Emd Millipore Corporation

Millipore Corporation

Millipore Investment Holdings, Ltd.

Ronald Tuccelli

Sebastien Cirou

Virginie Buisson

Jim E Kelly

Christopher Gillespie

Christine Abouayad El Idrissi

Melissa Holstein

John Caulmare

Salvatore Giglia

Gabriel Tkacik

Michael Joens

Luc Messier

Jibin Hao

Paul V McGrath

Roger Hill

Willem Franciscus Catherina Kools

Kristen Cotoni

Sébastien Cirou

Christine Abouayad El Idirissi

Methods of maintaining narrow residence time distributions in continuous flow systems, particularly applicable to virus inactivation such as during a protein purification process. Fluid sample is introduced into an axial flow channel and caused to flow therein in discrete packets or zones to minimize residence time distribution and axial dispersion. Embodiments described herein obviate or minimize the need for using large tanks or reservoirs for performing virus inactivation during a protein purification process; reduce the overall time required for virus inactivation, and/or reduce the overall physical space required to perform the virus inactivation operation during a protein purification process, which in turn reduces the overall footprint for the purification process.

Mechanical method of maintaining narrow residence time distributions in continuous flow systems

Method of maintaining narrow residence time distributions in continuous flow systems

The invention concerns a circuit comprising a bag () comprising two flexible films () and a press () comprising a first () and a second () shell clamping the bag to form pipes having a passage and edges (41); the first shell comprising a valve () which comprises a movable member () and a pad (), which pad has a resting configuration in which a second face () of the pad is concave and locally delimits a channel () and a pinching configuration in which the second face () is convex; said movable member and said pad being configured so that, when said valve is in closed position and said pad in pinching configuration, said passage is pinched by said movable member against said second shell channel and said edges () are pinched flat by said movable member against said second shell ().

Circuit for biological liquid comprising a pinch valve

The invention concerns a device comprising a circuit comprising a bag () comprising two flexible films (), a press () comprising a first shell () disposed upright on a front face of a base of the device and a second shell () mounted on said first shell, which shells clamp said bag to form conduits (); said press is provided with a system () for jamming at the location of a treatment zone () of the bag, which comprises a jamming member () provided with at least one jamming nipple () and a complementary jamming member () provided with a jamming channel () configured to receive said nipple; said jamming member () and complementary jamming member () and said bag () being configured in order for the latter to have a portion () in said treatment zone in which said films are jammed between said nipple and said channel.

Device for a biological liquid treatment installation

The invention relates to accelerated mixed gas integrity testing methods, devices, and systems for integrity testing wetted single and multi-layered porous materials, whereby the testing method is non-destructive to the porous materials being tested. The accelerated mixed gas integrity test method includes one or more of the following components: i) a permeate side gas purge component; ii) a permeate side volume reduction component; and iii) a permeate side circulation component. The invention is directed towards reducing the length of time necessary to complete the integrity testing of single and multi layered porous materials, elements and membranes.

Accelerated mixed gas integrity testing of porous materials

This invention provides for a method to control the pore size or bubble point of porous membranes made by phase inversion in a continuous manufacturing process by blending two or more solutions each capable of producing a porous membrane with different pore size or bubble point than the pore size or bubble point of the desired membrane, and blending these solutions by the method of this invention to produce the desired pore size or bubble point. This invention also provides for a method to monitor membrane pore size in a continuous process and adjust pore size during the continuous manufacturing process.

Method and system for controlling pore size of microporous phase inversion membranes

A cellulosic ultrafiltration membrane is provided having a microporous base resistant substrate and an ultrafiltration layer form of a cellulose ester or cellulose.

Cellulosic ultrafiltration membrane

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Winchester, MA, United States of America

Ronald Tuccelli