Preparation and characterization of bee venom-loaded PLGA particles for sustained release |
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Authors: | Min-Ho Park Hye-Suk Jun Jong-Woon Jeon Jin-Kyu Park Bong-Joo Lee Guk-Hyun Suh |
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Affiliation: | 1. College of Pharmacy and Institute of Drug Research and Development, Chungnam National University, Daejeon, South Korea;2. Wissen Co, Ltd, Daejeon, South Korea;3. College of Veterinary Medicine, Chonnam National University, Gwangju, South Korea |
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Abstract: | AbstractBee venom-loaded poly(lactic-co-glycolic acid) (PLGA) particles were prepared by double emulsion-solvent evaporation, and characterized for a sustained-release system. Factors such as the type of organic solvent, the amount of bee venom and PLGA, the type of PLGA, the type of polyvinyl alcohol, and the emulsification method were considered. Physicochemical properties, including the encapsulation efficiency, drug loading, particle size, zeta-potential and surface morphology were examined by Fourier transform infrared (FT-IR) spectroscopy, differential scanning calorimetry (DSC), and X-ray diffraction (XRD). The size of the bee venom-loaded PLGA particles was 500?nm (measured using sonication). Zeta-potentials of the bee venom-loaded PLGA particles were negative owing to the PLGA. FT-IR results demonstrated that the bee venom was completely encapsulated in the PLGA particles, indicated by the disappearance of the amine and amide peaks. In addition, sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) analysis indicated that the bee venom in the bee venom-loaded PLGA particles was intact. In vitro release of the bee venom from the bee venom-loaded PLGA particles showed a sustained-release profile over 1 month. Bee venom-loaded PLGA particles can help improve patients’ quality of life by reducing the number of injections required. |
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Keywords: | Bee venom PLGA sustained release microparticle |
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