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Encapsulation of salicylic acid in acylated low molecular weight chitosan for sustained release topical application
Author(s) -
Tiew Shu Xian,
Misran Misni
Publication year - 2017
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.45273
Subject(s) - chitosan , depolymerization , fourier transform infrared spectroscopy , amide , nuclear chemistry , dynamic light scattering , polymer , polymer chemistry , chemistry , materials science , organic chemistry , nanoparticle , chemical engineering , nanotechnology , engineering
Acylated low molecular weight chitosan was used to encapsulate salicylic acid (SA) for sustained release in topical delivery. Chitosan nanoparticles were prepared from the depolymerization of commercial chitosan and further acylated with short alkyl chains. The successful acylation of butyryl chitosan [low molecular weight chitosan (LMWC)‐B] were proved by Fourier transform infrared (FTIR) and 1 H‐NMR. Successful encapsulation of SA was observed by the shift of amide I band from 1648 cm −1 in LMWC‐B to 1641–1633 cm −1 in SA‐loaded LMWC‐B in FTIR analysis, which further confirmed with the size increment from dynamic light scattering and transmission electron microscopy analyses by comparing its unencapsulated LMWC‐B. SA release from LMWC‐B studied by Franz diffusion experiment followed Korsmeyer–Peppas model where the release component n value (0.502) indicated diffusion and polymer swelling were involved in release mechanism. The slow release study of SA showed the acylated chitosan exhibited sustained release property toward SA. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 45273.