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- Solid dispersion is able to release rapidly as an ameliorated technic. 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。
- Objective To optimize the method of preparing Dragon's blood solid dispersion . 目的确定制备龙血竭固体分散体的最佳方法。
- 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;
- Abstract: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。
- Objective To prepare the etodolac solid dispersion for enhancing its dissolution in vitro. 目的 制备依托度酸固体分散体,以提高依托度酸的溶出度。
- Objective To prepare apigenin (AP) solid dispersion and measure its dissolution in vitro. 目的 制备芹菜素固体分散体,并检测其体外溶出度。
- Conclusion The nifedipine-PEG solid dispersion could accelerate the in vitro drug dissolution. 结论 硝苯地平PEG固体分散体能加快药物的体外溶出速率。
- AIM Preparing the solid dispersion of anethole trithione so as to increase its solubility and dissolution rate. 目的制备茴三硫固体分散体,提高其溶解度和溶出速率。
- Objective:To improve the solubility and in vitro dissolution of isosorbide dinitrate(ISDN) solid dispersion. 目的:采用固体分散技术,提高硝酸异山梨酯在水中的溶解度和体外溶出速率。
- Conclusion The etodolac-PEG solid dispersion could enhance the drug dissolution in vitro. 结论 依托度酸PEG固体分散体能提高药物的体外溶出度。
- 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。
- Methods: The sulfamethoxazole solid dispersion was prepared.The dissolutions of the solid dispersion were detected. 方法:以固体分散技术制备磺胺甲恶唑固体分散体,并测定其体外溶出度。
- Aim Solid dispersion method was used to increase the solubility and dissolution rates of norfloxacin. 目的利用固体分散体技术,增加诺氟沙星的溶解度和溶出度。
- OBJECTIVE To study the formation and solubilization mechanism of cefuroxime axetil solid dispersion. 目的探讨头孢呋辛酯-聚维酮固态分散体形成和改善溶出的机制。
- OBJECTIVE To prepare nitrendipine solid dispersion using solvent evaporation-deposition method. 目的:采用溶剂蒸发-沉积法制备尼群地平固体分散体。
- OBJECTIVE To prepare vinpocetine solid dispersion and improve the dissolution of vinpocetine. 目的:制备长春西汀固体分散体,提高其溶出速度和程度。
- Abstract: OBJECTIVE To study the formation and solubilization mechanism of cefuroxime axetil solid dispersion. 摘 要: 目的 探讨头孢呋辛酯-聚维酮固态分散体形成和改善溶出的机制。
- Objective To investigate the stability of Nitrendipine solid dispersion pellets. 目的考察尼群地平固体分散体微丸的稳定性。
- Compared with the pure drug, the solubilities of HPMC-cisapride solid dispersion are increased by 239.4% in SGF, 132.6% in water, and 117.9% in SIF. 与西沙必利原料药相比; 固体分散体中药物在人工胃液、水和人工肠液中的溶解度分别提高了239.;4%25、132
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