Wan Hongshuang, Wang Shuangqing, Li Chuying, Zeng Bowen, Wu Hao, Liu Chao, Chen Liqing, Jin Mingji, Huang Wei, Zang Yingda, Zhang Dongming, Gao Zhonggao, Jin Zhehu
Keloid Research Center, Yanbian University Hospital, Yanji 133000, China.
State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.
Pharmaceutics. 2023 Aug 18;15(8):2157. doi: 10.3390/pharmaceutics15082157.
A keloid is a benign tumor manifested as abnormal fibroplasia on the surface of the skin. Curing keloids has become a major clinical challenge, and searching for new treatments and medications has become critical. In this study, we developed a LA67 liposome-loaded thermo-sensitive hydrogel (LA67-RL-Gel) with active targeting for treating keloids via peritumoral injection and explored the anti-keloid mechanism. Firstly, Arg-Gly-Asp (RGD) peptide-modified liposomes (LA67-RL) loaded with LA67 were prepared with a particle size of 105.9 nm and a Zeta potential of -27.4 mV, and an encapsulation efficiency of 89.6 ± 3.7%. We then constructed a thermo-sensitive hydrogel loaded with LA67-RL by poloxamer 407 and 188. The formulation was optimized through the Box-Behnken design, where the impact of the proportion of the ingredients on the quality of the hydrogel was evaluated entirely. The optimal formulation was 20.7% P407 and 2.1% P188, and the gelation time at 37 °C was 9.5 s. LA67-RL-Gel slowly released 92.2 ± 0.8% of LA67 at pH 6.5 PBS for 72 h. LA67-RL-Gel increased adhesion with KF cells; increased uptake; promoted KF cells apoptosis; inhibited cell proliferation; reduced α-SMA content; decreased collagen I, collagen III, and fibronectin deposition; inhibited angiogenesis; and modulated the keloid microenvironment, ultimately exerting anti-keloid effects. In summary, this simple, low-cost, and highly effective anti-keloid liposome hydrogel provides a novel approach for treating keloids and deserves further development.
瘢痕疙瘩是一种良性肿瘤,表现为皮肤表面异常的纤维增生。治愈瘢痕疙瘩已成为一项重大的临床挑战,寻找新的治疗方法和药物变得至关重要。在本研究中,我们开发了一种具有主动靶向性的载有LA67的脂质体热敏水凝胶(LA67-RL-Gel),通过瘤周注射治疗瘢痕疙瘩,并探索其抗瘢痕疙瘩机制。首先,制备了载有LA67的精氨酸-甘氨酸-天冬氨酸(RGD)肽修饰脂质体(LA67-RL),其粒径为105.9 nm,Zeta电位为-27.4 mV,包封率为89.6±3.7%。然后,我们用泊洛沙姆407和188构建了载有LA67-RL的热敏水凝胶。通过Box-Behnken设计对配方进行优化,全面评估了各成分比例对水凝胶质量的影响。最佳配方为20.7%的P407和2.1%的P188,37℃下的凝胶化时间为9.5 s。LA67-RL-Gel在pH 6.5的PBS中72小时缓慢释放92.2±0.8%的LA67。LA67-RL-Gel增加了与瘢痕疙瘩成纤维细胞(KF细胞)的黏附;增加了摄取;促进了KF细胞凋亡;抑制了细胞增殖;降低了α-平滑肌肌动蛋白(α-SMA)含量;减少了I型胶原、III型胶原和纤连蛋白的沉积;抑制了血管生成;并调节了瘢痕疙瘩微环境,最终发挥抗瘢痕疙瘩作用。总之,这种简单、低成本且高效的抗瘢痕疙瘩脂质体水凝胶为瘢痕疙瘩的治疗提供了一种新方法,值得进一步开发。