Prosonix is the world leader in use of ultrasonic pharmaceutical particle engineering technologies for the manufacture of high value pharmaceutical powders and Making Better Medicines. Our pipeline addresses the fast-growing market sectors of asthma, COPD and other respiratory disorders, as well as niche opportunities in orally and parentally delivered products. Prosonix proprietary technologies can be used for API manufacture at any scale.
Prosonitron™, DISCUS®, UMAX®, SAX™ and PRT based process technologies are proprietary “Solution-to-Particle” methods for controlling crystal size, shape and polymorph for APIs, aimed at Making Better Medicines. Technologies offer dose-to-dose uniformity, formulation consistency, stability and 200% performance increase of inhaled APIs compared to micronized. Combination particles of multiple APIs can be manufactured.
Power ultrasound facilitates controlled and reproducible crystal nucleation which is fundamental in controlling crystallization. Sonocrystallization delivers controlled nucleation and superior control of particle size, morphology, polymorphism, crystallinity and purity, and in doing so helps eliminate the need for troublesome external seeding and micronization for inhaled medicines.
Multipurpose laboratory equipment for sonocrystallization & sonochemistry are now available. These highly effective and flexible research tools facilitate 100ml – 100L operational capability in batch or continuous operation and can be integrated with automated laboratory reactors. The unique designs allow seamless transition and scale up to Prosonitron™ technology for commercial scale operation.
Prosonix provide cGMP & ATEX sonocrystallization Prosonitron™ ultrasonic process and reactor technology. They are aligned with emergent FDA “QbD” and “Design for Intent” philosophy. Our proprietary systems are of modular design for optimum flexibility and are an easy retro-fit to existing equipment. They are proven across scale in API production and can be seen as sustainable green technology.
| Prosonix Wins Poster Award at DDL-20 |
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| Written by Graham Ruecroft |
| Sunday, 13 December 2009 00:00 |
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Given the fact that the poster sessions at DDL-20 were peer reviewed, this success once again emphasizes that Prosonix is now truly participating at the highest level when it comes to respiratory drug delivery, and importantly, its manufacturing technologies - and most notably UMAX® which featured in the winning poster - are set to revolutionise the manufacture of structured pharmaceutical products for respiratory care, particularly asthma and Chronic Obstructive Pulmonary Disease (COPD). A warm thank-you and seasonal best wishes are extended to all participants at DDL-20, and particularly our clients present and anyone who viewed the poster. Prosonix thanks the organisers of DDL-20 for hosting a fantastic 20th anniversary symposium and hopes the next 20 years of inhalation therapy will be as rewarding as the last in establishing new technologies, medicines and understanding for combating respiratory disease. Please download a copy of the winning poster and for further information please contact Graham Ruecroft or David Hipkiss on +44(0)1865 784250 or Contact us http://www.ddl-conference.org.uk/index.php?q=home
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| Last Updated on Thursday, 18 March 2010 11:15 |
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| Prosonix has announced that it has entered into a multi-product co-development and licensing agreement with Trimel Biopharma (a subsidiary of Trimel Biopharma Holdings -Barbados) in order to collaborate in combining Prosonix' particle engineering technology and leadership with Trimel's award winning unit dose, single use, disposable dry powder inhaler technology. For further details please see the following and refer to the attached press release: |