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Volumn 130, Issue 2, 2008, Pages 457-459

Liposome encapsulation of conjugated polyelectrolytes: Toward a liposome beacon

Author keywords

[No Author keywords available]

Indexed keywords

1,2 DIOLEOYL 3 TRIMETHYLAMMONIOPROPANE; ELECTROLYTE; LIPOSOME; PHENYL GROUP; 3,3' DIOCTADECYLINDOCARBOCYANINE; 3,3'-DIOCTADECYLINDOCARBOCYANINE; CARBOCYANINE; FLUORESCENT DYE; POLY(2,5 METHOXY PROPYLOXY SULFONATE PHENYLENE VINYLENE); POLY(2,5-METHOXY-PROPYLOXY SULFONATE PHENYLENE VINYLENE); POLYVINYL DERIVATIVE; UNCLASSIFIED DRUG;

EID: 40149107623     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja076217b     Document Type: Article
Times cited : (34)

References (26)
  • 16
    • 3042817877 scopus 로고    scopus 로고
    • 2nd ed, Oxford University Press Inc, New York
    • Torchilin, V. P.; Weissig, V. Liposomes, 2nd ed.; Oxford University Press Inc.: New York, 2003; Vol. 264.
    • (2003) Liposomes , vol.264
    • Torchilin, V.P.1    Weissig, V.2
  • 20
    • 41449088273 scopus 로고    scopus 로고
    • -19 L, a 260 nM liposome solution will encapsulate a fraction of the total ap; 0.08 as determined by the product of the per liposome times the total number of liposome particles in solution.
    • -19 L, a 260 nM liposome solution will encapsulate a fraction of the total volume ≈ 0.08 as determined by the product of the volume per liposome times the total number of liposome particles in solution.
  • 21
    • 41449114534 scopus 로고    scopus 로고
    • Note that both the green and red traces have the same initial slope, that is, the samples in contact with DOPC have the same initial Stern-Volmer fluorescence quenching constant
    • Note that both the green and red traces have the same initial slope, that is, the samples in contact with DOPC have the same initial Stern-Volmer fluorescence quenching constant.
  • 26
    • 41449117161 scopus 로고    scopus 로고
    • Briefly, immobilization involved (a) the functionalization of glass coverslips with Vectabond reagent, (b) the covalent tethering of a 100/1 PEG (MW 5000)/biotin-PEG (MW 5000) mixture to the coverslip surface, (c) the assembly of a flow chamber, (d) a 10 min incubation of a streptavidin solution and (e) a 3-4 min incubation of the 5 pM liposome solution under study followed by a steady flow of buffer solution to remove all non-immobilized liposomes and non-encapsulated MPS-PPV.
    • Briefly, immobilization involved (a) the functionalization of glass coverslips with Vectabond reagent, (b) the covalent tethering of a 100/1 PEG (MW 5000)/biotin-PEG (MW 5000) mixture to the coverslip surface, (c) the assembly of a flow chamber, (d) a 10 min incubation of a streptavidin solution and (e) a 3-4 min incubation of the 5 pM liposome solution under study followed by a steady flow of buffer solution to remove all non-immobilized liposomes and non-encapsulated MPS-PPV.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.