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新型托烷司琼贴剂在大鼠抗癌药物诱导高岭土异食癖模型中的止吐作用。

The antiemetic effect of a novel tropisetron patch in anticancer agents-induced kaolin pica model using rats.

作者信息

Jeong Seung Wei, Cho Joong Woong, Hwang Jun Seok, Song Jin Deog, Shin Sunhee, Jang Ja Young, Hwang Seok-Yeon, Kim Okjin, Kim Jong-Choon, Kim Yun-Bae, Kang Jong-Koo

机构信息

Research and Development Center, Samyang Co. Ltd., Hwaam-dong, Daejeon 305-717, Korea; College of Veterinary Medicine and Research Institute of Veterinary Medicine, Chungbuk National University, Gaeshin-dong, Cheongju 361-763, Korea.

出版信息

Environ Toxicol Pharmacol. 2005 Jul;20(1):167-74. doi: 10.1016/j.etap.2004.12.065. Epub 2005 Feb 16.

Abstract

The efficacy of a novel transdermal patch containing tropisetron, a 5-hydroxytryptamine 3 (5-HT(3)) receptor antagonist, against emesis induced by anticancer agents were evaluated, in comparison with the effect of traditional tropisetron injection, in rats. The antiemetic effects were assessed via the inhibitory activity on the anticancer agent-induced kaolin-consuming behavior, a pica model representing vomiting in emesis-resistant rodents. The tropisetron patch (10mg/patch, 3.5cm(2)) was attached on the shaved back area of rats. Eight h later, each anticancer agent, cisplatin (10mg/kg, i.v.), cyclophosphamide (200mg/kg, i.p.) or doxorubicin (8mg/kg, i.v.), was administered, and thereafter, daily kaolin consumption was measured for 3 days. In comparison, the effect of daily injection of tropisetron (2mg/kg, i.v.), given 10min, 24 and 48h after the anticancer agent administration, was also evaluated. Kaolin intake greatly increased to 21, 17 and 10 folds of control ingestion on the first day after administration with the anticancer agents, cisplatin, cyclophosphamide and doxorubicin, respectively, and then gradually decreased to near control level on day 3. Such anticancer agent-induced increases in the kaolin consumption were remarkably attenuated by the attachment of tropisetron patch, resulting in the reduction to half levels, which is comparable to the efficacy of daily tropisetron injection. In particular, the blood concentration of tropisetron following patch attachment reached a maximum level of 30-40ng/ml in 12h and exhibited a plateau until detachment of the patch, in contrast to a rapid elimination with a half-life of 2.21h after injection of the drug. Taken together, it is suggested that the novel tropisetron patch could be a promising regimen for the relief of emesis, based on the long-term antiemetic effects on the diverse anticancer agents and the convenience to use the transdermal delivery system for the cancer patients who have difficulty in taking drugs due to surgical operation or gastrointestinal dysfunction.

摘要

在大鼠中,评估了一种含有5-羟色胺3(5-HT(3))受体拮抗剂托烷司琼的新型透皮贴剂对抗癌药物所致呕吐的疗效,并与传统托烷司琼注射剂的效果进行了比较。通过对代表抗呕吐啮齿动物呕吐的异食癖模型(即抗癌药物诱导的高岭土摄取行为)的抑制活性来评估其止吐效果。将托烷司琼贴剂(10mg/贴,3.5cm(2))贴于大鼠背部剃毛区。8小时后,分别静脉注射顺铂(10mg/kg)腹腔注射环磷酰胺(200mg/kg)或静脉注射阿霉素(8mg/kg),然后连续3天测量每日高岭土摄取量。作为对照,还评估了在给予抗癌药物后10分钟、24小时和48小时静脉注射托烷司琼(2mg/kg)的每日注射效果。给予抗癌药物顺铂、环磷酰胺和阿霉素后,第一天高岭土摄入量分别大幅增加至对照摄入量的21倍、17倍和10倍,然后在第3天逐渐降至接近对照水平。托烷司琼贴剂的贴敷显著减弱了这种抗癌药物诱导的高岭土摄取增加,使其减少至一半水平,这与每日注射托烷司琼的疗效相当。特别是,贴敷贴剂后托烷司琼的血药浓度在12小时内达到30-40ng/ml的最高水平,并在贴剂去除前保持稳定,这与注射药物后半衰期为2.21小时的快速消除形成对比。综上所述,基于对多种抗癌药物的长期止吐作用以及对于因手术或胃肠功能障碍而难以服药的癌症患者使用透皮给药系统的便利性,提示新型托烷司琼贴剂可能是一种有前景的缓解呕吐的给药方案。

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