Brown Desmond A, Venegas Berenice, Cooke Peter H, English Verrica, Chong Parkson Lee-Gau
Department of Biochemistry, Temple University School of Medicine, Philadelphia, PA 19140, USA.
Chem Phys Lipids. 2009 Jun;159(2):95-103. doi: 10.1016/j.chemphyslip.2009.03.004. Epub 2009 Apr 2.
The stability of liposomes made of the polar lipid fraction E (PLFE) isolated from the thermoacidophilic archaeon Sulfolobus acidocaldarius against autoclaving has been studied by using dynamic light scattering and transmission electron microscopy. PLFE lipids have structures distinctly different from those derived from eukaryotes and prokaryotes. PLFE lipids are bipolar tetraether molecules and may contain up to four cyclopentane rings in each of the two dibiphytanyl chains. In the pH range 4-10, PLFE-based archaeosomes, with and without polyethyleneglycol- and maleimide-lipids, are able to retain vesicle size, size distribution, and morphology through at least six autoclaving cycles. The cell growth temperature (65 degrees C vs. 78 degrees C), hence the number of cyclopentane rings in the hydrocarbon chains, does not affect this general conclusion. By contrast, at the same pH range, most conventional liposomes made of monopolar diester lipids and cholesterol or pegylated lipids cannot withhold vesicle size and size distribution against just one cycle of autoclaving. At pH<4, the particle size and polydispersity of PLFE-based archaeosomes increase with autoclaving cycles, suggesting that aggregation or membrane disruption may have occurred at extreme acidic conditions during heat sterilization. Under high salt conditions, dye leakage from PLFE archaeosomes due to autoclaving is significantly less than that from pegylated liposomes composed of conventional lipids. The ability to maintain vesicle integrity after multiple autoclaving cycles indicates the potential usefulness of utilizing PLFE-based archaeosomes as autoclavable and durable drug (including genes, peptides, vaccines, siRNA) delivery vehicles.
通过动态光散射和透射电子显微镜研究了从嗜热嗜酸古菌嗜酸热硫化叶菌中分离出的极性脂质组分E(PLFE)制成的脂质体对高压灭菌的稳定性。PLFE脂质的结构与真核生物和原核生物衍生的脂质结构明显不同。PLFE脂质是双极四醚分子,在两条二植烷链的每一条中可能含有多达四个环戊烷环。在pH值为4至10的范围内,含有和不含有聚乙二醇和马来酰亚胺脂质的基于PLFE的古脂质体能够通过至少六个高压灭菌循环保持囊泡大小、大小分布和形态。细胞生长温度(65摄氏度对78摄氏度),因此烃链中环戊烷环的数量,并不影响这一总体结论。相比之下,在相同的pH范围内,大多数由单极二酯脂质和胆固醇或聚乙二醇化脂质制成的传统脂质体在仅一个高压灭菌循环后就无法保持囊泡大小和大小分布。在pH<4时,基于PLFE的古脂质体的粒径和多分散性随高压灭菌循环次数增加,这表明在热灭菌过程中的极端酸性条件下可能发生了聚集或膜破坏。在高盐条件下,高压灭菌导致PLFE古脂质体的染料泄漏明显少于由传统脂质组成的聚乙二醇化脂质体。多次高压灭菌循环后保持囊泡完整性的能力表明,利用基于PLFE的古脂质体作为可高压灭菌且耐用的药物(包括基因、肽、疫苗、小干扰RNA)递送载体具有潜在的实用性。