Formation of curcumin nanoparticles via solution-enhanced dispersion by supercritical CO2

International Journal of Nanomedicine

Volumn 10, Issue , 2015, Pages 3171-3181

  Zhao, Zheng ^a   Xie, Maobin ^b   Li, Yi ^b   Chen, Aizheng ^c   Li, Gang ^d   Zhang, Jing ^b   Hu, Huawen ^b   Wang, Xinyu ^a   Li, Shipu ^a  

^a WUHAN UNIVERSITY OF TECHNOLOGY   (China)

^b HONG KONG POLYTECHNIC UNIVERSITY   (Hong Kong)

^c HUAQIAO UNIVERSITY   (China)

^d SOOCHOW UNIVERSITY   (China)

Author keywords

Crystalline sate; Curcumin; Dissolution rate; Solubility

Indexed keywords

CARBON DIOXIDE; CURCUMIN NANOPARTICLE; NANOPARTICLE; UNCLASSIFIED DRUG; CURCUMIN;

ARTICLE; CHEMICAL COMPOSITION; CONCENTRATION (PARAMETERS); DIFFERENTIAL SCANNING CALORIMETRY; DISSOLUTION; FLOW RATE; INFRARED SPECTROSCOPY; NANOFABRICATION; PARTICLE SIZE; POWDER; PRECIPITATION; SURFACE PROPERTY; TEMPERATURE SENSITIVITY; THERMOGRAVIMETRY; X RAY POWDER DIFFRACTION; CHEMISTRY; NANOTECHNOLOGY; PROCEDURES;

CARBON DIOXIDE; CURCUMIN; NANOPARTICLES; NANOTECHNOLOGY; PARTICLE SIZE;

EID: 84929430295     PISSN: 11769114     EISSN: 11782013     Source Type: Journal    
DOI: 10.2147/IJN.S80434     Document Type: Article

References (33)

1. Sun Y, Du L, Liu Y, et al. Transdermal delivery of the in situ hydrogels of curcumin and its inclusion complexes of hydroxypropyl-β-cyclodextrin for melanoma treatment. Int J Pharm. 2014;469(1):31–39.
2. Bhawana, Basniwal RK, Buttar HS, Jain VK, Jain N. Curcumin nano-particles: preparation, characterization, and antimicrobial study. J Agr Food Chem. 2011;59(5):2056–2061.
3. Yallapu MM, Jaggi M, Chauhan SC. Curcumin nanoformula-tions: a future nanomedicine for cancer. Drug Discov Today. 2012; 17(1–2):71–80.
4. Anand P, Kunnumakkara AB, Newman RA, Aggarwal BB. Bio-availability of curcumin: problems and promises. Mol Pharm. 2007; 4(6):807–818.
5. Takahashi M, Uechi S, Takara K, Asikin Y, Wada K. Evaluation of an oral carrier system in rats: bioavailability and antioxidant properties of liposome-encapsulated curcumin. J Agr Food Chem. 2009; 57(19):9141–9146.
6. Maiti K, Mukherjee K, Gantait A, Saha BP, Mukherjee PK. Curcumin-phospholipid complex: preparation, therapeutic evaluation and phar-macokinetic study in rats. Int J Pharm. 2007;330(1–2):155–163.
7. Marcolino VA, Zanin GM, Durrant LR, Benassi MDT, Matioli G. Interaction of curcumin and bixin with β-cyclodextrin: complexation methods, stability, and applications in food. J Agr Food Chem. 2011; 59(7):3348–3357.
8. Akhtar F, Rizvi MM, Kar SK. Oral delivery of curcumin bound to chi-tosan nanoparticles cured Plasmodium yoelii infected mice. Biotechnol Adv. 2012;30(1):310–320.
9. Gupta V, Aseh A, Rios CN, Aggarwal BB, Mathur AB. Fabrication and characterization of silk fibroin-derived curcumin nanoparticles for cancer therapy. Int J Nanomed. 2009;4(1):115–122.
10. Patel A, Hu YC, Tiwari JK. Synthesis and characterization of zein-curcumin colloidal particles. Soft Matter. 2010;6(24):6192–6199.
11. Jithan AV, Madhavi K, Madhavi M, Prabhakar K. Preparation and characterization of albumin nanoparticles encapsulating curcumin intended for the treatment of breast cancer. Int J Pharm Invest. 2011; 1(2):119–125.
12. Beloqui A, Coco R, Memvanga PB, Ucakar B, des Rieux A, Préat V. pH-sensitive nanoparticles for colonic delivery of curcumin in infam-matory bowel disease. Int J Pharm. 2014;473(1–2):203–212.
13. Yallapu MM, Gupta BK, Jaggi M, Chauhan SC. Fabrication of curcumin encapsulated PLGA nanoparticles for improved therapeutic effects in metastatic cancer cells. J Colloid Interf Sci. 2010;35(1):19–29.
14. Feng R, Song Z, Zhai G. Preparation and in vivo pharmacokinetics of curcumin-loaded PCL-PEG-PCL triblock copolymeric nanoparticles. Int J Nanomedicine. 2012;7:4089–4098.
15. Sun XZ, Williams GR, Hou XX, Zhu LM. Electrospun curcumin-loaded fibers with potential biomedical applications. Carbohyd Polym. 2013;94(1):147–153.
16. Merrell JG, McLaughlinb SW, Tie L, Laurencind CT, Chen AF, Nair LS. Curcumin loaded poly(ε-caprolactone) nanofibers: wound dressing with antioxidant and anti-infammatory properties. Clin Exp Pharmacol P. 2009;36(12):1149–1156.
17. Brahatheeswaran D, Mathew A, Aswathy RG, et al. Hybrid fuorescent curcumin loaded zein electrospun nanofibrous scaffold for biomedical applications. Biomed Mater. 2012;7(4):045001.
18. Tagami T, Imao Y, Ito S, Nakada A, Ozeki T. Simple and effective preparation of nano-pulverized curcumin by femtosecond laser ablation and the cytotoxic effect on C6 rat glioma cells in vitro. Int J Pharm. 2014;468(1–2):91–96.
19. Margulis K, Magdassi S, Lee HS, Macosko CW. Formation of curcumin nanoparticles by fash nanoprecipitation from emulsions. J Colloid Interface Sci. 2014;434:65–70.
20. Liu G, Wang W, Wang H, Jiang Y. Preparation of 10-hydroxycamptothecin proliposomes by the supercritical CO2 anti-solvent process. Chem Eng J. 2014;243:289–296.
21. Zhao Z, Chen AZ, Li Y, et al. Fabrication of silk fibroin nanoparticles for controlled drug delivery. J Nanopart Res. 2012;14(4):736–745.
22. Zhao Z, Li Y, Zhang Y, et al. Development of silk fibroin modifed poly(l-lactide)-poly(ethylene glycol)-poly(l-lactide) nanoparticles in supercritical CO2. Powder Technol. 2014;268:118–125.
23. Zhao Z, Li Y, Chen AZ, et al. Generation of silk fibroin nanoparticles via solution-enhanced dispersion by supercritical CO2. Ind Eng Chem Res. 2013;52(10):3752–3761.
24. Jin HY, Hemingway M, Xia F, Li NS, Zhao YP. Production of β-Carotene nanoparticles by the solution enhanced dispersion with enhanced mass transfer by ultrasound in supercritical CO2 (SEDS-EM). Ind Eng Chem Res. 2011;50(23):13475–13484.
25. Kalani M, Yunus R. Application of supercritical antisolvent method in drug encapsulation: a review. Int J Nanomedicine. 2011;6: 1429–1442.
26. Lee BM, Kim SJ, Lee BC, Kim HS, Kim H, Lee YW. Preparation of micronized β-HMX using supercritical carbon dioxide as antisolvent. Ind Eng Chem Res. 2011;50(15):9107–9115.
27. Wang Q, Guan YX, Yao SJ, Zhu ZQ. Microparticle formation of sodium cellulose sulfate using supercritical fuid assisted atomization introduced by hydrodynamic cavitation mixer. Chem Eng J. 2010;159:220–229.
28. Reverchon E, De Marco I. Supercritical antisolvent precipitation of cephalosporins. Powder Technol. 2006;164(3):139–146.
29. Su CS, Lo WS, Lien LH. Micronization of futicasone propionate using supercritical antisolvent process. Chem Eng Technol. 2011;34(4): 535–541.
30. Chen AZ, Li L, Wang SB, et al. Nanonization of methotrexate by solution-enhanced dispersion by supercritical CO2. J Supercrit Fluid. 2012;67:7–13.
31. Montes A, Tenorio A, Gordill MD, Pereyra C, Martinez de la Ossa EJ. Screening design of experiment applied to supercritical antisolvent precipitation of amoxicillin: exploring new miscible conditions. J Supercrit Fluid. 2010;51:399–403.
32. Song Z, Zhu W, Liu N, Yang F, Feng R. Linolenic acid-modifed PEG-PCL micelles for curcumin delivery. Int J Pharm. 2014;471(1–2):312–321.
33. Xie X, Tao Q, Zou Y, et al. PLGA nanoparticles improve the oral bioavailability of curcumin in rats: characterizations and mechanisms. J Agr Food Chem. 2011;59(17):9280–9289.