Publication:
Targeted gold nanohybrids functionalized with folate-hydrophobic-quaternized pullulan delivering camptothecin for enhancing hydrophobic anticancer drug efficacy

dc.contributor.authorLaksee S.
dc.contributor.authorSupachettapun C.
dc.contributor.authorMuangsin N.
dc.contributor.authorLertsarawut P.
dc.contributor.authorRattanawongwiboon T.
dc.contributor.authorSricharoen P.
dc.contributor.authorLimchoowong N.
dc.contributor.authorChutimasakul T.
dc.contributor.authorKwamman T.
dc.contributor.authorHemvichian K.
dc.date.accessioned2022-03-10T13:16:37Z
dc.date.available2022-03-10T13:16:37Z
dc.date.issued2021
dc.date.issuedBE2564
dc.description.abstractThis 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.
dc.format.mimetypeapplication/pdf
dc.identifier.citationPolymers. Vol 13, No.16 (2021)
dc.identifier.doi10.3390/polym13162670
dc.identifier.issn20734360
dc.identifier.other2-s2.0-85112697880
dc.identifier.urihttps://swu-dspace2.eval.plus/handle/123456789/4779
dc.language.isoeng
dc.rights.holderScopus
dc.subject.otherBiological organs
dc.subject.otherBiomimetics
dc.subject.otherCell death
dc.subject.otherControlled drug delivery
dc.subject.otherCytotoxicity
dc.subject.otherGold
dc.subject.otherHydrophobicity
dc.subject.otherMolecular biology
dc.subject.otherNanostructured materials
dc.subject.otherRespiratory system
dc.subject.otherAcidic conditions
dc.subject.otherAnticancer activities
dc.subject.otherApoptosis pathways
dc.subject.otherCamptothecin (CPT)
dc.subject.otherFolate receptor
dc.subject.otherHuman lung cancer cells
dc.subject.otherHuman lung cells
dc.subject.otherIntermolecular interactions
dc.subject.otherTargeted drug delivery
dc.titleTargeted gold nanohybrids functionalized with folate-hydrophobic-quaternized pullulan delivering camptothecin for enhancing hydrophobic anticancer drug efficacy
dc.typeArticle
dspace.entity.typePublication
swu.datasource.scopushttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85112697880&doi=10.3390%2fpolym13162670&partnerID=40&md5=6ce1cfd99faeb632837830093771fd2c

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