Glass slide adhesive
An adhesive and glass slide technology is applied in the field of slide glass anti-detachment treatment reagents, which can solve the problems of poor adhesion and weak wettability, and achieve the effects of improving wettability, firm bonding and low energy consumption.
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Embodiment 1
[0020] Weigh or measure each component according to the table below, and prepare a 100ml solution.
[0021] 3-Aminopropyltriethoxysilane (APTES) 0.010ml
[0022] Coconut Oil Fatty Acid Diethanolamide 0.200ml
[0023] Polyethylene glycol 200 0.010ml
[0024] Polyethylene glycol 4000 (density 1.212g / ml) 0.020g
[0025] Isopropanol 1.000ml
[0026] Ultrapure water make up 100ml
[0027] After mixing the components, stir to dissolve, soak the glass slide for 5-10 minutes, and let it dry.
[0028] 400 slides were processed for cytology and histology, and conventional staining and Feulgen staining were used. The results showed that the cell shedding rate of various preparation and staining methods was 0%; the wettability of liquid-based cytology preparation was poor; the cleanliness of the slide surface was poor after treatment.
Embodiment 2
[0030] Weigh or measure each component according to the table below, and prepare a 100ml solution.
[0031] 3-Aminopropyltriethoxysilane (APTES) 0.100ml
[0032] Polyvinylpyrrolidone (PVP) (density 1.23-1.29g / ml) 0.200g
[0033] Polyethylene glycol 200 0.005ml
[0034] Ethanol 0.500ml
[0035] Glycerol 1.650ml
[0036] Ultrapure water make up 100ml
[0037] After mixing the components, stir to dissolve, soak the glass slide for 5-10 minutes, and let it dry.
[0038] 400 slides were processed for cytology and histology, and conventional staining and Feulgen staining were used. The results showed that the cell shedding rate of various preparation and staining methods was 0%; the liquid-based cytology preparation had poor wettability; the surface cleanliness of the treated slide was good.
Embodiment 3
[0040] Weigh or measure each component according to the table below, and prepare a 100ml solution.
[0041] 3-Aminopropyltriethoxysilane (APTES) 0.020ml
[0042] Polyvinylpyrrolidone (PVP) (density 1.23-1.29g / ml) 0.300g
[0043] Polyethylene glycol 4000 (density 1.212g / ml) 0.010g
[0044] Isopropanol 2.000ml
[0045] Ultrapure water make up 100ml
[0046] After mixing the components, stir to dissolve, soak the glass slide for 5-10 minutes, and let it dry.
[0047] 400 slides were processed for cytology and histology, and conventional staining and Feulgen staining were used. The results showed that the cell shedding rate of various preparation and staining methods was 0%; the preparation of liquid-based cytology had strong wettability; the cleanliness of the surface of the slide was good after treatment.
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