[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"$f1wuXdmN4Jy5gDk9LIjC17nEvbHDgOUCsJ07X0iiEzuc":3},{"answer":4,"createTime":5,"id":6,"options":7,"origin":13,"question":20,"related":21,"source":32,"type":64},[],"2024-02-25 12:39:25",132436958,[8,9,10,11,12],"A+2.2S&le;15.0","A+S&gt;15.0","A+1.7S&le;15.0","A+1.7S&gt;15.0","A+2.2S&gt;15.0",{"count":14,"courseId":15,"courseImg":16,"courseName":17,"workId":18,"workName":19},9,"b20646fd0389d74970c30219538e7f57","https:\u002F\u002Ftihai-oss-cloud.itihey.com\u002Fimg\u002F6c42bcb478ddcfae4499f93840a5abdf.png","药物检测技术","a96571a5a1544807b2207b565cd08c3b","6.3 含量均匀度","某药品含量均匀度的限度为&plusmn;15%,若初试合格需满足()",[22,34,44,54,65,75,85,88,97],{"answer":23,"createTime":24,"id":25,"options":26,"question":31,"source":32,"type":33},[],"2024-02-25 12:39:24",132436934,[27,28,29,30],"小剂量固体制剂","非均相液体制剂","小剂量半固体制剂","单剂量固体制剂","下列需要检查含量均匀度的制剂是()","v1",1,{"answer":35,"createTime":24,"id":36,"options":37,"question":43,"source":32,"type":33},[],132436941,[38,39,40,41,42],"小剂量或单剂量的固体制剂,半固体制剂和非均相液体制剂的每片(个)含量符合标示量的程度","片剂,硬胶囊剂或注射用无菌粉末,每片(个)标示量不大于25mg","片剂、硬胶囊剂或注射用无菌粉末,主药含量不大于每片(个)质量25%","内容物非均一溶液的软胶囊、单剂量包装的口服混悬液","透皮贴剂、吸入剂和栓剂","含量均匀度指()",{"answer":45,"createTime":24,"id":46,"options":47,"question":53,"source":32,"type":33},[],132436947,[48,49,50,51,52],"对于小剂量的制剂,需要进行含量均匀度检查","含量均匀度是指制剂每片(个)含量偏离标示量的程度","凡是测定含量均匀度制剂,一般不再进行重量差异检查","含量均匀度检查所用方法和含量测定方法必须相同","除片剂和注射剂外,其他不需要进行含量均匀度检查","关于含量均匀度的检查说法正确的是()",{"answer":55,"createTime":24,"id":56,"options":57,"question":63,"source":32,"type":64},[],132436953,[58,59,60,61,62],"初试中以mg表示的标示量与测定均值之差","初试中以100表示的标示量与测定均值之差","初试中以100表示的标示量与测定均值之差的绝对值","复试中以100表示的标示量与测定均值之差的绝对值","复试中以100表示的标示量与测定均值之差","含量均匀度检查判别式(A+2.2S)中A表示()",0,{"answer":66,"createTime":5,"id":67,"options":68,"question":74,"source":32,"type":64},[],132436955,[69,70,71,72,73],"符合规定","不符合规定","合格","不合格","需要复试","含量均匀度复试判断结果时,当A&gt;0.25L时,若A+1.7S&gt;L,则结果判为()",{"answer":76,"createTime":5,"id":77,"options":78,"question":84,"source":32,"type":64},[],132436957,[79,80,81,82,83],"重量差异","崩解时限","含量均匀度","可见异物","溶出度","除另有规定外,片剂、硬胶囊剂、颗粒剂或散剂等,每一个单剂标示量小于25mg或主药含量小于每一个单剂重量25%者,应检查()",{"answer":86,"createTime":5,"id":6,"options":87,"question":20,"source":32,"type":64},[],[8,9,10,11,12],{"answer":89,"createTime":5,"id":90,"options":91,"question":96,"source":32,"type":64},[],132436959,[92,93,94,95],"所有片剂","小剂量片剂","大剂量片剂","有毒制剂","含量均匀度检查主要针对()",{"answer":98,"createTime":5,"id":99,"options":100,"question":103,"source":32,"type":64},[],132436960,[80,83,79,101,102],"鉴别实验","含量测定","《中国药典》规定,凡有含量均匀度测定的片剂可不进行()"]