英语释义

• a nonsteroidal anti-inflammatory drug (trade name Naprosyn) used in the treatment of arthritis and musculoskeletal inflammation and moderate pain

片语

Naproxen Granules萘普生颗粒

Naproxen Capsules萘普生胶囊

Naproxen impurities萘普生杂质

Naproxen Base翻译中国

naproxen ester萘普生酯

naproxen derivatives萘普生衍生物

Naproxen Suppositories萘普生栓

sodium naproxen萘普生钠

Naproxen Injection萘普生注射液

英汉例句

• 「For patients at high cardiovascular risk, naproxen is the drug of choice,」 Farkouh said. 「It has the best overall safety record.」

  对于处于心血管事件的高危患者，萘普生是他们的用药选择。该药总体上具有最安全的记录。

• The release test in vitro of sodium naproxen in the simulated human intestinal juice was conducted and these gels were used as carriers.

  并以两种水凝胶为载体，在模拟人体肠液环境下进行萘普生钠的体外释放实验。

• AIM: To observe the application effect of naproxen on postmenopausal women with intrauterine device.

  目的：观察萘普生栓在绝经后妇女取环中的作用。

• Overall, naproxen appeared to have the safest cardiovascular risk profile of the seven included in the review.

  总之，在这些研究中的七项风险预测表明，萘普生表现出最安全的心血管风险。

• Rofecoxib users had the highest event rates, while naproxen users had the lowest, even lower than non users.

  罗非考昔使用者的心血管事件发生率最高，而萘普生的发生率最低，甚至比不应用药物的人还要低。

• Objective: To investigate the feasibility of two enteric coating technologies for naproxen micro-pellets.

  前言：目的：考察萘普生肠溶微丸两种包衣工艺的可行性。

• The first part of this research involved the studies of NSAIDs-carprofen and naproxen .

  第一部份以研究NSAID药物包括卡普洛芬及那普洛辛。

• Recent developments in the catalytic asymmetric synthesis of non steroidal antiinflammatory drug naproxen is presented according to reaction types.

  按反应类型介绍了近几年来催化不对称合成非甾体消炎镇痛药萘普生的各种新方法。

• OBJECTIVE to prepare bilayer tablet, which consists of a metoclopramide rapid release layer and a naproxen sodium sustained release layer.

  目的制备由甲氧氯普胺速释层与萘普生钠缓释层组成的双层片。

• A newly intelligent drug delivery system was established to research the releasing of naproxen in the systems.

  建立一种新型的药物缓释系统，以研究抗炎药萘普生在该系统中的释放规律。

• A new technology was proposed to visually study the crystallization morphologies of naproxen particles synthesized by reaction-precipitation.

  采用毛细显微摄像技术对反应结晶法制备多形貌萘普生药物的晶体生长进行了直观、实时的观察和研究。

• AIM :To compare the effects of feprazone with naproxen on pain.

  目的：比较非普拉宗与萘普生止痛的疗效。

• METHODS: Using naproxen as internal standard, mycophenolic acid in plasma samples was determined by HPLC with protein precipitation.

  方法：以萘普生为内标，血浆用甲醇蛋白沉淀后直接进样。

• Objective: To study the preparation technique of naproxen pellets.

  目的：研究萘普生微丸的制备工艺。

• OBJECTIVE To develop naproxen enteric-coated pellets and evaluate its release characteristics in vitro.

  目的：研制萘普生肠溶微丸，评价其体外释药特性。

• The effects of concentration of acetic acid in the mobile phase was studied and the polymers were able to separate naproxen from the structurally similar molecular such as ibuprofen and ketoprofen .

  另外，在印迹柱上分离了与萘普生结构相似的布洛芬、酮洛芬，这进一步证实了制得的-萘普生分子印迹聚合物的高度专一识别性能。

• The active ingredient in Naprogesic is naproxen sodium.

  Naprogesic的活性成份是萘普生钠。

• The results indicated that anti-inflammatory and analgesic action was better than that of sodium naproxen injection and antondin injection (PP

  结果表明复方萘普生钠注射液的抗炎和镇痛作用均明显优于萘普生钠注射液和安痛定注射液（PP

• Pharmacokinetics on injection of sodium naproxen in experimental rabbits was studied in comparison with its capsules.

  以萘普生钠胶囊剂作对照，研究了萘普生的注射液在家兔体内的药代动力学。