Application of dielectrophoretic field-flow fractionation in environmental studies (Record no. 6546)

MARC details
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005 - DATE AND TIME OF LATEST TRANSACTION
control field 20260817162848.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 100531s2009 th uu|m rtt 0| a1eng d
035 ## - SYSTEM CONTROL NUMBER
System control number .b12077434
099 #9 - LOCAL FREE-TEXT CALL NUMBER (OCLC)
Classification number AIT Diss. no.EV-08-14
100 0# - MAIN ENTRY--PERSONAL NAME
Personal name Sittisak Pui-ock
245 10 - TITLE STATEMENT
Title Application of dielectrophoretic field-flow fractionation in environmental studies
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Pathum Thani, Thailand :
Name of publisher, distributor, etc. Asian Institute of Technology,
Date of publication, distribution, etc. 2008
300 ## - PHYSICAL DESCRIPTION
Extent 238 p. :
Other physical details ill.
490 1# - SERIES STATEMENT
Series statement Dissertation ;
Volume/sequential designation no. EV-08-14
500 ## - GENERAL NOTE
General note A dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Technical Science in Environmental Engineering and Management Inter-University Program on Environmental Toxicology, Technology and Management
502 ## - DISSERTATION NOTE
Dissertation note Thesis (Ph.D.) - Asian Institute of Technology - Chulabhorn Research Institute - Mahidol University, 2008
520 ## - SUMMARY, ETC.
Summary, etc. Earlier studies suggest dielectrophoretic techniques may be applicable for rapid detection of toxicity by exploiting changes induced in the dielectric properties of cells as a result of exposure to toxic agents. However, existing dielectric methods, including electrorotation and dielectrophoretic crossover frequency measurements, are inconvenient, tedious and lengthy. The aim of this study was to develop a practical and speedy dielectrophoretic approach to in vitro toxicity testing. To achieve this, the current study developed several innovations in dielectrophoresis combined with field-flow fractionation (dFFF) using flow cytometry for cell detection. In dFFF, a micro-patterned, nano-film electrode imposes electric forces on cells suspended in a parabolic flow profile as they pass through a thin chamber. Relative changes in the dFFF peak elution times, expressed as a dielectric response index D;, reveal the responses that occur in cell membrane area (capacitance) and ion permeability (conductivity) caused by toxicant exposure. For our purposes, cells were exposed to eight toxicants, each of different single or mixed modes of action. Cell responses were studied over the first 150 minutes of exposure. The selected toxicants include acrylonitrile, actinomycin D, carbon tetrachloride, endosulfan, N-nitroso-N-methylurea (NMU), paraquat dichloride, puromycin, and styrene oxide. The human-derived leukemia cell line HL-60 was used as the in vitro mammalian cell toxicity detection model. For all chemical treatments except actinomycin D, the Di of the HL-60 cells increased in a dose- and time- dependent manner. The sensitivity of the dFFF method was compared with both the cell viability assay for all toxicants studied and either mitochondrial potentiometric dye assay or DNA alkaline comet assay, depending on each toxicant's specific mode of action. Except for low doses of nucleic acid-targeting agents (actinomycin D and NMU), the dFFF method detected all toxicants with more sensitivity than the other assays, often up to 10⁵ times more sensitive than the viability approach. Based on the octanollwater partition (Kow) characteristics of the chemicals tested, the lipophilic chemicals (those with high log Kow) proved to be more easily detected in terms of the dFFF response index Di; than the hydrophilic chemicals (those with low log Kow). The dFFF method appeared to be especially sensitive to agents that directly damaged the plasma membrane or induced apoptosis in the cells. Notably, dFFF detected significant changes in the cell plasma membrane even at the earliest stage of apoptosis induction. In addition, dFFF more acutely detected changes in the plasma membrane of cells exposed to toxicants at doses too low to induce apoptosis or loss of cell viability. Intriguingly, the cells were still stimulated, leading to an increased cell membrane area, perhaps in the form of additional microvilli. A dFFF sample preparation protocol was also developed for testing the toxicity of environmental water samples. Finally, the flow cytometer was replaced by a laser light scatter detector. This device allows the dFFF method to be realized in a more portable, accessible, and cost-effective configuration. Based upon all the findings of this study, it is concluded that the dFFF technique merits further study as a potential rapid in vitro toxicant screening tool
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Dielectrophoresis
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Human ecology
General subdivision Study and teaching
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Mathuros Ruchirawat,
Relator term Chairperson
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Gascoyne, Peter R.C.,
Relator term Examination committee
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Preeda Pakpian,
Relator term Examination Committee
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Jutamaad Satayavivad,
Relator term Examination committee
710 2# - ADDED ENTRY--CORPORATE NAME
Corporate name or jurisdiction name as entry element Chulabhorn Research Institute,
Relator term Scholarship donor
710 2# - ADDED ENTRY--CORPORATE NAME
Corporate name or jurisdiction name as entry element Mahidol University,
Relator term Scholarship donor
710 2# - ADDED ENTRY--CORPORATE NAME
Corporate name or jurisdiction name as entry element Asian Institute of Technology Fellowship,
Relator term Scholarship donor
810 2# - SERIES ADDED ENTRY--CORPORATE NAME
Corporate name or jurisdiction name as entry element Asian Institute of Technology.
Title of a work Dissertation ;
Volume/sequential designation no. EV-08-14
856 ## - ELECTRONIC LOCATION AND ACCESS
Materials specified Full-Text
Uniform Resource Identifier <a href="http://203.159.5.9/ait-thesis/detail.php?q=B00538">http://203.159.5.9/ait-thesis/detail.php?q=B00538</a>
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902 ## - LOCAL DATA ELEMENT B, LDB (RLIN)
a 240329
998 ## - LOCAL CONTROL INFORMATION (RLIN)
Operator's initials, OID (RLIN) 0
Cataloger's initials, CIN (RLIN) 100531
First date, FD (RLIN) m
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945 ## - LOCAL PROCESSING INFORMATION (OCLC)
l mnait
945 ## - LOCAL PROCESSING INFORMATION (OCLC)
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942 ## - ADDED ENTRY ELEMENTS (KOHA)
Koha item type 22-AIT Thesis (Replacement)
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Koha item type 40-Archives
909 ## - LOCAL ITEMS USED
Barcode Barcode : 30050120725691
CREATED CREATED : 2012-08-16
RECORD Id RECORD # : i12686724
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Barcode Barcode : 30050160004239
CREATED CREATED : 2016-09-02
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Holdings
Withdrawn status Lost status Damaged status Not for loan Home library Current library Shelving location Date acquired Total checkouts Full call number Barcode Date last seen Copy number Price effective from Koha item type
      Available for Loans Asian Institute of Technology Library Asian Institute of Technology Library AIT Publications 17/08/2026   AIT Diss. no.EV-08-14 30050120725691 17/08/2026 3 17/08/2026 22-AIT Thesis (Replacement)
      Available for Loans Asian Institute of Technology Library Asian Institute of Technology Library Archives 17/08/2026   AIT Diss. no.EV-08-14 30050160004239 17/08/2026   17/08/2026 40-Archives
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