Handheld device for application of nanofiber matrix for wound care
Patent Information
- Authority / Receiving Office
- EP · EP
- Patent Type
- Applications
- Current Assignee / Owner
- MATREGENIX INC
- Filing Date
- 2024-08-15
- Publication Date
- 2026-06-24
AI Technical Summary
Current wound care treatments for severe burn wounds are often painful, require frequent bandage changes, and can lead to extended hospital stays, disfigurement, and disability, especially in lower to middle-income communities where access to proper care is limited.
A handheld device equipped with an electrospinning apparatus that generates a nanofiber matrix for wound dressing and tissue regeneration, allowing for contactless, rapid, and precise application of a nanofiber matrix that is transparent, gentle, and breathable, incorporating antimicrobial agents and biocompatible polymers.
The device enables pain-free or minimally painful wound treatment, accelerates tissue regeneration, reduces the risk of infection, and eliminates the need for traditional wound dressings and skin grafting, making it suitable for use in various settings, including hospitals, ambulances, and emergency situations.
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Figure US2024042587_20022025_PF_FP_ABST
Abstract
Description
HANDHELD DEVICE FOR APPLICATION OF NANOFIBER MATRIX FOR WOUND CARECROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application claims the benefit of U.S. Provisional Patent Application Serial Nos. 63 / 519,839, filed on August 15, 2023, and 63 / 624,280, filed on January 23, 2024, the disclosures of which are hereby incorporated in their entireties herein by reference.BACKGROUNDField of the Invention
[0002] The present disclosure relates to handheld devices for use in wound care.Description of the Related Art
[0003] Severe burn wounds are responsible for about 40,000 injuries requiring hospitalization each year in the United States. See Norbury, W ., et al. “Infection in Burns,” Surg. Infect. (Larchmt), 2016, 17(2), 250-5, doi: 10.1089 / sur.2013.134. It has been estimated that 10-12% of injuries in the military during conflicts are bum injuries. See Stokes, M. A.R., et al. “Burns in the Third World: An Unmet Need,” Ann. Burns Fire Disasters, 2017, 30(4), 243-46. As the bum care industry continues to develop new and better treatments, bum patients are becoming more aware of enhanced and diversified treatment alternatives that minimize the pain and inconvenience of changing bandages or enduring excruciating surgical procedures for skin grafting. Moreover, children under 16 account for approximately 26% of all admissions to bum center hospitals in the United States. See Am. Burn Ass’n, “Scald Statistics and Data Resources,” 2018, 1, available at: https: / / ameribum.org / wp-content / uploads / 2018 / 12 / nbaw2019_statsdataresources_120618-l.pdf.
[0004] Given the pain associated with wound treatment and the importance of a patient remaining still during treatment, a contactless and rapid therapeutic technique is highly desirable. In addition, non-fatal bum wounds contribute to extended hospital stays, disfigurement, and disability. According to the World Health Organization, burns are also a leading cause of loss in disability-adjusted life-years (DALYs) among lower to middle income countries. See Rybarczyk, M.M., et al. “A Systematic Review of Burn Injuries in Low- and Middle-Income Countries: Epidemiology in the WHO-Defined African Region,” Afr. J. Emerg. Med. 2017, 7(1), 30-37, doi:10.1016 / j.afjem.2017.01 .006. In lower to middle-income communities across America, constrained living circumstances and lack of access to rapid emergency responses or proper hospital care creates a risk of delayed treatment. Delayed access to burn wound treatment and emergency surgery increases the likelihood of disfigurement, sepsis, delayed healing, and increased mortality. Therefore, there is a significant need for a portable and easy-to-use wound dressing device that is readily accessible and can be used inside and outside of a hospital, in an ambulance, or at the site of the burn-causing accident.SUMMARY
[0005] The present disclosure describes a handheld device for application of a nanofiber matrix for wound care. In some implementations, the device includes an electrospinning apparatus to generate a nanofiber matrix for wound dressing and tissue regeneration.
[0006] In some implementations, the device may include a ring that is positioned over on in front of a needle or other nozzle used for electrospinning. The ring may be configured to narrow and focus the electrospinning jet, facilitating more accurate targeting of a patient’s wound.
[0007] In some implementations, the device may include a microcontroller that may be used to make real-time adjustments to electrospinning parameters during the electrospinning process.
[0008] In some implementations, the device may include an electro-centrifugal spinning apparatus. The electro-centrifugal spinning apparatus may include a spinneret that is operationally coupled to multiple nozzles for electro-centrifugal spinning. The electro-centrifugal spinning apparatus may further include a rotation arm that causes rotation of the nozzles.BRIEF DESCRIPTION OF THE DRAWINGS
[0009] FIG. 1 shows an embodiment of the disclosed device as an application gun that includes an electrospinning apparatus.
[0010] FIGS. 2A and 2B show embodiments of a ring positioned near the front of a nozzle of an embodiment of the disclosed device from which an electrospinning jet emerges when the device is in use.
[0011] FIG. 3 shows an embodiment of the disclosed electro-centrifugal spinning apparatus.
[0012] FIG. 4 shows a close-up sectional view of the embodiment shown in FIG. 3.
[0013] FIG. 5 shows an embodiment of the disclosed device as an applicator that includes an electrospinning apparatus.
[0014] FIG. 6 shows an example of a set of parameters that are communicatively coupled to a microcontroller, where operating parameters are adjusted algorithmically
[0015] FIG. 7A shows a schematic representation of the configuration of a convergent- divergent nozzle.
[0016] FIG. 7B shows an example of a convergent-divergent nozzle.DETAILED DESCRIPTION
[0017] The present disclosure describes a handheld device for application of an nanofiber matrix for wound care. In some implementations, the device includes an electrospinning apparatus to generate a nanofiber matrix for wound dressing and tissue regeneration. In some alternate implementations, the device uses electrospinning, centrifugal spinning, and electro-centrifugal spinning techniques to generate a nanofiber matrix for wound dressing and tissue regeneration.
[0018] The disclosed device generates a nanofiber matrix that is placed or adhered directly onto target tissues. This facilitates cellular adhesion, proliferation, and tissue regeneration. The handheld design enhances practicality for point-of-care applications, empowering healthcare professionals to administer precise and controlled treatments for tissue engineering and wound healing. The device may be used in regenerative medicine, wound care, and tissue engineering applications. Potential applications include, but are not limited to, treating chronic wounds, surgical interventions, and regenerating damaged tissues and organs.
[0019] In some implementations, a single-use, disposable solution ampule may be used with the device to apply a non-toxic, biocompatible polymer and highly efficacious antimicrobial additives to create a complex force-spun, water-soluble matrix that mimics natural soft tissue physiology on the nano- and cellular scale. The device may preferably apply a coating of a nanofiber matrix on the affected area which is transparent, gentle, and breathable. The nanofiber matrix may preferably incorporate antimicrobial agents. The nanofiber matrix may preferably be applied without contacting the burned tissue. Contactless application of the nanofiber matrix may preferably result in a pain-free or minimal pain treatment. Notably, application of the nanofiber matrix is gauze-free and adhesive-free, and does not require surgery. The application of thenanofiber matrix onto burned tissue may result in improved tissue regeneration and may overcome the painful steps of skin grafting and traditional wound dressing.
[0020] The disclosed device may be used to spray a nanofiber healing matrix onto wounds, mimicking natural skin and accelerating the healing process.
[0021] The device is preferably portable and may preferably be used in uncontrolled environments. This provides significant utility in emergency situations.
[0022] In some implementations, the nanofiber matrix may preferably incorporate one or more antibacterial additives. In some implementations, the one or more antibacterial additives include licorice extract.
[0023] The incorporation of antibacterial additives reduces the risk of infection without painful re-dressing or contact.
[0024] The nanofiber matrix is preferably transparent and lightweight, allowing for easy monitoring of the healing process.
[0025] The disclosed device may be used to apply a nanofiber matrix to the entire body in a single application. In some implementations, the device may be used to treat up to 1.9 m2of surface area in a single application, which corresponds to the entire body surface of an average adult human.
[0026] Use of the disclosed device to apply a nanofiber matrix allows for proper adherence even for hard-to-dress contours. Further, use of the disclosed device to apply a nanofiber matrix enables application of a wound dressing and healing coating that is specifically tailored to the needs of the burn patient with respect to wound size, wound geometry, degree of burning, and other patient-specific parameters without requiring large stocks of dressings of various shapes and sizes.
[0027] FIG. 1 shows an embodiment of the disclosed device that uses an electrospinning apparatus incorporated into a handheld application gun 10. The application gun 10 includes a high voltage power supply 20 having positive and negative electrodes (not labeled), where the positive electrode is operationally connected to a needle 30 via a housing that surrounds the needle (not labeled) and the negative electrode is connected to an external port (not labeled) to which an external ground may be attached. The application gun 10 includes a start button 40 which is used to start and stop the electrospinning process. The application gun 10 includes a voltage regulator 22 that regulates the voltage generated by the high voltage power supply 20. A controller 50 isoperationally connected to a display 52 that allows a user to monitor the voltage and other parameters. A battery 60 provides the necessary power for components that require power. A linear actuator 32 controls release of a solution for electrospinning from a syringe (not shown) that is housed in a syringe holder 34 into the needle 30. The start button 40 is operationally connected to the linear actuator 32.
[0028] The handheld gun design allows for intuitive usage, making the device suitable for various biomedical applications. The ergonomic grip of the handle ensures comfortable operation, while the controls and indicators may be strategically placed for effortless monitoring and adjustment.
[0029] In some implementations, the device uses an electrospinning apparatus that includes a high voltage power supply that generates voltages up to about 25 kV. This allows users to perform electrospinning from a reasonable distance from the application site of the electrospun nanofiber matrix. A user can create a nanofiber matrix without getting too close to the actual burnt tissue, which expands the range of possible applications.
[0030] In some other implementations, the device uses an electrospinning apparatus that includes a high voltage power supply that generates voltages up to about 10 kV. This allows the device to incorporate a smaller power supply and increases portability.
[0031] In some implementations, the electrical voltage output is proportional to the force applied when pressing the start button on the device. This enables a user to adjust the electrospinning intensity based on the pressure applied to the start button. This increases control over and precision of the electrospinning process.
[0032] In some implementations, the device includes an external port to which an external ground may be attached. The external ground may be linked to the patient to enhance safety by preventing unintended charge transfer to the patient during the nanofiber deposition process.
[0033] In some implementations, the device uses an electrospinning apparatus that includes a ring that may be positioned near the front of the needle or other nozzle used for electrospinning. The ring has the same positive charge as the needle or other nozzle. This ring narrows and focuses the electrospinning jet, facilitating more accurate targeting of the patient’s wound. By adjusting the distance between the ring and the tip of the nozzle, it is possible to adjust the width of the electrospinning jet. This adjustability allows a user to balance between focus and coverage, optimizing the balance for the specific application.
[0034] FIGS. 2A and 2B show embodiments of a ring 136 positioned at variable distances from the front of the needle 130 used for electrospinning.
[0035] In some implementations, a blower or heater is positioned exterior to the needle or other nozzle to enable pre-drying of fibers generated before the fibers contact the target. Pre-drying the fibers may cause the electrospun matrix to be more uniform and smooth by eliminating defects caused by residual moisture.
[0036] In some implementations, an ultrasonic or laser sensor is used to measure the spinning distance to allow for dynamic adjustment of the applied voltage. By ensuring the spinning distance remains within the optimal range and automatically shutting off the electric field when deviations beyond the optimal range occur, greater consistency in fiber production may be achieved.
[0037] In some implementations, ultrasonic waves are applied to the needle or other nozzle to facilitate overcoming the surface tension of the solution, leading to a more efficient and productive electrospinning process. Application of ultrasonic waves will not only increase output but also enhance the overall quality of the fibers produced.
[0038] In some alternate implementations, the device includes an electro-centrifugal spinning apparatus. The electro-centrifugal spinning apparatus is integrated into an application gun that is analogous to the application gun described above. The electro-centrifugal spinning apparatus may include a spinneret that is operationally coupled to multiple nozzles for electro-centrifugal spinning. In some implementations, the electro-centrifugal spinning apparatus may be configured to generate an electric field of up to 30 kV to charge the electro-centrifugally spun fibers and direct them toward a desired target. The electro-centrifugal spinning apparatus may further include a rotation arm that causes rotation of the nozzles and controlled ejection of the fibers. A power supply may be included to facilitate the application of an electric field during rotation to enhance fiber adhesion to targeted tissues or another desired target. The electro-centrifugal spinning apparatus may also include a user interface for adjusting rotation parameters, including electric field intensity and rotation speed.
[0039] FIG. 3 shows an embodiment of the disclosed electro-centrifugal spinning apparatus 210. A high voltage input connector 224 is connected to a power supply (not shown) for generating a high voltage during rotation. Multiple nozzles 230 are connected to a spinneret 236. A rotation arm 270 causes the nozzles to rotate around the spinneret when the apparatus is in use. Use of theelectro-centrifugal spinning apparatus generates multiple jets 290 for placement or adhesion onto a desired target.
[0040] In some implementations, the rotation arm may be controlled to adjust the spin rate across the multiple nozzles. The adjustable rotation speed precisely guides a polymer solution into the openings through centrifugal force. In addition, the fibers are charged via application of high voltage, facilitated by the rotated droplet shape of the polymer solution as it emerges from the nozzle. This allows breaking of the surface tension of the solution, significantly amplifying both the capacity and production efficiency of nanofibers.
[0041] FIG. 4 shows a close-up sectional view of the embodiment shown in FIG. 3, illustrating how a polymer solution being spun will be affected by rotation of the rotation arm when the polymer solution exits a nozzle.
[0042] By combining the precise control provided by electrospinning with the increased throughput provided by centrifugal spinning, the electro-centrifugal spinning apparatus allows for precise, efficient delivery of a nanofiber matrix to a desired target.
[0043] The nozzles are guiding modules for desired polymer matrices to coat the target surface and construct layered matrices. In implementations with multiple nozzles, the disclosed application gun has at least two integrated chambers. At least one chamber may be used for spinning a polymer solution and at least one chamber may be used for applying a suspension. The disclosed application gun may be used to apply both the suspension and the polymer solution simultaneously to construct layered matrices of suspension / polymer on the applied surfaces or apply the suspension and polymer solutions separately to provide an initial layer of polymer and a subsequent layer of the suspension. Both processes may be used repeatedly to achieve multilayered structures to build a desired thickness. This offers flexibility in constructing a desired matrix using different polymers and suspensions.
[0044] FIG. 5 shows an embodiment of the disclosed device that uses an electrospinning apparatus incorporated into a handheld applicator 310. The applicator 310 includes a high voltage power supply 320 having positive and negative electrodes (not labeled), where the positive electrode is operationally connected to a needle (not labeled) via a housing that surrounds the needle (not labeled) and the negative electrode is connected to an external port (not labeled) to which an external ground may be attached. The applicator 310 includes a switch 340 which is used to start and stop the electrospinning process by turning the power supply 320 on or off. Theapplicator 310 includes a voltage regulator (not labeled) that regulates the voltage generated by the high voltage power supply 320. A battery 360 provides the necessary power for components that require power. A battery charger and external power supply 324 is used to charges the battery and provide power to the circuit. A microcontroller 351 is operationally connected to a display 352 that allows a user to monitor the voltage, flow rate, battery status, and other parameters, and is also operationally connected to other components of the device to allow the user to control operating parameters. A linear actuator 332 controls release of a solution for electrospinning from a syringe 333 that is housed in a syringe holder (not labeled) into the needle. A directional ring 336 positioned near the front of the needle that has the same positive charge as the needle allows narrowing and focusing of the electrospinning jet. A step motor driver 337 provides mechanical control to actuate linear actuator 332. Microswitches 338 and 339 are operationally connected to the step motor driver 337 to provide for left and right adjustments thereof, respectively. A system switch 345 is used to turn the device on or off.
[0045] In some implementations, the device includes a microprocessor that is used to adjust operating parameters algorithmically. FIG. 6 shows an example of a set of parameters that are communicatively coupled to a microcontroller, where operating parameters are adjusted algorithmically. In some implementations, only a subset of the data inputs shown in FIG. 6 are used. In an illustrative implementation, the operating voltage and linear actuator are modulated by the measured voltage, the age of the polymer solution in the formulation ampule, and formulation calibration data through an algorithm that enables optimal performance. In some implementations, the polymer solution data is encoded via a bar code or QR code, while in other implementations the ampule is communicatively coupled to the microcontroller by, for example, an EEPROM or other non-volatile memory source.
[0046] In some implementations, the device includes a laser-enabled nanofiber thickness detection system. The thickness detection system enhances the precision and consistency of the nanofiber deposition process. A laser interacts with the nanofiber layer and measures the reflection, refraction, and interference patterns, enabling the system to accurately determine the thickness of the layer in real time. This not only ensures optimal nanofiber deposition but also allows for immediate adjustments, optimizing both quality and efficiency in application of the wound dressing.
[0047] In some implementations, the device includes a convergent-divergent nozzle. FIG. 7A shows a schematic representation of the configuration of a convergent-divergent nozzle. FIG. 7B shows an example of a convergent-divergent nozzle. The convergent-divergent nozzle is shaped to promote a polymer solution therein to adopt a cone shape.
[0048] In some implementations, the device is capable of being operated by user when the device is held by the user with one hand.
[0049] The polymer solution used for electrospinning or electro-centrifugal spinning may be a water or ethanol-based formulation that includes one or more of the polymer materials selected from the group consisting of polyvinyl alcohol (PVA), polyvinyl butyral (PVB), chitosan, collagen, hyaluronic acid (HA), B-silk, or a blend of any combination thereof. The formulation may further include an herbal extract that has antimicrobial properties, preferably licorice extract. The formulation may alternately or additionally include other biologies. The formulation may also further include antibiotics, painkillers, and / or other drugs.
[0050] By blending antimicrobials, antibiotics, painkillers, and / or other drugs or other biologies with the polymer solution, the nanofiber matrix generated may directly incorporate biologies for enhanced wound healing.
[0051] Biologies included in the polymer solution may include autologous or allogenic cell suspensions, including keratinocytes for epidermis regeneration, dermal fibroblasts for new extracellular matrix protein deposition, and / or melanocytes for natural pigmentation restoration. Biologies may additionally or alternately include platelet-rich plasma (PRP).
[0052] In some implementations, biologies may be blended with the polymer formulation in a single step, thereby allowing the biologies to be seamlessly incorporated into the nanofibers as they are spun. This method of blending will ensure a more uniform and effective distribution of the biologies within the nanofiber matrix, potentially improving the healing properties thereof. This single-step integration may streamline the process of including biologies in the nanofiber matrix, making it more efficient and potentially more effective in wound healing applications.
[0053] In some implementations, biologies may alternately be blended via sequential layering, where the disclosed device will sequentially apply multiple layers of material incorporating biologies and nanofibers. This may be achieved by having an additional nozzle for spraying biological substances (cells or PRP), followed by nanofiber spinning, and repeating the process as necessary.
[0054] In some implementations, biologies may alternately be applied using a different device, such as a syringe, if integration with the disclosed spinning device is not feasible.
[0055] In some implementations, the polymer solution may be used to deliver a non-toxic, non-reactive, and sustainable cosmetic PVA-based nanofiber matrix. The dissolution of PVA depends on solvent, temperature, and the extent of hydrolysis within the polymer. Additionally, solution parameters such as solution concentration, molecular weight, pH, salt, and surfactant molecules affect the morphology and diameter of electrospun PVA nanofibers. Thus, a series of PVA polymers (5-10% wt%) with selected molecular weight and degree of hydrolysis (60-99.9%), along with surfactants such as polyvinylpyrrolidone (PVP) and polysorbate, may be dissolved in a series of solvents such as water and water / ethanol mixtures (1 / 1, 2 / 1, and 3 / 1) to generate a PVA- based nanofiber matrix for cosmetic applications. Various active ingredients such as collagen peptides, vitamin A, and vitamin C, may also be blended into the polymer solution prior to spinning.Example
[0056] Licorice Extract Preparation. Licorice powder was mixed with a solvent consisting of ethanol and water in a 1 : 1 ratio, with a weight ratio of 1:3 powder / solvent. The mixture was placed in a sealed container and stirred continuously for 5 hours at ambient temperature, ensuring regular agitation to maximize the extraction of active compounds such as glycyrrhizin and flavonoids. Post-extraction, the mixture was filtered to separate the liquid extract from the solid residues, yielding a crude licorice extract. A rotary evaporator was used under reduced pressure to concentrate the liquid extract, resulting in a thick, concentrated extract.
[0057] Formulation / Solution Preparation. Polyvinyl alcohol (PVA) was dissolved in a water / ethanol mixture at a concentration of 9% wt / v with an 80:20 ratio at ambient temperature. To this solution, licorice extract prepared as described above was added at 0.1% wt / v, followed by the addition of phosphate-buffered saline (PBS) at 0.05% wt. / v. The entire mixture was then stirred on a magnetic stir plate for two hours to ensure homogeneity.
[0058] Electrospinning using Handheld Applicator. The prepared solution was loaded into a 5 mL syringe, which was then inserted into a handheld applicator. The applicator included a ring positioned to allow the syringe needle to be inserted through the ring, and 5 mm of the needle toextend beyond the ring. Electrospinning was performed at a flow rate of 500 pL / min, an applied voltage of 10 kV, and a distance of 10 cm between the applicator and the target surface.
[0059] In a typical electrospinning setup, a high voltage (typically above 15 kV is required to overcome the surface tension of the polymer solution and initiate spinning. Achieving such high voltage in a compact, handheld device is challenging, as a larger power supply must be used to generate higher voltages. A 10 kV power supply is generally insufficient for electrospinning, particularly with water-based solutions due to their low conductivity and low volatility, as these are critical parameters for successful electrospinning.
[0060] The example above shows successful electrospinning at a voltage of 10 kV. This was possible due to synergistic effects of the electrospinning parameters used, namely increased volatility of the solution generated by the addition of ethanol, increased conductivity generated by the use of PBS, and focusing of the electric field by use of a positively-charged ring. This approach allows for effective electrospinning in a handheld device at a reduced voltage, solving the key challenge of miniaturizing the power supply required while maintaining functionality.
[0061] Other experiments were carried out under similar conditions, without the use of PBS or ethanol and using a higher voltage of 25 kV during electrospinning. These handheld electrospinning devices required a larger power supply and therefore the devices were larger overall.Numbered Examples
[0062] Example 1. A method of applying a nanofiber matrix to a wound composed of electrospinning a polymer solution using a handheld electrospinning device to generate a nanofiber matrix, where the polymer solution includes: a. polyvinyl alcohol; b. licorice extract; c. phosphate-buffered saline; d. water; and e. ethanol; and where electrospinning is performed using an applied voltage of about 10 kV.
[0063] Example 2. A device for application of an electrospun nanofiber matrix to a wound that includes: a. a power supply; b. a syringe that includes a needle; anda microcontroller; where the power supply is operationally connected to the needle, where the microcontroller is configured to allow real-time adjustment of electrospinning parameters, and where the device may be operated by a user using one hand to hold the device.
[0064] Example 3. The device of Example 2 further including a ring positioned around or in front of the needle.
[0065] Example 4. The device of Example 3, where the ring is positioned around the needle.
[0066] Example 5. The device of Example 3, where the ring is positioned in front of the needle
[0067] Example 6. The device of any of Examples 3-5, where the ring is composed of a metal.
[0068] Example 7. A device for application of an electrospun nanofiber matrix to a wound that includes: a. a power supply; b. a syringe that includes a needle; c. a ring positioned around or in front of the needle; anda microcontroller; where the power supply is operationally connected to the needle, and where the device may be operated by a user using one hand to hold the device.
[0069] Example 8. The device of Example 7, where the ring is positioned around the needle.
[0070] Example 9. The device of Example 7, where the ring is positioned in front of the needle.
[0071] Example 10. A device for application of an electrospun nanofiber matrix to a wound that includes:a power supply; b. an electro-centrifugal spinning apparatus; and c. a microcontroller;where the power supply is operationally connected to the electro-centrifugal spinning apparatus, and where the device may be operated by a user using one hand to hold the device.
[0072] Example 11. The device of Example 10, where the electro-centrifugal spinning apparatus includes a spinneret that is operationally coupled to multiple nozzles for electrocentrifugal spinning.
[0073] Example 12. The device of Example 11, where the electro-centrifugal spinning apparatus further includes a rotation arm that enables rotation of the nozzles.
[0074] Example 13. The device of any of Examples 10-12, where the microcontroller is configured to allow real-time adjustment of electrospinning parameters.
[0075] The previous description of the disclosed embodiments is provided to enable any person skilled in the art to make or use the invention disclosed herein. Although the various inventive aspects are disclosed in the context of certain illustrated embodiments, implementations, and examples, it should be understood by those skilled in the art that the invention extends beyond the specifically disclosed embodiments to other alternative embodiments and / or uses of the invention and obvious modifications and equivalents thereof. In addition, while a number of variations of various inventive aspects have been shown and described in detail, other modifications that are within their scope will be readily apparent to those skilled in the art based upon reviewing this disclosure. It should be also understood that the scope of this disclosure includes the various combinations or sub-combinations of the specific features and aspects of the embodiments disclosed herein, such that the various features, modes of implementation, and aspects of the disclosed subject matter may be combined with or substituted for one another. The generic principles defined herein may be applied to other embodiments without departing from the spirit or scope of the disclosure. Thus, the present disclosure is not intended to be limited to the embodiments shown herein but is to be accorded the widest scope consistent with the principles and novel features disclosed herein.
[0076] Each of the foregoing and various aspects, together with those summarized above or otherwise disclosed herein, including the figures, may be combined without limitation to form claims for a device, apparatus, system, method of manufacture, and / or method of use.
[0077] All references cited herein are hereby expressly incorporated by reference.
Claims
CLAIMSWhat is claimed is:
1. A method of applying a nanofiber matrix to a wound comprising electrospinning a polymer solution using a handheld electrospinning device to generate a nanofiber matrix, wherein the polymer solution comprises: a. polyvinyl alcohol; b. licorice extract; c. phosphate-buffered saline; d. water; and e. ethanol; and wherein electrospinning is performed using an applied voltage of about 10 kV.
2. A device for application of an electrospun nanofiber matrix to a wound comprising: a. a power supply; b. a syringe that includes a needle; and c. a microcontroller; wherein the power supply is operationally connected to the needle, wherein the microcontroller is configured to allow real-time adjustment of electrospinning parameters, and wherein the device may be operated by a user using one hand to hold the device.
3. The device of Claim 2 further comprising a ring positioned around or in front of the needle.
4. The device of Claim 3, wherein the ring is positioned around the needle.
5. The device of Claim 3, wherein the ring is positioned in front of the needle.
6. The device of any of Claims 3-5, wherein the ring is composed of a metal.
7. A device for application of an electrospun nanofiber matrix to a wound comprising: a. a power supply; b. a syringe that includes a needle; c. a ring positioned around or in front of the needle; and d. a microcontroller; wherein the power supply is operationally connected to the needle, and wherein the device may be operated by a user using one hand to hold the device.
8. The device of Claim 7, wherein the ring is positioned around the needle.
9. The device of Claim 7, wherein the ring is positioned in front of the needle.
10. A device for application of an electrospun nanofiber matrix to a wound comprising: a. a power supply; b. an electro-centrifugal spinning apparatus; and c. a microcontroller; wherein the power supply is operationally connected to the electro-centrifugal spinning apparatus, and wherein the device may be operated by a user using one hand to hold the device.
11. The device of Claim 10, wherein the electro-centrifugal spinning apparatus comprises a spinneret that is operationally coupled to multiple nozzles for electro-centrifugal spinning.
12. The device of Claim 11, wherein the electro-centrifugal spinning apparatus further comprises a rotation arm that enables rotation of the nozzles.
13. The device of any of Claims 10-12, wherein the microcontroller is configured to allow real-time adjustment of electrospinning parameters.