Title of article
Evaluation of anti-metastatic potential of Cisplatin polymeric nanocarriers on B16F10 melanoma cells
Author/Authors
Shrikhande, Shruti S C.U. Shah College of Pharmacy - S.N.D.T. Women’s University, Santacruz (W), Mumbai 400049, India , Jain, Darshana S C.U. Shah College of Pharmacy - S.N.D.T. Women’s University, Santacruz (W), Mumbai 400049, India , Athawale, Rajani B C.U. Shah College of Pharmacy - S.N.D.T. Women’s University, Santacruz (W), Mumbai 400049, India , Bajaj, Amrita N SVKM’s Dr. Bhanuben Nanavati College of Pharmacy - V.M. Road, Vile Parle (W), Mumbai 400056, India , Goel, Peeyush Gude Lab, Cancer Research Institute, Advanced Centre for Treatment Research and Education in Cancer, Tata Memorial Centre, Kharghar, Navi Mumbai 410210, India , Kamran, Zahid Gude Lab, Cancer Research Institute, Advanced Centre for Treatment Research and Education in Cancer, Tata Memorial Centre, Kharghar, Navi Mumbai 410210, India , Nikam, Yuvraj Gude Lab, Cancer Research Institute, Advanced Centre for Treatment Research and Education in Cancer, Tata Memorial Centre, Kharghar, Navi Mumbai 410210, India , Gude, Rajiv Gude Lab - Cancer Research Institute - Advanced Centre for Treatment Research and Education in Cancer - Tata Memorial Centre - Kharghar, Navi Mumbai 410210, India
Pages
11
From page
341
To page
351
Abstract
Nanoparticles are being increasingly used in the field of cancer treatment due to their unique properties and advantages. The aim of the present research work was to prepare and characterize a polymeric albumin nanosystem for Cisplatin and evaluate its in-vitro efficacy against B16F10 melanoma. The developed nanoparticles were almost spherical in shape with a particle size in the range of 150–300 nm, low polydispersity values and about 80% drug entrapment efficiency. Albumin nanocarriers sustained the release of Cisplatin for more than 48 h, suggesting the reduction in dosing schedule for this drug. The results from in-vitro cell line studies indicated the dose dependent cytotoxic potential of drug loaded albumin nanoparticles, their potential to inhibit cell proliferation and induce morphological changes. In addition, these nanoparticles exhibited superiority to Cisplatin in hampering the cell migration. Developed nanoparticles caused cell cycle arrest along with time and concentration dependent cellular uptake in B16F10 cell line. These results signify that the prepared Cisplatin albumin nanoparticles could serve as a promising approach for B16F10 melanoma treatment.
Keywords
Cisplatin , Human serum albumin , B16F10 melanoma , Nanoparticles
Journal title
Astroparticle Physics
Serial Year
2015
Record number
2422714
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