

FOLLOWUS
a.Key Laboratory of Polymer Ecomaterials, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China
b.Jilin Biomedical Polymers Engineering Laboratory, Changchun 130022, China
c.School of Applied Chemistry and Engineering, University of Science and Technology of China, Hefei 230026, China
d.No. 1 Department of Neurology, China-Japan Union Hospital of Jilin University, Changchun 130033, China
e.Key Laboratory of Environmentally Friendly Chemistry and Applications of Ministry of Education and Key Laboratory of Polymeric Materials & Application Technology of Hunan Province, College of Chemistry, Xiangtan University, Xiangtan 411105, China
zxf7515@xtu.edu.cn (X.F.Z.)
ztang@ciac.ac.cn (Z.H.T.)
Received:19 November 2022,
Revised:2022-12-6,
Accepted:06 December 2022,
Online First:10 February 2023,
Published:01 August 2023
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Liu, Z. L.; Ren, X. T.; Huang, Y.; Sun, J. L.; Wang, X. S.; Zheng, M. F.; Cui, L. J.; Zhang, X. F.; Tang, Z. H. A novel CA4P polymeric nanoparticle for murine hepatoma therapy. Chinese J. Polym. Sci. 2023, 41, 1223–1229
Zhi-Lin Liu, Xi-Tong Ren, Yue Huang, et al. A Novel CA4P Polymeric Nanoparticle for Murine Hepatoma Therapy[J]. Chinese Journal of Polymer Science, 2023, 41(8): 1223-1229.
Liu, Z. L.; Ren, X. T.; Huang, Y.; Sun, J. L.; Wang, X. S.; Zheng, M. F.; Cui, L. J.; Zhang, X. F.; Tang, Z. H. A novel CA4P polymeric nanoparticle for murine hepatoma therapy. Chinese J. Polym. Sci. 2023, 41, 1223–1229 DOI: 10.1007/s10118-023-2921-7.
Zhi-Lin Liu, Xi-Tong Ren, Yue Huang, et al. A Novel CA4P Polymeric Nanoparticle for Murine Hepatoma Therapy[J]. Chinese Journal of Polymer Science, 2023, 41(8): 1223-1229. DOI: 10.1007/s10118-023-2921-7.
Combretastatin A4 phosphate (CA4P) is a potent vascular disrupting agent with good water solubility. However
it is only effective at high doses
which decreases clinical applicability. Herein
we designed stable CA4P polymeric nanoparticles (CA4P NPs) consisting of various cholesterol derivatives
and with a drug loading efficacy of 93%. The nanoparticles released CA4P in a sustained manner and achieved a 72% inhibition rate in the murine H22 liver tumor model
which was about 2.9-fold higher than that of free CA4P (24.6%). Furthermore
the carrier components of CA4P NPs were metabolized to arginine
cholesterol
ethanol and poly(ethylene glycol)
in vivo
; therefore
the CA4P NPs are safe and have significant potential for clinical translation.
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