z-logo
Premium
Sustained‐release ibuprofen prodrug particle: Emulsifier and initiator regulate the diameter and distribution
Author(s) -
Wang Jia,
Zhang Haixin,
Xu Jie,
Qian Hao,
Liu Rui,
Xu Zengchang,
Zhu Hongjun
Publication year - 2021
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.49779
Subject(s) - dispersity , ethylene glycol dimethacrylate , materials science , monomer , ethylene glycol , polymer chemistry , drug delivery , emulsion polymerization , fourier transform infrared spectroscopy , polymer , chemical engineering , methyl methacrylate , particle size , emulsion , chemistry , organic chemistry , methacrylic acid , nanotechnology , composite material , engineering
Polymers have played a vital part in the development of drug delivery systems (DDS). For DDS, having a controllable diameter and distribution are conducive to reproducibility of drug release behavior and efficacy. In this work, an ibuprofen prodrug (Ibu@PMMA) was synthesized by methyl methacrylate (MMA), ibuprofen monomer (Ibu@HEMA), and ethylene glycol dimethacrylate (EGDMA) via emulsion polymerization. The Ibu@PMMA exhibits spherical shapes, and its structural properties were characterized by NMR, FTIR, and SEM techniques. In addition, the hydrodynamic diameter and polydispersity index (PDI) of Ibu@PMMA were reduced by increasing the proportion of emulsifier. Meanwhile, by increasing the amount of initiator, the hydrodynamic diameter and PDI of Ibu@PMMA were decreased. Moreover, Ibu@PMMA exhibits good sustained‐release ability in vitro , which could be used as a potential delivery system for anti‐inflammatory agents.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom