4.7 Article

Development of a nanocapsule-loaded hydrogel for drug delivery for intraperitoneal administration

期刊

出版社

ELSEVIER
DOI: 10.1016/j.ijpharm.2022.121828

关键词

Intraperitoneal delivery; PEG hydrogel; Nanocapsule; Ovarian cancer; Localised drug; Localised drug delivery; Peritoneal metastases

资金

  1. Erasmus Mundus NanoFar project [2016-02-C5-EM]
  2. University of Santiago de Compostela, Spain
  3. Spanish Ministry of Sciences and Innovation [Feder Founds] [SAF2017-86634-R]
  4. Engineering and Physical Sciences Research Council EPSRC [EP/L01646X/1]
  5. CDT in Advanced Therapeutics and Nanomedicines
  6. University of Nottingham, UK

向作者/读者索取更多资源

A drug-loaded hydrogel has been developed for drug delivery into the peritoneal cavity. The hydrogel's stability and drug release properties were evaluated through in vitro and in vivo experiments. This hydrogel has potential applications as a biodegradable drug delivery system that can be implanted in the peritoneal cavity.
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 nano capsule (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 (R) 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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