Dripping pill is a dosage form of solid dispersion.
滴丸制剂是一种固体分散体。
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 Etodolac solid dispersion can significantly increase the dissolution rate.
结论依托度酸固体分散体能显著提高依托度酸的溶出速率。
Results: The in vitro dissolution rates of ISDN solid dispersion were faster than ISDN.
结果：固体分散体能加快药物的溶出速率，最佳比例为1∶7。
The present invention relates to a tanshinone solid dispersion and its preparation method.
本发明提供了一种丹参酮固体分散物及其制备方法。
Preparation methods had little effect on the dissolution rates of daidzein solid dispersion.
不同的固体分散体制备方法对药物的溶出度影响不大。
The results of DSC and PXRD showed that the quercetin in solid dispersion was amorphous form.
热差分析及粉末X衍射结果表明固体分散体中槲皮素呈非结晶形式；
RESULTS: X-ray diffraction methods showed that FD was numerous crystals existing in the solid dispersion.
结果：X射线衍射实验表明，此固态分散体中fd为无定型、无结晶。
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。
Conclusion The sample of Galactosylglucose and Gliclazide can form solid dispersion by high speed grinding.
结论乳糖和格列齐特一定比例下经高速研磨混合的样品形成了共熔体；
The dissolution of the solid dispersion was influenced by carrier ratio, surfactant ratio and dissolution media.
载体的用量、概况活性剂的用量和溶出介质对药物溶出有必然影响。
Aim In order to increase bioavailability of Artemisinin'S dosage form, solid dispersion of Artemisinin was prepared.
目的：研制青蒿素缓释固体分散物，提高其制剂的生物利用度。
Results:Acetaminophen combined with PEG 6000 by hydrogen bond, and acetaminophen was dispersed in solid dispersion.
结果：对乙酰氨基酚与PEG 6000之间存在氢键效应，对乙酰氨基酚高度分散在PEG 6000中。
Fenofibrate solid dispersion tablets were prepared by solvent melting method using PEG4000 and sodium lauryl sulfate.
PEG4000十烷硫酸钠体，溶剂-熔融制备非诺贝特固体散体，再适辅混合压片制非诺贝特固体散片。
Method: Bomeolum Syntheticum and PEG 6000 mixing preparative solid dispersion and packed capsules, toxicity was tested.
方法：将冰片用水溶性辅料聚乙二醇6000制成固体分散体，并填装入胶囊，进行毒理试验。
It is indicated that the solubility of Nisoldipine capsule is improved by the utilization of solid dispersion technology.
结果证明，采用固体分散技术能提高尼索地平的体外溶出度。
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。
Droppills were made by solid dispersion technology with the bases of PEG4000 and PEG6000, which has established the optimum moulding craft.
采用固体分散技术以聚乙二醇4000和聚乙二醇6000作为基质，甲基硅油作为冷却剂优化了滴丸成型工艺。
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 The solid dispersion method was adopted to enhance the dissolution rate of nifedipine (NFDP) which is a poorly water-soluble drug.
目的采用制剂技术提高难溶性药物硝苯地平体外溶出速率。
Conclusion: Raman spectrometry which is fast, direct and non-destructive is an ideal method in examining the dispersivity of solid dispersion.
结论：拉曼光谱法快速、直接、对样品无损伤，是一种新的理想的检查固体分散体分散性的方法。
Objective To prepare adefovir dipivoxil solid dispersion from poorly-soluble adefovir dipivoxil so as to improve its dissolution rate in vitro.
目的 将难溶性药物阿德福韦酯制备成固体分散体，以增加体外溶出度。
Conclusion: Raman spectrometry which is fast, direct and non-destructive is an ideal method for examining the dispersivity of solid dispersion.
结论：拉曼光谱法快速、直接、对样品无损伤，是一种新的理想的检查固体分散体分散性的方法。
It is prepared by supercritical extraction, flocculating and alcohol settling cyclodextrin investing and solid dispersion preparation technique.
该制剂的制备采用了超临界提取及絮凝醇沉的工艺及环糊精包埋与固体分散体制剂技术。
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。
Methods: the solid dispersion was prepared by solvent method. The solubility, the dissolution rate and the derivative thermogravimetry (DTG) were determined.
方法：采用溶剂法制备固体分散体，进行溶解度、溶出速率测定，导数热重分析(DTG)。
The solid dispersion technology was employed in research and development of Nisoldipine capsule. Further more, the dissolution rate was detected upon the capsule.
采用固体分散技术研究和制备了尼索地平胶囊，对其进行了溶出度测定。
The solid dispersion technology was employed in research and development of Nisoldipine capsule. Further more, the dissolution rate was detected upon the capsule.
采用固体分散技术研究和制备了尼索地平胶囊，对其进行了溶出度测定。
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