Version 2 2022-09-20, 11:34Version 2 2022-09-20, 11:34
Version 1 2022-09-15, 12:01Version 1 2022-09-15, 12:01
journal contribution
posted on 2022-09-20, 11:34authored bySeojin Jung, Seokhee Chang, Na-Eun Kim, Seong-O Choi, Yoon-Jae Song, Yue Yuan, Jooyoun Kim
A feasible strategy
of on-demand drug delivery for the treatment
of dermal inflammation under low-pH conditions is proposed, employing
zeolitic imidazolate framework-8 (ZIF-8) as a pH-responsive nanoparticle
and curcumin (CCM) as a model drug. To overcome the low bioavailability
of topically treated drug, a microneedle (MN) form is used to incorporate
CCM and ZIF-8. Taking advantage of the fact that ZIF-8 degrades under
acidic conditions, CCM is embedded in porous ZIF-8 nanoparticles such
that CCM is released when ZIF-8 comes into contact with an acidic
dermal fluid at the inflammation site, and this CCM-encapsulated ZIF-8
(CCMZIF) is incorporated into water-dissolvable poly(vinyl pyrrolidone)
MN. The ZIF-8 shows a high loading capacity (∼40.5%) of CCM
through chemical bonding and physical adsorption. From in vitro tests
with both a buffered solution and porcine skin, CCM from the CCMZIF
MN is released in a higher amount at pH 5.0 than at pH 7.4, demonstrating
the capability of the pH-responsive release of the drug when needed
at inflammatory sites. The analytical investigation conducted here
reveals that an acidic environment triggers the structural degradation
of ZIF-8, allowing the release of the chemically bonded CCM. Cytotoxicity
and stability tests demonstrate the good biocompatibility and bioavailability
of ZIF-8. This study highlights the analytical discussion of the encapsulation
and release mechanism of CCM in a ZIF-8-implemented MN drug delivery
platform. The results demonstrate an advanced on-demand therapeutic
strategy for skin disorder treatment.