期刊文献+

顺铂缓释剂瘤内治疗大鼠C_6胶质瘤实验观察 被引量:6

Efficacy of intratumoral administered cisplatin-impregnated biodegradable polymer for the treatment of C 6 glioma in the rat
原文传递
导出
摘要 目的 观察顺铂缓释剂瘤内用药治疗大鼠C6胶质瘤的生物学效应。方法 用几丁质做载体 ,与顺铂制成缓释剂型 ,进行瘤内植入治疗大鼠脑胶质瘤。结果 瘤内给予 1mg/m2 顺铂缓释剂无毒性 ,瘤内铂浓度比全身用药高 2~ 5 0倍 ,维持时间达 1月以上 ,血铂浓度比全身用药低 10~ 6 0倍 ,荷瘤鼠生存时间较单纯顺铂液瘤内或全身用药明显延长。结论 瘤内给予顺铂缓释剂的抗肿瘤效果优于局部和全身单纯顺铂液给药。 Objective To examine the benefit of local delivery of cisplatin via chitin a biodegradable polymer in the treatment of intracranial glioma in rats compared against intratumorally administered free cisplatin and systemic cisplatin.Methods The C 6 glioma rat model and healthy controls were used to determine toxicity and efficacy of cisplatin loaded polymers. Tissue distribution of cisplatin was tested after that cisplatin impregnated chitin was administered intralesionally and free cisplatin was given by systemic administration.Results Intratumoral chemotherapy with polymer impregnated 1 0mg/m 2 cisplatin resulted in a significant longer survival time in the C 6 glioma rat model, compared with the group treated with intralesionally administered free cisplatin, and 50mg/m 2 cisplatin by systemic administration (P<0 001, respectively). Tumor concentrations were 2~50 times higher after intratumoural administration of cisplatin impregnated biodegradable polymers than i. p. administration of cisplatin. Plasma and kideny concentrations after intratumoral administrations were 10~60 and 60~200 times lower than those measured after i. p. administration, respectively.Conclusions The local implantation of cisplatin impregnated biodegradable polymer, allowing the sustained release of high dose chemotherapy locally is effective treatment for intracranial C 6 glioma in the rat.
出处 《中华神经外科杂志》 CSCD 北大核心 2000年第2期91-93,共3页 Chinese Journal of Neurosurgery
关键词 顺铂 几丁质 瘤内化疗 脑胶质瘤 药物疗法 Chitin Cisplatin Intratumoral chemotherapy Glioma Sustained release drug
  • 相关文献

参考文献2

  • 1Eric P. Sipos,Betty Tyler,Steven Piantadosi,Peter C. Burger,H. Brem. Optimizing interstitial delivery of BCNU from controlled release polymers for the treatment of brain tumors[J] 1997,Cancer Chemotherapy and Pharmacology(5):383~389
  • 2T. Tomita. Interstitial chemotherapy for brain tumors: review[J] 1991,Journal of Neuro - Oncology(1):57~74

同被引文献35

  • 1徐海涛,袁先厚,马金阳,陈谦学,陈治标,黄书岚.壳聚糖及衍生物与大鼠脑的生物相容性研究[J].中华实验外科杂志,2005,22(4):463-464. 被引量:9
  • 2顾宇翔 陈衔城 王字倩.CHMI.脑内局部给药对大鼠脑组织的影响[J].中华临床医药杂志,2002,8:7743-7744.
  • 3Gen J, Strobel HW. Expression, induction and reguiation of the cytochrome P450 monooygenase system in the rat: glioma C6 cell line [j]. Brain Research, 1998,784: 276-283.
  • 4Weingert j, Thompsom R, Tyler B, et al. Local delivery of the topoisomerase 1 inhibitor captothecin prolongs survival in the rat intracranial 9L gliosareoma mode[J]. Int J Cancer 1995,62:605-609.
  • 5Qimin Z, Zheng X. Chml suppresses cell growth and induces apoptosis in multiple human tumor lines[j]. Anticancer research, 1999,19:2893-2899.
  • 6Zhan Q, Zhao SC, Xu Z. Antilumor activity of cytotropic heterogeneous molecular lipids (CHML) on human breast cancer xeno-graft in nude mice[ J ]. Anticancer Research, 2001,21 : 2477-2482.
  • 7Peter DL, Sheoidan PL, 13town WE. Animal model for brain tumors:historical perspectives and future directions[ J ]. J Neurosurg, 1994,80: 865-869.
  • 8YANG M B,TAMARGO R J,BREM H.Controlled delivery of 1,3-bis(2-chloroethl)-1-nitrosourea from ethylene-vinyl acetate copolymer.Cancer Res,1989,19:5103-5107.
  • 9Racine RJ,Steingart M,Mclntyre DC.Development of kindling-prone and kindling-resistant rats:selective breeding and electrophysiological studies[J].Epilepsy Res,1999,35 (3):183~195.
  • 10VandeVord PJ,Matthew HW,DeSilva SP,et al.Evaluation of the biocompatibility of a chitosan scaffold in mice[J].J Biomed Mater Res,2002,59(3):585~590.

引证文献6

二级引证文献16

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部