Figures and Tables

From the following article:

Carrier-mediated cellular uptake of pharmaceutical drugs: an exception or the rule?

Paul D. Dobson & Douglas B. Kell

Nature Reviews Drug Discovery 7, 205-220 (March 2008)

doi:10.1038/nrd2438

Figure 2 - Carrier-mediated cellular uptake of pharmaceutical drugs: an exception or the rule?

Figure 2

Comparisons between drug permeability in natural membranes and artificial systems, and their comparison with oil–water partition coefficients.

Figure 3 - Carrier-mediated cellular uptake of pharmaceutical drugs: an exception or the rule?

Figure 3

Comparisons between drug permeability in natural membranes and artificial systems, and their comparison with oil–water partition coefficients.

Figure 4 - Carrier-mediated cellular uptake of pharmaceutical drugs: an exception or the rule?

Figure 4

Multiple drug carriers in different tissues, all of which may need to be permeated.

Figure 5 - Carrier-mediated cellular uptake of pharmaceutical drugs: an exception or the rule?

Figure 5

Tissue-selective expression of solute carrier molecules, where brown colouration indicates presence of protein.

Table 1 - Carrier-mediated cellular uptake of pharmaceutical drugs: an exception or the rule?

Table 1

Some searchable databases for transporter molecules*

Table 2 - Carrier-mediated cellular uptake of pharmaceutical drugs: an exception or the rule?

Table 2

Overview of the human transporter superfamilies and families with possible/known roles in drug uptake

Table 3 - Carrier-mediated cellular uptake of pharmaceutical drugs: an exception or the rule?

Table 3

Examples of drug uptake by three of the most significant families of transporter

Table 4 - Carrier-mediated cellular uptake of pharmaceutical drugs: an exception or the rule?

Table 4

Some common drug substrates of the most prolific SLC transporter families*