Temperature-dependent interaction of thermo-sensitive polymer-modified liposomes with CV1 cells

被引:36
作者
Kono, K
Nakai, R
Morimoto, K
Takagishi, T
机构
[1] Univ Osaka Prefecture, Coll Engn, Dept Appl Mat Sci, Sakai, Osaka 5998531, Japan
[2] Univ Osaka Prefecture, Adv Sci & Technol Res Inst, Dept Appl Biosci, Sakai, Osaka 5998570, Japan
关键词
temperature-sensitive liposome; lower critical solution temperature; poly(N-acryloylpyrrolidine); poly(N-isopropylacrylamide); liposome-cell interaction; drug delivery system;
D O I
10.1016/S0014-5793(99)00975-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Egg yolk phosphatidylcholine liposomes modified with a copolymer of N-acryloylpyrrolidine and N-isopropylacrylamide having a lower critical solution temperature at ca, 40 degrees C were prepared and an effect of temperature on their interaction with CVI cells was investigated. The unmodified liposomes vc ere taken up by the cells approximately to the same extent after 3 h incubation at 37 and 42 degrees C, In contrast, uptake of the polymer-modified liposomes by CV1 cells decreased slightly at 37 degrees C but increased greatly at 42 degrees C, compared to the unmodified liposomes. Proliferation of the cells H as partly prohibited by the incubation with the unmodified liposomes encapsulating methotrexate at 37 and 42 degrees C. The treatment, with the polymer-modified liposomes containing methotrexate at 37 degrees C hardly effected the cell growth. However, the treatment at 42 degrees C inhibited the cell growth completely. It is considered that the highly hydrated polymer chains attached to the liposome surface suppressed the liposome-cell interaction below the lower critical solution temperature of the polymer but the dehydrated polymer chains enhanced the interaction above this temperature. Because interaction of the polymer-modified liposomes with cells can be controlled by the ambient temperature, these liposomes may have potential usefulness as efficient site-specific drug delivery systems. (C) 1999 Federation of European Biochemical Societies.
引用
收藏
页码:306 / 310
页数:5
相关论文
共 30 条
[1]   UPTAKE OF LIPOSOMES BY CULTURED MOUSE BONE-MARROW MACROPHAGES - INFLUENCE OF LIPOSOME COMPOSITION AND SIZE [J].
ALLEN, TM ;
AUSTIN, GA ;
CHONN, A ;
LIN, L ;
LEE, KC .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1061 (01) :56-64
[2]   TRIGGERED RELEASE OF HYDROPHILIC AGENTS FROM PLASMALOGEN LIPOSOMES USING VISIBLE-LIGHT OR ACID [J].
ANDERSON, VC ;
THOMPSON, DH .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1109 (01) :33-42
[3]  
CHONN A, 1992, J BIOL CHEM, V267, P18759
[4]   Grafted poly-(ethylene glycol) on lipid surfaces inhibits protein adsorption and cell adhesion [J].
Du, H ;
Chandaroy, P ;
Hui, SW .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1997, 1326 (02) :236-248
[5]   PHOTOINDUCED DESTABILIZATION OF BILAYER VESICLES [J].
FRANKEL, DA ;
LAMPARSKI, H ;
LIMAN, U ;
OBRIEN, DF .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1989, 111 (26) :9262-9263
[6]  
Guillet J.E., 1968, J. Macromol. Sci. Part A-Chem, V2, P1441, DOI DOI 10.1080/10601326808051910
[7]   Temperature sensitization of liposomes using copolymers of N-ispopropylacrylamide [J].
Hayashi, H ;
Kono, K ;
Takagishi, T .
BIOCONJUGATE CHEMISTRY, 1999, 10 (03) :412-418
[8]   Temperature-controlled release property of phospholipid vesicles bearing a thermo-sensitive polymer [J].
Hayashi, H ;
Kono, K ;
Takagishi, T .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1996, 1280 (01) :127-134
[9]   Temperature-dependent associating property of liposomes modified with a thermosensitive polymer [J].
Hayashi, H ;
Kono, K ;
Takagishi, T .
BIOCONJUGATE CHEMISTRY, 1998, 9 (03) :382-389
[10]   THE TARGETING OF IMMUNOLIPOSOMES TO TUMOR-CELLS (A431) AND THE EFFECTS OF ENCAPSULATED METHOTREXATE [J].
JONES, MN ;
HUDSON, MJH .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1152 (02) :231-242