Efficacy and Safety Evaluation of Pulsed Laser-Activated Injectable Hydrogel for Combined Photodynamic and Photothermal Therapy in Hypertrophic Scar Treatment

光热治疗 光动力疗法 医学 增生性瘢痕 激光治疗 激光器 皮肤病科 生物医学工程 材料科学 外科 纳米技术 化学 光学 物理 有机化学
作者
Xinling Zhang,Xuejie Gao,Yaqi Wei,Yi Zhang,Kun Zhang,Hongtao Chen,Lu Han,Mengjuan Mu,Chendong Ji,Hongyi Zhao
出处
期刊:Photodiagnosis and Photodynamic Therapy [Elsevier BV]
卷期号:: 104647-104647
标识
DOI:10.1016/j.pdpdt.2025.104647
摘要

To explore the efficacy and safety of pulsed laser-activated injectable hydrogel for combined photodynamic and photothermal therapy of hypertrophic scars. In this prospective study, indocyanine green (ICG) was used as a photosensitizer combined with hyaluronic acid (HA) to prepare ICG-HA hydrogel, and its photodynamic and photothermal properties were evaluated. The ex vivo photothermal experiments were conducted to assess the thermal effects on tissue integrity as a preliminary evaluation of safety. Human umbilical vein endothelial cells (HUVECs) were used as the experimental cell model to evaluate the in vitro effects of ICG-HA hydrogel under different therapies. A rabbit ear scar model (n=36) was established and randomly divided into 6 groups: ICG-HA hydrogels + single-pulse irradiation, single-pulse irradiation, ICG-HA hydrogels + continuous-pulse irradiation, continuous-pulse irradiation, ICG-HA hydrogels and control (n=6/group). Scar characteristics were monitored at 0, 1, 3, and 5 weeks using Ultrasound Doppler, colorimetry, VSS, and SEI assessments. At 1 and 5 weeks after ICG-HA hydrogels injection, histopathological analyses (hematoxylin and eosin (HE) staining, Masson's trichrome staining (MASSON) and CD31 immunohistochemical staining) were performed. The ICG-HA hydrogel exhibited favorable photodynamic and photothermal properties while maintaining structural integrity during laser therapy. In vitro cell experiments, using CCK-8 for metabolic activity and live/dead staining for membrane integrity, demonstrated that the combined PDT and PTT treatment significantly reduced cell metabolic activity and induced cell death compared to either PDT or PTT alone (P<0.001). In the rabbit ear scar model, the VSS results showed that at 3 and 5 weeks post-treatment, both the ICG-HA hydrogels + single-pulse irradiation group and the ICG-HA hydrogels + continuous-pulse irradiation group had significantly lower VSS scores compared to the control group (P<0.05), with the ICG-HA hydrogels + single-pulse irradiation group showing a more pronounced reduction (P<0.01 at 3 weeks and P<0.001 at 5 weeks). The similar trends were observed in the SEI scores. Colorimeter analysis revealed that, compared with the control group and the single-pulse irradiation group, the ICG-HA hydrogels + single-pulse irradiation group exhibited significantly lower color difference scores at 1, 3, and 5 weeks post-treatment (P<0.001, P<0.01 and P<0.001, respectively). HE staining results showed that, at 1 and 5 weeks post-treatment, the ICG-HA hydrogels + single-pulse irradiation group had the most significant reduction in scar thickness compared with all other groups (P<0.001). MASSON results indicated that, at 1 week post-treatment, the ICG-HA hydrogels + single-pulse irradiation group exhibited more orderly collagen alignment with significant consistency and sparser collagen distribution. CD31 immunohistochemical staining results demonstrated that, at 1 and 5 weeks post-treatment, the ICG-HA hydrogels + single-pulse irradiation group significantly reduced vascular density within the scar tissue (P<0.001). The ICG-HA hydrogel can effectively and safely synergize PDT and PTT to improve hypertrophic scar conditions under pulsed laser irradiation, especially single-pulse irradiation. This approach provides valuable reference for the clinical treatment in scar treatment.
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