Disposable Passive Electrochemical Microfluidic Device for Diagnosis of Congenital Disorders of Glycosylation
نویسندگان
چکیده
A disposable pump-free electrochemical microfluidic device made by using a multilayer lamination technique is proposed for diagnosis of glycosylation disorders. Thanks to the stacking polyethylene terephthalate (PET) films and double adhesive layers, it possible create geometry that allows filling tailored channels in fixed time. In main channel this passive device, necessary steps perform determination transferrin are performed: labeling protein with Os (VI) complex (electrochemical tag), washing water osmium residues detection adsorptive transfer stripping square wave voltammetry. Electrochemical released two signals: one from due carbohydrates at −0.9 V, other intrinsic signal glycoprotein amino acids +0.8 V. The ratio between them establishes an indicator degree (called index glycosylation). method was successfully applied analysis clinical samples patients congenital disorders glycosylation.
منابع مشابه
Congenital disorders of glycosylation.
Congenital disorders of glycosylation (CDG) are a rapidly growing group of genetic diseases that are due to defects in the synthesis of glycans and in the attachment of glycans to other compounds. Most CDG are multisystem diseases that include severe brain involvement. The CDG causing sialic acid deficiency of N-glycans can be diagnosed by isoelectrofocusing of serum sialotransferrins. An effic...
متن کاملCongenital disorders of glycosylation (CDG)
Congenital Disorders of Glycosylation (CDG) comprise permanently expanding group of inherited diseases caused by defects of multiple glycosylation pathways which disturb structure of many glycoconjugates classes. The first patients were described by Jaak Jaeken in 1980, in 1984 simple test was implemented to identify new cases. In 1995, fifteen years later, enzymatic defect was revealed as phos...
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متن کاملCongenital Disorders of Glycosylation: A Review
Congenital disorders of glycosylation (CDG) are a rapidly growing group of inborn erros of metabolism with abnormal glycosylation of proteins and lipids. Nearly 70 inborn errors of metabolism have been described due to congenital defects of glycosylation, present as clinical syndromes, affecting multiple systems, impacting nearly every organ. No specific tests are available yet for screening al...
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ژورنال
عنوان ژورنال: Analysis & sensing
سال: 2021
ISSN: ['2629-2742']
DOI: https://doi.org/10.1002/anse.202100038