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Drug-dendrimer complex

Jain NK, Gupta U. Application of dendrimer-drug complexation in the enhancement of drug solubility and bioavailability. Expert Opin Drug Metab Toxicol 2008 4 1035-52. [Pg.199]

P. Kolhe, E. Misra, R.M. Kannan, S. Kannan, M. lieh-Im, Drug complexation, in vitro release and cellular entry of dendrimers and hyperbranched polymers, InL J. Hiarm. 259 (2003) 143-160. [Pg.256]

Fig. 8 Nanosystems that may function as simultaneous drug delivery and imaging agents for targeting T cells (a) liposomal systems, (b) solid biodegradable nanoparticulates, and (c) macro-molecular dendrimer complexes. PEG polyethylene glycol, Gd-DTPA gadolininum-diethylene triamine penta acetic acid. (Adapted from [48])... Fig. 8 Nanosystems that may function as simultaneous drug delivery and imaging agents for targeting T cells (a) liposomal systems, (b) solid biodegradable nanoparticulates, and (c) macro-molecular dendrimer complexes. PEG polyethylene glycol, Gd-DTPA gadolininum-diethylene triamine penta acetic acid. (Adapted from [48])...
Devarakonda et al. (2005) compared the solubilization of niclosamide by complexing with polyamidoamine (PAMAM) dendrimers and CDs, and found the solubility of niclosamide was sig-niLcantly higher with PAMAM. However, the dissolution rate was lower with PAMAM compared to the CDs, which was owing to the strong interaction between niclosamide and PAMAM delayed the release of the drug from the complexes of dendrimers. [Pg.148]

Patri AK, Kukowska-Latallo IF, Baker Jr. Targeted drug dehvery with dendrimers comparison of the release kinehcs of covalently conjugated drug and non-covalent drug inclusion complex. Adv. Drug Delivery Rev. 2005 57 2203-2214. [Pg.288]

Wiwattanapatapee, R. Jee, R.D. Duncan, R. PAMAM dendrimers as a potential oral drug delivery system dendrimer complexes with piroxicam. Proc. Int. Symp. Control. Release Bioact. Mater. 1999, 26, 145-146. [Pg.889]

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See also in sourсe #XX -- [ Pg.881 ]



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