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Simple chitin-based cell culture platform for production of biopharmaceuticals.
Kida, Katsuhiko; Hatanaka, Daisuke; Minami, Masataka; Suzuki, Taiyo; Iwakami, Masashi; Kobayashi, Masaki; Hayashi, Hisato; Kawahara, Hiroharu; Horikawa, Masato; Kanaki, Tatsuro.
Affiliation
  • Kida K; Biological Research Laboratories, Nissan Chemical Corporation, Saitama, Japan. kidak@nissanchem.co.jp.
  • Hatanaka D; Materials Research Laboratories, Nissan Chemical Corporation, Chiba, Japan.
  • Minami M; Materials Research Laboratories, Nissan Chemical Corporation, Chiba, Japan.
  • Suzuki T; Materials Research Laboratories, Nissan Chemical Corporation, Chiba, Japan.
  • Iwakami M; Biological Research Laboratories, Nissan Chemical Corporation, Saitama, Japan.
  • Kobayashi M; Biological Research Laboratories, Nissan Chemical Corporation, Saitama, Japan.
  • Hayashi H; Head office, Nissan Chemical Corporation, Tokyo, Japan.
  • Kawahara H; Department of Creative Engineering, Material Chemistry Course, National Institute of Technology Kitakyushu College, Fukuoka, Japan.
  • Horikawa M; Head office, Nissan Chemical Corporation, Tokyo, Japan.
  • Kanaki T; Head office, Nissan Chemical Corporation, Tokyo, Japan.
Biotechnol Lett ; 45(10): 1265-1277, 2023 Oct.
Article in En | MEDLINE | ID: mdl-37606752
ABSTRACT

OBJECTIVES:

Gene therapy using viral vectors and antibody-based therapies continue to expand within the pharmaceutical market. We evaluated whether Cellhesion® VP, a chitin-based material, can be used as 3D culture platform for cell lines used for the production of antibodies and viral vectors.

RESULTS:

The results of Cell Counting Kit-8 assay and LDH assay revealed that Cellhesion® VP had no adverse effect to Human Embryonic Kidney (HEK) 293, A549 and Chinese hamster ovary (CHO) DG44-Interferon-ß (IFN) cells. Cell growth analyses showed that Cellhesion® VP supported the 3D culture of HEK293, A549 and CHO DG44- IFN-ß cells with a spherical morphology. Importantly, subculture of these cell lines on Cellhesion® VP was easily performed without trypsinization because cells readily transferred to newly added scaffold. Our data also suggest that CHO DG44-IFNß, cultured on Cellhesion® VP secreted IFNß stably and continuously during the culture period.

CONCLUSIONS:

Cellhesion® VP provides a simple and streamlined expansion culture system for the production of biopharmaceuticals.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biological Products Limits: Animals / Humans Language: En Journal: Biotechnol Lett Year: 2023 Document type: Article Affiliation country: Japan

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biological Products Limits: Animals / Humans Language: En Journal: Biotechnol Lett Year: 2023 Document type: Article Affiliation country: Japan