Ghent Research Group on Nanomedicines, Laboratory for General Biochemistry and Physical Pharmacy, Faculty of Pharmacy, Ghent University, Ottergemsesteenweg 460, 9000 Ghent, Belgium.
Department of Surgery, Laboratory of Experimental Surgery, Ghent University Hospital, De Pintelaan 185, 9000 Ghent, Belgium; Cancer Research Institute Ghent (CRIG), Ghent, Belgium.
Adv Drug Deliv Rev. 2017 Jan 1;108:13-24. doi: 10.1016/j.addr.2016.07.001. Epub 2016 Jul 13.
Intraperitoneal (IP) drug delivery represents an attractive strategy for the local treatment of peritoneal carcinomatosis (PC). Over the past decade, a lot of effort has been put both in the academia and clinic in developing IP therapeutic approaches that maximize local efficacy while limiting systemic side effects. Also nanomedicines are under investigation for the treatment of tumors confined to the peritoneal cavity, due to their potential to increase the peritoneal retention and to target drugs to the tumor sites as compared to free drugs. Despite the progress reported by multiple clinical studies, there are no FDA approved drugs or formulations for specific use in the IP cavity yet. This review discusses the current clinical management of PC, as well as recent advances in nanomedicine-based IP delivery. We address important challenges to be overcome towards designing optimal nanocarriers for IP therapy in vivo.
腹腔内(IP)药物输送代表了一种有吸引力的策略,可用于局部治疗腹膜癌病(PC)。在过去的十年中,学术界和临床医生都在努力开发 IP 治疗方法,这些方法最大限度地提高了局部疗效,同时限制了全身副作用。由于纳米药物具有增加腹膜保留和将药物靶向肿瘤部位的潜力,因此与游离药物相比,它们也被用于治疗局限于腹腔内的肿瘤。尽管多项临床研究报告了进展,但目前尚无 FDA 批准的专门用于 IP 腔的药物或制剂。这篇综述讨论了 PC 的当前临床管理,以及基于纳米医学的 IP 输送的最新进展。我们解决了在设计用于 IP 治疗的最佳纳米载体方面需要克服的重要挑战。