Kit for detecting urinary lactic acid, creatine and beta-hydroxybutyric acid in human urine simultaneously
A technology for detecting human bodies and kits, applied in biological testing, material inspection products, etc., can solve problems such as semi-quantitative detection, false positives, interference, etc., and achieve the effects of improving stability and accuracy, ensuring stability, and ensuring results
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Embodiment 1
[0070] Example 1 Urine Purification Device
[0071] Such as figure 1 As shown, the urine purification device is a titration container, including a filling chamber 2, the top of the filling chamber 2 has a liquid filling port 8, and a sealing cap 1 is provided at the liquid filling port 8. The chamber 2 is filled with a selective adsorbent 3, the bottom of the packing chamber 2 has a liquid outlet 6, the liquid outlet 6 is conical and protruding, and has a plug cap 7 at the protruding end. The bottom of the packing chamber 2 has a clamping membrane ring 4, and a filter membrane 5 is located below the clamping membrane ring 4.
Embodiment 2
[0072] Example 2 Detection Kit
[0073] Urine Purification Device
[0074] The structure of the urine purification device is the same as in Example 1. In this example, the selective specific adsorbent is an adsorbent composed of 0.5g neutral alumina and 0.3g of purified activated carbon, wherein the purified activated carbon is treated with 10% NaOH, and the selective adsorbent is baked at 70°C for 72 hours. activation. The activated adsorbent can completely absorb and remove interfering substances in urine such as bilirubin, vitamin C and other interfering substances.
[0075] Preparation of dry chemical reaction device
[0076] Prepare lactate oxidase pads:
[0077] The 3MM grade chromatographic paper of Whatman is used as the carrier, cut into discs with a diameter of 3.98mm, and the chromatographic paper carrier is prepared by 100U / ml lactate oxidase and pH=7.0, 100mmol / L piperazine-N, Soak in N-bis(2-ethanesulfonic acid) (PIPES) buffer for 2 hours, and dry at 20°C fo...
Embodiment 3
[0098] Urine Purification Device
[0099] The urine purification device is the same as in Example 1 in this example. The selective specific adsorbent of the present embodiment is an adsorbent composed of 0.4g neutral alumina and 0.2g purified activated carbon: wherein the purified activated carbon is treated with 10% NaOH, and the selective adsorbent is baked at 150°C for 36 hours. Activated, the activated adsorbent can completely absorb and remove interfering substances in urine such as bilirubin, vitamin C and other interfering substances.
[0100] Preparation of dry chemical reaction device
[0101] Prepare lactate oxidase pads:
[0102] The 3MM grade chromatographic paper of Whatman is used as the carrier, cut into discs with a diameter of 3.98mm, and the chromatographic paper carrier is made of 200U / ml lactate oxidase and pH=7.2, 100mmol / L piperazine-N, Soak in N-bis(2-ethanesulfonic acid) (PIPES) buffer for 2 hours, and dry at 20°C for 4 hours.
[0103] Prepare perox...
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