Li Weijun, Huang Zhaohua, MacKay J Andrew, Grube Stefan, Szoka Francis C
Department of Biopharmaceutical Sciences and Pharmaceutical Chemistry, University of California at San Francisco, San Francisco, CA 94143-0446, USA.
J Gene Med. 2005 Jan;7(1):67-79. doi: 10.1002/jgm.634.
We have studied the effects of the poly(ethylene glycol) (PEG) chain length and acyl chain composition on the pH-sensitivity of acid-labile PEG-diorthoester (POD) lipids. The optimal conditions are described for preparation of DNA plasmid encapsulated POD nanolipoparticles (NLPs) which mediate high gene delivery activity in vitro with moderate cytotoxicity.
A series of POD lipids with various PEG chain lengths (750, 2000, and 5000 Da) or acyl chains (distearoyl 18:0 or dioleoyl 18:1) were incorporated into DNA containing NLPs or model liposomes as a stealth and bioresponsive component. We investigated the collapse kinetics of the POD-stabilized liposomes when the PEG chain length was changed. We optimized a detergent dialysis method to encapsulate plasmid DNA into NLPs prepared from a mixture of the various POD lipids, cationic lipid and phosphatidylethanolamine lipid. A critical concentration (28 mM) of n-octyl-beta-D-glucopyranoside (OG) enabled high encapsulation of DNA plasmid into 100 nm particles with a neutral surface charge. The POD NLPs are stable at pH 8.5 but rapidly collapse (approximately 10 min) into aggregates at pH 5.0. In the detergent solution there is a metastable DNA-lipid intermediate that evolves into a stable NLP if the detergent is removed shortly after adding DNA to the lipid-detergent mixture. The rank order of transfection activity from NLPs containing PEG-lipid was POD 750 > POD 5000 = POD 2000 > non-pH-sensitive PEG-lipid. The particle size stability was in the reverse order. Binding of the NLPs to cells reached a maximum level by 12 hours. The POD NLPs had slightly less transfection activity but considerably lower cytotoxicity than the PEI-DNA polyplex.
Of the PEG-orthoester lipids tested, POD 2000 is the better choice for the preparation of sterically stabilized NLPs with a small particle diameter, good stability, low cytotoxicity, and satisfactory transfection activity.
我们研究了聚乙二醇(PEG)链长和酰基链组成对酸不稳定的PEG - 二原酸酯(POD)脂质pH敏感性的影响。描述了制备包裹DNA质粒的POD纳米脂质体(NLP)的最佳条件,该纳米脂质体在体外介导高基因传递活性且细胞毒性适中。
将一系列具有不同PEG链长(750、2000和5000 Da)或酰基链(二硬脂酰18:0或二油酰18:1)的POD脂质作为隐形和生物响应成分掺入含DNA的NLP或模型脂质体中。我们研究了PEG链长改变时POD稳定脂质体的塌陷动力学。我们优化了去污剂透析方法,将质粒DNA包裹到由各种POD脂质、阳离子脂质和磷脂酰乙醇胺脂质的混合物制备的NLP中。正辛基 - β - D - 葡萄糖苷(OG)的临界浓度(28 mM)能够使DNA质粒高包裹率地进入具有中性表面电荷的100 nm颗粒中。POD NLP在pH 8.5时稳定,但在pH 5.0时迅速塌陷(约10分钟)形成聚集体。在去污剂溶液中存在一种亚稳态的DNA - 脂质中间体,如果在将DNA添加到脂质 - 去污剂混合物后不久去除去污剂,它会演变成稳定的NLP。含PEG - 脂质的NLP的转染活性排序为POD 750 > POD 5000 = POD 2000 > 非pH敏感的PEG - 脂质。颗粒大小稳定性顺序相反。NLP与细胞的结合在12小时时达到最高水平。与PEI - DNA多聚体相比,POD NLP的转染活性略低,但细胞毒性低得多。
在所测试的PEG - 原酸酯脂质中,POD 2000是制备具有小粒径、良好稳定性、低细胞毒性和令人满意的转染活性的空间稳定NLP的更好选择。