Abstract
The purpose of this study was to develop a buccal paclitaxel delivery system using the thermosensitive polymer Pluronic F127 (PF127) and the mucoadhesive polymer polyethylene oxide (PEO). The anticancer agent paclitaxel is usually used to treat ovarian, breast, and non-small-cell lung cancer. To improve its aqueous solubility, paclitaxel was incorporated into an inclusion complex with (2,6-di-O-methyl)-β-cyclodextrin (DMβCD). The formation of the paclitaxel inclusion complex was evaluated using various techniques, including x-ray diffractometry (XRD), Fourier-transform infrared (FT-IR) spectrophotometry, differential scanning calorimetry (DSC), and scanning electron microscopy (SEM). Hydrogels were prepared using a cold method. Concentrations of 18, 20, and 23% (w/v) PF127 were dissolved in distilled water including paclitaxel and stored overnight in a refrigerator at 4°C. PEO was added at concentrations of 0.1, 0.2, 0.4, 0.8, and 1% (w/v). Each formulation included paclitaxel (0.5 mg/mL). The sol-gel transition temperature of the hydrogels was measured using the tube-inverting method. Drug release from the hydrogels was measured using a Franz diffusion cell containing pH 7.4 phosphate-buffered solution (PBS) buffer at 37°C. The cytotoxicity of each formulation was measured using the MTT assay with a human oral cancer cell (KB cell). The sol-gel transition temperature of the hydrogel decreased when PF127 was present and varied according to the presence of mucoadhesive polymers. The in vitro release was sustained and the release rate was slowed by the addition of the mucoadhesive polymer. The cytotoxicity of the blank formulation was low, although the drug-loaded hydrogel showed acceptable cytotoxicity. The results of our study suggest that the combination of a PF 127-based mucoadhesive hydrogel formulation and inclusion complexes improves the in vitro release and cytotoxic effect of paclitaxel.
Highlights
Paclitaxel is one of the most successful anticancer drugs discovered in the past few decades
Paclitaxel is poorly soluble in aqueous liquids due to its highly lipophilic properties [2]
Paclitaxel is solubilized in a mixture of ethanol and Cremophor EL, and causes serious side effects including neurotoxicity, hypersensitivity reactions and nephrotoxicity [3,4]
Summary
Paclitaxel is one of the most successful anticancer drugs discovered in the past few decades. Due to the cavity in this molecule, it is used to form inclusion complexes with many compounds, which prevents the oxidation of oils and volatilization of volatile flavors, and solubilizes insoluble compounds. It is used in the pharmaceutical field to form inclusion complexes with drug molecules to increase their aqueous solubility and stability [12,13], to enhance the water solubility and hydrolytic stability of curcumin [14], to improve photochemical and thermal stability [15], to mask unwanted characteristics, or to reduce side effects
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