Driscoll David F, Nehne Jorg, Peterss Horst, Klutsch Karsten, Bistrian Bruce R, Niemann Wilhelm
Department of Medicine, Nutrition/Infection Laboratory, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts.
Int J Pharm Compd. 2006 Jul-Aug;10(4):309-15.
In confirming the stability of lipid injectable emulsions, the United States Pharmacopeia has recently recommended that light scattering be used to determine the mean droplet size (i.e., fineness of the dispersion), and light obscuration or light extinction be used to quantify the extent of the large-diameter tail (i.e., coarseness of the dispersion). In confirming the results obtained by these two methods, the usefulness of a third method, differential interference contrast microscopy using an oil immersion technique was investigated. The physical stabilities of 95 different formulations made from 20% w/v lipid emulsions were evaluated by all three methods. A wide spectrum of globule-size distributions was investigated, measured by light obscuration and expressed as the volume-weighted percent of fat greater than 5 micrometers (PFAT5) from very fine (0.001%) to very coarse (0.596%) formulations. The responses obtained by the light scattering method did not reflect the values for the large-diameter tail (i.e., coalescence) seen with the less stable emulsions, whereas these differences were detectable using the differential interference contrast microscopy technique. It was concluded that differential interference contrast microscopy provides complementary data about the physical stability of lipid injectable emulsions and can be applied as a confirmatory evaluation to the methods proposed in United States Pharmacopeia Chapter 729.
在确认脂质注射乳剂的稳定性时,美国药典最近建议使用光散射来测定平均液滴大小(即分散体的细度),并使用光阻法或消光法来量化大直径尾部的程度(即分散体的粗糙度)。在确认这两种方法所获得的结果时,研究了第三种方法——使用油浸技术的微分干涉对比显微镜法的实用性。用这三种方法评估了由20% w/v脂质乳剂制成的95种不同配方的物理稳定性。研究了广泛的球粒大小分布,通过光阻法测量,并表示为大于5微米的脂肪的体积加权百分比(PFAT5),范围从非常细的(0.001%)到非常粗的(0.596%)配方。光散射法获得的结果没有反映出不稳定乳剂中出现的大直径尾部(即聚结)的值,而使用微分干涉对比显微镜技术可以检测到这些差异。得出的结论是,微分干涉对比显微镜提供了关于脂质注射乳剂物理稳定性的补充数据,可作为对美国药典第729章中提出的方法的确认性评估。