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Development of Norelgestromin Dissolving Bilayer Microarray Patches for Sustained Release of Hormonal Contraceptive.
Vora, Lalitkumar K; Tekko, Ismaiel A; Volpe Zanutto, Fabiana; Sabri, Akmal; Choy, Robert K M; Mistilis, Jessica; Kwarteng, Priscilla; Kilbourne-Brook, Maggie; Jarrahian, Courtney; McCarthy, Helen O; Donnelly, Ryan F.
Affiliation
  • Vora LK; School of Pharmacy, Medical Biology Centre, Queen's University Belfast, 97 Lisburn Road, Belfast BT9 7BL, UK.
  • Tekko IA; School of Pharmacy, Medical Biology Centre, Queen's University Belfast, 97 Lisburn Road, Belfast BT9 7BL, UK.
  • Volpe Zanutto F; School of Pharmacy, Medical Biology Centre, Queen's University Belfast, 97 Lisburn Road, Belfast BT9 7BL, UK.
  • Sabri A; School of Pharmacy, Medical Biology Centre, Queen's University Belfast, 97 Lisburn Road, Belfast BT9 7BL, UK.
  • Choy RKM; PATH, 2201 Westlake Avenue, Seattle, WA 98121, USA.
  • Mistilis J; PATH, 2201 Westlake Avenue, Seattle, WA 98121, USA.
  • Kwarteng P; PATH, 2201 Westlake Avenue, Seattle, WA 98121, USA.
  • Kilbourne-Brook M; PATH, 2201 Westlake Avenue, Seattle, WA 98121, USA.
  • Jarrahian C; PATH, 2201 Westlake Avenue, Seattle, WA 98121, USA.
  • McCarthy HO; School of Pharmacy, Medical Biology Centre, Queen's University Belfast, 97 Lisburn Road, Belfast BT9 7BL, UK.
  • Donnelly RF; School of Pharmacy, Medical Biology Centre, Queen's University Belfast, 97 Lisburn Road, Belfast BT9 7BL, UK.
Pharmaceutics ; 16(7)2024 Jul 17.
Article de En | MEDLINE | ID: mdl-39065643
ABSTRACT
Microarray patches (MAPs) offer a noninvasive and patient-friendly drug delivery method, suitable for self-administration, which is especially promising for low- and middle-income country settings. This study focuses on the development of dissolving bilayer MAPs loaded with norelgestromin (NGMN) as a first step towards developing a future potential drug delivery system for sustained hormonal contraception. The fabricated MAPs were designed with the appropriate needle lengths to penetrate the stratum corneum, while remaining minimally stimulating to dermal nociceptors. Ex vivo assessments showed that the MAPs delivered an average of 176 ± 60.9 µg of NGMN per MAP into excised neonatal porcine skin, representing 15.3 ± 5.3% of the loaded drug. In vivo pharmacokinetic analysis in Sprague Dawley rats demonstrated a Tmax of 4 h and a Cmax of 67.4 ± 20.1 ng/mL for the MAP-treated group, compared to a Tmax of 1 h and a Cmax of 700 ± 138 ng/mL for the intramuscular (IM) injection group, with a relative bioavailability of approximately 10% for the MAPs. The MAP-treated rats maintained plasma levels sufficient for therapeutic effects for up to 7 days after a single application. These results indicate the potential of NGMN-loaded dissolving bilayer MAPs, with further development focused on extending the release duration and improving bioavailability for prolonged contraceptive effects.
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Pharmaceutics Année: 2024 Type de document: Article Pays d'affiliation: Royaume-Uni Pays de publication: Suisse

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Pharmaceutics Année: 2024 Type de document: Article Pays d'affiliation: Royaume-Uni Pays de publication: Suisse