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基本药物在运往热带地区途中的稳定性。

Stability of essential drugs during shipment to the tropics.

作者信息

Hogerzeil H V, Battersby A, Srdanovic V, Stjernstrom N E

机构信息

World Health Organisation, Action Programme on Essential Drugs, Geneva-27, Switzerland.

出版信息

BMJ. 1992 Jan 25;304(6821):210-2. doi: 10.1136/bmj.304.6821.210.

Abstract

OBJECTIVE

To determine whether present methods of international transport of essential drugs by sea adversely affect their quality.

DESIGN

Controlled longitudinal study of drug shipments sent by sea from Unicef in Copenhagen to Lagos; to Mombasa and by land to Kampala; and to Bangkok. 11 essential drugs were stored in four locations on board the ships.

SETTING

Main shipping routes from Unicef, Copenhagen, to tropical countries.

MAIN OUTCOME MEASURES

Temperature and relative humidity in the test packs during the journey. Amount of active ingredient in the drugs before and after shipment.

RESULTS

Temperatures recorded within the test packs range from -3.5 degrees C to 42.4 degrees C and were 3-12 degrees C higher than the ambient temperature. Relative humidity within the packs ranged from 20% to 88%. Differences between the locations on board were negligible. Ergometrine injection, methylergometrine injection, and retinol capsules lost 1.5-5.8% of their activity. Ampoules of ergometrine showed a large variation in the amount of active ingredient after shipment, with three of 80 samples having concentrations 60% below those stated. Ampicillin, benzylpenicillin, phenoxymethylpenicillin, and tetracycline were not affected by transport.

CONCLUSIONS

Drugs were exposed to a much higher temperature and humidity than is recommended by the manufacturer, especially in tropical harbours and during inland transport. Except for ergometrine and methylergometrine the transport would not affect clinical effectiveness.

摘要

目的

确定目前基本药物的国际海上运输方式是否会对其质量产生不利影响。

设计

对从哥本哈根的联合国儿童基金会海运至拉各斯、蒙巴萨以及经陆路运输至坎帕拉和曼谷的药品进行对照纵向研究。11种基本药物存放在船上的4个位置。

地点

从哥本哈根的联合国儿童基金会至热带国家的主要航线。

主要观察指标

运输过程中测试包内的温度和相对湿度。运输前后药品中活性成分的含量。

结果

测试包内记录的温度范围为-3.5摄氏度至42.4摄氏度,比环境温度高3至12摄氏度。包内相对湿度范围为20%至88%。船上不同位置之间的差异可忽略不计。麦角新碱注射液、甲基麦角新碱注射液和视黄醇胶囊损失了1.5%至5.8%的活性。麦角新碱安瓿在运输后活性成分含量差异很大,80个样本中有3个的浓度比规定浓度低60%。氨苄西林、苄青霉素、苯氧甲基青霉素和四环素不受运输影响。

结论

药物所接触的温度和湿度远高于制造商推荐的水平,尤其是在热带港口和内陆运输期间。除麦角新碱和甲基麦角新碱外,运输不会影响临床疗效。

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