Injectable nanoparticle-loaded hydrogen system for local delivery of sodium alendronate

U. Posadowska, M. Parizek, E. Filova, M.K. Wlodarczyk-Biegun, M.M.G. Kamperman, L. Bacakova, E. Pamula

Research output: Contribution to journalArticleAcademicpeer-review

41 Citations (Scopus)

Abstract

Systemic administration of bisphosphonates, e.g. sodium alendronate (Aln) is characterized by extremely low bioavailability and high toxicity. To omit aforementioned drawbacks an injectable system for the intra-bone delivery of Aln based on Aln-loaded nanoparticles (NPs-Aln) suspended in a hydrogel matrix (gellan gum, GG) was developed. Aln was encapsulated in poly(lactide-co-glycolide) (PLGA 85:15) by solid–oil–water emulsification. Drug release tests showed that within 25 days all the encapsulated drug was released from NPs-Aln and the release rate was highest at the beginning and decreased with time. In contrast, by suspending NPs-Aln in a GG matrix, the release rate was significantly lower and more constant in time. The GG–NPs-Aln system was engineered to be easily injectable and was able to reassemble its structure after extrusion as shown by rheological measurements. Invitro studies showed that the GG–NPs-Aln was cytocompatible with MG-63 osteoblast-like cells and it inhibited RANKL-mediated osteoclastic differentiation of RAW 264.7 cells. The injectability, the sustained local delivery of small doses of Aln and the biological activity render the GG–NPs-Aln system promising for the local treatment of osteoporosis and other bone tissue disorders.
Original languageEnglish
Pages (from-to)31-40
JournalInternational Journal of Pharmaceutics
Volume485
Issue number1
DOIs
Publication statusPublished - 2015

Keywords

  • drug-delivery
  • osteoclast formation
  • controlled-release
  • bone
  • gellan
  • cytotoxicity
  • formulation
  • cells
  • microspheres
  • therapeutics

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