19
Views
24
CrossRef citations to date
0
Altmetric
Research Article

Transfer of protons from bulk solution to the surface of poly(L-lactide) microcapsules

, &
Pages 195-202 | Received 09 Apr 1986, Accepted 15 Apr 1986, Published online: 27 Sep 2008
 

Abstract

Excessive proton transfer from bulk solution to the surface of poly(L-lactide) microcapsules was observed. In acidic solutions of pH < 3.0, the zeta potential of the microcapsules became slightly positive, although poly(L-lactide) has only carbonyl groups and alcoholic hydroxyl groups which can be charged. In an NMR study, the signal of the water protons shifted towards a higher applied field with increasing interaction of water with the poly (L-lactide) microcapsule surface when the microcapsules were dispersed at low concentrations (up to 4x 10−3 per cent).

In solutions of pH 3.2–7.6, the observed values of the zeta potential were in good accordance with theoretical values calculated assuming that the charged groups distribute uniformly in the microcapsule wall. In this pH range, the average density of charged groups in the wall was estimated to be 0.04 m. The average volume occupied by one polymer unit (one poly(L-lactide) molecule) in the microcapsule membrane was estimated to be (35 Å)3, suggesting a rather tight polymer network in the poly(L-lactide) microcapsule membrane.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.