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Table 2 Histological findings for all treatment groups from Series 1 and Series 2

From: Long-term exposure to commercially available sunscreens containing nanoparticles of TiO2 and ZnO revealed no biological impact in a hairless mouse model

 

Group ID

Sunscreen

UVR kJ/m2

Number of mice per group

Number of mice that reached endpoint without AE

Total mice with AE

Mice with AE related to malignant or pre-malignant findings (histologically diagnosed)

Mice with AE related to non-malignant findings (histologically diagnosed)

Mice with AE, no necroscopy

Total mice at predetermined endpoint with malignant findings (histologically diagnosed)

Total mice at predetermined endpoint with non-malignant findings (histologically diagnosed)

Total mice at predetermined endpoint with no malignant or non-malignant findings

Series 1

Control-UVR

None

0

10

10

0

0

0

0

0

0

10

Control + UVR

None

29

10

6

4

4 (1 X CFS; 1 X CFS + SCC; 1 X LL; 1 X SCP)

0

0

1 (1 X SCP)

4a

1

ZnO-UVR

ZnO

0

10

10

0

0

0

0

0

1 (1 X PA)

9

ZnO + UVR

ZnO

29

10

5

5

1 (1 X LL)

2 (1 X N; 1 X HC)

2

1 (1 X CFS)

0

4

TiO2-UVR

TiO2

0

10

9

1

0

1 (1 X P)

0

0

0

9

TiO2 + UVR

TiO2

29

10

10

0

0

0

0

2 (2 X BAC)

1 (1 X PA)

7

Organic-UVR

Organic

0

10

9

1

1 (1 X LL)

0

0

0

0

9

Organic + UVR

Organic

29

10

9

1

0

0

1

1 (1 X LL)

0

8

Series 2

2-Control-UVR

None

0

10

10

0

0

0

0

0

0

10

2-Control + UVR

None

27

10

9

1

1 (1 X LL)

0

0

7 (1 X BAC; 4 X SCC; 1 X LL; 1 X CFS & SCP)

0

2

2-ZnO-UVR

ZnO

0

10

9

1

1 (1 X LL)

0

0

1 (1 X OS)

0

8

2-ZnO + UVR

ZnO

27

10

9

1

0

1 (1 X E)

0

0

0

9

  1. The predetermined endpoint for both groups was 36 weeks
  2. CODE: AE adverse event, BAC bronchioalveolar carcinoma, CFS cutaneous fibrosarcoma, E endometritis, HC haemolytic crisis, LL lymphocytic lymphoma, N nephropathy, OS osteosarcoma, P peritonitis, PA pulmonary adenoma, SCC squamous cell carcinoma, SCP squamous cell papilloma
  3. aNo malignant or non-malignant outcomes, but moderate to severe dermal hyperplasia and inflammation were histologically diagnosed in all four mice