Hemostatic dressing
a technology of hemostatic dressing and hemisphere, which is applied in the direction of drug compositions, peptide/protein ingredients, extracellular fluid disorder, etc., can solve the problems of reducing the interaction of the dressing components, reducing the effectiveness of the dressing in preventing hemorrhage, and not uncommon occurrence of excessive bleeding or fatal hemorrhage from an accessible site. , to achieve the effect of inhibiting the delamination of the layers
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Benefits of technology
Problems solved by technology
Method used
Examples
example 1
[0059] The example set forth below demonstrates that delamination of the dressings can be decreased by preparing a dressing in which the thrombin layer is not coextensive with the first and second fibrinogen layers. In this example, thrombin was dispensed onto the first fibrinogen layer in either of two configurations. In the conventional dressings, the thrombin fully covered the first fibrinogen layer (this configuration is referred to herein as “full” coverage). In the dressings of the invention, the thrombin was configured on top of the first fibrinogen layer as a single circle that was not coextensive with the first fibrinogen layer (this configuration is referred to herein as “circle” coverage).
[0060] To prepare the dressings, fibrinogen was formulated in a conventional manner: 35 mg / ml of total protein (TP) in Buffer D (100 mM NaCl, 1.1 mM CaCl2.H2O, 10 mM TrisHCl, 10 mM Sodium Citrate, 2% Sucrose, 2.8 mg / ml albumin, 0.52 mg / ml TWEEN-80, pH 7.2) containing albumin at 80 mg / g ...
example 2
[0080] The data set forth below in Table 2 demonstrate that delamination can be attributed to full coverage of the thrombin layer (or buffer) on the first fibrinogen layer. Dressings that were produced with thrombin applied such that the thrombin layer was not coextensive with the first fibrinogen layer generally passed the delamination appearance test (groups 9-11 and 13-16 in Table 2). Similarly, dressings that were produced with no middle layer, i.e., having only two fibrinogen layers, generally did not become delaminated, and the fibrinogen layers adhered tightly to each other.
[0081] In this example, fibrinogen was formulated as described above, and thrombin was formulated as described in Table 2. The fibrinogen layers (approx 1.2 mL) were applied using a programmable pipette, and the dressings were manufactured manually as described herein. The middle layer of the dressing (i.e., thrombin or fibrinogen) was applied either by spraying using an air brush or by pipetting. For eac...
PUM
Property | Measurement | Unit |
---|---|---|
diameter | aaaaa | aaaaa |
pH | aaaaa | aaaaa |
distance | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com