Zhang Li, Huang Tongzhou, Bi Jianing, Zheng Yingying, Lu Chao, Hui Qi, Wang Xiaojie, Lin Xiaohua
The Department of Dermatology of the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
School of Pharmacy of Wenzhou Medical University, Wenzhou, China.
Front Pharmacol. 2020 Feb 21;11:58. doi: 10.3389/fphar.2020.00058. eCollection 2020.
We developed a highly stable recombinant human acidic fibroblast growth factor (rh-aFGF) carbomer 940 hydrogel for wound healing. This study aimed to reveal toxicity target organs and the toxicity dose-response in the long-term administration of rh-aFGF carbomer 940 hydrogel in a rabbit skin wound model. New Zealand rabbits were topically administrated rh-aFGF carbomer 940 hydrogel at a daily dose of 900 IU/cm, 1,800 IU/cm, and 3,600 IU/cm for 28 days. Lyophilized rh-aFGF agent was used as the positive control group. General behavior, serum chemistry, skin irritation, immunogenicity, immunotoxicity, and histopathology were analyzed at designated time points. Results revealed that food intake, body weight, body temperature, heart rate, and eye examinations were all normal, suggesting no obvious toxicity induced by the rh-aFGF hydrogel. Medium and high dose rh-aFGF hydrogel groups and the positive control group displayed increased cell numbers in the local lymph nodes near the site of administration, likely caused mesenteric lymph node follicular hyperplasia, and this observation was alleviated after 14 days of recovery. Immunogenicity studies demonstrated that the serum antibody titer against rh-aFGF increased with the duration and number of drug applications but were not neutralization antibodies. After administration stopped, antibody titer decreased and disappeared in some mice. In summary, the safe dose for long-term administration of rh-aFGF carbomer 940 hydrogel for persistently damaged skin was 900 IU/cm, which is 10 times that of the proposed clinical dosing.
我们开发了一种用于伤口愈合的高度稳定的重组人酸性成纤维细胞生长因子(rh-aFGF)卡波姆940水凝胶。本研究旨在揭示在兔皮肤伤口模型中长期给予rh-aFGF卡波姆940水凝胶的毒性靶器官和毒性剂量反应。将新西兰兔每日分别以900 IU/cm、1800 IU/cm和3600 IU/cm的剂量局部给予rh-aFGF卡波姆940水凝胶,持续28天。冻干的rh-aFGF制剂用作阳性对照组。在指定时间点分析一般行为、血清生化、皮肤刺激性及免疫原性、免疫毒性和组织病理学。结果显示,食物摄入量、体重、体温、心率和眼部检查均正常,表明rh-aFGF水凝胶未诱导明显毒性。中、高剂量rh-aFGF水凝胶组和阳性对照组给药部位附近局部淋巴结中的细胞数量增加,可能导致肠系膜淋巴结滤泡增生,恢复14天后这种现象有所缓解。免疫原性研究表明,抗rh-aFGF的血清抗体滴度随药物应用的持续时间和次数增加,但不是中和抗体。停药后,部分小鼠的抗体滴度下降并消失。总之,对于持续受损皮肤长期给予rh-aFGF卡波姆940水凝胶的安全剂量为900 IU/cm,是建议临床给药剂量的10倍。