| pubmed-article:21137839 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:21137839 | lifeskim:mentions | umls-concept:C0441833 | lld:lifeskim |
| pubmed-article:21137839 | lifeskim:mentions | umls-concept:C0004927 | lld:lifeskim |
| pubmed-article:21137839 | lifeskim:mentions | umls-concept:C1280500 | lld:lifeskim |
| pubmed-article:21137839 | lifeskim:mentions | umls-concept:C0332621 | lld:lifeskim |
| pubmed-article:21137839 | lifeskim:mentions | umls-concept:C0598629 | lld:lifeskim |
| pubmed-article:21137839 | lifeskim:mentions | umls-concept:C0243072 | lld:lifeskim |
| pubmed-article:21137839 | pubmed:issue | 10 | lld:pubmed |
| pubmed-article:21137839 | pubmed:dateCreated | 2010-12-8 | lld:pubmed |
| pubmed-article:21137839 | pubmed:abstractText | The effect of hydrophobic octadecyl groups on pH-dependent aggregation behavior of polyaspartammide derivatives was studied. A series of pH-sensitive amphiphilic polymers with different degrees of octaceylamine (C18) substitution were synthesized through a successive graft reaction of octaceylamine, O-(2-aminoethyl)-O'-methylpolyethylene glycol, and 1-(3-aminopropyl)imidazole on polysuccinimide. Micelle-like nano-aggregates were formed in aqueous solution at pH > 6.8 and they showed different pH dependent aggregation behavior according to degree of substitution (DS) of the hydrophobic C18 chains. These polymers will have a potential application as carriers for pH-sensitive drug release in anticancer or intracellular delivery systems. | lld:pubmed |
| pubmed-article:21137839 | pubmed:language | eng | lld:pubmed |
| pubmed-article:21137839 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21137839 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:21137839 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21137839 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21137839 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21137839 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21137839 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21137839 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21137839 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21137839 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21137839 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21137839 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:21137839 | pubmed:month | Oct | lld:pubmed |
| pubmed-article:21137839 | pubmed:issn | 1533-4880 | lld:pubmed |
| pubmed-article:21137839 | pubmed:author | pubmed-author:LeeDoo SungDS | lld:pubmed |
| pubmed-article:21137839 | pubmed:author | pubmed-author:KimSung... | lld:pubmed |
| pubmed-article:21137839 | pubmed:author | pubmed-author:KimDukjoonD | lld:pubmed |
| pubmed-article:21137839 | pubmed:author | pubmed-author:SeoKwangwonK | lld:pubmed |
| pubmed-article:21137839 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:21137839 | pubmed:volume | 10 | lld:pubmed |
| pubmed-article:21137839 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:21137839 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:21137839 | pubmed:pagination | 6986-91 | lld:pubmed |
| pubmed-article:21137839 | pubmed:meshHeading | pubmed-meshheading:21137839... | lld:pubmed |
| pubmed-article:21137839 | pubmed:meshHeading | pubmed-meshheading:21137839... | lld:pubmed |
| pubmed-article:21137839 | pubmed:meshHeading | pubmed-meshheading:21137839... | lld:pubmed |
| pubmed-article:21137839 | pubmed:meshHeading | pubmed-meshheading:21137839... | lld:pubmed |
| pubmed-article:21137839 | pubmed:meshHeading | pubmed-meshheading:21137839... | lld:pubmed |
| pubmed-article:21137839 | pubmed:meshHeading | pubmed-meshheading:21137839... | lld:pubmed |
| pubmed-article:21137839 | pubmed:meshHeading | pubmed-meshheading:21137839... | lld:pubmed |
| pubmed-article:21137839 | pubmed:meshHeading | pubmed-meshheading:21137839... | lld:pubmed |
| pubmed-article:21137839 | pubmed:meshHeading | pubmed-meshheading:21137839... | lld:pubmed |
| pubmed-article:21137839 | pubmed:meshHeading | pubmed-meshheading:21137839... | lld:pubmed |
| pubmed-article:21137839 | pubmed:meshHeading | pubmed-meshheading:21137839... | lld:pubmed |
| pubmed-article:21137839 | pubmed:meshHeading | pubmed-meshheading:21137839... | lld:pubmed |
| pubmed-article:21137839 | pubmed:meshHeading | pubmed-meshheading:21137839... | lld:pubmed |
| pubmed-article:21137839 | pubmed:meshHeading | pubmed-meshheading:21137839... | lld:pubmed |
| pubmed-article:21137839 | pubmed:year | 2010 | lld:pubmed |
| pubmed-article:21137839 | pubmed:articleTitle | Effect of hydrophobic octadecyl groups on pH-sensitive aggregation behavior of imidazole-containing polyaspartammide derivatives. | lld:pubmed |
| pubmed-article:21137839 | pubmed:affiliation | Department of Chemical Engineering, Sungkyunkwan University, Suwon 440-746, Korea. | lld:pubmed |
| pubmed-article:21137839 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:21137839 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
