pH-Responsive Charge-Conversion Progelator Peptides

被引:23
作者
Carlini, Andrea S. [1 ,2 ,3 ]
Choi, Wonmin [2 ,3 ]
McCallum, Naneki C. [2 ,3 ]
Gianneschi, Nathan C. [1 ,2 ,3 ,4 ]
机构
[1] Univ Calif San Diego, Dept Chem & Biochem, 9500 Gilman Dr, La Jolla, CA 92093 USA
[2] Northwestern Univ, Int Inst Nanotechnol, Chem Life Proc Inst, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA
[3] Northwestern Univ, Simpson Querrey Inst, 2145 Sheridan Rd, Evanston, IL 60208 USA
[4] Northwestern Univ, Dept Mat Sci & Engn, Dept Biomed Engn & Pharmacol, 2145 Sheridan Rd, Evanston, IL 60208 USA
关键词
catheter; charge-conversion; hemocompatible; hydrogels; peptides; pH-responsive; self-assembly; HYDROGELS; ACIDOSIS;
D O I
10.1002/adfm.202007733
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A simple strategy for generating stimuli-responsive peptide-based hydrogels via charge-conversion of a self-assembling peptide (SAP) is described. These materials are formulated as soluble, polyanionic peptides, containing maleic acid, citraconic acid, or dimethylmaleic acid amide masking groups on each lysine residue, which do not form assemblies, but instead flow easily through high gauge needles and catheters. Acid-induced mask hydrolysis renews the zwitterionic nature of the peptides with concomitant and rapid self-assembly via beta-sheet formation into rehealable hydrogels. The use of different masks enables one to tune pH responsiveness and assembly kinetics. In anticipation of their potential for in vivo hydrogel delivery and use, progelators exhibit hemocompatibility in whole human blood, and their peptide components are shown to be noncytotoxic. Finally, demonstration of stimuli-induced self-assembly for dye sequestration suggests a simple, non-covalent strategy for small molecule encapsulation in a degradable scaffold. In summary, this simple, scalable masking strategy allows for preparation of responsive, dynamic self-assembling biomaterials. This work sets the stage for implementing biodegradable therapeutic hydrogels that assemble in response to physiological, disease-relevant states of acidosis.
引用
收藏
页数:9
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