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pubmed-article:18605754pubmed:abstractTextRelationships of electrostatic interaction and encapsulation between poly(amidoamine) (PAMAM) dendrimers and negatively charged drug molecules have been investigated by aqueous solubility and NMR ( (1)H NMR and two-dimensional nuclear Overhauser effect spectroscopy (2D-NOESY)) studies. PAMAM dendrimers significantly increased the solubilities of phenobarbital and sulfamethoxazole, but scarcely influenced those of primidone and trimethoprim. Moreover, (1)H NMR and 2D-NOESY measurements indicated that few phenobarbital or sulfamethoxazole molecules were entrapped in the cavities of low-generation dendrimers (generation 3, G3). These results suggest that external electrostatic interaction contributes more to the solubility enhancement of drugs than internal encapsulation.lld:pubmed
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pubmed-article:18605754pubmed:authorpubmed-author:LiYiwenYlld:pubmed
pubmed-article:18605754pubmed:authorpubmed-author:XuTongwenTlld:pubmed
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pubmed-article:18605754pubmed:authorpubmed-author:WuQinglinQlld:pubmed
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pubmed-article:18605754pubmed:dateRevised2010-11-18lld:pubmed
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pubmed-article:18605754pubmed:articleTitleExternal electrostatic interaction versus internal encapsulation between cationic dendrimers and negatively charged drugs: which contributes more to solubility enhancement of the drugs?lld:pubmed
pubmed-article:18605754pubmed:affiliationLaboratory of Functional Membranes, Department of Chemistry, University of Science and Technology of China, Hefei, Anhui 230026, China. yycheng@mail.ustc.edu.cnlld:pubmed
pubmed-article:18605754pubmed:publicationTypeJournal Articlelld:pubmed
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