Abstract: Described herein is a composition comprising a particle comprising a biodegradable and hydrolysable polymer, wherein a medicament for the treatment of a disease of the urinary tract is dispersed in the polymer, wherein the particle has a dimension of from 1 ?m to 30 ?m. Also described herein is a composition for the treatment of a disease, the composition comprising a particle comprising a biodegradable and hydrolysable polymer, wherein a medicament is dispersed in the polymer, wherein the particle has a dimension of from 1 ?m to 30 ?m, wherein the composition is for use in a method for treating the disease and the method involves the intracellular delivery of the particle or the medicament from the particle.

Abstract: A method of distributing microparticles is provided, the method comprising: providing a plurality of microparticles at an insertion site in a medium; applying ultrasound to the insertion site that generates gas bubbles by cavitation at cavitation nuclei located at the insertion site and drives movement of the gas bubbles such that the gas bubbles drive movement of the microparticles into a desired spatial distribution in the tumour. The method may be a method of treating a tumour, and the microparticles may comprise a radioisotope for treating the tumour. Microparticles for use in the treatment of a tumour by the method are also disclosed.

Abstract: Described herein is a composition comprising a particle comprising a biodegradable and hydrolysable polymer, wherein a medicament for the treatment of a disease of the urinary tract is dispersed in the polymer, wherein the particle has a dimension of from 1 ?m to 30 ?m. Also described herein is a composition for the treatment of a disease, the composition comprising a particle comprising a biodegradable and hydrolysable polymer, wherein a medicament is dispersed in the polymer, wherein the particle has a dimension of from 1 ?m to 30 ?m, wherein the composition is for use in a method for treating the disease and the method involves the intracellular delivery of the particle or the medicament from the particle.

Abstract: The invention provides a method of preparing a suspension of microbubbles for use in a carrier liquid, wherein the microbubbles have a gas core and a liquid shell, said liquid shell comprising magnetic nanoparticles, and wherein the microbubbles satisfy the following conditions: (i) the force due to buoyancy (FBW) of the microbubble in the carrier liquid is greater than the weight (W) of the microbubble; (ii) the magnetic force (FM) on the microbubble due to a magnetic field applied to the carrier liquid is greater than the combined weight (W) and force due to buoyancy (FBW) of the microbubble; (iii) said magnetic force (FM) on the microbubble is greater than the force due to viscous drag (FD) on the microbubble due to flow of the carrier liquid; and (iv) the scattering cross section (?scat) of the microbubble to ultrasound allows the microbubble to be detectable and rupturable on exposure to ultrasound.

Abstract: The invention provides a method of preparing a suspension of microbubbles for use in a carrier liquid, wherein the microbubbles have a gas core and a liquid shell, said liquid shell comprising magnetic nanoparticles, and wherein the microbubbles satisfy the following conditions: (i) the force due to buoyancy (FBW) of the microbubble in the carrier liquid is greater than the weight (W) of the microbubble; (ii) the magnetic force (FM) on the microbubble due to a magnetic field applied to the carrier liquid is greater than the combined weight (W) and force due to buoyancy (FBW) of the microbubble; (iii) said magnetic force (FM) on the microbubble is greater than the force due to viscous drag (FD) on the microbubble due to flow of the carrier liquid; and (iv) the scattering cross section (?scat) of the microbubble to ultrasound allows the microbubble to be detectable and rupturable on exposure to ultrasound.