Embodiments disclosed herein relate, in general, to a medical device and, more particularly, to a medical device having a multi-needle assembly.
Changes in environment have adverse effect on human health. The polluted air we breathe or exposure to UV radiations put humans at a higher risk of health issues such as, damage or loss of skin/tissues. Further, these health issues can alter tissue structures and/or functions which may further result in skin laxity, tightness, hair loss, etc. Several available medical tools facilitate delivery of aesthetic, and/or therapeutic compounds or formulations directly into the layers of the skin to overcome such tissue/skin conditions. However, such medical tools are not effective to overcome and/or reduce the tissue/skin disorders. For example, conventional micro needling treatment applies a patient's own plasma to the skin and then performs the micro needling to the skin, for example, facial skin, to have the serum penetrate the skin. In addition, these conventional devices attempt to infuse target areas of the skin such as, face and scalp, with concentrated stem cells, collagen and growth hormone extracted from the patient's own blood. However, these micro needling causes multiple facial punctures to stimulate plasma growth by damaging the superficial layers of the skin. These micro needling tools and its usage for treatments of skin/tissue disorders are not effective because the punctures in the superficial layers of the skin cause bleeding out to the surface. In addition, these micro needling tools do not penetrate plasma into the dermis and epidermis of a patient.
Moreover, conventional needle platform tools have a limited number of needles, for example, five or seven needles on the head to inject mesotherapy medications in order to dissolve fat. In addition, the platform space between needles are too distant, which is not beneficial for injecting plasma for skin and scalp injections. These needles are too long and thick (0.5 inches long & 27 gauge thick) to be used effectively for infiltrating epidermis of the skin with PRP (platelet rich plasma), hyaluronic acid and/or anti-inflammatory steroid.
Accordingly, it is desired to provide an improved medical tool for treatment of skin/tissue disorders and hair loss.
Embodiments of the present invention are directed to a medical device for the intracellular delivery of a therapeutic formulation to a predetermined site within a patient, according to an embodiment of the present invention. The medical device comprising a needle hub assembly such that the needle hub assembly is attached to a distal end of a syringe, the needle hub assembly comprising a hollow body; a platform; and a needle hub, wherein the needle hub comprising a plurality of needles disposed on the platform arranged in a predefined needle array, wherein the plurality of needles closely spaced, which and are inserted into the predetermined site within the patient for delivering the therapeutic formulation.
Embodiments of the present invention are directed to a medical device for the intracellular delivery of a therapeutic formulation to a predetermined site within a patient' skin and/or a scalp, according to an embodiment of the present invention. The medical device comprising a needle hub assembly such that the needle hub assembly is connected to a distal end of a syringe, the needle hub assembly comprising a hollow body; a platform; and a needle hub, wherein the needle hub comprising a plurality of needles disposed on the platform arranged in a linear pattern sequence, wherein the plurality of needles closely spaced, which are inserted into the predetermined site within the patient for delivering the therapeutic formulation.
Embodiments of the present invention are directed to a medical device for the intracellular delivery of a therapeutic formulation to a predetermined site within a patient, according to an embodiment of the present invention. The medical device comprising a needle hub assembly such that the needle hub assembly is connected to a distal end of a syringe, the needle hub assembly comprising a hollow body; a platform; and a needle hub, wherein the needle hub comprising a plurality of needles disposed on the platform arranged in a concentric circular pattern sequence, wherein the plurality of needles closely spaced and are inserted into the predetermined site within the patient for delivering the therapeutic formulation.
Embodiments of the present invention are directed to significantly reduce time, minimizing pain, and increasing medical formulation absorption efficiency to maximize effectiveness of treatment.
Embodiments in accordance with the present invention provide a medical device for a treatment of skin/tissue such as, skin lifting, reducing skin laxity, skin tightening, stimulate healthier follicles that produces firmer hair, etc.
Embodiments in accordance with the present invention further provide a medical device to inject ‘Platelet Rich Plasma” (PRP) into the epidermis in order to treat fine lines and wrinkles.
Embodiments in accordance with the present invention further provide a medical device having the needle hub assembly that comprises closely packed needles arranged in multiple rows and columns.
Embodiments in accordance with the present invention further provide a medical device having the needle hub assembly that comprises 16 closely packed needles arranged in a concentric circular pattern sequence.
Embodiments in accordance with the present invention further provide a medical device having the needle hub assembly that comprises 16 closely packed needles arranged in a linear pattern sequence.
Embodiments of the present invention may provide a number of advantages depending on its particular configuration. It is an object of the present invention to provide a medical device that may be effective in injecting medical formulations into the skin infusing the epidermis or dermis with Platelet Rich Plasma (PRP) proportional. Furthermore, the disclosed medical device comprises a plurality of needles in a small area that may be beneficial for injecting plasma for skin and scalp injections, infusing, penetrating the PRP into a targeted area only.
These and other advantages will be apparent from the present application of the embodiments described herein. The preceding is a simplified summary to provide an understanding of some embodiments of the present invention. This summary is neither an extensive nor exhaustive overview of the present invention and its various embodiments. The summary presents selected concepts of the embodiments of the present invention in a simplified form as an introduction to the more detailed description presented below. As will be appreciated, other embodiments of the present invention are possible utilizing, alone or in combination, one or more of the features set forth above or described in detail below.
The foregoing and other aspects of the embodiments disclosed herein are best understood from the following detailed description when read in connection with the accompanying drawings. For the purpose of illustrating the embodiments disclosed herein, there is shown in the drawings embodiments that are presently preferred, it being understood, however, that the embodiments disclosed herein are not limited to the specific instrumentalities disclosed. Included in the drawings are the following figures:
While embodiments of the present invention are described herein by way of example using several illustrative drawings, those skilled in the art will recognize the present invention is not limited to the embodiments or drawings described. It should be understood the drawings and the detailed description thereto are not intended to limit the present invention to the particular form disclosed, but to the contrary, the present invention is to cover all modification, equivalents and alternatives falling within the spirit and scope of embodiments of the present invention as defined by the appended claims.
The headings used herein are for organizational purposes only and are not meant to be used to limit the scope of the description or the claims. As used throughout this application, the word “may” is used in a permissive sense (i.e., meaning having the potential to), rather than the mandatory sense (i.e., meaning must). Similarly, the words “include”, “including”, and “includes” mean including but not limited to. To facilitate understanding, like reference numerals have been used, where possible, to designate like elements common to the figures.
Embodiments of the present invention will be described below in conjunction with exemplary medical equipment. Embodiments of the present invention are not limited to any particular type of medical equipment. Those skilled in the art will recognize the disclosed techniques may be used in any medical equipment in which it is desirable to inject medication in the layers of skin of a patient.
The phrases “at least one”, “one or more”, and “and/or” are open-ended expressions that are both conjunctive and disjunctive in operation. For example, each of the expressions “at least one of A, B and C”, “at least one of A, B, or C”, “one or more of A, B, and C”, “one or more of A, B, or C” and “A, B, and/or C” means A alone, B alone, C alone, A and B together, A and C together, B and C together, or A, B and C together.
The term “a” or “an” entity refers to one or more of that entity. As such, the terms “a” (or “an”), “one or more” and “at least one” can be used interchangeably herein. It is also to be noted that the terms “comprising”, “including”, and “having” can be used interchangeably.
Further, the proximal end 114 of the plunger 102 may include a thumbpress 118, in an embodiment of the present invention. The thumbpress 118 may be configured to push and/or pull the plunger 102 for receiving and/or injecting medical formulations at a predetermined site within a patient. In an embodiment of the present invention, the predetermined site within a patient may be, but not limited to, a skin, a scalp, and so forth. In an embodiment of the present invention, the plunger 102 may be made up of plastic. Embodiments of the present invention are intended to include or otherwise cover any material for the plunger 102, the plunger rod 112, and the thumbpress 118 including known, related art, and/or later developed technologies that may be beneficial to provide a robust structure.
Further, the distal end 116 of the plunger 102 may comprise the plunger piston 104. In an embodiment of the present invention, the plunger piston 104 may be removably attached to the distal end 116 of the plunger 102. The plunger piston 104 may be made up of, but not limited to, an elastomeric material. Embodiments of the present invention are intended to include or otherwise cover any material for the plunger piston 104 including known, related art, and/or later developed technologies. Furthermore, the plunger piston 104 may comprise a small opening such that the opening may be beneficial for the removal of air from the barrel 106 when the medical device 100 is in use.
Further, the barrel 106 may have a proximal end 120, a distal end 122 and a chamber 124, according to an embodiment of the present invention. The plunger 102 of the medical device 100 may be linearly pulled and/or pushed between the proximal end 120 and the distal end 122 within the barrel 106. The plunger piston 104 may be dimensioned to be frictionally slidable along an inner wall of the barrel 106. Further, the chamber 124 between the proximal end 120 and the distal end 122 of the barrel 106 may be used to retain medical formulations and/or other fluids. In an embodiment of the present invention, the chamber 124 may retain liquids such as, but not limited to, blood that is pulled out from a patient, medical formulations to be injected into the body of the patient, and so forth. In an embodiment of the present invention, the medical device 100 may comprise a measuring scale on the outer wall of the chamber 124 between the proximal end 120 and the distal end 122. The measuring scale may be used to measure the amount of the medical formulation in the chamber 124, in an embodiment of the present invention.
In an embodiment of the present invention, when the plunger 102 is pulled towards the proximal end 120 within the barrel 106, the medical formulation may be drawn into the chamber 124 of the barrel 106 of the medical device 100 from a medical container (not shown). In another embodiment of the present invention, when the plunger 102 is pushed from the proximal end 120 towards the distal end 122 within the barrel 106, the medical formulation may be pushed out from the chamber 124 of the barrel 106 of the medical device 100. The barrel 106 may be made up of, but is not limited to, plastic, glass, and so forth, in an embodiment of the present invention. Embodiments of the present invention are intended to include or otherwise cover any material for the barrel 106 including known, related art, and/or later developed technologies that may be beneficial to retain medical formulations. In one embodiment of the present invention, the medical formulation may be in a liquid form, which may be used to treat skin and/or tissue disorders in a patient.
According to an embodiment of the present invention, the proximal end 120 of the barrel 106 may comprise a finger flange 126. In another embodiment of the present invention, the finger flange 126 may be pre-fabricated along any portion of the barrel 106, or may be a separate component that is connected to or affixed to the barrel 106. The finger flange 126 may be configured to provide an interface for holding the medical device 100 while depressing the plunger 102 for injection of the medical formulation in the patient. Embodiments of the present invention are intended to include or otherwise cover any shape, size, and material for the finger flange 126 including known, related art, and/or later developed technologies.
Further, the distal end 122 of the barrel 106 may comprise a tip 128, according to an embodiment of the present invention. The tip 128 may be utilized to attach a needle hub assembly 108 with the barrel 106. In an embodiment of the present invention, the tip 128 may comprise a threaded male part (not shown) to receive the needle hub assembly 108. In another embodiment of the present invention, a luer locking arrangement (not shown) may be used such that the needle hub assembly 108 may be coupled with the barrel 106 just prior to use.
Further, the needle hub assembly 108 may comprise a plurality of needles 130, in an embodiment of the present invention. The needle hub assembly 108 may comprise an opening 132 to pass the medical formulation from the barrel 106 of the syringe 101 to the plurality of needles 130. The plurality of needles 130 may be disposed on a platform 134 of the needle hub assembly 108. In an embodiment of the present invention, the platform 134 of the needle hub assembly 108 may be, but is not limited to, a square platform. In another embodiment of the present invention, the platform 134 of the needle hub assembly 108 may be a circular platform. Embodiments of the present invention are intended to include or otherwise cover any shape for the platform 134 including known, related art, and/or later developed technologies. According to an embodiment of the present invention, the platform 134 may be but is not limited to, a flat platform.
In an embodiment of the present invention, each of the plurality of needles 130 may comprise an outlet (not shown) at a proximal end of the needle to receive the therapeutic formulation from the barrel 106. Further, each of the plurality of needles 130 comprising an opening at a distal end of the needle to deliver the therapeutic formulation at the predetermined site of a patients' skin or scalp. The plurality of needles 130 may be arranged in a multiple row and multiple column needle array 136 arranged on the platform 134. In an embodiment of the present invention, the plurality of needles 130 are arranged in a concentric circular pattern sequence. In another embodiment of the present invention, the plurality of needles 130 are arranged in a linear pattern sequence.
In one embodiment of the present invention, the needle array 136 may include 16 needles. In another embodiment, the needle array 136 may include any number of needles that may be beneficial, for example, to inject medical formulations such as, but not limited to, “Platelet Rich Plasma” in the epidermis of a patient simultaneously through the plurality of needles 130. In an embodiment of the present invention, the plurality of needles 130 may be placed in a 4×4 needle array on the platform 134. In a further embodiment of the present invention, the plurality of needles 130 may be placed in a 2×8 needle array on the platform 134. Further, the needle array 136 may be a disposable needle array, in one embodiment of the present invention. In another embodiment of the present invention, the needle array 136 may be a re-usable needle array.
Further, the needle cap 110 may be provided to seal the medical device 100 filled with the medical formulation or other liquid before storing and/or moving the medical device 100. In an embodiment of the present invention, the needle cap 110 may be made up of, but is not limited to, rigid plastic or other material known to person skilled in the art. According to an embodiment of the present invention, the shape of the needle cap 110 may be, but is not limited to a square or a circle. According to an embodiment of the present invention, the shape of the needle cap 110 may be, but not limited to, as per the shape of the needle hub assembly 108.
Further, the platform 406 may comprises a plurality of grooves 414 for accepting a plurality of needles 408. According to an embodiment of the present invention, the plurality of grooves 414 may be arranged in a 4×4 needle array sequence, and/or a linear pattern sequence. Further, the plurality of grooves 414 may be arranged in a 2×8 needle array sequence, and/or a linear pattern sequence, according to another embodiment of the present invention. According to an exemplary embodiment of the present invention, the plurality of grooves 414 may be arranged in a concentric circular pattern sequence. Furthermore, the grooves 414 may comprise an outlet 416. The outlet 416 may communicate with the barrel 106 of the syringe 101 to receive the medical formulation from the barrel 106 and transmit the medical formulation at a predetermined site of a patient from the opening of each of the plurality of needles 408 through the outlet 416.
Further, the needle hub assembly 306 comprises the lock 412 at the proximal end 400 of the needle hub assembly 306. In one embodiment of the present invention, the lock 412 may be, but is not limited to, a luer lock. In another embodiment of the present invention, the lock 412 may be any other lock that may be beneficial to attach the syringe 301 (not shown) of the medical device 100 to the needle hub assembly 306 of the medical device 100. More specifically, the lock 412 may attach the needle hub assembly 306 with the tip 128 (not shown) of the barrel 106 of the syringe 301 (not shown).
(PRP), hyaluronic acid and/or anti-inflammatory steroid. The needles may be arranged in a 4×4 array on the platform 700, in one embodiment. The platform 700 may be a 16 needle platform that may be disposable and screwed onto the medical device 100 to inject, for example, platelet rich plasma (PRP) in square footprints into the epidermis and dermis of the face, skin, and or scalp. The grooves 702 may be 0.0625 inch apart, in one embodiment of the present invention. In another embodiment of the present invention, a distance between the grooves 702 may be in a range of 0.055 inches to 0.075 inches. The needles may be closely placed to insure that the target area is properly infiltrated for best results. In one embodiment of the present invention, short 31 gauge needles may be used to infuse small areas such as crow's feet with PRP to regenerate healthy skin growth. In another embodiment of the present invention, slightly longer 30 gauge needle heads may be used to infiltrate underlying dermis to regenerate healthy deeper tissue growth. The medical device 100 with 16 needles head of 30 gauge needles may be used to inject the scalp to revitalize weak and dormant hair follicles to stimulate healthy hair growth.
Further, the platform 1206 may comprises a plurality of grooves 1214 for accepting the plurality of needles 1208. According to an embodiment of the present invention, the plurality of grooves 1214 may be arranged in a concentric circular pattern sequence. Furthermore, each of the plurality of grooves 1214 may comprise an outlet 1216. The outlet 1216 may communicate with the barrel 1104 of the medical device 1100 to receive the medical formulation from the barrel 1104 and transmit the medical formulation at a predetermined site of a patient from the opening of each of the plurality of needles 1208 through the outlet 1216.
Further, the needle hub assembly 1106 comprises the lock 1212 at the proximal end 1200 of the needle hub assembly 1106. In one embodiment of the present invention, the lock 1212 may be, but is not limited to, a luer lock. In another embodiment of the present invention, the lock 1212 may be any other lock that may be beneficial to attach the syringe 1101 of the medical device 1100 to the needle hub assembly 1106 of the medical device 1100. More specifically, the lock 1212 may attach the needle hub assembly 1106 with the tip (not shown) of the barrel 1104 of the syringe 1101.
Although the invention has been described with reference to exemplary embodiments, it is not limited thereto. Those skilled in the art will appreciate that numerous changes and modifications may be made to the preferred embodiments of the invention and that such changes and modifications may be made without departing from the true spirit of the invention. It is therefore intended that the appended claims be construed to cover all such equivalent variations as fall within the true spirit and scope of the invention.
The exemplary embodiments of this present invention have been described in relation to medical equipment. However, to avoid unnecessarily obscuring the present invention, the preceding description omits a number of known structures and devices. This omission is not to be construed as a limitation of the scope of the present invention. Specific details are set forth by use of the embodiments to provide an understanding of the present invention. It should however be appreciated that the present invention may be practiced in a variety of ways beyond the specific embodiments set forth herein.
A number of variations and modifications of the present invention can be used. It would be possible to provide for some features of the present invention without providing others.
The present invention, in various embodiments, configurations, and aspects, includes components, methods, processes, systems and/or apparatus substantially as depicted and described herein, including various embodiments, sub-combinations, and subsets thereof. Those of skill in the art will understand how to make and use the present invention after understanding the present disclosure. The present invention, in various embodiments, configurations, and aspects, includes providing devices and processes in the absence of items not depicted and/or described herein or in various embodiments, configurations, or aspects hereof, including in the absence of such items as may have been used in previous devices or processes, e.g., for improving performance, achieving ease and/or reducing cost of implementation.
The foregoing discussion of the present invention has been presented for purposes of illustration and description. It is not intended to limit the present invention to the form or forms disclosed herein. In the foregoing Detailed Description, for example, various features of the present invention are grouped together in one or more embodiments, configurations, or aspects for the purpose of streamlining the disclosure. The features of the embodiments, configurations, or aspects may be combined in alternate embodiments, configurations, or aspects other than those discussed above. This method of disclosure is not to be interpreted as reflecting an intention the present invention requires more features than are expressly recited in each claim. Rather, as the following claims reflect, inventive aspects lie in less than all features of a single foregoing disclosed embodiment, configuration, or aspect. Thus, the following claims are hereby incorporated into this Detailed Description, with each claim standing on its own as a separate embodiment of the present invention.
Moreover, though the description of the present invention has included description of one or more embodiments, configurations, or aspects and certain variations and modifications, other variations, combinations, and modifications are within the scope of the present invention, e.g., as may be within the skill and knowledge of those in the art, after understanding the present disclosure. It is intended to obtain rights which include alternative embodiments, configurations, or aspects to the extent permitted, including alternate, interchangeable and/or equivalent structures, functions, ranges or steps to those claimed, whether or not such alternate, interchangeable and/or equivalent structures, functions, ranges or steps are disclosed herein, and without intending to publicly dedicate any patentable subject matter.
This application claims the benefit of U.S. Provisional Application Ser. No. 62/781,225 filed Dec. 18, 2018, entitled “Medical Tool Having Needle Hub”, which is incorporated herein by reference in its entirety.
Number | Date | Country | |
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62781225 | Dec 2018 | US |