A flow cell for a dissolution test apparatus, Includes a cell mount, a filter head, a cylindrical cell casing connected with the cell mount and with the filter head via threads provided on respective ends of the cylindrical cell casing, and a sample cell received in the cell casing and co figured for receiving a sample.

A system for mixing solutions includes: a first container and at least one second container capable of containing solutions, each second container being capable of entirely containing the first container; means for displacing the first container and/or each second container capable of entirely immersing the first container in each second container; and rotational drive means for the first container so as to mix the solutions present in the first and second containers when the first container is entirely immersed in the solution present in the second container.

An apparatus (1) for dissolution testing comprises a tank (2) having a circular cylindrical outer body portion (21) with a transparent side wall and a circular cylindrical inner body portion (22) with a transparent side wall, wherein the inner body portion (22) is coaxially arranged with respect to the outer body portion (21) such that an outer interior (23) having a ring-shaped cross section is defined between the outer body portion (21) and the inner body portion (22) and an inner interior (24) having a circular cross section is defined inside the inner body portion. The apparatus (1) further comprises a plurality of dissolution vessels (4) arranged in the outer interior (23) of the tank and a heater assembly being arranged to heat a test media in the vessels (4) to a predefined temperature. The apparatus (1) according to the invention allows for a comparably precise monitoring of vessels (4) inside the tank (2) and/or an appropriate manipulation of the vessels (4) inside the tank (2).

An in vitro release testing method and system for testing the ability of formulations to deliver agents across a barrier membrane is disclosed. The method may comprise steps of providing a dosage of a semi-solid formulation containing the bioactive agent, a receptor solution, and a barrier membrane to separate the semi-solid formulation and the receptor solution. The receptor solution may be a biphasic solution or an immiscible solution. The semi-solid formulation may be contacted with one side of the barrier membrane and the receptor solution with the other side of the barrier membrane for a time sufficient to produce penetration of the barrier membrane by the semi-solid formulation. The receptor solution may be sampled and assayed to determine the concentration of the bioactive agent in the receptor solution.

The invention relates to a method for determining in vitro release rate of at least one active principle ingredient from at least one semisolid form.

An apparatus for monitoring the effective dissolving of a polymer when the use region is not accessible. The apparatus includes a pipe on which are inserted, consecutively: a pump, a flowmeter, a water or brine inlet mechanism for diluting the mother solution flowing in the pipe, a mixer capable of in-line homogenization of the diluted mother solution, a first tube calibrated to simulate the distance and the conditions for moving the diluted solution in the main pipe between the point where the mother solution is diluted and the use region, a mechanism capable of reducing the pressure of the diluted solution flowing in the pipe upstream of the first tube that is calibrated from 10 to 10000 kPa (from 0.1 to 100 bar), a second calibrated tube for creating a head loss, and a device for measuring differential pressure between the inlet and the outlet of the second calibrated tube.

This disclosure describes the results of the studies conducted to develop a dissolution method to monitor release profiles of hydrophobic active pharmaceutical ingredients such as ivermectin with or without pyrantel pamoate from a drug product made of complex matrix that includes, but is not limited to beef, tallow, corn cob and soy protein.

The invention concerns a method and system for determining dissolution properties of a particle. The method comprises providing into a vessel dissolution medium capable of dissolving the particle and providing the particle into said vessel in contact with the dissolution medium for dissolving the particle. According to the invention, the particle is trapped in a particle trapping zone formed at a predetermined location in the vessel, the particle trapping zone being formed preferably at least partially by continuous hydrodynamic motion of the dissolution medium. Residue of the particle is imaged while being trapped in said particle trapping zone for providing a plurality of sequential images of the particle residue. Finally, at least one dissolution property of the particle is determined based on the sequential images. The invention allows for dissolution rate, intrinsic dissolution rate and/or solubility of matter to be reliably determined from very small sample amounts and without manual affixation of samples.

An artificial gut simulator and methods are shown. In one example, the artificial gut simulator and methods provide accurate dissolution data by removing detected test sample material from the tester over time.

An analysis method and device including detecting at least one particle of matter in a fluid inside in a reaction chamber and correlating a change in the particle to a physicochemical property of the matter.