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Pharmaceutical Manufacturing and Packing Sourcer

Solving Solubility

Nanoparticles and new technologies enhance the bioavailability of poorly soluble drugs, writes Yann Bayeux at Pierre Fabre Medicament

Around two thirds of the products used in the pharmaceutical industry are in solid form, such as tablets and pills. Consequently, a lot of effort has been put into research on particle generation processes. The standard processes – crushing/milling and crystallisation/precipitation – are still the most commonly used. However, supercritical fluid (SCF) technologies present a new and interesting route for particle formation, which avoids most of the drawbacks of the traditional methods. Supercritical processes give micro or even nanoparticles with a narrow size distribution. They can also be used in co-process with excipients or host molecules like cyclodextrins.

USING SUPERCRITICAL CO2

The supercritical state is also known as the fourth state of matter. Above a certain critical temperature and pressure (30.7°C and 73.8 bar respectively for CO2), the boundaries between gas and liquid disappear. Beyond this critical point, the substance has the viscosity of a gas and the density of a liquid. Supercritical CO2 (scCO2) is the most commonly-used system in nanoparticle generation. The main reason is linked to the intrinsic solvent properties of the supercritical CO2: the viscosity of a gas, the density of liquid and the fact that the critical state of CO2 can be easily reached. The treatment is generally carried out at about 40°C and it allows us to handle temperature-sensitive molecules. Furthermore, CO2 is cheap, non-toxic, noninflammable, easily available and can also be recycled. Supercritical carbon dioxide is considered as a ‘green’ solvent; after depressurisation, it leaves no residue, unlike an organic solvent.


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Yann Bayeux graduated from the University of Caen, France, and received his MD in Chemistry in 2002. He is also an Engineering graduate of Ensi-Caen High School. Yann started his career with Courtage Analyses Services (CAS), where he was in charge of the quality control laboratory. In 2003, he left CAS to join Pierre Fabre Medicament with responsibility for creating and developing custom manufacturing activities. Yann is now in charge of marketing, communication and sales operations, and provides services in synthetic chemistry
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Yann Bayeux
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Industry Events

4th Annual Patient Recruitment and Retention in Clinical Trials

13-15 October 2008, Amsterdam

Patient recruitment is now consuming thirty percent of clinical trial time - more time than any other clinical trial activity - and almost half of all trial delays result from patient recruitment problems. As the recruiting culture becomes more sophisticated and the forces affecting patient enrollment grow more numerous and complex, pharmaceutical companies are striving to discover new strategies to facilitate enrollment in clinical trials. With increasing industry pressure to develop, test and market greater numbers of new drugs faster, pharmaceutical companies need to perform clinical trials as quickly as possible. Inefficient patient recruitment processes is a formidable barrier to pharmaceutical companies' success in launching new products. Improving the patient recruitment process is imperative to avoid wasted investments and eliminate costly delays in bringing new drugs to market -- today and even more so in the not-so-distant future. Improved patient recruitment presents one of the largest opportunities for pharmaceutical companies to eliminate delays in clinical trials, thereby making it possible to reduce time to market.  With patent time limits and large overheads meaning that any delays in the development timeline can be disastrous, a good understanding of how to successfully recruit patients for trials is vital for any company looking to succeed.
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