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Table 1 Properties of hydrogel contact lenses used in this study

From: A three-phase in-vitro system for studying Pseudomonas aeruginosa adhesion and biofilm formation upon hydrogel contact lenses

Proprietary name

ACUVUE 2

PROCLEAR

BIOFINITY

AIROPTIX

United States Adopted Name (USAN)

Etafilcon A

Omafilcon A

Comfilcon A

Lotrafilcon B

Manufacturer

Johnson & Johnson

Cooper Vision

Cooper Vision

CIBA Vision

Water content (%)

58

62

48

33

Ionic charge

Ionic

Non-ionic

Non-ionic

Non-ionic

Oxygen permeability (Dk)

22

27

128

110

Centre thickness (mm) -3.00 D

0.084

0.065

0.08

0.08

Oxygen transmissibility (Dk/t) at 35°C

33.3

42

160

138

Basis curve (mm)

8.7

8.6

8.6

8.6

Diameter (mm)

14.0

14.2

14.0

14.2

Surface treatment

None

None

None

25-nm-thick plasma coating with high refractive index

FDA Group

4 (Conventional hydrogel)

2 (Conventional hydrogel)

1 (Silicone hydrogel)α

1 (Silicone hydrogel)β

Replacement and wearing schedule*

Every 2 weeks (daily wear) OR six nights extended wear

Every 4 weeks (daily wear)

Every 4 weeks (daily, continuous OR flexible wear)

Every 4 weeks (daily wear) OR up to six nights extended wear

Principal monomers

HEMA, MA

HEMA, PC

FM0411M, HOB, IBM, M3U, NVP, TAIC, VMA

DMA, TRIS, siloxane monomer

  1. HEMA (poly-2-hydroxyethyl methacrylate); MA (methacrylic acid); PC (phoshoryl choline); DMA (N,N-dimethylacryl amide); TRIS (trimethylsiloxy silane); DMA, N,N-dimethylacrylamide; FM0411M (α-methacryloyloxyethyl iminocarboxyethyloxypropyl-poly(dimethylsiloxy)-butyldimethylsilane); HOB (2-hydroxybutyl methacrylate); IBM (isobornyl methacrylate); M3U αω -bis(methacryloyloxyethyl iminocarboxy ethyloxypropyl)-poly(dimethylsiloxane)-poly(trifluoropropylmethylsiloxane)-poly(ω methoxy- poly(ethyleneglycol)propylmethylsiloxane); NVP (N-vinyl pyrrolidone); TAIC (1,3,5-triallyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione); VMA (N-Vinyl-N-methylacetamide)
  2. α third silicone generation
  3. β first silicone generation
  4. *It is recommended that the CL wearer first be evaluated on a daily wear schedule. If successful, then a gradual introduction of extended wear can be followed as determined by the prescribing Eye Care Practitioner.