QbD) approach to develop fast-dissolving tablets using melt-dispersion paired with surface-adsorption method: formulation and pharmacokinetics of flurbiprofen melt-dispersion granules
    Vemula, Sateesh Kumar
    Daravath, Bhaskar
    Repka, Michael
    DRUG DELIVERY AND TRANSLATIONAL RESEARCH, 2023, 13 (12) : 3204 - 3222
  • [46] The Novel Quality by Design Concept in the Development and Validation of a Stability-Indicating RP-HPLC PDA Method for Estimating Terlipressin in an Injectable Dosage Form
    Salva, Charumathi
    Galla, Rajitha
    CHROMATOGRAPHIA, 2024, 87 (09) : 567 - 579
  • [47] Comprehensive stability-indicating method development of Avanafil Phosphodiesterase type 5 inhibitor using advanced Quality-by-Design approach
    Patel, Mital
    Kothari, Charmy
    JOURNAL OF ANALYTICAL SCIENCE AND TECHNOLOGY, 2020, 11 (01)
  • [48] Development and validation of an eco-friendly, stability-indicating UV spectroscopic method for trigonelline analysis in nanoformulation using quality by design approach
    Umarani, Adarsh C.
    Patil, Akshay K.
    Karadesai, Manikant B.
    Mandi, Praneeth N.
    Patil, Sneha B.
    Jalalpure, Sunil S.
    ANALYTICAL CHEMISTRY LETTERS, 2025, 15 (01) : 103 - 118
  • [49] Development and validation of a stability-indicating ultra-high-performance liquid chromatography method for the estimation of ibrutinib and trace-level quantification of related substances using quality-by-design approach
    Prasad, Shishir Kumar
    Kalpana, Divekar
    BIOMEDICAL CHROMATOGRAPHY, 2024, 38 (03)
  • [50] Application of a Quality by Design-based approach in development and validation of an RP-HPLC method for simultaneous estimation of methotrexate and mangiferin in dual drug-loaded liposomes
    Adin, Syeda Nashvia
    Gupta, Isha
    Aqil, Mohd.
    Mujeeb, Mohd.
    Najmi, Abul Kalam
    BIOMEDICAL CHROMATOGRAPHY, 2023, 37 (08)