4.6 Article

Levonorgestrel Microneedle Array Patch for Sustained Release Contraception: Formulation, Optimization and In Vivo Characterization

Journal

MOLECULES
Volume 27, Issue 7, Pages -

Publisher

MDPI
DOI: 10.3390/molecules27072349

Keywords

drug delivery; nanotechnology; contraception; levonorgestrel; liposomes; microneedle; sustained-release

Funding

  1. Bill & Melinda Gates Foundation, USA [OPP1184017, RD/0118-GATES00-001]
  2. Bill and Melinda Gates Foundation [OPP1184017] Funding Source: Bill and Melinda Gates Foundation

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This study developed a levonorgestrel liposome-loaded microneedle array patch for contraception, which showed better efficacy than the drug-loaded microneedle array patch. The sustained release behavior of levonorgestrel was observed for 28 days.
Background: The goal of this work was to develop a levonorgestrel liposome-loaded microneedle array patch for contraception. Methods: Levonorgestrel-loaded liposome was formulated by a solvent injection technique, characterized, and studied. Results: The formulated liposomes were characterized for particle size (147 +/- 8 nm), polydispersity index (0.207 +/- 0.03), zeta potential (-23 +/- 4.25 mV), drug loading (18 +/- 3.22%) and entrapment efficiency (85 +/- 4.34%). A cryo high-resolution transmission electron microscopy and cryo field emission gun scanning electron microscopy study showed spherical shaped particles with a smooth surface. The in vitro drug release and in vivo pharmacokinetic study showed sustained behaviour of Levonorgestrel for 28 days. Conclusion: The levonorgestrel liposome-loaded microneedle array patch showed better contraception than the drug-loaded microneedle array patch.

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