Objective: To prepare oxaprozin liposome.
目的：制备恶丙嗪脂质体。
Objective: To determine the content of oxaprozin.
目的：测定奥沙普秦含量。
CONCLUSION The gel of oxaprozin has good stability.
结论奥沙普秦凝胶剂稳定性良好。
The stability of oxaprozin gel was measured by stability experiment.
通过稳定性实验考察奥沙普秦凝胶的稳定性。
Objective to synthesize nonsteroidal anti-inflammatory drug oxaprozin.
目的合成非甾体类抗炎药奥沙普秦。
METHODS:The Oxaprozin gel which Carbomer 941 as excipient was prepared.
方法：以卡波姆941为辅料，制备呷恶丙嗪凝胶剂；
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。
OBJECTIVE To study the effects of enhancers on the transdermal delivery of oxaprozin.
目的研究促进剂对奥沙普秦渗透性的影响。
Objective To establish a HPLC method for determining the concentration of oxaprozin in human plasma.
目的建立奥沙普嗪血药浓度的高效液相色谱法(HPLC法)。
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。
Objective to evaluate the efficacy and safety of oxaprozin (OXP) and aspirin (asp) in the treatment of patients with postoperative dental surgery pain (PDSP).
目的比较研究口恶丙口秦(OXP)和肠溶阿司匹林(asp)治疗牙科手术后疼痛(pdsp)的疗效和安全性。
METHOD:Using simple cell method and snake skin as transdermal barrier, we determined the transdermal amount of oxaprozin in different Azone concentrations liniments.
方法：应用简单小室法，以蛇皮为透皮屏障，使用不同浓度的月桂氮酮，测量丙嗪的透皮吸收量。
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。
Three aspects of Oxaprozin are discussed in this article, Which inclnde the optimum design of reaction conditions, purification of the find product and preparation of the Calcium Salt.
本文讨论了（口恶）丙嗪合成条件的优化设计，产品的纯制方法及钙盐的制备方法。
CONCLUSIONS: The oxaprozin dispersible tablets was characteristic of rapid disintegration, uniform dispersion, fast and complete dissolution. It would be a new dosage form of developmental worth.
结论：卟恶丙嗪分散片比另两种市售片剂崩解快、分散均匀度好、溶出快而完全。
CONCLUSIONS: The oxaprozin dispersible tablets was characteristic of rapid disintegration, uniform dispersion, fast and complete dissolution. It would be a new dosage form of developmental worth.
结论：卟恶丙嗪分散片比另两种市售片剂崩解快、分散均匀度好、溶出快而完全。
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