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Pharmaceutical Manufacturing and Packing Sourcer
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| 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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AMRI Announces Preferred Provider Agreement with BioPontis Alliance LLC
AMRI, a global contract services organization, announced today that it has entered into a preferred provider agreement with BioPontis Alliance LLC. The agreement is aimed at supporting BioPontis’ mission to bridge the gap between early-stage research and technologies being discovered and developed in academia and other research entities. AMRI will provide its services in small molecule discovery, development, and manufacturing in BioPontis’ drug discovery research programs. The agreement also supports the need for proof-of-concept data that is required in the current pharmaceutical company licensing environment. The goal of BioPontis Alliance is to identify promising early stage product opportunities and utilize a preferred network of CROs and leading research companies to apply appropriate expertise to develop these opportunities enough to attract pharmaceutical company licensing partners.
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