Kwon Soonmin, Choi Hyunsu, Park Changhee, Choi Sangkee, Kim Eunha, Kim Sung Won, Kim Choung-Soo, Koo Heebeom
Department of Medical Life Sciences, Department of Biomedicine & Health Sciences, and Catholic Photomedicine Research Institute, College of Medicine, The Catholic University of Korea, 222 Banpo-daero, Seocho-gu, Seoul, 06591, Republic of Korea.
Biomater Sci. 2021 Jan 5;9(1):108-115. doi: 10.1039/d0bm01155j.
It is important to focus on urgent needs in clinics and develop optimal materials. For successful augmentation of vocal folds, the ideal filler should be injectable through a syringe, and should stably maintain its volume for a long time without toxicity. To achieve these criteria, a click chemistry-based PEG (polyethylene glycol) hydrogel was developed and applied for vocal fold augmentation in vivo. The PEG hydrogel enables fast gelation in vivo after injection and provides long-term stability. Azide- and dibenzocyclooctyne (DBCO)-modified 4-arm PEG were cross-linked by chemical conjugation via click chemistry and yielded gelation within several minutes. After subcutaneous injection into mice and rats, the PEG hydrogel showed higher stability after 1 month compared to the traditionally used calcium hydroxyapatite-carboxymethyl cellulose (CaHA-CMC) filler. In rabbit models with vocal fold paralysis, the PEG hydrogel stably fixed the paralyzed vocal fold in 4 months and minimized the glottic gap. It was an improved therapeutic result compared to CaHA-CMC, demonstrating the potential of a click chemistry-based PEG hydrogel for vocal fold therapy.
关注临床的迫切需求并开发出最佳材料很重要。对于成功的声带增强,理想的填充物应可通过注射器注射,并能长期稳定保持其体积且无毒。为达到这些标准,开发了一种基于点击化学的聚乙二醇(PEG)水凝胶并将其应用于体内声带增强。PEG水凝胶在注射后能在体内快速凝胶化并提供长期稳定性。通过点击化学进行化学共轭,使叠氮化物和二苯并环辛炔(DBCO)修饰的四臂PEG交联,并在几分钟内产生凝胶化。皮下注射到小鼠和大鼠体内后,与传统使用的羟基磷灰石-羧甲基纤维素(CaHA-CMC)填充物相比,PEG水凝胶在1个月后显示出更高的稳定性。在声带麻痹的兔模型中,PEG水凝胶在4个月内稳定地固定了麻痹的声带并使声门间隙最小化。与CaHA-CMC相比,这是一个改善的治疗结果,证明了基于点击化学的PEG水凝胶在声带治疗中的潜力。