6). Release profiles were characterized by lack http://www.selleckchem.com/products/chir-99021-ct99021-hcl.html of burst effect and relatively low release rate indicating efficient dye entrapment. Approximately 14.5%, 15.8%, and 17.2% of the dye was released at 6 h from NPs prepared using PLGA with copolymer ratio of 100:0 (F4), 75:25 (F5), and 50:50 (F6), respectively. FITC NPs with positive and negative zeta potential at 10% w/w loading (F10 and F12, respectively) were used. Exposure of skin samples to negatively charged NPs resulted in greater skin permeation of FITC despite the larger NPs size (367.0 versus 122.0 nm for F10 and F12, respectively, Fig. 7 and Table 1). The mean Q48 and flux values for F12

NPs were 0.24 ± 0.08 μg/cm2 and 0.35 ± 0.11 μg/cm2/h, respectively ( Table 2). These corresponded to mean Q48 and flux values of 0.09 ± 0.01 μg/cm2 and 0.12 ± 0.02 μg/cm2/h ALK inhibitor for the positively charged FITC NPs (F10), respectively. Differences

between Q48 and flux values for F10 and F12 were statistically significant (P < 0.05). Fig. 8 shows permeation profiles for Rh B and FITC encapsulated in 50:50 PLGA NPs at 10% w/w loading (F7 and F10, respectively, Table 1). Both formulations had similar particulate properties in terms of size (117.4 and 122.0 nm, respectively) and zeta potential (57 mV). Poorer permeation of FITC was observed with a significantly longer lag period (∼30 h) compared to Rh B NPs (∼6 h), suggesting a different permeation mechanism. A statistically significant 33.2-fold

and 35.8-fold difference in Q48 and flux values, respectively, was observed for Rh B compared to FITC. The Q48 and flux values for Rh B were 2.99 ± 0.26 μg/cm2 and 4.29 ± 0.42 μg/cm2/h, respectively. Significantly lower values (P < 0.05) for Q48 (0.09 ± 0.01 μg/cm2) and flux (0.12 ± 0.02 μg/cm2/h) were obtained for FITC. CLSM images of MN-treated porcine skin exposed to these two NP formulations (F7 and F10) for 48 h were obtained for both vertical sections (surface view of mechanically sectioned skin) and Z-stacks to determine the depth of dye permeation ( Fig. 9a–d). Rh B and FITC NPs applied to the MN-treated skin surface infiltrated the microchannels because as evidenced by the red and green intense fluorescence in Fig. 9a and b, respectively, with deeper penetration of Rh B. Individual NPs could not be visualized as their size was below the resolution limit of the confocal microscope [32] and [33]. This is in addition to deterioration of the resolution in real-case scenarios when imaging biological specimens, skin in this case, in which the light suffers several effects such as scattering [34]. While Rh B diffused laterally as indicated by red fluorescence around microchannels and in deeper skin layers ( Fig. 9a), FITC fluorescence was mainly restricted to microchannels ( Fig. 9b). Penetration depth profiles (Z-stacks, Fig.