Publications by authors named "Elif Seven"

Elevated dopamine (DA) levels in urine denote neuroblastoma, a pediatric cancer. Saccharide-derived carbon dots (CDs) were applied to assay DA detection in simulated urine (SU) while delineating the effects of graphene defect density on electrocatalytic activity. CDs were hydrothermally synthesized to vary graphene defect densities using sucrose, raffinose, and palatinose, depositing them onto glassy carbon electrodes (GCEs).

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Carbon dots (CDs) from glucose were synthesized using two of the most common bottom-up methods, namely, microwave assisted (MW) and hydrothermal carbonization (HT). Synthetic parameters such as reaction time, temperature, and precursor concentration were changed to study the effects of each parameter on CD size, structure, surface functionalities, charge, photoluminescence behavior, quantum yield, cytotoxicity, blood-brain barrier (BBB) crossing ability and bioimaging. A detailed analysis is performed to compare the structure and properties of the CDs synthesized in ten different conditions.

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Article Synopsis
  • Drug delivery across the blood-brain barrier (BBB) is a significant challenge in treating brain diseases due to its selective permeability, but carbon dots (CDs) have emerged as a promising solution for this issue.
  • CDs have shown success in penetrating the BBB, and their various structures and abundant surface functional groups make them versatile carriers for drugs targeting neurodegenerative diseases like Alzheimer's and brain tumors.
  • The review also discusses the mechanisms for transporting molecules across the BBB, recent advancements in using CDs for CNS disease treatment, and the potential future integration of artificial intelligence and nanorobots in CD-based drug delivery systems.
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  • The blood-brain barrier (BBB) significantly limits drug delivery to the central nervous system (CNS), often rendering therapeutics ineffective against brain tumors and neurological disorders.
  • Researchers have developed carbon dots from glucose (GluCD-F) that successfully cross the BBB in zebrafish and rats without needing additional targeting ligands, relying on glucose transporters for uptake in cells.
  • GluCD-F shows potential for targeting neurons within the CNS, suggesting its possible application as a drug delivery platform in treating neurodegenerative diseases and CNS-related conditions.
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  • Carbon dots (CDs), known for their low toxicity and high photoluminescence, have been synthesized from metformin (Met-CDs) using a microwave-assisted method.
  • The Met-CDs were thoroughly characterized with various spectroscopic and microscopic techniques, revealing their biocompatibility and low toxicity to both tumor and non-tumor cells.
  • Bioimaging studies indicated that Met-CDs can effectively penetrate cell membranes, particularly localizing in the mitochondria of cancer cells and crossing the blood-brain barrier in zebrafish, showcasing their potential for biomedical applications.
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Tumor microenvironment responsive drug delivery systems are potential approaches to reduce the acute toxicity caused by high-dose cancer chemotherapy. Notwithstanding the conventional nano-drug delivery systems, the redox and pH stimuli drug delivery systems are currently gaining attention. Therefore, the current study was designed to compare three different covalent carbon dots (C-dots) systems based on doxorubicin (dox) release profiles and cancer cell viability efficacy under acidic and physiological conditions.

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As a promising drug nanocarrier, carbon dots (CDs) have exhibited many excellent properties. However, some properties such as bone targeting and crossing the blood-brain barrier (BBB) only apply to a certain CD preparation with limited drug loading capacity. Therefore, it is significant to conjugate distinct CDs to centralize many unique properties on the novel drug nanocarrier.

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Despite the recent rigorous studies towards a possible cure, cancer still remains as one of the most daunting problems faced by the humanity. Currently utilized two-dimensional cancer models are known to have various insuperable limitations such as insufficient biomimicry of the heterogeneous conditions of tumors and their three-dimensional structures. Discrepancies between the laboratory models and the actual tumor environment significantly impair a thorough comprehension of the carcinogenesis process and development of successful remedies against cancer.

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Alzheimer's disease (AD) is an irreversible and progressive neurodegenerative disorder manifested by memory loss and cognitive impairment. Deposition of the amyloid β plaques has been identified as the most common AD pathology; however, the excessive accumulation of phosphorylated or total tau proteins, reactive oxygen species, and higher acetylcholinesterase activity are also strongly associated with Alzheimer's dementia. Several therapeutic approaches targeting these pathogenic mechanisms have failed in clinical or preclinical trials, partly due to the limited bioavailability, poor cell, and blood-brain barrier penetration, and low drug half-life of current regimens.

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  • Carbon dots (CDs) are tiny carbon nanoparticles (less than 10 nm) that can now form stable Langmuir monolayers at the air-subphase interface, which could advance our understanding of interface interactions and sensor development.
  • Amphiphilic CDs, created from saccharides, successfully exhibited all phases of a Langmuir monolayer—gas, liquid-expanded, liquid-condensed, and solid—with minimal hysteresis during compression-decompression cycles.
  • The optical properties of these CDs, including UV/vis absorption and consistent excitation-independent photoluminescence in the monolayer, indicate their potential utility in various applications.
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  • Breast cancer (BC) is the most common cancer among women and often lethal, with traditional treatments like surgery, chemotherapy, and radiotherapy having significant side effects that can limit their effectiveness.
  • New developments in nanoparticles (NPs) offer a targeted drug delivery system that aims to specifically target cancer cells while minimizing harm to healthy tissues, making it a promising alternative for BC treatment.
  • This study reviews recent research on NPs-mediated drug delivery systems, highlighting their advantages such as low toxicity, good compatibility, and effectiveness in bioimaging, and aims to guide future methods for enhanced BC treatments.
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  • A novel type of orange carbon dots (O-CDs) was created using citric acid and 1,2-phenylenediamine, and successfully incorporated into sodium polyacrylate (SPA) ink for 3D printing.
  • The O-CDs, measuring around 2 nm, exhibited unique emission properties that change with the solvent but not with the excitation source, and they were well-distributed in the SPA, minimizing aggregation.
  • This research marks a significant milestone as it is the first demonstration of using bare carbon dots as photoluminescent materials in 3D printing and introduces SPA as a viable 3D printing material.
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Methionine aminopeptidase (MetAP) is a dinuclear metalloprotease responsible for the cleavage of methionine initiator residues from nascent proteins. MetAP activity is necessary for bacterial proliferation and is therefore a projected novel antibacterial target. A compound library consisting of 294 members containing metal-binding functional groups was screened against Rickettsia prowazekii MetAP to determine potential inhibitory motifs.

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In this article, we explored the surface chemistry properties of a cholera toxin B (CTB) monolayer at the air-subphase interface and investigated the change in interfacial properties through in situ spectroscopy. The study showed that the impact of the blue shift was negligible, suggesting that the CTB molecules were minimally affected by the subphase molecules. The stability of the CTB monolayer was studied by maintaining the constant surface pressure for a long time and also by using the compression-decompression cycle experiments.

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The blood-brain barrier (BBB) is one of the most essential protection mechanisms in the central nervous system (CNS). It selectively allows individual molecules such as small lipid-soluble molecules to pass through the capillary endothelial membrane while limiting the passage of pathogens or toxins. However, this protection mechanism is also a major obstacle during disease state since it dramatically hinders the drug delivery.

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  • SULF1 is suggested to act as a tumor promoter in hepatocellular carcinoma (HCC) despite previous beliefs of it being a tumor suppressor, as demonstrated in a transgenic mouse model.
  • SULF1 overexpression leads to increased tumor incidence and lung metastases by activating the TGF-β/SMAD pathway, which enhances cell migration and invasiveness.
  • High levels of SULF1 in human HCC patients correlate with poorer survival rates and are related to TGF-β expression, indicating its potential as a biomarker for cancer progression.
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