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化疗药物与动脉内可降解淀粉微球(Spherex)联合应用的药代动力学原理。

Pharmacokinetic rationale for chemotherapeutic drugs combined with intra-arterial degradable starch microspheres (Spherex).

作者信息

Johansson C J

机构信息

Toxicology and Safety Assessment, Pharmacia and Upjohn AB, Helsingborg, Sweden.

出版信息

Clin Pharmacokinet. 1996 Sep;31(3):231-40. doi: 10.2165/00003088-199631030-00006.

Abstract

To enhance the effectiveness of regional treatment in patients with liver carcinoma, cytotoxic drugs may be combined with alternative therapeutic strategies such as partial vascular blockade using degradable starch microspheres (DSM). When DSM combined with a cytotoxic drug are infused through the hepatic artery, the steep drug concentration gradient to the tumour tissue results in higher tissue drug concentrations which may elicit an increased antitumour response. The co-injected drug should therefore possess an extensive extravascular distribution and possess a suitable dose-response relationship. Furthermore, the drug of choice should also have a high total body clearance with a large component of clearance outside the target compartment, should not interact with the spheres and should be given without inducing any back-flow. Under these assumptions, a reduced systemic exposure of a co-injected drug could be translated into an increased regional extraction ratio induced by the blood flow reduction.

摘要

为提高肝癌患者区域治疗的有效性,细胞毒性药物可与替代性治疗策略联合使用,如使用可降解淀粉微球(DSM)进行部分血管阻断。当将DSM与细胞毒性药物通过肝动脉注入时,肿瘤组织处陡峭的药物浓度梯度会导致更高的组织药物浓度,这可能引发更强的抗肿瘤反应。因此,共同注射的药物应具有广泛的血管外分布并具有合适的剂量反应关系。此外,所选择的药物还应具有较高的全身清除率,且在靶区室以外的清除占比很大,不应与微球相互作用,并且给药时不应引起任何逆流。在这些假设下,共同注射药物的全身暴露减少可转化为因血流减少而导致的区域摄取率增加。

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