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新型泵控制药物释放在胰腺癌治疗中的应用。

Pancreatic cancer therapy with a novel pump for controlled drug release.

机构信息

Department of Pharmacoepidemiology, Graduate School of Medicine and Public Health, Kyoto University, Sakyoku, Kyoto, Japan.

出版信息

Oncol Rep. 2010 Feb;23(2):365-70.

PMID:20043096
Abstract

Enhancing antitumor activity and minimizing treatment side effects are important issues in cancer therapy. One method to deal with these issues is the utilization of a drug delivery system (DDS). In this study, we developed a novel drug administration pump, a mechanically controlled DDS (M-DDS). The antitumor activity of 5-fluorouracil (5-FU) (15 or 30 mg/kg/day) was evaluated in comparison with systemic intraperitoneal (i.p.) administration for 7 days in a rat model of human pancreatic cancer. The M-DDS was superior to i.p. administration in enhancing antitumor activity and also prolonging median survival from 69 to 85 days at the lower drug dose (15 mg/kg/day). In addition, toxicities in liver, kidney and spleen were found in animals receiving i.p. administration, whereas rats receiving M-DDS treatment did not show these toxicities. The concentration of 5-FU in tumors 1 day after the completion of treatment was considerably higher in rats receiving M-DDS treatment. These results suggest that this novel M-DDS may be a powerful tool for the treatment of pancreatic cancer in combination with conventional chemotherapeutic drugs, offering strong antitumor activity with fewer toxicities. This novel M-DDS, consisting of a control circuit and drug reservoir/pump unit, may be a useful tool for the treatment not only of pancreatic cancer but also of various other accessible cancers for which there is no effective treatment, such as bile-duct and brain tumors.

摘要

提高抗肿瘤活性和最小化治疗副作用是癌症治疗中的重要问题。解决这些问题的一种方法是利用药物输送系统(DDS)。在这项研究中,我们开发了一种新型药物给药泵,即机械控制的 DDS(M-DDS)。我们评估了氟尿嘧啶(5-FU)(15 或 30mg/kg/天)的抗肿瘤活性,与在人胰腺癌细胞模型中连续 7 天进行全身腹腔内(i.p.)给药进行比较。M-DDS 在增强抗肿瘤活性方面优于 i.p.给药,并且在较低药物剂量(15mg/kg/天)下将中位生存时间从 69 天延长至 85 天。此外,接受 i.p.给药的动物出现了肝、肾和脾毒性,而接受 M-DDS 治疗的大鼠没有出现这些毒性。在治疗完成后 1 天,接受 M-DDS 治疗的大鼠肿瘤中 5-FU 的浓度明显更高。这些结果表明,这种新型 M-DDS 可能与传统化疗药物联合成为治疗胰腺癌的有力工具,具有更强的抗肿瘤活性和更少的毒性。这种新型 M-DDS 由控制电路和药物储存/泵单元组成,不仅可能是治疗胰腺癌的有用工具,而且可能是治疗其他没有有效治疗方法的可及性癌症的有用工具,例如胆管癌和脑肿瘤。

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