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使用干粉吸入器给药系统通过气管导管进行药物递送的体外评估。

In vitro assessment of drug delivery through an endotracheal tube using a dry powder inhaler delivery system.

作者信息

Everard M L, Devadason S G, Le Souëf P N

机构信息

Department of Respiratory Medicine, Princess Margaret Hospital for Children, Subiaco, Australia.

出版信息

Thorax. 1996 Jan;51(1):75-7. doi: 10.1136/thx.51.1.75.

Abstract

BACKGROUND

Jet nubulisers and metered dose inhalers are widely used to deliver aerosolised drugs to the lungs of intubated patients in adult intensive care units. Drug delivery using these systems has been shown to be inefficient and both forms of delivery have the potential to induce paradoxical bronchoconstriction in patients with reactive airways disease.

METHODS

Experiments were carried out to determine whether it was possible to deliver drug from a dry powder delivery system through an endotracheal tube. A 200 micrograms budesonide Turbohaler was enclosed in a chamber which allowed it to be inserted into a ventilator circuit. Experiments were performed with a multistage liquid impinger in which drug was drawn through the Turbohaler and endotracheal tube at 60 l/min providing an index of the maximum drug delivery achievable via this route. A second series of experiments was performed in which the Turbohaler was placed in a ventilator circuit using a Servo 900C volume cycled ventilator. Drug delivered from the Turbohaler during the inspiratory phase was collected on a filter placed between the end of a 9 mm endotracheal tube and a model lung. A tidal volume of 500 ml and inspiratory time of 0.5 seconds was used. Budesonide was assayed using an ultraviolet spectrophotometric assay.

RESULTS

Thirty percent of the nominal dose passed through the endotracheal tube and was collected in the multistage liquid impinger. Mean drug delivery to the filter in the ventilator circuit was 20%.

CONCLUSIONS

This in vitro study indicates that drugs from dry powder inhalers (in this case the Turbohaler) can be satisfactorily delivered through endotracheal tubes and that clinical evaluation of this technique is now indicated.

摘要

背景

喷射雾化器和定量吸入器被广泛用于在成人重症监护病房中向插管患者的肺部输送雾化药物。使用这些系统进行药物输送已被证明效率低下,并且这两种输送方式都有可能在患有反应性气道疾病的患者中诱发矛盾性支气管收缩。

方法

进行实验以确定是否可以通过气管内导管从干粉输送系统输送药物。将200微克布地奈德都保置于一个腔室中,该腔室使其能够插入呼吸机回路。使用多级液体冲击器进行实验,其中药物以60升/分钟的速度通过都保和气管内导管抽吸,提供通过该途径可实现的最大药物输送指数。进行了第二系列实验,其中使用Servo 900C容量控制呼吸机将都保置于呼吸机回路中。在吸气阶段从都保输送的药物收集在置于9毫米气管内导管末端和模型肺之间的过滤器上。使用500毫升的潮气量和0.5秒的吸气时间。使用紫外分光光度法测定布地奈德。

结果

标称剂量的30%通过气管内导管并收集在多级液体冲击器中。呼吸机回路中过滤器的平均药物输送量为20%。

结论

这项体外研究表明,干粉吸入器(在本案例中为都保)中的药物可以通过气管内导管令人满意地输送,现在需要对该技术进行临床评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aaa0/472804/f4190c8bd6fa/thorax00320-0084-a.jpg

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