IMPROVING SOLUBILITY AND DISSOLUTION OF A NATURAL PRODUCT APIGENIN VIA PREPARATION OF SOLID DISPERSION BY HOT MELT EXTRUSION

Authors

  • SOFI N. STIANI Department of Pharmaceutics and Pharmaceutical Technology, Padjadjaran University, Pharmacy Study Program, STIKes Salsabila, Serang Banten, Indonesia
  • TAOFIK RUSDIANA Department of Pharmaceutics and Pharmaceutical Technology, Padjadjaran University
  • ANAS SUBARNAS Department of Pharmacology and Clinical Pharmacy, Padjadjaran University

DOI:

https://doi.org/10.22159/ijap.2021.v13s3.10

Keywords:

Apigenin, Solid dispersion, Solubility, Hot melt extrusion

Abstract

Objective: Hot Melt Extrusion (HME) is one of the techniques for preparing a solid dispersion hydrophilic excipient known as a no solvents practical method to increase the solubility of drugs. Apigenin (APG) has properties that thermal stable with melting point 345-350 °C but very low solubility in the water around 1,35 µg/ml. The polymer is stable in the HME method are Soluplus and Kollidon VA 64. The study aims to optimize the kind of polymer in HME formulae to improve the solubility and dissolution rate of apigenin by solid dispersion using hot-melt extrusion.

Methods: Apigenin 10–50% w/w and Kollidon®VA 64 or Soluplus® and combination of Kollidon®VA 64 and Soluplus® were mixed, and the resulting blends extruded using a twin-screw extruder (Teach-Line ZK25T). Characterization of apigenin extrudates conducted using scanning electron microscopy, thermogravimetric analysis, differential scanning calorimetry, Fourier transform infrared spectroscopy, powder X-ray diffractometry, and dissolution.

Results: Solubility studies presented enhancement in apigenin of 10%/Soluplus®90%; 10% w/w apigenin/Kollidon®VA 64 (90%); and 33,3% w/w apigenin/Kollidon®VA 64 33,3% mix Soluplus® 33,3% increased more than 18,25; 16,18-and 8,52-fold in water, respectively. Furthermore dissolution studies showed enhancement in apigenin percent release of 10%/Soluplus®90%; 10% w/w apigenin/Kollidon®VA 64 90%; and 33,3% w/w apigenin/Kollidon®VA 64 33,3% mix Soluplus® 33,3% tablet apigenin HME up to 34,29%; 69,75% and 30,69%, respectively.

Conclusion: The formulation of 10% w/w Apigenin and 90% Soluplus® using hot-melt extrusion able to increase water solubility approximately 18,25-fold than raw material apigenin.

Downloads

Download data is not yet available.

References

1. Tang D, Chen K, Huang L, Li J. Pharmacokinetic properties and drug interactions of apigenin, a natural flavone. Expert Opin Drug Metab Toxicol 2017;13:323-30.
2. Sharafzadeh S, Alizadeh O. German and roman chamomile. J Appl Pharm Sci 2011;1:1-5.
3. Stiani SN, Fillah SM, Hanindhiya F, Subarnas A, Rusdiana T. Anticalculi activity of apigenin and celery (Apium graveolens L.) extract in rats induced by ethylene glycol–ammonium chloride. J Pharm Bioallied Sci 2019;11:556–61.
4. Li B, Robinson DH, Birt DF. Evaluation of properties of apigenin and [G-3H] apigenin and analytic method development. J Pharm Sci 1997;86:721-5.
5. Zhang J, Liu D, Huang Y, Gao Y, Qian S. Biopharmaceutics classification and intestinal absorption study of apigenin. Int J Pharm 2012;436:311-7.
6. Altamimi MA, Eljayat M, Alshehri M, Mohsin K, Ibrahim A, Maenazal A, et al. Utilizing spray drying technique to improve oral bioavailability of apigenin. Adv Powder Technol 2018;29:1676-84.
7. Dogra X, Dhyani A, Juyal D. Solid dispersion. Int J Pharm Sci Lett 2015;5:593-8.
8. Zhang J, Huang Y, Liu D, Gao Y, Qian S. Preparation of apigenin nanocrystals using supercritical antisolvent process for dissolution and bioavailability enhancement. Eur J Pharm Sci 2013;45:740-7.
9. Huang Y, Zu Y, Zhao X, Wu M, Feng Z, Deng Y, et al. Preparation of inclusion complex of apigenin-hydroxypropyl-?-cyclodextrin by using supercritical antisolvent process for dissolution and bioavailability enhancement. Int J Pharm 2016;512:921-30.
10. Ma XQ, Zhuang C, Wang BC, Huang YF, Chen Q, Lin N. Cocrystal of apigenin with higher solubility. Enhanced oral bioavailability and anti-inflammatory effect cryst. Growth Des 2019;19:5531-7.
11. Shakeel F, Haq N, Alshehri S. Solubility determination and thermodynamic data of apigenin in binary {Transcutol®?+? water} mixtures. Ind Crops Prod 2018; 116:56-63.
12. Telange DR, Patil AT, Pethe AM, Fegade H, Anand S, Dave VS. Formulation and characterization of an apigenin-phospholipid phytosome (APLC) for improved solubility, in vivo bioavailability, and antioxidant potential. Eur J Pharm Sci 2017;108:36-49.
13. Zhao L, Zhang L, Meng L, Wang J, Zhai G. Design and evaluation of a self-microemulsifying drug delivery system for apigenin. Drug Dev Ind Pharm 2013;39:662-9.
14. Zhang Z, Cui C, Wei F, Lv H. Improved solubility and oral bioavailability of apigenin via Soluplus/Pluronic F127 binary mixed micelles system. Drug Dev Ind Pharm 2017;43:1276-82.
15. Ding B, Chen H, Wang C, Zhai Y, Zhai G. Preparation and in vitro evaluation of apigenin loaded lipid nanocapsules. J Nanosci Nanotechnol 2013;13:6546-52.
16. Gao N, Guo M, Fu Q, He Z. Application of hot-melt extrusion to enhance the dissolution and oral bioavailability of oleanolic acid. Asian J Pharm Sci 2017;12:66-72.
17. Huang Y, Dai WG. Fundamental aspects of solid dispersion technology for poorly soluble drugs. Acta Pharm Sin B 2014;4:16-25.
18. Dhirendra K, Lewis S, Udupa N, Atin K. Solid dispersions: a review. Pak J Pharm Sci 2009;22:234-46.
19. Stiani SN, Rusdiana T, Subarnas A. Enhancing dissolution and bioavailability of purely water-insoluble natural compounds by solid dispersion with hot-melt extrusion technique. J Global Pharma Technol 2018;10:139-51.
20. Singhal S, Lohar VK, Arora V. Hot melt extrusion technique. Webmed Central Pharm Sci 2011;2:1-20.
21. Rachmaniar R, Panatarani C, Joni IM, Abdasah M, Rusdiana T. Enhancement of solubility and dissolution of ibuprofen microparticle prepared by ultrasonic spray drying. Marmara Pharm J 2017;21:783-92.
22. Chokshi R, Zia H. Hot-melt extrusion technique: a review. Iran J Pharm Res 2004;3:3–16.
23. Yulianto AN, Rusdiana T, Muchtaridi M, Subarnas A. Validation of UV-Vis spectrophotometry methode for analysis of apigenin in celery extract (Apium graveolens L.). Pharmaciana 2017;72:159.
24. Kolter M, Karl K. Suitability of plasticized polymers for hot-melt extrusion. Ex Act For Pharma Ing Serv 2010;24:2–6.
25. Ashour EA, Majumdar S, Alsheteli A, Alsulays B, Ashehri S, Feng X, et al. Hot melt extrusion as an approach to improve solubility, permeability and oral absorption of a psychoactive natural product, piperine. J Pharm Pharmacol 2016;68:989–98.
26. Yannian H, Zhao X, Zu Y, Wang L, Deng Y, Wu M, et al. Enhanced solubility and bioavailability of apigenin via preparation of solid dispersions of mesoporous silica nanoparticles. Iran J Pharm Res 2019;18:168-82.

Published

10-03-2021

How to Cite

STIANI, S. N., RUSDIANA, T., & SUBARNAS, A. (2021). IMPROVING SOLUBILITY AND DISSOLUTION OF A NATURAL PRODUCT APIGENIN VIA PREPARATION OF SOLID DISPERSION BY HOT MELT EXTRUSION. International Journal of Applied Pharmaceutics, 13(3), 47–52. https://doi.org/10.22159/ijap.2021.v13s3.10

Issue

Section

Original Article(s)

Most read articles by the same author(s)

1 2 > >>