Dual-responsive mesoporous poly-N-isopropylacrylamide-hydroxyapatite composite microspheres for controlled anticancer drug delivery
The advantages of mesoporous hydroxyapatite and the thermo-responsive property of poly-N-isopropylacrylamide make them attractive in drug delivery system, respectively. In this work, mesoporous poly-N-isopropylacrylamide-hydroxyapatite composite microspheres (PNIPAM-m-HAP) were synthesized, characte...
Gespeichert in:
Veröffentlicht in: | Journal of sol-gel science and technology 2021-03, Vol.97 (3), p.600-609 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | The advantages of mesoporous hydroxyapatite and the thermo-responsive property of poly-N-isopropylacrylamide make them attractive in drug delivery system, respectively. In this work, mesoporous poly-N-isopropylacrylamide-hydroxyapatite composite microspheres (PNIPAM-m-HAP) were synthesized, characterized and applied as a drug carrier. Doxorubicin was selected as a typical anticancer drug to study the in-vitro release characteristics of drug from PNIPAM-m-HAP in PBS. The release mechanism and release kinetics was also studied. Furthermore, the biocompatibility of the PNIPAM-m-HAP material was evaluated by MTT method. The experimental results depicted that the synthesized PNIPAM-m-HAP material was biocompatible, pH and thermo-responsive, which showed controlled release of doxorubicin.
Mesoporous hydroxyapatite and poly-N-isopropylacrylamide composite microspheres were synthesized, characterized and applied as a drug carrier for anticancer drug of doxorubicin, which showed controlled release of doxorubicin and dual response of pH and temperature.
Highlights
PNIPAM-m-HAP microspheres were synthesized, characterized and used as anticancer drug carrier.
PNIPAM-m-HAP was pH and thermo-responsive, which showed sustainable release of doxorubicin.
The release mechanism was studied and the biocompatibility of PNIPAM-m-HAP was evaluated. |
---|---|
ISSN: | 0928-0707 1573-4846 |
DOI: | 10.1007/s10971-020-05460-3 |