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35 results about "Terbutaline" patented technology

Terbutaline is used to treat wheezing and shortness of breath from lung problems (e.g., asthma, chronic obstructive pulmonary disease, bronchitis and emphysema).

Terbutaline conjugate and its preparation method and uses

InactiveCN101078725AIt takes a long time to make upSimple methodBiological testingElisa kitNew Zealand white rabbit
The invention discloses a coupling matter of terbutaline in general formula (I), constituted in coupling by terbutaline hapten and carrier matter generating immunogenicity, which is bovine serum albumin or ovalbumin. Whereinto, n is the number of terbutaline molecules combined with a bovine serum albumin molecule. Said n is integer from 1 to 15. cBSA is activated bovine serum albumin and the range of molecular weight is 66KDa-69KDa. The invention also discloses the preparation method of said coupling matter. Terbutaline is connected with carrier matter generating immunogenicity to combine the coupling matter which can induce animal immune system to generate antibody. By immunizing New Zealand white rabbit the coupling matter of terbutaline in invention prepares antiserum with value of more than 1:50,000. The lowest measuring limitation is 0.3ppb and IC50 is 9.25ppb. The invention is convenient, quick, special and accurate. It provides a foundation for preparing ELISA kit for detecting of terbutaline.
Owner:SHANDONG UNIV

Colloidal gold kit for detecting beta-stimulant drug and preparation method thereof

The invention discloses a colloidal gold kit for detecting a beta-stimulant drug. The kit comprises reagent strips and colloidal-gold marker micropores, the reagent strip comprises a base plate, a chromatography membrane, a sample pad arranged at two ends of the chromatography membrane, and an absorbent pad are arranged on the base plate in order, a quality control line C and a detection line arearranged on the chromatography membrane, the line C is coated with a goat-anti-mouse IgG antibody, the detection line comprises a T1 line and a T2 line, the T1 line is a ractopamine detection line, and is coated with a ractopamine antigen, the T2 line is the salbutamol, clenbuterol, brombuterol, tulobuterol, mabuterol, terbutaline, cimbuterol, clorprenaline, and cimaterol detection line, the T2 line is coated with a beta-stimulant antigen, the line C, the T1 line, and the T2 line present three parallel bands which are vertical to a long phase of a test paper strip, the colloidal-gold marker micropores contains a colloidal gold-labeled beta-stimulant polyclonal antibody and a ractopamine monoclonal antibody, by aiming at special objects of raw milk and fresh milk, ten drugs can be detectedat one time, a detection scope is enlarged, leak detection can be prevented, sensitivity is high, and stability is good.
Owner:杭州南开日新生物技术有限公司

Pretreatment method for rapid determination of beta-agonists in livestock and poultry meat through gas chromatography/mass spectrometry

The invention relates to a pretreatment method for rapid determination of beta-agonists in livestock and poultry meat through gas chromatography / mass spectrometry and discloses a simple, convenient, highly efficient and accurate pretreatment technology in determination of terbutaline, clenbuterol, salbutamol and ractopamine through gas chromatography / mass spectrometry. According to the method, a minced meat sample is ultrasonically extracted with 5% perchloric acid, then centrifuged at a speed of 10000 r / min for 15 min; then supernatant is enriched and purified with a WCX solid-phase extraction column; and detection is carried out after derivatization. The four agonists have good linearity in a range of 50 to 1000 [mu]g / L; correlation coefficient is more than 0.995; standard-added recovery rate is in a range of 84.32 to 103.15%; RSD is in a range of 1.35 to 4.78%; occurrence of false positive results is prevented; and lowest detection limit and the standard-added recovery rate meet current detection requirements at home and abroad.
Owner:QUZHOU QUALITY & TECH SUPERVISION & INSPECTION CENT

Preparation and application of bis [-6-oxo-(3-deoxgmonoester citrate-4)]-beta-cyclodextrin HPLC column material

The invention relates to the technical field of preparation and application of chiral high-performance liquid chromatography column materials, and discloses preparation and application of beta-CD-D2 high-performance liquid chromatography chiral column material. A high-performance liquid chromatography chiral column is prepared from beta-CD-D2 and is used for splitting chiral medicine enantiomers. The preparation and the application of the beta-CD-D2 high-performance liquid chromatography chiral column material comprise the following steps: 1, constructing a chiral environment by using beta-CD-D2, bonding the chiral environment with high-performance liquid chromatography silica beads into a fixed phase filler, then preparing the fixed phase filler into a chiral column, and applying the chiral column into high-performance liquid chromatography; 2, finding out an optional formula and an optional condition by using a proper characterization means, and optimizing the method and the condition; 3, establishing a preparation method of a salmeterol single enantiomer by using the prepared beta-CD-D2 chiral column, and splitting a chiral compound by using a cyclodextrins derivative for the first time; and 4, splitting drugs by using the prepared beta-CD-D2 chiral column, and establishing a method for splitting and qualitatively and quantitatively analyzing seven chiral drugs including salmeterol, terbutaline, procaterol, cetirizine, lamivudine, cefuroxime and ceftriaxone.
Owner:SOUTH CENTRAL UNIVERSITY FOR NATIONALITIES

Preparation and application of bis[-6-oxo-(3-deoxycitrate monoester-4)]-β-cyclodextrin hplc column material

The invention relates to the technical field of preparation and application of chiral high-performance liquid chromatography column materials, and discloses preparation and application of beta-CD-D2 high-performance liquid chromatography chiral column material. A high-performance liquid chromatography chiral column is prepared from beta-CD-D2 and is used for splitting chiral medicine enantiomers. The preparation and the application of the beta-CD-D2 high-performance liquid chromatography chiral column material comprise the following steps: 1, constructing a chiral environment by using beta-CD-D2, bonding the chiral environment with high-performance liquid chromatography silica beads into a fixed phase filler, then preparing the fixed phase filler into a chiral column, and applying the chiral column into high-performance liquid chromatography; 2, finding out an optional formula and an optional condition by using a proper characterization means, and optimizing the method and the condition; 3, establishing a preparation method of a salmeterol single enantiomer by using the prepared beta-CD-D2 chiral column, and splitting a chiral compound by using a cyclodextrins derivative for the first time; and 4, splitting drugs by using the prepared beta-CD-D2 chiral column, and establishing a method for splitting and qualitatively and quantitatively analyzing seven chiral drugs including salmeterol, terbutaline, procaterol, cetirizine, lamivudine, cefuroxime and ceftriaxone.
Owner:SOUTH CENTRAL UNIVERSITY FOR NATIONALITIES

Method for separating terbutaline enantiomers in extracted mode through hydrophobicity phase transferring chirality

The invention provides a method for separating terbutaline enantiomers in an extracted mode through hydrophobicity phase transferring chirality. Beta-cyclodextrin is used as an extraction agent, the terbutaline enantiomers serve as separated objects, the solubilizing performance of a hydrophobicity phase transferring agent for terbutaline in the organic phase is used, mass transferring efficiency is improved through the centrifugal acting force of a centrifugal extractor, mass transferring and reacting of the terbutaline enantiomers in the water phase and the organic phase are accelerated, extract-phase outlet purity and raffinate-phase outlet purity are greatly improved accordingly, and the extract-phase yield and the raffinate-phase yield are greatly increased accordingly. The method has the advantages that the extraction agent and the phase transferring agent are low in price and easy to get; extraction efficiency is high, and the separating speed is high; operation is flexible, and the environment-friendly effect and the efficient effect are achieved. By means of the method, the problem that the solubility of the terbutaline in the organic phase is poor is solved, and the problems that as for common extraction technologies, mass transferring efficiency is low, single-stage extraction is carried out, and purity and the yield are low are solved. Rapid and high-selectivity separation of the terbutaline can be achieved through multi-stage counter-current extraction.
Owner:HUNAN INSTITUTE OF SCIENCE AND TECHNOLOGY

Terbutaline, salbutamol, ractopamine, clenbuterol online immunoaffinity purification detecting device

The invention discloses a terbutaline, salbutamol, ractopamine, clenbuterol online immunoaffinity purification detecting device. Automatic sample loading and elution of immunoaffinity columns are realized through flow switching of three six-way valves; secondary enrichment purification and desalination are realized by the use of MCX columns; a purification solution can be directly introduced intoa tandem mass spectrometry detector, therefore, high-sensitivity detection of the four drugs based on automatic purification is realized. The immunoaffinity purification columns of the terbutaline, salbutamol, ractopamine, clenbuterol online immunoaffinity purification detecting device can be reused, and the automation of sample purification and analysis are realized, which can save money, save time, and save manpower; and the practicability is good.
Owner:ANIMAL & PLANT & FOOD INSPECTION CENT OF TIANJIN ENTRY EXIT INSPECTION & QUARANTINE BUREAU

Nine-link detection card for beta-incitant

The invention discloses a nine-link detection card for beta-incitant. The nine-link detection card comprises a shell and a detection card arranged in the shell, wherein the shell comprises an upper shell and a lower shell; a detection card accommodating cavity is formed between the upper shell and the lower shell; four corners of the lower shell are provided with bosses; the bosses are provided with clamping holes; the upper shell is provided with clamping posts corresponding to the bosses, and the clamping posts are matched with the clamping holes in the bosses; the detection card comprises a bottom plate; the middle of the top of the bottom plate is provided with nine reaction films; one side of each reaction film is provided with a sample pad and a structure release pad, and the other side of each reaction film is provided with a water absorption pad; the tops of the sample pads, the structure release pads and the water absorption pads are provided with fixing films; the parts, corresponding to the middles of the sample pads, of the fixing films are provided with sample feeding holes; nine sample pads and nine reaction films are arranged; the nine sample pads are respectively used for detecting the clenbuterol hydrochloride, ractopamine, salbutamol, cimbuterol, mabuterol, bombuterol, tulobuterol, terbutaline and clorprenaline in the beta-incitant; positions corresponding to the reaction films are observation areas.
Owner:BEOSON JIANGSU FOOD SAFETY TECH CO LTD
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