TY - JOUR
T1 - Chiral D-peptide supramolecular hydrogel for minimizing postoperative pancreatic fistula by devitalizing pancreatic enzymes
AU - Li, Xiao
AU - Wang, Yang
AU - Yuan, Juzheng
AU - An, Jiaze
AU - Yan, Siqi
AU - Wu, Weikang
AU - He, Wangxiao
AU - Yan, Jin
AU - Tao, Kaishan
N1 - Publisher Copyright:
© 2024 The Author(s)
PY - 2024/2/15
Y1 - 2024/2/15
N2 - Postoperative pancreatic fistula (POPF), is regarded as one of the most challenging complications following pancreatic and intestinal surgeries, posing significant risks to patients due to rapid tissue degradation caused by enzymes such as proteases and lipases released from the pancreas. The incorporation of D-enantiomerism into the backbone-side-chain connectivity and geometry of peptides offers a promising solution to enhance their resistance against proteases and lipases substantially. Therefore, this study successfully developed a chiral D-peptide supramolecular hydrogel known as CDPSH within a supramolecular hydrogel called LPSH. LPSH is composed of two peptides capable of self-assembling into intricate nanofibers that interweave into a mesh-like structure, facilitated by the presence of Ca2+ ions and blood coagulation factor FXIIIa. Remarkably, the hydrogel properties and mechanical characteristics of LPSH remained intact when incorporating D-enantiomerism, leading to the emergence of CDPSH. CDPSH exhibited a novel functionality by effectively inhibiting the enzymatic activities of trypsin, chymotrypsin, and lipase. Functioning as a self-healing physical barrier with resistance against proteolysis, CDPSH successfully encapsulated pancreatic fluid in rats with POPF. Furthermore, it significantly mitigated the inflammation caused by POPF while maintaining an excellent biosafety profile. In conclusion, the use of D-enantiomeric peptides in constructing supramolecular hydrogels not only provides a novel approach for creating biocompatible, biomimetic, and injectable hydrogels through peptide self-assembly but also introduces an innovative strategy for developing highly stable and multifunctional hydrogels with clinical applications.
AB - Postoperative pancreatic fistula (POPF), is regarded as one of the most challenging complications following pancreatic and intestinal surgeries, posing significant risks to patients due to rapid tissue degradation caused by enzymes such as proteases and lipases released from the pancreas. The incorporation of D-enantiomerism into the backbone-side-chain connectivity and geometry of peptides offers a promising solution to enhance their resistance against proteases and lipases substantially. Therefore, this study successfully developed a chiral D-peptide supramolecular hydrogel known as CDPSH within a supramolecular hydrogel called LPSH. LPSH is composed of two peptides capable of self-assembling into intricate nanofibers that interweave into a mesh-like structure, facilitated by the presence of Ca2+ ions and blood coagulation factor FXIIIa. Remarkably, the hydrogel properties and mechanical characteristics of LPSH remained intact when incorporating D-enantiomerism, leading to the emergence of CDPSH. CDPSH exhibited a novel functionality by effectively inhibiting the enzymatic activities of trypsin, chymotrypsin, and lipase. Functioning as a self-healing physical barrier with resistance against proteolysis, CDPSH successfully encapsulated pancreatic fluid in rats with POPF. Furthermore, it significantly mitigated the inflammation caused by POPF while maintaining an excellent biosafety profile. In conclusion, the use of D-enantiomeric peptides in constructing supramolecular hydrogels not only provides a novel approach for creating biocompatible, biomimetic, and injectable hydrogels through peptide self-assembly but also introduces an innovative strategy for developing highly stable and multifunctional hydrogels with clinical applications.
KW - D-enantiomerism
KW - Hydrogel
KW - Peptide
KW - Postoperative pancreatic fistula
KW - Supermolecule
UR - https://www.scopus.com/pages/publications/85183855904
U2 - 10.1016/j.cej.2024.149069
DO - 10.1016/j.cej.2024.149069
M3 - 文章
AN - SCOPUS:85183855904
SN - 1385-8947
VL - 482
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 149069
ER -