Abstract
The supramolecular interactions of the ocular drug tropicamide (TR) with cucurbit[7]uril (CB7) and cucurbit[8]uril (CB8) were investigated in aqueous solutions by using 1H NMR, ESI-MS and UV-vis spectroscopic techniques. The results indicate a 1:1 binding stoichiometry of TR with CB7 and CB8. The binding constants of TR in its protonated form were higher (e.g. K = 4 × 10 6M -1 with CB8) than in its neutral form (e.g. K = 1.4 × 10 4M -1 with CB8), which led to a complexation-induced increase in its pK a value of ca. 0.5 and 2 units with CB7 and CB8, respectively. In the presence of about 1% (w/v) CB8, the ionisation degree of 0.1% (w/v) TR was increased from 2% to 62% at neutral pH. The increase in the pK a value and thus stabilisation of the protonated TR species at neutral pH is discussed in the context of supramolecular drug delivery of ophthalmologic drugs.
| Original language | English |
|---|---|
| Pages (from-to) | 654-661 |
| Number of pages | 8 |
| Journal | Supramolecular Chemistry |
| Volume | 23 |
| Issue number | 9 |
| DOIs | |
| Publication status | Published - Sept 2011 |
Keywords
- Cucurbiturils
- Drug ionisation
- Host-guest complexes
- PK shifts
- Tropicamide
ASJC Scopus subject areas
- General Chemistry
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