174
Views
12
CrossRef citations to date
0
Altmetric
Research Article

Development and evaluation of co-formulated docetaxel and curcumin biodegradable nanoparticles for parenteral administration

, , &
Pages 725-736 | Received 03 Jan 2015, Accepted 03 May 2015, Published online: 31 Aug 2015

References

  • Peer D, Karp JM, Hong S, et al. Nanocarriers as an emerging platform for cancer therapy. Nat Nanotechnol 2007;2:751–760
  • Waterhouse DN, Gelmon KA, Klasa R, et al. Development and assessment of conventional and targeted drug combinations for use in the treatment of aggressive breast cancers. Curr Cancer Drug Targets 2006;6:455–489
  • DeSantis C, Ma J, Bryan L, Jemal A. Breast cancer statistics, 2013. CA Cancer J Clin 2014;64:52–62
  • Venishetty VK, Parikh N, Sistala R, et al. Application of validated RP-HPLC method for simultaneous determination of docetaxel and Ketoconazole in solid lipid nanoparticles. J Chromatogr Sci 2011;49:136–141
  • Wang L, Liu Z, Liu D, et al. Docetaxel-loaded-lipid-based-nanosuspensions (DTX-LNS): preparation, pharmacokinetics, tissue distribution and antitumor activity. Int J Pharm 2011;413:194–201
  • Jinturkar KA, Anish C, Kumar MK, et al. Liposomal formulations of etoposide and docetaxel for p53 mediated enhanced cytotoxicity in lung cancer cell lines. Biomaterials 2012;33:2492–2507
  • Galletti E, Magnani M, Renzulli ML, Botta M. Paclitaxel and docetaxel resistance: molecular mechanisms and development of new generation taxanes. Chem Med Chem 2007;2:920–942
  • Zhan Y, Chen Y, Liu R, et al. Potentiation of paclitaxel activity by curcumin in human breast cancer cell by modulating apoptosis and inhibiting EGFR signaling. Arch Pharmacal Res 2014;37:1086–1095
  • Mohan PR, Sreelakshmi G, Muralidharan CV. Water soluble complexes of curcumin with cyclodextrins: characterization by FT-Raman spectroscopy. Vib Spectrosc 2012;62:77–84
  • Bill MA, Baken C, Benson DM, et al. Curcumin induces pro-apoptotic effects against human melanoma cells and modulates the cellular response to immunotherapeutic cytokines. Mol Cancer Ther 2009;8:2726–2735
  • Gaurisankar SA, Das T. Anti cancer effects of curcumin: cycle of life and death. Cell Division 2008;3:14
  • 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;351:19–29
  • Aggarwal BB, Shishodia S, Takada Y, et al. Curcumin suppresses the paclitaxel-induced nuclear factor-κB pathway in breast cancer cells and inhibits lung metastasis of human breast cancer in nude mice. Clin Cancer Res 2005;11:7490–7498
  • Averineni RK, Shavi GV, Gurram AK, et al. PLGA 50:50 nanoparticles of paclitaxel: development, in vitro anti-tumor activity in BT-549 cells and in vivo evaluation. Bull Mater Sci 2012;35:319–326
  • Danhier F, Ansorena E, Silva JM, et al. PLGA-based nanoparticles: an overview of biomedical applications. J Control Release 2012;161:505–522
  • Kumari A, Yadav SK, Yadav SC. Biodegradable polymeric nanoparticles based drug delivery systems. Colloids Surf B Biointerfaces 2010;75:1–18
  • Zhou YZ, Alany RG, Chuang V, Wen J. Optimization of PLGA nanoparticles formulation containing L-DOPA by applying the central composite design. Drug Dev Ind Pharm 2013;39:321–330
  • Woodcock J. The concept of pharmaceutical quality. Am Pharm Rev 2004;7:10–15
  • US FDA. Guidance for industry: PAT-A framework for innovative pharmaceutical development, manufacturing, and quality assurance. Silver Spring, MD: US FDA; 2004
  • Singh B, Kumar R, Ahuja N. Optimizing drug delivery systems using systematic “design of experiments”. Part I: fundamental aspects. Crit RevTher Drug 2005;22:27–105
  • Upadhyay KK, Bhatt AN, Castro E, et al. In vitro and in vivo evaluation of docetaxel loaded biodegradable polymersomes. Macromol Biosci 2010;10:503–512
  • Li X, Wang D, Zhang J, Pan W. Preparation and pharmacokinetics of docetaxel based on nanostructured lipid carriers. J Pharm Pharmacol 2009;61:1485–1492
  • Singare DS, Marella S, Gowthamrajan K, et al. Optimization of formulation and process variable of nanosuspension: an industrial perspective. Int J Pharm 2010;402:213–220
  • Kwon HY, Lee JY, Choi SW, et al. Preparation of PLGA nanoparticles containing estrogen by emulsification–diffusion method. Colloid Surface B 2001;30:123–130
  • GC Na, Rajagopalan N. Use of charged phospholipids to reduce nanoparticle aggregation. US Patent 5,336,507, Google Patents, 1994
  • Papadopoulou V, Kosmidis K, Vlachou M, Macheras P. On the use of the weibull function for the discernment of drug release mechanisms. Int J Pharm 2006;309:44–50
  • Podczeck F. Comparison of in vitro dissolution profiles by calculating mean dissolution time (MDT) or mean residence time (MRT). Int J Pharm 1993;97:93–100
  • Rivolta I, Panariti A, Lettiero B, et al. Cellular uptake of coumarin-6 as a model drug loaded in solid lipid nanoparticles. J Physiol Pharmacol 2011;62:45–53
  • Gao H, Yang Z, Zhang S, et al. Ligand modified nanoparticles increases cell uptake, alters endocytosis and elevates glioma distribution and internalization. Sci Rep 2013;3:1–8
  • Italia J, Yahya M, Singh D, Kumar MR. Biodegradable nanoparticles improve oral bioavailability of amphotericin B and show reduced nephrotoxicity compared to intravenous Fungizone®. Pharm Res 2009;26:1324–1331
  • Fu K, Pack DW, Klibanov AM, Langer R. Visual evidence of acidic environment within degrading poly(lactic-co-glycolic acid) (PLGA) microspheres. Pharm Res 2000;17:100–106
  • Huang X, Zhou C, Wang H, et al. Pharmacokinetics, efficacy, and safety evaluation of docetaxel/hydroxypropyl-sulfobutyl-β-cyclodextrin inclusion complex. AAPS PharmSciTech 2011;12:665–672
  • Panyam J, Labhasetwar V. Biodegradable nanoparticles for drug and gene delivery to cells and tissue. Adv Drug Del Rev 2003;55:329–347
  • Schrijvers D, Wanders J, Dirix L, et al. Coping with toxicities of docetaxel (Taxotere™). Ann Oncol 1993;4:610–611
  • Avgoustakis K, Beletsi A, Panagi Z, et al. PLGA–mPEG nanoparticles of cisplatin: in vitro nanoparticle degradation, in vitro drug release and in vivo drug residence in blood properties. J Control Release 2002;79:123–135

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.