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- epirubicin glucuronide 表柔比星葡糖苷酸
- Methods The cell line transfected with E1A gene was treated by Epirubicin,Taxotere and 5-fluorouracil respectively. 方法通过PEI-Fe3O4纳米粒介导将E1A基因导入人乳腺癌细胞系MCF-7,经G418筛选获得稳定表达E1A的转染细胞(MCF-7-E1A)。
- Lee J S,Kim H J.A new anti-HIV:flavonoid glucuronide from Chrysanthemum morifolium[J].Planta Med,2003,69(9):859. 徐文斌;郭巧生;李彦农;等.;药用菊花不同栽培类型内在质量的比较研究[J]
- Urine pregnanediol 3 glucuronide (PdG) and follicular stimulating hormone(FSH) were measured by enzyme immunoassay(EIA). 酶免疫分析法测定尿样中的孕二醇 - 3-葡萄糖苷酸 (Pd G)和卵泡刺激素(FSH)。
- The standard dose intensity of epirubicin was defined as 20 mg/m2,the dose was 60mg/m2 given every three weeks. Efficacy and toxicity was evaluated. 表阿霉素按标准剂量每3周60mg/m2,剂量强度为20mg/m2,评估其客观疗效及毒副作用。
- With regard to tumor progression, BCG was also statistically superior to epirubicin (Peto OR=1.70, 95%CI=[1.16, 2.49], P=0.006). 在预防疾病进展方面;卡介苗同样优于表柔比星(PetoOR=1.;70;95%25CI=[1
- In the progesterone inactivated in the liver, into a surrogate glycol with the glucuronide by the combination of urine and feces from the bile. 体内的孕激素在肝脏中灭活，转变为孕二醇再与葡萄糖醛酸结合后由尿和胆汁随粪便排出。
- Objective To evaluate intravesical epirubicin instillation for preventing the recurrence of superficial bladder tumors after surgical management. 目的探讨表阿霉素膀胱灌注防治浅表性膀胱癌术后复发的疗效。
- Objectives:To study the efficiency and safety of instillation with epirubicin(EPI) to prevent) postoperative recurrence of superficial bladdercancer. 为了观察法玛新膀胱灌洗预防浅表性膀胱癌术后复发临床疗效。
- Patients receied a maximum of four treatment cycles.These consisted of epirubicin on day 1 and cisplatin on days 1 to 5 eery 3 weeks. 患者接受了最大量的四种循环治疗模式的治疗，其中包括每三周的第一天的表柔比星和第一天到第五天的顺铂。
- The pretreatment with Phe accelerated the metabolism of plasma Ace in mice,but the effect was unrelated to the conjunction with glucuronide and sulfate. Phe预处理明显加快小鼠血浆Ace消除，但该作用与葡萄糖醛酸和硫酸结合代谢反应无关。
- Method: To determine the DPPH free radical scavenging activity and assay of four bioactive components: baicalin, baicalein, wogonin and wogonin 7 O glucuronide by HPLC. 方法:测定清除DPPH自由基活性,并以HPLC法测定黄芩苷、黄芩素、汉黄芩苷和汉黄芩素的含量。
- Abstract ABSTRACT:Objective To evaluate the effect of combination of eicosapentaenoic acid (EPA) and epirubicin(EPI) on the human gastric carcinoma cell MGC-803 in vitro. 摘要 摘要：目的 评估二十碳五烯酸（EPA）联合表阿霉素（EPI）对人胃癌细胞株MGC-803的作用。
- Purpose: To study the short-term efficacy and toxicity of the neoajuvant chemotherapy with epirubicin (EPI) plus paclitaxel( TAX) in treatment of patients with breast cancer. 目的:研究表柔比星加紫杉醇新辅助化疗方案治疗乳腺癌的近期疗效及毒副反应。
- Epirubicin (EPI) is a broad-spectrum antitumor antibiotic drug.To reduce the amount of administration and side effects, EPI loaded nanoparticles were prepared by dialysis. 表阿霉素(EPI)是一种广谱的抗肿瘤抗生素类药物,临床上主要剂型为注射用表阿霉素冻干粉。
- Objective To evaluate the treatment of non-Hodgkin s lymphoma with combined regimen containing epirubicin as the main drug and to find an effective regimen with low toxicity. 目的评估表柔比星为主的联合方案治疗非霍奇金淋巴瘤的疗效。
- Objective:To observe the efficacy and toxicity of domestic epirubicin in treatment of non Hodgkin's lymphoma,breast cancer,and non small cell lung cancer. 目的:观察国产表柔比星为主的联合化疗方案治疗非霍奇金淋巴瘤、乳腺癌、非小细胞肺癌的疗效和不良反应。
- The test usually employed for testosterone abuse relies on measuring the ratio of two chemicals found in the urine: testosterone glucuronide (TG) and epitestosterone glucuronide (EG). 针对睾酮使用的检测通常是基于测量尿样中所发现的两种化学成分的比例，即睾酮葡糖苷酸（TG）和表睾酮葡糖苷酸（EG）的比例。
- On celline Aspc-1, the interactions between 5-fluorouracil and epirubicin ,cisplatin and epirubicin were both sligh antagonistic, which of5-fluorouracil and cisplatin was related with the drugs concentration but it was antagonistic at most concentration. 对细胞株ASpC一1，5一FU和DDP合用时的相互作用与药物浓度有关，但在大多数浓度下表现为拮抗作用，5一FU和E一ADM、DDP和E一ADM合用时在不同浓度均表现为轻度拮抗作用。
- Human breast carcinoma cells transfected by E1A gene was remarkably more sensitive to Epirubicin and Taxotere,but not sensititive to 5-flourouracil and sensitivity was increased by 11 times and 15 times compared with that of MCF-7 and MCF-7-vect cells. 转染E1A基因的人乳腺癌细胞(MCF-7-E1A)对表阿霉素和泰素帝的敏感性显著增加,与MCF-7和MCF-7-vect细胞系比较,MCF-7-E1A细胞对表阿霉素和泰素帝的敏感性增加11倍和15倍; 对5-氟尿嘧啶的增敏作用不明显。
