Comparative pharmacokinetic studies of borneol in mouse plasma and brain by different administrations

被引:35
作者
Zhao, Jing-yi [1 ]
Lu, Yang [1 ]
Du, Shou-ying [1 ]
Song, Xiao [1 ]
Bai, Jie [1 ]
Wang, Yue [1 ]
机构
[1] Beijing Univ Chinese Med, Sch Chinese Pharm, Dept Ind Pharm, Beijing 100102, Peoples R China
来源
JOURNAL OF ZHEJIANG UNIVERSITY-SCIENCE B | 2012年 / 13卷 / 12期
基金
中国国家自然科学基金;
关键词
Borneol; Intravenous administration; Intranasal administration; Oral administration; Pharmacokinetics; CENTRAL-NERVOUS-SYSTEM; INTRANASAL DELIVERY; NASAL ABSORPTION; IN-VIVO; GENIPOSIDE; MICE; RAT;
D O I
10.1631/jzus.B1200142
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Borneol, a monoterpenoid alcohol, is used widely, particularly in combined formulas for preventing and curing cardiovascular and cerebrovascular diseases in traditional Chinese medicine. In order to understand the blood and brain pharmacokinetics after intravenous, intranasal, or oral administration and to investigate the superiority and feasibility of intranasal administration, a simple gas chromatographic (GC) method with flame ionization detection (FID) was developed for the quantification of borneol. Blood samples and brain were collected from mice at 1, 3, 5, 10, 20, 30, 60, 90, and 120 min after intravenous, intranasal, or oral administration of borneol at a dosage of 30.0 mg/kg. Sample preparations were carried out by liquid-liquid extraction with an internal standard solution of octadecane. The pharmacokinetic parameters were calculated by the software of Kinetica. The calibration curves were linear in the range of 0.11-84.24 mu g/ml and 0.16-63.18 mu g/g for borneol in plasma and brain, respectively. The methodological and extraction recoveries were both in the range of 85%-115%. The intra-day and inter-day variabilities for plasma and brain samples were <= 5.00% relative standard deviation (RSD). The absolute bioavailabilities F of intranasal and oral administrations were 90.68% and 42.99%. The relative brain targeted coefficients Re of intranasal and oral administrations were 68.37% and 38.40%. The GC-FID method developed could be applied to determination and pharmacokinetic study. The borneol from injection was distributed and metabolized fast without absorption process. The borneol from oral administration was distributed more slowly and had the lowest absolute bioavailability. Nasal administration of borneol was quickly absorbed into the blood and brain, was easy to use and had a greater safety than infection, which makes it worthy of further development as an administration route for encephalopathy treatment.
引用
收藏
页码:990 / 996
页数:7
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