braised cuttle fish with wild mushrooms

1、

vent in upstream side of wedge

楔形闸板上游排泄口

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2、

b. upstream side of the north shore of navigable road;

北岸一侧为上行通航分道；

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3、

a securing means 33 that is capable of maintaining the upstream-side hose 11 in the extended state is provided.

具有在上游管部（11）处于拉伸状态下能够保持该拉伸状态的固定机构（33）。

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4、

when cleaning is performed, the securing means 33 maintains the upstream-side hose 11 in the extended state.

吸尘时，通过固定机构（33）把上游管部（11）保持在拉伸状态。

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5、

an absorbing layer absorbs the energy of microwave in n frequency areas and is installed at the upstream side.

吸收层吸收在N个频率范围之一内的微波能量，并设置于所述上游端。

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6、

conclusions the results showed that the percutaneous absorption of oxaprozin was a zero-order releasing kinetics through nonpolar channel, and 10% oleic acid plus 1% azone was the most effective one.

结论：奥沙普秦透皮吸收符合非极性通道释放的零级动力学方程，其中以10%油酸加1%月桂氮芯卓酮组成的混合促进剂作用最显著。

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7、

results the oxaprozin-peg 6000 solid dispersion was a simple-lower-eutectic compound. the oxaprozin was dispersed in peg 6000 as micro-crystallite form.

结果：卟恶丙嗪PEG6000固体分散体是一种简单低共熔混合物，卟恶丙嗪以超细结晶状态分散在PEG载体中。

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8、

conclusion: the method is used to determine the content of oxaprozin tablet and raw material medicine, which is simple, rapid, qualitative, accurate with satisfactory results.

结论：该法快速准确、操作方便，用于样品及原料药中的奥沙普秦的含量测定，结果令人满意。

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9、

studies on solubility of oxaprozin

恶丙嗪溶解性能的研究

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10、

aim an hplc method was established for the study on pharmacokinetics and bioequivalence of oxaprozin enteric tablet in healthy volunteers.

目的建立一种HPLC检测法，以测定人体血浆中奥沙普秦的药物浓度，并对两种奥沙普秦肠溶片生物等效性进行评价。

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11、

determination of oxaprozin gel by hplc

奥沙普秦凝胶剂的HPLC测定

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12、

preparation and determination of oxaprozin gel

恶丙嗪凝胶剂的制备及含量测定

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13、

the bioequivalence of oxaprozin enteric tablet in healthy volunteers measured with hplc

奥沙普秦肠溶片HPLC测定法及其人体生物等效性研究

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14、

objective: to compare the relative bioavailability of 2 kinds of domestic oxaprozin enteric tablets.

目的：比较2种国产奥沙普秦肠溶片的相对生物利用度。

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15、

phase iii trials of oxaprozin enteric coated tablet in treatment of rheumatoid arthritis

奥沙普秦肠溶片治疗类风湿关节炎的III期临床试验

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16、

methods: the permeation and release of oxaprozin gel was measured by using franz diffusion cell.

方法：采用Franz扩散池，进行奥沙普秦凝胶剂体外渗透性和释放度实验。

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17、

objective: to study the influence of oxaprozin on platelet aggregation and thrombosis in rabbits and rats.

目的：研究奥沙普嗪对家兔和大鼠血小板聚集和血栓形成的影响。

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18、

objective to synthesize nonsteroidal anti-inflammatory drug oxaprozin.

目的合成非甾体类抗炎药奥沙普秦。

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19、

study on pharmacodynamics and permeation of oxaprozin gel in vitro

奥沙普秦凝胶剂的体外渗透性及药效学

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20、

objective to prepare the complex between oxaprozin and hydrogenated phospholipid.

目的制备奥沙普秦氢化磷脂复合物。

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