Wound dressing
A method for controlling fiber cross-alignment in a nanofiber membrane, comprising: providing a multiple segment collector in an electrospinning device including a first and second segment electrically isolated from an intermediate segment positioned between the first and second segment, collectively presenting a cylindrical structure, rotating the cylindrical structure around a longitudinal axis proximate to an electrically charged fiber emitter; electrically grounding or charging edge conductors circumferentially resident on the first and second segment, maintaining intermediate collector electrically neutral; dispensing electrospun fiber toward the collector, the fiber attaching to edge conductors and spanning the separation space between edge conductors; attracting electrospun fiber attached to the edge conductors to the surface of the cylindrical structure, forming a first fiber layer; increasing or decreasing rotation speed of the cylindrical structure to alter the angular cross-alignment relationship between aligned nanofibers in adjacent layers, the rotation speed being altered to achieve a target relational angle.
1. A wound dressing comprising:
any of a medical fabric, a film, or a porous material;
a fiber membrane, comprising electrospun fiberizeable material in at least three adjacent layers of nanofibers, each layer comprising a plurality of aligned nanofibers oriented at oblique angles relative to nanofibers in adjacent layers, said plurality of aligned nanofibers in each layer extending from a first membrane edge to a second membrane edge,
wherein a plurality of aligned nanofibers in each layer cross a plurality of aligned nanofibers in adjacent layers at a plurality of distinct points of intersection, forming a crossing at each distinct point of intersection consisting of three crossing nanofibers extending directionally as six radials from each of said distinct points of intersection,
wherein relative cross-alignment angles between said six radials at each distinct point of intersection are in the range of 50 to 70 degrees, and said relative cross-alignment angles of said aligned nanofibers and spacing between said aligned nanofibers each have a specific average numerical value in said membrane and comprise a structure having porosity required for exudate flow from a wound, and
wherein said aligned nanofibers in each said layer comprise at least one of solid, hollow, or core-shell fiber.
2. The wound dressing of claim 1 , further comprising any combination of said fiber membrane, film, medical fabric, or porous material.
3. The wound dressing of claim 1 , further comprising any of an antimicrobial agent, hemostatic agent, analgesic agent, regenerative agent, immune modulator, oxygenating agent, and pH stabilizer.
4. The wound dressing of claim 1 , wherein said nanofibers comprise any one or combination of poly (lactic-co-glycolic acid) (PLGA), polyvinylpyrrolidone (PVP), poly(ethyleneoxide) (PEO), polyurethane (PU), PVP/cyclodextrin, polyvinyl alcohol (PVA), polycaprolactone (PCL), cellulose, PVP/ethyl cellulose, PVP/zein, cellulose acetate, hydroxypropyl methylcellulose (HPMC), and analogues thereof.
5. The wound dressing of claim 1 , wherein said nanofibers comprise an absorbable and biodegradable polymer that can be enzymatically or nonenzymatically decomposed, yields no toxic decomposition product, and has ability of releasing a drug.
6. The wound dressing of claim 1 , wherein said nanofibers further comprise a polymeric material and a chromogenic agent responsive to enzymatic activity.
7. The wound dressing of claim 6 , wherein said chromogenic agent is a dye presenting a color change response to said enzymatic activity produced by pathogens present on human skin, in a wound bed, in wound exudate, or in bodily fluid.
8. The wound dressing of claim 7 , wherein said enzymatic activity produces lipase.
9. The wound dressing of claim 7 , wherein said pathogens include at least Proteus mirabilis, Pseudomonas aeruginosa , and methicillin-resistant Staphylococcus aureus (MRSA).
10. A wound dressing, comprising:
any of a medical fabric, a film, and a porous material, or any combination thereof;
electrospun fiberizeable material in at least three adjacent layers of nanofibers, each layer comprising a plurality of aligned nanofibers oriented at oblique angles relative to nanofibers in adjacent layers, said plurality of aligned nanofibers in each layer extending from a first membrane edge to a second membrane edge,
wherein a plurality of aligned nanofibers in each layer cross a plurality of aligned nanofibers in adjacent layers at a plurality of distinct points of intersection, forming a crossing at each distinct point of intersection consisting of three crossing nanofibers extending directionally as six radials from each of said distinct points of intersection,
wherein relative cross-alignment angles between said six radials at each distinct point of intersection are in the range of 50 to 70 degrees, and said relative cross-alignment angles of said aligned nanofibers and spacing between said aligned nanofibers each have a specific average numerical value in said membrane,
wherein said nanofibers further comprise a polymeric material and a chromogenic agent responsive to enzymatic activity, and
wherein said nanofibers further comprise an absorbable and biodegradable polymer that can be enzymatically or nonenzymatically decomposed, yields no toxic decomposition product, and has ability of releasing a drug.
11. The wound dressing of claim 10 , wherein said chromogenic agent is a dye presenting a color change response to said enzymatic activity produced by pathogens present on human skin, in a wound bed, in wound exudate, or in bodily fluid.
12. The wound dressing of claim 11 , wherein said enzymatic activity produces lipase.
13. The wound dressing of claim 11 , wherein said pathogens include at least Proteus mirabilis, Pseudomonas aeruginosa , and methicillin-resistant Staphylococcus aureus (MRSA).
14. The wound dressing of claim 11 , wherein said aligned nanofibers in each said layer comprise at least one of solid, hollow, or core-shell fiber.
15. The wound dressing of claim 10 , wherein said nanofibers comprise any one or combination of poly (lactic-co-glycolic acid) (PLGA), polyvinylpyrrolidone (PVP), poly(ethyleneoxide) (PEO), polyurethane (PU), PVP/cyclodextrin, polyvinyl alcohol (PVA), polycaprolactone (PCL), cellulose, PVP/ethyl cellulose, PVP/zein, cellulose acetate, hydroxypropyl methylcellulose (HPMC), and analogues thereof.
16. The wound dressing of claim 11 , wherein said medical fabric is a woven or non-woven biomedical textile comprising organic or synthetic polymers.
17. The wound dressing of claim 11 , wherein said wound bed comprises any of full and partial thickness burns, ulcerated skin, punctured skin, and traumatized tissue.
18. The wound dressing of claim 11 , wherein said medical fabric and said porous material are absorbent.
19. The wound dressing of claim 18 , wherein said enzymatic activity produces lipase.
20. The wound dressing of claim 19 , wherein said pathogens include at least Proteus mirabilis, Pseudomonas aeruginosa , and methicillin-resistant Staphylococcus aureus (MRSA).