alexa Vitamin E-TPGS Stabilized Lapatinib Nanocrystals: In-vivo Pharmacokinetic And Pharmacodynamic Evaluation
ISSN 2472-1042

Pharmacoeconomics: Open Access
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11th World Congress on Pharmaceutical Sciences and Innovations in Pharma Industry
February 27-28, 2017 Amsterdam, Netherlands

Agrawal Satish, Hafsa Ahmad, Roshan Sikandar, Abhishek Arya and Anil Kumar Dwivedi
Central Drug Research Institute- CSIR, India
Posters & Accepted Abstracts: Pharmacoeconomics
DOI: 10.4172/2472-1042.C1.003
Abstract
Aim: The aim of this study is the development of vitamin E-TPGS stabilized Lapatinib Nanocrystals (LPT-NCs) to improve its anticancer activity. Methods: Nanocrystals were prepared through high pressure homogenization and the optimized formulation was further characterized on the basis of in-vitro and in-vivo evaluations. Results: Optimized formulation had 282.2±9.48 nm average particle size, 0.288±0.006 PDI and 33.63±3.59 mv zeta potential values. Microscopic examination displayed formation of rod shaped nano-sized crystals. DSC thermogram showed that crystallinity of Lapatinib was retained in formulation. Formulation significantly enhanced the saturation solubility of LPT in water. LPT-NCs were found to be stable during 4 months study period when stored at 4ºC. In-vivo pharmacokinetics study comprising of crude lapatinib suspension and LPT-NCs by oral route performed on healthy adult female Sprauge-Dawley rats demonstrated significant enhancement in AUC, Cmax and reduction in clearance of LPT in LPT-NCs treated group. Tumor regression study performed in 4T1 cells induced syngeneic breast cancer female BALB/c mice revealed significant reduction in tumor burden and overall improvement in survival in LPT-NCs treated group compared to crude Lapatinib suspension. Conclusion: LPT-NCs significantly enhanced anticancer activity of LPT by improving its oral bioavailability possibly due to solubility enhancement and P-gp inhibition.
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