A naked-eye liquid-phase colorimetric assay of simultaneous detect cysteine and lysine

2019 ◽  
Vol 160 ◽  
pp. 151-158 ◽  
Author(s):  
Zhonghua Xue ◽  
Lulu Xiong ◽  
Honghong Rao ◽  
Xiuhui Liu ◽  
Xiaoquan Lu
2017 ◽  
Vol 53 (60) ◽  
pp. 8407-8410 ◽  
Author(s):  
Huili Wang ◽  
Yun Zhang ◽  
Rongxing Li ◽  
Jinfang Nie ◽  
Afaf H. El-Sagheer ◽  
...  

This work describes a new class of gold nanoparticle-based liquid-phase colorimetric assay (GNP-LPCA) termed as two dimensional (2D) GNP-LPCA that enables quantitative detection of model analytes with naked eye.


2016 ◽  
Vol 52 (47) ◽  
pp. 7454-7457 ◽  
Author(s):  
Jinfang Nie ◽  
Tom Brown ◽  
Yun Zhang

This work describes a new point-of-care two dimensional liquid-phase colorimetric assay (2D LPCA) based on old iodine–starch complexation reaction firstly discovered in 1814 for simple, low-cost, portable, naked-eye detection and quantification of two model analytes.


The Analyst ◽  
2017 ◽  
Vol 142 (17) ◽  
pp. 3235-3240 ◽  
Author(s):  
Yaocai Wang ◽  
Luzhu Yang ◽  
Yanjun Wang ◽  
Wei Liu ◽  
Baoxin Li ◽  
...  

We proposed a sensitive colorimetric assay for detecting telomerase activity. The telomerase activity of 5 and 20 HeLa cell lysates can be detected via UV-vis spectroscopy and the naked eye, respectively.


2020 ◽  
Vol 12 (26) ◽  
pp. 3361-3367
Author(s):  
Wenshuai Li ◽  
Guorui Wu ◽  
Min Wang ◽  
Aiqin Yue ◽  
Weijun Du ◽  
...  

We propose a colorimetric assay based on the coupling of gap ligase chain reaction (Gap-LCR) with DNAzyme to detect the target GmSg-1 genes of class A soybean saponins with the naked eye, without the involvement of expensive instruments.


The Analyst ◽  
2019 ◽  
Vol 144 (2) ◽  
pp. 716-721 ◽  
Author(s):  
Qing Juan Guo ◽  
Zi Yu Pan ◽  
Chen Men ◽  
Wen Yi Lv ◽  
Hong Yan Zou ◽  
...  

Cu2−xSe nanoparticles grown in situ on reduced graphene oxide (Cu2−xSe/rGO) acted as an efficient nanozyme. Using the Cu2−xSe/rGO as a signal transducer, a colorimetric assay for cancer cells with the naked eye has been developed.


Nanomaterials ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 1470 ◽  
Author(s):  
Roman Lehmacher ◽  
Claus Feldmann

Nitrogen-containing C-dots were prepared by heating (160 °C, 1 h) 1,2,4,5-tetracyanobenzene (TCB) in polyethylene glycol 400 (PEG400). The as-prepared monocrystalline C-dots were 2–4 nm in diameter and contained 24.4 wt. % of nitrogen. They showed intense fluorescence under excitation at 400–500 nm as well as under excitation at 600–700 nm. In addition to an excitation-wavelength-depending emission at 400 to 650 nm, the emission spectra exhibited a strong emission peaking at 715 nm, whose position was independent from the wavelength of excitation. For this deep-red emission a remarkable quantum yield of 69% was detected. The synthesis of nitrogen-containing C-dotswas completely performed in the liquid phase. Moreover, the C-dots could be directly dispersed in water. The resulting aqueous suspensions of PEG400-stabilized nitrogen-containing C-dots also showed intense red emission that was visible to the naked eye.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
George S. Luka ◽  
Ephraim Nowak ◽  
Quin Robert Toyata ◽  
Nishat Tasnim ◽  
Homayoun Najjaran ◽  
...  

AbstractCryptosporidium, a protozoan pathogen, is a leading threat to public health and the economy. Herein, we report the development of a portable, colorimetric biosensing platform for the sensitive, selective and label/PCR-free detection of Cryptosporidium RNA using oligonucleotides modified gold nanoparticles (AuNPs). A pair of specific thiolated oligonucleotides, complementary to adjacent sequences on Cryptosporidium RNA, were attached to AuNPs. The need for expensive laboratory-based equipment was eliminated by performing the colorimetric assay on a micro-fabricated chip in a 3D-printed holder assembly. A smartphone camera was used to capture an image of the color change for quantitative analysis. The detection was based on the aggregation of the gold nanoparticles due to the hybridization between the complementary Cryptosporidium RNA and the oligonucleotides immobilized on the AuNPs surface. In the complementary RNA’s presence, a distinctive color change of the AuNPs (from red to blue) was observed by the naked eye. However, in the presence of non-complementary RNA, no color change was observed. The sensing platform showed wide linear responses between 5 and 100 µM with a low detection limit of 5 µM of Cryptosporidium RNA. Additionally, the sensor developed here can provide information about different Cryptosporidium species present in water resources. This cost-effective, easy-to-use, portable and smartphone integrated on-chip colorimetric biosensor has great potential to be used for real-time and portable POC pathogen monitoring and molecular diagnostics.


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