Langmuir monolayers of the long-chain alkyl derivatives of a nucleoside analogue and the formation of self-assembled nanoparticles

Colloids and Surfaces B: Biointerfaces

Volumn 42, Issue 1, 2005, Pages 45-51

  Jin, Yiguang ^a,b   Qiao, Yingxin ^b   Li, Miao ^a   Ai, Ping ^a   Hou, Xinpu ^b  

^a BEIJING INSTITUTE OF RADIATION MEDICINE   (China)

^b PEKING UNIVERSITY HEALTH SCIENCE CENTER   (China)

Author keywords

Acyclovir; Langmuir monolayers; Nanoparticles; Nucleoside analogues; Self assembly

Indexed keywords

CARBON; DERIVATIVES; ESTERIFICATION; HYDROGEN BONDS; LIPIDS; NANOSTRUCTURED MATERIALS; PHASE TRANSITIONS; SALTS; SELF ASSEMBLY; SODIUM;

18-CARBON LEGNTH (C18); ALKYL CHAINS; LANGMUIR MONOLAYERS; PARTICLE SIZE;

MONOLAYERS;

ACICLOVIR; ALKYL GROUP; CARBON; CHOLESTEROL; CRYSTALLIN; DIOCTADECYLASPARTATE SUCCINYLACICLOVIR; GUANINE; LIPID; NANOPARTICLE; NUCLEOSIDE DERIVATIVE; SODIUM; SOLVENT; STEARYLGLYCEROSUCCINYLACICLOVIR; TETRAHYDROFURAN; UNCLASSIFIED DRUG;

AIRFLOW; ALKYLATION; ARTICLE; COMPLEX FORMATION; CRYSTALLIZATION; DRUG FORMULARY; DRUG SOLUBILITY; DRUG SYNTHESIS; ELECTRIC POTENTIAL; ESTERIFICATION; GEL; HYDROGEN BOND; HYDROPHOBICITY; INJECTION; LANGMUIR BLODGETT FILM; MOLECULAR DYNAMICS; MOLECULAR INTERACTION; MOLECULAR MECHANICS; PARTICLE SIZE; PHASE TRANSITION; PRIORITY JOURNAL; REACTION ANALYSIS; RIGIDITY; SURFACE PROPERTY; SUSPENDED PARTICULATE MATTER; TECHNIQUE; WATER ANALYSIS; WATER FLOW;

ACYCLOVIR; ASPARTIC ACID; GLYCEROL; HYDROGEN BONDING; HYDROPHOBICITY; LIPIDS; LIPOSOMES; MICROSCOPY, ELECTRON; NANOSTRUCTURES; NUCLEOSIDES; OLEIC ACIDS; PARTICLE SIZE; SODIUM; STEARIC ACIDS; SUCCINIC ACID; SURFACE PROPERTIES;

EID: 15244351254     PISSN: 09277765     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.colsurfb.2005.02.001     Document Type: Article

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