Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/17208
Title: Targeted gold nanohybrids functionalized with folate-hydrophobic-quaternized pullulan delivering camptothecin for enhancing hydrophobic anticancer drug efficacy
Authors: Laksee S.
Supachettapun C.
Muangsin N.
Lertsarawut P.
Rattanawongwiboon T.
Sricharoen P.
Limchoowong N.
Chutimasakul T.
Kwamman T.
Hemvichian K.
Keywords: Biological organs
Biomimetics
Cell death
Controlled drug delivery
Cytotoxicity
Gold
Hydrophobicity
Molecular biology
Nanostructured materials
Respiratory system
Acidic conditions
Anticancer activities
Apoptosis pathways
Camptothecin (CPT)
Folate receptor
Human lung cancer cells
Human lung cells
Intermolecular interactions
Targeted drug delivery
Issue Date: 2021
Abstract: This study presented a green, facile and efficient approach for a new combination of targeted gold nanohybrids functionalized with folate-hydrophobic-quaternized pullulan delivering hydrophobic camptothecin (CPT-GNHs@FHQ-PUL) to enhance the efficacy, selectivity, and safety of these systems. New formulations of spherical CPT-GNHs@FHQ-PUL obtained by bio-inspired strategy were fully characterized by TEM, EDS, DLS, zeta-potential, UV-vis, XRD, and ATR-FTIR anal-yses, showing a homogeneous particles size with an average size of approximately 10.97 ± 2.29 nm. CPT was successfully loaded on multifunctional GNHs@FHQ-PUL via intermolecular interactions. Moreover, pH-responsive CPT release from newly formulated-CPT-GNHs@FHQ-PUL exhibited a faster release rate under acidic conditions. The intelligent CPT-GNHs@FHQ-PUL (IC50 = 6.2 µM) displayed a 2.82-time higher cytotoxicity against human lung cancer cells (Chago-k1) than CPT alone (IC50 = 2.2 µM), while simultaneously exhibiting less toxicity toward normal human lung cells (Wi-38). These systems also showed specific uptake by folate receptor-mediated endocytosis, exhibited excellent anticancer activity, induced the death of cells by increasing apoptosis pathway (13.97%), and arrested the cell cycle at the G0-G1 phase. The results of this study showed that the delivery of CPT by smart GNHs@FHQ-PUL systems proved to be a promising strategy for increasing its chemotherapeutic effects. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
URI: https://ir.swu.ac.th/jspui/handle/123456789/17208
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85112697880&doi=10.3390%2fpolym13162670&partnerID=40&md5=6ce1cfd99faeb632837830093771fd2c
ISSN: 20734360
Appears in Collections:Scopus 1983-2021

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