TY - JOUR
T1 - Water-soluble polyvinyl alcohol microspheres for temporary embolization
T2 - Development and in vivo characteristics in a pig kidney model
AU - Shomura, Yuzo
AU - Tanigawa, Noboru
AU - Shibutani, Mitsuo
AU - Wakimoto, Shinya
AU - Tsuji, Kazutoshi
AU - Tokuda, Takanori
AU - Terada, Jiro
AU - Kariya, Shuji
AU - Kojima, Hiroyuki
AU - Komemushi, Atsushi
AU - Sawada, Satoshi
PY - 2011/2
Y1 - 2011/2
N2 - Purpose To preliminarily examine whether solubility of water-soluble polyvinyl alcohol (PVA) microspheres in blood plasma changes in proportion to their degrees of saponification. The study also examined their feasibility as a temporary embolic agents in the pig renal artery. Materials and Methods Three types of PVA microspheres with the degrees of saponification of 97 mol% (S97), 98 mol% (S98), and 99 mol% (S99) were prepared. Seven kidneys in seven miniature pigs were embolized and divided into three groups so there would be at least two kidneys for each type of PVA. One animal in each group was euthanized immediately after angiography at 3 hours after embolization and the other one at 7 days after. In addition, one animal embolized with S99 microspheres was euthanized at 21 days after embolization. Results With S97 microspheres, the vascular network had recovered to the preembolic state by 3 hours after embolization. With S98 microspheres, blood flow in the third-order branch had been restored in the same period. With S99 microspheres, the second- and lower order branches remained occluded until 21 days. Histopathologic specimens harvested at 3 hours revealed only a trace of PVA for S97 microspheres. With S98 microspheres, the vascular lumen was still found to be filled with PVA gel. With S99 microspheres, swollen microspheres densely filled the vascular lumen even on day 21. Conclusions Dissolution process in vitro and the duration of arterial occlusion in vivo were possibly related to the degree of saponification of PVA. This result may support feasibility of PVA microspheres as a temporary embolic agent.
AB - Purpose To preliminarily examine whether solubility of water-soluble polyvinyl alcohol (PVA) microspheres in blood plasma changes in proportion to their degrees of saponification. The study also examined their feasibility as a temporary embolic agents in the pig renal artery. Materials and Methods Three types of PVA microspheres with the degrees of saponification of 97 mol% (S97), 98 mol% (S98), and 99 mol% (S99) were prepared. Seven kidneys in seven miniature pigs were embolized and divided into three groups so there would be at least two kidneys for each type of PVA. One animal in each group was euthanized immediately after angiography at 3 hours after embolization and the other one at 7 days after. In addition, one animal embolized with S99 microspheres was euthanized at 21 days after embolization. Results With S97 microspheres, the vascular network had recovered to the preembolic state by 3 hours after embolization. With S98 microspheres, blood flow in the third-order branch had been restored in the same period. With S99 microspheres, the second- and lower order branches remained occluded until 21 days. Histopathologic specimens harvested at 3 hours revealed only a trace of PVA for S97 microspheres. With S98 microspheres, the vascular lumen was still found to be filled with PVA gel. With S99 microspheres, swollen microspheres densely filled the vascular lumen even on day 21. Conclusions Dissolution process in vitro and the duration of arterial occlusion in vivo were possibly related to the degree of saponification of PVA. This result may support feasibility of PVA microspheres as a temporary embolic agent.
UR - http://www.scopus.com/inward/record.url?scp=79451473415&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=79451473415&partnerID=8YFLogxK
U2 - 10.1016/j.jvir.2010.10.015
DO - 10.1016/j.jvir.2010.10.015
M3 - Article
C2 - 21194968
AN - SCOPUS:79451473415
SN - 1051-0443
VL - 22
SP - 212
EP - 219
JO - Journal of Vascular and Interventional Radiology
JF - Journal of Vascular and Interventional Radiology
IS - 2
ER -