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Journal articles on the topic 'Polynorepinephrine'

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Author: Grafiati
Published: 10 March 2023

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1

Lu, Zhenzhen, Alon M. Douek, Ashley M. Rozario, Rico F. Tabor, Jan Kaslin, Bart Follink, and Boon Mian Teo. "Bioinspired polynorepinephrine nanoparticles as an efficient vehicle for enhanced drug delivery." Journal of Materials Chemistry B 8, no. 5 (2020): 961–68. http://dx.doi.org/10.1039/c9tb02375e.

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2

Taskin, Mehmet Berat, Ruodan Xu, Huiling Zhao, Xueqin Wang, Mingdong Dong, Flemming Besenbacher, and Menglin Chen. "Poly(norepinephrine) as a functional bio-interface for neuronal differentiation on electrospun fibers." Physical Chemistry Chemical Physics 17, no. 14 (2015): 9446–53. http://dx.doi.org/10.1039/c5cp00413f.

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3

Lu, Zhenzhen, Shahinur Acter, Boon M. Teo, and Rico F. Tabor. "Synthesis and characterisation of polynorepinephrine-shelled microcapsules via an oil-in-water emulsion templating route." Journal of Materials Chemistry B 9, no. 46 (2021): 9575–82. http://dx.doi.org/10.1039/d1tb01786a.

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4

Jiang, Xiumei, Yanfang Li, Ying Liu, Chunying Chen, and Menglin Chen. "Selective enhancement of human stem cell proliferation by mussel inspired surface coating." RSC Advances 6, no. 65 (2016): 60206–14. http://dx.doi.org/10.1039/c6ra11173d.

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The biocompatibility and cell adhesion properties of mussel inspired polydopamine and polynorepinephrine surface coatings on PCL fibers for human mesenchymal and human induced pluripotent stem cell derived mesenchymal stem cells were investigated.
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5

Liu, Xin, Zhuo Xie, Wei Shi, Zi He, Yang Liu, Huling Su, Yanan Sun, and Dongtao Ge. "Polynorepinephrine Nanoparticles: A Novel Photothermal Nanoagent for Chemo-Photothermal Cancer Therapy." ACS Applied Materials & Interfaces 11, no. 22 (May 15, 2019): 19763–73. http://dx.doi.org/10.1021/acsami.9b03458.

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6

Wu, Jia, Xue Xiao, Zhenqun Li, and Li Jia. "Enantioseparation of chiral β-blockers using polynorepinephrine-coated nanoparticles and chiral capillary electrophoresis." Analytical and Bioanalytical Chemistry 411, no. 10 (February 8, 2019): 2121–29. http://dx.doi.org/10.1007/s00216-019-01641-4.

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7

Baldoneschi, Veronica, Pasquale Palladino, Simona Scarano, and Maria Minunni. "Polynorepinephrine: state-of-the-art and perspective applications in biosensing and molecular recognition." Analytical and Bioanalytical Chemistry 412, no. 24 (March 20, 2020): 5945–54. http://dx.doi.org/10.1007/s00216-020-02578-9.

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8

Iwasaki, Takeshi, Yuki Tamai, Mikiya Yamamoto, Tatsuo Taniguchi, Keiki Kishikawa, and Michinari Kohri. "Melanin Precursor Influence on Structural Colors from Artificial Melanin Particles: PolyDOPA, Polydopamine, and Polynorepinephrine." Langmuir 34, no. 39 (September 5, 2018): 11814–21. http://dx.doi.org/10.1021/acs.langmuir.8b02444.

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9

Liu, Yang, Xu Nan, Wei Shi, Xin Liu, Zi He, Yanan Sun, and Dongtao Ge. "A glucose biosensor based on the immobilization of glucose oxidase and Au nanocomposites with polynorepinephrine." RSC Advances 9, no. 29 (2019): 16439–46. http://dx.doi.org/10.1039/c9ra02054c.

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10

Lu, Zhenzhen, Adam J. Quek, Shane P. Meaney, Rico F. Tabor, Bart Follink, and Boon Mian Teo. "Polynorepinephrine as an Efficient Antifouling-Coating Material and Its Application as a Bacterial Killing Photothermal Agent." ACS Applied Bio Materials 3, no. 9 (August 11, 2020): 5880–86. http://dx.doi.org/10.1021/acsabm.0c00578.

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11

Jędrzak, Artur, Maria Kuznowicz, Tomasz Rębiś, and Teofil Jesionowski. "Portable glucose biosensor based on polynorepinephrine@magnetite nanomaterial integrated with a smartphone analyzer for point-of-care application." Bioelectrochemistry 145 (June 2022): 108071. http://dx.doi.org/10.1016/j.bioelechem.2022.108071.

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12

Ganguly, Sayan, Poushali Das, Arka Saha, Malachi Noked, Aharon Gedanken, and Shlomo Margel. "Mussel-Inspired Polynorepinephrine/MXene-Based Magnetic Nanohybrid for Electromagnetic Interference Shielding in X-Band and Strain-Sensing Performance." Langmuir 38, no. 12 (March 14, 2022): 3936–50. http://dx.doi.org/10.1021/acs.langmuir.2c00278.

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13

Son, Eun Jin, Jae Hong Kim, Jong Wan Ko, and Chan Beum Park. "Catecholamine-functionalized graphene as a biomimetic redox shuttle for solar water oxidation." Faraday Discussions 198 (2017): 135–45. http://dx.doi.org/10.1039/c6fd00190d.

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In natural photosynthesis, solar energy is converted to chemical energy through a cascaded, photoinduced charge transfer chain that consists of primary and secondary acceptor quinones (i.e., QA and QB). This leads to an exceptionally high near-unity quantum yield. Inspired by the unique multistep architecture of charge transfer in nature, we have synthesized a catecholamine-functionalized, reduced graphene oxide (RGO) film as a redox mediator that can mimic quinone acceptors in photosystem II. We used polynorepinephrine (PNE) as a redox-shuttling chemical. We also used it to coat graphene oxide (GO) and to reduce GO to RGO. The quinone ligands in PNE, which are characterized by a charge transfer involving two electrons and two protons, acted as electron acceptors that facilitated charge transfer in photocatalytic water oxidation. Furthermore, PNE-coated RGO film promoted fast charge separation in [Ru(bpy)3]2+ and increased the activity of cobalt phosphate on photocatalytic water oxidation more than two-fold. The results suggest that our bio-inspired strategy for the construction of a forward charge transfer pathway can provide more opportunities to realize efficient artificial photosynthesis.
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14

Torrini, Francesca, Pasquale Palladino, Veronica Baldoneschi, Simona Scarano, and Maria Minunni. "Sensitive ‘two-steps’ competitive assay for gonadotropin-releasing hormone detection via SPR biosensing and polynorepinephrine-based molecularly imprinted polymer." Analytica Chimica Acta 1161 (May 2021): 338481. http://dx.doi.org/10.1016/j.aca.2021.338481.

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15

Liang, Ru-Ping, Cai-Yun Xiang, Jing-Wu Wang, and Jian-Ding Qiu. "Preparation of polynorepinephrine adhesive coating via one-step self-polymerization for enantioselective capillary electrochromatography coupled with electrogenerated chemiluminesense detection." Journal of Chromatography A 1284 (April 2013): 194–201. http://dx.doi.org/10.1016/j.chroma.2013.02.007.

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16

Qiu, Junlang, Guosheng Chen, Fang Zhu, and Gangfeng Ouyang. "Sulfonated nanoparticles doped electrospun fibers with bioinspired polynorepinephrine sheath for in vivo solid-phase microextraction of pharmaceuticals in fish and vegetable." Journal of Chromatography A 1455 (July 2016): 20–27. http://dx.doi.org/10.1016/j.chroma.2016.05.082.

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17

Lu, Zhenzhen, Boon M. Teo, and Rico Tabor. "Recent developments in polynorepinephrine: an innovative material for bioinspired coatings and colloids." Journal of Materials Chemistry B, 2022. http://dx.doi.org/10.1039/d2tb01335e.

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While applications of polydopamine (PDA) are exponentially growing, research concerning the closely related neurotransmitter derivative polynorepinephrine (PNE) is in paucity, even though norepinephrine shares dopamine’s ability to self-polymerize and form...
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18

Liu, Ying, Guoqiang Zhou, Zhu Liu, Mengyu Guo, Xiumei Jiang, Mehmet Berat Taskin, Zhongyang Zhang, et al. "Mussel Inspired Polynorepinephrine Functionalized Electrospun Polycaprolactone Microfibers for Muscle Regeneration." Scientific Reports 7, no. 1 (August 15, 2017). http://dx.doi.org/10.1038/s41598-017-08572-z.

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19

Torrini, Francesca, Laura Caponi, Andrea Bertolini, Pasquale Palladino, Francesca Cipolli, Alessandro Saba, Aldo Paolicchi, Simona Scarano, and Maria Minunni. "A biomimetic enzyme-linked immunosorbent assay (BELISA) for the analysis of gonadorelin by using molecularly imprinted polymer-coated microplates." Analytical and Bioanalytical Chemistry, January 13, 2022. http://dx.doi.org/10.1007/s00216-021-03867-7.

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AbstractAn original biomimetic enzyme-linked immunoassay (BELISA) to target the small peptide hormone gonadorelin is presented. This peptide has been recently listed among the substances banned in sports by the World Antidoping Agency (WADA) since its misuse by male athletes triggers testosterone increase. Hence, in response to this emerging issue in anti-doping controls, we proposed BELISA which involves the growth of a polynorepinephrine (PNE)–based molecularly imprinted polymer (MIP) directly on microwells. PNE, a polydopamine (PDA) analog, has recently displayed impressive performances when it was exploited for MIP preparation, giving even better results than PDA. Gonadorelin quantification was accomplished via a colorimetric indirect competitive bioassay involving the competition between biotinylated gonadorelin linked to the signal reporter and the unlabeled analyte. These compete for the same MIP binding sites resulting in an inverse correlation between gonadorelin concentration and the output color signal (λ = 450 nm). A detection limit of 277 pmol L−1 was achieved with very good reproducibility in standard solutions (avCV% = 4.07%) and in urine samples (avCV% = 5.24%). The selectivity of the assay resulted adequate for biological specimens and non-specific control peptides. In addition, the analytical figures of merit were successfully validated by mass spectrometry, the reference anti-doping benchtop platform for the analyte. BELISA was aimed to open real perspectives for PNE-based MIPs as alternatives to antibodies, especially when the target analyte is a poorly or non-immunogenic small molecule, such as gonadorelin. Graphical abstract
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20

Torrini, Francesca, Giada Goletta, Pasquale Palladino, Simona Scarano, and Maria Minunni. "A LysLysLys-tag as trigger in polynorepinephrine epitope imprinting: The case study of soluble PD-L1 detection in serum by optical-based sensing." Biosensors and Bioelectronics, October 2022, 114806. http://dx.doi.org/10.1016/j.bios.2022.114806.

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