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. 2019 Jul 1;31(4):403–413. doi: 10.5021/ad.2019.31.4.403

Fig. 3. Polydeoxyribonucleotide (PDRN) decreases wound area and wound depth in diabetic mice. (A) Color-coded surface topography image captured by a PRIMOSLITE optical 3D skin measuring device, (B) graph showing changes in wound area over time after injury. In +Leprdb/+Leprdb mice, the reduction of the wound area in the PDRN-injected group occurred more rapidly than in the phosphate-buffered saline (PBS)-injected group. In both m+/+Leprdb mice and +Leprdb/+Leprdb mice, the wound area decreased faster than in controls, but this difference was not significant. (C) Graph showing changes in wound depth over time after injury. The PDRN-injected +Leprdb/+Leprdb mice recovered at a rate similar to that of PDRN-injected m+/+Leprdb mice, but the recovery of the wound depth was delayed in the PBS-injected +Leprdb/+Leprdb mice. The wound depth of the PBS-injected group was significantly different from that of the PDRN-injected group on days 6 and 9 (*p<0.05) in +Leprdb/+Leprdb mice.

Fig. 3