Shape Memory Polymer Nasolacrimal Duct Insertion Member
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Solution Overview
Problem
Existing nasolacrimal duct insertion devices lack a passage for proper tear discharge, leading to stagnation and a high risk of infection, especially after dacryocystoplasty, where the tube occupies most of the tear discharge passage.
Innovation Solution
A nasolacrimal duct insertion member comprising a shape memory polymer with a melting point suitable for bio-implantation, allowing for easy insertion and expansion to facilitate smooth tear discharge without the need for post-operative removal.
Engineering Contradictions & Design Principles
Engineering Contradiction Analysis
1Reliability
If a conventional silicone tube is inserted into the nasolacrimal duct, then the duct can be kept open, but the tube occupies most of the tear discharge passage causing tear stagnation and infection risk
Solution Approach 1:
The insertion member is made of a porous polymer material that allows tears to pass through the tube wall itself, creating multiple discharge pathways. This porous structure eliminates tear stagnation while maintaining duct patency, as tears can flow through the porous matrix rather than being blocked by a solid tube interior
Solution Approach 2:
The insertion member uses a flexible porous polymer shell that can be compressed to a thin profile for easy insertion, then expands to provide structural support. The thin film structure minimizes the space occupied in the duct while still maintaining patency, leaving more room for tear flow
2Strength
If a rigid metallic probe structure is used to keep the duct open, then structural support is provided, but insertion difficulty and patient discomfort increase
Solution Approach 1:
The insertion member transitions from a flexible, compressible state during insertion to a rigid, supportive state after deployment. The porous polymer structure allows compression to a small profile for easy insertion, then expands within the duct to provide the necessary structural support, dynamically adapting its mechanical properties
Solution Approach 2:
The insertion member is designed as a flexible shell that can be compressed to a thin film state for minimally invasive insertion, then expands to form a rigid-like supportive structure. This flexible shell approach eliminates the need for rigid metallic probes while providing equivalent structural support
3Reliability
If a tube is maintained in the duct for three to six months, then the duct remains patent, but the need for post-operative removal adds complexity and risk
Solution Approach 1:
The insertion member is made of a polymer with a phase transition temperature near body temperature, allowing it to be inserted in a soft, flexible state and then transition to a rigid, supportive state. This parameter change eliminates the need for removal, as the material naturally adapts to the physiological environment
Solution Approach 2:
The insertion member is designed as a single-use, biodegradable polymer device that serves its function temporarily to establish duct patency, then naturally degrades and is eliminated by the body. This disposable approach eliminates complex removal procedures while maintaining duct patency during the critical healing period
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
The shape memory polymer insertion member can be easily inserted into the nasolacrimal duct, expand to widen obstructed or narrowed ducts, and ensure proper tear discharge, reducing the risk of infection and eliminating the need for post-operative removal.
Implementation Method 1
a shape memory polymer with a melting point suitable for bio-implantation
Implementation Method 2
The shape memory polymer insertion member can be easily inserted into the nasolacrimal duct, expand to widen obstructed or narrowed ducts
Data Source
AI summary
The present invention relates to a nasolacrimal duct insertion member comprising a shape memory polymer for treatment of nasolacrimal duct obstruction/stenosis, wherein the shape memory polymer comprises a crosslinkable functional group, such that the nasolacrimal duct insertion member has a melting point suitable for implantation into a living body.


