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Treatment liquid for use in desorption of steroid included in cyclodextrin

A technology of steroids and treatment liquids, applied in the field of treatment liquids, which can solve the problems of signal intensity drop, inability to exclude batch differences, infection risks, etc., and achieve high-precision results

Pending Publication Date: 2020-04-21
FUJIREBIO CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, in the case of using serum-based standard solutions, batch-to-batch variations from raw materials, risk of infection cannot be ruled out
[0004] Therefore, in the preparation of the standard solution, a buffer solution containing proteins such as bovine serum albumin is also used instead of serum. In this case, the steroid contained in the standard solution shows a tendency to decompose over time. Its signal strength drop becomes a problem
In addition, hydrophobic steroids are easily adsorbed to the components and containers of the standard solution, which will also cause a decrease in the signal intensity during measurement.

Method used

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  • Treatment liquid for use in desorption of steroid included in cyclodextrin
  • Treatment liquid for use in desorption of steroid included in cyclodextrin
  • Treatment liquid for use in desorption of steroid included in cyclodextrin

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1-1

[0089] [Example 1-1] Cyclodextrin to the inspection of inclusion effect of aldosterone

[0090] In this example, aldosterone was used as the antigen, and a buffer-based standard solution was used as the standard solution. Specifically, firstly, cyclodextrins (α-cyclodextrin (αCD), β-cyclodextrin (βCD), hydroxypropyl β-cyclodextrin (HPβCD), hydroxypropyl β-cyclodextrin (HPβCD), Aldosterone was added to a diluted solution of γ-cyclodextrin (γCD) to prepare an aldosterone solution (standard solution) at about 500 pg / mL. The matrix composition of the above dilution was set as "50mM MOPS (pH7.2), 150mM NaCl, 0.1%NaN 3 ".

[0091] For each aldosterone solution, anti-aldosterone antibody-conjugated particles (anti-aldosterone antibody-conjugated magnetic particles (antibody-conjugated particles) The assay was carried out by a two-step method of phosphatase-labeled anti-aldosterone antibody (enzyme-labeled antibody). Specifically, it follows the steps (a) to (f) below.

[0092] (...

Embodiment 1-2

[0099] [Example 1-2] Inspection of the Stabilizing Effect of HPβCD on Aldosterone

[0100] In this example, aldosterone was used as the antigen, and the standard solution of the buffer matrix was used as the standard solution. Specifically, aldosterone was first added to a diluted solution to which HPβCD was added at a concentration of 0.1% or 1%, to prepare an approximately 300 pg / mL aldosterone solution (standard solution). The matrix composition of the above dilution is set as "100mM HEPES (pH7.5), 150mM NaCl, 0.5%BSA, 0.1%NaN 3 ".

[0101]The obtained aldosterone solutions (approximately 300 pg / mL aldosterone solution) were stored at -80°C, 4°C, 25°C, and 37°C for 45 days, respectively, and then used for measurement. For each preserved aldosterone solution, anti-aldosterone antibody-conjugated particles (anti-aldosterone antibody-conjugated magnetic particles (antibody-conjugated particles) prepared by a conventional method) and alkaline phosphatase-labeled anti-aldoster...

Embodiment 1-3

[0109] [Example 1-3] Effect of decomplexing aldosterone from HPβCD-1

[0110] In this example, aldosterone was used as the antigen, and a buffer-based standard solution was used as the standard solution. Specifically, first, add aldosterone to the following standard solution dilution (with HPβCD), prepare about 1600pg / mL aldosterone solution (1600pg / mL CD (+) standard solution), and use the following defatted serum as a mock test Aldosterone was added to a sample diluent to prepare an approximately 1600 pg / mL aldosterone solution (1600 pg / mL sample (simulated test sample)). As the above standard solution dilution (with HPβCD), use "50mM MOPS (pH7.2), 150mM NaCl, 1%HPβCD, 0.1%NaN 3 ", as the above-mentioned defatted serum, "DDC Mass Spect Gold (serum free of steroid hormones and cholesterol and TG, manufactured by Veritas Corporation)" was used.

[0111] In addition, 12 kinds of surfactants [sodium deoxycholate (manufactured by Fujifilm Wako Pure Chemical Industries, Ltd.), N...

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Abstract

It was found that by treating a standard solution containing a steroid included in a cyclodextrin with a surfactant in a method for immunologically quantifying a steroid, is possible to desorb the steroid from the cyclodextrin, deviation in the behavior of an antigen-antibody reaction in a specimen (a test sample) and the standard solution is thereby minimized, and the precision of quantificationof the steroid is thus significantly improved.

Description

technical field [0001] The present invention relates to a treatment liquid for decomplexing steroid contained in cyclodextrin, which contains a surfactant as an active ingredient. In addition, the present invention relates to the use of the treatment solution for immunological quantification of steroids. Background technique [0002] When immunologically quantifying the target substance (antigen) contained in the sample (test sample), the signal intensity of the antigen-antibody reaction of the sample and the signal of the antigen-antibody reaction of the standard solution containing the target substance at a specified concentration are usually separately measured. intensity and compare their measured values. In order to perform this quantification with high accuracy, it is necessary to make the behavior of the antigen-antibody reaction in the sample and the standard solution as consistent as possible. [0003] For example, in the case of immunological quantification of st...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): G01N33/53G01N33/74G01N33/92
CPCG01N33/92G01N33/5306G01N33/5436G01N33/548G01N2400/18G01N2496/25G01N33/743
Inventor 吉见达成照山杏子
Owner FUJIREBIO CO LTD