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Volumn 6, Issue 8, 2010, Pages 952-959

Liposome destabilization by a 2,7-diazapyrenium derivative through formation of transient pores in the lipid bilayer

Author keywords

Fluorescent probes; Lipid bilayers; Liposomes; Molecular dynamics simulations

Indexed keywords

BI-LAYER; COMPUTATIONAL DATA; DIAZAPYRENIUM; FLUORESCENT PROBES; HYDROPHOBIC AND HYDROPHILIC; INTERCALATORS; LIPOSOME DESTABILIZATION; MOLECULAR DYNAMICS SIMULATIONS; WATER MOLECULE;

EID: 77951215301     PISSN: 16136810     EISSN: 16136829     Source Type: Journal    
DOI: 10.1002/smll.200902306     Document Type: Article
Times cited : (14)

References (87)
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    • At pH 7.4 the trianionic and highly fluorescent form of carboxyfluorescein prevails over the others ([trianionic]/[dianionic]=5). Therefore, for the sake of simplicity, carboxyfluorescein has been indicated throughout the paper as CF3.
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    • At pH 7.4 the tetra-anionic and highly fluorescent form of calcein prevails over the others ([tetranionic]/[trianionic]=100). Therefore, for the sake of simplicity, calcein has been indicated throughout the paper as CL4
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    • Unlikely kinetic stability measurements upon addition of positive fluorescent probes, such as methylene blue and ethidium bromide, could not be performed because these probes could not be appreciably entrapped in the liposomes at the self-quenching concentration (1.0-10-4 and 1.0-10-2 M, respectively).
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.