L-Lysine-Modified pNIPAm-co-GMA Copolymer Hydrogel for pH- and Temperature-Responsive Drug Delivery and Fluorescence Imaging Applications.

Autor: Santhamoorthy M; School of Chemical Engineering, Yeungnam University, Gyeongsan 38541, Republic of Korea., Vanaraj R; School of Chemical Engineering, Yeungnam University, Gyeongsan 38541, Republic of Korea., Thirupathi K; Department of Physics, Government Arts and Science College for Women, Karimangalam 635111, Dharmapuri, Tamil Nadu, India., Ulagesan S; Division of Fisheries Life Sciences, Pukyong National University, Nam-gu, Busan 48513, Republic of Korea., Nam TJ; Institute of Fisheries Sciences, Pukyong National University, Gijang-gun, Busan 46041, Republic of Korea., Phan TTV; Center for Advanced Chemistry, Institute of Research and Development, Duy Tan University, 03 Quang Trung, Hai Chau, Danang 550000, Vietnam.; Faculty of Environmental and Chemical Engineering, Duy Tan University, 03 Quang Trung, Hai Chau, Danang 550000, Vietnam., Kim SC; School of Chemical Engineering, Yeungnam University, Gyeongsan 38541, Republic of Korea.
Jazyk: angličtina
Zdroj: Gels (Basel, Switzerland) [Gels] 2023 Apr 25; Vol. 9 (5). Date of Electronic Publication: 2023 Apr 25.
DOI: 10.3390/gels9050363
Abstrakt: The development of dual-stimuli-responsive hydrogels attracts much research interest owing to its unique stimuli-responsive characteristics. In this study, a poly-N-isopropyl acrylamide-co-glycidyl methacrylate-based copolymer was synthesized by incorporating N-isopropyl acrylamide (NIPAm) and a glycidyl methacrylate (GMA) monomer. The synthesized copolymer, pNIPAm-co-GMA was further modified with L-lysine (Lys) functional units and further conjugated with fluorescent isothiocyanate (FITC) to produce a fluorescent copolymer pNIPAAm-co-GMA-Lys hydrogel (HG). The in vitro drug loading and dual pH- and temperature-stimuli-responsive drug release behavior of the pNIPAAm-co-GMA-Lys HG was investigated at different pH (pH 7.4, 6.2, and 4.0) and temperature (25 °C, 37 °C, and 45 °C) conditions, respectively, using curcumin (Cur) as a model anticancer drug. The Cur drug-loaded pNIPAAm-co-GMA-Lys/Cur HG showed a relatively slow drug release behavior at a physiological pH (pH 7.4) and low temperature (25 °C) condition, whereas enhanced drug release was achieved at acidic pH (pH 6.2 and 4.0) and higher temperature (37 °C and 45 °C) conditions. Furthermore, the in vitro biocompatibility and intracellular fluorescence imaging were examined using the MDA-MB-231 cell line. Therefore, we demonstrate that the synthesized pNIPAAm-co-GMA-Lys HG system with temperature- and pH-stimuli-responsive features could be promising for various applications in biomedical fields, including drug delivery, gene delivery, tissue engineering, diagnosis, antibacterial/antifouling material, and implantable devices.
Databáze: MEDLINE