Abstract

Background: Post embolization aneurysm reccurence is still a drawback in endovascular coiling for cerebral aneuryms. That stimulated reaearch into new promising embolic materials, as the Thermoreversible Gelation Polymer (TGP) when used as cell culture medium with its temperature related properties. We evaluated proliferative properties of fibroblast cell cultures in association with metalic coils. Methods: Intial assessment of cell viability was done for 3T3 (mouse fibroblast) and A172 (glioma cell) lines for 6 and 16 days in TGP solid phase and media. After that TGP was liquified and cell attachment confirmed. Next, fibroblasts were cultivated under the same conditions adding Guglielmi detachable coils for 24 h and 3 days with TGP, evaluating cell attachment and proliferation on coils. Last, the time course of cell proliferation was evaluated, comparing cell numbers on equal coil surface areas for 1,3,5,7,10,14 and 21 days in TGP. Electron microscopy was used for cell assessment on the coils. Results: Fibroblasts survive and show satisfactory viability in TGP. In liquefied TGP after 6 days and 16days, both cell types temporally extended processes and attached on flask`s bottom. Next after 24 h and 3 days fibroblast cultivation with coils in TGP, cells extended processes and attached to coils, indicating some proliferation and clustering. Last, the day 1 attached cell numbers on coils cultivated in TGP gradually decreased until day 10 and later increased again to just below day 1 level. However, both fibroblast and glioma cells in TGP did not extend processes, move or proliferate, and had spherical shape while in solid TGP. Conclusion: Fibroblasts attachment and long survival on coils in TGP may facilitate aneurysm treatment to achieve better volume embolization rate and improve intra-aneurysmal thrombus organization.

Highlights

  • Subarachnoid haemorrhage (SAH) due to rupture of cerebral aneurysm is a significant cause of morbidity and mortality throughout the world [1]

  • The contributing factors to prevent recanalisation are high volume embolization rate, promotion of thrombus organization in the aneurysm and endothelialial coverige of the occluded aneurysm orifice [6].Volume embolization ratio greater than 25% was necessary to achieve stability in large and wide-neck aneurysms treated by detachable platium coil embolization [7] and currently it is a routine goal during treatment

  • Fibloblasts accelarated early histlogical profliferation/maturation compared to controls [9,10].At the completion of the process, tissues obliterating the aneurysm neck orifice were usually covered by neoendothelial membrane [11], replacing the surface of the initial fresh thrombus [12]

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Summary

Introduction

Subarachnoid haemorrhage (SAH) due to rupture of cerebral aneurysm is a significant cause of morbidity and mortality throughout the world [1]. Endovascular therapy becomes increasingly popular alternative to surgical clipping because of being less invasive and the accumulation of results indicating similar or better outcomes [4,5] It has been less effective in wide-neck or large/giant aneurysms. The contributing factors to prevent recanalisation are high volume embolization rate, promotion of thrombus organization in the aneurysm and endothelialial coverige of the occluded aneurysm orifice [6].Volume embolization ratio greater than 25% was necessary to achieve stability in large and wide-neck aneurysms treated by detachable platium coil embolization [7] and currently it is a routine goal during treatment. In some wide-neck or large/giant aneurysms, the thurombus induced by coil placement remains poorly organized after 3 weeks from treatment. We evaluated proliferative properties of fibroblast cell cultures in association with metalic coils

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