RT info:eu-repo/semantics/article
T1 Intestinal Permeability of ß-Lapachone and Its Cyclodextrin Complexes and Physical Mixtures
A1 Echezarreta López, María Magdalena
A1 Mangas-Sanjuan, Victor
A1 Gutiérrez-Nieto, Jorge
A1 Gonzá´lez-Álvarez, Isabel
A1 González-Álvarez, Marta
A1 Casabó, Vicente-Germán
A1 Bermejo, Marival
A1 Landin, Mariana
A2 Ingeniería Química y Tecnología Farmacéutica
AB Background and objectives b-Lapachone (bLAP) is a promising, poorly soluble, antitumoral drug. bLAP combination with cyclodextrins (CDs) improves its solubility and dissolution but there is not enough information about the impact of cyclodextrins on bLAP intestinal permeability. The objectives of this work were to characterize bLAP intestinal permeability and to elucidate cyclodextrins effect on the dissolution properties and on the intestinal permeability. The final goal was to evaluate CDs influence on the oral absorption of bLAP. Methods Binary systems (physical mixtures and inclusion complexes) including bLAP and CDs (b-cyclodextrin: bCD, random-methyl-b-cyclodextrin: RMbCD and sulfobutylether-b-cyclodextrin: SBEbCD) have been prepared and analysed by differential scanning calorimetry. bLAP (and its combinations with CDs) absorption rate coefficients and effective permeability values have been determined in vitro in MDCK or MDCK-Mdr1 monolayers and in situ in rat by a closed loop perfusion technique. Results DSC results confirmed the formation of the inclusion complexes. bLAP–CDs inclusion complexes improve drug solubility and dissolution rate in comparison with physical mixtures. bLAP presented a high permeability value which can provide complete oral absorption. Its oral absorption is limited by its low solubility and dissolution rate. Cyclodextrin (both as physical mixtures and inclusion complexes) showed a positive effect on the intestinal permeability of bLAP. Complexation withCDsdoesnotreduce bLAP intestinal permeability in spite of the potential negative effect of the reduction in free fraction of the drug. Conclusions The use of RMbCD or SBEbCD inclusion complexes could benefit bLAP oral absorption by enhancing its solubility, dissolution rate and permeability.
YR 2015
FD 2015
LK http://riull.ull.es/xmlui/handle/915/37317
UL http://riull.ull.es/xmlui/handle/915/37317
LA en
NO Proyecto financiado por el proyecto: Diseño de formulaciones de fármacos de baja hidrosolubilidad mediante herramientas de Inteligencia Artificial (SAF 2012-39878-C02-01) del Ministerio de Ciencia e Innovación.
DS Repositorio institucional de la Universidad de La Laguna
RD 01-nov-2024