

FOLLOWUS
a.School of Biomedical Sciences and Engineering, South China University of Technology, Guangzhou International Campus, Guangzhou 511442, China
b.National Engineering Research Center for Tissue Restoration and Reconstruction, and Guangdong Provincial Key Laboratory of Biomedical Engineering, and Key Laboratory of Biomedical Materials of the Ministry of Education, South China University of Technology, Guangzhou 510006, China
chenjunbin@scut.edu.cn (J.B.C.)
yangxz@scut.edu.cn (X.Z.Y.)
Received:29 July 2026,
Accepted:13 September 2026,
Online First:11 November 2026,
Published:2026-10
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Xiao, Z. K.; Wang, J. H.; Chen, J. B.; Yang, X. Z. Polymers with intrinsically therapeutic activity: from membrane-targeted cytotoxicity to receptor-topology remodeling. Chinese J. Polym. Sci. https://doi.org/10.1007/s10118-026-3891-3
Ze-Kai Xiao, Ji-Hong Wang, Jun-Bin Chen, et al. Polymers with Intrinsically Therapeutic Activity: from Membrane-targeted Cytotoxicity to Receptor-topology Remodeling[J/OL]. Chinese Journal of Polymer Science, 2026, 441-23.
Xiao, Z. K.; Wang, J. H.; Chen, J. B.; Yang, X. Z. Polymers with intrinsically therapeutic activity: from membrane-targeted cytotoxicity to receptor-topology remodeling. Chinese J. Polym. Sci. https://doi.org/10.1007/s10118-026-3891-3 DOI:
Ze-Kai Xiao, Ji-Hong Wang, Jun-Bin Chen, et al. Polymers with Intrinsically Therapeutic Activity: from Membrane-targeted Cytotoxicity to Receptor-topology Remodeling[J/OL]. Chinese Journal of Polymer Science, 2026, 441-23. DOI: 10.1007/s10118-026-3891-3.
Polymers with intrinsic therapeutic activity have redefined the role of macromolecules in medicine. Unlike conventional polymeric carriers
which primarily improve solubility
prolong circulation
or control drug release
these polymers directly engage in therapeutic processes through their chemical structures
physical organization
multivalent interactions
and stimulus-responsive behaviors. In this review
we discuss the four representative classes of therapeutic polymers. Membrane-active polymers eradicate pathogens
disrupt biofilms
and kill tumor cells by exploiting their charge
hydrophobicity
chain conformation
and disease-associated membrane vulnerability. Immunomodulatory polymers activate or redirect protective immunity by engaging innate immune sensors
glycan-recognition pathways
and engineered immune-cell interfaces. Anti-inflammatory polymers resolve pathological inflammation by scavenging reactive oxygen species
regulating macrophage polarization
inhibiting pyroptosis
and remodeling damaged tissue microenvironments. Receptor-topology-remodeling multivalent polymers reorganize cell surface receptors through nanoscale ligand spacing
receptor crosslinking
mechanical force
and programmable clustering to induce apoptosis or rewire signaling. Taken together
these examples establish that polymer architecture itself can determine therapeutic outcomes across a wide spectrum of conditions
including infection
cancer
inflammatory diseases
and immune-mediated disorders. By comparing these mechanisms
we highlight how macromolecular design parameters
including valency
degradability
assembly state
and disease-triggered activation
can translate into therapeutic potential. We further delineated the key design principles and translational challenges for this emerging class of polymer-based therapeutics.
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