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Nanocarriers and the delivered drug: effect interference due to intravenous administration.
Vlasova, Maria A; Rytkönen, Jussi; Riikonen, Joakim; Tarasova, Olga S; Mönkäre, Juha; Kovalainen, Miia; Närvänen, Ale; Salonen, Jarno; Herzig, Karl-Heinz; Lehto, Vesa-Pekka; Järvinen, Kristiina.
Afiliación
  • Vlasova MA; Faculty of Health Sciences, School of Pharmacy, University of Eastern Finland, 70211 Kuopio, Finland. Electronic address: maria.vlasova@uef.fi.
  • Rytkönen J; Faculty of Health Sciences, School of Pharmacy, University of Eastern Finland, 70211 Kuopio, Finland.
  • Riikonen J; Faculty of Science and Forestry, Department of Applied Physics, University of Eastern Finland, 70211 Kuopio, Finland. Electronic address: joakim.riikonen@uef.fi.
  • Tarasova OS; Department of Human and Animal Physiology, M.V. Lomonosov Moscow State University, Moscow 119234, Russia. Electronic address: ost.msu@gmail.com.
  • Mönkäre J; Faculty of Health Sciences, School of Pharmacy, University of Eastern Finland, 70211 Kuopio, Finland.
  • Kovalainen M; Faculty of Health Sciences, School of Pharmacy, University of Eastern Finland, 70211 Kuopio, Finland.
  • Närvänen A; Faculty of Health Sciences, School of Pharmacy, University of Eastern Finland, 70211 Kuopio, Finland.
  • Salonen J; Department of Physics and Astronomy, University of Turku, 20014 Turku, Finland. Electronic address: jarno.salonen@utu.fi.
  • Herzig KH; Institute of Biomedicine & Biocenter of Oulu, University of Oulu, 90014 Oulu, Finland. Electronic address: karl-heinz.herzig@oulu.fi.
  • Lehto VP; Faculty of Science and Forestry, Department of Applied Physics, University of Eastern Finland, 70211 Kuopio, Finland. Electronic address: vesa-pekka.lehto@uef.fi.
  • Järvinen K; Faculty of Health Sciences, School of Pharmacy, University of Eastern Finland, 70211 Kuopio, Finland. Electronic address: kristiina.jarvinen@uef.fi.
Eur J Pharm Sci ; 63: 96-102, 2014 Oct 15.
Article en En | MEDLINE | ID: mdl-24964293
ABSTRACT
Intravenously administered nanocarriers are widely studied to improve the delivery of various therapeutic agents. However, recent in vivo studies have demonstrated that intravenously administered nanocarriers that do not contain any drug may affect cardiovascular function. Here we provide an example where the drug and the nanocarrier both affect the same cardiovascular parameters following intravenous administration. The peptide ghrelin antagonist (GhA) increases arterial pressure, while thermally hydrocarbonized porous silicon nanoparticles (THCPSi) transiently decrease it, as assessed with radiotelemetry in conscious rats. As a result, intravenous administration of GhA-loaded THCPSi nanoparticles partially antagonized GhA activity arterial pressure was not increased. When the cardiovascular effects of GhA were blocked with atenolol pretreatment, GhA-loaded nanoparticles reduced arterial pressure to similar extent as drug-free nanoparticles. These data indicate that the biological activity of a drug delivered within a nanocarrier may be obscured by the biological responses induced by the nanocarrier itself.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Péptidos / Portadores de Fármacos / Sistema Cardiovascular / Artefactos / Nanopartículas Idioma: En Revista: Eur J Pharm Sci Asunto de la revista: FARMACIA / FARMACOLOGIA / QUIMICA Año: 2014 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Péptidos / Portadores de Fármacos / Sistema Cardiovascular / Artefactos / Nanopartículas Idioma: En Revista: Eur J Pharm Sci Asunto de la revista: FARMACIA / FARMACOLOGIA / QUIMICA Año: 2014 Tipo del documento: Article