Folate receptor-targeted dendrimer-methotrexate conjugate for inflammatory arthritis

  • Rong Qi
  • , Istvan Majoros
  • , Asish C. Misra
  • , Alisa E. Koch
  • , Phil Campbell
  • , Hubert Marotte
  • , Ingrid L. Bergin
  • , Zhengyi Cao
  • , Sascha Goonewardena
  • , Jingga Morry
  • , Shuai Zhang
  • , Michael Beer
  • , Paul Makidon
  • , Alina Kotlyar
  • , Thommey P. Thomas
  • , James R. Baker

Producción científica: Articlerevisión exhaustiva

51 Citas (Scopus)

Resumen

Generation 5 (G5) poly(amidoamide) (PAMAM) dendrimers are synthetic polymers that have been broadly applied as drug delivery carriers. Methotrexate (MTX), an anti-folate metabolite, has been successfully used as an anti-inflammatory drug to treat rheumatoid arthritis (RA) in the clinic. In this study, we examine the therapeutic efficacy of G5 PAMAM dendrimer methotrexate conjugates (G5-MTX) that also have folic acid (FA) conjugated to the G5-MTX (G5-FA-MTX) to target inflammation-activated folate receptors overexpressing macrophages. These cells are thought to play an important role in the development of RA. With G5 serving as a control, the in vitro binding affinities of G5-FA-MTX and G5-MTX to activated macrophages were assessed in RAW264.7, NR8383 and primary rat peritoneal macrophages. The results indicated that the binding of either conjugate to macrophages was concentration- and temperature-dependent and could be blocked by the presence of 6.25 mM free FA (p < 0.005). The preventive effects of G5-MTX and G5-FA-MTX conjugates on the development of arthritis were explored on an adjuvant-induced inflammatory arthritis model and had similar preventive effects in inflammatory arthritis at a MTX equivalent dose of 4.95 -mol/kg. These studies indicated that when multiples of MTX are conjugated on dendritic polymers, they specifically bind to folate receptor overexpressing macrophages and have comparable anti-inflammatory effects to folate targeted MTX conjugated polymers.

Idioma originalEnglish (US)
Páginas (desde-hasta)1370-1384
Número de páginas15
PublicaciónJournal of Biomedical Nanotechnology
Volumen11
N.º8
DOI
EstadoPublished - ago 1 2014
Publicado de forma externa

ASJC Scopus subject areas

  • General Medicine

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