A single oral dose of celecoxib-loaded solid lipid nanoparticles for treatment of different developmental stages of experimental schistosomiasis mansoni

•Formulation and characterization of celecoxib-loaded solid lipid nanoparticles.•Solid lipid nanoparticles enhanced the antischistosomal effect of celecoxib.•20 mg/kg in a single oral dose of celecoxib-loaded solid lipid nanoparticles showed antischistosomal effects.•Juveniles were marked affected.•...

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Veröffentlicht in:Acta tropica 2022-05, Vol.229, p.106342-106342, Article 106342
Hauptverfasser: Ibrahim, Eman Ibrahim, Abou-El-Naga, Iman Fathy, El-Temsahy, Mona Mohamed, Elsawy, Eman Sheta Ali, Makled, Shaimaa, Mogahed, Nermine Mogahed Fawzy Hussein
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Sprache:eng
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Zusammenfassung:•Formulation and characterization of celecoxib-loaded solid lipid nanoparticles.•Solid lipid nanoparticles enhanced the antischistosomal effect of celecoxib.•20 mg/kg in a single oral dose of celecoxib-loaded solid lipid nanoparticles showed antischistosomal effects.•Juveniles were marked affected.•Celecoxib-loaded solid lipid nanoparticles induced tegumental damage. Schistosomiasis, a neglected tropical parasitic disease, is associated with severe pathology, mortality and economic loss. The treatment and control of schistosomiasis depends mainly on a single dose of praziquantel (PZQ). Drug repurposing and nanomedicine attract great attention to improve anti-schistosomal therapy. Previously, we reported that celecoxib (CELE), the non-steroidal anti-inflammatory drug, showed potent anti-schistosomal efficacy in an oral dose of 20 mg/kg/day for five days against different developmental stages of Schistosoma mansoni (S. mansoni) infection in mice. The aim of the current study was to shorten the duration of CELE treatment to reach an effective single oral dose against different developmental stages of S. mansoni infection using solid lipid nanoparticles (SLNs) as nano-carriers. The latter enhance the solubility, bioavailability and drug delivery and hence can decrease the frequency of administration which is of great clinical value. CELE-loaded SLNs showed good colloidal properties, high entrapment efficiency and drug loading, sustained biphasic release pattern with excellent storage stability. The used regimen was efficient against different developmental stages of S. mansoni infection with the most pronounced effect against the juvenile stage where the worm load, the hepatic egg count and the intestinal egg count were reduced by 86.39%, 91.45% and 90.11%, respectively. Meanwhile, when targeting the invasive and the adult stages, it induced reduction in the worm load by 73.55% and 78.22%, the hepatic egg count by 69.99% and 75.39% and the intestinal egg count by 77.57% and 79.89%, respectively. Additionally, CELE-loaded SLNs caused extensive tegumental damage of adult worms and marked improvement in the liver pathology. [Display omitted]
ISSN:0001-706X
1873-6254
DOI:10.1016/j.actatropica.2022.106342