CN103105488B - 一种氨基脲(sem)衍生化试剂及其使用方法 - Google Patents
一种氨基脲(sem)衍生化试剂及其使用方法 Download PDFInfo
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- CN103105488B CN103105488B CN201210586467.XA CN201210586467A CN103105488B CN 103105488 B CN103105488 B CN 103105488B CN 201210586467 A CN201210586467 A CN 201210586467A CN 103105488 B CN103105488 B CN 103105488B
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- semicarbazides
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- benzoic acid
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- 150000003349 semicarbazides Chemical class 0.000 title claims abstract description 55
- 238000001212 derivatisation Methods 0.000 title claims abstract description 28
- 239000003153 chemical reaction reagent Substances 0.000 title claims abstract description 19
- 238000000034 method Methods 0.000 title claims description 30
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims abstract description 50
- 150000003384 small molecules Chemical class 0.000 claims abstract description 27
- 239000005711 Benzoic acid Substances 0.000 claims abstract description 25
- 235000010233 benzoic acid Nutrition 0.000 claims abstract description 25
- 238000001514 detection method Methods 0.000 claims abstract description 20
- 241001597008 Nomeidae Species 0.000 claims abstract description 18
- 150000001299 aldehydes Chemical class 0.000 claims description 19
- YBJHBAHKTGYVGT-ZKWXMUAHSA-N (+)-Biotin Chemical compound N1C(=O)N[C@@H]2[C@H](CCCCC(=O)O)SC[C@@H]21 YBJHBAHKTGYVGT-ZKWXMUAHSA-N 0.000 claims description 18
- 108010001336 Horseradish Peroxidase Proteins 0.000 claims description 11
- 238000002965 ELISA Methods 0.000 claims description 9
- 102000004160 Phosphoric Monoester Hydrolases Human genes 0.000 claims description 9
- 108090000608 Phosphoric Monoester Hydrolases Proteins 0.000 claims description 9
- 239000003513 alkali Substances 0.000 claims description 9
- 229960002685 biotin Drugs 0.000 claims description 9
- 235000020958 biotin Nutrition 0.000 claims description 9
- 239000011616 biotin Substances 0.000 claims description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 6
- 238000002835 absorbance Methods 0.000 claims description 5
- 229940126619 mouse monoclonal antibody Drugs 0.000 claims description 5
- 102000004169 proteins and genes Human genes 0.000 claims description 5
- 108090000623 proteins and genes Proteins 0.000 claims description 5
- LTMHDMANZUZIPE-AMTYYWEZSA-N Digoxin Natural products O([C@H]1[C@H](C)O[C@H](O[C@@H]2C[C@@H]3[C@@](C)([C@@H]4[C@H]([C@]5(O)[C@](C)([C@H](O)C4)[C@H](C4=CC(=O)OC4)CC5)CC3)CC2)C[C@@H]1O)[C@H]1O[C@H](C)[C@@H](O[C@H]2O[C@@H](C)[C@H](O)[C@@H](O)C2)[C@@H](O)C1 LTMHDMANZUZIPE-AMTYYWEZSA-N 0.000 claims description 4
- LTMHDMANZUZIPE-PUGKRICDSA-N digoxin Chemical compound C1[C@H](O)[C@H](O)[C@@H](C)O[C@H]1O[C@@H]1[C@@H](C)O[C@@H](O[C@@H]2[C@H](O[C@@H](O[C@@H]3C[C@@H]4[C@]([C@@H]5[C@H]([C@]6(CC[C@@H]([C@@]6(C)[C@H](O)C5)C=5COC(=O)C=5)O)CC4)(C)CC3)C[C@@H]2O)C)C[C@@H]1O LTMHDMANZUZIPE-PUGKRICDSA-N 0.000 claims description 4
- 229960005156 digoxin Drugs 0.000 claims description 4
- LTMHDMANZUZIPE-UHFFFAOYSA-N digoxine Natural products C1C(O)C(O)C(C)OC1OC1C(C)OC(OC2C(OC(OC3CC4C(C5C(C6(CCC(C6(C)C(O)C5)C=5COC(=O)C=5)O)CC4)(C)CC3)CC2O)C)CC1O LTMHDMANZUZIPE-UHFFFAOYSA-N 0.000 claims description 4
- GOUHYARYYWKXHS-UHFFFAOYSA-N 4-formylbenzoic acid Chemical compound OC(=O)C1=CC=C(C=O)C=C1 GOUHYARYYWKXHS-UHFFFAOYSA-N 0.000 claims description 3
- 241000283973 Oryctolagus cuniculus Species 0.000 claims description 3
- 108010090804 Streptavidin Proteins 0.000 claims description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- MHMNJMPURVTYEJ-UHFFFAOYSA-N fluorescein-5-isothiocyanate Chemical compound O1C(=O)C2=CC(N=C=S)=CC=C2C21C1=CC=C(O)C=C1OC1=CC(O)=CC=C21 MHMNJMPURVTYEJ-UHFFFAOYSA-N 0.000 claims description 3
- 238000010353 genetic engineering Methods 0.000 claims description 3
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 claims description 3
- 229920002704 polyhistidine Polymers 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims 3
- 108090001008 Avidin Proteins 0.000 claims 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 2
- HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical compound OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 claims 2
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims 2
- 229960002885 histidine Drugs 0.000 claims 2
- 239000002798 polar solvent Substances 0.000 claims 2
- 239000000376 reactant Substances 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
- 238000003118 sandwich ELISA Methods 0.000 abstract description 9
- 230000035945 sensitivity Effects 0.000 abstract description 5
- 238000000746 purification Methods 0.000 abstract description 4
- 238000002360 preparation method Methods 0.000 abstract description 2
- 230000009467 reduction Effects 0.000 abstract description 2
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 abstract 2
- IAIWVQXQOWNYOU-FPYGCLRLSA-N nitrofural Chemical compound NC(=O)N\N=C\C1=CC=C([N+]([O-])=O)O1 IAIWVQXQOWNYOU-FPYGCLRLSA-N 0.000 description 10
- 229960001907 nitrofurazone Drugs 0.000 description 8
- 230000005477 standard model Effects 0.000 description 8
- 239000000047 product Substances 0.000 description 7
- 239000002253 acid Substances 0.000 description 5
- 241001465754 Metazoa Species 0.000 description 4
- 239000003814 drug Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 210000001519 tissue Anatomy 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- UQLDLKMNUJERMK-UHFFFAOYSA-L di(octadecanoyloxy)lead Chemical compound [Pb+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O UQLDLKMNUJERMK-UHFFFAOYSA-L 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 108090000790 Enzymes Proteins 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000007405 data analysis Methods 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- 238000009396 hybridization Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000006228 supernatant Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 108050001427 Avidin/streptavidin Proteins 0.000 description 1
- -1 Furacilin metabolite semicarbazides Chemical class 0.000 description 1
- 208000031320 Teratogenesis Diseases 0.000 description 1
- 239000005557 antagonist Substances 0.000 description 1
- 238000009360 aquaculture Methods 0.000 description 1
- 244000144974 aquaculture Species 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 230000000711 cancerogenic effect Effects 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 231100000315 carcinogenic Toxicity 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000009514 concussion Effects 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 239000003547 immunosorbent Substances 0.000 description 1
- 238000001294 liquid chromatography-tandem mass spectrometry Methods 0.000 description 1
- 230000001404 mediated effect Effects 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 210000003205 muscle Anatomy 0.000 description 1
- 238000002703 mutagenesis Methods 0.000 description 1
- 231100000350 mutagenesis Toxicity 0.000 description 1
- 244000144977 poultry Species 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910021642 ultra pure water Inorganic materials 0.000 description 1
- 239000012498 ultrapure water Substances 0.000 description 1
- 239000000273 veterinary drug Substances 0.000 description 1
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- Peptides Or Proteins (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
Abstract
Description
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Families Citing this family (3)
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CN106093379A (zh) * | 2016-06-08 | 2016-11-09 | 中国科学院广州生物医药与健康研究院 | 一种氨基脲衍生化试剂及其快速检测卡 |
CN106831498B (zh) * | 2017-01-12 | 2018-10-30 | 广州润坤生物科技有限公司 | 呋喃西林代谢物sem衍生化半抗原、人工抗原的制备方法及其应用 |
CN109696553A (zh) * | 2018-12-20 | 2019-04-30 | 江苏美正生物科技有限公司 | 一种适用于氨基残留物的高灵敏elisa检测方法 |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101320037A (zh) * | 2008-06-25 | 2008-12-10 | 江南大学 | 快速检测呋喃西林代谢物的胶体金层析试纸条的制备方法 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2007024735A2 (en) * | 2005-08-19 | 2007-03-01 | Charm Sciences, Inc. | Method and antibodies for detecting nitrofuran |
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Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
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CN101320037A (zh) * | 2008-06-25 | 2008-12-10 | 江南大学 | 快速检测呋喃西林代谢物的胶体金层析试纸条的制备方法 |
Non-Patent Citations (5)
Title |
---|
ELISA detection of semicarbazide based on a fast sample pretreatment method.;Zhiyuan Fang, et al.;《Chem. Commun.》;20130523;第49卷(第55期);第6164-6466页 * |
ELISA for semicarbazide and its application for screening in food contamination.;M.Vass, et al.;《ANALYTICA CHIMICA ACTA》;20071215;第608卷(第1期);第87页左栏第10行,第88页左栏第10行-右栏第3行,第89页左栏第24-34行,图1 * |
Enzyme immunoassay for semicarbazide-The nitrofuran metabolite and food contaminant.;Kevin M.Cooper, et al.,;《ANALYTICA CHIMICA ACTA》;20070419;第592卷(第1期);第64-71页 * |
Protein Biotinylation.;Giuliano Elia;《Current Protocols in Protein Science》;20100401;第3章 第3.6单元:图3.6.1 * |
生物素-亲和素系统试剂及其应用的研究Ⅸ活化长臂生物素的合成及其应用;沈定仁,等;《上海免疫学杂志》;19871028;第7卷(第5期);第267页左栏第10-17行,第2667页右栏第26行-第268页右栏第6行,第270页右栏第1-18行,图1 * |
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Effective date of registration: 20160922 Address after: 101102, Tongzhou District, Beijing, Qiao Town, King Sheng, four South 15 street, 20, two Patentee after: BEIJING XINKAIYUAN PHARMACEUTICAL TECHNOLOGY CO.,LTD. Address before: 351200 No. 112 West Licheng Road, Licheng street, Xianyou County, Fujian Province, China Patentee before: Dai Xinmin |
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Denomination of invention: A Semicarbamide (SEM) Derivatization Reagent and Its Usage Method Effective date of registration: 20230829 Granted publication date: 20160330 Pledgee: Industrial Bank Co.,Ltd. Beijing Pinggu Branch Pledgor: BEIJING XINKAIYUAN PHARMACEUTICAL TECHNOLOGY CO.,LTD. Registration number: Y2023110000364 |
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