Kappa carrageenan/PEG-CuO nanoparticles as a multifunctional nanoplatform: digital colorimetric biosensor and anticancer drug nanocarrier
Özet
The development of green multifunctional nanoformulation has been given great attention with unique anticancer activity and ultra-sensitive sensing properties in biomedical applications. This study investigated the smartphone-integrated colorimetric dopamine sensing platform and the anticancer activity of Kappa Carrageenan/PEG-CuO nanoparticles (κCA/PEG-CuO NPs). The characterization of the prepared κCA/PEG-CuO NPs was conducted using scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), X-ray diffraction analysis (XRD), zeta-potential, Fourier transform infrared spectroscopy (FTIR), and ultraviolet–visible (UV–Vis) techniques. The surface characterization revealed that the obtained NPs had a spherical surface in the particle-size range of 5–10 nm. With a high coefficient of correlation (R2 = 0.982), the digital colorimetric κCA/PEG-CuO NPs-based biosensor detected dopamine in a wide concentration range of 0.1–100 µM and a low limit of detection (LOD) of 504 nM in 0.1 M phosphate buffer solution (PBS) (pH 7.4). In addition, the cytotoxicity of the prepared κCA/PEG-CuO NPs in living cells (HepG2 hepatocellular carcinoma), MIA PaCa-2 pancreatic cancer cells, and HUVEC (human umbilical vein endothelial cells) was investigated, which proved that κCA/PEG-CuO NPs exhibited high anticancer activity against MIA PaCa-2 pancreatic cancer cells. In conclusion, experimental results showed that multifunctional κCA/PEG-CuO NPs are both a promising biosensor for dopamine detection and an effective nanocarrier for pancreatic cancer therapy. © 2022, The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature.
Anahtar Kelimeler
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Karabatak, Aysun | |
| dc.contributor.author | Danışman-Kalındemirtaş, Ferdane | |
| dc.contributor.author | Tan, Ezgi | |
| dc.contributor.author | Erdem-Kuruca, Serap | |
| dc.contributor.author | Karakuş, Selcan | |
| dc.date.accessioned | 2026-10-18T20:27:48.698047540Z | |
| dc.date.available | 2026-10-18T20:27:48.698047540Z | |
| dc.date.issued | 2022 | |
| dc.description.abstract | The development of green multifunctional nanoformulation has been given great attention with unique anticancer activity and ultra-sensitive sensing properties in biomedical applications. This study investigated the smartphone-integrated colorimetric dopamine sensing platform and the anticancer activity of Kappa Carrageenan/PEG-CuO nanoparticles (κCA/PEG-CuO NPs). The characterization of the prepared κCA/PEG-CuO NPs was conducted using scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), X-ray diffraction analysis (XRD), zeta-potential, Fourier transform infrared spectroscopy (FTIR), and ultraviolet–visible (UV–Vis) techniques. The surface characterization revealed that the obtained NPs had a spherical surface in the particle-size range of 5–10 nm. With a high coefficient of correlation (R2 = 0.982), the digital colorimetric κCA/PEG-CuO NPs-based biosensor detected dopamine in a wide concentration range of 0.1–100 µM and a low limit of detection (LOD) of 504 nM in 0.1 M phosphate buffer solution (PBS) (pH 7.4). In addition, the cytotoxicity of the prepared κCA/PEG-CuO NPs in living cells (HepG2 hepatocellular carcinoma), MIA PaCa-2 pancreatic cancer cells, and HUVEC (human umbilical vein endothelial cells) was investigated, which proved that κCA/PEG-CuO NPs exhibited high anticancer activity against MIA PaCa-2 pancreatic cancer cells. In conclusion, experimental results showed that multifunctional κCA/PEG-CuO NPs are both a promising biosensor for dopamine detection and an effective nanocarrier for pancreatic cancer therapy. © 2022, The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature. | |
| dc.description.sponsorship | This work was supported by Scientific Research Projects Coordination Unit of Istanbul University-Cerrahpasa under Project Number: 36118. | |
| dc.identifier.doi | 10.1007/s00339-022-05802-8 | |
| dc.identifier.eissn | 1432-0630 | |
| dc.identifier.issn | 0947-8396 | |
| dc.identifier.issue | 8 | |
| dc.identifier.scopus | 2-s2.0-85133696880 | |
| dc.identifier.startpage | 661 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/ebyu/12954 | |
| dc.identifier.volume | 128 | |
| dc.identifier.wos | WOS:000824890400003 | |
| dc.language.iso | en | |
| dc.publisher | Springer Science and Business Media Deutschland GmbH | |
| dc.relation.ispartof | Applied Physics A: Materials Science and Processing | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | Cisplatin | |
| dc.subject | Dopamine biosensor | |
| dc.subject | Multifunctional nanoparticle | |
| dc.subject | Pancreatic cancer | |
| dc.subject | Biosensors | |
| dc.subject | Color | |
| dc.subject | Colorimetry | |
| dc.subject | Cytology | |
| dc.subject | Diseases | |
| dc.subject | Drug delivery | |
| dc.subject | Endothelial cells | |
| dc.subject | Fourier transform infrared spectroscopy | |
| dc.subject | High resolution transmission electron microscopy | |
| dc.subject | Medical applications | |
| dc.subject | Nanoparticles | |
| dc.subject | Neurophysiology | |
| dc.subject | Particle size | |
| dc.subject | Particle size analysis | |
| dc.subject | Scanning electron microscopy | |
| dc.subject | X ray photoelectron spectroscopy | |
| dc.subject | X ray powder diffraction | |
| dc.subject | Anticancer activities | |
| dc.subject | Cis-platin | |
| dc.subject | CuO nanoparticles | |
| dc.subject | Dopamine | |
| dc.subject | Kappa carrageenan | |
| dc.subject | Multi-functional nanoparticles | |
| dc.subject | Nanocarriers | |
| dc.subject | Pancreatic cancers | |
| dc.subject | Amines | |
| dc.title | Kappa carrageenan/PEG-CuO nanoparticles as a multifunctional nanoplatform: digital colorimetric biosensor and anticancer drug nanocarrier | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| rdl.citation.scopus | 13 | |
| rdl.citation.wos | 12 | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.wos.index | Science Citation Index Expanded (SCI-EXPANDED) |
