[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"$fDrv3HwxyhOhU40U1FTpr8TgXDKj_wBeO-zLWDqGUCN0":3},{"answer":4,"createTime":5,"id":6,"options":7,"origin":13,"question":20,"related":21,"source":32,"type":33},[],"2026-06-02 02:36:36",132689020,[8,9,10,11,12],"口服吸收迅速","属一室分布模型","口服药物未经肝门脉吸收","口服的生物利用度低","口服吸收完全",{"count":14,"courseId":15,"courseImg":16,"courseName":17,"workId":18,"workName":19},16,"ec893d7e811b03e920247aef5390f04a","https:\u002F\u002Ftihai-oss-cloud.itihey.com\u002Fimg\u002F077210f6d991c0881781af75bb05cf0c.jpg","药理学","cc7741b65736452b8d92bb5f92f4c1e3","药动学自测题","某药物在口服和静注相同剂量后的时量曲线下面积相等,表明其",[22,34,44,47,57,67,77,87,97,107],{"answer":23,"createTime":5,"id":24,"options":25,"question":31,"source":32,"type":33},[],132689018,[26,27,28,29,30],"加速药物在体内的分布","对药物的主动转运有影响","是可逆的","是永久性的","促进药物排泄","药物与血浆蛋白结合","v1",0,{"answer":35,"createTime":5,"id":36,"options":37,"question":43,"source":32,"type":33},[],132689019,[38,39,40,41,42],"代谢快慢","分布","与血浆蛋白结合","作用持续时间","起效快慢","药物肝肠循环影响了药物在体内的",{"answer":45,"createTime":5,"id":6,"options":46,"question":20,"source":32,"type":33},[],[8,9,10,11,12],{"answer":48,"createTime":5,"id":49,"options":50,"question":56,"source":32,"type":33},[],132689021,[51,52,53,54,55],"弱碱性药在酸性环境中","在碱性环境中解离型药","在酸性环境中解离型药","弱酸性药在酸性环境中","弱酸性药在碱性环境中","下列易被转运的条件是",{"answer":58,"createTime":5,"id":59,"options":60,"question":66,"source":32,"type":33},[],132689022,[61,62,63,64,65],"7个半衰期","5个半衰期","以上都不是","2个半衰期","1个半衰期","某药达稳态血浓度,中途停药,再达稳态血浓度时间还需要",{"answer":68,"createTime":5,"id":69,"options":70,"question":76,"source":32,"type":33},[],132689023,[71,72,73,74,75],"不受饱和及竞争性抑制影响","不耗能量","转运需载体","从高浓度侧向低浓度侧转运","膜两侧浓度达平衡时停止","下列药物被动转运的错误项是",{"answer":78,"createTime":5,"id":79,"options":80,"question":86,"source":32,"type":33},[],132689024,[81,82,83,84,85],"作用增强","作用完全改变","作用消除","无变化","作用减弱","经肝药酶代谢的药物与肝药酶诱导剂合用后其效应可",{"answer":88,"createTime":5,"id":89,"options":90,"question":96,"source":32,"type":33},[],132689025,[91,92,93,94,95],"按一级动力学消除","按零级动力学消除","经肠道排出","经肝代谢消除","经肾排出","体内药物浓度超出其代谢消除能力时其消除方式是",{"answer":98,"createTime":5,"id":99,"options":100,"question":106,"source":32,"type":33},[],132689026,[101,102,103,104,105],"药物的水溶性","药物的解离度","化学结构","分子量大小","药物的脂溶性","体液的pH可影响药物跨膜转运,主要是改变其",{"answer":108,"createTime":5,"id":109,"options":110,"question":116,"source":32,"type":33},[],132689027,[111,112,113,114,115],"辅酶Ⅱ","葡萄糖醛酸转移酶","水解酶","细胞色素P450酶系统","单胺氧化酶","促进药物生物转化的主要酶系统是"]