Table 2.
Ref. | Materials | Strut thickness | Eluting | Animal type | n | Vessel implantation site | Follow-up duration | Monitoring | Results |
---|---|---|---|---|---|---|---|---|---|
[94] | Pure Fe | 100–120 μm | – | New Zealand white rabbits |
16 | Descending aorta | 6, 12, 18 months | Angiography | No thromboembolic complications, neointimal proliferation, pronounced inflammatory response, and systemic toxicity |
[104] | Pure Fe | 120 μm | – | Minipigs | 27 | Descending aorta | 1–360 days | Histomorphometry and quantitative angiography analysis |
No signs of iron overload or iron-related organ toxicity and evidence for local toxicity |
[105] | Pure Fe | – | – | Juvenile domestic pigs | 8 | Proximal left anterior descending, left circumflex artery, or right coronary artery | 28 days | Histochemistry, vessel morphometry |
Safe, without inflammation. Brownish tinge. No excessive endothelization |
[99] | Pure Fe and nitrided Fe | 120 μm | – | Minipigs | 18 | Left and right iliac arteries | 1, 3, 6 and 12 months | Histological examination | No thrombosis, decreased inflammation |
[95] | Nitrided Fe | 70 μm | – | Minipigs | 8 Fe; 8 CoCr | Coronary artery | 28 days | Coronary angiography, endothelialization and histological observation | No signs of organ toxicity |
[17] | Fe-0.07 N | 90 μm | – | New Zealand white rabbits | 78 | Abdominal aorta | 7 days; 1, 4, 6, 9, 12, 24 and 36 months |
Endothelialization and histopathologic observation | No adverse events, homogeneous endothelial coverage, slight inflammatory response |
[101] | Pure Fe – polymer (MPS) | 50 μm | Sirolimus | Small Guizhou pigs |
15 | Left anterior descending coronary artery and right coronary artery | 6, 12 months | Micro-CT, angiography and Optical coherence tomography | No inflammation and good degradation profile of MPS |
[89] | PLA coated Fe (MPS) | 53 μm | Sirolimus | Minipigs | 74 MP S; 68 CoCr |
Left anterior descending coronary artery and right coronary artery | 1, 3, 6, 12, 24 months | Micro-CT, optical coherence tomography, endothelialization and histopathologic observation | No significant impact on endothelial cells and smooth muscle cells on MPS. No thrombosis observed |
[100] | Nitrided iron stents | 70 μm | – | Rabbits | 6 | Right femoral artery | 1 and 6 months | Radiographs; cell proliferation and viability | Decreased the neointimal hyperplasia by inhibiting VSMC proliferation induced by corroded granules |
[103] | Pure Fe | 54 μm | – | Diabetic new Zealand white rabbits | 7 Fe 7 stainless S316L |
Right femoral artery | 6 months | Radiographs; endothelial cell proliferation and viability | Increased in iron-stent degradation and inflammation; decreased re-endothelialization. |