4.7 Article

Facile and green synthesis of pullulan derivative-stabilized Au nanoparticles as drug carriers for enhancing anticancer activity

Journal

CARBOHYDRATE POLYMERS
Volume 198, Issue -, Pages 495-508

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.carbpol.2018.06.119

Keywords

Au nanoparticles; Pullulan derivatives; Cytotoxicity; PABA-QP; Chago cells; Doxorubicin

Funding

  1. Ratchadapisak Sompoch Endowment Fund (2016)
  2. Chulalongkorn University [CU-59-037-AM]
  3. Science Achievement Scholarship of Thailand (SAST) [CU-06-2555, CU-02-2557]

Ask authors/readers for more resources

In this work, we report for the first time AuNPs reduced/stabilized/capped with modified para-aminobenzoic acid-quat188-pullulan (PABA-QP) as excellent nanocarriers for delivery of doxorubicin to enhance the activity and safety of these systems. Spherical AuNPs@PABA-QP obtained by facile and green synthesis under optimum conditions were characterized by UV-VIS, TEM, EDS, SAED, XRD, ATR-FTIR and zeta-potential analyses and showed a narrow size distribution of 13.7 +/- 1.9 nm. DOX was successfully loaded onto AuNPs@PABA-QP via intermolecular interactions with high drug loading. DOX-AuNPs@PABA-QP (IC50 = 0.39 mu M) showed a 2.1-fold higher cytotoxicity against Chago cells than DOX alone (IC50 = 0.82 mu M), while exhibiting less cytotoxicity against normal cells (Wi-38). Moreover, DOX-AuNPs@PABA-QP also demonstrated high intracellular uptake by endocytosis, arrested in S and G2-M phases of the cell cycle (total S/G2-M increased to approximately 18.0%), induced excellent cytotoxicity, and increased the fraction of late-apoptotic cells (18.6%). Consequently, it is suggested that the novel combination of DOX-AuNPs@PABA-QP has the potential to be developed for human cancer treatment.

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