paracetamol

Paracetamol ( Par ) ip accelerated the formation of liver malondialdehyde ( MDA ) , in-creased the content of serum MDA , and enhanced the activity of serum alanine transaminase ( ALT ) in the dose-response and time - response relationships .

在量－效和时－效关系上，醋氨酚（Par）ip能加速肝脏丙二本醛（MDA）生成，增加血清MDA含量，同时提高血清丙氨酸转氨酶（ALT）活性。

Take two paracetamol and try to sleep .

服两片扑热息痛，好好睡一觉。

Do you have any paracetamol ?

你有扑热息痛吗？

I often take paracetamol at work if I get a bad headache

工作中头疼得厉害时，我常服用扑热息痛。

I took 2 paracetamol .

我吃了两片扑热息痛。

Study on quantitative control in TABLET-MAKING using paracetamol as model drug

以扑热息痛为模型药物对片剂生产量化控制的研究

Comparison with two methods for determination of paracetamol in granules of sugar

氨金黄敏颗粒（含糖）中对乙酰氨基酚含量测定方法的比较

METHODS : To analyse the market of paracetamol at home and abroad .

方法：对扑热息痛国内外市场状况进行全面分析。

Preparation of paracetamol hollow type suppository and its quality research

对乙酰氨基酚中空栓的研制及其质量考查

Take two paracetamol s and try to sleep .

服两片扑热息痛，好好睡一觉。

The application of new accessories and techniques in the preparation of Paracetamol Tablets

新辅料及新工艺在对乙酰氨基酚片中的应用

In trials the test predicted how well men would respond to paracetamol .

在试验中，尿检预测了人们代谢对乙酰氨基酚的过程。

Paracetamol sustained release pellets were prepared using melt method .

采用熔融法制备了对乙酰氨基酚缓释微丸。

Study of Paracetamol Molecularly Imprinted Polymers Applied to Solid Phase Extraction

扑热息痛分子印迹聚合物应用于固相萃取的研究

The stability studies of paracetamol solution and ATP injection by linear non-isothermal method

用线性变温法研究扑热息痛溶液和三磷酸腺苷注射液的稳定性

Studies of Selective Enrichment and Recognized Characteristics of Paracetamol Molecular Template Polymer

药物扑热息痛分子模板聚合物的选择性富集与识别特性研究

A rapid and exclusive method for the identification of paracetamol tablets was established .

建立对乙酰氨基酚片快速、专属的鉴别方法。

The method is applied to the analysis of paracetamol in the diluted urine samples .

该方法已用于尿样中扑热息痛的分析测定。

β - CD interact with paracetamol and form inclusion compound in water .

在水溶液中β-环糊精能够与扑热息痛发生相互作用，生成包结复合物。

Results : The retention times of paracetamol was 4.448 min.

结果：对乙酰氨基酚的保留时间为4.448min。

Group B was treated with paracetamol .

B组予扑热息痛口服；

Market Analysis of Paracetamol

扑热息痛市场分析

Study on Pharmacology and Pharmacokinetics of 10 % Paracetamol Injection in Rabbit

10%扑热息痛注射液的药理及兔体内动力学研究

Relative Bioavailability of Paracetamol Soft Capsules and Tablets in Human

对乙酰氨基酚软胶囊与片剂的人体相对生物利用度研究

Methods : Paracetamol hollow type suppository was produced by the model of HTS .

方法：用中空栓模具，制备了对乙酰氨基酚中空栓。

Studies on effect of potassium glycyrrhizate on stability of paracetamol

甘草酸钾对扑热息痛稳定性影响的研究

OBJECTIVE : To study crospovidone effect on the dissolution rate of paracetamol tablets .

目的：研究崩解剂交联聚维酮对对乙酰氨酚片溶出度的影响。

Study on interaction between potassium glycyrrhizate and compound paracetamol using differential scanning calorimetry

甘草酸钾与复方对乙酰氨基酚相互作用的差示扫描量热法研究

Group C was treated with diazepam , paracetamol and lidocaine .

C组予安定、扑热息痛口服，利多卡因表面麻醉。

Establishment of Microbial Limit Test for Compound Paracetamol and Amantadine Hydrochloride Preparations

复方氨酚烷胺制剂的微生物限度检查方法的建立