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吉非替尼乳剂单次与多次给药后在大鼠体内的药动学研究                                                                 Δ


        李 莹 ,文 周 ,马风伟 ,刘志刚 ,田 驰 ,刘治芳 ,程泽能 (1.贵阳学院食品与制药工程学院,贵阳
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        550005;2.中南大学湘雅药学院,长沙 410013;3.贵阳市花溪区市场监督管理局,贵阳 550025;4.长沙医学院
        药学院,长沙 410013)
        中图分类号 R969.1          文献标志码 A          文章编号 1001-0408(2020)01-0048-05
        DOI   10.6039/j.issn.1001-0408.2020.01.09
        摘   要   目的:研究吉非替尼乳剂单次和多次给药后在大鼠体内的药动学特征。方法:将大鼠分为单次给药组和多次给药组。单
        次给药组大鼠分为吉非替尼原料药组(50 mg/kg)和吉非替尼乳剂组(50 mg/kg),每组6只,灌胃给药1次。多次给药组大鼠分为吉
        非替尼原料药组(50 mg/kg)和吉非替尼乳剂组(50 mg/kg),每组8只,连续灌胃给药7 d,每天1次。吉非替尼原料药组大鼠于给药
        前和给药后1、2、2.5、3、3.5、3.75、4、4.25、4.5、6、8、12和24 h取血0.3 mL,吉非替尼乳剂组大鼠于给药前和给药后(多次给药组为给
        药7 d后)2、4、6、8、9、10、11、12、13、14、16、24、36和48 h取血0.3 mL,采用高效液相色谱法测定大鼠血浆中吉非替尼的血药浓度,
        绘制药-时曲线,并用 DAS 2.0 软件拟合药动学参数。结果:单次给药后,与吉非替尼原料药组 tmax[(2.67±0.75)h]、MRT0-24 h
        [ (8.68±0.91)h]、MRT0-∞[(14.20±3.45)h]比较,吉非替尼乳剂组tmax[(8.33±4.41)h]、MRT0-48 h[(15.00±1.60)h]、MRT0-∞[(17.60±
        2.66)h]均显著增加(P<0.05)。多次给药后,与吉非替尼原料药组 tmax[(6.79±3.75)h]、AUC0-48 h[(41.10±8.92)mg·h/L]、Vz/F
        [ (16.30±5.45)L/kg]、CLz/F[(0.94±0.19)L/(h·kg)]、MRT0-48 h[(10.10±0.36)h]比较,吉非替尼乳剂组Vz/F[(44.20±30.30)L/kg]、
        CLz/F[(1.89±1.56)L/(h·kg)]、MRT0-48 h[(16.20±2.52)h]均显著增加(P<0.05),AUC0-48 h[(38.70±26.20)mg·h/L]显著减少(P<
        0.05),tmax[(10.40±3.25)h]增加,但差异无统计学意义。结论:与吉非替尼原料药比较,单次和多次给药吉非替尼乳剂,均可延长
        药物的达峰时间;本研究结果可为吉非替尼新型给药系统的研究提供参考。
        关键词 吉非替尼;乳剂;单次;多次;高效液相色谱法;药动学;大鼠

        Pharmacokinetic Study on Single and Multiple Administration of Gefitinib Emulsion in Rats
        LI Ying ,WEN Zhou ,MA Fengwei ,LIU Zhigang ,TIAN Chi ,LIU Zhifang ,CHENG Zeneng(1.Food and
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        Pharmaceutical Engineering Institute, Guiyang University, Guiyang 550005, China;2.Xiangya School of
        Pharmaceutical Sciences,Central South University,Changsha 410013,China;3.Market Supervision Bureau of
        Guiyang Huaxi District,Guiyang 550025;4.College of Pharmacy,Changsha Medical University,Changsha
        410013,China)
        ABSTRACT    OBJECTIVE:To study pharmacokinetic characteristics of single dose and multiple dose administration of Gefitinib
        emulsion in rats. METHODS:The rats were divided into single administration group and multiple administration group. Single
        administration group was subdivided into Gefitinib raw medicine group(50 mg/kg,i.g.)and Gefitinib emulsion group(50 mg/kg,
        i.g.),with 6 rats in each group,gavage once. Multiple administration group were subdivided into Gefitinib raw medicine group
        (50 mg/kg)and Gefitinib emulsion group(50 mg/kg),with 8 rats in each group;they were given relevant medicine intragastricaly
        for consecutive 7d,once a day. 0.3 mL blood of rats in Gefitinib raw medicine group was taken before medication and 1,2,2.5,
        3,3.5,3.75,4,4.25,4.5,6,8,12 and 24 h after medication;0.3 mL blood of rats in Gefitinib emulsion group was taken
        before medication and 2,4,6,8,9,10,11,12,13,14,16,24,36 and 48 h after administration(Multiple administration
        group is after 7 d of administration). HPLC method was used to determine the plasma concentration of gefitinib in rat,and plasma
        concentration-time curves were drawn. Pharmacokinetic parameters were fitted by using DAS 2.0 software. RESULTS:After single
        administration,compared with the tmax[(2.67±0.75)h],MRT0-24 h [(8.68±0.91)h],MRT0- ∞ [(14.20±3.45)h] of Gefitinib raw
        medicine group,tmax [(8.33±4.41)h],MRT0-48 h [(15.00±1.60)h],MRT0-∞ [(17.60±2.66)h] of Gefitinib emulsion group were
        increased significantly(P<0.05). After multiple administration,compared with the tmax [(6.79±3.75)h],AUC0-48 h [(41.10±8.92)
                                                            mg·h/L],Vz/F [(16.30±5.45)L/kg],CLz/F [(0.94±0.19)
            Δ 基金项目:贵州省科技厅基础研究计划项目(No.黔科合基础                  L/(h·kg)],MRT0-48 h [(10.10 ± 0.36) h] of Gefitinib raw
        〔2019〕1013)号;2019年度贵阳市科学技术局-贵阳学院科技专项资金
                                                            medicine group,Vz/F [(44.20±30.3)L/kg],CLz/F[(1.89±
        项目(No.GYU-KYZ〔2019-2020〕PT16-05);2015 年湖南省教育厅科
                                                            1.56) L/(h·kg)],MRT0-48 h [(16.20 ± 2.52) h] of Gefitinib
        研项目(No.15C0160)
            * 硕 士 研 究 生 。 研 究 方 向 :药 剂 学 与 药 动 学 。 电 话 :0851-  emulsion group were increased significantly (P<0.05) ,
        85403091。E-mail:463492650@qq.com                    AUC0-48 h [(38.70±26.20)mg·h/L] was decreased significantly
            # 通信作者:教授,博士。研究方向:新药临床前药动学及早期临                 (P<0.05),and tmax [(10.40±3.25)h] was increased,without
        床试验。电话:0731-82650446。E-mail:chengzn@csu.edu.cn      statistical  significance.  CONCLUSIONS: Compared  with


        ·48  ·  China Pharmacy 2020 Vol. 31 No. 1                                    中国药房    2020年第31卷第1期
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