Department of Applied Science, University of California, Davis. Davis, CA 95616, USA.
Chemphyschem. 2012 Jan 16;13(1):314-22. doi: 10.1002/cphc.201100573. Epub 2011 Oct 19.
Lipid molecules in water form uni- or multilamellar vesicles in polydisperse form. Herein, we present energetic considerations for their equilibrium morphological organization. Our formulation provides elemental energy diagrams, which explain the polydispersity and account for the structural diversity. These energy diagrams describe the ranges of core radius (r(c)) and number of lamellae (N) that result in the formation of stable vesicles under specific conditions, thus providing prescriptions for the design of vesicles tailored for specific properties, including stability, cargo capacity, and resistance to deformation by osmotic stress. We deduced key design criteria as follows: 1) designing highly stable unilamellar vesicles requires low bending rigidity lipids and dimensions exceeding a few hundred nm in radii; 2) very large unilamellar vesicles (r(c)>several tens of microns) are not stable for typical lipids; lipids with higher bending rigidity are required; 3) the distribution of the stable size of vesicles is proportional to the bending rigidity; 4) for the case of multilamellar vesicles, vesicles with more than a few hundred layers usually exhibit greater structural integrity than those with lower degrees of lamellarity, especially when the core radii are small (<100 nm); 5) for osmotically stressed vesicles, the energy contributed by even a small concentration gradient (>mM) is the most dominant factor in the free energy, suggesting active response by vesicles (e.g., poration) to release osmotic stress; and 6) vesicles with a core radius of a few hundred nm and more than hundred lamellae are more resistant to deformation by osmotic stress, thus making them more suited to applications involving osmotic pressure gradients, such as in drug delivery.
在水中,脂质分子以多分散形式形成单或多层囊泡。在此,我们提出了关于它们平衡形态组织的能量考虑因素。我们的配方提供了基本的能量图,这些能量图解释了多分散性,并解释了结构多样性。这些能量图描述了在特定条件下形成稳定囊泡的核心半径(r(c))和层数(N)范围,从而为设计具有特定性质的囊泡提供了处方,包括稳定性、载药量和抵抗渗透压变形的能力。我们推导出了以下关键设计标准:1)设计高度稳定的单层囊泡需要低弯曲刚度脂质和半径超过几百纳米的尺寸;2)非常大的单层囊泡(r(c)>几十微米)对于典型脂质不稳定;需要具有更高弯曲刚度的脂质;3)稳定囊泡尺寸的分布与弯曲刚度成正比;4)对于多层囊泡,层数超过几百层的囊泡通常比层状程度较低的囊泡具有更高的结构完整性,尤其是当核心半径较小时(<100nm);5)对于渗透压胁迫的囊泡,即使是很小浓度梯度(>mM)的能量贡献也是自由能中最主要的因素,这表明囊泡会主动响应(例如,穿孔)以释放渗透压胁迫;6)半径为几百纳米且层数超过几百层的囊泡对渗透压变形的抵抗力更强,因此更适合涉及渗透压梯度的应用,如药物输送。