• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

用于间质化疗的三周缓释卡氮芥亲水聚乳酸-羟基乙酸共聚物微球:对人胶质母细胞瘤细胞的研发及活性

Three weeks release BCNU loaded hydrophilic-PLGA microspheres for interstitial chemotherapy: Development and activity against human glioblastoma cells.

作者信息

Esther Gil-Alegre María, González-Alvarez Isabel, Gutiérrez-Paúls Laura, Torres-Suárez Ana Isabel

机构信息

Department of Pharmacy and Pharmaceutical Technology, Complutense University of Madrid, Spain.

出版信息

J Microencapsul. 2008 Dec;25(8):561-8. doi: 10.1080/02652040802075799.

DOI:10.1080/02652040802075799
PMID:18608792
Abstract

The aim of this study is the development of microspheres of BCNU for intracranial administration, as an alternative to marketed novel Gliadel Implant in the treatment of brain tumours. H poly-lactide-co-glycolide biodegradable microspheres of BCNU with a mean size of 33.5 + or - 1.8 microm were obtained by an oil-in-water emulsion solvent evaporation method. Their small size would allow their intracranial administration through a needle by cerebral stereotaxia if tumour recurrence occurs, without a surgical intervention, as Gliadel needs. BCNU was released from these microspheres during 21 days, mainly by a mechanism of diffusion from the polymer matrix (K = 2.91 mg days(-(1/2))). The cytotoxic effects of these microspheres on human glioblastoma cells were demonstrated all through 21 days and the value of percentage of viable cells was less than 40%. These microspheres should be commercialized as a freeze-dried product to keep at -20 degrees C. Three hundred and twenty milligrams of microspheres contain 61.6 mg of BCNU, the same amount of BCNU contained in 1600 mg or eight wafers of Gliadel usually implanted after the tumour resection.

摘要

本研究的目的是开发用于颅内给药的卡莫司汀微球,作为市售新型格利雅得植入剂治疗脑肿瘤的替代方案。通过水包油乳液溶剂蒸发法获得了平均粒径为33.5±1.8微米的卡莫司汀聚丙交酯-乙交酯可生物降解微球。如果肿瘤复发,其小尺寸将允许通过脑立体定向术经针进行颅内给药,而无需像格利雅得那样进行手术干预。卡莫司汀在21天内从这些微球中释放,主要通过从聚合物基质扩散的机制(K = 2.91毫克·天^(-1/2))。这些微球对人胶质母细胞瘤细胞的细胞毒性作用在21天内均得到证实,活细胞百分比值小于40%。这些微球应以冻干产品形式商业化,保存在-20℃。320毫克微球含有61.6毫克卡莫司汀,与肿瘤切除后通常植入的1600毫克或八片格利雅得中所含的卡莫司汀量相同。

相似文献

1
Three weeks release BCNU loaded hydrophilic-PLGA microspheres for interstitial chemotherapy: Development and activity against human glioblastoma cells.用于间质化疗的三周缓释卡氮芥亲水聚乳酸-羟基乙酸共聚物微球:对人胶质母细胞瘤细胞的研发及活性
J Microencapsul. 2008 Dec;25(8):561-8. doi: 10.1080/02652040802075799.
2
Biodegradable wafers releasing Temozolomide and Carmustine for the treatment of brain cancer.可生物降解的载替莫唑胺和卡莫司汀的水凝胶用于脑肿瘤的治疗。
J Control Release. 2019 Feb 10;295:93-101. doi: 10.1016/j.jconrel.2018.12.048. Epub 2018 Dec 31.
3
BCNU-loaded poly(D, L-lactide-co-glycolide) wafer and antitumor activity against XF-498 human CNS tumor cells in vitro.负载卡莫司汀的聚(D,L-丙交酯-共-乙交酯)薄片及其对XF-498人中枢神经系统肿瘤细胞的体外抗肿瘤活性。
Int J Pharm. 2003 Jan 30;251(1-2):1-12. doi: 10.1016/s0378-5173(02)00543-4.
4
Sustainable release of carmustine from biodegradable poly[((D,L))-lactide-co-glycolide] nanofibrous membranes in the cerebral cavity: in vitro and in vivo studies.可生物降解的聚[(D,L)-丙交酯-co-乙交酯]纳米纤维膜在脑室内的卡莫司汀可持续释放:体外和体内研究。
Expert Opin Drug Deliv. 2013 Jul;10(7):879-88. doi: 10.1517/17425247.2013.758102. Epub 2013 Jan 7.
5
Internal morphology of poly(D,L-lactide-co-glycolide) BCNU-loaded microspheres. Influence on drug stability.载有卡莫司汀的聚(D,L-丙交酯-共-乙交酯)微球的内部形态。对药物稳定性的影响。
Eur J Pharm Biopharm. 1998 Jan;45(1):31-9. doi: 10.1016/S0939-6411(97)00120-3.
6
Monitoring the effects of BCNU chemotherapy Wafers (Gliadel) in glioblastoma multiforme with proton magnetic resonance spectroscopic imaging at 3.0 Tesla.使用3.0特斯拉质子磁共振波谱成像监测卡莫司汀化疗晶片(Gliadel)对多形性胶质母细胞瘤的疗效。
J Neurooncol. 2007 Mar;82(1):103-10. doi: 10.1007/s11060-006-9254-6. Epub 2006 Sep 22.
7
Enhancement of the stability of BCNU using self-emulsifying drug delivery systems (SEDDS) and in vitro antitumor activity of self-emulsified BCNU-loaded PLGA wafer.使用自乳化药物递送系统(SEDDS)增强卡莫司汀(BCNU)的稳定性以及载有BCNU的聚乳酸-羟基乙酸共聚物(PLGA)自乳化薄片的体外抗肿瘤活性
Int J Pharm. 2005 Sep 14;301(1-2):6-14. doi: 10.1016/j.ijpharm.2005.03.034.
8
Local immunotherapy with interleukin-2 delivered from biodegradable polymer microspheres combined with interstitial chemotherapy: a novel treatment for experimental malignant glioma.由可生物降解聚合物微球递送白细胞介素-2的局部免疫疗法联合间质化疗:一种治疗实验性恶性胶质瘤的新方法。
Neurosurgery. 2003 Apr;52(4):872-9; discussion 879-80. doi: 10.1227/01.neu.0000053211.39087.d1.
9
Efficacy of BCNU and paclitaxel loaded subcutaneous implants in the interstitial chemotherapy of U-87 MG human glioblastoma xenografts.卡莫司汀和紫杉醇负载皮下植入物在U-87 MG人胶质母细胞瘤异种移植瘤间质化疗中的疗效。
Int J Pharm. 2002 May 15;238(1-2):111-21. doi: 10.1016/s0378-5173(02)00061-3.
10
Gliadel wafer in initial surgery for malignant glioma: long-term follow-up of a multicenter controlled trial.用于恶性胶质瘤初次手术的Gliadel薄片:一项多中心对照试验的长期随访
Acta Neurochir (Wien). 2006 Mar;148(3):269-75; discussion 275. doi: 10.1007/s00701-005-0707-z. Epub 2006 Feb 17.

引用本文的文献

1
Emerging insights into barriers to effective brain tumor therapeutics.新兴的关于脑肿瘤治疗效果障碍的见解。
Front Oncol. 2014 Jul 21;4:126. doi: 10.3389/fonc.2014.00126. eCollection 2014.
2
BCNU/PLGA microspheres: a promising strategy for the treatment of gliomas in mice.BCNU/PLGA 微球:一种治疗小鼠脑胶质瘤的有前途的策略。
Chin J Cancer Res. 2014 Feb;26(1):81-8. doi: 10.3978/j.issn.1000-9604.2014.02.01.
3
Local delivery of cannabinoid-loaded microparticles inhibits tumor growth in a murine xenograft model of glioblastoma multiforme.
局部递送大麻素负载微球抑制多形性胶质母细胞瘤小鼠异种移植模型中的肿瘤生长。
PLoS One. 2013;8(1):e54795. doi: 10.1371/journal.pone.0054795. Epub 2013 Jan 22.
4
Nano to micro delivery systems: targeting angiogenesis in brain tumors.纳米至微米级递送系统:靶向脑肿瘤中的血管生成
J Angiogenes Res. 2010 Oct 8;2(1):20. doi: 10.1186/2040-2384-2-20.
5
Antiangiogenic therapy and mechanisms of tumor resistance in malignant glioma.抗血管生成治疗与恶性脑胶质瘤肿瘤耐药的机制。
J Oncol. 2010;2010:251231. doi: 10.1155/2010/251231. Epub 2010 Apr 11.