Stabilization of lipid/DNA complexes during the freezing step of the lyophilization process: the particle isolation hypothesis

被引:146
作者
Allison, SD [1 ]
Molina, MDC [1 ]
Anchordoquy, TJ [1 ]
机构
[1] Univ Colorado, Sch Pharm, Ctr Pharmaceut Biotechnol, Denver, CO 80262 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2000年 / 1468卷 / 1-2期
关键词
stabilization; gene delivery; nonviral vector; lyophilization; freezing; formulation;
D O I
10.1016/S0005-2736(00)00251-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The instability of nonviral vectors in aqueous suspensions has stimulated an interest in developing lyophilized formulations for use in gene therapy. previous work has demonstrated a strong correlation between the maintenance of particle size and retention of transfection rates. Our earlier work has shown that aggregation of nonviral vectors typically occurs during the freezing step of the lyophilization process, and that high concentrations of sugars are capable of maintaining particle size. This study extends these observations, and demonstrates that glass formation is not the mechanism by which sugars protect lipid/DNA complexes during freezing. We also show that polymers (e.g,, hydroxyethyl starch) are not capable of preventing aggregation despite their ability to form glasses at relatively high subzero temperatures. Instead, our data suggest that it is the separation of individual particles within the unfrozen fraction that prevents aggregation during freezing, i.e., the particle isolation hypothesis. Furthermore, we suggest that the relatively low surface tension of mono- and disaccharides, as compared to starch, allows phase-separated particles to remain dispersed within the unfrozen excipient solution, which preserves particle size and transfection rates during freezing. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:127 / 138
页数:12
相关论文
共 40 条
[1]
Counteracting effects of thiocyanate and sucrose on chymotrypsinogen secondary structure and aggregation during freezing, drying, and rehydration [J].
Allison, SD ;
Dong, AC ;
Carpenter, JF .
BIOPHYSICAL JOURNAL, 1996, 71 (04) :2022-2032
[2]
Allison SD, 2000, J PHARM SCI, V89, P682, DOI 10.1002/(SICI)1520-6017(200005)89:5<682::AID-JPS14>3.3.CO
[3]
2-R
[4]
Anchordoquy TJ, 1999, BIOPHARM-APPL T BIO, V12, P42
[5]
Anchordoquy TJ, 1999, BIOPHARM-APPL T BIO, V12, P46
[6]
Anchordoquy TJ, 2000, J PHARM SCI, V89, P289, DOI 10.1002/(SICI)1520-6017(200003)89:3<289::AID-JPS1>3.3.CO
[7]
2-E
[8]
Stability of lipid/DNA complexes during agitation and freeze-thawing [J].
Anchordoquy, TJ ;
Girouard, LG ;
Carpenter, JF ;
Kroll, DJ .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1998, 87 (09) :1046-1051
[9]
Maintenance of transfection rates and physical characterization of lipid/DNA complexes after freeze-drying and rehydration [J].
Anchordoquy, TJ ;
Carpenter, JF ;
Kroll, DJ .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1997, 348 (01) :199-206
[10]
ANDERSON WF, 1995, SCI AM, V273, P124