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1.
Biosens Bioelectron ; 157: 112144, 2020 Jun 01.
Artigo em Inglês | MEDLINE | ID: mdl-32250927

RESUMO

In vitro fertilization (IVF) is the most common assisted reproductive technology used to treat infertility. Embryo selection for transfer in IVF cycles relies on the morphological evaluation by embryologists, either by conventional microscopic assessment or more recently by time-lapse imaging systems. Despite the introduction of time-lapse imaging improvements in IVF success rates have failed to materialize, therefore alternative approaches are needed. Recent studies have shown that embryos resulting in successful pregnancy differ in their secretome and metabolism compared to embryos that fail to implant, suggesting that molecular analysis of embryo culture medium could assist in non-invasive single embryo selection. However, this approach has yet to be adopted clinically due to the lack of appropriate highly sensitive screening technologies needed to assess volume-limited samples. Here we report the detection of hCGß, IL-8 and TNFα from conditioned culture media of single human embryos using electrochemical impedance spectroscopy. The impedimetric immunosensors revealed that morphologically non-viable embryos produce higher levels of IL-8 and TNFα, associated with abnormal cell division and cell death, respectively. More importantly, hCGß detection was able to discriminate apparently morphologically identical viable embryos. This work brings an objective dimension to embryo selection, which could overcome the major limitations of morphology-based embryo selection for implantation. Future work should include the validation of these biomarkers in a large patient cohort.


Assuntos
Gonadotropina Coriônica Humana Subunidade beta/análise , Meios de Cultivo Condicionados/metabolismo , Embrião de Mamíferos/metabolismo , Interleucina-8/análise , Fator de Necrose Tumoral alfa/análise , Técnicas Biossensoriais/métodos , Linhagem Celular , Gonadotropina Coriônica Humana Subunidade beta/metabolismo , Meios de Cultivo Condicionados/análise , Técnicas de Cultura Embrionária , Implantação do Embrião , Desenvolvimento Embrionário , Feminino , Fertilização in vitro , Humanos , Imunoensaio/métodos , Interleucina-8/metabolismo , Gravidez , Fator de Necrose Tumoral alfa/metabolismo
2.
ACS Appl Mater Interfaces ; 11(8): 8470-8482, 2019 Feb 27.
Artigo em Inglês | MEDLINE | ID: mdl-30694644

RESUMO

Hybrid diamond-graphite nanoplatelet (DGNP) thin films are produced and applied to label-free impedimetric biosensors for the first time, using avidin detection as a proof of concept. The DGNPs are synthesized by microwave plasma chemical vapor deposition through H2/CH4/N2 gas mixtures in a reproducible and rapid single-step process. The material building unit consists of an inner two-dimensional-like nanodiamond with preferential vertical alignment covered by and covalently bound to nanocrystalline graphite grains, exhibiting {111}diamond||{0002}graphite epitaxy. The DGNP films' morphostructural aspects are of interest for electrochemical transduction, in general, and for Faradaic impedimetric biosensors, in particular, combining enhanced surface area for biorecognition element loading and facile Faradaic charge transfer. Charge transfer rate constants in phosphate buffer saline/[Fe(CN)6]4- solution are shown to increase up to 5.6 × 10-3 cm s-1 upon N2 addition to DGNP synthesis. For the impedimetric detection of avidin, biotin molecules are covalently bound as avidin specific recognition elements on (3-aminopropyl)triethoxysilane-functionalized DGNP surfaces. Avidin quantification is attained within the 10-1000 µg mL-1 range following a logarithmic dependency. The limits of detection and of quantitation are 1.3 and 6.4 µg mL-1 (19 and 93 nM), respectively, and 2.3 and 13.8 µg mL-1 (33 and 200 nM) when considering the nonspecific response of the sensors.


Assuntos
Avidina/análise , Técnicas Biossensoriais/métodos , Diamante/química , Grafite/química , Nanoestruturas/química , Técnicas Eletroquímicas , Ferricianetos/química , Gases/química , Limite de Detecção , Propilaminas/química , Silanos/química
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