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Copyright ©2013 Baishideng.
World J Pharmacol. Mar 9, 2013; 2(1): 1-17
Published online Mar 9, 2013. doi: 10.5497/wjp.v2.i1.1
Figure 1
Figure 1 Structure of the eye. Credit: National Eye Institute, National Institutes of Health.
Figure 2
Figure 2 Routes of ocular drug delivery.
Figure 3
Figure 3 Disposition of drugs in the eye.
Figure 4
Figure 4 Role of efflux and influx transporters in ocular absorption.
Figure 5
Figure 5 hSMVT cDNA was generated by reverse transcription polymerase chain reaction amplification of total RNA from ARPE-19 cells (lane 2). Aliquots of polymerase chain reaction products were analyzed by gel electrophoresis on 0.8% agarose. Ethidium bromide staining of the gel showed a approximately 862 bp band corresponding. Reproduced with permission from[176].
Figure 6
Figure 6 Quantitative uptake of doxorubicin in Y-79 cells using doxorubicin, doxorubicin-loaded in polymeric micelles, folate conjugated polymeric micelles and folate conjugated polymeric micelles in presence of folic acid. aP < 0.05. Reproduced with permission from[186].
Figure 7
Figure 7 Cell viability studies of doxorubicin in ARPE-19 cells following treatment with doxorubicin and folate conjugated polymeric micelles. Reproduced with permission from[186].
Figure 8
Figure 8 Reverse transcription polymerase chain reaction analysis of folate receptor-α, reduce folate carrier, proton coupled folate transporter. GAPDH: Glyceraldehyde 3-phosphate dehydrogenase. Reproduced with permission from[180]. FR: Folate receptors; RFC: Reduced folate carrier; PCFT: Proton-coupled folate transporter.
Figure 9
Figure 9 Western blotting analysis of folate receptor-α and proton coupled folate transporter. Reproduced with permission from[180]. FR: Folate receptors; PCFT: Proton-coupled folate transporter.