“…This may originate from the lower potential to form interaction between PAAM hydrogel and the luteinizing hormone, and the higher diffusability of the drug through the abdominal hairless rat skin; thus a larger diffusion coefficient was obtained. In general, we may conclude that the diffusion coefficient of a drug in transdermal delivery system depends on several factors: the chemical composition of the drug, the molecular weight of the drug, and the size of the drug, the polymer matrix, the drug-matrix interaction, and the experimental set-up, as shown in Table 2 (Attwood et al, 1981;Chen & Chien, 1996;Valento et al, 2000;Ferreira et al, 2001;Vankov, 2004), and a further studied is needed.…”