Faculty of Pharmacy, University of Veterinary and Pharmaceutical Sciences, Palackeho 1/3, 61242 Brno, Czech Republic.
Molecules. 2012 Sep 13;17(9):11067-78. doi: 10.3390/molecules170911067.
The absorption, distribution, biotransformation and excretion of a drug involve its transport across cell membranes. This process is essential and influenced by the characteristics of the drug, especially its molecular size and shape, solubility at the site of its absorption, relative lipid solubility, etc. One of the progressive ways for increasing bioavaibility is a nanoparticle preparation technique. Cholesterol, cholestenolone and pregnenolone acetate as model active pharmaceutical ingredients and some of the commonly used excipients as nanoparticle stabilizers were used in the investigated precipitation method that was modified and simplified and can be used as an effective and an affordable technique for the preparation of nanoparticles. All 120 prepared samples were analyzed by means of dynamic light scattering (Nanophox). The range of the particle size of the determined 100 nanoparticle samples was from 1 nm to 773 nm, whereas 82 samples contained nanoparticles of less than 200 nm. Relationships between solvents and used excipients and their amount are discussed.
药物的吸收、分布、生物转化和排泄涉及药物跨细胞膜的转运。这个过程是必不可少的,受到药物特性的影响,特别是其分子大小和形状、吸收部位的溶解度、相对脂溶性等。增加生物利用度的一种渐进方法是纳米颗粒制备技术。胆固醇、胆甾烯酮和醋酸孕烯醇酮作为模型活性药物成分和一些常用的赋形剂作为纳米颗粒稳定剂,用于研究中改进和简化的沉淀方法,可作为制备纳米颗粒的有效且经济实惠的技术。所有 120 个制备的样品都通过动态光散射(Nanophox)进行了分析。确定的 100 个纳米颗粒样品的粒径范围为 1nm 至 773nm,而 82 个样品含有小于 200nm 的纳米颗粒。讨论了溶剂与所用赋形剂及其用量之间的关系。