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 | … | |
| gdc.author.scopusid | 58188838300 | |
| gdc.author.scopusid | 58189517500 | |
| gdc.author.scopusid | 57192172269 | |
| gdc.author.scopusid | 58189346900 | |
| gdc.author.scopusid | 58188478400 | |
| gdc.author.scopusid | 36474168400 | |
| gdc.author.scopusid | 57220544824 | |
| gdc.author.wosid | Köse, Sıla Naz/HZH-5954-2023 | |
| gdc.author.wosid | YANDIM, Cihangir/AAA-2250-2021 | |
| gdc.bip.impulseclass | C4 | |
| gdc.bip.influenceclass | C5 | |
| gdc.bip.popularityclass | C4 | |
| gdc.coar.access | metadata only access | |
| gdc.coar.type | text::journal::journal article | |
| gdc.collaboration.industrial | false | |
| 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 | |
| gdc.index.type | WoS | |
| gdc.index.type | Scopus | |
| gdc.oaire.diamondjournal | false | |
| gdc.oaire.impulse | 9.0 | |
| gdc.oaire.influence | 2.7308924E-9 | |
| gdc.oaire.isgreen | true | |
| gdc.oaire.keywords | Life sciences; biology | |
| gdc.oaire.keywords | info:eu-repo/classification/ddc/570 | |
| gdc.oaire.keywords | 570 | |
| gdc.oaire.keywords | biology | |
| gdc.oaire.keywords | ddc:570 | |
| gdc.oaire.keywords | 540 | |
| gdc.oaire.keywords | Life sciences | |
| gdc.oaire.popularity | 8.797415E-9 | |
| gdc.oaire.publicfunded | false | |
| gdc.openalex.collaboration | International | |
| gdc.openalex.fwci | 3.1137 | |
| gdc.openalex.normalizedpercentile | 0.91 | |
| gdc.openalex.toppercent | TOP 10% | |
| gdc.opencitations.count | 6 | |
| gdc.plumx.crossrefcites | 8 | |
| gdc.plumx.mendeley | 11 | |
| gdc.plumx.scopuscites | 11 | |
| gdc.scopus.citedcount | 11 | |
| gdc.virtual.author | Yandım, Cihangir | |
| gdc.virtual.author | Alp, Burçak | |
| gdc.virtual.author | Köse, Sıla Naz | |
| gdc.wos.citedcount | 11 | |
| relation.isAuthorOfPublication | dcc90be4-1500-42cd-856d-16623e9ec3da | |
| relation.isAuthorOfPublication | a02839f9-9689-4d55-90ef-09cac1030bba | |
| relation.isAuthorOfPublication | 59362908-71a3-4b7c-8b16-d1f2f1fced5f | |
| relation.isAuthorOfPublication.latestForDiscovery | dcc90be4-1500-42cd-856d-16623e9ec3da | |
| relation.isOrgUnitOfPublication | ea0c3216-9cb2-4b28-8b85-9cf129e0036d | |
| relation.isOrgUnitOfPublication | f07c2219-8f05-4f62-93be-5d2ae67a8477 | |
| relation.isOrgUnitOfPublication | 26a7372c-1a5e-42d9-90b6-a3f7d14cad44 | |
| relation.isOrgUnitOfPublication | e9e77e3e-bc94-40a7-9b24-b807b2cd0319 | |
| relation.isOrgUnitOfPublication.latestForDiscovery | ea0c3216-9cb2-4b28-8b85-9cf129e0036d |
Files
Original bundle
1 - 1 of 1
