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Hybrid Microneedle-Mediated Transdermal Delivery of Atorvastatin Calcium-Loaded Polymeric Micelles for Hyperlipidemia Therapy.

Authors :
Ou Yang MW
Hu LF
Feng YH
Li X
Peng J
Yu R
Zhang CY
Chen BZ
Guo XD
Source :
ACS applied bio materials [ACS Appl Bio Mater] 2024 Jun 17; Vol. 7 (6), pp. 4051-4061. Date of Electronic Publication: 2024 May 24.
Publication Year :
2024

Abstract

Hyperlipidemia has been a huge challenge to global health, leading to the cardiovascular disease, hypertension, and diabetes. Atorvastatin calcium (AC), a widely prescribed drug for hyperlipidemia, faces huge challenges with oral administration due to poor water solubility and hepatic first-pass effects, resulting in low therapeutic efficacy. In this work, we designed and developed a hybrid microneedle (MN) patch system constructed with soluble poly(vinyl alcohol) (PVA) and AC-loaded polymeric micelles (AC@PMs) for transdermal delivery of AC to enhance the hyperlipidemia therapy. We first prepared various AC@PM formulations self-assembled from mPEG-PLA and mPEG-PLA-PEG block copolymers using a dialysis method and evaluated the physicochemical properties in combination with experiment skills and dissipative particle dynamics (DPD) simulations. Then, we encapsulated the AC@PMs into the PVA MN patch using a micromold filling method, followed by characterizing the performances, especially the structural stability, mechanical performance, and biosafety. After conducting in vivo experiments using a hyperlipidemic rat model, our findings revealed that the hybrid microneedle-mediated administration exhibited superior therapeutic efficacy when compared to oral delivery methods. In summary, we have successfully developed a hybrid microneedle (MN) patch system that holds promising potential for the efficient transdermal delivery of hydrophobic drugs.

Details

Language :
English
ISSN :
2576-6422
Volume :
7
Issue :
6
Database :
MEDLINE
Journal :
ACS applied bio materials
Publication Type :
Academic Journal
Accession number :
38790078
Full Text :
https://doi.org/10.1021/acsabm.4c00399