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多柔比星和伊立替康载药微球治疗脑胶质瘤的实验研究:大鼠模型中的初步研究。

Doxorubicin and irinotecan drug-eluting beads for treatment of glioma: a pilot study in a rat model.

机构信息

International Neuroscience Institute GmbH, Hannover, Germany.

出版信息

J Mater Sci Mater Med. 2010 Apr;21(4):1393-402. doi: 10.1007/s10856-009-3803-4. Epub 2010 Feb 17.

Abstract

Despite some progress in therapy, the prognosis of patients with malignant gliomas remains poor. Local delivery of cytostatics to the tumour has been proven to be an efficacious therapeutic approach but which nevertheless needs further improvements. Drug Eluting Beads (DEB), have been developed as drug delivery embolisation systems for use in trans-arterial chemoembolisation. We tested in a rat model of malignant glioma, whether DEB, loaded with doxorubicin or irinotecan, may be used for local treatment of brain tumours. Unloaded and drug loaded DEB were implanted into the brains of healthy and tumour bearing BD IX rats followed by histological investigations and survival assessment. Intracerebral implantation of unloaded DEB caused no significant local tissue damage, whilst both doxorubicin and irinotecan DEB improved survival time significantly. However, a significant local toxicity was found after the implantation of doxorubicin DEB but not with irinotecan DEB. We concluded that irinotecan appears to be superior in terms of the risk-benefit ratio and that DEB may be used for local treatment of brain tumours.

摘要

尽管在治疗方面取得了一些进展,但恶性胶质瘤患者的预后仍然很差。局部向肿瘤递送细胞抑制剂已被证明是一种有效的治疗方法,但仍需要进一步改进。载药微球(DEB)已被开发为用于经动脉化疗栓塞的药物输送栓塞系统。我们在恶性胶质瘤的大鼠模型中进行了测试,载有阿霉素或伊立替康的 DEB 是否可用于脑肿瘤的局部治疗。将未载药和载药的 DEB 植入健康和荷瘤 BDIX 大鼠的大脑中,然后进行组织学研究和生存评估。未载药 DEB 的颅内植入不会引起明显的局部组织损伤,而阿霉素和伊立替康 DEB 均可显著延长生存时间。然而,在植入阿霉素 DEB 后会发现明显的局部毒性,但植入伊立替康 DEB 则没有。我们得出结论,伊立替康在风险效益比方面似乎更具优势,DEB 可用于脑肿瘤的局部治疗。

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