瘢痕疙瘩
纤维连接蛋白
脂质体
化学
泊洛沙姆
Zeta电位
细胞
材料科学
纳米技术
医学
生物化学
聚合物
外科
纳米颗粒
共聚物
有机化学
作者
Hongshuang Wan,Li Wang,Chuying Li,Bowen Zeng,Hao Wu,Chao Liu,Liqing Chen,Mingji Jin,Wei Huang,Yingda Zang,Dongming Zhang,Zhonggao Gao,Zhehu Jin
出处
期刊:Pharmaceutics
[Multidisciplinary Digital Publishing Institute]
日期:2023-08-18
卷期号:15 (8): 2157-2157
被引量:3
标识
DOI:10.3390/pharmaceutics15082157
摘要
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.
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