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含微载体的水凝胶基质用于地塞米松递送以预防顺铂诱导的听力损失。

Hydrogel Matrix Containing Microcarriers for Dexamethasone Delivery to Protect Against Cisplatin-Induced Hearing Loss.

作者信息

Dindelegan Maximilian G, Blebea Cristina M, Perde-Schrepler Maria, Necula Violeta, Maniu Alma A, Pascalau Violeta, Popa Catalin, Susman Sergiu, Gherman Luciana M, Buzoianu Anca D

机构信息

Department of Clinical Pharmacology, "Iuliu Hațieganu" University of Medicine and Pharmacy, Cluj-Napoca, ROU.

Department of Surgery - Practical Abilities, "Iuliu Hațieganu" University of Medicine and Pharmacy, Cluj-Napoca, ROU.

出版信息

Cureus. 2024 Oct 9;16(10):e71142. doi: 10.7759/cureus.71142. eCollection 2024 Oct.

Abstract

A functional hydrogel containing biopolymer microcarriers loaded with dexamethasone was developed to address the hearing loss that results from cisplatin ototoxicity. The drug delivery platform was tested both in vitro in the HEI-OC1 inner ear cell line and in vivo in a rat animal model. The newly described formula offered prolonged release of the contained dexamethasone for up to six days and transformed into a solid state at body temperature, thus counteracting its clearing through the Eustachian tube when injected into the middle ear. When tested in vitro, the inner ear cells exposed to cisplatin showed significantly higher viability at 48 hours when seeded on hydrogel containing dexamethasone-loaded microparticles than the cells treated with free dexamethasone. In the rat in vivo model, the ears of the rats treated with the hydrogel formulation presented better hearing thresholds after cisplatin administration than contralateral ears treated with free dexamethasone. The ears of the rats treated with microcarriers without inclusion in the functional hydrogel obtained better results than the dexamethasone treatment group but not as good as the hydrogel-containing microcarrier group. Histological assessment of the rats' inner ears showed better integrity of the structures and lower apoptosis in the microcarrier-treated groups than in the control group. Overall, the newly described microcarrier of dexamethasone offers better protection against cisplatin-induced hearing loss than free dexamethasone, especially when contained in a functional hydrogel formulation.

摘要

为解决顺铂耳毒性导致的听力损失问题,研发了一种含有负载地塞米松的生物聚合物微载体的功能性水凝胶。该药物递送平台在体外的HEI-OC1内耳细胞系以及体内的大鼠动物模型中均进行了测试。新描述的配方可使所含地塞米松延长释放长达六天,并在体温下转变为固态,从而在注入中耳时抵消其通过咽鼓管的清除。在体外测试时,接种在含有负载地塞米松微粒的水凝胶上的内耳细胞,在48小时时暴露于顺铂后的活力显著高于用游离地塞米松处理的细胞。在大鼠体内模型中,用该水凝胶制剂治疗的大鼠耳朵在给予顺铂后的听力阈值比用游离地塞米松治疗的对侧耳朵更好。用不含功能性水凝胶的微载体治疗的大鼠耳朵比地塞米松治疗组取得了更好的结果,但不如含微载体的水凝胶组。对大鼠内耳的组织学评估显示,与对照组相比,微载体治疗组内耳结构的完整性更好,细胞凋亡更低。总体而言,新描述的地塞米松微载体比游离地塞米松能更好地预防顺铂诱导的听力损失,尤其是当它包含在功能性水凝胶制剂中时。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/051d/11463264/034670b1e779/cureus-0016-00000071142-i01.jpg

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