dc.description.abstract | Dissolving microneedles have gained interest due to their ability to encapsulate
and release drug formulations upon dissolution. These devices are composed of soluble
materials or biodegradable polymers, allowing controlled drug delivery. Chitosan, a
significant component in dissolving microneedles, has been widely used due to its high
biodegradability and biocompatibility. However, studies have yet to explore how the
molecular weight of chitosan affects transdermal distribution utilizing dissolving
microneedles. This research aimed to study the impact of chitosan molecular weight on
the fabrication of chitosan microneedles for transdermal drug delivery. Nine
microneedle types were fabricated using Polyvinyl alcohol /polyvinylpyrrolidone
(PVA/PVP) solution as a supporting base, yielding nine different microneedle types.
The study compared morphologies, characteristics, mechanical properties, skin
insertion, cytotoxicity, and drug release profiles using Rhodamine B as the model drug.
This information can be applied to the formulation of dissolving microneedles for
transdermal drug delivery. Chitosan from different molecular weights and
concentrations was successfully fabricated into microneedles using the double-casting
method. The shape, mechanical strength, and insertion characteristics of chitosan
microneedles were greatly influenced by their molecular weight. At 3%(w/v)
concentrations, low, medium, and high molecular weight chitosan microneedles
demonstrated high mechanical strength. With an insertion depth of 0.52 mm, the 3%
light weight chitosan microneedle (3LW) displayed the greatest skin penetration
through PARAFILM. 3LW demonstrated the highest mechanical strength and insertion
properties. It was utilized to analyze the cytotoxicity and drug release profile of the
microneedles. Within 10 minutes, there was an initial burst release, which was followed
by a slow release over time. At a concentration of 3% (w/v), which was used to form
3LW, low-weight chitosan was found to be low-toxic. | en_US |