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机译:通过亲脂性前药掩模掩模方法提高环状RGD六峰肽的口服生物利用度:从肺膜到牙细胞途径重定向肽肠道渗透率
Hebrew Univ Jerusalem Inst Drug Res Sch Pharm Fac Med POB 12065 IL-91120 Jerusalem Israel;
Hebrew Univ Jerusalem Inst Drug Res Sch Pharm Fac Med POB 12065 IL-91120 Jerusalem Israel;
Hebrew Univ Jerusalem Inst Drug Res Sch Pharm Fac Med POB 12065 IL-91120 Jerusalem Israel;
Tech Univ Munich Inst Adv Study Lichtenbergstr 4 D-85748 Garching Germany;
Tech Univ Munich Inst Adv Study Lichtenbergstr 4 D-85748 Garching Germany;
Tech Univ Munich Inst Adv Study Lichtenbergstr 4 D-85748 Garching Germany;
Hebrew Univ Jerusalem Inst Chem Hebrew Univ Edmond Safra Campus Givat Ram Campus IL-91904;
Hebrew Univ Jerusalem Inst Chem Hebrew Univ Edmond Safra Campus Givat Ram Campus IL-91904;
Tech Univ Munich Inst Adv Study Lichtenbergstr 4 D-85748 Garching Germany;
Hebrew Univ Jerusalem Inst Drug Res Sch Pharm Fac Med POB 12065 IL-91120 Jerusalem Israel;
oral bioavailability; peptides; intestinal permeability; RGD integrin inhibitor; prodrug; enterocytes; metabolic stability; pharmacokinetics;
机译:通过亲脂性前药掩模掩模方法提高环状RGD六峰肽的口服生物利用度:从肺膜到牙细胞途径重定向肽肠道渗透率
机译:主动乳糜泻对麦醇溶蛋白的细胞旁和跨细胞肠通透性
机译:在C6胶质瘤模型中通过微泡增强诊断超声通过跨细胞和旁细胞途径增加血脑肿瘤屏障通透性
机译:增强亲水性药物的口服递送:设计和评估紧密连接调节剂和环肽前药。
机译:胰高血糖素样肽2增强小鼠跨细胞和旁细胞途径的肠上皮屏障功能
机译:胰高血糖素样肽2增强小鼠跨细胞和旁细胞途径的肠上皮屏障功能