• Objective To research relativity of diabetes and C-peptide release test.

    目的研究糖尿病与C -肽释放试验的相关性。

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  • Objective:To establish a hemoglobin release test and to approach its significance.

    目的:建立血红蛋白释放试验,明确方法,探讨其意义。

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  • Objective To study the effect of blood sampling with puncture trocar on insulin and C peptide release test.

    目的探讨套管针采血对胰岛素和C肽测定结果的影响。

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  • The liver function, kidney function, blood fat, insulin release test, serum uric acid and body mass index(BMI)were determined in all cases.

    均查肝功,肾功,血脂,胰岛素释放试验,血尿酸和体重指数(BMI)。

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  • Oral glucose tolerance test and insulin release test were carried out to measure plasma glucose concentrations, serum insulin concentrations and serum FFA levels.

    口服葡萄糖耐量试验和胰岛素释放试验,测定血浆葡萄糖浓度、血清胰岛素浓度、FFA水平。

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  • Conclusion: 131i uptake test can show the ability of I uptake for thyroid only and KCl4 release test can reflect the activity of TPO for thyroxin anabolic process.

    结论:摄131i试验仅表示甲状腺组织的摄取功能,过氯酸钾释放试验反映的是甲状腺激素合成过程中过氧化物酶活性。

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  • FDA clears apheresis platelets collected with certain systems for routine storage and patient transfusion up to 7 days when tested with a microbial detection system release test.

    FDA明确了经过微生物检测系统释放检验后,用于常规储存和病人输血的单采血小板保存时间可增加为七天。

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  • Among hemolysis three tests, the positive rates of direct coombs test, free antibody test and antibody release test were 44%(88/200), 28%(56/200) and 62.5%(125/200) respectively.

    溶血三项试验中直接抗人球蛋白试验阳性88例,阳性率为44%(88/200),血清游离抗体试验阳性56例,阳性率为28%(56/200),抗体释放试验阳性125例,阳性率为62.5%(125/200)。

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  • Methods BALB/c mice were immunized by subcutaneous injection of polypeptides from HCV core region, and the CTL activity of mouse spleen cells was detected by the LDH release test.

    方法将HCV核心区多肽皮下注射免疫BALB/c小鼠,用乳酸脱氢酶释放实验检测小鼠脾细胞CTL活性。

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  • Conclusion: Microcapsules containing drugs prepared by the optimum conditions had shown good reproducibility, process stability, and good sustained action by in vitro release test.

    结论:以最佳工艺条件制备的含药微囊,重复性好,工艺稳定,同时体外释放试验表明,该微囊具有较好的缓释作用。

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  • Methods Ultraviolet spectrophotometry and release test were applied to determine the release of cefixime in cefixime sustained-release tablets under different media and time points.

    方法用紫外分光光度法和释放度试验,考察头孢克肟缓释片在不同释放介质中不同释放时间的累积释放度。

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  • Methods Ultraviolet spectrophotometry and release test were applied to determine the release of cefixime in cefixime sustained-release tablets under different media and time points.

    方法用紫外分光光度法和释放度试验,考察头孢克肟缓释片在不同释放介质中不同释放时间的累积释放度。

    youdao

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