solid dispersion发音

意思翻译

固态分散体

相似词语短语

solid───n.固体；立方体；n.(Solid)人名；(瑞典)索利德；adj.固体的；可靠的；立体的；结实的；一致的

dispersion───n.散布；[统计][数]离差；驱散

friable solid───易碎固体

dispersion relation───[物][核]色散关系；分散关系；频散关系

dispersion interaction───弥散相互作用；弥散相互酌

dispersion parameter───[冶]分散度参数

zet solid───凝固

platonic solid───柏拉图立体；正多面体；柏拉图立体; 正多面体

solid color───n.纯色；单色，纯色

双语使用场景

Dripping pill is a dosage form of solid dispersion.───滴丸制剂是一种固体分散体。

CONCLUSION Itraconazole solid dispersion can significantly increase it's solubility and dissolution rate.───结论：伊曲康唑固体分散体能明显提高伊曲康唑的溶解度及体外溶出速率。

Result: solid dispersion method can effective promoting the dissolution.───结果：该法能很好的促进药物的释放。

CONCLUSION: Ethylcellulose is suitable to be sustained release solid dispersion excipient.───结论：乙基纤维素适合作缓释型固体分散物载体。

Setting up the topic by that, solid dispersion was studied to innovate on its dosage-form.───以此立题，研究索法酮固体分散体，对其剂型进行创新研究。

Methods Etodolac solid dispersion was prepared with PEG as carrier by solvent-fusion method and identified by differential thermal analysis.───方法选用聚乙二醇为载体，采用溶剂-熔融法制备依托度酸固体分散体，通过差热分析对固体分散体进行鉴定。

Objective To prepare vinpocetine( VIN ) solid dispersion(SD) and improve the dissolution profile of vinpocetine.───目的采用固体分散体技术改善长春西汀（VIN）的体外溶出特性。

METHODS Using the orthogonal design, it was prepared nifedipine solid dispersion by melting method, then filling into hard capsule.───方法：熔融法制备硝苯地平固体分散体并灌装于硬胶囊中，采用正交设计试验优化处方。

Results: The results showed that solid dispersion give much higher improvement than physical mixture in the dissolution rate.───结果体外实验结果表明，固体分散体对尼莫地平溶出度的提高大大优于物理混合物。

英语使用场景

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.