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作 者:陆瑾 展冠军[2] 郭立玮[3] LU Jin;ZHAN Guanjun;GUO Liwei(Nanjing Dachang Hospital,Nanjing 210048,China;Zhongda Hospital,Southeast University,Nanjing 210009,China;Nanjing University of Chinese Medicine,Nanjing 210023,China)
机构地区:[1]南京市大厂医院,南京210048 [2]东南大学附属中大医院,南京210009 [3]南京中医药大学,南京210023
出 处:《中国现代应用药学》2019年第18期2280-2284,共5页Chinese Journal of Modern Applied Pharmacy
摘 要:目的将α-细辛脑制备成聚乙二醇-聚乳酸-α-细辛脑纳米粒(PEG-PLA-α-细辛脑纳米粒),考察其表面性能及鼻腔给药后的鼻纤毛毒性。方法采用有机溶剂挥发法将α-细辛脑制备成PEG-PLA-α-细辛脑纳米粒。纳米粒度定位仪、透射电镜、差示扫描量热仪及X射线衍射法对PEG-PLA-α-细辛脑纳米粒进行表征;透析法研究PEG-PLA-α-细辛脑体外释放行为;大鼠模型考察PEG-PLA-α-细辛脑纳米粒鼻腔给药后的鼻纤毛毒性。结果PEG-PLA-α-细辛脑纳米粒平均粒径为172.3 nm,PDI指数0.256,载药量10.70%,包封率59.36%;α-细辛脑主要以分子分散的形式存在于PEG-PLA-α-细辛脑纳米粒中;PEG-PLA-α-细辛脑纳米粒中α-细辛脑的体外释放行为符合Ritger-peppas拟合方程;PEG-PLA-α-细辛脑纳米粒鼻腔给药后对鼻纤毛无明显的毒性。结论有机溶剂挥发法制备的PEG-PLA-α-细辛脑纳米粒可用于鼻腔给药。OBJECTIVE To prepareα-asarone into polyethylene glycol-polylactic acid-α-asarone nanoparticles(PEG-PLA-α-asarone nanoparticles),and investigate the surface properties of PEG-PLA-α-asarone nanoparticles and the nasal cilia toxicity after nasal administration.METHODSα-Asarone was prepared into PEG-PLA-α-asarone nanoparticles by organic solvent evaporation method.PEG-PLA-α-asarone nanoparticles were characterized by nano-particle size locator,transmission electron microscope,differential scanning calorimeter and X-ray diffraction method.In vitro release behavior of PEG-PLA-α-asarone nanoparticles was studied by dialysis method.The rat model was used to investigate the nasal cilia toxicity of PEG-PLA-α-asarone nanoparticles after nasal administration.RESULTS The average particle size of PEG-PLA-α-asarone nanoparticles was 172.3 nm,the PDI index was 0.256,the drug loading was 10.70%,and the entrapment efficiency was 59.36%.The characterization results showed thatα-asarone was mainly in the form of molecular dispersion exist in PEG-PLA-α-asarone nanoparticles.In vitro release behavior ofα-asarone in PEG-PLA-α-asarone nanoparticles was in accordance with the Ritger-peppas fitting equation.The result of nasal cilia toxicity study showed that PEG-PLA-α-asarone nanoparticles had no apparent toxicity to nasal cilia after nasal administration.CONCLUSION PEG-PLA-α-asarone nanoparticles prepared by volatilization of organic solvents method can be used for nasal administration.
关 键 词:PEG-PLA-α-细辛脑纳米粒 鼻腔给药 表征 鼻纤毛毒性
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