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. 2019 Apr 15;10:1735. doi: 10.1038/s41467-019-09587-y

Fig. 7.

Fig. 7

In vitro catheter injection of low-viscosity progelators. a Complex viscosity of KLDLCyclic (blue triangles) and KFDFCyclic (blue circles) progelators reveal >20× decrease in comparison to corresponding unmodified KLDL (black triangles) and KFDF (black circles) self-assembling peptides (SAPs). b Schematic illustrating catheter applicability of KLDL and KFDF SAPs vs that of enzyme-responsive KLDLCyclic and KFDFCylic progelators. Injection of SAP hydrogels causes clogging. Clipart adapted from Servier’s Medical Art database (https://smart.servier.com). c Experimental setup of progelator (2 mol% labeled) catheter injection test. Peptide was (1) loaded in a 1 mL syringe, (2) mounted on a syringe pump, and (3) flowed at 0.6 mL min−1 through the inner nitinol tubing (27 G) of a MyoStar transendocardial injection catheter. The catheter was (4) submerged in a circulating water bath heated to 37 °C. The collection tube (5) before (top) and after (bottom) injection shows successful injection. d Photographs of KLDLCyclic and KFDFCyclic progelators (2 mol% labeled) after catheter injection into an empty vial (left) or a vial containing thermolysin (right), demonstrating that injection does not disrupt enzyme responsiveness. Progelator formulated as 10 mM in 1× Dulbecco's phosphate-buffered saline (DPBS; pH 7.4) and treated with 1:4500 enzyme/substrate molar ratio