Examples of 'drug particles' in a sentence
Meaning of "drug particles"
The phrase 'drug particles' refers to tiny constituent particles or molecules of pharmaceutical drugs. These particles are crucial in drug delivery systems, as they determine how the drug interacts with the body and its effectiveness. Understanding the behavior and characteristics of drug particles is essential for developing effective medications
How to use "drug particles" in a sentence
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drug particles
Sterilization of glucocorticoid drug particles for pulmonary delivery.
Small drug particles are likely to agglomerate.
The substrate can be pellets or tablets or drug particles.
Small drug particles tend to agglomerate.
A still further subject are the coated drug particles.
Certain drug particles have a bitter or otherwise unpleasant taste.
Upon reconstitution in water the drug particles dissolved completely.
The drug particles are provided on the surface of the balloon.
Methods of producing monodisperse drug particles are known in the art.
Said drug particles also show good flow properties.
Lactose particles appear to be of a size similar to that of drug particles.
These small drug particles will have a tendency to agglomerate.
The coating layer preferably further contains drug particles.
The drug particles may be in a crystalline phase or in an amorphous phase.
It is also important to control the properties of the drug particles.
See also
No solid drug particles are evident on visual or light microscopic examination.
Another method of application of the drug particles is to use electrostatic attraction.
Solid drug particles are evident on visual and light microscopic examination.
Granules generally comprise drug particles and require further processing.
The resulting lipid suspension is free from precipitated drug particles.
A spray gun nozzle deposits drug particles on the rotating stent.
Drug particles are sprayed through a nozzle connected with an air flow inlet.
Micronization is the process by which solid drug particles are reduced in size.
The encapsulated drug particles are bound to particles of a thickening agent by means of a binder.
This positioning can reduce the deposition of drug particles on the sensor.
Using smaller drug particles tended to yield more fines in the granules.
This results in an improved wettability of hydrophobic drug particles through polar interactions.
Examples of the drug particles include particles of the active ingredients exemplified above.
This peak includes both the surfactant aggregates and drug particles.
This is significant as smaller drug particles result in greater bioavailability of the drug.
Similar shortcomings have been encountered using liposomal formulations to coat drug particles.
One embodiment utilizes microencapsulated drug particles retained within a permeable barrier.
This process results in an increase in the size distribution of the drug particles.
It can broaden the surface área of drug particles by reducing their size.
Drug particles that are not microencapsulated are preferable from the standpoint of rapid dissolution.
Changes in the surface nature of the drug particles results in a change in product performance.
After drug release the surface is more porous because of disappearance of drug particles.
It will be appreciated that the drug particles are subsequently carried into the lung.
These carrier particles are very much larger than the drug particles in size.
Conventionally these finely divided drug particles are made by techniques such as micronization or grinding.
The solid form may also include an excipient as part of the drug particles themselves.
The particles of the invention are drug particles suitable for use in inhalation therapy.
This process provides more passive sites for adhesion of the micronized drug particles.
Individual loratadine drug particles should be prevalent throughout the dispersion at this point.
Such powders may contain aggregated nanoparticulate drug particles having a surface modifier.
Microencapsulated drugs are drug particles or droplets which have been coated with a protective coating material.
Schematic depiction of a balloon surface coated with nanocrystalline drug particles and tracer particles.
Preferably the drug particles are spray-dried.
The solubility of the drug falls to the point where solid drug particles are formed.
Preferably, the drug particles are a solid at normal temperatures.
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Particles thus entangled will behave identically
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