Abstract
Using biodegradable polymeric nanoparticles as model systems for drug and gene delivery, this chapter describes commonly used methods for preparing and characterizing nanoparticles. This chapter focuses on emulsion solvent evaporation-based methods for encapsulating hydrophilic as well as lipophilic drugs in polymeric nanoparticles. In order to describe methods for preparing nanoparticles, we have chosen poly(lactide) (PLA)/poly(lactide-co-glycolide) (PLGA) as the carrier materials for nanoparticles intended for drug and gene delivery. Nanoparticles intended for drug and gene delivery can be characterized for various parameters including particle size, size distribution, morphology, zeta potential, drug loading, syringeability and injectability, in vitro drug release, and stability. Methods for the measurement of these parameters, which influence the performance characteristics of nanoparticles in vivo, are also discussed in this chapter.
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Acknowledgments
This work was supported in part by the NIH grant EY018940. The authors are thankful to lab members including Puneet Tyagi, Shelley Durazo, Ruchit Trivedi, and Dr. Jiban Jyoti Panda and past lab member Dr. Sarath Yandrapu for helpful discussions during the preparation of this chapter.
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Kulkarni, S.S., Kompella, U.B. (2013). Nanoparticles for Drug and Gene Delivery in Treating Diseases of the Eye. In: Gilger, B. (eds) Ocular Pharmacology and Toxicology. Methods in Pharmacology and Toxicology. Humana Press, Totowa, NJ. https://doi.org/10.1007/7653_2013_11
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DOI: https://doi.org/10.1007/7653_2013_11
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