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DOI: 10.3791/62685-v
Su Yin Chaw1,2, Tina Tzee Ling Wong3,4, Subbu Venkatraman2,5, Ann-Marie Chacko1
1Laboratory for Translational and Molecular Imaging, Cancer and Stem Cell Biology Programme,Duke-NUS Medical School, 2School of Materials Science and Engineering,Nanyang Technological University, 3Singapore National Eye Centre, 4Singapore Eye Research Institute, 5Material Science & Engineering,National University of Singapore
We present a protocol for the use of fiberoptic confocal laser microendoscopy (CLM) to non-invasively study the spatio-temporal distribution of liposomes in the eye after subconjunctival injection.
This protocol facilitates screening of new formulations to better understand how modifications affect their tissue residence times, which is critical in designing an optimal drug delivery system. This technique is noninvasive and allows realtime imaging, which reduces the excessive use of animals for sampling. Drug delivery systems can be redesigned for imaging and therapeutic applications by simply including the therapeutic drug and the imaging moiety in one nano-carrier.
This has useful applications in both treating cancer and infectious disease. Demonstrating the procedure will be Rasha Msallam, a senior research fellow from my laboratory. To begin with, two hours before subconjunctival injection, inject the mouse intravenously via tail with 2.5 milligrams per kilogram of Evans blue, or EB.After sedating the mouse with 5%isoflurane, transfer the mouse to a nose cone and maintain sedated mouse on a heating pad.
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