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1.
Talanta ; 225: 122021, 2021 Apr 01.
Article in English | MEDLINE | ID: mdl-33592751

ABSTRACT

Frequent on-line and automated monitoring of multiple protein biomarkers level secreted in the culture media during tissue growth is essential for the successful development of Tissue Engineering and Regenerative Medicine (TERM) products. Here, we present a low-cost, rapid, reliable, and integrable anion-exchange membrane-(AEM) based multiplexed sensing platform for this application. Unlike the gold-standard manual ELISA test, incubation/wash steps are optimized for each target and precisely metered in microfluidic chips to enhance selectivity. Unlike optical detection and unreliable visual detection for the ELISA test, which require standardization for every usage, the AEM ion current signal also offers robustness, endowed by the pH and ionic strength control capability of the ion-selective membrane, such that a universal standard curve can be used to calibrate all runs. The electrical signal is enhanced by highly charged silica nanoparticle reporters, which also act as hydrodynamic shear amplifiers to enhance selectivity during wash. This AEM-based sensing platform is tested with vascular protein biomarkers, Endothelin-1 (ET-1), Angiogenin (ANG) and Placental Growth Factor (PlGF). The limit of detection and three-decade dynamic range are comparable to ELISA assay but with a significantly reduced assay time of 1 h vs 7 h, due to the elimination of calibration and blocking steps. Optimized protocol for each target renders the detection highly reliable with more than 98% confidence. The multiplexed detection capability of the platform is also demonstrated by simultaneous detection of ET-1, ANG and PlGF in 40 µl of the vascular endothelial cell culture supernatants using three-membrane AEM sensor and the performance is validated against ELISA.


Subject(s)
Hydrodynamics , Silicon Dioxide , Biomarkers , Enzyme-Linked Immunosorbent Assay , Placenta Growth Factor
2.
Med Clin North Am ; 104(4): 631-646, 2020 Jul.
Article in English | MEDLINE | ID: mdl-32505257

ABSTRACT

"Acute venous thromboembolism is a common disease seen by nearly all hospitalists. The advent of low molecular weight heparin (LMWH) several decades ago ushered in the era of early hospital discharge and home treatment. More recently, the direct oral anticoagulants (DOACs) have further simplified outpatient treatment and some offer treatment without parenteral therapy. Use of DOACs for cancer-associated venous thromboembolism is emerging and is a welcome evolution of care to spare oncologic patients the burden of daily LMWH injections."


Subject(s)
Anticoagulants/therapeutic use , Venous Thromboembolism/therapy , Venous Thrombosis/therapy , Administration, Oral , Anticoagulants/adverse effects , Hemorrhage/chemically induced , Heparin, Low-Molecular-Weight/therapeutic use , Humans , Neoplasms/complications , Pulmonary Embolism/therapy , Risk Assessment , Surgical Procedures, Operative , Venous Thromboembolism/etiology , Venous Thrombosis/etiology , Vitamin K/antagonists & inhibitors
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