3D DLP-printed cannabinoid microneedles patch and its pharmacokinetic evaluation in rats.
Document Type
Article
Publication Date
4-24-2024
Abstract
OBJECTIVE: The objective of the present study was to enhance the bioavailability of cannabidiol (CBD) using 3D Digital Light Processing (DLP)-printed microneedle (MN) transdermal drug delivery system.
METHODS: CBD MN patch was fabricated and optimized using 3D DLP printing using CBD (8% w/v), Lithium phenyl-2,4,6-trimethylbenzoylphosphinate (LAP) (0.49% w/v), distilled water (20% w/v), and poly (ethylene glycol) dimethacrylate 550 (PEGDAMA 550) (up to 100% w/v). CBD MNs were characterized for their morphology, mechanical strength, in vitro release study, ex vivo permeation study, and in vivo pharmacokinetic (PK) profile.
KEY FINDINGS: Microscopic images showed that sharp CBD MNs with a height of ~800 μm, base diameter of ~250 μm, and tip with a radius of curvature (RoC) of ~15 μm were successfully printed using optimized printing parameters. Mechanical strength studies showed no significant deformation in the morphology of CBD MNs even after applying 0.5N/needle force. Ex vivo permeation study showed significant (P < .0001) permeation of CBD in the receiving media as compared to CBD patch (control). In vivo PK study showed significantly (P < .05) enhanced bioavailability in the case of CBD MN patch as compared to CBD subcutaneous inj. (control).
CONCLUSION: Overall, systemic absorption of CBD was significantly enhanced using 3D-printed MN drug delivery system.
Publication Title
The Journal of Pharmacy and Pharmacology
PubMed ID
38656627
Recommended Citation
Bagde, Arvind; Mosley-Kellum, Keb; Spencer, Shawn; and Singh, Mandip, "3D DLP-printed cannabinoid microneedles patch and its pharmacokinetic evaluation in rats." (2024). PCOM Scholarly Works. 2257.
https://digitalcommons.pcom.edu/scholarly_papers/2257
DOI: https://doi.org/10.1093/jpp/rgae043
Comments
This article was published in Journal of Pharmacy and Pharmacology.
The published version is available at https://doi.org/10.1093/jpp/rgae043.
Copyright © 2024 The Author(s) 2024. Published by Oxford University Press on behalf of the Royal Pharmaceutical Society.