1
INTRODUCTION
In the mid-1990s, hydrogen peroxide and chlorine-
based contact lens cleaning systems had a
predominant stance in the market, comprising almost
half of all cleaning regimes prescribed.
1, 2
Since then,
the two-step hydrogen peroxide, requiring a second
neutralization step, and chlorine-based systems have
become virtually obsolete and the one-step hydrogen
peroxide systems have experienced a drastic drop in
use due to the growing popularity of multipurpose
solutions.
1, 2
Multipurpose solutions now account for
over 85%
1, 2
of the market for contact lens cleaning
and disinfection solutions and for many years
have been the preference of patients due to their
simplicity, ease of use, and speed of use. However,
in recent years there have been two worldwide
recalls of multipurpose solutions due to microbial
keratitis outbreaks
3–5
and there have been reports
of an increased prevalence of corneal staining with
the use of polyhexamethyl biguanide (PHMB)
6–8
containing multipurpose solutions when combined
with certain lenses. Due to these factors, there has
been a resurgence of interest in hydrogen peroxide
Current Eye Research, 2012; Early Online: 1–10
© 2012 Informa Healthcare USA, Inc.
ISSN: 0271-3683 print/1460-2202 online
DOI: 10.3109/02713683.2012.682636
Received 13 February 2012; revised 28 March 2012; accepted 01 April 2012
Correspondence: Holly Lorentz, Centre for Contact Lens Research, School of Optometry, University of Waterloo, 200, University Avenue
West, Waterloo, Ontario, Canada N2L 3G1. Phone: (519) 888-4567 Extn 31349. Fax: (519) 884–8769. E-mail: hmelchin@uwaterloo.ca
ORGINAL ARTICLE
Using an In Vitro Model of Lipid Deposition to Assess the
Eficiency of Hydrogen Peroxide Solutions to Remove
Lipid from Various Contact Lens Materials
Holly Lorentz
1
, Miriam Heynen
1
, Helen Tran
1
, and Lyndon Jones
1
1
Centre for Contact Lens Research, School of Optometry, University of Waterloo, Waterloo, Ontario, Canada
ABSTRACT
Purpose: To test the ability of two commercially available hydrogen peroxide disinfection solutions, one con-
taining a surfactant and one without, to remove lipid from various contact lens materials using in vitro radio-
chemical experiments.
Methods: Etailcon A, senoilcon A and balailcon A contact lens materials were incubated in an artiicial tear solu-
tion (ATS) containing a mixture of lipids, proteins, mucin and either
14
C-cholesterol or
14
C-phosphatidylcholine
for 8 h. Following incubation, the lenses were removed, rinsed, and placed for 16 h in either a surfactant-
containing peroxide solution (ClearCare
®
), a peroxide solution devoid of a surfactant (AOSept
®
) or stored
without solution (control). This process was repeated every day for 1 week. The lenses were extracted with
a previously optimized extraction protocol, evaporated, re-suspended, luor added and counted for their
radioactive signals. Masses of lipids deposited were calculated based on standard calibration curves, the
disinfection solutions were compared and repeated measures ANOVA and post hoc statistical analysis was
completed using Statistica 9.
Results: The results of this experiment found that daily disinfection with hydrogen peroxide solutions reduced
the amount of cholesterol and phosphatidylcholine deposited on the three contact lens materials exam-
ined, however in many cases the reduction in deposition was less than 15% when compared to the control.
Disinfection with the solution containing the surfactant (ClearCare), resulted in the least deposited cholesterol
and phosphatidylcholine for all materials, however not all of the comparisons were statistically signiicant.
Conclusions: Overall, ClearCare hydrogen peroxide disinfection solution containing Pluronic 17R4 removed
the most lipid from lenses when compared to the non-surfactant containing AOSept or the control, for both
lipids and all lens materials. However, the differences found were quite small at times and whether these dif-
ferences are clinically signiicant are yet to be determined.
Keywords: contact lens, lipid, disinfection solutions, hydrogen peroxide
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