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David Morton

Publications and source records attributed to David Morton.

5 recordsLinked to original sources

Active and intelligent inhaler device development.

The dry powder inhaler, which has traditionally relied on the patient's inspiratory force to deaggregate and deliver the active agent to the target region of the lung, has been a successful delivery device for the provision of locally active agents for the treatment of conditions such as asthma and chronic obstructive pulmonary disease (COPD). However, such devices can suffer from poor delivery characteristics and/or poor reproducibility. More recently, drugs for systemic delivery and more high value compounds have been put into DPI devices. Regulatory, dosing, manufacturing and economic concerns have demanded that a more efficient and reproducible performance is achieved by these devices. Recently strategies have been put in place to produce a more efficient DPI device/formulation combination. Using one novel device as an example the paper will examine which features are important in such a device and some of the strategies required to implement these features. All of these technological advances are invisible, and may be irrelevant, to the patient. However, their inability to use an inhaler device properly has significant implications for their therapy. Use of active device mechanisms, which reduce the dependence on patient inspiratory flow, and sensible industrial design, which give the patient the right clues to use, are important determinants of performance here.

Drug Delivery Systems↗

[Humane endpoints as a replacement for the estimation of lethality rates in the potency testing of rabies vaccines]

Vaccines are successfully used to prevent rabies infections in humans and animals. The quality requirements for these products are high. After licensing it is still necessary for batch release to perform animal challenge tests to demonstrate the potency of the vaccines. In these experiments it is registered how many animals in the immunised groups die or show symptoms of rabies within a defined time frame. An ECVAM working group has examined whether clinical signs can be used in challenge tests for vaccine control to replace lethality as criterion. The severe distress and the typical signs of the disease made the rabies infection a promising example for this study. Clinical signs, body temperature and body weight were the criteria used to define humane endpoints. It could be shown, that the reduction of body weight and the appearance of typical clinical signs are suitable to define humane endpoints. Pain and distress could be considerably reduced by the implementation of these criteria in to the legal requirements for potency tests of rabies vaccines.

Journal Article↗