Micro- and Nanofluidic Systems for Trace Analysis of Biological Samples

2010 ◽  
pp. 111-131
Author(s):  
Debashis Dutta
Keyword(s):  
Biological Samples ◽  
Trace Analysis

The trace analysis of musk xylene in biological samples: Problems associated with its ubiquitous occurrence

Chemosphere ◽  
1994 ◽  
Vol 29 (3) ◽  
pp. 477-484 ◽  
Author(s):  
Karin S. Helbling ◽  
Peter Schmid ◽  
Christian Schlatter
Keyword(s):  
Biological Samples ◽  
Trace Analysis ◽  
Musk Xylene

NiO–ZrO2 nanocomposite modified electrode for the sensitive and selective determination of efavirenz, an anti-HIV drug

RSC Advances ◽  
2015 ◽  
Vol 5 (50) ◽  
pp. 40057-40064 ◽  
Author(s):  
Neeta Thapliyal ◽  
Nadir S. E. Osman ◽  
Harun Patel ◽  
Rajshekhar Karpoormath ◽  
Rajendra N. Goyal ◽  
...  
Keyword(s):  
Modified Electrode ◽  
Biological Samples ◽  
Trace Analysis ◽  
Selective Determination ◽  
Highly Sensitive ◽  
Anti Hiv

A highly sensitive NiO–ZrO2 nanocomposite modified electrode was fabricated for trace analysis of efavirenz in pharmaceutical and biological samples.

Fluorescence Labelling in trace analysis of biological samples

1981 ◽  
Vol 217 ◽  
pp. 491-507 ◽  
Author(s):  
Wolfgang Voelter ◽  
Reinhard Huber ◽  
Karl Zech
Keyword(s):  
Biological Samples ◽  
Trace Analysis ◽  
Fluorescence Labelling

An Efficient Statistic for Determining the Diameter of Thin Sectioned Uniform Spheres from Measurements of Biological Samples

1974 ◽  
Vol 32 ◽  
pp. 114-115
Author(s):  
W. R. Schucany ◽  
G. H. Kelsoe ◽  
V. F. Allison
Keyword(s):  
Biological Samples ◽  
Traditional Method ◽  
Cell Types ◽  
Accurate Estimation ◽  
Morphological Identification ◽  
Sectioned Material ◽  
Maximal Diameter ◽  
Similar Cell

Accurate estimation of the size of spheroid organelles from thin sectioned material is often necessary, as uniquely homogenous populations of organelles such as vessicles, granules, or nuclei often are critically important in the morphological identification of similar cell types. However, the difficulty in obtaining accurate diameter measurements of thin sectioned organelles is well known. This difficulty is due to the extreme tenuity of the sectioned material as compared to the size of the intact organelle. In populations where low variance is suspected the traditional method of diameter estimation has been to measure literally hundreds of profiles and to describe the “largest” as representative of the “approximate maximal diameter”.

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