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Nanoparticle Formation

Nanoparticle Formation

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Pharmaceutical R&D scientists use combinatorial chemistry and modeling to mimic natural mediators. These hydrophobic substances are synthesized locally, avoiding absorption and distribution issues. To address solubility challenges, formulators employ various drug delivery systems like solid dispersions, microemulsions, liposomes, and nanostructured particles.
Nanoparticle Formation

Publication

Pharmaceutical research and development scientists have applied combinatorial chemistry and molecular modeling techniques to develop drug compounds with properties more closely resembling natural mediators in the body. Many of these natural mediators are hydrophobic substances and are synthesized at or near the site of action; thus they do not need to overcome the absorption, distribution, metabolism, and excretion issues associated with administered drugs. To overcome the challenges of absorption and distribution resulting from hydrophobicity and poor solubility, formulators have developed drug delivery systems such as solid dispersions, microemulsions, self-emulsifying systems, complexation, liposomes, and nanostructured particles created using particle-size reduction and particle-formation techniques.

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