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基于脱细胞羊膜的热敏性阴道水凝胶可提高利托君疗效并减少早产治疗中的全身副作用。

Decellularized amnion membrane-based thermosensitive vaginal hydrogel enhances ritodrine efficacy and reduces systemic side effects in preterm birth treatment.

作者信息

Xin Yu, Chen Yue, Zhu Xiaojun, Zhang Ying, Kong Maiqi, Jiang Huidi, Li Xiao, Fei Weidong, Zheng Caihong

机构信息

Women's Hospital, Zhejiang University School of Medicine, Hangzhou 310006, China; Research Center for Clinical Pharmacy, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, China.

Women's Hospital, Zhejiang University School of Medicine, Hangzhou 310006, China.

出版信息

Acta Biomater. 2025 Jul 1;201:212-228. doi: 10.1016/j.actbio.2025.06.024. Epub 2025 Jun 16.

Abstract

Preterm birth remains a major cause of maternal and neonatal mortality, primarily due to the lack of effective clinical interventions. Ritodrine, a typical β-adrenoceptor agonist with low cost and proven clinical efficacy, faces restrictions in many developed countries because of its systemic side effects. To overcome the clinical limitations of ritodrine, this study developed a decellularized amnion membrane (dAM)-derived thermosensitive hydrogel for vaginal delivery of ritodrine (dAM@Rit). The resulting dAM@Rit exhibited favorable temperature sensitivity, optimal rheological properties, sustained drug release, low cytotoxicity, and high biocompatibility. In vivo fluorescence analyses confirmed the uterine-specific distribution of the drugs through the vaginal delivery of dAM@Rit, facilitated by the uterine first-pass effect. Pharmacodynamic evaluation revealed that dAM@Rit maintenance therapy reduced the preterm birth rate due to the anti-inflammatory properties of dAM and the β-adrenoceptor antagonizing effect of ritodrine. Notably, the dAM@Rit formulation also substantially mitigated ritodrine-induced adverse reactions, such as pulmonary edema and rhabdomyolysis. In conclusion, our findings offered a promising strategy to optimize the clinical application of ritodrine for managing preterm birth while minimizing its systemic side effects. STATEMENT OF SIGNIFICANCE: 1. This study designed a thermosensitive hydrogel for the vaginal delivery of ritodrine, achieving targeted uterine drug delivery through the uterine first-pass effect. 2. The hydrogel utilizes decellularized amnion membrane (dAM) as its matrix, which not only exhibits high biocompatibility but also enhances the therapeutic efficacy of ritodrine through its anti-inflammatory properties, synergistically treating premature labor. 3. Compared with intravenous or oral administration, the dAM-based vaginal hydrogel significantly reduces the adverse effects of ritodrine on both mothers and fetuses, offering a safer alternative for the management of preterm birth. 4. This work demonstrates the application of human amniotic membrane-derived biomaterial for pregnancy-related diseases, highlighting the importance of balancing efficacy and safety in clinical applications.

摘要

早产仍然是孕产妇和新生儿死亡的主要原因,主要是由于缺乏有效的临床干预措施。利托君是一种典型的β -肾上腺素能受体激动剂,成本低且临床疗效已得到证实,但由于其全身性副作用,在许多发达国家受到限制。为了克服利托君的临床局限性,本研究开发了一种用于经阴道递送利托君的脱细胞羊膜(dAM)衍生的热敏水凝胶(dAM@Rit)。所得的dAM@Rit表现出良好的温度敏感性、最佳的流变学性质、持续的药物释放、低细胞毒性和高生物相容性。体内荧光分析证实,通过子宫首过效应,经阴道递送dAM@Rit可实现药物在子宫内的特异性分布。药效学评价显示,由于dAM的抗炎特性和利托君的β -肾上腺素能受体拮抗作用,dAM@Rit维持治疗降低了早产率。值得注意的是,dAM@Rit制剂还显著减轻了利托君引起的不良反应,如肺水肿和横纹肌溶解。总之,我们的研究结果提供了一种有前景的策略,可优化利托君在治疗早产中的临床应用,同时将其全身性副作用降至最低。重要意义声明:1. 本研究设计了一种用于经阴道递送利托君的热敏水凝胶,通过子宫首过效应实现靶向子宫药物递送。2. 该水凝胶利用脱细胞羊膜(dAM)作为其基质,不仅具有高生物相容性,还通过其抗炎特性增强了利托君的治疗效果,协同治疗早产。3. 与静脉注射或口服给药相比,基于dAM的阴道水凝胶显著降低了利托君对母亲和胎儿的不良反应,为早产管理提供了更安全的选择。4. 这项工作展示了人羊膜衍生生物材料在妊娠相关疾病中的应用,强调了在临床应用中平衡疗效和安全性的重要性。

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