Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14365/4667
Title: Characterization of cisplatin loaded hydrophilic glycol chitosan modified eumelanin nanoparticles for potential controlled-release application
Authors: Atik, Aleyna
Günal, Tuğce
Acar Bozkurt, Pınar
Kose, Sila Naz
Alp, Burcak
Yandım, Cihangir
Kaleli, Nurettin Mete
Keywords: Natural melanin nanoparticles
Eumelanin
Glycol chitosan
Cisplatin
Nanoparticle drug delivery
Super Case II Transport
Drug-Delivery
Melanin Nanoparticles
Natural Melanin
Cancer-Therapy
Nanomaterials
Mechanisms
Nanomedicine
Efficacy
Models
Films
Publisher: Elsevier
Abstract: Free liquid cytotoxic substances, such as cisplatin (CDDP), have been widely administered for the conventional chemotherapy treatment of cancer patients. However, this classical approach has several drawbacks, including high dosage requirements, poor bioavailability, low therapeutic index, and geno-/cyto-toxicity resulting in several adverse side effects that constrain patient compliance and clinical outcomes. Such downsides can be improved by replacing conventional drugs with advanced nanocomposite-drug conjugates. In line with this, our study aimed to characterize a novel potential drug nano delivery system, so-called hydrophilic glycol chitosan (HGC) coated melanin nanoparticles (MNPs), to improve the abovementioned constraints in the case of classical chemotherapy drug cisplatin. Following the production of MNP-based nanocomplexes by a single-step mixing, essential physical and chemical characterizations were performed. The nanoformulations generated here were spherically shaped with an optimum size range (between 100 and 200 nm) and exhibited comparable drug loading capacities (21.7% +/- 0.5 for the CDDP-MNPs and 24.7% +/- 0.4 for HGC/CDDP-MNPs) and remarkable entrapment efficiencies (93.2% +/- 2.0 for CDDP-MNPs and 94.9% +/- 1.1 for HGC/CDDP-MNPs) as a biopolymer. Notably, the cell viability assay showed that MNP-based nanocarriers could inhibit the proliferation of liver cancer cells in a more prolonged fashion compared to free CDDP. The TGA and FTIR-ATR analyses confirmed the compatibility between CDDP and its nanocarrier MNP. The Super Case II Transport was primarily in charge of controlling CDDP release from both matrices as a result of polymer relaxation and swelling of HGC-CDDP-MNPs and CDDP-MNPs, which is highly preferred because it enables simple manipulation of the nanocarrier properties to suit the disease biology. All of these findings point to the natural MNP-based nanoformulation's superiority as a prospective and cutting-edge chemotherapeutic nano-delivery technology.
URI: https://doi.org/10.1016/j.jddst.2023.104440
https://hdl.handle.net/20.500.14365/4667
ISSN: 1773-2247
2588-8943
Appears in Collections:Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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