Table 5.
Drug | Method Used | Loading Conditions | Results | Ref. |
---|---|---|---|---|
ANTIHISTAMINES AND MAST CELL STABILISERS | ||||
Cromolyn sodium | Unmodified commercial hydrogel and silicone hydrogel materials |
20 mg/mL solution for 50 h |
In vitro: Alphafilcon A (1147 ± 146 μg/lens). |
Karlgard 2003 [160] |
Ketotifen fumarate | Unmodified commercial hydrogel and silicone hydrogel materials |
2.5 mg/mL solution or 24 h |
In vitro: Etafilcon (284.5 ± 29.8 μg/lens) Balafilcon A (227.6 ± 14.7 μg/lens). |
Soluri 2012 [172] |
Ketotifen fumarate | Soaking Combined acrylic acid, acrylamide, N-vinyl 2- pyrrolidinone and polyethylene glycol (200) dimethacrylate molecularly imprinted pHEMA gels |
Soaking in ‘concentrated’ ketotifen solutions until equilibrium |
In vitro: Increased ketotifen loading into gels 6- to 8-fold. 8% of the total amount of drug released after 4 days. Presence of lysozyme: further extended-release times 5-fold. In vivo: Imprinted contact lens: increase 4 and 50 times compared to nonimprinted lenses and eye drops, respectively. |
Venkatesh 2007 [173] Ali 2007 [174] Venkatesh 2008 [175] Tieppo 2012 [99] |
Ketotifen fumarate | Model DMA, MA-PDMS-MA, TRIS, hydrogel contact lenses |
1.945 mg/mL solutions for five days |
In vitro: hydrophilic phases exhibited faster release. In vivo: 19.53 μg/mL in tear film after 24 h of lens wearing. |
Xu 2011 [176] |
Olopatadine hydrochloride | Combined acrylic acid, acrylamide, 2- acrylamide-2-methyl- propane sulfonic acid and benzyl methacrylate molecularly imprinted pHEMA materials |
0.2 or 10 mg/mL solutions for 20 days |
In vitro: Sustain release for upward of 24 h. |
González-Chomon 2016 [177] |
DMA: N, N-dimethyl acrylamide, MA-PDMS-MA: methacrylated polydimethylsiloxanes, pHEMA: poly-2-hydroxyl ethyl methacrylate, TRIS: tris(trimethyl siloxy) silyl-propyl methacrylate.