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Fine structures of self-assembled beta-cyclodextrin/Pluronic in dilute and dense systems: a small angle X-ray scattering study.
Shih, Kuo-Chih; Li, Chi-Yen; Li, Wen-Hsien; Lai, Hsi-Mei.
Affiliation
  • Shih KC; Department of Agricultural Chemistry, National Taiwan University, No. 1, Roosevelt Rd., Sec. 4, Taipei 10617, Taiwan. hmlai@ntu.edu.tw.
Soft Matter ; 10(38): 7606-14, 2014 Oct 14.
Article in En | MEDLINE | ID: mdl-25121472
The evolution of the fine structures of self-assembled polypseudorotaxane (PPR) in Pluronic (PL F108) solutions containing dilute to dense beta-cyclodextrin (ß-CD) was illustrated for the first time by small angle X-ray scattering (SAXS). Dense ß-CD (∼19 w/v%) was found feasible to be dispersed in 24% citric acid solution. 5% of PL F108 formed cylindrical micelles of 1 nm in radius and 8 nm in length in the presence of 24% citric acid through the dehydration of citric acid and citrate. PPR was formed through host-guest interaction between PL F108 and ß-CD. In dilute ß-CD system (1%), the single chains of PPR with separated ß-CD stacks on PL F108 were formed. The numbers of ß-CD in each stack increased from 1 to 4 on increasing ß-CD concentration to 9%. In a dense ß-CD system, PPR condensed to correlated structures majorly composed of two unit blocks through the hydrogen bonds between PPRs. Two distinguishable correlated domains with correlation lengths of 50 nm (marked α-phase) and 46 nm (marked ß-phase) along the chains, but without fine periodic structure within each individual domain, were identified in the 10% ß-CD solution. Periodic stacking of ß-CD in the domains developed in the 12% solution. As ß-CD concentration increased from 12 to 19%, the correlated heights of α and ß phases reduced from 41 and 32 nm to 30 and 10 nm, respectively. There were 48 ß-CDs that stabilized on each PL F108 chain in the 19% ß-CD system, which is in good agreement with stoichiometry.

Full text: 1 Database: MEDLINE Language: En Year: 2014 Type: Article

Full text: 1 Database: MEDLINE Language: En Year: 2014 Type: Article