SoluBest has developed a proprietary nanotechnology platform (Solumer TM)
for significantly improving the bioperformance of poorly soluble and
insoluble. The versatile solubilization technology is widely applicable to
numerous off-patent (or soon to be off-patent) drugs and NCEs. Rapid
screening times allow the identification of suitable candidates in a few
short weeks. Feasibility studies to clinical batch preparation can proceed
in under 6 months. A significant advantage of the technology stems from
its use of readily available equipment for a process consisting of a few
simple steps, making scale-up safe, robust, rapid, and inexpensive. The
company’s strategy focuses on the development of novel drug
formulations that can be performed in collaboration with API
manufacturers, generic and brand pharmaceutical companies, biotechs,
and drug delivery firms. For more information, visit SoluBest at
www.solubest.com.
Pharmaburst TM is the first and ONLY patented off-the-shelf co-processed
excipient system for fast-dissolving ODT applications in the
pharmaceutical market. It is now being used in a wide variety of new and
generic drug applications by many leading multi-nationals and several top
generic companies. Pharmaburst is the only ODT platform included in the
USFDA’s Inactive Ingredient Guide (IIG List). Since its inception, several
grades of Pharmaburst have been introduced to meet specific formulation
needs. A brand new version with superior performance and cost
effectiveness will be launched. Oral dispersible drugs containing
Pharmaburst have been successfully launched in regulated and
developing markets around the world for indications such as migraine,
allergy, analgesics, anxiety, oncology, schizophrenia, depression,
Parkinson's, etc. SPI Pharma has a fully integrated drug development
program that utilizes its functionally superior excipients, proprietary
delivery platforms, and enhanced APIs. For more information, visit SPI
Pharma at www.spipharma.com.
Drug Delivery Technology June 2009 Vol 9 No 6
Xcelience is the premier source for unsurpassed quality in drug
development services. The company brings together the industry's most
experienced and talented scientists, consistently and efficiently moving
compounds through the research and development continuum to
regulatory approval. Since 1997, the Tampa-based laboratory has been
developing formulations for clients throughout the pharmaceutical
industry. Xcelience's unique corporate structure creates project teams
that work intensively with each client, bringing an extension of their own
organization into the Xcelience lab. The lab uses only state-of-the-art
equipment, highlighted by the patented Xcelodose®, which fills API
directly to capsules (Xcelodose is a registered trademark of Capsugel
BVBA). This and other technologies give Xcelience unparalleled speed to
market without compromising its absolute commitment to quality. For
more information, contact Xcelience at (608) 643-4444 or visit
www.xcelience.com.
Gateway BioPharma’s solubilization platform offers a compelling
approach to overcome solubility challenges, accelerate drug
development, and improve patient outcomes. Our platform will
advance the way a wide array of compounds are manufactured and
administered to patients. At the core is a suite of novel particle
engineering technologies that produce superior nanostructured
particles with high surface area, providing rapid dissolution, improved
physical stability, and exceptional bioavailability when compared to
conventional formulation technologies. We take a portfolio approach
to solving solubilization issues, based on well-characterized and
scalable controlled particle growth technologies, regardless of the
delivery objectives for a particular drug. Both Controlled Precipitation
and Ultra-Rapid Freezing are used in order to optimize compound
solubility and long-term stability. For more information, contact
Gateway BioPharma at (512) 891-1216 or visit
www.gatewaybio.com.