| Bioactive Materials | |
| Viscosity and degradation controlled injectable hydrogel for esophageal endoscopic submucosal dissection | |
| Shiming Yang1  Tongchuan Wang2  Lu Liu2  Yu Huang2  Chaoqiang Fan2  Shuang Liu2  Wei Wang2  Weichao Hu2  Kaige Xu3  Malcolm Xing3  | |
| [1] Corresponding author.;Department of Gastroenterology, Xinqiao Hospital, Army Medical University, NO.183, Xinqiao Street, Shapingba District, Chongqing City, 400037, People's Republic of China;Department of Mechanical Engineering, Biochemistry and Medical Genetics, University of Manitoba, Winnipeg MB, R3T 2N2, Manitoba, Canada; | |
| 关键词: Injectable hydrogel; Controllable gelation and viscosity; Esophageal submucosal liquid cushion; Early esophageal cancer; Pig model; | |
| DOI : | |
| 来源: DOAJ | |
【 摘 要 】
Endoscopic submucosal dissection (ESD) is a common procedure to treat early and precancerous gastrointestinal lesions. Via submucosal injection, a liquid cushion is created to lift and separate the lesion and malignant part from the muscular layer where the formed indispensable space is convenient for endoscopic incision. Saline is a most common submucosal injection liquid, but the formed liquid pad lasts only a short time, and thus repeated injections increase the potential risk of adverse events. Hydrogels with high osmotic pressure and high viscosity are used as an alternate; however, with some drawbacks such as tissue damage, excessive injection resistance, and high cost. Here, we reported a nature derived hydrogel of gelatin-oxidized alginate (G-OALG). Based on the rheological analysis and compare to commercial endoscopic mucosal resection (EMR) solution (0.25% hyaluronic acid, HA), a designed G-OALG hydrogel of desired concentration and composition showed higher performances in controllable gelation and injectability, higher viscosity and more stable structures. The G-OALG gel also showed lower propulsion resistance than 0.25% HA in the injection force assessment under standard endoscopic instruments, which eased the surgical operation. In addition, the G-OALG hydrogel showed good in vivo degradability biocompatibility. By comparing the results acquired via ESD to normal saline, the G-OALG shows great histocompatibility and excellent endoscopic injectability, and enables create a longer-lasting submucosal cushion. All the features have been confirmed in the living both pig and rat models. The G-OALG could be a promising submucosal injection agent for esophageal ESD.
【 授权许可】
Unknown