TY - GEN
T1 - Therapeutic contact lenses via biomimetic imprinting
AU - Venkatesh, Siddarth
AU - Ali, Maryam
AU - Sizemore, Stephen P.
AU - Zhang, Jeney B.
AU - Byrne, Mark E.
PY - 2006/12/1
Y1 - 2006/12/1
N2 - A biomimetic approach has been exercised to design and synthesize novel contact lenses, to tackle the unmet need for the controlled loading and release of therapeutics on the surface of the eye. This work will demonstrate the formation and characterization of novel lenses with controlled loading and release of ocular Hlantihistamines and antibiotics. Since ocular bioavailability of topical drugs is very poor (typically less than 7% is absorbed by the eye), a high dosage is needed which typically prohibits contact lens use and warrants multiple dosages a day. Controlling and tailoring the release of drugs via novel contact lenses with significantly enhanced loading can solve these problems with increased drug bioavailability, less irritation to eye tissue, and reduced eye and body side effects. Conventional soft contact lenses typically do not work due to a lack of sufficient drug loading and poor control of drug release. This new class of recognitive intelligent biomaterials is designed by incorporating motifs with structural and molecular homology to biological receptor docking sites and has a strong potential to work with a wide spectrum of drugs and impact the administration of a number of ocular therapies. Gels of multiple binding points with varying functionalities outperformed gels formed with fewer types of functionality and showed the greatest loading potential (i.e., up to 6 times more than control lenses) with mechanical and optical properties comparable to conventional lenses. Dynamic drug release profiles under in vitro physiological conditions demonstrated that release rates can be tailored via type and amount of functionality and a viable therapeutic concentration of drug can be delivered at a constant rate for extended periods from 16 hours to over a week depending on formulation.
AB - A biomimetic approach has been exercised to design and synthesize novel contact lenses, to tackle the unmet need for the controlled loading and release of therapeutics on the surface of the eye. This work will demonstrate the formation and characterization of novel lenses with controlled loading and release of ocular Hlantihistamines and antibiotics. Since ocular bioavailability of topical drugs is very poor (typically less than 7% is absorbed by the eye), a high dosage is needed which typically prohibits contact lens use and warrants multiple dosages a day. Controlling and tailoring the release of drugs via novel contact lenses with significantly enhanced loading can solve these problems with increased drug bioavailability, less irritation to eye tissue, and reduced eye and body side effects. Conventional soft contact lenses typically do not work due to a lack of sufficient drug loading and poor control of drug release. This new class of recognitive intelligent biomaterials is designed by incorporating motifs with structural and molecular homology to biological receptor docking sites and has a strong potential to work with a wide spectrum of drugs and impact the administration of a number of ocular therapies. Gels of multiple binding points with varying functionalities outperformed gels formed with fewer types of functionality and showed the greatest loading potential (i.e., up to 6 times more than control lenses) with mechanical and optical properties comparable to conventional lenses. Dynamic drug release profiles under in vitro physiological conditions demonstrated that release rates can be tailored via type and amount of functionality and a viable therapeutic concentration of drug can be delivered at a constant rate for extended periods from 16 hours to over a week depending on formulation.
UR - http://www.scopus.com/inward/record.url?scp=80053792385&partnerID=8YFLogxK
M3 - Conference contribution
AN - SCOPUS:80053792385
SN - 081691012X
SN - 9780816910120
T3 - AIChE Annual Meeting, Conference Proceedings
BT - 2006 AIChE Annual Meeting
T2 - 2006 AIChE Annual Meeting
Y2 - 12 November 2006 through 17 November 2006
ER -