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Encapsulation of Curcumin in Diblock Copolymer Micelles for Cancer Therapy Publisher Pubmed



Alizadeh AM1 ; Sadeghizadeh M2 ; Najafi F3 ; Ardestani SK4 ; Erfanimoghadam V5 ; Khaniki M6 ; Rezaei A7 ; Zamani M2 ; Khodayari S8 ; Khodayari H8 ; Mohagheghi MA1
Authors
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Authors Affiliations
  1. 1. Cancer Research Center, Tehran University of Medical Sciences, Tehran, 14197-33141, Iran
  2. 2. Department of Genetics, School of Biological Sciences, Tarbiat Modares University, Tehran, 14115-137, Iran
  3. 3. Department of Resin and Additives, Institute for Color Science and Technology, Tehran, 16765-654, Iran
  4. 4. Immunology Lab, Institute of Biochemistry and Biophysics, University of Tehran, Tehran, 13145-1384, Iran
  5. 5. Department of Biotechnology, Faculty of Advanced Medical Technology, Golestan University of Medical Sciences, Gorgan, 49175-553, Iran
  6. 6. Department of Pathology, School of Medicine, Tehran University of Medical Sciences, Tehran, 14197-33141, Iran
  7. 7. School of Biological Science, Damghan University, Damghan, 36716-41167, Iran
  8. 8. Cancer Model Research Center, Tehran University of Medical Sciences, Tehran, 14197-33141, Iran

Source: BioMed Research International Published:2015


Abstract

Application of nanoparticles has recently promising results for water insoluble agents like curcumin. In this study, we synthesized polymeric nanoparticle-curcumin (PNPC) and then showed its efficiency, drug loading, stability, and safety. Therapeutic effects of PNPC were also assessed on two cell lines and in an animal model of breast cancer. PNPC remarkably suppressed mammary and hepatocellular carcinoma cells proliferation (P < 0.05). Under the dosing procedure, PNPC was safe at 31.25 mg/kg and lower doses. Higher doses demonstrated minimal hepatocellular and renal toxicity in paraclinical and histopathological examinations. Tumor take rate in PNPC-treated group was 37.5% compared with 87.5% in control (P < 0.05). Average tumor size and weight were significantly lower in PNPC group than control (P < 0.05). PNPC increased proapoptotic Bax protein expression (P < 0.05). Antiapoptotic Bcl-2 protein expression, however, was lower in PNPC-treated animals than the control ones (P < 0.05). In addition, proliferative and angiogenic parameters were statistically decreased in PNPC-treated animals (P < 0.05). These results highlight the suppressing role for PNPC in in vitro and in vivo tumor growth models. Our findings provide credible evidence for superior biocompatibility of the polymeric nanocarrier in pharmacological arena together with an excellent tumor-suppressing response. © 2015 Ali Mohammad Alizadeh et al.
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