Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 4 de 4
Filter
Add more filters










Database
Language
Publication year range
1.
Sensors (Basel) ; 20(12)2020 Jun 23.
Article in English | MEDLINE | ID: mdl-32585936

ABSTRACT

The significant improvement of quality of life achieved over the last decades has stimulated the development of new approaches in medicine to take into account the personal needs of each patient. Precision medicine, providing healthcare customization, opens new horizons in the diagnosis, treatment and prevention of numerous diseases. As a consequence, there is a growing demand for novel analytical devices and methods capable of addressing the challenges of precision medicine. For example, various types of sensors or their arrays are highly suitable for simultaneous monitoring of multiple analytes in complex biological media in order to obtain more information about the health status of a patient or to follow the treatment process. Besides, the development of sustainable sensors based on natural chemicals allows reducing their environmental impact. This review is concerned with the application of such analytical platforms in various areas of medicine: analysis of body fluids, wearable sensors, drug manufacturing and screening. The importance and role of naturally-occurring compounds in the development of electrochemical multisensor systems and arrays are discussed.


Subject(s)
Biosensing Techniques , Precision Medicine , Body Fluids , Diagnosis , Humans , Pharmaceutical Preparations , Wearable Electronic Devices
2.
J Pharm Biomed Anal ; 150: 67-71, 2018 Feb 20.
Article in English | MEDLINE | ID: mdl-29216587

ABSTRACT

Quantification of proteins is a key biochemical assay in molecular biology, biotechnology, medicine and pharmacology. Protein quantification protocols can be based on spectrophotometry, enzyme-linked immunosorbent assay, mass spectrometry or quantitative immunoblotting depending on analyte. In case of immobilized protein these methods require suitable sample preparation. Thus, sophisticated analysis becomes even more complex, expensive and time-consuming. Such drawbacks are highly undesirable in industry. In this study we propose a new approach for evaluation of immobilized protein concentration based on application of bio-assisted potentiometric multisensor system. Surface-immobilized recombinant protein A from Staphylococcus aureus (SpA, expressed in Escherichia coli), which is commonly used as affinity ligand immobilized to stationary phase (сhromatography media) for monoclonal antibody purification was employed as the model object. Chromatography media samples containing different amounts of immobilized SpA were analyzed. Proteinase K from Tritirachium album was employed as a bio-transducer. We demonstrated that the suggested approach provides information about immobilized SpA concentration with 0.8mg/ml accuracy in the range 1-6.7mg/ml and within just 16min. Moreover, the proposed procedure requires no expensive materials and equipment and no bio-transducer immobilization. This method has potential of application for fast monitoring of other immobilized proteins in different tasks.


Subject(s)
Enzyme-Linked Immunosorbent Assay/methods , Immobilized Proteins/chemistry , Potentiometry/methods , Staphylococcal Protein A/chemistry , Endopeptidase K/chemistry , Immobilized Proteins/analysis , Recombinant Proteins/analysis , Recombinant Proteins/chemistry , Reproducibility of Results , Staphylococcal Protein A/analysis
3.
Talanta ; 156-157: 87-94, 2016 Aug 15.
Article in English | MEDLINE | ID: mdl-27260439

ABSTRACT

Recombinant proteins became essential components of drug manufacturing. Quality control of such proteins is routine task, which usually requires a lot of time, expensive reagents, specialized equipment and highly educated personnel. In this study we propose a new concept for protein purity evaluation that is based on application of bio-assisted potentiometric multisensor system. The model object for analysis was recombinant protein A from Staphylococcus aureus (SpA), which is commonly used for monoclonal antibody purification. SpA solutions with different amount of host cell related impurities (Escherichia coli, bacterial lysate) were analyzed. Two different bio-transducers were employed: proteinase K from Tritirachium album and baker's yeast Saccharomyces cerevisiae. It was shown that both bio-transducers are able to induce changes in pure and lysate-contaminated SpA samples. Different products of yeast digestion and proteolysis with proteinase of pure SpA and lysate were detected with size exclusion high-performance liquid chromatography (SE-HPLC). The induced changes of chemical composition are detectible with potentiometric multisensor system and can be related to SpA purity through projection on latent structures (PLS) regression technique. The proposed method allows for estimation of the impurity content with 12% accuracy using proteinase K and 16% accuracy using baker's yeast. The suggested approach could be useful for early contamination warning at initial protein purification steps. The analysis requires no expensive materials and equipment, no bio-material immobilization, and its duration time is comparable with other commonly used methods like chromatography or electrophoresis though the main part of this time is related to the sample preparation.


Subject(s)
Biosensing Techniques/instrumentation , Potentiometry/instrumentation , Saccharomyces cerevisiae/metabolism , Staphylococcal Protein A/analysis , Biosensing Techniques/methods , Endopeptidase K/metabolism , Equipment Design , Fungi/enzymology , Potentiometry/methods , Proteolysis , Recombinant Proteins/analysis , Recombinant Proteins/metabolism , Staphylococcal Protein A/metabolism , Staphylococcus aureus/chemistry , Staphylococcus aureus/metabolism
4.
J Nanosci Nanotechnol ; 11(10): 9003-11, 2011 Oct.
Article in English | MEDLINE | ID: mdl-22400293

ABSTRACT

Surfaces of constituent parts of biosensors based on single wall carbon nanotube layer were investigated and compare for properly functioning and faulty biosensors. Though the original technology is acceptable for changing of the selectivity, only glucose sensitive biosensors are investigated. Based on the results of the study, a correlation between the features of the nanoscale structures and parameters of amperiometric biosensors for assemblage of which an innovative approach is described. Original template of the electrodes has been prepared on a base of single wall carbon nanotube layer deposited on the supporting polycarbonate membrane. Original immobilisation of enzymes within special membrane allows functional modification of biosensors being accomplished by simple replacement of the enzymatic membrane. The original technology leads to a novel family of biosensors acceptable for detection of wide range of carbohydrates. The morphology and the local electric properties of the constituent parts of the biosensors are characterized by scanning probe microscopy. The sensitivity, selectivity and stability are described for typical types of the biosensors.


Subject(s)
Biosensing Techniques , Electrodes , Nanotubes, Carbon/chemistry , Carbohydrates/chemistry , Enzymes, Immobilized/chemistry , Glucose/chemistry , Microscopy, Scanning Probe/methods , Polycarboxylate Cement/chemistry , Sensitivity and Specificity
SELECTION OF CITATIONS
SEARCH DETAIL
...