Distribution in brain of liposomes after convection enhanced delivery; modulation by particle charge, particle diameter, and presence of steric coating

被引:145
作者
MacKay, JA
Deen, DF
Szoka, FC
机构
[1] Univ Calif San Francisco, Dept Biopharmaceut Sci, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Joint Grad Grp Bioengn, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Brain Tumor Res Ctr, Dept Neurol Sci, San Francisco, CA 94143 USA
[5] Univ Calif Berkeley, Berkeley, CA 94720 USA
关键词
cationic lipid; DNA; PEG; rodent; tumor; rat;
D O I
10.1016/j.brainres.2004.12.007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We have investigated the role of diameter, charge, and steric shielding on the brain distribution of liposomes infused by convection enhanced delivery (CED) using both radiolabeled and fluorescent-labeled particles. Liposomes of 40 and 80-nm diameter traveled the same distance but penetrated significantly less than a 10-kDa dextran; whereas 200-nm-diameter liposomes penetrated less than 80 nm liposomes. A neutral liposome shielded by polyethylene glycol (PEG; 2 kDa; 10% by mole) penetrated significantly farther than an unshielded liposome. Even when shielded with PEG, positive surface charge (10% by mole) significantly reduced the penetration radius compared to a neutral or negative charged liposome (10% by mole). A mathematical CED model including a term for liposome cell binding was applied to analyze the radius of particle penetration. Neutral liposomes had a binding constant of k = 0.0010 +/- 0.0002 min(-1), whereas for positive charged liposomes k increased 50-fold. The binding constant was independently verified using a degradable lipid radiolabel that eliminated from the brain with a 9.9 +/- 2.0 h half-life, equivalent to the calculated elimination constant k = 0.0012 +/- 0.0002 min(-1). During CED, liposomes accumulated in a subpopulation of perivascular cells within the brain. A non-degradable lipid radiolabel showed that lipid components remained within these perivascular brain cells for at least 2 days. To reduce this uptake, 100-fold molar excess of non-labeled liposomes were co-infused with labeled liposomes, which significantly increased liposome penetration. These studies suggest that optimization of therapeutic CED using particles such as drug-loaded liposomes, polymeric nanoparticles, non-viral DNA complexes, and viruses will require a strategy to overcome particle binding and clearance by cells within the CNS. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:139 / 153
页数:15
相关论文
共 50 条
[1]  
ABRA RM, 1982, RES COMMUN CHEM PATH, V37, P199
[2]   Convection-enhanced delivery of AAV vector in parkinsonian monkeys;: In vivo detection of gene expression and restoration of dopaminergic function using pro-drug approach [J].
Bankiewicz, KS ;
Eberling, JL ;
Kohutnicka, M ;
Jagust, W ;
Pivirotto, P ;
Bringas, J ;
Cunningham, J ;
Budinger, TF ;
Harvey-White, J .
EXPERIMENTAL NEUROLOGY, 2000, 164 (01) :2-14
[3]  
BARTLETT GR, 1959, J BIOL CHEM, V234, P466
[4]   Gene transfer to rodent brain with recombinant adenoviral vectors: Effects of infusion parameters, infectious titer, and virus concentration on transduction volume [J].
Betz, AL ;
Shakui, P ;
Davidson, BL .
EXPERIMENTAL NEUROLOGY, 1998, 150 (01) :136-142
[5]   CONVECTION-ENHANCED DELIVERY OF MACROMOLECULES IN THE BRAIN [J].
BOBO, RH ;
LASKE, DW ;
AKBASAK, A ;
MORRISON, PF ;
DEDRICK, RL ;
OLDFIELD, EH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (06) :2076-2080
[6]   Intracerebral clysis in a rat glioma model [J].
Bruce, JN ;
Falavigna, A ;
Johnson, JP ;
Hall, JS ;
Birch, BD ;
Yoon, JT ;
Wu, EX ;
Fine, RL ;
Parsa, AT .
NEUROSURGERY, 2000, 46 (03) :683-691
[7]   Liposome-mediated transfer of the bcl-2 gene results in neuroprotection after in vivo transient focal cerebral ischemia in an animal model [J].
Cao, YJ ;
Shibata, T ;
Rainov, NG .
GENE THERAPY, 2002, 9 (06) :415-419
[8]   New approach to tumor therapy for inoperable areas of the brain: chronic intraparenchymal drug delivery [J].
Carson, BS ;
Wu, QZ ;
Tyler, B ;
Sukay, L ;
Raychaudhuri, R ;
DiMeco, F ;
Clatterbuck, RE ;
Olivi, A ;
Guarnieri, M .
JOURNAL OF NEURO-ONCOLOGY, 2002, 60 (02) :151-158
[9]   Variables affecting convection-enhanced delivery to the striatum: a systematic examination of rate of infusion, cannula size, infusate concentration, and tissue-cannula sealing time [J].
Chen, MY ;
Lonser, RR ;
Morrison, PF ;
Governale, LS ;
Oldfield, EH .
JOURNAL OF NEUROSURGERY, 1999, 90 (02) :315-320
[10]   Low-pH-sensitive PEG-stabilized plasmid-lipid nanoparticles: Preparation and characterization [J].
Choi, JS ;
MacKay, JA ;
Szoka, FC .
BIOCONJUGATE CHEMISTRY, 2003, 14 (02) :420-429