The preparation of silybin-phospholipid complex and the study on its pharmacokinetics in rats

被引:287
作者
Xiao, YY [1 ]
Song, YM [1 ]
Chen, ZP [1 ]
Ping, QN [1 ]
机构
[1] China Pharmaceut Univ, Nanjing, Jiangsu, Peoples R China
关键词
silybin-phospholipid complex; silybin-N-methylglucamine; physicochemical properties; oral bioavailability; pharmacokinetics; silybin;
D O I
10.1016/j.ijpharm.2005.10.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of the present study was to find a way of prepare silybin-phospholipid complex to make oral bioavailability of silybin increase and to study its physicochemical properties and to compare the pharmacokinetic characteristics and bioavailability after oral administration of silybin-phospholipid complex and silybin-N-methylglucamine in rats. Using ethanol as a reaction medium, silybin and phospholipids were resolved into the medium, after the organic solvent was removed under vacuum condition, silybin-phospholipid complex was formed. The new complex's physicochemical properties including scanning electron microscopy (SEM), transmission electron microscopy (TEM), differential scanning calorimetry (DSC), solubility, dissolution, etc., were tested. The concentrations of silybin after oral administration of silybin-phospholipid complex and silybin-N-methylglucamine at different time in rats were determined by RP-HPLC. The pharmacokinetic parameters were computed by software program 3p97. Our data showed that silybin and phospholipids in the silybin-phospholipid complex were combined by non-covalent-bond, not forming a new compound and the solubility of silybin-phospholipid complex in water and in n-octanol was effectively enhanced. We found that mean plasma concentration-time curve of silybin after oral administration of silybin-phospholipid. complex and silybin-N-methylglucamine in rats was both in accordance with open single-compartment model with first-order absorption. Pharmacokinetic parameters of silybin in rats were T-max 10 and 5 min; C-max 126.72 and 104.29 ng ml(-1); AUC(0-infinity) 1020.33 and 235.81 ng ml(-1) h, respectively. The bioavailability of silybin in rats was increased remarkably after oral administration of silybin-phospholipid complex comparing to silybin-N-methylglucamine. This was mainly due to an impressive improvement of the lipophilic property of silybin-phospholipid complex and improvement of the biological effect of silybin. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:77 / 82
页数:6
相关论文
共 7 条
[1]   PHARMACOKINETIC STUDIES ON IDB-1016, A SILYBIN-PHOSPHATIDYLCHOLINE COMPLEX, IN HEALTHY-HUMAN SUBJECTS [J].
BARZAGHI, N ;
CREMA, F ;
GATTI, G ;
PIFFERI, G ;
PERUCCA, E .
EUROPEAN JOURNAL OF DRUG METABOLISM AND PHARMACOKINETICS, 1990, 15 (04) :333-338
[2]   MEMBRANE EFFECTS OF ANTI-INFLAMMATORY AGENTS .2. INTERACTION OF NON-STEROIDAL ANTI-INFLAMMATORY DRUGS WITH LIPOSOME AND PURPLE MEMBRANES [J].
HWANG, SB ;
SHEN, TY .
JOURNAL OF MEDICINAL CHEMISTRY, 1981, 24 (10) :1202-1211
[3]   Analysis of the active components of silymarin [J].
Kvasnicka, F ;
Bíba, B ;
Sevcík, R ;
Voldrich, M ;
Krátká, J .
JOURNAL OF CHROMATOGRAPHY A, 2003, 990 (1-2) :239-245
[4]   AN NMR AND DSC STUDY OF THE INTERACTION OF PHOSPHOLIPID-VESICLES WITH SOME ANTIINFLAMMATORY AGENTS [J].
LASONDER, E ;
WERINGA, WD .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1990, 139 (02) :469-478
[5]   COMPARATIVE BIOAVAILABILITY OF SILIPIDE, A NEW FLAVANOLIGNAN COMPLEX, IN RATS [J].
MORAZZONI, P ;
MAGISTRETTI, MJ ;
GIACHETTI, C ;
ZANOLO, G .
EUROPEAN JOURNAL OF DRUG METABOLISM AND PHARMACOKINETICS, 1992, 17 (01) :39-44
[6]   Effects of silymarin, a natural hepatoprotector, in periparturient dairy cows [J].
Tedesco, D ;
Tava, A ;
Galletti, S ;
Tameni, M ;
Varisco, G ;
Costa, A ;
Steidler, S .
JOURNAL OF DAIRY SCIENCE, 2004, 87 (07) :2239-2247
[7]   THE INTERACTIONS OF PHOSPHOLIPID-VESICLES WITH SOME ANTI-INFLAMMATORY AGENTS [J].
VENEMA, FR ;
WERINGA, WD .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1988, 125 (02) :484-492