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Design and physicochemical characterisation of novel dissolving polymeric microneedle arrays for transdermal delivery of high dose, low molecular weight drugs.
McCrudden, Maelíosa T C; Alkilani, Ahlam Zaid; McCrudden, Cian M; McAlister, Emma; McCarthy, Helen O; Woolfson, A David; Donnelly, Ryan F.
Afiliación
  • McCrudden MT; Queen's University, Belfast School of Pharmacy, 97 Lisburn Road, Belfast BT9 7BL, UK.
  • Alkilani AZ; Queen's University, Belfast School of Pharmacy, 97 Lisburn Road, Belfast BT9 7BL, UK; School of Pharmacy, Zarqa University, Zarqa 132222, Jordan.
  • McCrudden CM; Queen's University, Belfast School of Pharmacy, 97 Lisburn Road, Belfast BT9 7BL, UK.
  • McAlister E; Queen's University, Belfast School of Pharmacy, 97 Lisburn Road, Belfast BT9 7BL, UK.
  • McCarthy HO; Queen's University, Belfast School of Pharmacy, 97 Lisburn Road, Belfast BT9 7BL, UK.
  • Woolfson AD; Queen's University, Belfast School of Pharmacy, 97 Lisburn Road, Belfast BT9 7BL, UK.
  • Donnelly RF; Queen's University, Belfast School of Pharmacy, 97 Lisburn Road, Belfast BT9 7BL, UK. Electronic address: r.donnelly@qub.ac.uk.
J Control Release ; 180: 71-80, 2014 Apr 28.
Article en En | MEDLINE | ID: mdl-24556420
We describe formulation and evaluation of novel dissolving polymeric microneedle (MN) arrays for the facilitated delivery of low molecular weight, high dose drugs. Ibuprofen sodium was used as the model here and was successfully formulated at approximately 50% w/w in the dry state using the copolymer poly(methylvinylether/maleic acid). These MNs were robust and effectively penetrated skin in vitro, dissolving rapidly to deliver the incorporated drug. The delivery of 1.5mg ibuprofen sodium, the theoretical mass of ibuprofen sodium contained within the dry MN alone, was vastly exceeded, indicating extensive delivery of the drug loaded into the baseplates. Indeed in in vitro transdermal delivery studies, approximately 33mg (90%) of the drug initially loaded into the arrays was delivered over 24h. Iontophoresis produced no meaningful increase in delivery. Biocompatibility studies and in vivo rat skin tolerance experiments raised no concerns. The blood plasma ibuprofen sodium concentrations achieved in rats (263µgml(-1) at the 24h time point) were approximately 20 times greater than the human therapeutic plasma level. By simplistic extrapolation of average weights from rats to humans, a MN patch design of no greater than 10cm(2) could cautiously be estimated to deliver therapeutically-relevant concentrations of ibuprofen sodium in humans. This work, therefore, represents a significant progression in exploitation of MN for successful transdermal delivery of a much wider range of drugs.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polímeros / Antiinflamatorios no Esteroideos / Ibuprofeno / Sistemas de Liberación de Medicamentos / Microinyecciones Límite: Animals / Humans / Male Idioma: En Revista: J Control Release Asunto de la revista: FARMACOLOGIA Año: 2014 Tipo del documento: Article Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polímeros / Antiinflamatorios no Esteroideos / Ibuprofeno / Sistemas de Liberación de Medicamentos / Microinyecciones Límite: Animals / Humans / Male Idioma: En Revista: J Control Release Asunto de la revista: FARMACOLOGIA Año: 2014 Tipo del documento: Article Pais de publicación: Países Bajos