Characterization of Cisplatin Loaded Hydrophilic Glycol Chitosan Modified Eumelanin Nanoparticles for Potential Controlled-Release Application

dc.contributor.author Atik, Aleyna
dc.contributor.author Günal, Tuğce
dc.contributor.author Acar Bozkurt, Pınar
dc.contributor.author Kose, Sila Naz
dc.contributor.author Alp, Burcak
dc.contributor.author Yandım, Cihangir
dc.contributor.author Kaleli, Nurettin Mete
dc.date.accessioned 2023-06-19T20:56:10Z
dc.date.available 2023-06-19T20:56:10Z
dc.date.issued 2023
dc.description.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. en_US
dc.identifier.doi 10.1016/j.jddst.2023.104440
dc.identifier.issn 1773-2247
dc.identifier.issn 2588-8943
dc.identifier.scopus 2-s2.0-85152966464
dc.identifier.uri https://doi.org/10.1016/j.jddst.2023.104440
dc.identifier.uri https://hdl.handle.net/20.500.14365/4667
dc.language.iso en en_US
dc.publisher Elsevier en_US
dc.relation.ispartof Journal of Drug Delivery Science and Technology en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Natural melanin nanoparticles en_US
dc.subject Eumelanin en_US
dc.subject Glycol chitosan en_US
dc.subject Cisplatin en_US
dc.subject Nanoparticle drug delivery en_US
dc.subject Super Case II Transport en_US
dc.subject Drug-Delivery en_US
dc.subject Melanin Nanoparticles en_US
dc.subject Natural Melanin en_US
dc.subject Cancer-Therapy en_US
dc.subject Nanomaterials en_US
dc.subject Mechanisms en_US
dc.subject Nanomedicine en_US
dc.subject Efficacy en_US
dc.subject Models en_US
dc.subject Films en_US
dc.title Characterization of Cisplatin Loaded Hydrophilic Glycol Chitosan Modified Eumelanin Nanoparticles for Potential Controlled-Release Application en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id Köse, Sıla Naz/0000-0003-2358-1605
gdc.author.id YANDIM, Cihangir/0000-0002-2050-6186
gdc.author.institutional
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gdc.author.wosid Köse, Sıla Naz/HZH-5954-2023
gdc.author.wosid YANDIM, Cihangir/AAA-2250-2021
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gdc.coar.access metadata only access
gdc.coar.type text::journal::journal article
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gdc.description.department İEÜ, Mühendislik Fakültesi, Genetik ve Biyomühendislik Bölümü en_US
gdc.description.departmenttemp [Atik, Aleyna; Gunal, Tugce; Kaleli-Can, Gizem] Izmir Democracy Univ, Dept Biomed Engn, TR-35140 Izmir, Turkiye; [Bozkurt, Pinar Acar; Kaleli, Nurettin Mete] Ankara Univ, Sci Fac, Dept Chem, TR-06100 Ankara, Turkiye; [Kose, Sila Naz; Yandim, Cihangir] Izmir Univ Econ, Fac Engn, Dept Genet & Bioengn, TR-35330 Izmir, Turkiye; [Alp, Burcak] Izmir Univ Econ, Dept Biomed Engn, TR-35330 Izmir, Turkiye; [Kabay, Gozde] Karlsruhe Inst Technol, Inst Funct Interfaces IFG, D-76344 Karlsruhe, Germany en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q1
gdc.description.volume 84 en_US
gdc.description.wosquality Q1
gdc.identifier.openalex W4366247581
gdc.identifier.wos WOS:000983830900001
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gdc.oaire.keywords Life sciences; biology
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gdc.opencitations.count 6
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gdc.scopus.citedcount 11
gdc.virtual.author Yandım, Cihangir
gdc.virtual.author Alp, Burçak
gdc.virtual.author Köse, Sıla Naz
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