Figures & data
Figure 3 H&E stained skin sections in an acute toxicity study (× 40). A) Negative control; B) AgNO3 group: reduced thickness of epidermis and increased regular collagen fiber in papillary layer and mononuclear inflammation; C) Low-dose nanosilver group with reduced thickness of epidermis, reduced thickness of papillary layer, and regular collagen fibers; D) High-dose nanosilver group with reduced thickness of epidermis, reduced thickness of papillary layer, and irregular collagen fibers.
![Figure 3 H&E stained skin sections in an acute toxicity study (× 40). A) Negative control; B) AgNO3 group: reduced thickness of epidermis and increased regular collagen fiber in papillary layer and mononuclear inflammation; C) Low-dose nanosilver group with reduced thickness of epidermis, reduced thickness of papillary layer, and regular collagen fibers; D) High-dose nanosilver group with reduced thickness of epidermis, reduced thickness of papillary layer, and irregular collagen fibers.](/cms/asset/d99edaec-1352-4c8e-b294-cf081a33275f/dijn_a_17065_f0003_c.jpg)
Table 1 Dermal histopathologic changes in acute study
Figure 4 H&E stained skin sections in subchronic toxicity (× 40). A) Normal skin in control group; B) AgNO3 group with reduced thickness of dermis and epidermis, increased Langerhans cells, inflammation, decreased thickness of papillary zone layer, and increased collagen levels of dermis layer; C) Skin abnormalities in low-dose nanosilver group; D) Skin abnormalities in high-dose nanosilver group; E) Highest level of dermal toxicity (see text for further details).
![Figure 4 H&E stained skin sections in subchronic toxicity (× 40). A) Normal skin in control group; B) AgNO3 group with reduced thickness of dermis and epidermis, increased Langerhans cells, inflammation, decreased thickness of papillary zone layer, and increased collagen levels of dermis layer; C) Skin abnormalities in low-dose nanosilver group; D) Skin abnormalities in high-dose nanosilver group; E) Highest level of dermal toxicity (see text for further details).](/cms/asset/a94e9861-ac70-48bf-a6e1-8d48d301b79d/dijn_a_17065_f0004_c.jpg)
Table 2A Dermal histopathologic changes in subchronic test
Table 2B Liver histopathologic changes in subchronic test
Table 2C Histopathologic changes of the spleen in subchronic test
Figure 5 H&E stained liver sections in subchronic toxicity (× 40). A) Normal liver in control group; B) AgNO3 group with hepatic cord deformation; C) Overproduction of Kupffer cells and degeneration of hepatocytes in low-dose nanosilver group; D) Overproduction of Kupffer cells and degeneration of hepatocyte in medium-dose nanosilver group; E) Liver necrosis in nanosilver high-dose group.
![Figure 5 H&E stained liver sections in subchronic toxicity (× 40). A) Normal liver in control group; B) AgNO3 group with hepatic cord deformation; C) Overproduction of Kupffer cells and degeneration of hepatocytes in low-dose nanosilver group; D) Overproduction of Kupffer cells and degeneration of hepatocyte in medium-dose nanosilver group; E) Liver necrosis in nanosilver high-dose group.](/cms/asset/005afd43-59d8-403e-9dce-58c3183eea5f/dijn_a_17065_f0005_c.jpg)
Figure 6 H&E stained spleen sections in subchronic toxicity study (× 40). A) Normal spleen in control group. B) Thin red capsule with inflammation and white pulp hypertrophy in AgNO3 group; C) Thin capsules with inflammation, accumulation of red blood cells (RBC), and white pulp atrophy in low-dose nanosilver group; D) Thin capsules with inflammation, accumulation of RBC, and white pulp atrophy in medium-dose nanosilver group; E) The highest levels of red pulp inflammation, white pulp atrophy, and thinnest capsule in high-dose nanosilver group.
![Figure 6 H&E stained spleen sections in subchronic toxicity study (× 40). A) Normal spleen in control group. B) Thin red capsule with inflammation and white pulp hypertrophy in AgNO3 group; C) Thin capsules with inflammation, accumulation of red blood cells (RBC), and white pulp atrophy in low-dose nanosilver group; D) Thin capsules with inflammation, accumulation of RBC, and white pulp atrophy in medium-dose nanosilver group; E) The highest levels of red pulp inflammation, white pulp atrophy, and thinnest capsule in high-dose nanosilver group.](/cms/asset/c1f15bed-b790-4d5a-bc4a-ac2ba439fdf3/dijn_a_17065_f0006_c.jpg)