许多方法可用于促进药物的经皮吸收。
Many approaches have been used to promote the drug percutaneous absorption.
目的研究利多卡因凝胶的经皮吸收动力学以及药效学。
Aim To study the cutaneous permeation kinetics and pharmacodynamics of lidocaine gel.
目的：介绍组织工程化皮肤在药物经皮吸收研究中的应用。
Objective: To introduce the use of tissue engineering skin in percutaneous drug absorption.
目的研究双氯芬酸钾(DP)脂质体制剂的制备及体外的经皮吸收特点。
Objective to study the preparation of topical liposomal diclofenac potassium (DP) formulation and the percutaneous absorption in vitro.
本发明提供一种含有抑制在使用部位发生液体流下的经皮吸收药物的气雾剂。
The invention provides an aerosol containing penetration drug preventing fluid flowing down at a use location.
结论载药脂质体凝胶剂可显著促进药物经皮吸收，为经皮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.
目的研制格列美脲凝胶骨架控释贴剂，并评价其经皮吸收对正常大鼠的降血糖作用。
OBJECTIVE To prepare glimepiride gel-matrix controlled-release patch and to investigate its antihyperglycemic effects in normal rats after transdermal absorption.
研究氧化型染发剂主要成分对苯二胺（PPD）氧化产物经皮吸收后对小鼠的亚慢性毒作用。
To study the subchronic toxicity to mice caused by the oxidized product of paraphenylenediamine(PPD).
该经皮吸收制剂具有使用方便、安全、有效、涂布性好、无刺激性和无中枢性副作用的优点。
The preparation of the invention has the advantages of convenient use, safety, high effectiveness, good spreading property and no irritation and nerve central side effect.
相比较，经皮吸收雌激素组中，胰岛素抵抗相关参数并无明显改变，但血糖-胰岛素抵抗比率下降。
In contrast, no significant changes in insulin resistance parameters were observed after transdermal estrogen, except for a decrease in the glucose-insulin resistance ratio.
无毒而高溶血活性的烷基糖苷可能用于制药和化妆品工业改变药物动力学过程和提高有效物的经皮吸收。
Alkyl glucoside without poison and with high haemolysis active can be used to change the dynamics process of effective matter and raise the skin absorption in the medicine and cosmetic industry.
含有精油作为活性成分的睡眠诱导物用组合物，含有该组合物的经皮吸收型睡眠诱导物，以及它们的制备方法。
Composition for inducing sleep comprising essential oils as active ingredients, a percutaneous pharmaceutical agent comprising thereof, and a process for producing thereof.
物质经皮作用全过程：经皮渗透、皮肤吸收、在作用部位积聚。
The process of dermal delivery includes penetration, skin absorption, and accumulation in the action site.
结论：1,2 -丙二醇，月桂氮卓芯酮—胰岛素传递体经皮给药系统可进一步提高胰岛素传递体的透皮吸收效率，降低血糖。
CONCLUSION Transfersulin system with azone and 1, 2-propanediol can improve the penetration efficiency on mice skin and eliminate the blood glucose.
经皮给药制剂是一种有着广阔市场前景的给药途径，但皮肤使多数药物难以渗透吸收。
Transdermal drug delivery systems (TDDS) have broad market prospects. However, transdermal delivery is limited by the inability of the large majority of drugs to cross skin.
结论胰岛素经皮电渗较胰岛素皮下注射给药吸收速度慢，两种给药方法胰岛素的消除过程相近。
CONCLUSION the absorption rate in the subcutaneous injection group was faster than the three groups of transdermal delivery, but the elimination was the same in all the groups.
结论胰岛素经皮电渗较胰岛素皮下注射给药吸收速度慢，两种给药方法胰岛素的消除过程相近。
CONCLUSION the absorption rate in the subcutaneous injection group was faster than the three groups of transdermal delivery, but the elimination was the same in all the groups.
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