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|Title:||Formulation of modified microspheres based on cyclodextrin-lactic acid polymers||Authors:||Kassab, Rima
|Affiliations:||Department of Chemistry
Department of Chemistry
|Keywords:||Poly L-lactic acid
|Subjects:||Amphotericin B||Issue Date:||2008||Part of:||Jordan journal of chemistry||Volume:||3||Issue:||4||Start page:||433||End page:||437||Abstract:||
Polymers, based on Poly L-lactic acid (L-PLA) and coupled with β-Cyclodextrin (β-CD), have been used for the preparation of microspheres for drug encapsulation. The strategy was based on the modification of the terminal carboxylic group of L-PLA (73.000) by coupling it with a β-CD in the presence of the peptide coupling agents: DCC/HOBT. The degree of functionalisation was found to be 80%. Characterizations of the new product were carried out using 1 H NMR, gel permeation chromatography, and acid base titration. The size of the functionalized microspheres was determined to be 211 µm by Dynamic Light Scattering (DLS). Amphotericin B (AmB), a polyenic antifungal molecule, has been incorporated in L-PLA coupled with β-CD microspheres. The maximal quantity of AmB encapsulated, reported to 100 mg of the microspheres, was 7.2 mg (encapsulation ratio 60% by mol).
|URI:||https://scholarhub.balamand.edu.lb/handle/uob/2016||Open URL:||Link to full text||Type:||Journal Article|
|Appears in Collections:||Department of Chemistry|
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