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Pharmacokinetics study of a supersaturatable self-microemulsifying drug delivery system for ellagic acid by UHPLC-Q-TOF-MS Cover

Pharmacokinetics study of a supersaturatable self-microemulsifying drug delivery system for ellagic acid by UHPLC-Q-TOF-MS

Open Access
|Apr 2021

References

  1. 1. G. Quan, B. Niu, V. Singh, Y. Zhou, C. Wu, X. Pan and C. Wu, Supersaturable solid self-microemulsifying drug delivery system: precipitation inhibition and bioavailability enhancement, Int. J. Nanomed.12 (2017) 8801–8811; https://doi.org/10.2147/IJN.S14971710.2147/IJN.S149717
  2. 2. N. T. Tung, C. S. Tran, H. A. Nguyen, T. D. Nguyen, S. C. Chi, D. V. Pham, Q. D. Bui and X. H. Ho, Formulation and biopharmaceutical evaluation of supersaturatable self-nanoemulsifying drug delivery systems containing silymarin, Int. J. Pharm.555 (2019) 63–76; https://doi.org/10.1016/j.ijpharm.2018.11.03610.1016/j.ijpharm.2018.11.036
  3. 3. Z. Q. Chen, Y. Liu, J. H. Zhao, L. Wang and N. P. Feng, Improved oral bioavailability of poorly water-soluble indirubin by a supersaturatable self-microemulsifying drug delivery system, Int. J. Nanomed.7 (2012) 1115–1125; https://doi.org/10.2147/IJN.S2876110.2147/IJN.S28761
  4. 4. J. M. Landete, Ellagitannins, ellagic acid and their derived metabolites: A review about source, metabolism, functions and health, Food Res. Int.44 (2011) 1150–1160; https://doi.org/10.1016/j.foodres.2011.04.02710.1016/j.foodres.2011.04.027
  5. 5. F. Lei, D. M. Xing, L. Xiang, Y. N. Zhao, W. Wang, L. J. Zhang and L. J. Du, Pharmacokinetic study of ellagic acid in rat after oral administration of pomegranate leaf extract, J. Chromatogr. B796 (2003) 189–194; https://doi.org/10.1016/S1570-0232(03)00610-X10.1016/S1570-0232(03)00610-X
  6. 6. A. W. R. Hamad, W. M. Al-Momani, S. Janakat and S. A. Oran, Bioavailability of ellagic acid after single dose administration using HPLC, Par. J. Stat.8 (2009) 1661–1664; https://DOI:10.3923/pjn.2009.1661.166410.3923/pjn.2009.1661.1664
  7. 7. L. Yan, P. Yin, C. Ma and Y. Liu, Method development and validation for pharmacokinetic and tissue distributions of ellagic acid using ultrahigh performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS), Molecules19 (2014) 18923–18935; https://doi:10.3390/molecules19111892310.3390/molecules191118923627145925412040
  8. 8. J. Wang, D. Zheng, Y. Wang, C. Zhang and X. Sun, Pharmacokinetics study of Erhuang decoction extracts in rats by HPLC-MS/MS, J. Chromatogr. B1059 (2017) 35–42; https://doi.org/10.1016/j.jchromb.2017.05.01910.1016/j.jchromb.2017.05.01928570935
  9. 9. G. R. Valicherla, M. Riyazuddin, S. Shahi, A. P. Gupta, A. A. Syed, A. Husain and J. R. Gayen, LCESI-MS/MS assay development and validation of a novel antidiabetic peptide PSTi8 in mice plasma using SPE: An application to pharmacokinetics, J. Pharm. Biomed. Anal.180 (2019) 113074; https://doi.org/10.1016/j.jpba.2019.11307410.1016/j.jpba.2019.11307431891874
  10. 10. V. Ferrone, M. Carlucci, P. Palumbo and G. Carlucci, Bioanalytical method development for quantification of ulifloxacin, fenbufen and felbinac in rat plasma by solid-phase extraction (SPE) and HPLC with PDA detection, J. Pharm. Biomed. Anal.123 (2016) 205–212; https://doi.org/10.1016/j.jpba.2016.01.06210.1016/j.jpba.2016.01.06226898973
  11. 11. D. Zheng, C. Lv, X. Sun, J. Wang and Z. Zhao, Preparation of a supersaturatable self-microemulsion as drug delivery system for ellagic acid and evaluation of its antioxidant activities, J. Drug Deliv. Sci. Technol.53 (2019) 101209; https://doi.org/10.1016/j.jddst.2019.10120910.1016/j.jddst.2019.101209
  12. 12. G. Z. Pei, W. Chen, H. Zhang and G. H. Li, Pharmacokinetics of ellagic acid tablets in rabbits, Chin. J. Exp. Tradit. Med. Formulae18 (2012) 136–138; https://doi.org/10.13422/j.cnki.syfjx.2012.12.047
  13. 13. C. Sun, Y. Gui, R. Hu, J. Chen, B. Wang, Y. Guo, W. Lu, X. Nie, Q. Shen, S. Gao and W. Fang, Preparation and Pharmacokinetics Evaluation of Solid Self-Microemulsifying Drug Delivery System (SSMEDDS) of Osthole, AAPS PharmSciTech19 (2018) 2301–2310; https://doi.org/10.1208/s12249-018-1067-310.1208/s12249-018-1067-329845504
  14. 14. J. Jinno, N. Kamada, M. Miyake, K. Yamada, T. Mukai, M. Odomi, H. Toguchi, G. G. Liversidge, K. Higaki and T. Kimura, Effect of particle size reduction on dissolution and oral absorption of a poorly water-soluble drug, cilostazol, in beagle dogs, J. Controll. Release111 (2006) 56–64; https://doi.org/10.1016/j.jconrel.2005.11.01310.1016/j.jconrel.2005.11.01316410029
  15. 15. H. Mu, R. Holm and A. Müllertz, Lipid-based formulations for oral administration of poorly water-soluble drugs, Int. J. Pharm.453 (2013) 215–224; https://doi.org/10.1016/j.ijpharm.2013.03.05410.1016/j.ijpharm.2013.03.05423578826
DOI: https://doi.org/10.2478/acph-2021-0031 | Journal eISSN: 1846-9558 | Journal ISSN: 1330-0075
Language: English
Page range: 679 - 687
Accepted on: Sep 22, 2020
Published on: Apr 3, 2021
Published by: Croatian Pharmaceutical Society
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year
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© 2021 Jinglong Wang, Liqun Fan, Lihua Zhang, Dandan Zheng, Yingzi Wang, Xiao Sun, Yonghui Ji, published by Croatian Pharmaceutical Society
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.