Dry Spray Hemostatic System Using Synthetic Platelets
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Solution Overview
Problem
Current methods for controlling hemorrhaging in traumatic injuries, such as those in the central nervous system, are inadequate as they often result in uncontrolled bleeding due to the limitations of platelet substitutes, external hemostatic agents, and the challenges of administering recombinant factor VIIa, which is expensive and requires refrigeration, necessitating a new approach for immediate and effective hemostasis.
Innovation Solution
Development of dry spray compositions comprising co-block polymers coupled with water-soluble polymers and peptides, specifically RGD sequences, that act as synthetic platelets for targeted hemostasis, providing quick and even distribution at the wound site, stability at room temperature, and specific aggregation properties to prevent non-specific thrombosis.
Engineering Contradictions & Design Principles
Engineering Contradiction Analysis
1Reliability
If allogeneic platelets are administered to control hemorrhaging, then bleeding can be halted, but platelets have short shelf life and can cause graft versus host disease, alloimmunization, and transfusion-associated lung injuries
Solution Approach 1:
The patent creates synthetic platelets that replicate the hemostatic functions of natural platelets without using actual biological platelets. These synthetic platelets are composed of fibrinogen-coated microcapsules based on albumin, copying the essential clotting function while avoiding all transfusion-related complications such as graft versus host disease, alloimmunization, and transfusion-associated lung injuries.
Solution Approach 2:
The synthetic platelets use albumin as a base material, which is inexpensive, readily available, and has a long shelf life compared to natural platelets. The microcapsule structure allows these synthetic platelets to be stored without refrigeration and administered when needed, eliminating the short shelf life problem of natural platelets while maintaining effective hemostasis.
2Reliability
If recombinant factor VIIa is administered intravenously to augment hemostasis, then bleeding control can be achieved, but it requires refrigeration, is expensive, and has mixed results making it challenging to administer in the field
Solution Approach 1:
The synthetic platelets use albumin as a base material, which is inexpensive, readily available, and has a long shelf life compared to natural platelets. The microcapsule structure allows these synthetic platelets to be stored without refrigeration and administered when needed, eliminating the short shelf life problem of natural platelets while maintaining effective hemostasis.
Solution Approach 2:
The patent replaces the complex biochemical cascade required for natural hemostasis with a simplified mechanical approach: fibrinogen-coated microcapsules that directly bind to exposed collagen at the injury site and recruit platelets through physical adsorption and specific binding, bypassing the need for recombinant factor VIIa and its associated refrigeration and cost issues.
3Productivity
If spray on hemostatic systems are developed for quick and even distribution, then application to difficult-to-contact areas is enabled, but the system needs to be non-toxic, stable at room temperature, and avoid non-specific thrombosis
Solution Approach 1:
The synthetic platelets are designed with localized functionality: fibrinogen coating on the microcapsule surface provides specific binding affinity for exposed collagen at the injury site, while the albumin core provides structural stability. This localized functional design ensures that hemostatic activity is concentrated exactly where needed (at the collagen-exposed wound bed) rather than systemically throughout the bloodstream, preventing non-specific thrombosis.
Solution Approach 2:
The synthetic platelets combine multiple materials with complementary properties: albumin provides a biocompatible, stable core structure; fibrinogen coating provides specific binding to collagen and platelet recruitment; and the microcapsule structure provides controlled delivery. This composite material design achieves both effective localized hemostasis and systemic safety.
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 dry spray compositions significantly reduce bleeding time in trauma models by acting as synthetic platelets, offering a stable, effective, and easily applicable solution for hemostasis, even in hard-to-reach areas, with the potential to improve tissue preservation and functional outcomes.
Implementation Method 1
nanoparticles that act essentially as synthetic platelets and are stable at room temperature
Implementation Method 2
The ultimate step, clot formation, is the conversion of fibrinogen, a large, soluble plasma protein produced by the liver and normally present in the plasma, into fibrin, an insoluble, threadlike molecule
Implementation Method 3
Spray on hemostatic systems have many advantages such as quick and even distribution over a broad coverage area
Data Source
AI summary
The invention provides for dry spray compositions comprising co-polymers comprising a core, water-soluble polymer and a peptide.


