NZ613852B2 - Contact lens cleaning system with monitor - Google Patents
Contact lens cleaning system with monitor Download PDFInfo
- Publication number
- NZ613852B2 NZ613852B2 NZ613852A NZ61385212A NZ613852B2 NZ 613852 B2 NZ613852 B2 NZ 613852B2 NZ 613852 A NZ613852 A NZ 613852A NZ 61385212 A NZ61385212 A NZ 61385212A NZ 613852 B2 NZ613852 B2 NZ 613852B2
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- New Zealand
- Prior art keywords
- sensor
- cleaning
- solution
- rate
- processing device
- Prior art date
Links
- 238000004140 cleaning Methods 0.000 title claims abstract description 256
- 238000006386 neutralization reaction Methods 0.000 claims abstract description 49
- 239000003054 catalyst Substances 0.000 claims abstract description 48
- 230000005591 charge neutralization Effects 0.000 claims abstract description 47
- 230000001264 neutralization Effects 0.000 claims abstract description 47
- 238000004891 communication Methods 0.000 claims abstract description 23
- 230000003472 neutralizing Effects 0.000 claims abstract description 12
- 238000006243 chemical reaction Methods 0.000 claims description 49
- MHAJPDPJQMAIIY-UHFFFAOYSA-N hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 48
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 30
- 229910052697 platinum Inorganic materials 0.000 claims description 15
- 239000007789 gas Substances 0.000 claims description 14
- 230000000875 corresponding Effects 0.000 claims description 4
- 239000000243 solution Substances 0.000 description 216
- 230000000249 desinfective Effects 0.000 description 35
- 238000000034 method Methods 0.000 description 31
- 238000004659 sterilization and disinfection Methods 0.000 description 24
- 150000002978 peroxides Chemical class 0.000 description 23
- 239000003570 air Substances 0.000 description 19
- 238000005259 measurement Methods 0.000 description 12
- 238000009529 body temperature measurement Methods 0.000 description 9
- 239000000203 mixture Substances 0.000 description 8
- 230000003287 optical Effects 0.000 description 7
- 238000003780 insertion Methods 0.000 description 6
- 150000002500 ions Chemical class 0.000 description 6
- 206010055116 Chemical eye injury Diseases 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 239000003990 capacitor Substances 0.000 description 4
- 101700087049 chup-1 Proteins 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 239000011780 sodium chloride Substances 0.000 description 4
- 239000008174 sterile solution Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 244000052616 bacterial pathogens Species 0.000 description 3
- 230000004397 blinking Effects 0.000 description 3
- 239000000882 contact lens solution Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000006011 modification reaction Methods 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 239000012080 ambient air Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000001934 delay Effects 0.000 description 2
- 230000001419 dependent Effects 0.000 description 2
- 230000000994 depressed Effects 0.000 description 2
- 201000009910 diseases by infectious agent Diseases 0.000 description 2
- 238000011067 equilibration Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000004973 liquid crystal related substance Substances 0.000 description 2
- 230000005236 sound signal Effects 0.000 description 2
- 241000229754 Iva xanthiifolia Species 0.000 description 1
- 101700015817 LAT2 Proteins 0.000 description 1
- 241000120694 Thestor Species 0.000 description 1
- 210000003932 Urinary Bladder Anatomy 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K [O-]P([O-])([O-])=O Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 230000003197 catalytic Effects 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 230000002596 correlated Effects 0.000 description 1
- 230000003247 decreasing Effects 0.000 description 1
- 230000000881 depressing Effects 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000007519 figuring Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000000813 microbial Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 230000003389 potentiating Effects 0.000 description 1
- 230000002250 progressing Effects 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000006479 redox reaction Methods 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 230000001954 sterilising Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- -1 temperature changes Chemical class 0.000 description 1
- 230000001960 triggered Effects 0.000 description 1
- 238000002604 ultrasonography Methods 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 230000003442 weekly Effects 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L12/00—Methods or apparatus for disinfecting or sterilising contact lenses; Accessories therefor
- A61L12/08—Methods or apparatus for disinfecting or sterilising contact lenses; Accessories therefor using chemical substances
- A61L12/12—Non-macromolecular oxygen-containing compounds, e.g. hydrogen peroxide or ozone
- A61L12/124—Hydrogen peroxide; Peroxy compounds
- A61L12/128—Hydrogen peroxide; Peroxy compounds neutralised with catalysts
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0078—Compositions for cleaning contact lenses, spectacles or lenses
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3947—Liquid compositions
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N7/00—Analysing materials by measuring the pressure or volume of a gas or vapour
- G01N7/14—Analysing materials by measuring the pressure or volume of a gas or vapour by allowing the material to emit a gas or vapour, e.g. water vapour, and measuring a pressure or volume difference
- G01N7/18—Analysing materials by measuring the pressure or volume of a gas or vapour by allowing the material to emit a gas or vapour, e.g. water vapour, and measuring a pressure or volume difference by allowing the material to react
-
- G—PHYSICS
- G02—OPTICS
- G02C—SPECTACLES; SUNGLASSES OR GOGGLES INSOFAR AS THEY HAVE THE SAME FEATURES AS SPECTACLES; CONTACT LENSES
- G02C13/00—Assembling; Repairing; Cleaning
- G02C13/008—Devices specially adapted for cleaning contact lenses
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S134/00—Cleaning and liquid contact with solids
- Y10S134/901—Contact lens
Abstract
Disclosed is a contact lens cleaning system (150) with a contact lens holder and a vial (3) adapted to contain the contact lens holder, a cleaning solution (120) and a catalyst capable of neutralizing the cleaning solution (120). A sensor provides data on a rate of neutralization of the cleaning solution (120) and a processing device in communication with the sensor receives the rate of neutralization data from the sensor. A display is in communication with the processing device and provides cleaning efficacy information based on the rate of neutralization data. ution (120) and a processing device in communication with the sensor receives the rate of neutralization data from the sensor. A display is in communication with the processing device and provides cleaning efficacy information based on the rate of neutralization data.
Description
CONTACT LENS CLEANING SYSTEM WITH MONITOR
CROSS REFERENCE TO RELATED APPLICATIONS
The present application claims the benefit of U.S. Provisional Application Nos.
61/445,910, filed on February 23, 2011 and 61/547,598, filed October 14, 2011. The foregoing
applications are hereby incorporated by reference herein in their entirety.
INCORPORATION BY REFERENCE
All publications and patent applications mentioned in this specification are herein
incorporated by reference to the same extent as if each individual publication or patent
ation was ically and individually indicated to be incorporated by reference.
FIELD
The present invention relates generally to system for ng and disinfecting
contact lenses and method of use thereof. In s emboidments, the invention is directed to a
system that monitors the cleaning solution neutralization process using a on sensor and
compares the measured values with theoretical values. Embodiments of the invention ine
if the process is ding properly or not, based on the measurements obtained by the on
sensor, and notifies the user of the status of the neutralization.
BACKGROUND
Any discussion of the prior art throughout the specification should in no way be
considered as an admission that such prior art is widely known or forms part of common general
knowledge in the field.
[0004a] There are two main types of chemical disinfection systems for contact lenses,
multipurpose and hydrogen peroxide-based s. Hydrogen peroxide-based systems are
often preferred, due to its rapid kill of ial contaminants, preservative-free packaging, low
user sensitivity, and neutralization to natural by-products, such as water and oxygen. The
disadvantage of the hydrogen peroxide-based systems are that they e memorization of
what time the disinfection time was started and figuring out when the neutralization process is
complete. Also, if too much time has elapsed since the en peroxide solution has been
neutralized, the sterile solution can eventually become re-infected and foster microbial .
One of the main reasons why users switch from hydrogen peroxide-based systems to
multipurpose is e hydrogen peroxide-based systems require users to calculate when the
ideal usage time is for each time that they disinfect their contact lenses, without knowledge of
how effective the platinum catalyst is working; that is, enough elapsed time has passed to ensure
the peroxide has been fully neutralized, to avoid chemical conjunctivitis and keratitis, and short
enough elapsed time to ensure microbes have not re-infected the sterile solution.
An example of a contact lens cleaning and ization system is described in U.S.
Patent No. 4,687,997. This ng system requires insertion of the lenses into a disinfecting
solution for a preset time period followed by insertion into a lizing solution for a second
preset time period. A first indicator shows a steady light while the disinfectant is in the cleaning
case and a second indicator when the lizing solution is in the case. The system
distinguishes the disinfecting on from the neutralizing solution by measuring the electrical
tivity of the solution within the cleaning case. After a ermined amount of time,
both lights flash to indicate the item has been disinfected and neutralized, respectively. This
system does not monitor the efficacy of cleaning, disinfecting or neutralization of the solutions,
however; the tor lights flash to show completion of the disinfecting and neutralization
cycles solely in response to the passage of time.
Another example of a cleaning and sterilization system is described in U.S. Patent
No. 6,183,705. The system uses ultrasonic waves to clean contact lenses, and heat to disinfect
contact lens solution medium. The system includes a housing, control circuit assembly,
ultrasonic waveguide, a heating rod with two electrodes and a graduated cleaning cup that is
operated using the automatic l t. The control circuit includes a microprocessor for
controlling the heating rod and the ultrasonic waveguide. The microprocessor operates the
ultrasound transducer for a preset time, then stops. After a rest time, the microprocessor heats
the cleaning solution to a preset temperature of 90º C as measured by a temperature sensor, then
turns off the heating rod, allowing the lenses to soak in the hot solution for another preset time.
Once again, this system does not monitor the efficacy of the cleaning solution; the cleaning
process always proceeds along the same preset time intervals, and the indicator lights merely
show which stage the cleaning process is in.
SUMMARY OF THE DISCLOSURE
Embodiments of the t invention use a hydrogen peroxide solution for cleaning
and disinfecting soft (hydrophilic) and rigid gas permeable contact lenses, and uses a platinum
disk for peroxide neutralization. Neutralization is required to convert hydrogen peroxide to
water and oxygen, so the residual solution on the contact will not irritate the eye during t
lens ion. The system monitors the cleaning solution within the , and guides the user
through the contact lens cleaning process with lights and/or textual directions.
The system may also monitor the internal and external temperatures and verify that
the hydrogen de solution is neutralizing properly. The monitoring is done by verifying
the exothermic peroxide-neutralization process is occurring at an acceptable rate. Causes of
poor neutralization can include old or expired peroxide solution, poorly stored cleaning solution,
extreme solution temperatures, or the um disc has decreased catalytic ability. The device
can determine if the user accidently used a bottle of saline solution, instead of a bottle of
hydrogen de solution. If a bottle of saline solution is used instead of a bottle of hydrogen
peroxide solution, the cleaning and disinfection of the contact lenses will not occur increasing
the risk of infection of the eye. Additionally, the device zes the desire to rinse the
contacts with saline solution after cleaning and prior to insertion in to the eye; if hydrogen
peroxide was enly used instead of saline solution, chemical conjunctivitis or keratitis may
Embodiments of the t invention lly relate to an apparatus for cleaning
and disinfecting contact lenses. Provided herein are apparatus, systems and methods for use
with a cleaning solution used to clean a medical device in which one or more messages are
displayed to encourage compliance with the normal medical device ng protocol.
The following embodiments, aspects and variations thereof are exemplary and
illustrative are not intended to be limiting in scope.
In one embodiment, a contact lens cleaning system includes a contact lens holder; a
vial adapted to contain the t lens holder and a cleaning solution; a reaction sensor adapted
to monitor a chemical reaction rate of the cleaning solution; a processing device in
communication with the reaction sensor to receive a reaction signal from the reaction sensor;
and a display in communication with the processing device, the processing device being adapted
to operate the y to provide cleaning cy information based on the reaction signal. A
catalyst element may be disposed within the vial and d to react with the cleaning solution.
The reaction sensor may be a temperature sensor. The temperature sensor may be disposed in a
cap covering the vial or e of the vial. The processing device may be adapted to determine
a temperature change rate from the reaction signal.
In an embodiment, the system may determine ng efficacy by comparing the
temperature change rate to a theoretical temperature change rate. The system may include an
ambient ature sensor disposed outside of the vial and may e a temperature of air
surrounding the vial. The processing device may display cleaning efficacy information based on
a temperature signal from the ambient temperature sensor. The system may e a use
r communicating with the processing device. The processing device may display
information corresponding to the number of cleaning uses of the cleaning system.
The reaction sensor may be a re sensor. The system may include a caddy to
support the vial. The display may be disposed within the caddy. T he display may be disposed
in a cap on the vial. The system may include a solution sensor disposed within the vial. The
processing device may determine the presence of cleaning solution within the vial based on a
- 3a -
signal from the solution sensor. The on sensor may include an electrode and/or a capacitive
sensor.
] In another embodiment, a method for cleaning a contact lens and displaying cleaning
efficacy information includes receiving a contact lens into a contact lens holder, receiving
cleaning solution into a vial, wherein the vial containing the contact lens and contact lens holder,
determining a chemical reaction rate of the ng solution and cleaning efficacy information
based on the chemical reaction rate, and displaying the cleaning efficacy information.
The vial may also contain a catalyst and the chemical reaction rate may include a rate
of chemical reaction between the ng on and the catalyst. The determining step may
include monitoring temperature, monitoring temperature of the cleaning solution, monitoring
temperature exterior to the vial, calculating a temperature change rate, comparing the
temperature change rate to a theoretical temperature change rate, and/or monitoring temperature
within the vial.
The method may include monitoring t temperature outside of the vial, such
that the determining step includes determining the chemical reaction rate from the temperature
within the vial and the ambient temperature. The method may e counting a number of
contact lens cleaning uses and may y information related to the number of contact lens
cleaning uses. The determining step may e monitoring pressure within the via]. The
method may include determining r there is cleaning on in the vial prior to the step of
determining a chemical reaction rate.
In another embodiment, the tus may include a cap assembly configured to
attach to a contact lens cup, a contact lens holder extending from the cap assembly into the cup, a
solution sensor attached to the cap assembly and configured to determine the presence of a
solution within the cup, and a first temperature sensor attached to the cap ly, a display and
a microcontroller within the cap. The microcontroller may communicate with the solution
sensor, the first temperature sensor and the y.
The solution sensor may be a pair of electrodes that measures conductivity or a
capacitive sensor. The apparatus may e a catalyst for neutralizing the solution and the
solution may be hydrogen peroxide. The first temperature sensor may be a couple or a
thermistor and may be positioned to measure a temperature of the solution or of air surrounding
the cup.
The apparatus may include a second temperature . A second temperature
sensor may be positioned to measure a temperature of air surrounding the cup and may
communicate with the microcontroller. The microcontroller may be adapted to receive
conductivity data from the electrodes, solution temperature data from the first temperature
sensor, and air temperature data from the second temperature sensor. The microcontroller may
output a signal based on the data.
The signal output by the microcontroller may drive an LED on the y and may
e a text display on the display.
] The text display may be provided through a liquid crystal display. A capacitive touch
sensor may be attached to the cap assembly. The apparatus may include a battery for powering
the microcontroller.
In another embodiment, a method for cleaning a contact lens and displaying a status
ofthe cleaning process may include receiving a contact lens into a contact lens . A contact
lens ng solution may be received into a contact lens cup, and a determination is made
whether there is cleaning solution in the cup. If cleaning solution is present in the cup, the
method may include measuring the temperature of the cleaning solution. The status of the
cleaning may be determined based on the cleaning solution temperature. The status of the
cleaning may be displayed.
[00023] The temperature of air surrounding the cup may be measured. The status of the
cleaning may be determined based on the measured air temperature and displayed on an LED
display. The status may be displayed on a message display. Determining the status ofthe
cleaning may e measuring conductivity within the cup. Monitoring of the ng
solution may be initialized by a capacitive touch sensor.
[00024] In r embodiment, an apparatus for cleaning and disinfecting contact lenses may
include a cap assembly, a contact lens holder, a cleaning solution, a st, a first temperature
, a display, and a ontroller. The cap ly is configured to attach to a contact
lens cup. The contact lens holder extends from the cap assembly into the cup. The cleaning
solution is contained within the cup. The catalyst is contained within the cup and configured to
neutralize the cleaning solution. The first temperature sensor is attached to the cap assembly.
The microcontroller is within the cap and communicates with the first temperature sensor and the
display.
In another embodiment, there is provided apparatus, systems and methods for use
with a cleaning solution used to clean a medical device in which one or more es are
displayed. The messages may inform the user about the cleaning protocol or the condition ofthe
cleaning system, and may encourage compliance with proper cleaning ols, including
messages about when it is safe to use the l device, when a cleaning system should be
replaced, and, in some cases, to consult a healthcare professional.
] Another embodiment provides for an apparatus which is adapted for use with a
cleaning solution used to clean a medical device, the apparatus including a r, a processing
device in communication with the trigger and which provides a count of the number of times the
trigger has been d, and a display device in communication with the processing device
wherein the y device displays a message based on the count. In certain embodiments, the
medical device can be a contact lens. For example, the display device can display the message
“Please replace your case and solution” when a certain count has been reached, for example
when the count is 180, which would be the count at six months of daily use.
] Another embodiment provides for an apparatus which is adapted for use with a
cleaning on used to clean a medical device and may include a sensor that measures a
property ofthe cleaning solution or a nearby area or the l device; a processing device in
communication with the detector; a display device in communication with the processing device,
wherein the display device displays a message based on the ty of the cleaning solution or a
nearby area or the medical device. In certain embodiments, the cleaning solution comprises
hydrogen peroxide. In n embodiments, the medical device is a contact lens. In certain
embodiments, the sensor is a temperature , an electronic sensor, a pressure sensor, a sound
sensor, an optical sensor, or a gas sensor. In certain embodiments, the processing device
compares an input signal from the sensor to one or more preset values, and provides one or more
output signals depending on the comparison to the display device. In certain embodiments, the
display device is a light (e.g. an LED) or a liquid crystal display.
Another embodiment provides for an apparatus which is adapted for use with a
cleaning solution used to clean a medical device, sing a ature sensor that measures
the temperature profile of the cleaning solution or nearby area during the cleaning cycle; a
processing device in communication with the temperature sensor and storing in memory an
acceptable temperature profile range; a timer; and a display device in communication with the
processing device, wherein different messages are displayed on the display device depending on
whether the ature sensor measures a ature profile that falls within or outside of the
acceptable temperature profile range.
r ment provides for an apparatus which is adapted for use with a
cleaning solution used to clean a medical device and which provides a message to a user,
comprising a means for measuring a property of the cleaning solution or a nearby area or the
medical device; a processing means for (a) accepting an input signal; (b) providing a comparison
ofthe input signal to one or more preset values; and (c) providing one or more output signals
depending on the comparison; and a means for displaying a message, wherein the message is
based on the output .
Another embodiment provides for a method of monitoring t compliance with a
protocol for cleaning a medical device with a cleaning solution, the method comprising obtaining
-6'—
data by measuring a property of the cleaning solution or a nearby area or the medical device, and
displaying one or more messages according to the data. In some embodiments, the data may be
provided to a medical professional.
[00030a] According to a first aspect of the invention there is provided a contact lens cleaning
system comprising:
a contact lens holder;
a vial adapted to contain the contact lens holder and a cleaning solution, n a
st is capable of neutralizing the cleaning solution;
a sensor capable of providing data on a rate of neutralization of the cleaning
solution;
a sing device in ication with the sensor to receive the rate of
neutralization data from the sensor; and
a display in communication with the processing device, the processing device being
adapted to operate the display to provide cleaning efficacy information based on the rate of
neutralization data.
[00030b] ing to a second aspect of the invention there is ed a contact lens
cleaning system comprising:
a contact lens holder;
a vial d to n the contact lens holder and a cleaning solution, wherein a
catalyst is capable of neutralizing the cleaning solution;
a sensor capable of providing data on a characteristic of the neutralization of the
cleaning solution;
a processing device in communication with the sensor to e the data from the
sensor and determine an approximate rate of lization using the data; and
a display in ication with the processing device, the processing device being
adapted to operate the display to provide cleaning efficacy information based on the
approximate rate of neutralization.
[00030c] According to a third aspect of the invention there is provided a contact lens cleaning
system comprising:
a contact lens holder;
a vial d to contain the contact lens holder and a cleaning solution, wherein a
catalyst is capable of neutralizing the cleaning on;
a conductivity sensor capable of generating conductivity data related to a rate of
neutralization of the cleaning solution;
a sing device in communication with the conductivity sensor to obtain the
conductivity data and determine an approximate rate of neutralization using the conductivity
data; and
a y in communication with the processing device, the processing device being
adapted to operate the display to provide cleaning efficacy information based on the
approximate rate of neutralization.
[00030d] It is an object of the present invention to overcome or ameliorate at least one of the
disadvantages of the prior art, or to provide a useful alternative.
[00030e] Unless the context y es otherwise, throughout the description and the
, the words “comprise”, “comprising”, and the like are to be construed in an ive
sense as opposed to an exclusive or exhaustive sense; that is to say, in the sense of “including,
but not limited to”.
BRIEF DESCRIPTION OF THE DRAWINGS
The novel features of the invention are set forth with particularity in the claims that
follow. A better understanding of the features and advantages of the present invention will be
ed by reference to the following detailed description that sets forth illustrative
embodiments, in which the principles of the ion are utilized, and the accompanying
gs of which:
FIGs. 1A-1B illustrate an ary contact lens storage system.
FIGs. 2A-2B illustrate another exemplary contact lens storage system.
illustrates an exemplary operational flowchart.
FIGs. 4A-4B illustrate another exemplary contact lens storage system.
rates another exemplary operational flowchart.
FIGs. 6A-6B illustrate a top view and a side view, respectively, of another contact
lens storage system.
illustrates a side perspective view of a contact lens ng case and monitor.
illustrates a side view of the contact lens cap, lens basket, and platinum
catalyst.
illustrates a top perspective view of the contact lens cap showing the main
internal components.
illustrates another top perspective view of the contact lens cap g an
LED configuration.
- 7a -
] illustrates another top perspective view of the contact lens cap showing a
LCD configuration.
illustrates the rate of temperature increase of solution over time.
illustrates the rate of dependence on initial on temperatures.
illustrates the determination of equation of formula slope and y-intercept.
illustrates the ination of rate in which air heats the solution inside
contact lens case.
] illustrates an example of thermistor RC time to temperature conversion.
illustrates a block diagram of a cleaning device for a medical device.
- 7b -
illustrates a block diagram of an exemplary temperature sensing contact lens
cleaning case.
FIGS. B illustrates another exemplary operational flowchart.
illustrates r exemplary t lens storage system.
FIGS. 18A-18B illustrate a side View and top View, respectively, the cleaning case of
.
DETAILED DESCRIPTION
The present invention relates to a system and method for monitoring the efficacy and
status of a contact lens cleaning process, such as in systems using hydrogen de and a
neutralizing catalyst. One goal of the invention is to provide the user with an improved
determination ofwhen the catalyst has reduced the peroxide concentration low enough to allow
insertion ofthe contact lenses into the eye. The improved determination, which traditionally was
done solely based on d time and uncorrected for on temperature, may greatly reduce
the risk of chemical ctivitis cause by ntal peroxide burns of the eye. Accidental
burns may be caused by incorrect usage of the hydrogen de disinfection system, the use of
expired peroxide solutions, poorly stored disinfection solution, extreme disinfection solution
temperatures, rinsing contacts with hydrogen peroxide prior to insertion, or the use of a platinum
catalyst has sed tic ability.
Without knowledge ofhow effective the platinum catalyst is at neutralizing the
cleaning solution, users may need to calculate when the safe usage time is for each instance that
they disinfect their t lenses. That is, the user may need to determine when enough time
has elapsed to ensure the peroxide has been fully neutralized, to avoid chemical conjunctivitis,
and short enough elapsed time to ensure microbes have not re-infected the sterile solution. The
present invention automatically does the ations for the user, so the user does not have to;
and the device evaluates the effectiveness of the chemical reaction that is taking place during the
neutralization.
[00055] The system includes a cap assembly configured to attach to a contact lens cup or vial.
Examples ofcleaning cases that include a cap and contact lens cup or vial are well known in the
literature and may include other features not shown herein. Examples of such cases can be found
in US. Patent Nos. 4,637,919, 4,750,610, 5,186,317, 5,366,078, 5,558,846, 5,609,284,
,609,837, and 992. Commercial examples of such cases are found in or included as parts
ofthe AOSBPT® Disposable Cup & Disc (CIBA VISION®) and CLEAR CARE® (CIBA
VISION®) systems.
A on sensor may be attached to the cap assembly and configured to determine
the presence of a solution within the cup. In some embodiments, the system may e a
reaction sensor. The reaction sensor may be adapted to monitor a chemical reaction rate of the
cleaning solution. The reaction sensor may be implemented as a ature sensor, an electric
sensor, a pressure sensor, a sound sensor, an optical sensor, or a gas sensor. The system may
include a first temperature sensor attached to the cap assembly and a y. A first temperature
sensor may be implemented as a first reaction sensor and may be configured to measure the
temperature of the solution. The system may further include a second on sensor in the form
of a second temperature sensor configured to measure the temperature of the air surrounding the
cup. The cap assembly may e a microcontroller. The microcontroller may communicate
with a reaction sensor, the solution detector, the capacitive touch sensor, the solution sensor, the
first temperature sensor, a second ature sensor, and/or the display, and send an output
signal based on the data.
In certain aspects, the apparatus, systems and methods described herein may have the
following advantages. In certain aspects, they may provide a convenient reminder to the user
regarding whether cleaning is occurring or progressing normally, when it is safe to use the
medical device, or when the medical device should be replaced. In embodiments where the
apparatus, system or methods are used with a contact lens r, they may improve user
compliance with the procedures of cleaning contact lenses as well as improve safety and
cleanliness ofthe lenses. In certain aspects, using the apparatus, systems and methods described
herein may increase the likelihood that lenses have been cleaned properly, may decrease the
likelihood that contact lenses will be re-infected after the cleaning procedure, or may decrease
the likelihood that lenses will irritate the eye after being cleaned. For example, for tus in
which hydrogen peroxide-based ng solutions are used, the apparatus described herein may
indicate to the user if the solution is potent (that is, if there is sufficient peroxide in the solution
to clean the lens within the specified time), ifthe normal cleaning cycle is complete and the
lenses are safe to be placed in the eye, if the catalyst used to consume hydrogen peroxide is
functioning properly or needs to be replaced, and other aspects of the cleaning protocol. In yet
other aspects, apparatus bed herein for use with a t lens cleaning system may display
a signal or e that the user should t his or her optician or eye-care professional. In
certain aspects, using the contact lens e s described herein may increase patient or
user compliance with the normal lens cleaning protocol or other s of his or her eye care.
Although some of the aforementioned ages pertain to contact lens cleaning systems, these
advantages may also pertain to corresponding apparatus, systems and methods adapted to be
used to clean other medical devices, including dentures, endoscopes, ers, ports, and so
forth.
The term “caddy” refers to an apparatus adapted for use with a cleaning solution used
to clean a medical device. In certain embodiments, a caddy may be an apparatus into or onto
which a te cleaning case may be removably placed. In other embodiments, a caddy may
also be the cleaning case, ie. cleaning solution may be poured ly into parts of the caddy.
] The term “cleaning solution” refers to any liquid cleaning or disinfecting solution
used to clean medical devices such as contact lenses. Cleaning solutions may or may not include
hydrogen peroxide or other peroxide nds. Cleaning solutions may also include other
ingredients. Examples of cleaning solutions which may be used in accordance with the systems
described herein include, without limitation, AOSEPT® Disinfectant (CIBA VISION®) and
CLEAR CARE® (CIBA VISION®).
The term “cleaning system” refers to a cleaning solution and accompanying devices,
such as a catalyst used to consume hydrogen peroxide in peroxide-based cleaning solutions.
[00061] The term “property” refers to a al, chemical, electrical, optical, or other
property, as well as a profile ofthat ty over time.
Unless specifically noted otherwise herein, the definitions of the terms used are
standard definitions used in the art of organic synthesis and pharmaceutical sciences. Exemplary
embodiments, aspects and variations are illustrated in the figures and drawings, and it is intended
that the embodiments, aspects and variations, and the figures and drawings disclosed herein are
to be considered illustrative and not limiting.
] FIGS. lA-B show caddy 150 and cleaning case 110. Referring to , caddy
150 comprises caddy case 151, indicator 152, and display panel 154. Caddy case 151 may be
made out ofan appropriate material, e.g. a plastic or r type of material, which is well
known in the art. Indicator 152 may be a light or an LED (light emitting diode), and display
panel may be an LCD (liquid l display) or a r display panel capable of displaying text
and/or graphical images either in color or black/white/grayscale. A display may be an indicator
such as a light or an LED or a display panel such as an LCD. These components and structures
are also well known in the art.
[00064] In some embodiments, caddy 150 may include a mechanism for providing an audio
indication ofthe solution status, ature ring, and other information. For e,
caddy case may include one or more speakers and a controller or sor. The one or more
speakers may output audio from an acoustic signal provided by the controller or processor. The
controller or processor may receive temperature or other data from one or more sensors. An
audio message may be provided based on the data provided by the sensors. For example, the
caddy 150 may provide an audio alert indicating the time remaining in the neutralization process,
the neutralization process is complete, the caddy is ecting the contact lens, disinfection was
successful or unsuccessful, the solution is not detected and other messages. Hence, the system of
the present invention may provide audio alerts in place or in on to visual or tactive alerts to
communicate events or ions d to contact lens, the solution, and other aspects of the
present technology.
Referring to , a separate and partially disassembled cleaning case 110 is
shown. Cleaning case 110 may comprise such elements as cap 112, support beam 114, basket
116 and catalyst 118, and cylinder 120. Contact lenses, 117, are also shown. es of
ng cases are well known in the literature and may include other features not shown herein,
or modifications ofthe features shown herein. As shown, cleaning case 110 may be fully
assembled by reversibly affixing (e.g. by screwing, snapping, form-fitting, friction fitting, etc.)
includes
cap 112 onto cylinder 120. The cylinder 120 of the embodiment illustrated in
threads or screws 3 for affixing cap 112. The cylinder 120 of the embodiment illustrated in 1B includes s or screws 3 for affixing cap 112. Once fully assembled, the cleaning case
may be ably placed in or on the caddy.
Referring to , caddy 150 is shown in perspective side view, in which caddy
case 151, indicator 152, and display panel 154 are also shown. shows a cross-sectional
view of caddy 150 and trigger 160, which are electronically connected to processing device 170,
which is connected to and powered by power source 180. sing device 170 is also
electronically connected to indicator 152 and display panel 154. Trigger 160 is positioned such
that it is tripped under normal operation when cleaning case 110 is placed in or on caddy 150.
ng the trigger advances a counter within the processing device to provide a count.
Processing device 170 may be a logic circuit, integrated circuit chip, or microprocessor, e.g.
computing chip, or a plurality or combination thereof. Similarly, a processor may take the form
of a logic circuit, integrated circuit chip, or microprocessor, e.g. a computer chip, or a plurality or
combination thereof. Power source 180 may be a battery, e.g. a rechargeable y or other
type of battery lly used in small electronic devices. In some embodiments, the power
source may be a power source external to the caddy, e.g. a household 110 V or r source. A
small transformer, not shown, may also be .
] Referring to various aspects of operation of certain embodiments of a caddy
are shown. The process begins at step 301 after contact lenses and cleaning solution are placed
in a cleaning case (e.g. cleaning case 110, ). At this time, the fully assembled cleaning
case should be placed into the base unit. A trigger (e.g. trigger 160, ) and the processing
device to which it is connected (e.g. processing device 170, ) can be used to determine if
the contact lens case has been placed into the base unit at step 302. If a cleaning case has been
placed n, then a counter in the processing device may advance the count by one at step 304;
if not, then the system may be placed in “stand by” mode at step 303. If the count reaches a
n preset indicator value at step 305, then the system can display a message such as “Please
replace case and solution” at step 307. The preset tor or other values may be stored in a
memory unit, which may be part of the sing device.
For example, if lens cleaning cases and solutions typically have a useful life of about
six months, then the indicator value can be set at 180 (assuming daily cleaning for six months).
Other indicators values can be set, multiple indicators can be set for different messages, and the
indicator values can be changed. When the count reaches an indicator value, the system can
y an appropriate message to the user to encourage use of a new cleaning case and solution,
thereby ing compliance with proper lens cleaning protocols. This ure is
represented by step 308. At this time, the systems can be reset, i.e. the counter can be reset to a
zero value, for example by the user depressing a button or switch on the base unit (not shown) or
via an external computing device (also not shown). Referring back to step 305, if the indicator
has not yet been reached, then the user can continue normal operation of the cleaning system and
may use it for a subsequent ng at step 306.
es may be in the form of a light, such as that from an LED or similar light, an
audible signal such as a chime, bell, voice recording, etc., a tactile signal such as a Braille dot, or
indicators ying other signals. In one embodiment, when an indicator value in a processing
device is reached, a red light is displayed. In another embodiment, a green tight is yed
before the indicator value is reached, and when the indicator value is reached, the green light is
turned offand a red light is on. Similarly, an audio signal such as a bell, chime, or suitable voice
recording can be triggered when the indicator value is reached.
[00070] Messages may also take the form of a text message or graphical depiction, which may
be displayed on an LCD. One example of a text message is “Please replace your case and
solution” which can be displayed when a counter reaches a n preset value, indicating that
the solution and/or catalysts may be nearing the end of its useful lifetime. One example of a
graphical depiction is a graphical representation of a cleaning case or a bottle of cleaning
solution. More examples and details of messages are described below.
Additional examples of messages include the following: “Thank You for using Clear
Care Lens Solution;” “You can trust your eyes to AOSEPT ®;” “Your contact lenses are being
disinfected;” “It will take six hours before your contact lens are ready for use;” “Your contact
lenses are ready for use;” “Please remove them only after you have washed your hands with soap
and water;” e discard your contact lens solution as the solution is no longer ;” “It is
now six months since your contact lens case was purchased. Please see your Optometrist.”
In various embodiments, a contact lens storage system can measure a property of (a)
the cleaning solution, (b) the area near the cleaning solution (also referred to as a nearby area)
(e.g. the gaseous ace above the cleaning solution) or (c) one or more of the medical
devices being cleaned. Examples of properties of the cleaning solution include temperature,
electrical conductivity, color, UV/Vis absorbance, and profiles f (e.g. temperature vs. time,
etc.). Examples of properties of the nearby area include pressure, sound (e.g. sound generated by
bursting bubbles at the solution/air interface), temperature, and profiles thereof. Examples of
properties ofthe medical devices e ction, dispersion or other property. Such
measurement can, via known calculations and/or comparisons in a processing device, be the
basis of one or more messages relating to whether the cleaning solution is , working
properly, needs to be replaced, if the lenses are clean and ready to be d for use, etc.
FIGS. 4A and 4B illustrate an embodiment of a contact lens storage system 400,
showing cleaning case 110 removeably placed in base unit 450 (also referred to as a caddy
herein). Referring to , in this embodiment, base unit case 151 (also referred to as a
caddy case herein) and display panel 154 are shown, as described above. Also in this
embodiment, there are two indicators 152A and 152B which may be, for example, a red light and
a green light, as described above. Depicted by dotted lines in this view are power source 180
(described above), temperature sensor 492, and circuit board 495.
shows cleaning case 110 ably placed in base unit 450 of contact lens
storage system 400 in a View in which certain features are hidden from view and certain other
features are described . Upon insertion of cleaning case 110 into the base unit 450, trigger
460 may be tripped and roller 461 may be deflected downward. Roller 461 may be a ball, disc,
or similar component. Trigger 460 may be, for example, a mechanical switch (such as shown in
) or an optical switch such as a combination of a LED IR emitter and photo detector (not
shown). ature sensor 492 may be situated such that it can monitor the temperature or
ature changes (i.e. temperature profile) of the cleaning solution during the cleaning cycle.
Optional thermistor, 494, may be present in certain embodiments to measure the nearby
temperature (e.g. the temperature external to the cleaning case). Trigger 460 and temperature
sensor 492 are connected to processing device 170 and all are powered by power source 180.
this embodiment, processing device 170 is also connected to port 490. Port 490 may be, for
e, a USB port to connect the system to a computer, smart-phone, or similar device. A
wireless tion (e.g. a BLUETOOTH®) may also be used.
Typically, when hydrogen peroxide is introduced to cleaning case 110 containing
catalyst 118, a chemical reaction occurs in which the st chemically reduces, and thereby
consumes, the peroxide. Complete ption of the peroxide is ended before
inserting a lens into the eye, since ever trace amounts of peroxide can be very painful to the eye.
Heat is generated during this chemical reaction. The rate and degree of temperature increase
during the on and decrease after the reaction can be measured and will be a function of the
amount ofperoxide in the solution and the amount of available catalyst since catalyst material,
typically a metal such as platinum, is also oxidized during the reaction. Thus, in one
embodiment, changes in the temperature or temperature profile (i.e. the shape of a temperature
vs. time curve) of the cleaning solution can be correlated to changes in the quality of the cleaning
on (e.g. amount of peroxide present) or the catalyst (how much catalyst is still available).
A sing device can then be programmed to compare the temperature or temperature profile
with a preset value. Thus, ent messages can be yed on the display device depending
on whether the temperature sensor measures a temperature profile that falls within or outside of
the acceptable temperature profile range.
Referring to various aspects of operation of certain embodiments of a contact
lens storage system are shown. The process begins at step 501 after contact lenses and cleaning
solution are placed in a cleaning case (e.g. cleaning case 110, ). At this time, the
cleaning case should be inserted in the base unit. A trigger (e.g. trigger 460, ) and the
processing device to which it is connected can be used to determine if the contact lens case has
been placed into the base unit at step 502. If a cleaning case has been placed therein, a e
such as “Disinfecting” can be yed on a display panel (e.g. display panel 154, ) at
step 503. Ifno cleaning case has been placed in the base unit, the display panel can display a
message such as “Standing By” at step 507 and the base unit can be said to be in “standby
mode”. After the trigger has been tripped, the ature profile of the solution in the ng
case can be measured to determine if it falls within an acceptable temperature profile range at
step 504. If“No” then a message such as “Disinfection unsuccessful. Please replace case and
solution.” can be yed at step 505, after which the case can be removed at step 506 and the
“Standing By” message can be displayed at step 507. If the temperature is found to be increasing
within an acceptable range, then a timer can begin counting to a preset m disinfection
time (“MDT”) time for normal disinfection of a pair of contact lenses at step 508. At this time, a
“Disinfection working properly” message can be displayed. This message can remain displayed
as long as long as the elapsed time is not greater than the minimum disinfection time at step 510.
Once the d time (“ET”) equals the minimum disinfection time at step 510, a “Safe to Wear
Lenses” or “Disinfection Complete” message may be displayed at step 511. For example, the
minimum disinfection time can be set at 6 hours. Other minimum disinfection times can be set
according to such factors as how long it takes to measure the temperature profile, the size and
shape of the lens case and catalyst, and the recommended minimum time of disinfection
specified by the ng system (e.g., CLEAR CARE®, etc.). If the case is then d at step
512, the base unit is returned to standby mode. If the case is not removed at step 512, then the
timer continues to count. When the elapsed time ed by the timer reaches a preset upper
limit of safe storage time (“SST”) at step 514, a message such as “Please t the disinfection
process” can be displayed at step 515; if not, the “Safe to Wear Lenses” message can remain
displayed. For e, the upper limit of SST may be about 18 hours, about 24 hours, about 7
days, or another time depending on the cleaning system used. Since after this time the risk of re-
infection may increase, it may be advisable to remove the lenses from the cleaning case before
this time. As will be appreciated by persons having ordinary skill in the art, the processing
device, which can include one or more memory units, can store the values such as the d
time, the safe storage time, etc. and can perform the above-described comparisons and
calculations.
] Referring to FIGs. 6A-B, an embodiment where the caddy itself receives the cleaning
solution (i.e. where there is no te cleaning case) is shown. Referring to , caddy
800 in side view is shown, including caddy case 851, made of plastic or some other suitable
material, indicator 852, control buttons 853A and 853B, display 854, reservoirs 820A and 820B,
and caps 812A and 812B, which may be reversibly affixed (e.g. by screwing, snapping, form-
fitting, friction fitting, etc.) to caddy case 851. Certain of these components are shown in side
view in . This caddy may include features illustrated in the other embodiments, and not
explicitly shown here, such as a trigger, a timer, a processing device or a power source. The
caddy shown in FIGS. 6A-B may also include a reaction sensor such as a temperature sensor, an
electronic sensor, a pressure , a sound sensor, or a gas . For example, caddy 800
in caps
may include a ature sensor of the type shown in , or a pressure sensor (e.g.
812A-B) ofthe type shown in FIGS. 17-18. The caddy may also include buttons or tabs under a
portion ofwhere the caps are placed which are depressed when the caps have been reversibly
affixed to the case. When depressed, a signal can then be sent to the processing device to begin a
timer or display a message, similar to the trigger described above.
illustrates a side perspective View of a contact lens cleaning case and monitor
according to one embodiment of the invention. The embodiment of has a t lens cup
1 which is filled with buffered hydrogen peroxide solution to the fill line 2.
rates a side view of the contact lens cap, lens basket, and platinum
catalyst. The contact lens cup 1 uses a screw 3 to secure it to the screw cap 4 of . The
solution temperature sensor 5 monitors the temperature of the solution over time during the
hydrogen neutralization process. In s embodiments, the solution temperature sensor 5 may
be a thermistor or a thermocouple. Using a solution sensor 6, the ontroller (not shown)
senses that the contact lenses are immersed into the solution and initiates the monitoring process.
The solution sensor 6 may include two electrodes, one of which is shown on the support beam of
. Solution sensor 6 may be located adjacent or near a top portion of lens basket 7 (not
shown). The solution sensor may be a pair of conductivity electrodes. In various embodiments,
when the presence of the solution is sensed using conductivity, the microcontroller 11 may
supply power to one electrode and measures current at the other electrode. If current flows from
one ode to the other, the microcontroller ines the cap is placed into solution. The
solution sensor may also be a capacitive sensor. In various embodiments, when the presence of
the solution is sensed using capacitance sensors, the microcontroller may measure the capacitive
load. An example of simple way to measure capacitance is through the use ofan RC circuit,
where the charging or discharging time of the effective capacitor is ed by the
microcontroller; sed capacitance correlates with sed time. Examples of capacitive
solution sensors can be found in U.S. Patent Nos. 2,409,073, 5,145,323, and 5,238,369.
A pair of contact lens baskets 7 holds the contacts in place during the cleaning
process. A platinum catalyst 8 neutralizes the hydrogen peroxide solution, which is an
exothermic process. The basket hinge 9 allows the contact lens basket 7 to open, which allows
the ts to be attached or removed.
illustrates a top View of the contact lens cap showing the main internal
components. The main internal components of the contact lens cap may include a
microcontroller 11, a reaction sensor such as an external temperature sensor 13, and a battery 12.
The capacitive touch sensor 10 wakes the microcontroller 11 from low-power sleep mode. The
capacitive touch sensor 10, commonly used in many hand-held devices such as cell phone
capacitive touch s, may communicate with the microcontroller 11 to identify hand touch.
The microcontroller 11 may measure the capacitive load of the touch sensor 10. When a
conductive object, such as a finger, gets in close proximity to a touch sensor, the capacitive load
changes. Examples oftouch s can be found in U.S. Patent Nos. 4,186,392, 4,736,191, and
,650,597. A battery 12 es power to the device.
The al ature sensor 13 measures the temperature ofthe air around the
cup 1 and corrects for external g or cooling of the solution. In various embodiments, the
external temperature sensor 13 may be a thermistor or a thermocouple. An e how the
microcontroller 11 may measure temperature through the use of a thermistor, is with the use of
an RC circuit. The thermistor (for example a 33k NTC-type), which has variable resistance with
-16—
respect to ature, may be connected in parallel with a capacitor of known, fixed
capacitance (for example 1000pF). The ontroller initially charges the capacitor to a
specific higher voltage (for example, imately 4.5V). When the l voltage is reached,
the charging process is d, and time is measured for the thermistor to rge the
capacitor to a specific lower voltage (for example, approximately 1.4V). Since resistance of the
stor is dependent on temperature, temperature can be easily calculated by the
microcontroller 11 by time measurements n the higher and lower voltages. Measurement
results from this example are illustrated in .
In one embodiment, the microcontroller 11 may measure ature through the use
of a thermocouple by ing the current generated by the thermocouple, which is composed
oftwo dissimilar thermoelectric characteristics. The current is converted to the digital signal, by
an analog—to—digital converter, for the microcontroller to process. Since current is dependent on
temperature, the microcontroller 11 can ate the temperature based on this current.
Examples of a thermocouple can be found in US. Patent Nos. 2,985,949 and 307.
rates a top View of the contact lens cap showing a display using an LED
configuration. The LED colored light or lights 14 of indicate(s) the status ofthe
solution. illustrates a top View of the contact lens cap showing a display using an LCD
configuration. The optional LCD display 15 may supplement or replace the LED light or lights
in communication of the status of the solution or device to the user. The status ofthe solution or
device may include text which reads “analyzing the solution’s cleaning process”, “wait for
solution to complete ng process”, “safe to insert contacts into eye”, “contacts unsafe to
insert contacts into eye, redo cleaning process”, “cleaning process not functioning properly,
replace on and/or case”, and “battery low”. The indications may be done by a colored LED
light or lights such as for example red, yellow, orange, green, and short messages on the optional
LCD display. The short messages may include “BATT”, “WAIT”, “OK”, “REDO”, “BAD”,
“USE”, “SAFE”, “LOW”, “CLEANING”, “ANALYZE”, “REPLACE”. In some embodiments,
an indication may be provided as an audio signal.
EXAMPLE 1
The exothermic reaction monitored by the reaction sensor of this invention can be
illustrated by this example. The contact lens case was a 20 mm diameter and a 2 mm thick
plastic-walled reaction vessel such as the one shown in The contact lens case was
thermally insulated from the environment to negate external temperature influence. The case
was filled with 10 ml of disinfection solution (a solution of3% hydrogen peroxide, 0.85%
sodium de, onic acid, and phosphate ) at an initial ature of 20.0°C. The
contact lens cap contained a cogwheel-shaped, platinum catalyst disc (comparable to the
common ~lO.4 cm2/1150pg platinum catalyst currently commercially available and used in
contact lens care). The thermal gradient was ed over time with an imbedded
thermocouple. For a 20°C solution, the temperature lly increased at a rate of approximately
°C per minute. Since the solution’s peroxide concentration decreases over time, the rate of
temperature change (exothermic reaction) begins to slow. One competing event is that
exothermic reactions rate with an increase in temperature. The resulting reproducible
temperature profile is illustrated in which can be predicted with the mathematical
formula:
RATE (20°C) = rate of temperature change without contribution from external air
temperature influence, when the solution in at 20°C (Celsius/minute).
The formula may also be expressed as:
RATE (20°C) = (0.00009 x TIME3) — 4 x TIMEZ) — (0.0248 x TIME) + 1.5611
where TIME is the on time (minutes).
Although the curve appears to be polynomial, linear approximation can also be used for simpler
calculations:
RATE (20°C) = (-0.124 x TIME) + 1.6725
[00086] The experiment described above was repeated at different initial on
temperatures. illustrates the reaction rate’s dependence on initial solution temperatures.
As shown in , the exothermic reaction is ent on the initial temperature of the
solution. A decrease in initial solution temperature has a decrease in rate oftemperature change
over time, while an increase in temperature has an accelerated rate of temperature change over
time. illustrates the determination of equation of formula slope and y-intercept. As
shown in , the slope and y-intercept of these graphs are fairly linear with t to initial
solution temperature. Thus, a simple mathematical calculation can be used to predict the
temperature rate ge at any time point for a given initial solution temperature.
RATE (1) = rate of temperature change without contribution from external air
temperature influence (Celsius/minute).
The formula may also be expressed as:
RATE(1) =(((—0.008 x IST)+0.037) x TIME) + ((0.039 x IST)+0.821)
-18—
Where IST is the initial solution temperature (Celsius) and TIME is the reaction time (minutes).
Since the mathematical calculation does not account for the external air temperature
warming the contact lens case, one can easily correct for this. The experiment bed above
was performed at multiple ambient air temperatures. illustrates the determination of the
effect of ambient air temperatures on the heat of the solution inside contact lens case during the
exothermic disinfection process. The effect was found to be linear with respect to the
instantaneous temperature difference between the air temperature and solution temperature. The
cooling effect also fits this equation, where the air temperature was lower than the solution
temperature, although a negative value. Thus, the overall rate is:
RATE (2) = rate of change of solution temperature without contribution from the
exothermic neutralization reaction (Celsius/minute) (rate that air heats solution)
The formula may be expressed as:
RATE(2) = 0.056 x (CET — CST)
Where CST is the current solution ature us) and CET is the t external
temperature us).
The THERORETICAL RATE may then be calculated as the overall rate of change of
solution temperature. The tical rate may be sed as:
ETICAL RATE = RATE(l) + RATE(2)
THERORETICAL RATE = (-0.008 x IST + 0.037) x TIME + (0.039 x IST + 0.821) +
0.056 x (CET — CST)
This equation only fits a specific contact case design, solution formulation,
peroxide concentration, and catalyst design and quality. This is advantageous, since an
ally high or low peroxide concentration and/or a ion in quality ofthe platinum
catalyst can be easily identified by a comparison of theoretical and actual temperature
measurements.
A method for using the device may begin when a user places t lenses into
40 the contact lens baskets 7 of the contact lens cap 4, and closes the baskets 7. The contact lens
case cup (reaction vessel) 1 is filled with hydrogen peroxide disinfection/cleaning solution up to
the fill line 2. The contact lens cap 4 is grasped by the user’s hand. The user’s hand is sensed by
\_19‘
the capacitive touch sensor 10, which wakes the microcontroller 11 from wer mode. The
microcontroller 11 then monitors the solution sensor 6 to sense when the contacts lenses are
immersed in to the solution. For purposes of discussion, conductivity electrodes are used as an
example ofthe solution sensor. The exemplary solution sensor is not intended to be limiting.
The microcontroller 11 may sense when the contact lenses are immersed because the solution
contains ions which allow electricity to flow from one electrode to the other. Since the
tivity electrodes 6 are d near or above the solution temperature sensor 5, contact
lenses, and fill line 2, there is confirmation that there is sufficient on added to the contact
lens case cup (reaction vessel) 1. The conductivity electrodes 6 signal the microcontroller 11 to
initiate the monitoring of the contact lens solution and to start the reaction timer. For example,
the microcontroller 11 may cause a yellow LED light 14 to blink rapidly or a display to provide
the message “ANALYZE” on the LCD display 15. The microcontroller 11 would then take an
l solution temperature ement (IST). In various embodiments, the ontroller 11
thermistor or thermocouple 5 at
may take a solution temperature measurement with a solution
1.5 minutes and 0.5 minutes and take the ence ofthese two numbers (ACTUAL RATE);
the microcontroller 11 will also take a measurements at 1.0 minute (TIME = 1.0) with solution
stor or thermocouple 5 (CST), and a measurement with external temperature sensor 13
(CET). The values may be used in the following example equation:
THEORETICAL RATE = (-0.008 x IST + 0.037) x TIME + (0.039 x IST + 0.821) + 0.056 x
(CET — CST)
For example, if the ACTUAL RATE is within +/— 20% of the TICAL
RATE, the device fies that the solution and platinum catalyst are performing as expected;
the device may then slowly blink a yellow LED light 14 or display “CLEANING” on the LCD
display 15 . For example, if the ACTUAL RATE is not within +/- 20% of the THEORETICAL
RATE, the device identifies that the solution and platinum catalyst are not performing as
expected; the device may blink a red LED light 14 or display “REDO” or “BAD” on the LCD
display 15.
[00091] Ifthe device identified that the solution and platinum catalyst are performing as
ed, a specific time will be d to elapse which is appropriate for the complete
neutralization of the hydrogen peroxide at the given solution temperature (approximately 6 hours
at 20°C). At this point, the contacts are considered ready to wear, and the device may then
slowly blink a green LED light 14 or display “USE” or “SAFE” or “WEAR” on the LCD display
15. If the conductivity electrodes 6 and capacitive touch sensor 10 do not sense that the screw
cap 4 was removed from the contact lens cup 1 which contains the neutralized solution, the
device may then slowly blink a green LED light 14 up to the point where the contact lens are not
longer safe to place into the eye at the given solution ature (approximately 7 days at
°C). At this point, the device may then slowly blink a red LED light 14 or display “REDO” on
the LCD display 15.
The device may also count the number of times the cleaning process was
preformed, and blink a red LED light 14 or display “BAD” or “REPLACE” on the LCD display
after the maximum number of uses was exceeded. An audio indication may also be provided
to indicate the maximum number of uses was exceeded. The device may also count the number
of days that have elapsed alter the l use, and blink a red LED light 14 or display “BAD” or
“REPLACE” on the LCD display 15 after the maximum number of days was ed.
illustrates a block diagram of a cleaning device 700 for a medical device.
Cleaning device 700 has a microcontroller 704 that is powered by the power supply 702. The
microcontroller 704 controls and icates with the display/user interface 701, reaction
sensor 703, and memory 705. The device’s ion m and user data is stored on the
microcontroller 704. The
memory 705, and the information is accessed on demand by the
microcontroller’s program may be initiated by a signal from the reaction sensor 703 or from a
signal from the user, via the display/user interface 701, such as a display touch screen. The
microcontroller 704 takes readings from the sensor over time, makes calculations with the
measurements and the data stored in the , and displays a result on the display/user
interface 701.
illustrates a block diagram of an exemplary temperature sensing t lens
cleaning case 706. The cleaning case 706 has a microcontroller 708 that is powered by the
711 to sense when
power supply 713. The microcontroller 708 monitors the solution sensor
on is present. When the microcontroller 708 determines that solution is present, readings
from air temperature sensor 709 and on temperature sensor 710 are obtained. These
readings, combined with calibration data stored in the memory 712, are converted to temperature
measurements by the microcontroller 708. The microcontroller 708 then stores these historical
temperature measurements in the memory 712 for later retrieval. After a specific duration, the
temperature measurements are recalled from the memory 712 by the microcontroller 708. The
microcontroller 708 determines what signals should be sent to display 707.
FIGS. l6A-B illustrate an example of an operational flow chart for using a three light
LED y configuration. The flow of operation described herein is for illustrative purposes
and is not intended to be limiting. In various embodiments, the process begins at step 720 when
the cleaning case (e.g. ng vial and cap ) is powered on. In some
embodiments, the device is normally in low-power sleep mode at step 721 to preserve limited
battery life. The device may wake up from low—power sleep mode every 1 to 3 seconds for a
period of a few microseconds to sense if cleaning solution has been added to the device at step
722. If no solution is detected, the device goes back into sleep mode. If solution is detected, the
device blinks the yellow LED quickly at step 723. For example, the device LED may blink
twice per . Quick blinking may te the device is determining if the cleaning solution
and system are functioning properly. The device delays 5 to 15 seconds before taking a baseline
ature measurement at step 724, to allow for ature equilibration of the cleaning
solution, vial, and cap. After equilibration, l solution and atmospheric temperature
measurements are taken at step 725. The solution temperature is used as a reference point, in
which future on ature rates can be determined. Since the cleaning solution can
either be heated by the exothermic chemical reaction or the heat from the nment, it is
useful to take atmospheric temperature ements. Once the air temperature is known,
atmospheric heating of the solution can be factored out, thereby giving a more accurate
ement of chemical heating. The device routinely detects if the cap is continuously
immersed in solution at step 726.
If no solution is detected at step 726, the LED will blink red at step 730, indicating
that the cleaning process has been interrupted and that it is unsafe to place the contact lenses into
the eye. The red blinking LED continues to blink for 30 seconds, followed by return to low-
power sleep mode at the start of the sequence. If solution is detected, the microcontroller delays
for 30 seconds at step 727. Solution and atmospheric temperature measurements are re-sampled
or taken at step 728. The device routinely detects if the cap is continuously immersed in solution
at step 729, and the s proceeds if solution is detected. Theoretical temperature rate is
ated at step 732 from the solution temperature measurements and corrected by the
atmospheric temperature measurements. If the actual temperature rate is not within 20% of the
calculated theoretical ature rate at step 733, then the LED blinks red to indicate that the
lenses are not safe to insert into the eye at step 741. After 30 seconds, the device may ue
to wait until no solution is detected at step 742, and then the process returns to start at step 743.
If the actual temperature rate is within 20% ofthe calculated theoretical temperature
rate at step 733, then the device blinks the yellow LED slowly at step 734, for example once per
2 to 3 seconds. The purpose of the slowly blinking is to indicate that the device has determined
that the cleaning solution and system are functioning properly, and the device is cleaning the
contact lenses. The device detects if the cap is continuously immersed in solution at step 735. If
solution is detected, the device proceeds to allow 6 hours for the cleaning solution to complete
the cleaning/neutralization cycle at step 736. If 6 hours has elapsed, the device blinks the green
LED slowly at step 737, which indicates to the user that the device has finished the cleaning
/neutralization cycle, and the contact lenses are safe to insert into the eye. The device continues
to blink the green LED until no solution is ed at step 738, where it returns to the start at
step 743. If solution is ued to be detected at step 738, and 7 days has elapsed at step 739,
then the LED blinks red at step 740 to indicate that it is no longer safe to insert the contact lenses
into the eye. This is due to a ility that microbes may have re-infected the sterile solution.
The red LED will continue to blink until no solution is ed at step 744.
illustrates an embodiment of a system 600 comprising a cleaning case 610
and a caddy 680, in which pressure in the headspace above the cleaning solution is measured
within the cleaning case, and messages based on the pressure profile are displayed on the caddy.
Cleaning case 610 includes cap 630 and may also e aforementioned components, not
shown here, such as a basket for holding contact lenses, a catalyst, and others. In this
embodiment, cap 630 es case ts 650A and 650B. Also shown is caddy 680, which
includes features described above such as caddy case 151, indicators 152A and 152B, and
display panel 154. Also shown are caddy contacts 670A and 670B.
Still referring to , case contacts 650A and 650B make electrical contact with
caddy contacts 670A and 670B when the case is placed in caddy 680. In this way there is an
electrical communication n the case and the caddy to enable other features of this system.
Cleaning case 610 also includes cylinder 620, which may have an orienting component for
rotationally positioning the cleaning case once it is placed in the caddy such that case contacts
650A and 650B make proper t to caddy contacts 670A and 670B. Such orienting
component may be a fin, such as fin 621 shown, or may be a groove, bump, dimple, or similar
structure. In such case, the caddy will also include a corresponding receiver, not shown, which
can receive or mate with the structure on the cylinder. Such receiver can be a groove, fin, dimple
or notch, and is not shown in the figure. For example, caddy 680 can include a groove to receive
fin 621 when case 610 is placed in the caddy. Other mechanisms for properly orienting the case
in the caddy may be easily envisaged.
ing to A, certain ents and additional features ofthe embodiment
ofthe cleaning case illustrated in are shown. A shows a side view of cap 630 of
the cleaning case shown in .
As explained above, when a peroxide-based cleaning solution and catalyst are used,
an oxidation-reduction reaction occurs. During this on, oxygen bubbles are generated at
the catalyst. These bubbles float to the surface ofthe on, whereupon oxygen gas is
released. If the cap makes a reasonably gas-tight seal onto the cylinder, pressure in the
headspace above the solution will increase as gas is released. Fresh solutions and catalysts will
generate more gas than old ones. Messages informing a user about the quality and useful life of
the cleaning solution and catalyst can be generated using these concepts.
Still referring to A, cap 630 includes several components which can measure
the pressure of gas generated by the reaction of a peroxide with a catalyst, i.e. a reaction sensor
in the form of a pressure sensor. Internal port 632 allows gas from headspace 631 to enter
bladder 633 where it pushes against diaphragm 634. As the pressure builds, diaphragm 634
pushes against shorting bar 636, which is disposed against spring 638 towards cap top 643 until
it contacts pins 646A and 646B. Pins 646A and 646B are connected to wires 640A and 640B,
tively, which are connected to case contacts 650A and 650B, tively.
3] After a cleaning cycle is initiated and case 610 is placed in caddy 680 (), gas
is ted by the chemical reaction. When shorting bar 636, which is electrically conductive,
contacts pins 646A—B, an electrical tion is made between the two pins and a connecting to
a logic chip is completed. Thus, a signal can be sent to a processing device so that a message can
be displayed and/or a timer can also be started to display messages at a later time. For example,
upon shorting bar 636 making a connection to pins 646A and 646B, a message such as “Your
Contact Lenses are Being d” can be yed, e.g. in display 154 (). At this time
a timer can count to a specified time, e.g. 6 hours, at which time a message such as “Your
Contact Lenses are Clean and Ready for Use” can be displayed. atives can be easily
ged.
Referring again to A, external port 642 allows air to escape as diaphragm 634
and shorting bar 636 are disposed towards cap top 643. Cap 630 may also include an overflow
port 644 opened by overflow valve 648. In some cases when the pressure in the headspace
exceeds a certain amount, such a system can allow excess gas to escape from the headspace.
B shows a top-down view of the cap shown in A. This view shows
shorting bar 636, spring 63 8, external port 642, overflow port 644, pins 646A-B, and case
contacts 650A-B. In the embodiment shown in FIGS. 18A-B, the shorting bar 636 is shown as a
disc, however it may take any other riate shapes, such as that of a pin or rod, an oval, etc.
The examples above describe in detail embodiments in which the temperature of the
solution is measured with a temperature sensor, and another embodiment in which pressure of
gas generated by a reaction of peroxide with a catalyst is measured by a pressure .
However, this disclosure encompasses onal embodiments wherein other ways of measuring
or sensing a property using a sensor may be used. Such sensors may be, for example and without
limitation, an electronic sensor (which includes a sensor of conductivity, voltage, or other
electronic properties, e.g. between two electrodes), a sound sensor, an optical sensor, or a gas
sensor. For example, in one embodiment, a caddy may e two electrodes (the catalyst can
be one electrode) which contact the cleaning solution. Differences in the conductivity or e
over time as the reaction of peroxide with the catalyst progresses can be measured using a
reaction sensor and used to initiate a timer or display one or more messages, as described above.
In other embodiments, other types of sensors may be used to drive similar processes.
Also provided are methods of monitoring patient compliance with a protocol for
cleaning a medical device with a cleaning solution, the methods comprising ing data by
measuring a property of the cleaning solution or a nearby area or the medical device, and
displaying one or more messages according to the data. The data ed from the
measurements (“measurement data”) may be compared to preset data stored in memory, and the
one or more message may be based on a ison between the measurement data and the
preset data. In some embodiments, the data may be provided to a medical professional. For
example, in one method, data from measuring the temperature or temperature profile of a
cleaning case may be obtained and ed to preset data, e.g. an acceptable temperature
profile range (see discussion of above). If the measurement data is within the acceptable
then a
range, a message such as “Disinfection working properly” can be yed; if not,
ofcleaning
message such as “Disinfection unsuccessful” can be displayed. Data for a series
events can be stored over time. This data can be provided to or accessed by the user or a
healthcare professional such as, in embodiments where the medical device is a contact lens, an
optician. For example, the user or medical professional can access the data with a computer,
smartphone, or similar computing . The data may provide a history of the user’s cleaning
regimens over a certain time, e.g. six months or a year. With this method, the user and an
can monitor and improve compliance with the cleaning protocol.
Any ofthe apparatus or systems (e.g. caddies) or methods described herein may have
the following onal features or components. They may include a first sensor and a second
sensor, wherein the first and second sensors are each one of the sensors described above
(thermal, optical, etc.) and wherein the first sensor measures a property relating to the
oxidation/reduction reaction of the peroxide and catalyst (e.g. temperature changes, conductivity
or e changes n electrodes, re, sound, etc.) and the second sensor measures a
certain “signature” of the solution. The signature may be, for example, a unique optical
absorptivity of one supplier’s cleaning solution absent in other cleaning solutions. The caddy
can be programmed to operate only when this ture” is ed. Thus, a caddy can be
made to operate only when a ular supplier’s cleaning solution is used. In some
embodiments, the apparatus or system can include a selector switch or similar input device in
which the user selects the frequency at which they replace their contact lenses. For example, a
selector switch can include s for daily, weekly, bi—weekly, or monthly replacement. Such
a selection, which can also be made with a computer or similar device, can send a signal to the
processing device so that a message can be yed suggesting the user replace his or her
contact lenses.
While a number of exemplary embodiments, aspects and variations have been
provided herein, those of skill in the art will recognize certain modifications, permutations,
additions and combinations and certain sub-combinations of the embodiments, aspects and
variations. It is intended that the ing claims are reted to include all such
modifications, permutations, additions and combinations and certain sub-combinations of the
embodiments, aspects and variations are within their scope. This, in the context of this
disclosure, although a temperature sensor and a pressure sensor may not be structural
lents, in that a temperature sensor may measure temperature using an infrared detector and
a pressure sensor may measure pressure of a gas, in the context of measuring a property of a
cleaning solution, the area near a cleaning or one or more of the medical devices being cleaned, a
temperature sensor and a re sensor may be equivalent structures.
Claims (32)
1. A contact lens cleaning system comprising: a contact lens holder; a vial adapted to n the contact lens holder and a cleaning solution, wherein a catalyst is capable of neutralizing the cleaning solution; a sensor capable of ing data on a rate of neutralization of the cleaning solution; a processing device in communication with the sensor to receive the rate of neutralization data from the ; and a display in communication with the processing device, the processing device being adapted to operate the display to provide cleaning efficacy information based on the rate of neutralization data.
2. The system of claim 1 n the sensor is a ature sensor.
3. The system of claim 2 wherein the ature sensor is disposed in a cap covering the vial.
4. The system of claim 2 wherein the ature sensor is disposed outside of the vial.
5. The system of any one of the preceding claims 2 to 4 wherein the processing device is d to determine a temperature change rate from the rate of neutralization data.
6. The system of claim 5 wherein the processing device is further adapted to determine cleaning efficacy by comparing the temperature change rate to a theoretical temperature change rate.
7. The system of claim 6 further comprising an ambient temperature sensor disposed outside of the vial and adapted to measure a temperature of air surrounding the vial, the processing device being further adapted to determine cleaning efficacy using a temperature signal from the ambient temperature sensor to correct for ambient temperature affect to the approximate rate of temperature change as compared to the theoretical temperature change rate.
8. The system of any one of the preceding claims further comprising a use counter communicating with the sing device, the sing device being further adapted to display ation corresponding to the number of cleaning uses of the cleaning system.
9. The system of any one of the preceding claims wherein the sensor is a pressure sensor.
10. The system of any one of the preceding claims further comprising a caddy adapted to support the vial.
11. The system of claim 10 wherein the display is ed within the caddy.
12. The system of any one of the preceding claims wherein the display is ed in a cap on the vial.
13. The system of any one of the preceding claims further comprising a solution sensor disposed within the vial, the processing device being further adapted to determine the presence of cleaning on within the vial based on a signal from the solution sensor.
14. The system of claim 13 wherein the solution sensor comprises an electrode.
15. The system of claim 13 wherein the solution sensor comprises a capacitive sensor.
16. The system of any one of the preceding claims wherein the catalyst comprises um.
17. The system of any one of the preceding claims n the cleaning solution comprises hydrogen peroxide.
18. A contact lens cleaning system comprising: a contact lens holder; a vial adapted to contain the contact lens holder and a cleaning solution, wherein a catalyst is capable of neutralizing the cleaning on; a sensor capable of providing data on a characteristic of the neutralization of the cleaning solution; a processing device in communication with the sensor to receive the data from the sensor and determine an approximate rate of neutralization using the data; and a display in communication with the processing device, the processing device being d to operate the y to provide ng efficacy information based on the approximate rate of neutralization.
19. The system according to claim 18, wherein the characteristic of the chemical reaction is temperature resulting from heat produced by the neutralization of the cleaning solution, and wherein the sensor is a temperature sensor.
20. The system ing to claim 19, wherein the sing device is further adapted to determine cleaning efficacy by comparing the approximate rate of temperature change to a theoretically determined rate of temperature change for the neutralization of the cleaning
21. The system according to claim 20 further comprising an ambient temperature sensor disposed outside of the vial and adapted to measure a temperature of air surrounding the vial, the processing device being further d to determine cleaning efficacy using a temperature signal from the ambient ature sensor to correct for ambient temperature affect to the approximate rate of temperature change as compared to the tically determined rate of temperature change.
22. The system according to any one of the preceding claims 18 to 21, wherein the characteristic of the neutralization of the ng on is re resulting from a gas product from the neutralization, and wherein the sensor is a pressure sensor.
23. The system according to claim 22, wherein the processing device is further adapted to determine cleaning efficacy by comparing the approximate rate of pressure change to a theoretically determined rate of pressure change for the neutralization.
24. The system according to any one of the preceding claims 18 to 23 wherein the catalyst comprises platinum.
25. The system according to any one of the preceding claims 18 to 24 wherein the cleaning solution comprises hydrogen peroxide.
26. The system according to claim 18, wherein the teristic of the neutralization of the cleaning solution is conductivity resulting from the neutralization of the cleaning solution, and wherein the sensor is a tivity sensor.
27. The system according to claim 26, wherein the processing device is further d to determine cleaning efficacy by comparing the approximate rate of tivity change to a tically determined rate of conductivity change for the neutralization of the cleaning solution.
28. The system of any one of the preceding claims 18 to 27 n the sensor is a conductivity sensor.
29. The system of claim 28 wherein the processing device is adapted to ine a conductivity change rate from the rate of lization data.
30. The system of claim 29 wherein the processing device is further adapted to determine cleaning efficacy by ing the conductivity change rate to a theoretical conductivity change rate.
31. A contact lens cleaning system comprising: a contact lens holder; a vial adapted to contain the contact lens holder and a cleaning solution, wherein a catalyst is capable of neutralizing the cleaning solution; a conductivity sensor capable of generating conductivity data related to a rate of neutralization of the cleaning solution; a processing device in ication with the conductivity sensor to obtain the conductivity data and determine an approximate rate of neutralization using the conductivity data; and a display in communication with the processing device, the processing device being adapted to operate the display to provide cleaning efficacy information based on the approximate rate of neutralization.
32. A contact lens cleaning system according to any one of the preceding claims substantially as herein described with reference to any one of the embodiments of the invention rated in the accompanying drawings and/or examples.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201161445910P | 2011-02-23 | 2011-02-23 | |
US61/445,910 | 2011-02-23 | ||
US201161547598P | 2011-10-14 | 2011-10-14 | |
US61/547,598 | 2011-10-14 | ||
PCT/US2012/026249 WO2012116138A2 (en) | 2011-02-23 | 2012-02-23 | Contact lens cleaning system with monitor |
Publications (2)
Publication Number | Publication Date |
---|---|
NZ613852A NZ613852A (en) | 2015-09-25 |
NZ613852B2 true NZ613852B2 (en) | 2016-01-06 |
Family
ID=
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