A Pharmacokinetic Study of Sixteen Major Bioactive Components of Jinshui-Huanxian Granules in Pulmonary Fibrosis Model and Control Rats Using Orbitrap Fusion Mass Spectrometry

被引:1
作者
Zhang, Weiwei [1 ,2 ]
Wan, Yan [3 ]
Sun, Shuding [1 ,4 ]
Xie, Yang [4 ,5 ]
Zhao, Di [1 ,4 ]
Li, Bing [1 ,3 ]
Li, Jiansheng [4 ,5 ]
Tian, Yange [1 ,4 ]
Feng, Suxiang [1 ,4 ]
机构
[1] Henan Univ Chinese Med, Acad Chinese Med Sci, Zhengzhou 450003, Peoples R China
[2] Univ Strasbourg, Fac Chem, F-67008 Strasbourg, France
[3] Henan Univ Chinese Med, Coll Pharm, Zhengzhou 450003, Peoples R China
[4] Henan Prov & Educ Minist PR China, Collaborat Innovat Ctr Chinese Med & Resp Dis, Zhengzhou 450046, Peoples R China
[5] Henan Univ Chinese Med, Affiliated Hosp 1, Zhengzhou 450003, Peoples R China
基金
中国国家自然科学基金;
关键词
Jinshui-Huanxian granules (JHGs); pharmacokinetic; pulmonary fibrosis (PF); bioactive compounds; Orbitrap Fusion MS; BIOAVAILABILITY; PROTOCOL; EXPOSURE;
D O I
10.3390/molecules28186492
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
Jinshui-Huanxian granules (JHGs), a Chinese herbal compound prescription, have shown a therapeutic effect in reducing lung tissue damage, improving the degree of pulmonary fibrosis, replenishing lungs and kidneys, relieving cough and asthma, reducing phlegm, and activating blood circulation. However, these active compounds' pharmacokinetics and metabolic processes were unclear. This study aimed to compare the pharmacokinetics, reveal the metabolic dynamic changes, and obtain the basic pharmacokinetic parameters of 16 main bioactive compounds after intragastric administration of JHGs in control and pulmonary fibrosis (PF) model rats by using Orbitrap Fusion MS. After administration of JHGs, the rat plasma was collected at different times. Pretreating the plasma sample with methanol and internal standard (IS) solution carbamazepine (CBZ), and it was then applied to a C18 column by setting gradient elution with a mobile phase consisting of methanol 0.1% formic acid aqueous solution. Detection was performed on an electrospray ionization source (ESI), and the scanning mode was SIM. Pharmacokinetic parameters were analyzed according to the different analytes' concentrations in plasma. The matrix effect was within the range of 79.01-110.90%, the extraction recovery rate was 80.37-102.72%, the intra-day and inter-day precision relative standard deviation (RSD) was less than 7.76%, and the stability was good, which met the requirements of biological sample testing. The method was validated (r >= 0.9955) and applied to compare the pharmacokinetic profiles of the control group and PF model group after intragastric administration of the JHGs. The 16 analytes exhibited different pharmacokinetic behaviors in vivo. In the pathological state of the PF model, most of the components were more favorable for metabolism and absorption, and it was more meaningful to study the pharmacokinetics. Above all, this study provided an essential reference for exploring the mechanism of action of JHGs and guided clinical medication as well.
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页数:22
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共 36 条
[1]   Chemistry, pharmacokinetics, pharmacology and recent novel drug delivery systems of paeonol [J].
Adki, Kaveri M. ;
Kulkarni, Yogesh A. .
LIFE SCIENCES, 2020, 250
[2]   A Chinese Herbal Formula Ameliorates Pulmonary Fibrosis by Inhibiting Oxidative Stress via Upregulating Nrf2 [J].
Bai, Yunping ;
Li, Jiansheng ;
Zhao, Peng ;
Li, Ya ;
Li, Meng ;
Feng, Suxiang ;
Qin, Yanqin ;
Tian, Yange ;
Zhou, Tiqiang .
FRONTIERS IN PHARMACOLOGY, 2018, 9
[3]   Idiopathic Pulmonary Fibrosis and Lung Transplantation: When it is Feasible [J].
Balestro, Elisabetta ;
Cocconcelli, Elisabetta ;
Tine, Mariaenrica ;
Biondini, Davide ;
Faccioli, Eleonora ;
Saetta, Marina ;
Rea, Federico .
MEDICINA-LITHUANIA, 2019, 55 (10)
[4]   Multiple Biological Effects of an Iridoid Glucoside, Catalpol, and Its Underlying Molecular Mechanisms [J].
Bhattamisra, Subrat Kumar ;
Yap, Kah Heng ;
Rao, Vikram ;
Choudhury, Hira .
BIOMOLECULES, 2020, 10 (01)
[5]   Anti-inflammatory and immunoregulatory effects of icariin and icaritin [J].
Bi, Zhangyang ;
Zhang, Wei ;
Yan, Xiaoyan .
BIOMEDICINE & PHARMACOTHERAPY, 2022, 151
[6]   Intestinal Absorption Mechanisms of Prenylated Flavonoids Present in the Heat-Processed Epimedium koreanum Nakai (Yin Yanghuo) [J].
Chen, Yan ;
Zhao, Yan Hong ;
Jia, Xiao Bin ;
Hu, Ming .
PHARMACEUTICAL RESEARCH, 2008, 25 (09) :2190-2199
[7]   Peiminine Attenuates Acute Lung Injury Induced by LPS Through Inhibiting Lipid Rafts Formation [J].
Du, Boxiang ;
Cao, Liang ;
Wang, Kai ;
Miu, Juanjuan ;
Yao, Lei ;
Xu, Zhihua ;
Song, Jie .
INFLAMMATION, 2020, 43 (03) :1110-1119
[8]   Absolute bioavailability and dose-dependent pharmacokinetic behaviour of dietary doses of the chemopreventive isothiocyanate sulforaphane in rat [J].
Hanlon, Natalya ;
Coldham, Nick ;
Gielbert, Adriana ;
Kuhnert, Nikolai ;
Sauer, Maurice J. ;
Kingi, Laurie J. ;
Ioannides, Costas .
BRITISH JOURNAL OF NUTRITION, 2008, 99 (03) :559-564
[9]   Dose-Dependent Bioavailability and CYP3A Inhibition Contribute to Non-Linear Pharmacokinetics of Voriconazole [J].
Hohmann, Nicolas ;
Kocheise, Franziska ;
Carls, Alexandra ;
Burhenne, Juergen ;
Weiss, Johanna ;
Haefeli, Walter E. ;
Mikus, Gerd .
CLINICAL PHARMACOKINETICS, 2016, 55 (12) :1535-1545
[10]   Development of Paeonol Liposomes: Design, Optimization, in vitro and in vivo Evaluation [J].
Huang, Shan ;
Zhai, Bingtao ;
Fan, Yu ;
Sun, Jing ;
Cheng, Jiangxue ;
Zou, Junbo ;
Zhang, Xiaofei ;
Shi, Yajun ;
Guo, Dongyan .
INTERNATIONAL JOURNAL OF NANOMEDICINE, 2022, 17 :5027-5046