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Sökning: id:"swepub:oai:DiVA.org:ltu-11190" > Influence of polyme...

Influence of polymeric microcarriers on the in-vivo intranasal uptake of an anti-migraine drug for brain targeting

Gavini, Elisabetta (författare)
Department of Chemistry and Pharmacy, University of Sassari
Rassu, Giovanna (författare)
Department of Chemistry and Pharmacy, University of Sassari
Ferraro, Luca (författare)
Department of Experimental and Clinical Medicine, Pharmacology Section, University of Ferrara
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Beggiato, Sarah (författare)
Department of Experimental and Clinical Medicine, Pharmacology Section, University of Ferrara
Alhalaweh, Amjad (författare)
Luleå tekniska universitet,Medicinsk vetenskap
Velaga, Sitaram (författare)
Luleå tekniska universitet,Medicinsk vetenskap
Marchetti, Nichola (författare)
Department of Chemistry, University of Ferrara
Bandiera, Pasquale (författare)
Department of Biomedical Sciences, University of Sassari
Giunchedi, Paolo (författare)
Department of Chemistry and Pharmacy, University of Sassari
Dalpiaz, Alessandro (författare)
Department of Pharmaceutical Sciences, University of Ferrara
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 (creator_code:org_t)
Elsevier BV, 2013
2013
Engelska.
Ingår i: European journal of pharmaceutics and biopharmaceutics. - : Elsevier BV. - 0939-6411 .- 1873-3441. ; 83:2, s. 174-183
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • The objective of this study was to investigate the effect of polymeric microcarriers on the in-vivo intranasal uptake of an anti-migraine drug for brain targeting. Mucoadhesive powder formulations consisted of antimigraine drug, zolmitriptan, and chitosans (various molecular weights and types) or hydroxypropyl methylcellulose (HPMC). Their suitability for nasal administration was evaluated by in-vitro and ex-vivo mucoadhesion and permeation tests. The formulations based on chitosan glutamate (CG) or HPMC were tested in-vivo because they showed good mucoadhesive properties and altered the permeation rate of the drug. The in-vivo results from intravenous infusion and nasal aqueous suspension of the drug or nasal particulate powders were compared. The plasmatic AUC values obtained within 8 h following intravenous administration appeared about three times higher than those obtained by nasal administration, independent of the formulations. Zolmitriptan concentrations in the cerebrospinal fluid obtained from nasal and intravenous administrations were respectively 30 and 90 times lower than the concentrations of the drug in the blood. Thus, nasal administration potentiated the central zolmitriptan activity allowing a reduction of the drug peripheral levels, with respect to the intravenous administration. Among nasally administered formulations, CG microparticles showed the highest efficacy in promoting the central uptake of zolmitriptan within 1 h.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Hälsovetenskap -- Annan hälsovetenskap (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Health Sciences -- Other Health Sciences (hsv//eng)

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Health Science
Hälsovetenskap

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