scholarly journals Adenosine Triphosphate Measurement in Deep Sea Using a Microfluidic Device

Micromachines ◽  
2018 ◽  
Vol 9 (8) ◽  
pp. 370 ◽  
Author(s):  
Tatsuhiro Fukuba ◽  
Takuroh Noguchi ◽  
Kei Okamura ◽  
Teruo Fujii

Total ATP (adenosine triphosphate) concentration is a useful biochemical parameter for detecting microbial biomass or biogeochemical activity anomalies in the natural environment. In this study, we describe the development and evaluation of a new version of in situ ATP analyzer improved for the continuous and quantitative determination of ATP in submarine environments. We integrated a transparent microfluidic device containing a microchannel for cell lysis and a channel for the bioluminescence L–L (luciferin–luciferase) assay with a miniature pumping unit and a photometry module for the measurement of the bioluminescence intensity. A heater and a temperature sensor were also included in the system to maintain an optimal temperature for the L–L reaction. In this study, the analyzer was evaluated in deep sea environments, reaching a depth of 200 m using a remotely operated underwater vehicle. We show that the ATP analyzer successfully operated in the deep-sea environment and accurately quantified total ATP within the concentration lower than 5 × 10−11 M.

Author(s):  
Tatsuhiro Fukuba ◽  
Kei Okamura ◽  
Teruo Fujii
Keyword(s):  

2019 ◽  
Vol 11 (31) ◽  
pp. 3943-3957
Author(s):  
Imma Tolosa ◽  
Carlos Guitart ◽  
Marianela Mesa-Albernas ◽  
Carolina Funkey ◽  
Roberto Cassi

A large volume sampling technique is used to develop and validate a home-made SPE system connected to a particle collector in situ pump for high sample pre-concentration and determination of petroleum hydrocarbons and their 13C/12C isotope ratio.


2021 ◽  
Vol 332 ◽  
pp. 129506
Author(s):  
Inmaculada Ortiz-Gómez ◽  
Víctor Toral-López ◽  
Francisco J. Romero ◽  
Ignacio de Orbe-Payá ◽  
Antonio García ◽  
...  

2011 ◽  
Vol 27 (2) ◽  
pp. 183 ◽  
Author(s):  
Keiichi FUJIMORI ◽  
Kenta TSUJIMOTO ◽  
Takayo MORIUCHI-KAWAKAMI ◽  
Yasuhiko SHIBUTANI ◽  
Masato UEDA ◽  
...  
Keyword(s):  

1961 ◽  
Vol 38 (4) ◽  
pp. 545-562 ◽  
Author(s):  
L. Kecskés ◽  
F. Mutschler ◽  
I. Glós ◽  
E. Thán ◽  
I. Farkas ◽  
...  

ABSTRACT 1. An indirect paperchromatographic method is described for separating urinary oestrogens; this consists of the following steps: acidic hydrolysis, extraction with ether, dissociation of phenol-fractions with partition between the solvents. Previous purification of phenol fraction with the aid of paperchromatography. The elution of oestrogen containing fractions is followed by acetylation. Oestrogen acetate is isolated by re-chromatography. The chromatogram was developed after hydrolysis of the oestrogens 'in situ' on the paper. The quantity of oestrogens was determined indirectly, by means of an iron-reaction, after the elution of the iron content of the oestrogen spot, which was developed by the Jellinek-reaction. 2. The method described above is satisfactory for determining urinary oestrogen, 17β-oestradiol and oestriol, but could include 16-epioestriol and other oestrogenic metabolites. 3. The sensitivity of the method is 1.3–1.6 μg/24 hours. 4. The quantitative and qualitative determination of urinary oestrogens with the above mentioned method was performed in 50 pregnant and 9 non pregnant women, and also in 2 patients with granulosa cell tumour.


2015 ◽  
Vol 49 (6) ◽  
pp. 613-620 ◽  
Author(s):  
Masahiro Yamamoto ◽  
Hitoshi Kodamatani ◽  
Yuriko Kono ◽  
Akinori Takeuchi ◽  
Ken Takai ◽  
...  

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