Encapsulation of Curcumin in Diblock Copolymer Micelles for Cancer Therapy

Author:

Alizadeh Ali Mohammad1,Sadeghizadeh Majid2,Najafi Farhood3,Ardestani Sussan K.4,Erfani-Moghadam Vahid5,Khaniki Mahmood6,Rezaei Arezou7,Zamani Mina2,Khodayari Saeed8,Khodayari Hamid8,Mohagheghi Mohammad Ali1

Affiliation:

1. Cancer Research Center, Tehran University of Medical Sciences, Tehran 14197-33141, Iran

2. Department of Genetics, School of Biological Sciences, Tarbiat Modares University, Tehran 14115-137, Iran

3. Department of Resin and Additives, Institute for Color Science and Technology, Tehran 16765-654, Iran

4. Immunology Lab, Institute of Biochemistry and Biophysics, University of Tehran, Tehran 13145-1384, Iran

5. Department of Biotechnology, Faculty of Advanced Medical Technology, Golestan University of Medical Sciences, Gorgan 49175-553, Iran

6. Department of Pathology, School of Medicine, Tehran University of Medical Sciences, Tehran 14197-33141, Iran

7. School of Biological Science, Damghan University, Damghan 36716-41167, Iran

8. Cancer Model Research Center, Tehran University of Medical Sciences, Tehran 14197-33141, Iran

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 inin vitroandin vivotumor growth models. Our findings provide credible evidence for superior biocompatibility of the polymeric nanocarrier in pharmacological arena together with an excellent tumor-suppressing response.

Funder

Tehran University of Medical Sciences and Health Services

Publisher

Hindawi Limited

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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