COMPOSITION FOR REMOVING NOISE FROM MRI AND PAD USING THE SAME
20210132172 · 2021-05-06
Assignee
Inventors
Cpc classification
A61B5/055
HUMAN NECESSITIES
International classification
G01R33/565
PHYSICS
A61B5/00
HUMAN NECESSITIES
Abstract
Provided are a composition for removing noise from an MRI, including a compound having a hydrogen bond, and a pad using the same, wherein the composition is applied in a non-invasive way causing no side effects in the human body, the composition is not toxic and thus is safe, the composition is used in the manner of covering an area requiring diagnosis or being attached to an MRI apparatus, and thus has the advantages of improving images of a relatively wide range, and obtaining more accurate image information than restoration of a distorted image by a program, and the composition is expected to be easily commercialized by companies because the costs required to manufacture the composition are low.
Claims
1. A composition for removing noise from an MRI image, comprising: a compound having a functional group capable of hydrogen bonding.
2. The composition according to claim 1, wherein the composition improves the quality of an MRI image.
3. The composition according to claim 1, wherein the compound is one or more selected from the group consisting of water (H.sub.2O), amyl alcohol (C.sub.5H.sub.11OH), butyl alcohol (CH.sub.3CH.sub.2CH.sub.2OH), ethanol (C.sub.2H.sub.5OH), methyl alcohol (CH.sub.3OH), ethylene glycol (OHCH.sub.2CH.sub.2OH), formaldehyde (HCHO), nitrobenzene (C.sub.6H.sub.5NO.sub.2), propylene glycol (OH(CH.sub.2).sub.3H), hydrogen peroxide (H.sub.2O.sub.2), acetic acid (CH.sub.3COOH), acetic anhydride (C.sub.4H.sub.6O.sub.3), butanic acid (C.sub.3H.sub.7COOH), benzenesulfonic acid (C.sub.6H.sub.5SO.sub.3H), benzoic acid (C.sub.6H.sub.5COOH), chromic acid (H.sub.2CrO.sub.4), citric acid (C.sub.6H.sub.8O.sub.7H.sub.2O), hexafluorosilicic acid (H.sub.2SiF.sub.6), fluoroboric acid (HBF.sub.4), formic acid (HCOOH), hydrochloric acid (HCl), hydrocyanic acid (HCN), hydrofluoric acid (HF), hypochlorous acid (HClO), lactic acid (CH.sub.3CHOHCOOH), maleic acid ((CHOOH).sub.2), nitric acid (HNO.sub.3), oleic acid (C.sub.18H.sub.34O.sub.2), phosphoric acid (H.sub.3PO.sub.4), perchloric acid (HClO.sub.4), sulfuric acid (H.sub.2SO.sub.4), stearic acid (C.sub.17H.sub.35COOH), trichloroacetic acid (CCl.sub.3COOH), ammonia (NH.sub.4OH), sodium hydrogen carbonate (NaHCO.sub.3), ammonium carbonate ((NH.sub.4).sub.2CO.sub.3), ammonium chloride ((NH.sub.4).sub.2Cl), ammonium nitride (NH.sub.4NO.sub.3), ammonium persulfate ((NH.sub.4).sub.2S.sub.2O.sub.8), glycerin (C.sub.3H.sub.8O.sub.3), ammonium sulfate ((NH4).sub.2SO.sub.4) and ammonium bicarbonate (NH.sub.4HCO.sub.3).
4. The composition according to claim 1, wherein the noise is generated by a metal inserted into the body.
5. A pad for removing noise from an MRI image, comprising the composition of claim 1.
6. The pad according to claim 5, which improves the quality of an MRI image.
7. The pad according to claim 5, further comprising a cover accommodating the composition.
8. The pad according to claim 5, which is transformable into a shape of the human body.
9. The pad according to claim 5, which is attachable/detachable to a main body coil, a shim coil, an RF coil, an array coil, a surface coil, a spine coil, a head coil, an extremity coil or a torso coil for an MRI apparatus.
10. A coil for an MRI apparatus into which the composition of claim 1 is injected.
11. The coil according to claim 10, which is one or more selected from the group consisting of a main body coil, a shim coil, an RF coil, an array coil, a surface coil, a spine coil, a head coil, an extremity coil or a torso coil for an MRI apparatus.
12. A method of removing noise from an MRI image using a composition comprising a compound having a functional group capable of hydrogen bonding.
13. The method according to claim 12, wherein the compound is one or more selected from the group consisting of water (H.sub.2O), amyl alcohol (C.sub.5H.sub.11OH), butyl alcohol (CH.sub.3CH.sub.2CH.sub.2H), ethanol (C.sub.2H.sub.5OH), methyl alcohol (CH.sub.3OH), ethylene glycol (OHCH.sub.2CH.sub.2OH), formaldehyde (HCHO), nitrobenzene (C.sub.6H.sub.5NO.sub.2), propylene glycol (OH(CH.sub.2).sub.3H), hydrogen peroxide (H.sub.2O.sub.2), acetic acid (CH.sub.3COOH), acetic anhydride (C.sub.4H.sub.6O.sub.3), butanic acid (C.sub.3H.sub.7COOH), benzenesulfonic acid (C.sub.6H.sub.5SO.sub.3H), benzoic acid (C.sub.6H.sub.5COOH), chromic acid (H.sub.2CrO.sub.4), citric acid (C.sub.6H.sub.8O.sub.7H.sub.2O), hexafluorosilicic acid (H.sub.2SiF.sub.6), fluoroboric acid (HBF.sub.4), formic acid (HCOOH), hydrochloric acid (HCl), hydrocyanic acid (HCN), hydrofluoric acid (HF), hypochlorous acid (HClO), lactic acid (CH.sub.3CHOHCOOH), maleic acid ((CHOOH).sub.2), nitric acid (HNO.sub.3), oleic acid (C.sub.18H.sub.34O.sub.2), phosphoric acid (H.sub.3PO.sub.4), perchloric acid (HClO.sub.4), sulfuric acid (H.sub.2SO.sub.4), stearic acid (C.sub.17H.sub.35COOH), trichloroacetic acid (CCl.sub.3COOH), ammonia (NH.sub.4OH), sodium hydrogen carbonate (NaHCO.sub.3), ammonium carbonate ((NH.sub.4).sub.2CO), ammonium chloride ((NH.sub.4).sub.2Cl), ammonium nitride (NH.sub.4NO.sub.3), ammonium persulfate ((NH.sub.4).sub.2S.sub.2O.sub.8), glycerin (C.sub.3H.sub.8O.sub.3), ammonium sulfate ((NH4).sub.2SO.sub.4) and ammonium bicarbonate (NH.sub.4HCO.sub.3).
14. A method of obtaining a noise-reduced MRI image, comprising: manufacturing a pad including a compound having a functional group capable of hydrogen bonding; attaching the pad to a desired region of a subject; and obtaining an MRI image in the desired region using an MRI apparatus.
15. The method according to claim 14, wherein the compound is one or more selected from the group consisting of water (H.sub.2O), amyl alcohol (C.sub.5H.sub.11OH), butyl alcohol (CH.sub.3CH.sub.2CH.sub.2OH), ethanol (C.sub.2H.sub.5OH), methyl alcohol (CH.sub.3OH), ethylene glycol (OHCH.sub.2CH.sub.2OH), formaldehyde (HCHO), nitrobenzene (C.sub.6H.sub.5NO.sub.2), propylene glycol (OH(CH.sub.2).sub.3OH), hydrogen peroxide (H.sub.2O.sub.2), acetic acid (CH.sub.3COOH), acetic anhydride (C.sub.4H.sub.6O.sub.3), butanic acid (C.sub.3H.sub.7COOH), benzenesulfonic acid (C.sub.6H.sub.5SO.sub.3H), benzoic acid (C.sub.6H.sub.5COOH), chromic acid (H.sub.2CrO.sub.4), citric acid (C.sub.6H.sub.8O.sub.7H.sub.2O), hexafluorosilicic acid (H.sub.2SiF.sub.6), fluoroboric acid (HBF.sub.4), formic acid (HCOOH), hydrochloric acid (HCl), hydrocyanic acid (HCN), hydrofluoric acid (HF), hypochlorous acid (HClO), lactic acid (CH.sub.3CHOHCOOH), maleic acid ((CHOOH).sub.2), nitric acid (HNO.sub.3), oleic acid (C.sub.18H.sub.34O.sub.2), phosphoric acid (H.sub.3PO.sub.4), perchloric acid (HClO.sub.4), sulfuric acid (H.sub.2SO.sub.4), stearic acid (C.sub.17H.sub.35COOH), trichloroacetic acid (CCl.sub.3COOH), ammonia (NH.sub.4OH), sodium hydrogen carbonate (NaHCO.sub.3), ammonium carbonate ((NH.sub.4).sub.2CO.sub.3), ammonium chloride ((NH.sub.4).sub.2Cl), ammonium nitride (NH.sub.4NO.sub.3), ammonium persulfate ((NH.sub.4).sub.2S.sub.2O.sub.8), glycerin (C.sub.3H.sub.8O.sub.3), ammonium sulfate ((NH4).sub.2SO.sub.4) and ammonium bicarbonate (NH.sub.4HCO.sub.3).
16. (canceled)
Description
DESCRIPTION OF DRAWINGS
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MODES OF THE INVENTION
[0043] Hereinafter, the present invention will be described in detail with reference to the following examples or the accompanying drawings. However, the examples or the description of the drawings merely explain exemplary embodiments of the present invention, and the scope of the present invention is not intended to be limited or narrowly interpreted by the description of the present invention.
[Example 1] Preparation and Methods of Experiment
[0044] 1-1. Manufacture of the Acetic Acid Pad
[0045] Since acetic acid is easy to purchase and harmless to the human body and to investigate whether the removal of noise from an MRI image and an image quality-improving effect can be obtained using the acetic acid, a pad was manufactured using a naturally obtained concentration of acetic acid prepared from fruit juice.
[0046] A small amount of glycerin was mixed with fruit juice acetic acid, and a thickening agent was used to easily attach the mixture to a patient's implant site. Here, the used thickening agent refers to a mixture of glycerin (ultrasound gel component) and a common thickening component, and the thickening agent can be replaced with an ultrasound gel.
[0047] As shown in
[0048] Afterward, as shown in
[0049] 1-2. Comparison Experiment Before/after Use of Acetic Acid Pad
[0050] To overcome the limits of a human body experiment, as shown in
[0051] More specifically, using specified protocol T1 Fat Saturation (Fov 240×207, TR 750 ms, TE 12 ms, Thickness 4 mm, Gap 1.5 mm), an international standard phantom was used as a target, and observation was performed before and after the use of a fruit juice acetic acid component pad. After the test, images of the region of interest (ROI) sites were obtained using MacroView (INFINITT) and a workstation ROI (contrast HU-value; M-view v 5.4.10.61).
[0052] After the phantom experiment, a patient observation test was performed before and after the use of the acetic acid pad, and thus images were obtained.
[Example 2] Confirmation of Experiment Results for Phantoms Before/after Use of Acetic Acid Pad
[0053] For international standard quality control (QC), that is, checking of the improvement of apparatus quality, an experiment was performed using the international standard QC phantom according to the method described in Example 1-2, and then a common phantom image, and the ROI mean values of a water pad and an acetic acid pad were compared. As a result, as shown in
TABLE-US-00001 TABLE 1 Type ROI mean value Common phantom 2029 Water pad 2318 Acetic acid pad 2364
[0054] In addition, as shown in
[Example 3] Confirmation of Experiment Results for Patients Before/after Use of Acetic Acid Pad
[0055] To compare the images with noise caused by a metallic material before and after the use of an acetic acid pad, patients were observed according to the method described in Example 1-2. Here, to compare the objective measurement data on the effect of using an acetic acid pad, the ROI mean value of the minimum and maximum standard deviations in an image quality contrast was compared.
[0056] As a result, as shown in
TABLE-US-00002 TABLE 2 ROI mean value Before pad use After pad use Drawing (left panel of a drawing) (right panel of a drawing) FIG. 5A 380 533 FIG. 5B 462 599 FIG. 5C 852 1011
[0057] Moreover,
[Example 4] Confirmation of the Effect of Removing Noise from MRI Image of the Pad Including a Compound Having a Functional Group Capable of Hydrogen Bonding
[0058] As shown in Example 3, human images were obtained before and after the use of a pad consisting of acetic acid as a component, and to confirm the MRI image noise-removing effect of each pad filled with citric acid, sodium hydrogen carbonate, ethanol or glycerin, which has a high hydrogen content, for example, acetic acid, a region of interest (ROI) mean value in the image was measured using the phantom manufactured herein.
[0059] An acetic acid, citric acid, sodium hydrogen carbonate, ethanol or glycerin concentration of 0% represents water (H.sub.2O.sub.2), and an MRI image was obtained by targeting a component containing hydrogen, as a criterion for image acquisition, the natural state, water (H.sub.2O), has been standardized according to MRI periodic inspection and international standard inspection.
[0060] 4-1. Confirmation of Removal of Noise from MRI Image Using Water (H.sub.2O) and Acetic Acid
[0061] According to the method described in Example 1-1, a pad was manufactured by filling a pad with acetic acid (CH.sub.3COOH), and an MRI image was measured.
[0062] As a result, as shown in
TABLE-US-00003 TABLE 3 Concentration of acetic acid (CH.sub.3COOH) ROI mean value (Mean) 0% (H.sub.2O) 1119 20% 1147 40% 1798 60% 1868 80% 1935 100% 2004
[0063] 4-2. Confirmation of Removal of Noise from MRI Image Using Citric Acid
[0064] In addition, according to the method described in Example 1-1, a pad was manufactured by filling a pad with citric acid (C.sub.6H.sub.8O.sub.7H.sub.2O), and an MRI image was measured.
[0065] As a result, as shown in
TABLE-US-00004 TABLE 4 Concentration of citric acid (C.sub.6H.sub.8O.sub.7H.sub.2O) ROI mean value (Mean) 0% (H.sub.2O) 1480 20% 1698 40% 1702 60% 1734 80% 1762 100% 1797
[0066] 4-3. Confirmation of Removal of Noise from MRI Image Using Sodium Hydrogen Carbonate
[0067] According to the method described in Example 1-1, a pad was manufactured by filling a pad with sodium hydrogen carbonate (NaHCO.sub.3), and an MRI image was measured.
[0068] As a result, as shown in
TABLE-US-00005 TABLE 5 Concentration of sodium hydrogen ROI mean value carbonate (NaHCO.sub.3) (Mean) 0% (H.sub.2O) 1216 20% 1439 40% 1653 60% 1622 80% 1734 100% 1730
[0069] 4-4. Confirmation of Removal of Noise from MRI Image Using Ethanol
[0070] According to the method described in Example 1-1, a pad was manufactured by filling a pad with ethanol (C.sub.2H.sub.5OH), and an MRI image was measured.
[0071] As a result, as shown in
TABLE-US-00006 TABLE 6 Concentration of ethanol (C.sub.2H.sub.5OH) ROI mean value (Mean) 0% (H.sub.2O) 1519 20% 1636 40% 2168 60% 5691 80% 8655 100% 14979
[0072] 4-5. Confirmation of Removal of Noise from MRI Image Using Glycerin
[0073] According to the method described in Example 1-1, a pad was manufactured by filling a pad with glycerin (C.sub.3H.sub.8O.sub.3), and an MRI image was measured.
[0074] As a result, as shown in
TABLE-US-00007 TABLE 7 Concentration of glycerin (C.sub.3H.sub.8O.sub.3) ROI mean value (Mean) 0% (H.sub.2O) 1397 20% 1488 40% 1503 60% 1538 80% 1702 100% 1712
[0075] It should be understood by those of ordinary skill in the art that the above description of the present invention is exemplary, and the exemplary embodiments disclosed herein can be easily modified into other specific forms without departing from the technical spirit or essential features of the present invention. Therefore, the exemplary embodiments described above should be interpreted as illustrative and not limited in any aspect.
INDUSTRIAL APPLICABILITY
[0076] The present invention relates to a composition for removing MRI noise using a compound having a functional group capable of hydrogen bonding and a pad using the same, and the composition or pad according to the present invention reduces noise caused by a metal implant in the acquisition of MRI images, has an excellent image enhancement effect, is cheap and economical, has no toxicity in a human body and thus is safe. For this reason, the composition can be used as a component of an image diagnostic device in the field of medical devices, and is expected to be effectively used to acquire noise-removed MRI images in the field of diagnostic radiology.