Temperature- and pH-Responsive Poly(NIPAM-<i>co</i>-HEMA-<i>co</i>-AAm) Nanogel as a Smart Vehicle for Doxorubicin Delivery; Combating Colorectal Cancer

Temperature- and pH-Responsive Poly(NIPAM-<i>co</i>-HEMA-<i>co</i>-AAm) Nanogel as a Smart Vehicle for Doxorubicin Delivery; Combating Colorectal Cancer

In this project, a new class of temperature- and pH-sensitive hydrogel consisting of <i>N</i>-isopropyl acrylamide (NIPAM), hydroxyethyl methacrylate (HEMA), and acrylamide (AAm) was prepared via a controlled route through the reversible addition–fragmentation chain-transfer (RAFT) polym...

Full description

Saved in:
Bibliographic Details
Main Authors: Soheila Ghasemi, Mehdi Najafi, Mohammad Doroudian, Banafsheh Rastegari, Abbas Behzad-Behbahani, Hadis Soltanimehr, Fatemeh Farjadian
Format: Article
Language:English
Published: MDPI AG 2025-03-01
Series:Gels
Subjects:
hydrogel
smart vehicle
RAFT polymerization
PNIPAM
doxorubicin
drug delivery
Online Access:https://www.mdpi.com/2310-2861/11/4/227
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:In this project, a new class of temperature- and pH-sensitive hydrogel consisting of <i>N</i>-isopropyl acrylamide (NIPAM), hydroxyethyl methacrylate (HEMA), and acrylamide (AAm) was prepared via a controlled route through the reversible addition–fragmentation chain-transfer (RAFT) polymerization process. Poly(ethyleneglycol) dimethacrylate (PEG-DMA) was used as a long-chain hydrophilic and biocompatible crosslinking agent. The hydrogel structure was confirmed by different characteristic techniques such as <sup>1</sup>H NMR, FT-IR, and SEC, and the morphology and particle diameters were checked via the scanning electron microscopy (SEM) and dynamic light scattering (DLS) methods. Afterward, the as-prepared hydrogel, poly(NIPAM-<i>co</i>-HEMA-<i>co</i>-AAm), was loaded with doxorubicin (DOX) to be used as a temperature- and pH-triggered delivery carrier. The prepared system released DOX slowly at 37 °C and neutral pH, but increased DOX release significantly at 42 °C and acidic pH. The anti-cancer efficiencies of free DOX, hydrogel, and the DOX–hydrogel conjugate were tested in vitro using human colorectal adenocarcinoma HT-29 cell lines. Cytotoxicity evaluation of free DOX compared with the DOX–hydrogel conjugate revealed that more cancer cells were killed with increasing concentration. Moreover, the DOX-mediated apoptosis and ROS levels showed the beneficial effects of poly(NIPAM-<i>co</i>-HEMA-<i>co</i>-AAm) hydrogel for cancer drug delivery. Generally, the results suggest that this system can be a potential candidate for designing drug delivery systems.
ISSN:2310-2861

Similar Items