Enhanced permeation retention effect

Ultrafiltration of heterogenous colloidal suspensions such as citrus juice is complex and many factors other than molecular weight contribute to fouling and permeation. For example, low MW aroma compounds were unevenly distributed in the permeate and retentate in UF in 500 kd MWCO system (10). The authors observed that the 500 kd MWCO UF removed all suspended solids, including pectin and PE. If PE is complexed to pectate in an inactive complex, then it is conceivable that release of PE from pectin with cations will enhance permeation in UF. At optimum salt concentration, less PE activation was observed at lower pH values than at higher pH (15). In juice systems, it is difficult to separate the effect of juice particulates on PE activity. Model studies with PE extracts allows UF in the absence of large or insoluble particulates and control of composition of the ultrafilter. In... 

By utilizing polymerization in the miniemulsion system, larger HPG analogues can be created by linking several HPG units to a nanoparticle in order to obtain an optimum diameter of 50 nm [116], This size range is considered to be ideal for drug delivery carriers that may accumulate in tumors or inflamed tissue by the enhanced permeation and retention effect (EPR) [52],... 

Deposition of polyelectrolytes Lajimi et al. [56] explored the surface modification of nanofiltration cellulose acetate (CA) membranes by alternating layer-by-layer deposition of acidic chitosan (CHI) and sodium alginate (AEG) as the cationic and anionic polyelectrolyte, respectively. The supporting CA membranes were obtained by a phase separation process from acetone/formamide. The permeation rate of salted solutions was found to be higher than that of pure water. The rejection of monovalent salt was decreased, while that of divalent salt remained constant so that the retention ratio increased. Increasing the concentration of feed solutions enhanced this selectivity effect. 

Dermac SR-38 is one of a series of oxazolidinones, cyclic urethane compounds, evaluated as transdermal enhancers. The compound was designed to mimic natural skin lipids (such as ceramides), to be nonirritating, and to be rapidly cleared from the systemic circulation following absorption. In animal and human safety studies, Dermac SR-38 demonstrated a good skin tolerance (no observed irritancy or sensitization at levels of 1-10 wt% moderate to severe irritation in rabbit at 100%), and a low degree of acute toxicity (LD50(rat oral) > 5.0g/kg). The compound was evaluated for its ability to enhance the human skin permeation of diverse drugs from dermal and transdermal delivery systems. Data for minoxidil indicated an enhancer concentration-dependent effect for permeation enhancement. Dermac SR-38 was also found to enhance the skin retention of both retinoic acid when applied in Retin A cream, and dihydroxyacetone when applied in a hydrophilic cream. ... 

This is unfortunate because the theoretical advantage of nanosystems is their small size, allowing freer movement than microspheres in the circulation, including the lymph and in tissues. Flow rates are important not least in the determination of the possibility of nanoparticle interaction with endothelial receptors prior to internalization, or indeed in the decoupling of carriers and receptors due to shear forces. Flow of nanoparticles is a vital element in extravasation and in the enhanced permeation and retention (EPR) effect. What is the influence of nanoparticle size on particle flow in the circulation And, with the advent of CNTs in particular, what is the influence of shape on flow and fate CNTs certainly behave differently in the blood from spherical C60 fidlerenes. CNTs activate human platelets and induce them to aggregate, whereas their spherical analogues do not... 

Decreased lymphatic drainage keeps the carriers in the tumor. This passive targeting mechanism has been called the enhanced permeation and retention (EPR) effect and was first identified by Maeda et al. [98,99]. Numerous studies have shown that the EPR effect results in passive accumulation of macromolecules and nanosized particulates (e.g., polymer conjugates, polymeric micelles, dendrimers, and liposomes) in solid tumor tissues, increasing the therapeutic index while decreasing side effects. Figure 4 describes the concept of passive tumor targeting by EPR effects. 

Then it appeared that conjugation of drugs with a polymer or macromolecule enhanced its passive distribution in favour to tumour tissue. This enhanced permeation and retention (EPR) effect was explained by differences... 

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