Mesna Powder Mixing Device for Stable Surgical Dissection
Find Innovative SolutionsGenerate Solutions
Solution Overview
Problem
Current Mesna solutions in liquid form are unstable due to oxidation, require cumbersome handling, and lack concentration flexibility, leading to reduced efficacy and increased health risks and costs in surgical tissue separation procedures.
Innovation Solution
A device with separate chambers for Mesna powder and sterile physiological saline solution, allowing immediate mixing and delivery of Mesna solution at desired concentrations, eliminating the need for stabilizing agents and reducing oxidation risks, while enabling controlled and isotonic delivery during surgery.
Engineering Contradictions & Design Principles
Engineering Contradiction Analysis
1Reliability
If Mesna is stored in liquid form in glass containers, then it requires stabilizers and anti-oxidants to prevent oxidation, but this increases contamination risk, surgery time, and patient health risks
Solution Approach 1:
The patent replaces the need for stabilizers and anti-oxidants by storing Mesna in an inert environment (lyophilized powder form) that prevents oxidation, eliminating harmful additives from the final solution
Solution Approach 2:
The patent extracts and removes the harmful stabilizers and anti-oxidants from the Mesna solution by using lyophilized powder that dissolves in sterile water to create a stabilizer-free solution
2Stability of the object's composition
If commercial Mesna solutions are used, then they are stabilized with pH adjustment agents and additives, but this increases cost and presents health risks to patients
Solution Approach 1:
The patent changes the physical state parameter of Mesna from liquid to lyophilized powder, and adjusts the concentration parameter to provide flexible dosing options ranging from 5% to 50% Mesna in sterile water
Solution Approach 2:
The patent eliminates harmful additives by using lyophilized powder stored in an inert state that dissolves in sterile water to create a pure Mesna solution without pH adjustment agents or stabilizers
3Ease of operation
If Mesna solution is transferred from glass containers to delivery devices, then it increases contamination risk and surgery time, but this is necessary for delivery to target tissue
Solution Approach 1:
The patent merges the storage and delivery functions into a single integrated device where lyophilized Mesna powder is stored in a cartridge that connects directly to a syringe containing sterile water, eliminating the need for separate transfer steps
Solution Approach 2:
The patent performs preliminary preparation by pre-packaging lyophilized Mesna powder in sterile cartridges and pre-filling syringes with sterile water before surgery, so that only a simple connection and mixing step is needed during the procedure
4Adaptability or versatility
If commercial Mesna vials are used, then concentration is fixed and practitioner can only dilute, but this limits flexibility when higher concentrations are needed
Solution Approach 1:
The patent provides concentration flexibility by offering cartridges with different Mesna powder concentrations (5%, 10%, 20%, 30%, 40%, 50%) and allowing practitioners to adjust the volume of sterile water added to achieve the desired final concentration
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 device stabilizes Mesna, reduces surgical time, minimizes tissue damage, and lowers costs by providing a flexible concentration option, enhancing surgical precision and safety with immediate and controlled delivery of Mesna solution.
Implementation Method 1
a first chamber for housing the solute, a second chamber for housing the solvent... and are in fluid communication with each other upon disruption of said separation means thereby forming the solution
Data Source
Figure 1A
Figure 1B~1C
Figure 1D
AI summary
The invention provides a device for delivering a solution to tissues and/or organs, the solution comprising at least one solvent and at least one solute. The device comprises at least one chamber (8) which comprises sodium 2-mercaptoethanesulfonate in powder form. A method comprising the steps of dissolving the solute in the solvent inside the device thereby obtaining the solution, and delivering immediately the obtained solution to said tissues and/or organs to facilitate dissection is described.