• 目的研制阿西美辛脂质体凝胶进行评价

    OBJECTIVE To prepare and evaluate a liposome hydrogel acemetacin (ACM).

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  • 目的制备利多卡因脂质体凝胶建立质量控制方法

    OBJECTIVE: to prepare lidocaine liposome gel and to establish its quality control method.

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  • 目的制备含有鬼臼毒素(PPT)的脂质体凝胶比较两者的性能

    Objective to prepare two different liposome gels containing podophyllotoxin (PPT) and compare their pharmaceutical properties.

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  • 释放面积,桨搅拌速度释放介质影响脂质体凝胶溶蚀及药物的释放。

    Drug release rate was significantly influenced by release area, stirring speed of peddles and the sorts of dispersion mediums respectively.

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  • 结论载药脂质体凝胶可显著促进药物吸收,吸收药物的理想载体

    CONCLUSION Liposomal gel has the ability to enhance LDH transcutaneous permeation. It is effective vehicle for transdermal therapeutic drugs.

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  • 目的研究盐酸丁卡因质体以及脂质体凝胶制备方法考察脂质体脂质体凝胶药物释放影响

    OBJECTIVE to study the methods of preparation of hydrochloride tetracaine liposome and liposome gel and to determine the liberation of drug from them.

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  • 目的为了增加洛韦皮肤中的滞留量,提高局部生物利用度制备阿昔洛棕榈酸酯脂质体凝胶剂。

    OBJECTIVE to prepare the acyclovir ACV palmitate liposome gel in order to raise ACV concentration in the skin and enhance the topical bioavailability of ACV.

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  • 方法乙醇注入法制盐酸卡因质体,研法制备脂质体凝胶透析测定盐酸丁卡因脂质体以及脂质体凝胶药物释放

    METHOD Prepare the hydrochloride tetracaine liposome by ethanol injection method, prepare hydrochloride tetracaine liposome gel by mixing method, and determine the liberation of drug by dialysis.

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  • 维生素D2质体可使维生素D2皮肤滞留,而且脂质体凝胶脂质体凝胶剂在皮肤层中维生素D2滞留量多

    The multilamellar vesicles detained a higher amount of vitamin D2 than the unilamillar vesicles in skin. The amount of vitamin D2 in the receiver cell did not increase significantly.

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  • 方法通过均匀实验设计优化利多卡因质体的处方制备工艺,蒸发-超声法制备LDH脂质体,再用卡波普基质制成凝胶剂;

    The LDH liposome was prepared by the reverse-phase evaporation and ultrasound method, the carbopol was added as a support base for the preparation of the liposomeal gel.

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  • 目的考察葡聚糖凝胶法测定质体包封率影响因素。

    OBJECTIVE To determine the trap efficiency of liposomes using Sephadex.

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  • 采用高效凝胶渗透色谱法(HPGPC)测定古糖酯质体封率。

    The encapsulation efficiency of PGS liposomes were determined by high performance gel permeation chromatography (HPGPC).

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  • 目的考察葡聚糖凝胶测定质体包封率影响因素。

    OBJECTIVE To determine the trap efficiency of liposomes using Sephadex. METHOD Tegafur liposomes was used as the model drug.

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  • 目的考察葡聚糖凝胶测定质体包封率影响因素。

    OBJECTIVE To determine the trap efficiency of liposomes using Sephadex. METHOD Tegafur liposomes was used as the model drug.

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