• 采用篮法研究体外释放特征

    Its release characteristics were studied by rotating basket.

    youdao

  • 结果显示体外释放缓慢

    The results showed release in vitro was slow.

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  • 填充胶囊制剂比较体外释放行为

    After filling capsules, compare the release behavior in vitro with that of the reference preparation.

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  • 结果直接反映微球体外释放情况。

    Results: Immediate release method can reflect in vitro release of micro-spheres.

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  • 目的研究阿昔洛韦眼用凝胶体外释放特性

    OBJECTIVE:To study the drug-releasing characteristics of acyclovir eye gel in vitro.

    youdao

  • 目的建立甲氨缓释植入剂体外释放方法

    Objective: To establish the in vitro release method of the sustained-release implant of methotrexate.

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  • 目的制备胸腺五肽微球体外释放进行考察

    OBJECTIVE To prepare thymopentin microspheres and investigate the drug release in vitro.

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  • 药物体外释放渗透受到多种处方因素的调节。

    The drug release and permeation were observed to be dependent on some factors.

    youdao

  • 黏附体外释放两个指标筛选优化处方

    The formulation was optimized using adhesive force and in vitro release as two evaluation parameters.

    youdao

  • 目的测定硝酸甘油贴膜含量均匀度体外释放

    Objective To determine the content uniformity and controlled release characteristics of transdermal nitroglycerin in vitro.

    youdao

  • 一级动力学模型对微球的体外释放情况拟合精度高。

    The first order dynamic model could describe the release process in vitro perfectly.

    youdao

  • 目的研究自制盐酸左旋沙丁胺醇缓释片体外释放度。

    Objective To study the in vitro dissolution rate of levalbuterol hydrochloride sustained released tablets.

    youdao

  • 结果:香荷药体外释放行为符合一级动力学方程

    RESULTS Releasing in vitro of the strip conforms to first order kinetics equation.

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  • 目的考察连巴布膏的体外释放透皮行为和规律。

    Objective: To investigate the regularity of Yulian Cataplasm in vitro release and transdermal behaviors.

    youdao

  • 目的考察硫酸长春新碱脂质体体外释放度及其药效

    Objective To investigate the release rate and pharmacodynamics in vitro of of vincristine sulfate liposomes.

    youdao

  • 目的制备美沙拉嗪缓释片剂评价体外释放特性

    OBJECTIVE: To prepare sustained release tablets and evaluate its drug release property.

    youdao

  • 药物树脂制备体外释放缓释包衣都进行了研究

    The research work was composed of preparation and releasing and coating.

    youdao

  • 结论方法用于甲氨蝶呤植入剂的体外释放测试。

    Conclusion: the dissolution method may be used to assess the drug delivery in vitro of methotrexate implants.

    youdao

  • 前言:目的:研究盐酸氨溴索渗透控释片体外释放度。

    Objective: To study the in vitro release rate of ambroxol HCl osmotic pump controlled release tablets.

    youdao

  • 前言:目的:建立一种适用于长效药物体外释放方法

    Objective: To establish a novel release method of sustained-release medications in vitro.

    youdao

  • 目的制备葛根素肠溶纳米粒体外释放度进行考察。

    Aim To prepare puerarin enteric nanoparticles and investigate their release rate in vitro.

    youdao

  • 目的评价醋黄酮缓释片的缓释效果并考察其体外释放规律

    OBJECTIVE To prepare sustained-release Hippophae rhamnoides(TFH) tablet and evaluate the rule of drug release property.

    youdao

  • 目的考察麝香保p H依赖型梯度药微丸体外释放度。

    Object To investigate the release of pH dependent gradient releasing heart protecting musk pellets (GRHPMP) in vitro.

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  • 目的探讨因素他克莫温度敏感眼用凝胶体外释放影响。

    Objective to study the factors that influence the release of tacrolimus from the thermosensitive ophthalmic gel.

    youdao

  • 体外释放试验结果表明胶乳分散体用于缓释制剂的包衣。

    The results showed that this colloidal aqueous dispersions could be used to prepare sustained release formulation.

    youdao

  • 目的研制维生素c微囊并制成缓释片剂,评价体外释放特性。

    OBJECTIVE To prepare vitamin C sustained-release tablets and determine their in vitro release rate.

    youdao

  • 目的制备醋酸地塞米松凝胶剂考察质量体外释放特征

    Objective: To prepare the dexamethasone acetate gel and investigate its quality and the character of its release in vitro.

    youdao

  • 本文简要介绍了几种控释骨架药物体外释放行为评价方法

    A few of evaluation methods for drug release in vitro of sustained-controlled matrix tablets were introduced in this review.

    youdao

  • 结果表明甲纤维素卡波对阻滞胶囊体外释放影响较大

    The results showed that the amount of HPMC and Carbomer had remarkable effects on the in vitro release of capsules.

    youdao

  • 结论黄酮缓释片缓释效果显著,体外释放符合布尔分布模型。

    CONCLUSION The TFH tablet has sustained release property in vitro. The drug release pattern is in accord with Weibull distribution.

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