Drug Formulation and Delivery Services
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| Encapsulation Method | Size Range (μm) | Format |
| Single- and twin-screw extrusion | 1,000+ | Implant |
| Submerged nozzle | 700 6,000 | Microcapsule |
| Centrifugal extrusion | 125 3,000 | Microcapsule or microsphere |
| Rotating disk | 35 1,000 | Microcapsule or microsphere |
| Spray drying | 5 150 | Glass, microcapsule, or microsphere |
| Suspension coating | 100 10,000 | Microcapsule, coated implants |
| Interfacial polymerization | 1 500 | Microcapsule |
| Phase separation/coacervation | 1 500 | Microcapsule |
| Solvent evaporation | 0.1 5,000 | Nano- or microsphere or capsule |
| Nanoprecipitation (pat.pend.) | 0.2 0.9 | Drug particle or nanocapsule |
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SwRI scientists have created stable taste-masked enteric-coated and sustained release oral formulations for Institute clients, such as this transparent nanosuspension. |
Using the SwRI-NASDEL capsule-gel mucosal delivery technology, medical personnel can deliver cytotoxic compounds to the patient without irritating or upsetting the nasal epithelium. |
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The Institute can test particle formulations with analytical capabilities including:
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Scientists utilize the SwRI-developed rotating disc process to encapsulate liquids and solids, forming microcapsules or microspheres. |
The Institute has developed a variety of materials for controlled delivery of therapeutic aids, such as this implantable coated fiber (left). Releaserate is modulated by the drugs physical properties or the implant material or porosity, providing release durations of up to six months. |
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SwRI has experience with a wide range of techniques for drug delivery, including the following:
Oral Using a variety of methods, SwRI scientists create stable taste-masked, enteric-coated and sustained release oral formulations that conform to current Good Manufacturing Practices (cGMP) standards. Using its cGMP suites, Institute scientists can prepare the micro- or nanoparticles for filling into hard gelatin capsules or compression into tablets.
Ocular SwRI-developed controlled-release microand nano-particles and implants allow drug delivery in the vitreous, conjunctiva, and anterior portions of the eye.
Nasal and Mucosal The Institute has developed a controlled-release nasal delivery technology (SwRINASDEL ) that does not irritate the nasal mucosa.
Subcutaneous (implant or depot) SwRI has developed controlled-release formulations in the form of depot and subcutaneous implants ranging from a fraction of a millimeter to several millimeters. Release rate and duration vary, according to client requirements.
Topical SwRI has experience in developing creams, ointments, and gels for a variety of compounds, including nano-particle-containing gels for cellular delivery of interfering RNA.
Intravenous and intramuscular (IV and IM) SwRI has developed traditional isotonic mixture IV and IM formulations, as well as nanosuspensions not immediately cleared by the reticular endothelial system for controlled release formulations.
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Scientists developed innovative techniques for surfactant -free nanoprecipitation. |
Institute scientists develop a variety of formulations capable of delivering therapeutic drugs via ocular pathways. Transparent nanosuspensions of coated particles or pure drug can be applied to the vitreous humor without disturbing the field of vision. |
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This brochure was originally published in February 2007. For more information about
Drug Formulation and Delivery Services, contact
Dr. Joseph McDonough, Synthesis and Drug Delivery Section, Chemistry
and Chemical Engineering Division, Southwest Research Institute, P.O. Drawer 28510,
San Antonio, Texas 78228-0510, Phone (210) 522-3670, Fax (210) 522-4632.
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