Home Preparation of Nano-curcumin with Enhanced Dissolution Using Ultrasonic-Assisted Supercritical Anti-solvent Technique
Article
Licensed
Unlicensed Requires Authentication

Preparation of Nano-curcumin with Enhanced Dissolution Using Ultrasonic-Assisted Supercritical Anti-solvent Technique

  • Fatemeh Zabihi , Na Xin , Jingfu Jia , Tao Cheng and Yaping Zhao EMAIL logo
Published/Copyright: August 18, 2015

Abstract

Curcumin is the main gradient of “Turmeric” a famous Indian spice and food additive. The marvelous nutritional and medicinal effects of curcumin made it a good alternative to some conventional drugs and food flavoring or coloring materials. However, the low solubility of curcumin is a challenging hindrance which should be seriously addressed. In this work, we prepared nano-curcumin with enhanced aqueous dispersion and dissolution rate. Ultrasonic-assisted supercritical anti-solvent (UA-SAS) technique was used to convert the commercial curcumin to uniform distributed nano-particles with the average size of 20 nm and yielding of 65%. The effect of process parameters including pressure, temperature, solution flow rate, and nature of organic solvent on the average particle size and yielding of products was investigated. The morphology, size, and crystalline pattern of processed curcumin particles were characterized by scanning electron microscopy, mean particle size analyzer, and X-ray diffraction. The champion specimen was achieved when the supercritical fluid was employed at 16 MPa and 35°C. Aqueous suspension of processed nano-curcumin can be stable for more than 2 months. In vitro dissolution experiments showed a remarkable enhancement in dissolution rate of UA-SAS-treated curcumin respecting to the commercial curcumin powder.

Funding statement: Funding: This research was supported by the Funding of National Natural Science Foundation of China (20976103), Chinese Postdoctoral Funding (2013M541521), and the Interdisciplinary (Engineering–Medical) Research Funding of Shanghai Jiaotong University (Grant No. YG2011MS30).

Acknowledgments

We are thankful to the Instrumental Analysis Center of SJTU for assistance on SEM analysis.

References

1. Basniwal RK, Buttar SH, Jain KV. Curcumin nanoparticles preparation, characterization, and antimicrobial study. J Agric Food Chem 2011;59:2056–61.10.1021/jf104402tSearch in Google Scholar PubMed

2. Yallapu MM, Jaggi M, Chauhan SC. Curcumin self-assembly: a novel approach to improve curcumin delivery and its therapeutic efficacy in prostate cancer cells. Macromol Biosci 2010;10:1141–51.10.1002/mabi.201000084Search in Google Scholar PubMed

3. Kakran M, Sahoo NG, Li Tan L. Preparation of nanoparticles of poorly water-soluble antioxidant curcumin by antisolvent precipitation methods. J Nanopart Res 2013;14:757–68.10.1007/s11051-012-0757-0Search in Google Scholar

4. Liu J, Chen S, Song L, Huang GS. Recent progress in studying curcumin and its nano-preparations for cancer therapy. Curr Pharm 2013;11:1974–93.10.2174/1381612811319110003Search in Google Scholar

5. Tsai YM, Chien CF, Lin LC, Tsai TH. Curcumin and its nano-formulation: the kinetics of tissue distribution and blood-brain barrier penetration. Int J Pharm 2011;416:331–8.10.1016/j.ijpharm.2011.06.030Search in Google Scholar PubMed

6. Douglas PL. Precipitation of pharmaceuticals using a supercritical anti‐solvent (SAS) technique: a preliminary study. Can J Chem Eng 2011;89:529–35.10.1002/cjce.20427Search in Google Scholar

7. Zu S, Yung L, Huang L, Ma C, Wang C. Micronization of taxifolin by supercritical antisolvent process and evaluation of radical scavenging activity. Int J Mol Sci 2012;13:8869–81.10.3390/ijms13078869Search in Google Scholar PubMed PubMed Central

8. Reverchon E, Marco I. Mechanisms controlling supercritical antisolvent precipitate morphology. J Chem Eng 2011;169:358–70.10.1016/j.cej.2011.02.064Search in Google Scholar

9. Chu J, Lee H, Kim H, Lee YU. Recrystallization of tetracycline hydrochloride using supercritical anti-solvent process. Korean J Chem Eng 2009;26:1119–24.10.1007/s11814-009-0186-7Search in Google Scholar

10. Wang Y, Pfeffer R, Dave R. Polymer encapsulation of fine particles by a supercritical antisolvent process. AIChE 2005;51:440–455.11.10.1002/aic.10323Search in Google Scholar

11. Kalantarian P, Najafabadi AR, Haririan I, Vatanara A, Yamini Y, Darabi M, et al. Preparation of 5-fluorouracil nanoparticles by supercritical antisolvents for pulmonary delivery. Int J Nanomedicine 2010;5:763–70.10.2147/IJN.S12415Search in Google Scholar PubMed PubMed Central

12. Zabihi F, Xin N, Jia J, Chen T, Zhao Y. Polymeric coating of fluidizing nano-curcumin via anti-solvent supercritical method for sustained release. Ind Eng Chem Res 2014;53:6569–74.10.1016/j.supflu.2014.02.021Search in Google Scholar

13. Zabihi F, Xin N, Jia J, Chen T, Zhao Y. High yield and high loading preparation of curcumin – PLGA nanoparticles using a modified supercritical antisolvent technique. Ind Eng Chem Res 2014;53:6569–74.10.1021/ie404215hSearch in Google Scholar

14. Zabihi F, Yang M, Leng Y, Zhao Y. PLGA–HPMC nanoparticles prepared by a modified supercritical anti-solvent technique for the controlled release of insulin. J Supercrit Fluids 2015;99:15–22.10.1016/j.supflu.2015.01.023Search in Google Scholar

15. Jin H, Hemingway M, Guptab RB, Xia F, Zhao Y. Preparation of thalidomide nano-flakes by supercritical antisolvent with enhanced mass transfer. Particuology 2013;10:17–23.10.1016/j.partic.2011.05.003Search in Google Scholar

16. Liu PS, Chen GF. Porous materials, processing and applications, 1st ed. Oxford, UK- Waltham, USA: Butterworth-Heinmann, 2014:464–83.Search in Google Scholar

17. Kim S, Lee S, Park JS, Woo SJ. Micronization of cilostazol using supercritical anti-solvent (SAS) process: effect of process parameters. Powder Technol 2007;177:64–70.10.1016/j.powtec.2007.02.029Search in Google Scholar

18. Cao Z, Sun L, Cao L, He Y. Production of ursolic acid nanoparticles by supercritical antisolvent precipitation. Adv Mater Res 2011;233:2210–14.10.4028/www.scientific.net/AMR.239-242.2210Search in Google Scholar

19. Kalani M, Yunus R. Effect of supercritical fluid density on nano-encapsulated drug particle size using the supercritical anti-solvent method. Int J Nanomedicine 2012;7:2165–72.10.2147/IJN.S29805Search in Google Scholar PubMed PubMed Central

20. Zu S, Yang L, Huang J, Chunhui J, Wang W, Zhao C, et al. Micronization of taxifolin by supercritical antisolvent process and evaluation of radical scavenging activity. Int J Mol Sci 2012;13:8869–81.10.3390/ijms13078869Search in Google Scholar PubMed PubMed Central

21. Gopalan B, Goto M, Kodama A, Hirose T. Supercritical carbon dioxide extraction of turmeric (curcuma longa). J Agric Food Chem 2000;48:2189–92.10.1021/jf9908594Search in Google Scholar PubMed

22. Badens E, Boutin O, Charbit L. Laminar Jet dispersion and jet atomization in pressurized carbon dioxide. J Supercrit Fluids 2005;36:81–90.10.1016/j.supflu.2005.03.007Search in Google Scholar

23. Rantakyla M, Jantti M, Aaltonen O, Hurme M. The effect of initial drop size on particle size in the supercritical antisolvent precipitation (SAS) technique. J Supercrit Fluid 2002;24:251–63.10.1016/S0896-8446(02)00034-7Search in Google Scholar

24. Kim MS, Song HS, Park HJ, Hwang SJ. Effect of solvent type on the nanoparticle formation of atorvastatin calcium by the supercritical antisolvent process. Chem Pharm Bull 2012;60:543–7.10.1248/cpb.60.543Search in Google Scholar PubMed

25. Ho DL, Glinka CJ. Effects of solvent solubility parameters on organ clay dispersions. Chem Mater 2003;15:1309–12.10.1021/cm0217194Search in Google Scholar

26. Marcus Y. The properties of solvents, 1st ed. Wiley Series in Solution Chemistry. New York-USA: John Wiley & Sons, 1998.Search in Google Scholar

27. Wang P, Anderko A. Modeling phase equilibria and speciation in mixed-solvent electrolyte systems. Fluid Phase Equilib 2001;186:103–22.10.1016/j.fluid.2004.06.008Search in Google Scholar

28. Sun M, Zhai X, Fan Z, Ma Y, Zhang R, Yang X. The influence of co-solvents on the stability and bioavailability of rapamycin formulated in self-microemulsifying drug delivery systems. Drug Dev Ind Pharm 2011;37:986–94.30.10.3109/03639045.2011.553618Search in Google Scholar PubMed

29. Chouhan R, Bajpai AK. Real time in vitro studies of doxorubicin release from PHEMA nanoparticles. J Nanobiotech 2009;7:1–10.10.1186/1477-3155-7-5Search in Google Scholar PubMed PubMed Central

30. Asare-Addo K, Conway RB, Larhrib H, Levina M, Rajabi-Siahboomi A, Tetteh J, et al. The effect of pH and ionic strength of dissolution media on in-vitro release of two model drugs of different solubilities from HPMC matrices. Coll Surf B Biointer 2013;111:384–91.10.1016/j.colsurfb.2013.06.034Search in Google Scholar PubMed

31. Kundu RD, Swarnakar S, Ramamurthy T, Chowdhury A, Nair GB, Hu C, et al. Preparation, characterization, and in vitro release investigation of lutein/zein nanoparticles via solution enhanced dispersion by supercritical fluids. J Food Eng 2012;109:545–52.10.1016/j.jfoodeng.2011.10.025Search in Google Scholar

32. Toropainen T, Leppänen J, Matilainen L, Velaga S, Jarho P, Carlfors J, et al. Crystal structure changes of gamma-cyclodextrin after the SEDS process in supercritical carbon dioxide affect the dissolution rate of complexed budesonide. Pharm Res 2007;24:1058–66.10.1007/s11095-006-9227-7Search in Google Scholar PubMed

Published Online: 2015-8-18
Published in Print: 2015-10-1

©2015 by De Gruyter

Downloaded on 12.11.2025 from https://www.degruyterbrill.com/document/doi/10.1515/ijfe-2015-0105/html
Scroll to top button