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基于非离子表面活性剂、胆固醇和聚乙二醇 - 胆固醇共轭物的新型空间稳定囊泡。

New sterically stabilized vesicles based on nonionic surfactant, cholesterol, and poly(ethylene glycol)-cholesterol conjugates.

作者信息

Beugin S, Edwards K, Karlsson G, Ollivon M, Lesieur S

机构信息

Equipe Physico-Chimie des Systèmes Polyphasés, URA CNRS 1218, Université Paris-Sud, Châtenay-Malabry, France.

出版信息

Biophys J. 1998 Jun;74(6):3198-210. doi: 10.1016/S0006-3495(98)78026-9.

DOI:10.1016/S0006-3495(98)78026-9
PMID:9635773
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1299660/
Abstract

Monomethoxypoly(ethylene glycol) cholesteryl carbonates (M-PEG-Chol) with polymer chain molecular weights of 1000 (M-PEG1000-Chol) and 2000 (M-PEG2000-Chol) have been newly synthesized and characterized. Their aggregation behavior in mixture with diglycerol hexadecyl ether (C16G2) and cholesterol has been examined by cryotransmission electron microscopy, high-performance gel exclusion chromatography, and quasielastic light scattering. Nonaggregated, stable, unilamellar vesicles were obtained at low polymer levels with optimal shape and size homogeneity at cholesteryl conjugate/ lipids ratios of 10 mol% M-PEG1000-Chol or 5 mol% M-PEG2000-Chol, corresponding to the theoretically predicted brush conformational state of the PEG chains. At 20 mol% M-PEG1000-Chol or 10 mol% M-PEG2000-Chol, the saturation threshold of the C16G2/cholesterol membrane in polymer is exceeded, and open disk-shaped aggregates are seen in coexistence with closed vesicles. Higher levels up to 30 mol% lead to the complete solubilization of the vesicles into disk-like structures of decreasing size with increasing PEG content. This study underlines the bivalent role of M-PEG-Chol derivatives: while behaving as solubilizing surfactants, they provide an efficient steric barrier, preventing the vesicles from aggregation and fusion over a period of at least 2 weeks.

摘要

新合成并表征了聚合物链分子量为1000(M-PEG1000-Chol)和2000(M-PEG2000-Chol)的单甲氧基聚(乙二醇)胆固醇碳酸酯(M-PEG-Chol)。通过低温透射电子显微镜、高效凝胶排阻色谱和准弹性光散射研究了它们与二甘油十六烷基醚(C16G2)和胆固醇混合物中的聚集行为。在低聚合物水平下,当胆固醇共轭物/脂质比为10 mol% M-PEG1000-Chol或5 mol% M-PEG2000-Chol时,获得了非聚集、稳定的单层囊泡,其形状和尺寸均匀性最佳,这与PEG链的理论预测刷状构象状态相对应。在20 mol% M-PEG1000-Chol或10 mol% M-PEG2000-Chol时,聚合物中C16G2/胆固醇膜的饱和阈值被超过,并且在与封闭囊泡共存时可以看到开放的盘状聚集体。高达30 mol%的更高水平会导致囊泡完全溶解为尺寸随PEG含量增加而减小的盘状结构。这项研究强调了M-PEG-Chol衍生物的双重作用:虽然它们表现为增溶表面活性剂,但它们提供了有效的空间位垒,可在至少2周的时间内防止囊泡聚集和融合。

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本文引用的文献

1
Effect of polyethyleneglycol-phospholipids on aggregate structure in preparations of small unilamellar liposomes.聚乙二醇磷脂对小单层脂质体制剂中聚集体结构的影响。
Biophys J. 1997 Jul;73(1):258-66. doi: 10.1016/S0006-3495(97)78066-4.
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Interaction of polyethyleneglycol-phospholipid conjugates with cholesterol-phosphatidylcholine mixtures: sterically stabilized liposome formulations.聚乙二醇 - 磷脂缀合物与胆固醇 - 磷脂酰胆碱混合物的相互作用:空间稳定脂质体制剂
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Effects of polyethyleneglycol chain length and phospholipid acyl chain composition on the interaction of polyethyleneglycol-phospholipid conjugates with phospholipid: implications in liposomal drug delivery.聚乙二醇链长和磷脂酰基链组成对聚乙二醇-磷脂缀合物与磷脂相互作用的影响:对脂质体药物递送的意义
Pharm Res. 1996 May;13(5):710-7. doi: 10.1023/a:1016091314940.
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Determination of the thickness of the fixed aqueous layer around polyethyleneglycol-coated liposomes.聚乙二醇包被脂质体周围固定水层厚度的测定。
J Drug Target. 1995;3(4):283-9. doi: 10.3109/10611869509015957.
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Interfacial thickness of liposomes containing poly(ethylene glycol)-cholesterol from electrophoresis.通过电泳法测定含聚乙二醇-胆固醇脂质体的界面厚度。
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Liposomes with detachable polymer coating: destabilization and fusion of dioleoylphosphatidylethanolamine vesicles triggered by cleavage of surface-grafted poly(ethylene glycol).具有可分离聚合物涂层的脂质体:表面接枝聚乙二醇的裂解引发二油酰磷脂酰乙醇胺囊泡的去稳定化和融合
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