Publication: Targeted gold nanohybrids functionalized with folate-hydrophobic-quaternized pullulan delivering camptothecin for enhancing hydrophobic anticancer drug efficacy
| dc.contributor.author | Laksee S. | |
| dc.contributor.author | Supachettapun C. | |
| dc.contributor.author | Muangsin N. | |
| dc.contributor.author | Lertsarawut P. | |
| dc.contributor.author | Rattanawongwiboon T. | |
| dc.contributor.author | Sricharoen P. | |
| dc.contributor.author | Limchoowong N. | |
| dc.contributor.author | Chutimasakul T. | |
| dc.contributor.author | Kwamman T. | |
| dc.contributor.author | Hemvichian K. | |
| dc.date.accessioned | 2022-03-10T13:16:37Z | |
| dc.date.available | 2022-03-10T13:16:37Z | |
| dc.date.issued | 2021 | |
| dc.date.issuedBE | 2564 | |
| dc.description.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. | |
| dc.format.mimetype | application/pdf | |
| dc.identifier.citation | Polymers. Vol 13, No.16 (2021) | |
| dc.identifier.doi | 10.3390/polym13162670 | |
| dc.identifier.issn | 20734360 | |
| dc.identifier.other | 2-s2.0-85112697880 | |
| dc.identifier.uri | https://swu-dspace2.eval.plus/handle/123456789/4779 | |
| dc.language.iso | eng | |
| dc.rights.holder | Scopus | |
| dc.subject.other | Biological organs | |
| dc.subject.other | Biomimetics | |
| dc.subject.other | Cell death | |
| dc.subject.other | Controlled drug delivery | |
| dc.subject.other | Cytotoxicity | |
| dc.subject.other | Gold | |
| dc.subject.other | Hydrophobicity | |
| dc.subject.other | Molecular biology | |
| dc.subject.other | Nanostructured materials | |
| dc.subject.other | Respiratory system | |
| dc.subject.other | Acidic conditions | |
| dc.subject.other | Anticancer activities | |
| dc.subject.other | Apoptosis pathways | |
| dc.subject.other | Camptothecin (CPT) | |
| dc.subject.other | Folate receptor | |
| dc.subject.other | Human lung cancer cells | |
| dc.subject.other | Human lung cells | |
| dc.subject.other | Intermolecular interactions | |
| dc.subject.other | Targeted drug delivery | |
| dc.title | Targeted gold nanohybrids functionalized with folate-hydrophobic-quaternized pullulan delivering camptothecin for enhancing hydrophobic anticancer drug efficacy | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| swu.datasource.scopus | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85112697880&doi=10.3390%2fpolym13162670&partnerID=40&md5=6ce1cfd99faeb632837830093771fd2c |