Ion pairing between drug and carrier can be influenced by the ionic strength of release medium. Li et al. [10] examined the effects of release medium on DS release from PLNPs. In their study, verapamil hydrochloride (VRP) was added into PLNPs to form a complex with DS, and the VRP-DS complex interacted with PLNPs. It was anticipated that counter ions in the release medium may interact with the sulfate groups on DS and alter DS-VRP complexes, affecting DS release kinetics of PLNPs. Indeed, when the ionic strength of the release medium increased from 0 to 0.15M NaCl, the release rates Inhibitors,research,lifescience,medical of DS increased significantly (Figure 4(c)). Our simulations show that ΔG increases

from −5.1 × 10−21J in DDI water to 0.64 Inhibitors,research,lifescience,medical × 10−21J in 0.5mM NaCl and to 4.9 × 10−21J in 0.015M NaCl and 3.36 × 10−21J in 0.15M NaCl. The rate constant of dissociation also steadily increases from 0.005/hr in DDI water to 0.023/hr

in 0.15M NaCl. In contrast, no significant changes in kS are observed. Therefore, the model the site suggests that the ionic strength of the release medium strongly affects the DS-VRP-PLNP association and disassociation, but not the DS diffusivity in PLNP. The chemical composition of NPs is another important determinant of release kinetics. Mittal et al. [12] analyzed the composition Dovitinib FLT3 inhibitor influence on estradiol release from PLGA NPs. In general, release may be mediated through both drug Inhibitors,research,lifescience,medical diffusion and matrix degradation. When high molecular weight PLGA was used to prepare NPs, however, release was largely mediated through the diffusion process. Inhibitors,research,lifescience,medical Furthermore, increasing lactide content reduced release rate (Figure 4(d)). When the PLA/PGA ratio increases from 50:50 to 65:35 and to 85:15, ΔG decreases from −1.7 to −2.4 and to −3.9 × 10−21J, explaining the decreasing magnitude of initial burst release. Negative ΔG in all cases suggests a strong interaction between estradiol

and PLGA, responsible for sustained release. In addition, Inhibitors,research,lifescience,medical a reduction in koff (from 0.02 to 0.004 and 0.007day−1) is consistent with the observed decrease in steady release. Particle size also strongly influences drug release through mediating both diffusion and matrix degradation. As shown in Figure 4(e), it takes 3 and 18 days to release 50% savoxepine from PLA NPs of 303nm and 671nm in size, respectively [13]. In (1), which describes the diffusion and convection process, kS is proportional Anacetrapib to the surface-to-volume ratio (A/V 1/r), if the rate constant k1 is independent of particle size r. Therefore, if release is dominated by the diffusion/convection process, doubling particle size will double the time for releasing drug at the same percentage. Thus, the diffusion process alone cannot explain the size effects observed in savoxepine release from PLA NPs. The simulation reveals a comparable kS (1.44 versus 1.79day−1) in both cases. In contrast, a large difference in ΔG (−0.61 versus −5.52 × 10−21J) suggests a stronger interaction between savoxepine and larger PLA NPs.