Comparison of Ulinastatin, Gabexate Mesilate, and Nafamostat Mesilate in Preservation Solution for Islet Isolation

Author:

Noguchi Hirofumi123,Naziruddin Bashoo24,Jackson Andrew24,Shimoda Masayuki5,Fujita Yasutaka1,Chujo Daisuke1,Takita Morihito1,Peng Han2,Sugimoto Koji1,Itoh Takeshi1,Kobayashi Naoya3,Ueda Michiko6,Okitsu Teru7,Iwanaga Yasuhiro7,Nagata Hideo6,Liu Xiaoling6,Kamiya Hiroki6,Onaca Nicholas3,Levy Marlon F.13,Matsumoto Shinichi1

Affiliation:

1. Baylor All Saints Medical Center, Baylor Research Institute, Fort Worth, TX, USA

2. Institute of Biomedical Studies, Baylor University, Waco, TX, USA

3. Department of Gastroenterological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan

4. Baylor Regional Transplant Institute, Dallas & Fort Worth, TX, USA

5. Division of Cardiology, Department of Internal Medicine, Baylor University Medical Center, Baylor Heart and Vascular Institute, Dallas, TX, USA

6. Second Department of Surgery, Fujita Health University, Toyoake, Aichi, Japan

7. Transplantation Unit, Kyoto University Hospital, Kyoto, Japan

Abstract

For islet transplantation, maintaining organ viability after pancreas procurement is critically important for optimal graft function and survival. We recently reported that islet yield was significantly higher in the modified ET-Kyoto (MK) solution, which includes a trypsin inhibitor (ulinastatin), compared with the UW solution, and that the advantages of MK solution are trypsin inhibition and less collagenase inhibition. In this study, we compared ulinastatin with other trypsin inhibitors, gabexate mesilate, and nafamostat mesilate, in preservation solution for islet isolation. Ulinastatin was easily dissolved in ET-Kyoto solution, while ET-Kyoto with gabexate mesilate and nafamostat mesilate became cloudy immediately after addition. Although there were no significant differences in islet yield among the three groups, viability was significantly higher for the MK group than for the GK group or the NK group. The stimulation index was significantly higher for the MK group than for the GK group. In summary, there are no other trypsin inhibitors that are more effective than ulinastatin. Based on these data, we now use ET-Kyoto solution with ulinastatin for clinical islet transplantation.

Publisher

SAGE Publications

Subject

Transplantation,Cell Biology,Biomedical Engineering

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