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Electrospun tetracycline hydrochloride drug

Kenawy et al. studied the potential of electrospun fiber mats as drug delivery system for the release of tetracycline hydrochloride (Kenawy et al. 2002). Electrospun PEVA + PLA blended fibers were 1—3 pm in diameter while the PLA fibers were around 3-6 pm. Srinivasan and Reneker 1995 examined the crystal structure and morphology of the electrospun Kevlar fibers (Srinivasan and Reneker 1995). Fibers from 40 nm to a few hundreds of nanometers were produced. [Pg.217]

Rather than drag coating onto electrospun surface, Kenawy et al. [51] have examined the behavior of nanofibers composed of PLA and poly (ethylene-acetate co-vinyl) (PEVA) with incorporated drag. The fibers were prepared by dissolving the polymer with tetracycline hydrochloride drag, thereby producing polymeric fibers. This experimentation demonstrates a constant drug release over 5 days from the polymer nanofibers in electrospun PEVA and 50/50 PLA/PEVA mats. [Pg.297]

Electrospun fiber mats explored as drug delivery vehicles using tetracycline hydrochloride as the model drug. [Pg.299]

Numerous other biodegradable polymers that can be electrospun can be applied in wound healing, for example, PLA and block-copolymer derivatives, PCL, chitin, and chitosan. Using tetracycline hydrochloride as a model drug, it was shown that the release kinetics can be adjusted... [Pg.176]


See other pages where Electrospun tetracycline hydrochloride drug is mentioned: [Pg.228]    [Pg.248]    [Pg.135]    [Pg.275]    [Pg.249]    [Pg.301]    [Pg.377]    [Pg.381]    [Pg.135]   


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