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Rapid Evaluation of Anti-inflammatory Effect of Geniopicroside

Received: 9 May 2023    Accepted: 26 May 2023    Published: 29 May 2023
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Abstract

Skin acts as a barrier and is an important part of body immune system. External physical, biochemical and other stimuli might cause skin inflammation. Drugs and cosmetics have been developed for skin inflammation treatment. At present, the tests of skin inflammation are mainly conducted on animal and 2D cell models. The former might bring problems such as ethics and authenticity, while the latter cannot fully represent the complex micro-environment of the human body. Microfluidic based Organ-on- a- chips technology provides a new method for drug and cosmetic ingredient screening. Skin-on-a-chip (SOC) has been designed for constructing in vitro skin models. In this paper, a SOC was developed to culture skin-like models in vitro. We tested the differentiation of SOC cultured skin model, and the results showed that its stratum corneum was well differentiated. It indicates that the skin tissue cultured by the SOC bears some similarities to human skin, which can be used for subsequent drug testing. We tested the anti-inflammatory effect of gentiopicroside and compared with dexamethasone. The results showed that 5μg/ml~50μg/ml of gentiopicroside had similar anti-inflammatory effect to 1μM of dexamethasone.

Published in American Journal of Bioscience and Bioengineering (Volume 11, Issue 1)
DOI 10.11648/j.bio.20231101.12
Page(s) 7-13
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2023. Published by Science Publishing Group

Keywords

Skin, Microfluidic Technology, Anti-inflammatory

References
[1] Gauglitz GG, Schauber J. Skin: architecture and function. Dermal Replacements in General, Burn, and Plastic Surgery: Tissue Engineering in Clinical Practice. 2013: 1-11.
[2] Liu Z, Han X, Qin L. Recent progress of microfluidics in translational applications. Advanced Healthcare Materials. 2016, 5 (8): 871-888.
[3] Nys G, Fillet M. Microfluidics contribution to pharmaceutical sciences: From drug discovery to post marketing product management. Journal of Pharmaceutical and Biomedical Analysis. 2018, 159: 348-362.
[4] Cui P, Wang S. Application of microfluidic chip technology in pharmaceutical analysis: A review. Journal of Pharmaceutical Analysis. 2019, 9 (4): 238-247.
[5] Bhise NS, Gray RS, Sunshine JC, et al. The relationship between terminal functionalization and molecular weight of a gene delivery polymer and transfection efficacy in mammary epithelial 2-D cultures and 3-D organotypic cultures. Biomaterials. 2010, 31 (31): 8088-8096.
[6] Chong SZ, Evrard M, Ng LG. Lights, Camera, and Action: Vertebrate Skin Sets the Stage for Immune Cell Interaction with Arthropod-Vectored Pathogens. Frontiers in Immunology. 2013, 4: 286.
[7] Wagner I, Materne E-M, Brincker S, et al. A dynamic multi-organ-chip for long-term cultivation and substance testing proven by 3D human liver and skin tissue co-culture. Lab Chip. 2013, 13 (18): 3538-3547.
[8] Maschmeyer I, Lorenz AK, Schimek K, et al. A four-organ-chip for interconnected long-term co-culture of human intestine, liver, skin and kidney equivalents. Lab Chip. 2015, 15 (12): 2688-2699.
[9] Ramadan Q, Ting FC. In vitro micro-physiological immune-competent model of the human skin. Lab Chip. 2016, 16 (10): 1899-1908.
[10] Sasaki N, Tsuchiya K, Kobayashi H. Photolithography-free skin-on-a-chip for parallel permeation assays. Sens Mater. 2019, 31 (1): 107-115.
[11] Wufuer M, Lee G, Hur W, et al. Skin-on-a-chip model simulating inflammation, edema and drug-based treatment. Scientific Reports. 2016, 6 (1): 37471.
[12] Song HJ, Lim HY, Chun W, et al. Fabrication of a pumpless, microfluidic skin chip from different collagen sources. Journal of Industrial and Engineering Chemistry. 2017, 56: 375-381.
[13] Jusoh N, Ko J, Jeon NL. Microfluidics-based skin irritation test using in vitro 3D angiogenesis platform. APL Bioengineering. 2019, 3 (3): 036101.
[14] Gledhill K, Guo Z, Umegaki-Arao N, et al. Melanin transfer in human 3D skin equivalents generated exclusively from induced pluripotent stem cells. PLoS One. 2015, 10 (8): e0136713.
[15] Sriram G, Alberti M, Dancik Y, et al. Full-thickness human skin-on-chip with enhanced epidermal morphogenesis and barrier function. Materials Today. 2018, 21 (4): 326-340.
[16] Lee S, Jin S-P, Kim YK, et al. Construction of 3D multicellular microfluidic chip for an in vitro skin model. Biomedical Microdevices. 2017, 19: 1-14.
[17] Lukács B, Bajza Á, Kocsis D, et al. Skin-on-a-chip device for ex vivo monitoring of transdermal delivery of drugs—design, fabrication, and testing. Pharmaceutics. 2019, 11 (9): 445.
[18] Zhao L, Ye J, Wu G-t, et al. Gentiopicroside prevents interleukin-1 beta induced inflammation response in rat articular chondrocyte. J Ethnopharmacol. 2015, 172: 100-107.
[19] Huang X-J, Li J, Mei Z-Y, et al. Gentiopicroside and sweroside from Veratrilla baillonii Franch. induce phosphorylation of Akt and suppress Pck1 expression in hepatoma cells. Biochemistry and Cell Biology. 2016, 94 (3): 270-278.
[20] Liu S-b, Zhao R, Li X-s, et al. Attenuation of reserpine-induced pain/depression dyad by gentiopicroside through downregulation of GluN2B receptors in the amygdala of mice. Neuromolecular Med. 2014, 16: 350-359.
[21] Chou C, Pan S, Teng C, et al. Pharmacological evaluation of several major ingredients of Chinese herbal medicines in human hepatoma Hep3B cells. European Journal of Pharmaceutical Sciences. 2003, 19 (5): 403-412.
[22] Shankar E, Goel A, Gupta K, et al. Plant flavone apigenin: an emerging anticancer agent. Current Pharmacology Reports. 2017, 3: 423-446.
[23] Lee S, Jin S-P, Kim YK, et al. Construction of 3D multicellular microfluidic chip for an in vitro skin model. Biomedical Microdevices. 2017, 19 (2): 22.
[24] Kitagawa N, Inai Y, Higuchi Y, et al. Inhibition of JNK in HaCaT cells induced tight junction formation with decreased expression of cytokeratin 5, cytokeratin 17 and desmoglein 3. Histochem Cell Biol. 2014, 142 (4): 389-399.
[25] Wilson VG. Growth and differentiation of HaCaT keratinocytes. Methods Mol Biol. 2014, 1195: 33-41.
[26] Srivastava SS, Alam H, Patil SJ, et al. Keratin 5/14-mediated cell differentiation and transformation are regulated by TAp63 and Notch-1 in oral squamous cell carcinoma-derived cells. Oncol Rep. 2018, 39 (5): 2393-2401.
Cite This Article
  • APA Style

    Zijia Liu, Yidong Tu, Tianbi Duan, Zhi Lv, Ruixue Yin, et al. (2023). Rapid Evaluation of Anti-inflammatory Effect of Geniopicroside. American Journal of Bioscience and Bioengineering, 11(1), 7-13. https://doi.org/10.11648/j.bio.20231101.12

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    ACS Style

    Zijia Liu; Yidong Tu; Tianbi Duan; Zhi Lv; Ruixue Yin, et al. Rapid Evaluation of Anti-inflammatory Effect of Geniopicroside. Am. J. BioSci. Bioeng. 2023, 11(1), 7-13. doi: 10.11648/j.bio.20231101.12

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    AMA Style

    Zijia Liu, Yidong Tu, Tianbi Duan, Zhi Lv, Ruixue Yin, et al. Rapid Evaluation of Anti-inflammatory Effect of Geniopicroside. Am J BioSci Bioeng. 2023;11(1):7-13. doi: 10.11648/j.bio.20231101.12

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  • @article{10.11648/j.bio.20231101.12,
      author = {Zijia Liu and Yidong Tu and Tianbi Duan and Zhi Lv and Ruixue Yin and Hongbo Zhang},
      title = {Rapid Evaluation of Anti-inflammatory Effect of Geniopicroside},
      journal = {American Journal of Bioscience and Bioengineering},
      volume = {11},
      number = {1},
      pages = {7-13},
      doi = {10.11648/j.bio.20231101.12},
      url = {https://doi.org/10.11648/j.bio.20231101.12},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.bio.20231101.12},
      abstract = {Skin acts as a barrier and is an important part of body immune system. External physical, biochemical and other stimuli might cause skin inflammation. Drugs and cosmetics have been developed for skin inflammation treatment. At present, the tests of skin inflammation are mainly conducted on animal and 2D cell models. The former might bring problems such as ethics and authenticity, while the latter cannot fully represent the complex micro-environment of the human body. Microfluidic based Organ-on- a- chips technology provides a new method for drug and cosmetic ingredient screening. Skin-on-a-chip (SOC) has been designed for constructing in vitro skin models. In this paper, a SOC was developed to culture skin-like models in vitro. We tested the differentiation of SOC cultured skin model, and the results showed that its stratum corneum was well differentiated. It indicates that the skin tissue cultured by the SOC bears some similarities to human skin, which can be used for subsequent drug testing. We tested the anti-inflammatory effect of gentiopicroside and compared with dexamethasone. The results showed that 5μg/ml~50μg/ml of gentiopicroside had similar anti-inflammatory effect to 1μM of dexamethasone.},
     year = {2023}
    }
    

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  • TY  - JOUR
    T1  - Rapid Evaluation of Anti-inflammatory Effect of Geniopicroside
    AU  - Zijia Liu
    AU  - Yidong Tu
    AU  - Tianbi Duan
    AU  - Zhi Lv
    AU  - Ruixue Yin
    AU  - Hongbo Zhang
    Y1  - 2023/05/29
    PY  - 2023
    N1  - https://doi.org/10.11648/j.bio.20231101.12
    DO  - 10.11648/j.bio.20231101.12
    T2  - American Journal of Bioscience and Bioengineering
    JF  - American Journal of Bioscience and Bioengineering
    JO  - American Journal of Bioscience and Bioengineering
    SP  - 7
    EP  - 13
    PB  - Science Publishing Group
    SN  - 2328-5893
    UR  - https://doi.org/10.11648/j.bio.20231101.12
    AB  - Skin acts as a barrier and is an important part of body immune system. External physical, biochemical and other stimuli might cause skin inflammation. Drugs and cosmetics have been developed for skin inflammation treatment. At present, the tests of skin inflammation are mainly conducted on animal and 2D cell models. The former might bring problems such as ethics and authenticity, while the latter cannot fully represent the complex micro-environment of the human body. Microfluidic based Organ-on- a- chips technology provides a new method for drug and cosmetic ingredient screening. Skin-on-a-chip (SOC) has been designed for constructing in vitro skin models. In this paper, a SOC was developed to culture skin-like models in vitro. We tested the differentiation of SOC cultured skin model, and the results showed that its stratum corneum was well differentiated. It indicates that the skin tissue cultured by the SOC bears some similarities to human skin, which can be used for subsequent drug testing. We tested the anti-inflammatory effect of gentiopicroside and compared with dexamethasone. The results showed that 5μg/ml~50μg/ml of gentiopicroside had similar anti-inflammatory effect to 1μM of dexamethasone.
    VL  - 11
    IS  - 1
    ER  - 

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Author Information
  • School of Mechanics, East China University of Science and Technology, Shanghai, China

  • Shanghai Inoherb Ltd., Shanghai, China

  • Shanghai Inoherb Ltd., Shanghai, China

  • Shanghai Inoherb Ltd., Shanghai, China

  • School of Mechanics, East China University of Science and Technology, Shanghai, China

  • School of Mechanics, East China University of Science and Technology, Shanghai, China

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