Lee Hee Su, Kim Junsik, Lee Eun Ji, Park Soo Jin, Mun Jaehee, Paik Haerin, Oh Soo Hyun, Park Sunwoo, Ryu Soomin, Lim Whasun, Song Gwonhwa, Kim Hee Seung, Lee Jung Chan
Interdisciplinary Program in Bioengineering, Seoul National University Graduate School, Seoul 08826, Republic of Korea.
Department of Obstetrics and Gynecology, Seoul National University Hospital, Seoul 03080, Republic of Korea.
Cancers (Basel). 2020 Mar 9;12(3):633. doi: 10.3390/cancers12030633.
Pressurized intraperitoneal aerosol chemotherapy (PIPAC) has been suggested as an alternative option for treating peritoneal carcinomatosis (PC). Even with its clinical advantages, the current PIPAC system still suffers from limitations regarding drug distribution area and penetration depth. Thus, we evaluated the new PIPAC system using a novel prototype, and compared its performance to the results from previous studies related with the current MIP indirectly because the system is currently not available for purchase in the market. The developed prototype includes a syringe pump, a nozzle, and controllers. Drug distribution was conducted using a methylene blue solution for performance test. For penetration depth evaluation, an ex-vivo experiment was performed with porcine tissues in a 3.5 L plastic box. Doxorubicin was sprayed using the novel prototype, and its penetration depth was investigated by confocal laser scanning microscopy. The experiment was repeated with varying nozzle levels from the bottom. The novel prototype sprays approximately 30 μm drug droplets at a flow rate of 30 mL/min with 7 bars of pressure. The average diameter of sprayed region with concentrated dye was 18.5 ± 1.2 cm, which was comparable to that of the current MIP (about 10 cm). The depth of concentrated diffusion (DCD) did not differ among varying nozzle levels, whereas the depth of maximal diffusion (DMD) decreased with increasing distance between the prototype and the bottom (mean values, 515.3 μm at 2 cm; 437.6 μm at 4 cm; 363.2 μm at 8 cm), which was comparable to those of the current MIP (about 350-500 μm). We developed a novel prototype that generate small droplets for drug aerosolization and that have a comparably wide sprayed area and depth of penetration to the current MIP at a lower pressure.
腹腔内加压气溶胶化疗(PIPAC)已被提议作为治疗腹膜癌(PC)的一种替代选择。尽管具有临床优势,但当前的PIPAC系统在药物分布区域和渗透深度方面仍存在局限性。因此,我们使用一种新型原型评估了新的PIPAC系统,并将其性能与之前有关当前MIP的研究结果进行了间接比较,因为该系统目前在市场上无法购买。所开发的原型包括一个注射泵、一个喷嘴和控制器。使用亚甲蓝溶液进行药物分布以进行性能测试。为了评估渗透深度,在一个3.5升的塑料盒中对猪组织进行了离体实验。使用新型原型喷洒阿霉素,并通过共聚焦激光扫描显微镜研究其渗透深度。从底部改变喷嘴高度重复该实验。新型原型在7巴压力下以30毫升/分钟的流速喷洒约30微米的药滴。浓缩染料喷洒区域的平均直径为18.5±1.2厘米,与当前MIP的直径(约10厘米)相当。不同喷嘴高度下的浓缩扩散深度(DCD)没有差异,而最大扩散深度(DMD)随着原型与底部之间距离的增加而减小(平均值,2厘米时为515.3微米;4厘米时为437.6微米;8厘米时为363.2微米),这与当前MIP的深度(约350 - 500微米)相当。我们开发了一种新型原型,它能产生用于药物雾化的小液滴,并且在较低压力下具有与当前MIP相当的宽喷洒面积和渗透深度。