腹膜腔
药物输送
乙二醇
体内
自愈水凝胶
药品
纳米囊
PEG比率
药理学
化学
生物医学工程
医学
外科
纳米技术
材料科学
纳米颗粒
高分子化学
有机化学
生物技术
经济
生物
财务
作者
Bhanu Teja Surikutchi,Rebeca Obenza-Otero,Emanuele Russo,Mischa Zelzer,Irene Golán‐Cancela,José A. Costoya,José Crecente‐Campo,Marı́a José Alonso,Maria Marlow
标识
DOI:10.1016/j.ijpharm.2022.121828
摘要
Intraperitoneal (IP) drug delivery of chemotherapeutic agents, administered through hyperthermal intraperitoneal chemotherapy (HIPEC) and pressurized intraperitoneal aerosolized chemotherapy (PIPAC), is effective for the treatment of peritoneal malignancies. However, these therapeutic interventions are cumbersome in terms of surgical practice and are often associated with the formation of peritoneal adhesions, due to the catheters inserted into the peritoneal cavity during these procedures. Hence, there is a need for the development of drug delivery systems that can be administered into the peritoneal cavity. In this study, we have developed a nanocapsule (NCs)-loaded hydrogel for drug delivery in the peritoneal cavity. The hydrogel has been developed using poly(ethylene glycol) (PEG) and thiol-maleimide chemistry. NCs-loaded hydrogels were characterized by rheology and their resistance to dilution and drug release were determined in vitro. Using IVIS® to measure individual organ and recovered gel fluorescence intensity, an in vivo imaging study was performed and demonstrated that NCs incorporated in the PEG gel were retained in the IP cavity for 24 h after IP administration. NCs-loaded PEG gels could find potential applications as biodegradable, drug delivery systems that could be implanted in the IP cavity, for example at a the tumour resection site to prevent recurrence of microscopic tumours.
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