首页> 外文期刊>Chemical and Pharmaceutical Bulletin >Deposits from Creams Containing 20% (w/w) Urea and Suppression of Crystallization (Part 2): Novel Analytical Methods of Urea Accumulated in the Stratum Corneum by Tape stripping and Colorimetry
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Deposits from Creams Containing 20% (w/w) Urea and Suppression of Crystallization (Part 2): Novel Analytical Methods of Urea Accumulated in the Stratum Corneum by Tape stripping and Colorimetry

机译:含20%(w / w)尿素的乳膏中的沉淀物和结晶的抑制作用(第2部分):通过剥离和比色法测定角质层中尿素的新分析方法

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The transfer of urea from a urea formulation to the stratum corneum varies with the formulation base and form, and impacts the formulation’s therapeutic effect. Consequently, determining the amount of urea transferred is essential for developing efficient formulations. This study assessed a simple method for measuring the amount of urea accumulated in the stratum corneum. Conventional methods rely on labeling urea used in the formulation with radiocarbon (14C) or other radioactive isotopes (RIs), retrieving the transferred urea from the stratum corneum by tape stripping, then quantitating the urea. The handling and use of RIs, however, is subject to legal regulation and can only be performed in sanctioned facilities, so methods employing RIs are neither simple nor convenient. We therefore developed a non-radiolabel method “tape stripping-colorimetry (T-C)” that combines tape stripping with colorimetry (urease–glutamate dehydrogenase (GLDH)) for the quantitative measurement of urea. Urea in the stratum corneum is collected by tape stripping and measured using urease-GLDH, which is commonly used to measure urea nitrogen in blood tests. The results indicate that accurate urea measurement by the T-C method requires the application of 1400?mg (on hairless rats) of a 20% urea solution on a 50?cm2 (5×10?cm) area. Further, we determined the amount of urea accumulated in the stratum corneum using formulations with different urea concentrations, and the time course of urea accumulation from formulations differing in the rate of urea crystallization. We demonstrate that the T-C method is simple and convenient, with no need for 14C or other RIs.
机译:尿素从尿素配方到角质层的转移随配方基础和形式的不同而变化,并影响配方的治疗效果。因此,确定转移的尿素量对于开发有效的配方至关重要。这项研究评估了一种简单的方法来测量角质层中累积的尿素量。常规方法依赖于用放射性碳( 14 C)或其他放射性同位素(RIs)标记制剂中使用的尿素,通过胶带剥离从角质层中回收转移的尿素,然后定量尿素。但是,RI的处理和使用受法律法规的约束,并且只能在受制裁的设施中执行,因此采用RI的方法既不简单也不方便。因此,我们开发了一种非放射性标记方法“胶带剥离比色法(T-C)”,该方法将胶带剥离与比色法(脲酶-谷氨酸脱氢酶(GLDH))结合起来用于尿素的定量测量。通过胶带剥离收集角质层中的尿素,并使用尿素酶-GLDH进行测量,后者通常在血液测试中用于测量尿素氮。结果表明,通过TC方法准确测量尿素需要在50?cm 2 (5×10?cm)的区域上应用1400?mg(无毛大鼠)的20%尿素溶液。 。此外,我们使用不同尿素浓度的配方确定了角质层中尿素的蓄积量,以及不同尿素结晶速率的配方中尿素蓄积的时间过程。我们证明了T-C方法简单方便,不需要 14 C或其他RI。

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