Safety evaluation of paclitaxel-eluting biliary metal stent with sodium caprate in porcine biliary tract

Sung Ill Jang, Seok Jeong, Don Haeng Lee, Kun Na, Sugeun Yang, Dong Ki Lee

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1 Citation (Scopus)

Abstract

Background/Aims: Metallic stents designed to relieve malignant biliary obstruction are susceptible to occlusive tumor ingrowth or overgrowth. In a previous report, we described metallic stents covered with paclitaxel-incorporated membrane (MSCPM-I, II) to prevent occlusion from tumor ingrowth via antitumor effect. This new generation paclitaxeleluting biliary stent is further endowed with sodium caprate (MSCPM-III) for enhanced drug delivery. The purpose of this study is to examine the safety of its drug delivery system in the porcine biliary tract. Methods: MSCPM-III (10% [wt/vol] paclitaxel) and covered metal stents (CMSs) were endoscopically inserted in porcine bile ducts in vivo. Histologic biliary changes, levels of paclitaxel released, and various serum analytes (albumin, alkaline phosphate, aspartate transaminase, alanine transaminase, total protein, total bilirubin, and direct bilirubin) were assessed. Results: Based on the intensity of reactive inflammation and fibrosis, changes in porcine biliary epithelium secondary to implanted MSCPMIII were deemed acceptable (i.e., safe). Histologic features in the MSCPM-III and CMS groups did not differ significantly. In a related serum analysis, paclitaxel release from MSCPMIII stents was below the limit of detection for 28 days. Biochemical analyses were also similar for the two groups, and no evidence of hepatic or renal toxicity was found in animals receiving MSCPM-III stents. Conclusions: In a prototypic porcine trial, this newly devised metal biliary stent incorporating both paclitaxel and sodium caprate appears to be safe in the porcine bile duct.

Original languageEnglish
Pages (from-to)471-478
Number of pages8
JournalGut and liver
Volume13
Issue number4
DOIs
Publication statusPublished - 2019

Bibliographical note

Funding Information:
This work was supported by the following programs: (1) the Technology Innovation Program (10044021, Development of nonvascular drug eluting stent for treatment of gastrointestinal disease), funded by the Ministry of Trade, Industry & Energy (MI, Korea); (2) Grants from the Korean Heath Industry Development Institute (KHIDI) and the National Center of Efficacy Evaluation for the Development of Health Products Targeting Digestive Disorders (NCEED); and (3) the Basic Science Research Program through the National Research Foundation of Korea (NRF) (2017R1A2A2A07001272) and a World Class Smart Lab (WCSL) research grant from Inha University.

Publisher Copyright:
© 2019 Editorial Office of Gut and Liver. All rights reserved.

All Science Journal Classification (ASJC) codes

  • Hepatology
  • Gastroenterology

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