Biomedical Engineering Reference
In-Depth Information
47. The volume of aliquot withdrawn depends on the drug solubility
and the analytical technique being used for quantification.
48. The time points selected should be such that they are able to
provide information about both initial burst release and com-
plete release of the drug from the nanoparticles.
49. To ensure there is no change in the overall volume of the release
medium in the centrifuge tubes over the length of the study,
aliquot withdrawn at any point of time must be replaced with
an equal volume of the same buffer. Moreover, the buffer
should be previously equilibrated to 37 C to maintain physio-
logical conditions. In cumulative drug release analysis, the
volumes removed should be corrected for.
50. If the nanoparticles do not pass through a 32G needle, 30G
needle can be used.
Acknowledgments
This work was supported in part by the NIH grant EY018940. The
authors are thankful to lab members including Puneet Tyagi, Shel-
ley 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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