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High-Performance Thin-Layer Chromatographic Analysis of Eugenol in Developed Nanoemulsion Gel and Nanoparticles: Validation of a Stability-Indicating Method

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
High-performance thin-layer chromatography (HPTLC) method for the quantification of eugenol from nanostructured drug delivery systems was successfully developed and validated. The mobile phase consisted of n-hexane:acetone (7:3, v/v), and the densitometric scanning was performed in the absorbance mode at 280 nm. The method was valid with respect to linearity and range, accuracy, precision, specificity, detection limit (DL), and quantitation limit (QL). The linearity of the method was established by a correlation coefficient value of 0.9930 ± 0.0013. The precision was tested by checking intra-day (repeatability) and inter-day (intermediate precision) variations. The method was established to be precise by low relative standard deviation (RSD) values for different concentration of eugenol. The results of the recovery studies of eugenol from preanalyzed samples demonstrated the accuracy of the method. The specificity of the developed method for the analysis of eugenol in the nanoemulsion gel and nanoparticles samples was confirmed by comparing the spectra obtained in standard and sample analysis. The DL and QL were determined to be 31.41 and 95.17 ng band−1, respectively, for the HPTLC method. The forced degradation studies revealed on eugenol established the effectiveness of the developed and validated method. The developed and validated HPTLC method was found to be a stability-indicating one, as indicated by the results of forced degradation studies, for its use during the accelerated stability studies of the nanoemulsion gels and nanoparticles of eugenol.
Rocznik
Strony
571--582
Opis fizyczny
Bibliogr. 20 poz., rys., tab.
Twórcy
autor
  • Department of Pharmaceutics, Faculty of Pharmacy, Jamia Hamdard, Hamdard Nagar, New Delhi — 110 062, India
autor
  • Department of Pharmacognosy and Phytochemistry, Faculty of Pharmacy, Jamia Hamdard, Hamdard Nagar, New Delhi - 110062, India
autor
  • Department of Pharmacognosy and Phytochemistry, Faculty of Pharmacy, Jamia Hamdard, Hamdard Nagar, New Delhi - 110062, India
autor
  • Department of Pharmacognosy and Phytochemistry, Faculty of Pharmacy, Jamia Hamdard, Hamdard Nagar, New Delhi - 110062, India
autor
  • Department of Pharmacognosy and Phytochemistry, Faculty of Pharmacy, Jamia Hamdard, Hamdard Nagar, New Delhi - 110062, India
autor
  • Department of Pharmacognosy and Phytochemistry, Faculty of Pharmacy, Jamia Hamdard, Hamdard Nagar, New Delhi - 110062, India
autor
  • Department of Pharmaceutics, Faculty of Pharmacy, Jamia Hamdard, Hamdard Nagar, New Delhi — 110 062, India
Bibliografia
  • [1] K. Pramod, S.H. Ansari, and J. Ali, Nat. Prod. Commun., 5, 1999–2006 (2010)
  • [2] L. Levi, G.C. Walker, and L.I. Pugsley, Can. Med. Assoc. J., 91, 781–785 (1964)
  • [3] C.L. Gopu, S. Aher, H. Mehta, A.R. Paradkar, and K.R. Mahadik, Phytochem. Anal., 19, 116–121 (2008)
  • [4] ICH Q1A (R2), Stability Testing of New Drug Substances and Products, 2000
  • [5] P. Alam, J. Gupta, S. Firdouse, A. Firdouse, and J. Afshan, Pharm. Globale, 10, 1–3 (2012)
  • [6] K.C. Patra and K.J. Kumar, J. Planar Chromatogr., 23, 293–297 (2010)
  • [7] S. Shailajan, M. Yeragi, and A. Purohit, Int. J. Pharm. Sci. Rev. Res., 9, 146–151 (2011)
  • [8] S. Anandjiwala, J. Kalola, and M. Rajani, J. AOAC Int., 89, 1467–1474 (2006)
  • [9] J.K. Lalla, P.D. Hamrapurkar, and A. Singh, J. Planar Chromatogr., 20, 135–138 (2007)
  • [10] S.B. Pathak, K. Niranjan, H. Padh, and M. Rajani, Chromatographia, 60, 241–244 (2004)
  • [11] M.L. Rusu, C. Marutoiu, I. Sandu, D. Tita, I. Gogoasa, C. Barbu, and A. Popescu, J. Planar Chromatogr., 20, 139–140 (2007)
  • [12] A. Saraswathy, R. Shakila, and K.N. Sunilkumar, Pharmacogn. J., 2, 211–215 (2010)
  • [13] K. Dhalwal, V.M. Shinde, K.R. Mahadik, and A.G. Namdeo, J. Sep. Sci., 30, 2053–2058 (2007)
  • [14] K. Pramod, S. Shanavas, S.H. Ansari, and J. Ali, Adv. Sci. Lett., 10, 1–13 (2012)
  • [15] C.P. Reis, R.J. Neufeld, A.J. Ribeiro, and F. Veiga, Nanomed.: Nanotechnol. Biol. and Med., 2, 8–21 (2006)
  • [16] K. Pramod, S.H. Ansari, and J. Ali, Adv. Sci. Eng. Med. (2013) (In Press)
  • [17] ICH Q2 (R1), Validation of Analytical Procedures: Text and Methodology, 2005
  • [18] P. Hamrapurkar, P. Patil, M. Phale, M. Gandhi, and S. Pawar, Pharm. Methods, 2, 15–20 (2011)
  • [19] M. Friedman, N. Kozukue, and L.A. Harden, J. Agric. Food Chem., 48, 5702–5709 (2000)
  • [20] M.W. Sabaa and R.R. Mohamed, Polym. Degrad. Stab., 92, 587–595 (2007)
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-785be2f5-97f7-417a-bf70-da8034f417e7
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