1. Field of Invention
The present invention relates to a biosensor, and more particularly to a biosensor that allows blood to react thoroughly with a reactive layer, so test results are accurate.
2. Description of the Related Art
Generally, a patient who needs to do periodic blood tests (such as blood sugar measurement, triglyceride measurement, cholesterol measurement, high-density lipoprotein measurement, low-density lipoprotein measurement, etc.) uses a biosensor that incorporates a biosensor detector allowing the patient to determine his or her physical condition virtually anywhere.
US publication No. 20030202906 disclosed a biosensor comprising a sensor strip. The sensor strip is folded to form a base and a cover. The base has an upper surface, two sides, an end, a distal end, a reactive layer and two electrodes. The reactive layer is mounted on the upper surface of the base. The electrodes are mounted on the upper surface of the base respectively near the sides of the base and each electrode is formed from the reactive layer to the sensing end of the base. The cover is shorter than the base, is bonded to the upper surface of the base, is flush with the distal end, covers the reactive layer of the base and leaves the sensing end of the base exposed. The cover has a lower surface and a through hole. The through hole is defined through the cover in a center of the corresponding reactive layer and between the electrodes.
When the biosensor is used, a drop of blood or other liquid sample is dropped through the through hole onto the reactive layer. Blood reacts with the reactive layer to generate electrons. The electrons will move between the electrodes and become a circuit with an electric current. Then, the sensing end of the base is inserted into a biosensor detector to detect the electric current and display a test result.
However, the conventional biosensor has a significant shortcoming. The through hole being formed in the center of the reactive layer and between the electrodes allows blood dropped on the reactive layer to react with the reactive layer to contact the electrodes and allow electrons to move immediately between the electrodes before the blood reacts thoroughly with the reactive layer. Therefore, the electric current is unstable, and the test results are not accurate, which can lead to undetected traumatic physical conditions and may lead to death.
US publication No. 20050252769 disclosed another conventional biosensor. The structure of the conventional biosensor is similar to that of the conventional biosensor described above, but the through hole of the cover is formed in one side of the cover and near one of the electrodes. Therefore, a drop of blood or other liquid sample is dropped in the through hole and then moves from the side that the through hole is located toward another side to contact another electrode.
However, the distance between two electrodes is too short to allow a sufficient period of time for reaction making the reactive layer react with the liquid sample thoroughly.
To overcome the shortcomings, the present invention provides a biosensor to mitigate or obviate the aforementioned.
The primary objective of the present invention is to provide a biosensor that allows blood to react thoroughly with a reactive layer, so test results are accurate.
To achieve the objective, a biosensor in accordance with the present invention is a sensor strip that is folded to form a base and a cover. The base has sides, a reactive layer and two electrodes. One of the electrodes is mounted longitudinally on the base, extends from the base to the cover and is covered with insulating materials. The other electrode is mounted on the base from an end of the base to the reactive layer. The cover bonds to and is shorter than the base and has a sample notch. The sample notch is formed in one side of the cover, corresponds to the reactive layer and is near the electrode on the reactive layer. A sample reacts thoroughly with the reactive layer because the anode on the cover takes time to transfer electrons therefore accurate test results are obtained.
Other objectives, advantages and novel features of the invention will become more apparent from the following detailed description when taken in conjunction with the accompanying drawings.
With reference to
With further reference to
The reactive layer (11) is mounted on the upper surface of the base (10) adjacent to one side of the base (10). For the biosensor to detect blood sugar, the reactive layer (11) may comprise a composition including: (A) an enzyme (such as glucose oxidase, etc.); (B) enzyme protectors (such as albumin, dextrin, dextran, amino acid, etc.); (C) a conductive medium (such as potassium, etc.); (D) surfactant (such as triton X-100, triton X-405, triton X-114, sodium lauryl sulfate, tween 20 (polyoxyethylenesorbitan monolaurate), tween 40 (polyoxyethylenesorbitan monopalmitate), tween 60 (polyoxyethylenesorbitan monostearate), tween 80 (polyoxyethylenesorbitan monooleate), another water-soluble surfactant, a cleaning agent, etc.); (E) a buffer that is salt (such as phosphate, etc.); and (F) water (such as distilled water).
The margin (15) is a space, is formed on the upper surface of the base (10) between the other side of the base (10) and the reactive layer (11).
The electrodes (12, 13) are mounted on the upper surface of the base (10) and extend to the sensing end of the base (10). The electrodes (12, 13) are an anode (12) and a cathode (13).
The anode (12) is a strip, is formed longitudinally on the base (10), extends from the sensing end of the base (10) toward the cover (20) via the folding line (30) and has a proximal end and a distal end and an intermediate section (121). The proximal end of the anode (12) is at the sensing end of the base (10). The distal end is at the cover (20). The anode (12) formed through the margin (15) so that the intermediate section (121) is located in the margin (15). The intermediate section (121) in the margin (15) is covered with insulating materials. The anode (12) on the cover (20) overlaps on the insulating materials when the sensor strip is folded to partially insulate the intermediate section (121) in the margin (15) and the reactive layer (11).
With further reference to
With further reference to
The cathode (13) is a strip, is shorter than the anode (12), is formed longitudinally on the base (10) and has a proximal end and a distal end. The proximal end of the cathode (13) is at the sensing end of the base (10). The distal end is mounted on the reactive layer (11).
The identifying electrode (14) is formed between the anode (12) and the cathode (13) without contacting the reactive layer (11) and allows a biosensor detector to recognize which test the biosensor performs (including, but not limited, to blood sugar measurement, triglyceride measurement, cholesterol measurement, high-density lipoprotein measurement, low-density lipoprotein measurement). The identifying electrode (14) has a proximal end and a distal end. The proximal end of the identifying electrode (14) is at the sensing end of the base (10). The distal end is mounted near the reactive layer (11).
The cover (20) is shorter than the base (10), is bonded to the upper surface of the base (10), covers the reactive layer (11) of the base (10) and exposes the sensing end of the base (10) and the proximal ends of the anode (12), the cathode (13) and the identifying electrode (14), which are inserted into a biosensor detector for detecting the electrodes (12, 13) and the identifying electrode (14). The cover (20) has two sides, a lower surface and a sample notch (22). The lower surface has a silver electrode membrane (21), a gap (15′) and adhesive layers (23). The silver electrode membrane (21) corresponds to the reactive layer (11) of the base (10) and has two ends. The gap (15′) is formed between the silver electrode membrane (21) and the anode (12) on the cover (20). The adhesive layers (23) are mounted on the lower surface of the cover (20), respectively overlap the ends of the silver electrode membrane (21), overlap partially on the intermediate section (121) of the anode (12) on the cover (20) and bond to the upper surface of the base (10). The sample notch (22) is formed in one side of the cover (20), corresponds to the reactive layer (11) of the base (10), is near the cathode (13) and allows blood or another liquid sample to be dropped on the reactive layer (11). The sample notch (22) comprises a semicircular notch (221) and a triangular notch (222). The semicircular notch (221) has a chord and an arc. The chord is flush with one side of the cover (20). The triangular notch (222) is formed from a center of the arc of the semicircular notch (221) toward the other side of the cover (20).
After the blood or another liquid sample is dropped on the reactive layer (11) through the sample notch (22), the blood or other liquid sample flows on and reacts with the reactive layer (11) from the semicircular notch (221) toward of the margin (15), which is guided by the triangular notch (222) to generate electrons.
At the first embodiment of the present invention, the blood or other liquid sample contacts the anode (12) in the margin (15) from the interval between two insulating layers (16), so the electrons allow the anode (12) and the cathode (13) to generate an electric current that is detected by the biosensor detector. It is noted that because the base (10) and the cover (20) are folded, part of the electron transfers through the silver electrode membrane (21) via the gap (15′) to contact the anode (12) on the cover (20). The electrons also transmit from the anode (12) on the cover (20) to the biosensor detector.
At the second embodiment of the present invention, the blood or other liquid sample cannot contact the intermediate section (121) of the anode (12) in the margin (15) because the insulating layer (16′) covers the intermediate section (121) in the margin (15) thoroughly. Accordingly the electrons transfers through the silver electrode membrane (21) via the gap (15′) and only contact the anode (12) on the cover (20) and an electric current from the anode (12) on the cover (20) transmits to the biosensor detector.
Therefore, the blood or other liquid sample reacts thoroughly with the reactive layer (11) because the anode (12) on the cover (20) takes time to transfer the electrons to the biosensor detector to obtain accurate test results.
Even though numerous characteristics and advantages of the present invention have been set forth in the foregoing description, together with details of the structure and function of the invention, the disclosure is illustrative only. Changes may be made in detail, especially in matters of shape, size and arrangement of parts within the principles of the invention to the full extent indicated by the broad general meaning of the terms in which the appended claims are expressed.
Number | Date | Country | Kind |
---|---|---|---|
097213709 | Aug 2008 | TW | national |