Reflux-free cannula for convection-enhanced high-speed delivery of therapeutic agents

套管 回流 医学 琼脂糖 体内 台盼蓝 麻醉 生物医学工程 外科 色谱法 化学 体外 病理 生物 生物技术 生物化学 疾病
作者
Michal T. Krauze,Ryuta Saito,Charles O. Noble,Matyas Tamas,John Bringas,John W. Park,Mitchel S. Berger,Krystof S. Bankiewicz
出处
期刊:Journal of Neurosurgery [American Association of Neurological Surgeons]
卷期号:103 (5): 923-929 被引量:234
标识
DOI:10.3171/jns.2005.103.5.0923
摘要

Object. Clinical application of the convection-enhanced delivery (CED) technique is currently limited by low infusion speed and reflux of the delivered agent. The authors developed and evaluated a new step-design cannula to overcome present limitations and to introduce a rapid, reflux-free CED method for future clinical trials. Methods. The CED of 0.4% trypan blue dye was performed in agarose gel to test cannula needles for distribution and reflux. Infusion rates ranging from 0.5 to 50 µl/minute were used. Agarose gel findings were translated into a study in rats and then in cynomolgus monkeys (Macaca fascicularis) by using trypan blue and liposomes to confirm the efficacy of the reflux-free step-design cannula in vivo. Results of agarose gel studies showed reflux-free infusion with high flow rates using the step-design cannula. Data from the study in rats confirmed the agarose gel findings and also revealed increasing tissue damage at a flow rate above 5-µl/minute. Robust reflux-free delivery and distribution of liposomes was achieved using the step-design cannula in brains in both rats and nonhuman primates. Conclusions. The authors developed a new step-design cannula for CED that effectively prevents reflux in vivo and maximizes the distribution of agents delivered in the brain. Data in the present study show reflux-free infusion with a constant volume of distribution in the rat brain over a broad range of flow rates. Reflux-free delivery of liposomes into nonhuman primate brain was also established using the cannula. This step-design cannula may allow reflux-free distribution and shorten the duration of infusion in future clinical applications of CED in humans.

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