solid dispersion的意思
solid dispersion中文翻譯:
固態分散體
solid───n.固體;立方體;n.(Solid)人名;(瑞典)索利德;adj.固體的;可靠的;立體的;結實的;一致的
dispersion───n.散布;[統計][數]離差;驅散
friable solid───易碎固體
dispersion relation───[物][核]色散關系;分散關系;頻散關系
dispersion interaction───彌散相互作用;彌散相互酌
dispersion parameter───[冶]分散度參數
zet solid───凝固
platonic solid───柏拉圖立體;正多面體;柏拉圖立體; 正多面體
solid color───n.純色;單色,純色
Dripping pill is a dosage form of solid dispersion.───滴丸制劑是一種固體分散體。
CONCLUSION Itraconazole solid dispersion can significantly increase it's solubility and dissolution rate.───結論:伊曲康唑固體分散體能明顯提高伊曲康唑的溶解度及體外溶出速率。
Result: solid dispersion method can effective promoting the dissolution.───結果:該法能很好的促進藥物的釋放。
CONCLUSION: Ethylcellulose is suitable to be sustained release solid dispersion excipient.───結論:乙基纖維素適合作緩釋型固體分散物載體。
Setting up the topic by that, solid dispersion was studied to innovate on its dosage-form.───以此立題,研究索法酮固體分散體,對其劑型進行創新研究。
Methods Etodolac solid dispersion was prepared with PEG as carrier by solvent-fusion method and identified by differential thermal analysis.───方法選用聚乙二醇為載體,采用溶劑-熔融法制備依托度酸固體分散體,通過差熱分析對固體分散體進行鑒定。
Objective To prepare vinpocetine( VIN ) solid dispersion(SD) and improve the dissolution profile of vinpocetine.───目的采用固體分散體技術改善長春西汀(VIN)的體外溶出特性。
METHODS Using the orthogonal design, it was prepared nifedipine solid dispersion by melting method, then filling into hard capsule.───方法:熔融法制備硝苯地平固體分散體并灌裝于硬膠囊中,采用正交設計試驗優化處方。
Results: The results showed that solid dispersion give much higher improvement than physical mixture in the dissolution rate.───結果體外實驗結果表明,固體分散體對尼莫地平溶出度的提高大大優于物理混合物。
Method: The solid dispersion method was used , dissolution was determined in vitro.
Due to aqueous insolubility of silymarin, the solid dispersion was prepared by the solvent method using PVP K30 as the hydrophilic carrier matrix.
OBJECTIVE To prepare etoposide solid dispersion to enhance the dissolution rate.
Objective To prepare apigenin (AP) solid dispersion and measure its dissolution in vitro.
OBJECTIVE To prepare vinpocetine solid dispersion and improve the dissolution of vinpocetine.
Fenofibrate solid dispersion tablets were prepared by solvent melting method using PEG 4000 and sodium lauryl sulfate.
Conclusion Etodolac solid dispersion can significantly increase the dissolution rate.
AIM Preparing the solid dispersion of anethole trithione so as to increase its solubility and dissolution rate.
Method: Solid dispersion systems of ursolic acid in PVP-K30 or Poloxamer 188 were prepared by co-evaporation of the drug and PVP-K30 or Poloxamer 188 ethanol solution.
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