| CPC A61L 15/24 (2013.01) [A61L 29/08 (2013.01); A61L 29/12 (2013.01); A61L 29/14 (2013.01); A61L 31/10 (2013.01); A61L 31/12 (2013.01); A61L 31/14 (2013.01); G02C 7/04 (2013.01)] | 11 Claims |
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1. A method of manufacturing a medical device comprising a substrate and a hydrophilic polymer layer, comprising the steps of:
placing the substrate in a solution containing a hydrophilic polymer and a normal salt in an amount ranging from 3.0 to 20% by mass; and
heating the solution at a temperature ranging from 50° C. to 140° C.,
wherein the normal salt contains one or more selected from the group consisting of BaSO4, BaCO3, CaSO4, CaCO3, (CH3COO)2Ca, NaCl, Na2CO3, Na2SO4, NaNO3, CH3COONa, KCl, K2SO4, K2CO3, KNO3, CH3COOK, LiCl, LiSO4, LiCO3, LiNO3, and CH3COOLi, and
wherein the hydrophilic polymer comprises an amide group and an acidic group.
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