4.8 Article

Gingipain-Responsive Thermosensitive Hydrogel Loaded with SDF-1 Facilitates In Situ Periodontal Tissue Regeneration

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 31, 页码 36880-36893

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c08855

关键词

periodontitis; Porphyromonas gingivalis; gingipain; smart materials; antibacterial agents; controlled release; stromal cell derived factor-1

资金

  1. National Natural Science Foundation of China [81873716, 81901009, 82001055]
  2. Shandong Provincial Natural Science Foundation [ZR2020QH158]
  3. China Postdoctoral Science Foundation [2019M662371]
  4. School of Stomatology, Shandong University [2019QNJJ03]
  5. Construction Engineering Special Fund of Taishan Scholars of Shandong Province [ts20190975]
  6. Rongxiang Regenerative Medicine Foundation of Shandong University [2019SDRX-14]
  7. Collaborative Innovation Center of Technology and Equipment for Biological Diagnosis and Therapy in Universities of Shandong, The National Key Research and Development Program of China [2017YFA0104604]

向作者/读者索取更多资源

An intelligent gingipain-responsive hydrogel was synthesized for on-demand drug delivery, showing excellent biocompatibility and promoting PDLSCs proliferation, migration, and osteogenic differentiation. Antibacterial testing demonstrated that the hydrogel released SAMP stressfully in response to gingipain stimulation, effectively inhibiting the growth of Porphyromonas gingivalis.
Existing local drug delivery systems for periodontitis suffer from poor antibacterial effect and unsatisfied periodontal regeneration. In this study, a smart gingipain-responsive hydrogel (PEGPD@SDF-1) was synthesized as an environmentally sensitive carrier for on-demand drug delivery. The PEGPD@SDF-1 hydrogel was synthesized from polyethylene glycol diacrylate (PEG-DA) based scaffolds, dithiothreitol (DTT), and a novel designed functional peptide module (FPM) via Michael-type addition reaction, and the hydrogel was further loaded with stromal cell derived factor-1 (SDF-1). The FPM exhibiting a structure of anchor peptide-short antimicrobial peptide (SAMP)anchor peptide could be cleaved by gingipain specifically, and the SAMP was released out of the hydrogel for antibacterial effect in response to gingipain. The hydrogel properties were characterized by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), swelling ratio analysis, degradation evaluation, and release curve description of the SAMP and SDF-1. Results in vitro indicated the PEGPD@SDF-1 hydrogel exhibited preferable biocompatibility and could promote the proliferation, migration, and osteogenic differentiation of periodontal ligament stem cells (PDLSCs). Antibacterial testing demonstrated that the PEGPD@SDF-1 hydrogel released the SAMP stressfully in response to gingipain stimulation, thereby strongly inhibiting the growth of Porphyromonas gingivalis. Furthermore, the study in vivo indicated that the PEGPD@SDF-1 hydrogel inhibited P. gingivalis reproduction, created a low-inflammatory environment, facilitated the recruitment of CD90+/CD34- stromal cells, and induced osteogenesis. Taken together, these results suggest that the gingipain-responsive PEGPD@SDF-1 hydrogel could facilitate in situ periodontal tissue regeneration and is a promising candidate for the on-demand local drug delivery system for periodontitis.

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