solid dispersion的例句大全

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。

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Method: The solid dispersion method was used , dissolution was determined in vitro.

方法: 采用固体分散体制备头孢克肟口含片, 测定其体外溶出度进行评价.

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the processes, characteristics, influence factors and applications of new technology for solid dispersion preparation are introduced.

介绍了固体分散法制剂工艺的类别，及其特点、过程、影响因素和应用等。

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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。

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OBJECTIVE To prepare etoposide solid dispersion to enhance the dissolution rate.

目的制备依托泊苷固体分散体,改善依托泊苷的溶出度.

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Dissolution rate of Aciclovir solid dispersion and its relative bioavailability in human

固体分散无环鸟苷胶囊剂溶出度及人体内生物利用度

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preliminary investigation on interphase mass transfer in agitated liquid-liquid-solid dispersion

搅拌槽中液-液-固三相传质的实验研究

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Study on the solid dispersion of ACV preparation

无环鸟苷固体分散体的研究

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differential scanning calorimetry indicated that hyperin was existed in amorphous form in solid dispersion.

固体分散体差示热扫描结果表明，金丝桃苷在固体分散体里以非晶型形式存在。

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Objective: To enhance the dissolution rate of Curcumin ( Cur) by solid dispersion technique.

目的：利用固体分散技术提高难溶性药物姜黄素的体外溶出速率。

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study on dissolution test method of silybin solid dispersion capsules

水飞蓟宾卵磷脂分散体胶囊剂溶出度测定方法的研究

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Conclusion Solid dispersion is able to release rapidly as an ameliorated technic.

结论固体分散体有速释作用,可考虑用固体分散技术改进降酶灵胶囊的制备工艺.

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CONCLUSION: The types of carriers and drug-carrier ratio had great effect on the characteristics of in vitro dissolution and enthalpy change of lornoxicam solid dispersion.

结论：载体类型及药物载体比例影响氯诺昔康固体分散体的体外溶出特性及热焓变化。

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results solid dispersion dissolutions of pvp and peg at 45 min were 9.7 and 7.5 times as much as material drug, respectively. characteristic melting peak of cryptotanshinone in dta curve of solid dispersion disappeared.

结果PVP及PEG固体分散体在45min的溶出度分别达到原料药的9.7倍和7.5倍，固体分散体的DTA曲线中隐丹参酮的特征熔融峰消失。

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Studies on formation and solubilizing mechanism of oleanolic acid solid dispersion

齐墩果酸固体分散体形成和增溶机制研究

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preparation and evaluation of nimesulide solid dispersion

尼美舒利固体分散体的制备及其性质考察

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results the oxaprozin-peg 6000 solid dispersion was a simple-lower-eutectic compound. the oxaprozin was dispersed in peg 6000 as micro-crystallite form.

结果：卟恶丙嗪PEG6000固体分散体是一种简单低共熔混合物，卟恶丙嗪以超细结晶状态分散在PEG载体中。

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studies on the absorption kinetics of acemetacin solid dispersion in rats' intestine

阿西美辛固体分散体大鼠在体肠道吸收动力学的研究

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objective to improve in vitro release of acemetacin, the technology of solid dispersion was used and acemetacin was prepared as solid dispersion.

目的：利用固体分散技术制备阿西美辛固体分散体，增加其溶解度和溶出速度。

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Conclusion: Solid dispersion improved the stability and dissolution of compound hawthorn dropping pills.

结论: 复方山楂滴丸固体分散体提高了药物稳定性和溶解性.

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