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miami1169691746.pdf (768.27 KB)
ETD Abstract Container
Abstract Header
Fluorescent Determination of Cardiolipin using 10-N-nonyl Acridine Orange
Author Info
Kaewsuya, Pakritsadang
Permalink:
http://rave.ohiolink.edu/etdc/view?acc_num=miami1169691746
Abstract Details
Year and Degree
2007, Master of Science, Miami University, Chemistry and Biochemistry.
Abstract
Cardiolipin (CL) plays an essential role as a marker for cell apoptosis. Quantitative detection of phospholipids (PLs) by UV absorbance is problematic due to the presence of only isolated double bonds in the structure. Although 10-N-nonyl acridine orange (NAO) has been utilized for fluorescent detection of liposomes and mitochondria through its interaction with CL, specific quantitative determination of CL in solution using NAO is uncommon. In this work, we have developed a fluorescence quenching method for CL using NAO. The optimum excitations are 499 and 518 nm at low and high NAO concentration, respectively. The optimum emissions are varied from 518 to 530 nm. The interaction of sodium n-dodecyl sulfate (SDS), sometimes used for lipid extraction from cells, and other PLs such as phosphatidic acid (PA), phosphatidylcholine (PC), phosphatidylethnolamine (PE), phosphatidylglycerol (PG), phosphatdiylserine (PS), sphingomyelin (SM) and cholesterol, with NAO is investigated. The fluorescence intensity of 0.5 µM NAO signal is strongly quenched by SDS below 25% methanol in water. With a methanol content above 50%, no quenching of NAO by SDS or the PLs with the exception of PG above 8 µM is observed. Using 50-50 methanol-water, the fluorescence as a function of reaction time for the NAO-CL interaction is quite stable from 3 to at least 15 min. Concentrations of 5, 10, 20, and 50 µM NAO are considered and 20 µM NAO provides a linear fluorescence response from 0.2 – 10 µM CL. The detection limit is 0.2 µM and the limit of quantification is 0.6 µM. Acridine orange (AO) and phenosafranin (PSF) dyes are less effective as fluorescent probes for CL. CL in whole cell and membrane samples is quantitatively determined by standard addition to be in the 0.2-1.5 µM range. The increase of CL as compared to the controls is not significantly different in all samples subjected to cell death using staurosporine.
Committee
Neil Danielson (Advisor)
Pages
85 p.
Subject Headings
Chemistry, Analytical
Keywords
Fluorescence
;
Cardiolipin
;
Phospholipids
;
10-Nonyl acridine orange
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Citations
Kaewsuya, P. (2007).
Fluorescent Determination of Cardiolipin using 10-N-nonyl Acridine Orange
[Master's thesis, Miami University]. OhioLINK Electronic Theses and Dissertations Center. http://rave.ohiolink.edu/etdc/view?acc_num=miami1169691746
APA Style (7th edition)
Kaewsuya, Pakritsadang.
Fluorescent Determination of Cardiolipin using 10-N-nonyl Acridine Orange.
2007. Miami University, Master's thesis.
OhioLINK Electronic Theses and Dissertations Center
, http://rave.ohiolink.edu/etdc/view?acc_num=miami1169691746.
MLA Style (8th edition)
Kaewsuya, Pakritsadang. "Fluorescent Determination of Cardiolipin using 10-N-nonyl Acridine Orange." Master's thesis, Miami University, 2007. http://rave.ohiolink.edu/etdc/view?acc_num=miami1169691746
Chicago Manual of Style (17th edition)
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Document number:
miami1169691746
Download Count:
2,204
Copyright Info
© 2007, all rights reserved.
This open access ETD is published by Miami University and OhioLINK.