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mitomycin C
Journal of Materials Chemistry B · 2025 · IF 5.7

Poly (L-lactic acid)/Gelatin microfiber membrane loaded with Mitomycin C promoting bladder defect repair by anti-fibrosis and anti-bacteria

Lunjie Zhao,Jianyou Xia,Congcong Yang,Jianping Tao,Shanfu Zhang,Wentao Hu,Chen Zhang,Jiuwu Zhang,Qiang Li,Yujie Xu

When the bladder is affected by factors such as tumors, tuberculosis, and trauma, its normal structure and function will be damaged inescapably. At this point, bladder replacement or enlargement surgery becomes necessary to restore its structure and improve the patient's quality of life. Traditional bladder reconstruction surgery, specifically ileum augmentation cystoplasty, has a complex surgical process, along with relatively large operative wounds and intestinal obstruction complications. There is an urgent need for bladder replacement material. Over the past decade, synthetic bladder scaffolds have emerged as alternatives; however, most fail to simultaneously address postoperative fibrosis and bacterial infection. To overcome these challenges, we developed an electrospinning poly (L-lactic acid)/gelatin (PLLA/GEL) microfiber membrane loaded with mitomycin C (MMC). By optimizing the PLLA/GEL ratio (7:3), the membrane had both good rigidity and excellent elasticity. The MMC-loaded fibers demonstrated sustained drug release, effectively inhibiting E. coli and S. aureus in vitro. In rat partial cystectomy models, the PLLA/GEL/MMC group showed reducing collagen III deposition through TGF-β/Smad2 pathway inhibition, enhancing urothelium regeneration and promoting angiogenesis. Notably, the membrane-maintained cell viability for both urothelial cells and smooth muscle cells over 7 days, confirming biocompatibility. These findings highlight a promising potential of the PLLA/GEL/MMC microfiber membrane not only as a material for bladder tissue engineering but also as a tool for therapeutic intervention that addresses multiple facets of bladder healing and regeneration.

研究领域: 生物医学工程 · 组织工程 · 药理学
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Nanoscale · 2016 ·Vol. 9 ·期 1 ·334-340 · IF 7.76

Mitomycin C-treated human-induced pluripotent stem cells as a safe delivery system of gold nanorods for targeted photothermal therapy of gastric cancer

Meng Yang,Yanlei Liu,Wenxiu Hou,Xiao Zhi,Chunlei Zhang,Xinquan Jiang,Fei Pan,Yuming Yang,Jian Ni,Daxiang Cui

Human-induced pluripotent stem cells (iPS) possess an intrinsic tumor tropism ability. However, iPS cells are impeded in clinical applications of tumor therapy due to the formation of teratomas and their survival in normal organs such as the liver, lungs, spleen and kidneys. Mitomycin C (MMC) can overcome this limitation by suppressing iPS proliferation. Herein, we fabricated a safe delivery system of iPS cells treated with MMC loading with gold nanorods (AuNRs) for the targeted photothermal treatment of gastric cancer. Our results showed that the tumor cells were efficiently killed by the heat generated from the gold nanorods, and the iPS cells ultimately died due to the action of MMC seven days after the photothermal treatment. This suggested that pre-treated iPS cells with MMC can be used as a novel and safe approach for targeted tumor therapy. This paves the road for clinical translation in the future.

研究领域: 生物医学工程 · 癌症研究 · 纳米技术 · 干细胞生物学
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