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1.
Expert Syst Appl ; 183: 115401, 2021 Nov 30.
Artigo em Inglês | MEDLINE | ID: mdl-34149202

RESUMO

The COVID-19 outbreak has catastrophically affected both public health system and world economy. Swift diagnosis of the positive cases will help in providing proper medical attention to the infected individuals and will also aid in effective tracing of their contacts to break the chain of transmission. Blending Artificial Intelligence (AI) with chest X-ray images and incorporating these models in a smartphone can be handy for the accelerated diagnosis of COVID-19. In this study, publicly available datasets of chest X-ray images have been utilized for training and testing of five pre-trained Convolutional Neural Network (CNN) models namely VGG16, MobileNetV2, Xception, NASNetMobile and InceptionResNetV2. Prior to the training of the selected models, the number of images in COVID-19 category has been increased employing traditional augmentation and Generative Adversarial Network (GAN). The performance of the five pre-trained CNN models utilizing the images generated with the two strategies has been compared. In the case of models trained using augmented images, Xception (98%) and MobileNetV2 (97.9%) turned out to be the ones with highest validation accuracy. Xception (98.1%) and VGG16 (98.6%) emerged as models with the highest validation accuracy in the models trained with synthetic GAN images. The best performing models have been further deployed in a smartphone and evaluated. The overall results suggest that VGG16 and Xception, trained with the synthetic images created using GAN, performed better compared to models trained with augmented images. Among these two models VGG16 produced an encouraging Diagnostic Odd Ratio (DOR) with higher positive likelihood and lower negative likelihood for the prediction of COVID-19.

2.
RSC Adv ; 10(7): 3951-3959, 2020 Jan 22.
Artigo em Inglês | MEDLINE | ID: mdl-35492677

RESUMO

Wide band gap metal oxides are ideally suited for inorganic optoelectronic devices. While zinc oxide is a commonly used n-type material, there is still a lot of ongoing work for finding suitable p-type oxides. In this work, we describe a two-step route to formulate a stable and conducting p-type nickel oxide (NiO) nanofluid. NiO nanoparticles were synthesised using a bottom-up wet chemical approach and dispersed in ethylene glycol to form a nanofluid. The viscosity and surface tension of the nanofluid were optimised for printing. The printing was done using an extrusion-based direct writer. The NiO nanofluid was printed onto an aluminum-doped zinc oxide layer and annealed at different temperatures. Electrical characterisation of the junction was used to extract the junction barrier for carriers across the interface. The resulting heterojunction was found to exhibit rectifying behaviour, with the highest rectification ratio occurring at an annealing temperature of 250 °C. This annealing temperature also resulted in the lowest junction barrier height, and was in excellent agreement with theoretically predicted values. The development of a printed p-type ink will help in the realisation of oxide-based printed electronic devices.

3.
Cells ; 1(3): 313-24, 2012 Jul 25.
Artigo em Inglês | MEDLINE | ID: mdl-24710478

RESUMO

Cryopreserved peripheral blood mononuclear cells (PBMC) constitute an important component of immune monitoring studies as they allow for efficient batch- testing of samples as well as for the validation and extension of original studies in the future. In this study, we systematically test the permutations of PBMC thawing practices commonly employed in the field and identify conditions that are high and low risk for the viability of PBMC and their functionality in downstream ELISPOT assays. The study identifies the addition of ice-chilled washing media to thawed cells at the same temperature as being a high risk practice, as it yields significantly lower viability and functionality of recovered PBMC when compared to warming the cryovials to 37 °C and adding a warm washing medium. We found thawed PBMC in cryovials could be kept up to 30 minutes at 37 °C in the presence of DMSO before commencement of washing, which surprisingly identifies exposure to DMSO as a low risk step during the thawing process. This latter finding is of considerable practical relevance since it permits batch-thawing of PBMC in high-throughput immune monitoring environments.

4.
Eur J Pharmacol ; 668(1-2): 99-106, 2011 Oct 01.
Artigo em Inglês | MEDLINE | ID: mdl-21749863

RESUMO

Substantial evidences suggest that lipoxygenase-catalyzed products have a strong influence on the development and progression of human cancers. The dietary phytochemical resveratrol has become a focus of intense research owing to its roles in cancer prevention. A single tail vein injection of 7,12-dimethylbenz(a)anthracene (DMBA) was given at a dose of 0.5mg/0.2 ml oil emulsion/100g body weight at 50 days of age of female Sprague-Dawley rats. Rats were treated with resveratrol from 2 weeks before DMBA injection (5 weeks of animal age) and continued to 24 weeks of the experimentation at a dose of 100 µg/rat in the diet. We observed that resveratrol acts as a potent 5-lipoxygenase (5-LOX) inhibitor obtained from natural sources. Our result indicated that resveratrol is a strong antioxidant in reducing lipid peroxidation and preventing DNA damage. It significantly decreased the extent of DNA strand break, inhibited abnormal cell proliferation as evidenced by BrdU labeling index and also induced apoptosis in carcinogen-challenged rat mammary tissue. Increased TGF-ß1 expression in resveratrol treated rats is thought to be one of the factors inducing apoptosis to suppress DMBA-induced mammary carcinogenesis.


Assuntos
9,10-Dimetil-1,2-benzantraceno/toxicidade , Araquidonato 5-Lipoxigenase/metabolismo , Inibidores de Lipoxigenase/farmacologia , Neoplasias Mamárias Experimentais/induzido quimicamente , Neoplasias Mamárias Experimentais/tratamento farmacológico , Estilbenos/farmacologia , Animais , Apoptose/efeitos dos fármacos , Proliferação de Células/efeitos dos fármacos , Ciclina D1/metabolismo , Quebras de DNA/efeitos dos fármacos , Feminino , Regulação Neoplásica da Expressão Gênica/efeitos dos fármacos , Marcação In Situ das Extremidades Cortadas , Leucotrieno B4/biossíntese , Peroxidação de Lipídeos/efeitos dos fármacos , Inibidores de Lipoxigenase/uso terapêutico , Glândulas Mamárias Animais/efeitos dos fármacos , Glândulas Mamárias Animais/metabolismo , Glândulas Mamárias Animais/patologia , Neoplasias Mamárias Experimentais/metabolismo , Neoplasias Mamárias Experimentais/patologia , NF-kappa B/metabolismo , Ratos , Ratos Sprague-Dawley , Resveratrol , Estilbenos/uso terapêutico , Fator de Crescimento Transformador beta1/metabolismo
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