Issue 18, 2018

Synthesis of poly(l-lactide)/β-cyclodextrin/citrate network modified hydroxyapatite and its biomedical properties

Abstract

Hydroxyapatite (HA) was modified by the chelation of citric acid and Ca2+ on the surface of HA, followed by cross-linking between the hydroxyl groups of β-cyclodextrin (β-CD) and citrate, and then further in situ ring-opening polymerization of L-lactide over the hydroxyl groups. The modification of HA adjusted its surface properties and reduced the particle size. The synthesized PLA-CD-HA-72 exhibited the good adhesion of mesenchymal stem cells (MSCs) of Wistar rats, higher viability of MSCs and larger osteoinductivity. The results indicated that the PLA-CD-HA-72 possessed a rather large biocompatibility and bioactivity, and it could be a promising candidate as a bone tissue engineering material.

Graphical abstract: Synthesis of poly(l-lactide)/β-cyclodextrin/citrate network modified hydroxyapatite and its biomedical properties

Supplementary files

Article information

Article type
Letter
Submitted
11 Mar 2018
Accepted
23 Jun 2018
First published
25 Jun 2018

New J. Chem., 2018,42, 14729-14732

Synthesis of poly(L-lactide)/β-cyclodextrin/citrate network modified hydroxyapatite and its biomedical properties

W. Yi, L. Li, H. He, Z. Hao, B. Liu, Z. Chao and Y. Shen, New J. Chem., 2018, 42, 14729 DOI: 10.1039/C8NJ01194J

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