論文

査読有り
2020年8月30日

Blood retention and antigenicity of polycarboxybetaine-modified liposomes

International Journal of Pharmaceutics
  • Ryujin, T.
  • ,
  • Shimizu, T.
  • ,
  • Miyahara, R.
  • ,
  • Asai, D.
  • ,
  • Shimazui, R.
  • ,
  • Yoshikawa, T.
  • ,
  • Kishimura, A.
  • ,
  • Mori, T.
  • ,
  • Ishida, T.
  • ,
  • Katayama, Y.

586
開始ページ
119521
終了ページ
119521
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1016/j.ijpharm.2020.119521

Zwitterionic polycarboxybetaines (PCBs) have gained attention as alternative stealth polymers whose liposomal formulation and protein conjugates were reported not to elicit anti-polymer antibodies. Here, we studied the blood retention and antigenicity of liposomes modified with PCBs focusing on their chemical structures and doses. We compared PCBs with either 1 or 3 (PCB1 or PCB3) spacer carbons between the carboxylate and ammonium groups. PCB3-modified liposomes had a short blood retention, whereas PCB1-modified liposomes demonstrated extended blood retention that was somewhat superior to PEGylated liposome. This confirmed the excellent non-fouling nature of PCB1 reported previously. Interestingly, PCB1-liposome as well as PCB3-liposome elicited specific IgMs toward each PCB. The dose-dependent production of specific IgMs to PCB-liposomes was similar to that of PEGylated liposome, i.e., high doses of PCB-liposomes reduced the production of specific IgMs, termed immunological tolerance. These results indicate the importance of investigating the effect of dose to clarify the existence of antigenicity of stealth polymers.

リンク情報
DOI
https://doi.org/10.1016/j.ijpharm.2020.119521
URL
https://web.db.tokushima-u.ac.jp/cgi-bin/edb_browse?EID=366302
URL
https://www.ncbi.nlm.nih.gov/pubmed/32561308
URL
https://www.scopus.com/record/display.url?eid=2-s2.0-85086721197&origin=inward
ID情報
  • DOI : 10.1016/j.ijpharm.2020.119521
  • ISSN : 1873-3476
  • ISSN : 0378-5173
  • ORCIDのPut Code : 97728637
  • SCOPUS ID : 85086721197

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