Abstract: A physiological sensing device for the measurement of pCO2 includes a closed chamber bounded, at least partially, by a carbon dioxide permeate e membrane (12). There are two electrodes (10) within the chamber. The chamber contains a substantially electrolyte-free liquid in contact with electrodes (10) and the membrane (12). The liquid contains a non-ionic excipient in order to prevent egress of water due to an osmotic gradient across the membrane (12) in use.

Abstract: Method and apparatus for continuous infusion to a subject of dispersions in which the dispersed phase is susceptible to flotation or sedimentation. The dispersion is controllably delivered from an upper or lower extremity of an essentially vertically positioned delivery vessel, e.g. syringe 2, and is then admixed with flushing medium, e.g. from infusion minibag 8, prior to administration to the subject. Vertical positioning of the delivery device maximises the distance through which flotation or sedimentation may occur, thereby substantially reducing the effects of separation over a given period of time compared to use of a corresponding horizontal delivery vessel such as a syringe placed in a conventional syringe driver.

Abstract: A physiological sensing device comprises, in combination a sensor (4) for the measurement of the partial pressure of carbon dioxide (pCO2), a body temperature sensor (5) and a heart rate and oxygen saturation sensor (54). The sensor device can be used to continuously monitor the vital signs of a patient.

Abstract: A physiological sensing device comprises an electrical sensor (4) for insertion into the tissue of a live animal and which measures the partial pressure of carbon dioxide in the animal tissue. The device also includes an electrical cable (6) connected electrically at its distal end to the sensor (4). The cable (6) is surrounded by a sheath (28). The sheath (28) has several flexible portions (30) separated by longitudinal slits (29). Movement of the proximal end of the sheath (28) towards its distal end shortens the distance between the ends of the flexible portions (30) and causes them to bow outwardly. The sensor (4) can be retained in animal tissue by the bowed flexible portions (30).

Abstract: A physiological sensing device for the measurement of pCO2 includes a closed chamber bounded, at least partially, by a carbon dioxide permeate e membrane (12). There are two electrodes (10) within the chamber. The chamber contains a substantially electrolyte-free liquid in contact with electrodes (10) and the membrane (12). The liquid contains a non-ionic excipient in order to prevent egress of water due to an osmotic gradient across the membrane (12) in use.

Abstract: A change in the surface properties of apparatus for pharmaceutical preparation results from steam sterilisation. This change may be avoided by the use of apparatus with more hydrophilic post-sterilisation surfaces, e.g. those of gold.

Abstract: Method and apparatus for continuous infusion to a subject of dispersions in which the dispersed phase is susceptible to flotation or sedimentation. The dispersion is controllably delivered from an upper or lower extremity of an essentially vertically positioned. delivery vessel, e.g. syringe 2, and is then admixed with flushing medium, e.g. from infusion minibag 8, prior to administration to the subject. Vertical positioning of the delivery device maximises the distance through which flotation or sedimentation may occur, thereby substantially reducing the effects of separation over a given period of time compared to use of a corresponding horizontal delivery vessel such as a syringe placed in a conventional syringe driver.

Abstract: The invention provides a process for the preparation of gas-containing vesicles wherein a mixture of gas, liquid and vesicle membrane forming material is passed through a zone in which it is subject to shear forces exerted by surfaces moving relative to each other at a speed of at least 20 m/s.

Abstract: A change in the surface properties of apparatus for pharmaceutical preparation results from steam sterilization. This change may be avoided by the use of apparatus with more hydrophilic post-sterilization surfaces, e.g. those of gold.

Abstract: An invention provides a process for the selection from a particulate pharmaceutical product of particles of a preselected size, said process comprising (i) obtaining a substantially homogeneous suspension of said particulate pharmaceutical product in a fluid suspension medium which is immiscible with said product and is of different density to said product, (ii) carrying out a size selection procedure to set an effective lower or upper size limit on the articles in the final particulate product, wherein step (ii) comprises either allowing said suspension to settle for a predetermined period, separating said suspension into a first and second component in a predetermined volume ratio, said first component deriving from an upper layer of said suspension and said second component deriving from a lower layer of said suspension, adding further suspension medium to said first component where said medium is more dense than the pharmaceutical product or to said second component where said medium is less dense than th