结论：A胶囊和B胶囊的溶出速度较快。
CONCLUSION: The dissolution speed of a and B capsules was faster.
目的：制备尼群地平固体分散体，增加其溶解度和溶出速度。
OBJECTIVE To improve the solubility and dissolution of nitrendipine by preparing its solid dispersions.
制备了吲哚美辛肠溶分散片，考察辅料对其崩解时限及溶出速度的影响。
Indomethacin enteric dispersible tablets were prepared, and factors affected disintegration time and dissolution rate were studied.
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。
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替硝唑固体分散体，增加替硝唑溶解度和溶出速度。
OBJECTIVE: to prepare tinidazole solid dispersion using the technology of solid dispersion, and to increase the dissolubility and the dissolution rate of tinidazole.
溶出度试验结果表明微粉化片溶出度达到中国药典普通片质量要求，比进口胶囊剂溶出速度快。
The dissolution test showed that they were accorded with the China Pharmacopia and quicker than that of the imported capsules.
为了适应临床需要，使制剂崩解、溶出速度快、奏效迅速，本实验系统地开展了脑得生分散片的研究。
This study has been done systematically on the extraction, purifying the active component of Naodesheng and preparation, etc.
目的：药物溶出度系指药物从片剂或胶囊等固体制剂或半国体制剂在规定的溶剂中溶出的速度和程度。
Objective: Drug dissolution is rate and degree of dissolution which is from solid dosage forms such as tablets and capsules so on at specified solvent.
氧化铜矿石的浸出过程主要受浸出剂与溶出物在矿石中的渗流与扩散速度的影响。
The process of leaching depends on the seeping and diffusing velocity of leaching agent and resultant.
氧化铜矿石的浸出过程主要受浸出剂与溶出物在矿石中的渗流与扩散速度的影响。
The process of leaching depends on the seeping and diffusing velocity of leaching agent and resultant.
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