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   <subfield code="a">Role of different vehicles in carotenoids delivery and their influence on cell viability, cell cycle progression, and induction of apoptosis in HeLa cells</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Poorigali Sowmya, Bangalore Arathi, Kariyappa Vijay, Vallikannan Baskaran, Rangaswamy Lakshminarayana]</subfield>
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   <subfield code="a">The objective of the present study was to determine the role of different vehicles in carotenoids delivery and their influence on cell viability, cell cycle progression and induction of apoptosis in HeLa cells. Cells (5×103) were treated with different concentrations (25-100µM) of β-carotene (BC) or lutein (L) or astaxanthin (AST) dissolved in 0.5% of tetrahydrofuran (THF), dimethylsulfoxide (DMSO), and fetal bovine serum (FBS), respectively. The effect of delivery vehicle on carotenoids uptake, cytotoxicity, oxidative status, cell cycle distribution, and apoptosis was examined after 48h of incubation. The results shown that, cell viability reduced significantly in a dose- and time-dependent manner irrespective of carotenoid delivered in vehicles. Cellular uptake of BC delivered in THF was higher by 49.1, 29.7% and L delivered through THF was higher by 41.7 and 37.5% than DMSO and FBS, respectively. While, AST delivered through DMSO was higher by 36.1 and 43.7% than the THF and FBS, respectively. In case of cells treated either with BC or L delivered through THF and AST in DMSO decreased the glutathione and increased the malondialdehyde levels. The net increase in the G 2/M phase percentage of cell cycle progression was observed in carotenoid-treated cells. The % induction of apoptosis by BC or L delivered with THF and AST in DMSO was higher than other treated groups. In conclusion, choice of suitable vehicle for specific carotenoids delivery is essential that in turn may influence on cell proliferation and cell-based assays.</subfield>
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   <subfield code="a">Springer Science+Business Media New York, 2015</subfield>
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   <subfield code="a">Carotenoids</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Cytotoxicity</subfield>
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   <subfield code="a">Cell cycle</subfield>
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   <subfield code="a">Apoptosis</subfield>
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   <subfield code="a">HeLa cells</subfield>
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   <subfield code="a">AST : Astaxanthin</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">BC : β-Carotene</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">BHT : Butylated hydroxytoluene</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">DMSO : Dimethyl sulfoxide</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">DTNB : 5, 5-dithiobis (2-nitrobenzoic acid)</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">FBS : Fetal bovine serum</subfield>
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   <subfield code="a">GR : Glutathione reductase</subfield>
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   <subfield code="a">L : Lutein</subfield>
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   <subfield code="a">MDA : Malondialdehyde</subfield>
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   <subfield code="a">MEM : Minimal essential medium</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">MTT : 3-[4, 5-dimethylthiazol-2-yl]-2, 5- diphenyltetrazolium bromide</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">NADPH : Nicotinamide adenine dinucleotide phosphate oxidase</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">NEAA : Non-essential amino acid</subfield>
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   <subfield code="a">THF : Tetrahydrofuran</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">TMP : Tetramethoxypropane</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Sowmya</subfield>
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   <subfield code="u">Department of Biotechnology, Bangalore University, Jnana Bharathi Campus, 560 056, Bengaluru, India</subfield>
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