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Therapeutic Delivery of CO

Adjei, H. (1997). Inhalation Delivery of Therapeutic Peptides and Proteins. J.A. Majors Co., Atlanta, GA. [Pg.89]

Chemical PEs have recently been studied for increasing transdermal delivery of ASOs or other polar macromolecules [35]. Chemically induced transdermal penetration results from a transient reduction in the barrier properties of the stratum corneum. The reduction may be attributed to a variety of factors such as the opening of intercellular junctions due to hydration [36], solubilization of the stratum corneum [37, 38], or increased lipid bilayer fluidization [39, 40]. Combining various surfactants and co-solvents can be used to achieve skin penetration, purportedly resulting in therapeutically relevant concentrations of ASO in the viable epidermis and dermis [41]. In summary, it appears feasible to deliver ASO to the skin using a number of different delivery techniques and formulations. [Pg.254]

The selective activation of compounds with potential therapeutic effects and the controlled delivery of bioactive molecules triggered by light are topics of intensely growing interest (6,197-200). Besides the search for light-sensitive prodrugs activated by photochemical cleavage, isomerization or photoredox processes (201-203), especially the release of small molecules such as NO, CO, CS2, and H2S, have attracted a lot of interest in the past years (204-208). [Pg.275]

Wiradharma N, Tong YW, Yang Y-Y (2009) Self-assembled oligopeptide nanostructures for co-delivery of drug and gene with synergistic therapeutic effect. Biomaterials 30 3100-3109... [Pg.208]


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