Application of biopharmaceutics classification system (BCS) in drug transport studies across human respiratory epithelial cell monolayers

被引:8
作者
Hyun-Jong Cho
Prabagar Balakrishnan
Hongxia Lin
Min-Koo Choi
Dae-Duk Kim
机构
[1] College of Pharmacy, Sunchon National University, Sunchon
[2] College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul
[3] College of Pharmacy, Dankook University, Cheon-an
基金
新加坡国家研究基金会;
关键词
BCS; Dose number; HNE cell monolayers; NHBE cell monolayers; P[!sub]app[!/sub] value; Physicochemical properties;
D O I
10.1007/s40005-012-0020-9
中图分类号
学科分类号
摘要
Transport studies of model drugs were conducted across the human nasal epithelial (HNE) and normal human bronchial epithelial (NHBE) cell monolayers cultured by air-liquid interface method. Physicochemical properties (e. g., molecular weight, calculated partition coefficient, dose number) of model drugs were quoted from literatures and apparent permeability coefficients (Papp) across the HNE and NHBE cell monolayers were directly measured. A linear relationship was observed between the Papp values of model drugs in the HNE and NHBE cell monolayers. As the molecular weight of model drugs increased, the Papp showed a decreasing pattern while the increase of partition coefficients resulted in the increment of Papp. These results indicated that the transport of model drugs across both cell monolayers followed mainly the passive diffusion mechanism, although substrates mediated by drug transporters showed a deviating pattern. It was also interesting to note that almost all model drugs could be grouped into the same biopharmaceutics classification system as that classified by the human intestinal permeability when the Papp was plotted as a function of dose number (D0) of each drug. © 2012 The Korean Society of Pharmaceutical Sciences and Technology.
引用
收藏
页码:147 / 153
页数:6
相关论文
共 26 条
[1]  
Abe K., Irie T., Uekama K., Enhanced nasal delivery of luteinizing hormone releasing hormone agonist buserelin by oleic acid solubilized and stabilized in hydroxypropyl-beta-cyclodextrin, Chem Pharm Bull, 43, pp. 2232-2237, (1995)
[2]  
Bai S., Yang T., Abbruscato T.J., Ahsan F., Evaluation of human nasal RPMI 2650 cells grown at an air-liquid interface as a model for nasal drug transport studies, J Pharm Sci, 97, pp. 1165-1178, (2008)
[3]  
Cho H.J., Choi M.K., Lin H., Kim J.S., Chung S.J., Shim C.K., Kim D.D., Expression and functional activity of P-glycoprotein in passaged primary human nasal epithelial cell monolayers cultured by the air-liquid interface method for nasal drug transport study, J Pharm Pharmacol, 63, pp. 385-391, (2011)
[4]  
Costantino H.R., Illum L., Brandt G., Johnson P.H., Quay S.C., Intranasal delivery: physicochemical and therapeutic aspects, Int J Pharm, 337, pp. 1-24, (2007)
[5]  
Densmore C.L., Orson F.M., Xu B., Kinsey B.M., Waldrep J.C., Hua P., Bhogal B., Knight V., Aerosol delivery of robust polyethyleneimine-DNA complexes for gene therapy and genetic immunization, Mol Ther, 1, pp. 180-188, (2000)
[6]  
Forbes B., Shah A., Martin G.P., Lansley A.B., The human bronchial epithelial cell line 16HBE14o: as a model system of the airways for studying drug transport, Int J Pharm, 257, pp. 161-167, (2003)
[7]  
Fuchs S., Hollins A.J., Laue M., Schaefer U.F., Roemer K., Gumbleton M., Lehr C.M., Differentiation of human alveolar epithelial cells in primary culture: morphological characterization and synthesis of caveolin-1 and surfactant protein-C, Cell Tissue Res, 311, pp. 31-45, (2003)
[8]  
Grainger C.I., Greenwell L.L., Lockley D.J., Martin G.P., Forbes B., Culture of Calu-3 cells at the air interface provides a representative model of the airway epithelial barrier, Pharm Res, 23, pp. 1482-1490, (2006)
[9]  
Hermens W.A., Deurloo M.J., Romeyn S.G., Verhoef J.C., Merkus F.W., Nasal absorption enhancement of 17 beta-estradiol by dimethyl-beta-cyclodextrin in rabbits and rats, Pharm Res, 7, pp. 500-503, (1990)
[10]  
Hinchcliffe M., Illum L., Intranasal insulin delivery and therapy, Adv Drug Deliv Rev, 35, pp. 199-234, (1999)