International Journal of Pharmaceutical Investigation, 2013, 3, 3, 119-125.
DOI: 10.4103/2230-973X.119212
Published: October 2013
Type: Original Article
Authors:
Jacob Shiny
Department of Pharmaceutics, Mother Teresa College of Pharmacy, Osmania University, Hanamkonda, Warangal, India.
Thadkapally Ramchander
Department of Pharmaceutics, Mother Teresa College of Pharmacy, Osmania University, Hanamkonda, Warangal, India.
Puchchakayala Goverdhan
Department of Pharmacology, Vaagdevi College of Pharmacy Kakatiya University, Hanamkonda, Warangal, India.
Mohammad Habibuddin
Alliance Institute of Advanced Pharmaceutical and Health Sciences, Jawaharlal Nehru Technical University Hyderabad, Ameerpet, Hyderabad, Andhra Pradesh, India.
Jithan Venkata Aukunuru
Department of Pharmaceutics, Mother Teresa College of Pharmacy, Osmania University, Hanamkonda, Warangal, India.
ABSTRACT
Objective: The objective of this study was to develop a novel 1 month depot paclitaxel (PTX) microspheres that give a sustained and complete drug release. Materials and Methods: PTX loaded microspheres were prepared by o/w emulsion solvent evaporation technique using the blends of poly(lactic-co-glycolic acid) (PLGA) 75/25, polycaprolactone 14,000 and polycaprolactone 80,000. Fourier transform infrared spectroscopy was used to investigate drug excipient compatibility. Compatible blends were used to prepare F1-F6 microspheres, the process was characterised and the optimum formulation was selected based on the release. Optimised formulation was characterised for solid state of the drug using the differential scanning calorimetry (DSC) studies, surface morphology using the scanning electron microscopy (SEM), in vivo drug release, in vitro in vivo correlation (IVIVC) and anticancer activity. Anticancer activity of release medium was determined using the cell viability assay in Michigan Cancer Foundation (MCF-7) cell line. Results: Blend of PLGA with polycaprolactone (Mwt 14,000) at a ratio of 1:1 (F5) resulted in complete release of the drug in a time frame of 30 days. F5 was considered as the optimised formulation. Incomplete release of the drug resulted from other formulations. The surface of the optimised formulation was smooth and the drug changed its solid state upon fabrication. The formulation also resulted in 1-month drug release in vivo. The released drug from F5 demonstrated anticancer activity for 1-month. Cell viability was reduced drastically with the release medium from F5 formulation. A 100% IVIVC was obtained with F5 formulation suggesting the authenticity of in vitro release, in vivo release and the use of the formulation in breast cancer. Conclusions: From our study, it was concluded that with careful selection of different polymers and their combinations, PTX 1 month depot formulation with 100% drug release and that can be used in breast cancer was developed.
Keywords: Blends, Complete release, Microspheres, Paclitaxel, Polycaprolactone, Polylactide-co-glycolide.