SwePub
Sök i LIBRIS databas

  Utökad sökning

id:"swepub:oai:DiVA.org:kth-200409"
 

Sökning: id:"swepub:oai:DiVA.org:kth-200409" > Biodistribution of ...

Biodistribution of biodegradable polymeric nano-carriers loaded with busulphan and designed for multimodal imaging

Asem, Heba (författare)
KTH,Funktionella material, FNM,Karolinska Institutet (KI), Sweden
Zhao, Ying (författare)
Karolinska Institutet
Ye, Fei (författare)
visa fler...
Barrefelt, Asa (författare)
Abedi-Valugerdi, Manuchehr (författare)
Karolinska Institutet
El-Sayed, Ramy (författare)
El-Serafi, Ibrahim (författare)
Karolinska Institutet
Abu-Salah, Khalid M. (författare)
Hamm, Jorg (författare)
Muhammed, Mamoun (författare)
Karolinska Institutet,KTH,Funktionella material, FNM
Hassan, Moustapha (författare)
visa färre...
 (creator_code:org_t)
2016-12-19
2016
Engelska.
Ingår i: Journal of Nanobiotechnology. - : BioMed Central (BMC). - 1477-3155. ; 14:1
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Background: Multifunctional nanocarriers for controlled drug delivery, imaging of disease development and follow-up of treatment efficacy are promising novel tools for disease diagnosis and treatment. In the current investigation, we present a multifunctional theranostic nanocarrier system for anticancer drug delivery and molecular imaging. Superparamagnetic iron oxide nanoparticles (SPIONs) as an MRI contrast agent and busulphan as a model for lipophilic antineoplastic drugs were encapsulated into poly (ethylene glycol)-co-poly (caprolactone) (PEG-PCL) micelles via the emulsion-evaporation method, and PEG-PCL was labelled with VivoTag 680XL fluorochrome for in vivo fluorescence imaging. Results: Busulphan entrapment efficiency was 83% while the drug release showed a sustained pattern over 10 h. SPION loaded-PEG-PCL micelles showed contrast enhancement in T-2*-weighted MRI with high r(2)* relaxivity. In vitro cellular uptake of PEG-PCL micelles labeled with fluorescein in J774A cells was found to be time-dependent. The maximum uptake was observed after 24 h of incubation. The biodistribution of PEG-PCL micelles functionalized with VivoTag 680XL was investigated in Balb/c mice over 48 h using in vivo fluorescence imaging. The results of real-time live imaging were then confirmed by ex vivo organ imaging and histological examination. Generally, PEG-PCL micelles were highly distributed into the lungs during the first 4 h post intravenous administration, then redistributed and accumulated in liver and spleen until 48 h post administration. No pathological impairment was found in the major organs studied. Conclusions: Thus, with loaded contrast agent and conjugated fluorochrome, PEG-PCL micelles as biodegradable and biocompatible nanocarriers are efficient multimodal imaging agents, offering high drug loading capacity, and sustained drug release. These might offer high treatment efficacy and real-time tracking of the drug delivery system in vivo, which is crucial for designing of an efficient drug delivery system.

Ämnesord

NATURVETENSKAP  -- Biologi -- Mikrobiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Microbiology (hsv//eng)

Nyckelord

Biodegradable polymer
Drug delivery
Magnetic resonance imaging
In vivo fluorescence imaging
Biodistribution
Busulphan
Cancer

Publikations- och innehållstyp

ref (ämneskategori)
art (ämneskategori)

Hitta via bibliotek

Till lärosätets databas

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy