LingLing Zhao

Find an error

Name: 赵玲玲
Organization: Ningbo University , China
Department:
Title: Lecturer(PhD)
Co-reporter:Lingling Zhao, Lijing Niu, Hongze Liang, Hui Tan, Chaozong Liu, and Feiyan Zhu
ACS Applied Materials & Interfaces November 1, 2017 Volume 9(Issue 43) pp:37563-37563
Publication Date(Web):October 10, 2017
DOI:10.1021/acsami.7b09395
pH and glucose dual-responsive injectable hydrogels were prepared through the cross-linking of Schiff’s base and phenylboronate ester using phenylboronic-modified chitosan, poly(vinyl alcohol) and benzaldehyde-capped poly(ethylene glycol). Protein drugs and live cells could be incorporated into the hydrogels during the in situ cross-linking, displaying sustained and pH/glucose-triggered drug release from the hydrogels and cell viability and proliferation in the three-dimensional hydrogel matrix as well. Hence, the hydrogels with insulin and fibroblasts were considered as bioactive dressings for diabetic wound healing. A streptozotocin-induced diabetic rat model was used to evaluate the efficacy of hydrogel dressings in wound repair. The results revealed that the incorporation of insulin and L929 in the hydrogels could promote neovascularization and collagen deposition and enhance the wound-healing process of diabetic wounds. Thus, the drug- and cell-loaded hydrogels have promising potential in wound healing as a medicated system for various therapeutic proteins and live cells.Keywords: diabetic foot ulcers; drug delivery system; glucose responsive; injectable hydrogel; pH responsive; wound dressing; wound healing;
Co-reporter:Juan Li;Weiqiong Hu;Yajuan Zhang;Hui Tan;Xiaojun Yan;Hongze Liang
Journal of Polymer Science Part A: Polymer Chemistry 2015 Volume 53( Issue 10) pp:1235-1244
Publication Date(Web):
DOI:10.1002/pola.27556

ABSTRACT

Injectable hydrogels with pH and glucose triggered drug release capability were synthesized based on biocompatible phenylboronic modified chitosan and oxidized dextran through the formation of covalent imine bond and phenylboronate ester. Rheological characterization demonstrated that the gelation rate was rapid, and the moduli of the hydrogels were able to be tuned with chemical composition as well as pH and glucose concentration of the polymer solution. Anticancer drugs could be incorporated inside the hydrogel through the in situ gel forming process and undergo a controlled release by altering pH or glucose concentration. The hydrogels had good biocompatibility with viable and proliferated cells cultured in the three dimensional matrix, and the cell proliferation was suppressed when a small amount of DOX was added, which is benefit for the application of the hydrogels as smart anticancer drug delivery system. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015, 53, 1235–1244

Phosphine oxide, (3-bromopropyl)diphenyl-