Hosoya Osamu, Chono Sumio, Saso Yuko, Juni Kazuhiko, Morimoto Kazuhiro, Seki Toshinobu
Hokkaido College of Pharmacy, 7-1 Katsuraoka-cho, Otaru, Hokkaido 047-0264, Japan.
J Pharm Pharmacol. 2004 Dec;56(12):1501-7. doi: 10.1211/0022357044878.
The diffusion coefficient (D) of peptide and protein drugs needs to be determined to examine the permeability through biological barriers and to optimize delivery systems. In this study, the D values of fluorescein isothiocyanate (FITC)-labelled dextrans (FDs) and peptides were determined and the permeability through a porous membrane was discussed. The observed D values of FDs and peptides, except in the case of insulin, were similar to those calculated based on a relationship previously reported between the molecular weight and D of lower-molecular-weight compounds, although the molecular weight range was completely different. The observed D value of insulin was between the calculated values for the insulin monomer and hexamer. The permeability of poly-lysine and insulin through the membrane was determined and the observed values were compared with predicted values by using the relationship between molecular weight and D and an equation based on the Renkin function. The observed permeability of insulin through the membrane was between that of the predicted permeability for the insulin monomer and hexamer. For the permeation of insulin, the determination of D was useful for estimating the permeability because of the irregular relationship between molecular weight and D. The methodology used in this study will be useful for a more quantitative evaluation of the absorption of peptide and protein drugs applied to mucous membranes.
为了研究肽类和蛋白质药物透过生物屏障的渗透性并优化给药系统,需要测定其扩散系数(D)。在本研究中,测定了异硫氰酸荧光素(FITC)标记的葡聚糖(FDs)和肽的D值,并讨论了它们透过多孔膜的渗透性。除胰岛素外,所观察到的FDs和肽的D值与根据先前报道的低分子量化合物分子量与D之间的关系计算得到的值相似,尽管分子量范围完全不同。胰岛素的观察到的D值介于胰岛素单体和六聚体的计算值之间。测定了聚赖氨酸和胰岛素透过膜的渗透性,并将观察值与利用分子量与D之间的关系以及基于Renkin函数的方程预测的值进行了比较。胰岛素透过膜的观察到的渗透性介于胰岛素单体和六聚体预测的渗透性之间。对于胰岛素的渗透,由于分子量与D之间的不规则关系,D的测定对于估计渗透性很有用。本研究中使用的方法将有助于更定量地评估应用于粘膜的肽类和蛋白质药物的吸收情况。