Atıf İçin Kopyala
AMASYA G., BAKAR ATEŞ F., Wintgens V., Amiel C.
INTERNATIONAL JOURNAL OF PHARMACEUTICS, cilt.592, 2021 (SCI-Expanded)
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Yayın Türü:
Makale / Tam Makale
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Cilt numarası:
592
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Basım Tarihi:
2021
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Doi Numarası:
10.1016/j.ijpharm.2020.119994
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Dergi Adı:
INTERNATIONAL JOURNAL OF PHARMACEUTICS
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Derginin Tarandığı İndeksler:
Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, Aquatic Science & Fisheries Abstracts (ASFA), BIOSIS, Biotechnology Research Abstracts, CAB Abstracts, Chemical Abstracts Core, EMBASE, International Pharmaceutical Abstracts, MEDLINE, Veterinary Science Database
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Anahtar Kelimeler:
Solid lipid nanoparticles (SLN), Layer by layer assembly, Oppositely charged beta-cyclodextrin polymers (poly-beta-CDs), Core-corona structure, Surface modified SLN, CONTROLLED DRUG-DELIVERY, VITRO RELEASE KINETICS, PLA NANOPARTICLES, SLN, CARRIERS, PACLITAXEL, STABILITY, DESIGN, NLC
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Ankara Üniversitesi Adresli:
Evet
Özet
This study aims to design and characterize the layer-by-layer assembly of core-corona nanoarchitecture for novel surface-modified solid lipid nanoparticles. Oppositely charged beta-cyclodextrin polymers were used to build corona structure onto lipid core, and the particle size, polydispersity index, and zeta potential of SLN with polymer layers were evaluated. Morphology of surface-modified SLN was identified using TEM. The effect of polymer coating on drug release pattern was investigated by in-vitro release studies. The biocompatibility of the novel SLN systems was assessed on various healty cell lines using in vitro cytotoxicity assay.