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Transdermal Delivery of Iron Using Soluble Microneedles: Dermal Kinetics and Safety.
Modepalli, Naresh; Shivakumar, H Nanjappa; McCrudden, Maeliosa T C; Donnelly, Ryan F; Banga, Ajay; Murthy, S Narasimha.
Afiliación
  • Modepalli N; The University of Mississippi School of Pharmacy, Mississippi 38677.
  • Shivakumar HN; Institute for Drug Delivery and Biomedical Research, Bangalore, India; KLE's University College of Pharmacy, Bangalore, India.
  • McCrudden MT; School of Pharmacy, Queen's University Belfast, Belfast, UK.
  • Donnelly RF; School of Pharmacy, Queen's University Belfast, Belfast, UK.
  • Banga A; College of Pharmacy, Mercer University, Atlanta, Georgia 30341.
  • Murthy SN; The University of Mississippi School of Pharmacy, Mississippi 38677; Institute for Drug Delivery and Biomedical Research, Bangalore, India. Electronic address: murthy@olemiss.edu.
J Pharm Sci ; 105(3): 1196-200, 2016 Mar.
Article en En | MEDLINE | ID: mdl-26928401
ABSTRACT
Currently, the iron compounds are administered via oral and parenteral routes in patients of all ages, to treat iron deficiency. Despite continued efforts to supplement iron via these conventional routes, iron deficiency still remains the most prevalent nutritional disorder all over the world. Transdermal replenishment of iron is a novel, potential approach of iron replenishment. Ferric pyrophosphate (FPP) was found to be a suitable source of iron for transdermal replenishment. The safety of FPP was assessed in this project by challenging the dermal fibroblast cells with high concentration of FPP. The cell viability assay and reactive oxygen species assay were performed. The soluble microneedle array was developed, incorporated with FPP and the kinetics of free iron in the skin; extracellular fluid following dermal administration of microneedle array was investigated in hairless rats. From the cell based assays, FPP was selected as one of the potential iron sources for transdermal delivery. The microneedles were found to dissolve in the skin fluid within 3 hours of administration. The FPP concentration in the dermal extracellular fluid declined after complete dissolution of the microneedle array. Overall, the studies demonstrated the safety of FPP for dermal delivery and the feasibility of soluble microneedle approach for transdermal iron replenishment therapy.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Piel / Absorción Cutánea / Sistemas de Liberación de Medicamentos / Difosfatos / Hierro Límite: Animals / Humans Idioma: En Revista: J Pharm Sci Año: 2016 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Piel / Absorción Cutánea / Sistemas de Liberación de Medicamentos / Difosfatos / Hierro Límite: Animals / Humans Idioma: En Revista: J Pharm Sci Año: 2016 Tipo del documento: Article