The degree of saponification, which is a dissolution
characteristic
of poly(vinyl alcohol) (PVA), is used to blend PVA to prepare a hydrogel
microneedle (MN) patch. The MN patch was manufactured with an adjustable
disassembly time using a molding process, and it was confirmed to
have morphological stability and excellent needle formation. The permeability
of the gelatin sheet, which is analogous to the skin elasticity coefficient
of a real human, was confirmed. The penetration ratio had a very high
value of 100% and sufficient physical properties to penetrate the
skin. In the disassembly experiment, the MN patch was produced with
ratios of lower:higher saponification of 6:4 (PVA6), 7:3 (PVA7), 8:2
(PVA8), 9:1 (PVA9), and 10:0 (PVA10). Degradation did not occur for
PVA6 and PVA7 but occurred for PVA8, PVA9, and PVA10. A cytotoxicity
test to investigate its suitability for use in the human body confirmed
the cell viability of 80% or more and nontoxic properties. Therefore,
sufficient cell viability was confirmed when compared to the existing
products.