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Pharmacokinetic Drug Interaction Studies of Irinotecan and Its Active Metabolite SN-38 with P-gp Inhibitors

Abstract第6-7页
Introduction第7-15页
    1.1. Background第7-9页
    1.2. Metabolism and excretion of irinotecan第9-11页
    1.3. Role of drug efflux transporters in irinotecan disposition第11-13页
    1.4. The Oral Route for Irinotecan Administration第13-14页
    1.5. HPLC Assay of Irinotecan and SN-38第14页
    1.6. The Aim of this Work第14-15页
Experimental Part第15-28页
    1. Materials第15-16页
    2. High Performance Liquid Chromatographic Analysis of Irinotecan and SN-38第16-22页
        2.1 Instruments第16页
        2.2 Chromatographic Conditions for intestinal perfusion samples第16-17页
            2.2.1. Mobile phase composition and preperation第16页
            2.2.3. Instrument adjustment第16页
            2.2.4. Preparation of Stock and Standard Solutions第16页
            2.2.5. Sample Preparation第16-17页
        2.3 Chromatographic Conditions for analysis of blood samples第17-18页
            2.3.1. Mobile phase composition and preperation第17页
            2.3.3. Instrument adjustment第17页
            2.3.4. Preparation of Stock and Standard Solutions第17页
            2.3.5. Sample Preparation第17-18页
        2.4. HPLC Method validation for the intestinal perfusion experiments第18-20页
            2.4.1 Specificity第18页
            2.4.2 Linearity第18-19页
            2.4.3 Accuracy and precision第19页
            2.4.4 Recovery第19页
            2.4.5. Stability studies第19-20页
            2.4.6 Lower limits of detection and quantification第20页
        2.5. HPLC Method validation for the in vivo pharmacokinetic experiments第20-22页
            2.5.1 Specificity第20-21页
            2.5.2 Linearity第21页
            2.5.3 Accuracy and precision第21页
            2.5.4 Recovery第21页
            2.5.5. Stability studies第21-22页
            2.5.6 Lower limits of detection and quantification第22页
    3. In Situ Single Pass Intestinal Perfusion experiments第22-25页
        3.1. Animals第22页
        3.2 preperation of the Perfusion Solution第22-23页
        3.3. Improved In Situ Single Pass Intestinal Perfusion Experiments第23-25页
        3.4. Data Analysis and Statistics第25页
    4. In Vivo Pharmacokinetic experiments第25-28页
        4.1. Animals第25-26页
        4.2. Animals grouping and drug dosage第26页
        4.3. Drug solutions preparation第26页
        4.4. Blood sampling第26-27页
        4.5. Pharmaco kinetic Data Analysis第27-28页
Results and Discussions第28-51页
    1. High Performance Liquid Chromatographic analysis of irinotecan and 第28-34页
        1.1 Chromatographic Method for analysis of perfusion samples第28-31页
            1.1.1 Specificity第28-29页
            1.1.2 Linearity第29页
            1.1.3 Accuracy and precision第29-30页
            1.1.4 Recovery第30页
            1.1.5 Stability第30-31页
            1.1.6 Lower limits of detection and quantification第31页
        1.2 Chromatographic Method for analysis of plasma samples第31-34页
            1.2.1 Specificity第31-32页
            1.2.2 Linearity第32-33页
            1.2.3 Accuracy and precision第33页
            1.2.4 Recovery第33-34页
            1.2.5 Stability第34页
            1.2.6 Lower limits of detection and quantification第34页
    2. Rat's Single Pass Intestinal Perfusion Experiments第34-45页
        2.1. Irinotecan-verapamil interaction第35-36页
        2.2. Irinotecan Excipients Interaction第36-43页
            2.2.1. Cremophor EL第36-39页
            2.2.2. Tween 80第39-41页
            2.2.3. PEG 400第41-43页
        2.3. Irinotecan-Grapefruit interaction第43-45页
    3. In vivo Pharmacokinetic experiments第45-51页
        3.1 Cremophor El-irinotecan interaction第47-48页
        3.2. Tween 80-irinotecan interaction第48-50页
        3.3. Grapefruit-irinotecan interaction第50-51页
Conclusions第51-52页
Acknowledgments第52页
Publications第52-53页
References第53-59页
Review第59-63页
References第63-67页

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