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Development of An Enzyme-Linked Immunosorbent Assay for Determination of the Furaltadone Etabolite,3-Amino-5-Morpholinomethyl-2-Oxazolidinone(AMOZ) in Animal Tissues 被引量:2
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作者 LUO Peng Jie JIANG Wen Xiao +6 位作者 BEIER Ross C. SHEN Jian Zhong JIANG Hai Yang MIAO Hong ZHAO Yun Feng CHEN Xia WU Yong Ning 《Biomedical and Environmental Sciences》 SCIE CAS CSCD 2012年第4期449-457,共9页
Objective To determine 3-amino-5-morpholinomethyl-2-oxazolidinone (AMOZ) residues released from protein bound AMOZ in animal tissues. Methods Polyclonal and monoclonal antibodies were produced in this study. A rapid... Objective To determine 3-amino-5-morpholinomethyl-2-oxazolidinone (AMOZ) residues released from protein bound AMOZ in animal tissues. Methods Polyclonal and monoclonal antibodies were produced in this study. A rapid, sensitive, and specific competitive direct enzyme-linked immunosorbent assay (cdELISA) was developed. Results Rabbit polyclonal antibodies were used in the optimized cdELISA method, and exhibited negligible cross-reactivity with other compounds structurally related to AMOZ. The IC50 of the polycional antibody was 0.16 ng/mL The method limit of detection in four different types of animal and fish tissues was less than 0.06 μg/kg. Recoveries ranged from 80% to 220% for fortified samples with the coefficient of variation values less than 15%. The results of the cdELISA method were in good agreement with the results from an established liquid chromatography-tandem mass spectrometry confirmatory method used for AMOZ residues. Conclusion The cdELISA method developed in the present study is a convenient practical tool for screening large numbers of animal and fish tissue samples for the the detection of released protein bound AMOZ residues. 展开更多
关键词 AMOZ animal tissue ELISA Fish tissue Furaltadone
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A Systematic Review of Animal and Clinical Studies on the Use of Scaffolds for Urethral Repair 被引量:3
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作者 祁娜 李文娇 田虹 《Journal of Huazhong University of Science and Technology(Medical Sciences)》 SCIE CAS 2016年第1期111-117,共7页
Replacing urethral tissue with functional scaffolds has been one of the challenging problems in the field of urethra reconstruction or repair over the last several decades. Various scaffold materials have been used in... Replacing urethral tissue with functional scaffolds has been one of the challenging problems in the field of urethra reconstruction or repair over the last several decades. Various scaffold materials have been used in animal studies, but clinical studies on use of scaffolds for urethral repair are scarce. The aim of this study was to review recent animal and clinical studies on the use of different scaffolds for urethral repair, and to evaluate these scaffolds based on the evidence from these studies. Pub Med and OVID databases were searched to identify relevant studies, in conjunction with further manual search. Studies that met the inclusion criteria were systematically evaluated. Of 555 identified studies, 38 were included for analysis. It was found that in both animal and clinical studies, scaffolds seeded with cells were used for repair of large segmental defects of the urethra, such as in tubular urethroplasty. When the defect area was small, cell-free scaffolds were more likely to be applied. A lot of pre-clinical and limited clinical evidence showed that natural or artificial materials could be used as scaffolds for urethral repair. Urinary tissue engineering is still in the immature stage, and the safety, efficacy, cost-effectiveness of the scaffolds are needed for further study. 展开更多
关键词 material/scaffold urethral repair tissue engineering/regenerative medicine animal models clinical studies
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Tectona grandis (Teak Tree) Young Leaf Extract as a Histological Stain
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作者 Cecilia Smith-Togobo Adam Abdul Fatau +4 位作者 Magalys Cuba Lopez Felix Kpor David Larbi Simpong George Osei Yiadom Emmanuel Akomanin Asiamah 《Journal of Biomedical Science and Engineering》 CAS 2023年第2期17-41,共25页
Stains are applied to impart contrast to the tissue and identify particular features of interest. However, the use of synthetic dyes as staining reagents has been associated with significant human health challenges an... Stains are applied to impart contrast to the tissue and identify particular features of interest. However, the use of synthetic dyes as staining reagents has been associated with significant human health challenges and pollution of the ecosystem. These developments have necessitated a shift towards using natural dyes that are eco-friendlier and readily available. We investigated the staining reaction patterns of teak tree leaves (Tectona grandis) dye extracts and explored their suitability as a cytoplasmic stain in micromorphological assessments. Dye extracts were prepared using acetone, methanol, and ethanol as solvents from air-dried (under shade) teak tree young leaves. The dye extracts were applied as a counterstain and evaluated against eosin in formalin-fixed paraffin-embedded (FFPE) bovine tissue sections at varying concentrations and different staining times. Teak tree leaves (Tectona grandis) dye extracts produced relatively varying staining intensities of reddish-brown cytoplasmic coloration when used on bovine tissue at different concentrations and staining times comparable to eosin and with blue-purple hematoxylin nuclear stain. The present study showed that Tectona grandis leaf dye extracts provide an excellent cytoplasmic staining pattern and can be used as an alternative counterstain in routine H&E staining techniques. 展开更多
关键词 Histology CYTOPLASM Plant Extract Tectona grandis Leaves Formalin-Fixed Paraffin-Embedded tissues Natural Dye STAINING Cytoplasmic Stain animal tissues Staining Reaction
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克伦特罗残留的GC-MS确证分析及应注意事项
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作者 刘琪 叶妮 王树槐 《分析测试学报》 CAS CSCD 北大核心 2004年第z1期214-216,共3页
  克伦特罗(clenbuterol,C12H18Cl2N2O)属β兴奋剂类,俗称为瘦肉精,畜牧业上可作为生长促进剂,其药物残留对人类健康有危害,我国农业部将其列为食品动物禁止使用的兽药[1].对于动物组织、尿中盐酸克伦特罗残留的测定,一般是先用酶联...   克伦特罗(clenbuterol,C12H18Cl2N2O)属β兴奋剂类,俗称为瘦肉精,畜牧业上可作为生长促进剂,其药物残留对人类健康有危害,我国农业部将其列为食品动物禁止使用的兽药[1].对于动物组织、尿中盐酸克伦特罗残留的测定,一般是先用酶联免疫检测法进行筛选,由于酶联法存在假阳性问题,对检测结果呈阳性的样品需再用气相色谱-质谱法进行确证检测.…… 展开更多
关键词 GC - MS animal tissues Clenbuterol residue
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