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2,5-二酮-3,6-二(N-富马酰基-4-氨基丁基)哌嗪(FDKP)载胰岛素微球的制备及表征
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作者 杨晨 王祺玥 +1 位作者 涂家生 孙春萌 《药学研究》 CAS 2016年第12期703-708,728,共7页
目的制备并表征载胰岛素的2,5-二酮-3,6-二(N-富马酰基-4-氨基丁基)哌嗪(FDKP)微球。方法以FDKP作为载体,制备载胰岛素微球(FDKP-INS),利用Box-Behnken试验设计对载药微球的载药量及粒径进行筛选。使用扫描电子显微镜(SEM)对微球形态进... 目的制备并表征载胰岛素的2,5-二酮-3,6-二(N-富马酰基-4-氨基丁基)哌嗪(FDKP)微球。方法以FDKP作为载体,制备载胰岛素微球(FDKP-INS),利用Box-Behnken试验设计对载药微球的载药量及粒径进行筛选。使用扫描电子显微镜(SEM)对微球形态进行观察,同时以差示扫描量热法(DSC)考察胰岛素与FDKP间相互作用。结果最优处方工艺条件为:混悬液p H值为4.56,投药比为15.97%(W/W),搅拌时间为2.4 h,在此工艺条件下制备的微球载药量为13.23%,粒径为4.515μm,与预测值接近;显示扫描图谱表明,胰岛素与FDKP间存在相互作用;扫描电子显微镜显示空白FDKP微球外形呈玫瑰花球形状,形态较完整,且表面呈现多孔隙,载药微球表面较平滑,胰岛素填充入空白微球孔隙中。结论经过优化的处方工艺所制得的载胰岛素FDKP微球具有良好的外观性状和较高的载药量。 展开更多
关键词 fdkp 胰岛素 载药微球 BOX-BEHNKEN试验设计 吸附作用
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Formulation optimization and in vitro antibacterial ability investigation of azithromycin loaded FDKP microspheres dry powder inhalation 被引量:2
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作者 Qiyue Wang Liang Ge +4 位作者 Lu Wang Ying Xu Si Miao Guiping Yu Yan Shen 《Chinese Chemical Letters》 SCIE CAS CSCD 2021年第3期1071-1076,共6页
Azithromycin loaded fumaryl diketopiperazine(FDKP)dry powder inhalation was designed and prepared for the treatment of community-acquired pneumonia.The solubility of FDKP and stability of azithromycin solution was inv... Azithromycin loaded fumaryl diketopiperazine(FDKP)dry powder inhalation was designed and prepared for the treatment of community-acquired pneumonia.The solubility of FDKP and stability of azithromycin solution was investigated.Formulation of azithromycin loaded FDKP microparticle was investigated and optimized by the single factor experiment.High-pressure homogenization and spray drying conditions were also optimized to prepare the particles by spray drying azithromycin dissolved FDKP microparticle suspension at pH 4.5.The in vitro antibacterial efficiency and in vitro dispersion performance was also investigated to confirm the antibacterial efficiency,dispersion and deposition behavers.FDKP/azithromycin mass ratio(3:2)was the optimized formulation of azithromycin loaded FDKP microparticle with the maximal drug loading efficiency.High-pressure homogenization and spray drying conditions were also optimized.The in vitro antibacterial results indicated that only with the antibiotic concentration higher than mutant prevention concentration could totally inhibit the reproduction of bacteria.In vitro dispersion performance of azithromycin loaded FDKP microparticles(AZM@FDKP-MPs)also shows remarkable improvement of dispersion and deposition behavers of AZM.AZM@FDKP-MPs dry powder inhalation as a targeting delivery route has better potential for lung infection treatment. 展开更多
关键词 AZITHROMYCIN fdkp Formulation optimization In vitro antibacterial efficiency Streptococcus pneumoniae
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