

FOLLOWUS
a.College of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022, China
b.School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing 100081, China
c.National Engineering Research Center for Colloidal Materials & Key Laboratory of Special Functional Aggregated Materials, Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China
chm_liss@ujn.edu.cn (S.S.L.)
chm_zhuxl@ujn.edu.cn (X.L.Z.)
Received:27 September 2025,
Accepted:13 November 2025,
Online First:22 January 2026,
Published:05 February 2026
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Xie, C.; Li, L. Y.; Li, S. S.; Zong, C. Y.; Jiang, X. B.; Zhu, X. L.; Feng, S. Y.; Kong, X. Z. Poly(hydroxy urethane-siloxane) pressure-sensitive adhesive: synthesis, characterization and its usage for skin-contact sensors. Chinese J. Polym. Sci. 2026, 44, 536–548
Chao Xie, Ling-Yi Li, Shu-Sheng Li, et al. Poly(hydroxy urethane-siloxane) Pressure-sensitive Adhesive: Synthesis, Characterization and Its Usage for Skin-contact Sensors[J]. Chinese Journal of Polymer Science, 2026, 44(2): 536-548.
Xie, C.; Li, L. Y.; Li, S. S.; Zong, C. Y.; Jiang, X. B.; Zhu, X. L.; Feng, S. Y.; Kong, X. Z. Poly(hydroxy urethane-siloxane) pressure-sensitive adhesive: synthesis, characterization and its usage for skin-contact sensors. Chinese J. Polym. Sci. 2026, 44, 536–548 DOI: 10.1007/s10118-025-3503-7.
Chao Xie, Ling-Yi Li, Shu-Sheng Li, et al. Poly(hydroxy urethane-siloxane) Pressure-sensitive Adhesive: Synthesis, Characterization and Its Usage for Skin-contact Sensors[J]. Chinese Journal of Polymer Science, 2026, 44(2): 536-548. DOI: 10.1007/s10118-025-3503-7.
Poly(hydroxy urethane-siloxane) pressure-sensitive adhesives (PHUSi) were synthesized through the reaction of cyclic carbonate-functionalized polysiloxanes with diamines. PHUSi exhibits high biocompatible and adhesive performance
suitable for medical applications
such as flexible electrocardiogram devices.
Silicone-based pressure-sensitive adhesives (Si-PSAs) are valued for their thermal stability
flexibility
and biocompatibility
but their weak bonding strength restricts high-performance use. Polyurethane-modified Si-PSAs enhance adhesion
however diisocyanates remain essential. The raw materials of isocyanates are toxic
and their synthesis involves phosgene. To make up for those shortcomings
a series of poly(hydroxy urethane-siloxane) PSAs
named as PHUSi here
were synthesized through the ring-opening reaction of cyclic carbonate-functionalized polysiloxanes (PSi
x
-VEC
z
) with various aliphatic diamines. The PSi
x
-VEC
z
precursors were prepared
via
the hydrosilylation of hydrogen-containing polysiloxanes (PSi
x
-H
y
) with 4-vinyl-1
3-dioxolan-2-one (VEC). The chemical structures of PSi
x
-H
y
PSi
x
-VEC
z
and PHUSi were characterized
and bonding properties of PHUSi were systematically evaluated. The influence of architectures on adhesive performance was elucidated through comprehensive analyses
including rheology
crosslink density assessment
and so on. These studies revealed that the tailored design of PHUSi adhesives combine the advantages of traditional Si-PSAs
with enhanced adhesion while eliminating isocyanate toxicity. The optimized PHUSi formulation achieved remarkable 180° peel strength (76.5 N/m on skin) and maximum probe tack force (1.61 N)
enabling secure 24 h attachment of flexible sensors to skin. These properties make PHUSi particularly suitable for medical applications
as demonstrated by successful implementation in flexible electrocardiogram devices
offering a biocompatible
high-performance adhesive.
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