Study on the safety and efficacy of micro-perfusion device for preserving isolated porcine limbs
10.12464/j.issn.1674-7445.2025318
- VernacularTitle:微型灌注仪保存猪离断肢体安全性有效性研究
- Author:
Pengkai LI
1
;
Zhaodi MI
2
;
Shen LI
2
;
Man YUAN
1
;
Xiwei PENG
1
;
Jia LÜ
1
;
Sice WANG
1
;
Zhibo JIA
2
;
Xiangyu SONG
1
;
Yixuan ZHU
2
;
Chonghui LI
3
;
Moling XIAO
1
;
Wenjing XU
3
;
Jiang PENG
1
Author Information
1. Research Institute of Orthopaedic Medicine Department, the Fourth Medical Center of the Chinese People's Liberation Army, Beijing 100853, China.
2. Research Institute of Orthopaedic Medicine Department, the Fourth Medical Center of the Chinese People's Liberation Army, Beijing 100853, China;null.
3. null.
- Publication Type:OriginalArticle
- Keywords:
Perfusion device;
Miniature;
Normothermic machine perfusion;
Static cold storage;
Amputated limb preservation;
Limb replantation;
Ischemia-reperfusion injury;
Inflammation
- From:
Organ Transplantation
2026;17(3):422-431
- CountryChina
- Language:Chinese
-
Abstract:
Objective To evaluate the safety and efficacy of a self-developed micro-normothermic machine perfusion (NMP) system (micro-perfusion device) for preserving isolated porcine limbs. Methods Five healthy Landrace pigs were selected, and their left and right forelimbs were randomly divided into the NMP group and static cold storage (SCS) group. The NMP group was perfused with the self-developed micro-perfusion device and polymerized hemoglobin perfusate for 32 hours at normothermia, while the SCS group was preserved at 4 ℃. Hemodynamic parameters such as perfusion pressure and flow were monitored. The pH value, partial pressure of oxygen (PO2), lactic acid (Lac), creatine kinase (CK) and lactate dehydrogenase (LDH) in the perfusate were measured. Hematoxylin-eosin staining was used to assess the muscle tissue structure, terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling was employed to evaluate muscle cell apoptosis, and immunohistochemistry staining was applied to detect the expressions of tumor necrosis factor (TNF)-α and interleukin (IL)-6. A mixed-effects model was used to analyze the effects of time and treatment methods on tissue structure, cell apoptosis and inflammatory factors. Results The device could stably maintain a perfusion pressure of (69±15) mmHg and a flow rate of (117±42) mL/min. The pH value and electrolytes of the perfusate were generally stable, with PO2 maintained at a high level. Lac was maintained at 5.38(3.81, 6.45) mmol/L, while CK and LDH increased over time. After 32 hours of perfusion in the NMP group, both the myocyte spacing and apoptosis rate were better than those in the SCS group. Mixed-effects model analysis showed that there were statistically significant differences in the effects of NMP treatment and SCS treatment on myocyte spacing and apoptosis rate per unit time (both P < 0.05). There were no statistically significant differences in TNF-α and IL-6 between the two groups, and mixed-effects model analysis showed no statistically significant differences in the effects of NMP treatment and SCS treatment on TNF-α and IL-6 per unit time (both P > 0.05). Conclusions The micro-perfusion device used in this study may achieve 32-hour normothermic preservation in a porcine limb amputation model, maintain basic metabolism and ionic homeostasis, reduce muscle structural damage and cell apoptosis without inducing additional inflammatory responses. This technology is expected to significantly extend the time window for replantation of amputated limbs in disaster rescue and long-distance transportation, providing an important technical basis for clinical translation and subsequent replantation research.
