Optical Interferometry for Tear Film Thickness Measurement

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Current methods for diagnosing and evaluating dry eye syndrome are imperfect and lack precision, particularly in measuring tear film thickness and lipid layer thickness after ophthalmic formula application, which is crucial for ocular surface health and drug delivery optimization.

Innovation Solution

A method and device using wavelength-dependent optical interferometry to measure tear film thickness, allowing for the accurate diagnosis of dry eye causes and the evaluation of ophthalmic formula effects on tear film layers, including aqueous and lipid layers, before and after application, enabling the selection of appropriate therapeutic products.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If current diagnostic methods (symptom assessment, fluorescein staining, TBUT) are used, then diagnosis can be performed, but measurement precision and accuracy are insufficient

Engineering Contradiction:
Improvetear film thickness measurement precisionVSAvoiddiagnostic device complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent replaces mechanical and chemical diagnostic methods (fluorescein staining, Schirmer test) with optical interferometry. The optical system uses wavelength-dependent interferometry to measure tear film thickness non-invasively, eliminating the need for chemical dyes and manual assessment procedures while achieving superior measurement precision.

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

Solution Approach 2:

The patent changes the measurement parameter from qualitative/semi-quantitative assessments (staining intensity, break-up time) to precise quantitative optical interference patterns. By measuring the wavelength-dependent reflectance spectrum, the system derives exact tear film thickness values, transforming subjective diagnostic parameters into objective numerical data.

Inventive Principle:
Principle #35Parameter changes

2Reliability

If fluorescein staining is used to assess tear film, then diagnosis can be performed, but the presence of fluorescein changes tear film properties making measurements non-physiological

Engineering Contradiction:
Improvephysiological accuracy of measurementVSAvoidsimplicity of diagnostic procedure
Core Design Contradiction:
ReliabilityVSEase of operation

Solution Approach 1:

The patent substitutes chemical staining methods with purely optical measurement. The optical interferometry system measures tear film thickness without introducing any foreign substances, ensuring that the tear film remains in its natural physiological state throughout the measurement process.

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

Solution Approach 2:

The patent uses optical interference patterns as an intermediary to measure tear film properties. Instead of directly interacting with the tear film through chemical dyes, the system uses light waves that reflect off the tear film interfaces, creating interference patterns that encode thickness information without altering the tear film composition.

Inventive Principle:
Principle #24Intermediary (Mediator)

3Measurement precision

If TBUT measurement with fluorescein instillation is used, then tear film stability can be assessed, but reflex tearing is stimulated preventing accurate measurement

Engineering Contradiction:
Improvetear film break-up time measurement precisionVSAvoidreflex tearing stimulation
Core Design Contradiction:
Measurement precisionVSObject-affected harmful factors

Solution Approach 1:

The patent replaces the chemical stimulation method (fluorescein instillation) with a non-invasive optical measurement approach. The interferometric system measures tear film thickness and stability without stimulating the ocular surface, thereby preventing reflex tearing and maintaining natural tear film physiology throughout the measurement.

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

4Loss of information

If multiple diagnostic tests are performed to evaluate tear film adequately, then comprehensive diagnosis is achieved, but time and resources are consumed

Engineering Contradiction:
Improvecompleteness of tear film assessmentVSAvoiddiagnostic time
Core Design Contradiction:
Loss of informationVSLoss of time

Solution Approach 1:

The patent creates a universal diagnostic platform that performs multiple tear film assessments simultaneously. The optical interferometry system measures aqueous layer thickness, lipid layer thickness, and tear film stability in a single integrated procedure, replacing the need for multiple separate tests (fluorescein staining, Schirmer test, TBUT measurement) and providing comprehensive tear film evaluation in one measurement session.

Inventive Principle:
Principle #6Universality (Multi-functionality)

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

This approach provides precise and accurate measurements of tear film layers, allowing for effective diagnosis and treatment of dry eye conditions, improving ocular surface health and optimizing ophthalmic dosage forms.

Implementation Method 1

employing an optical interferometer to measure tear film layer thickness

Methodology Applied
Scientific EffectOptical interference: Interference

Data Source

PatentUS7959293B2Methods and devices for measuring tear film and diagnosing tear disorders
Publication Date: 2011.06.14 JOHNSON & JOHNSON SURGICAL VISION INC
  • US7959293B2 patent drawing
  • US7959293B2 patent drawing
  • US7959293B2 patent drawing

AI summary

Methods and devices measure eye blinks and tear film lipid and aqueous layer thickness before and following ophthalmic formula application onto the ocular surface, especially wherein the ophthalmic formula is an artificial tear. The methods and devices are suitable for dry eye diagnosis. The methods and devices are suitable for use to evaluate ophthalmic formula effects on the tear film and to use such information to diagnose ophthalmic formula treatment of ocular disease conditions such as dry eye in the absence of contact lens wear or post-surgical eye drop treatment and diagnosis. The methods and devices are also suitable for use in the optimization of ophthalmic drug dosage forms and sustained drug release.