Laboratory of General Biochemistry and Physical Pharmacy, Faculty of Pharmaceutical Sciences, Ghent University, 9000 Ghent, Belgium.
Cancer Research Institute Ghent (CRIG), 9000 Ghent, Belgium.
ACS Appl Mater Interfaces. 2020 Jul 1;12(26):29024-29036. doi: 10.1021/acsami.0c05554. Epub 2020 Jun 22.
Intra-abdominal dissemination of peritoneal nodules, a condition known as peritoneal carcinomatosis (PC), is typically diagnosed in ovarian cancer patients at the advanced stages. The current treatment of PC consists of perioperative systemic chemotherapy and cytoreductive surgery, followed by intra-abdominal flushing with solutions of chemotherapeutics such as cisplatin and oxaliplatin. In this study, we developed cisplatin-loaded polyarginine-hyaluronic acid nanoscale particles (Cis-pARG-HA NPs) with high colloidal stability, marked drug loading efficiency, unimpaired biological activity, and tumor-targeting ability. Injected Cis-pARG-HA NPs showed enhanced antitumor activity in a rat model of PC, compared to injection of the free cisplatin drug. The activity of Cis-pARG-HA NPs could even be further improved when administered by an intra-abdominal aerosol therapy, referred to as pressurized intraperitoneal aerosol chemotherapy (PIPAC). PIPAC is hypothesized to ensure a more homogeneous drug distribution together with a deeper drug penetration into peritoneal tumor nodules within the abdominal cavity. Using fluorescent pARG-HA NPs, this enhanced nanoparticle deposit on tumors could indeed be observed in regions opposite the aerosolization nozzle. Therefore, this study demonstrates that nanoparticles carrying chemotherapeutics can be synergistically combined with the PIPAC technique for IP therapy of disseminated advanced ovarian tumors, while this synergistic effect was not observed for the administration of free cisplatin.
腹腔内播散的腹膜结节,即腹膜癌病(PC),通常在卵巢癌晚期患者中诊断。目前,PC 的治疗包括围手术期全身化疗和细胞减灭术,然后用顺铂和奥沙利铂等化疗药物进行腹腔冲洗。在这项研究中,我们开发了负载顺铂的聚精氨酸-透明质酸纳米颗粒(Cis-pARG-HA NPs),具有高胶体稳定性、显著的药物负载效率、未受损的生物活性和肿瘤靶向能力。与注射游离顺铂药物相比,注射 Cis-pARG-HA NPs 可增强 PC 大鼠模型的抗肿瘤活性。当通过腹腔内气溶胶治疗(称为加压腹腔内气溶胶化疗(PIPAC))给药时,Cis-pARG-HA NPs 的活性甚至可以进一步提高。PIPAC 被假设可以确保更均匀的药物分布,同时更深入地渗透到腹腔内的腹膜肿瘤结节中。使用荧光 pARG-HA NPs,可以观察到在气溶胶化喷嘴相对的区域,增强的纳米颗粒沉积在肿瘤上。因此,本研究表明,携带化疗药物的纳米颗粒可以与 PIPAC 技术协同用于治疗播散性晚期卵巢肿瘤的 IP 治疗,而对于游离顺铂的给药则没有观察到这种协同作用。