微球
乙醇酸
粒径
化学
乳酸
剂型
药物输送
PLGA公司
色谱法
生物医学工程
化学工程
核化学
材料科学
有机化学
生物化学
体外
医学
细菌
物理化学
工程类
生物
遗传学
作者
Ngo Giao Thong,B. Ha,Bui Thi Thuong,Nguyễn Thanh Hải,Thi Hai Yen Tran
标识
DOI:10.1080/03639045.2024.2433621
摘要
Objective Poly(lactic-co-glycolic acid) microsphere containing leuprolide acetate - an extended-release drug delivery system whose characteristics (i.e. loading capacity, particle size and initial burst phase) depend on processing parameters.Methods Microspheres were prepared by water/oil/water double-emulsion solvent evaporation method; drug content in microspheres was determined by high-performance liquid chromatography (HPLC); peptide concentration in the release medium was measured by fluorescence spectrometer; particle size and particle size distribution were measured by laser diffraction method; interaction between poly(lactic-co-glycolic acid) (PLGA) and leuprolide acetate (LA) was determined by differential scanning calorimetry (DSC) and Fourier-transform infrared spectroscopy (FTIR).Results DSC curves and assay results proved LA adsorption ability of PLGA film. FTIR spectra proved ionic interactions between positive charged LA molecules and negative charged PLGA chains in phosphate buffer pH 7.4. Ten processing parameters including LA concentration (mg/mL), PLGA concentration (mg/mL), W1/O ratio (v/v), the first homogenization time (min), the first homogenization speed (rpm), O/W2 ratio (v/v), PVA concentration of W2 phase (mg/ml), the second homogenization time (s), the volume of diluted solution (ml) and nitrogen aeration time (min) have impacts on loading capacity, particle size and initial burst phase of microspheres. The release exponent (n) of Korsmeyer-Peppas model was 0.3571 (lower than 0.43), indicating that Fickian diffusion manipulated release kinetics of initial burst phase.Conclusions Processing parameter modification contributes to small microspheres with high loading capacity and controlled initial burst phase.
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