Institute of Analytical and Environmental Sciences, National Tsing Hua University, Hsinchu, 30013, Taiwan.
Graduate Institute of Biomedical Engineering, Chang Gung University, Taoyuan, 33302, Taiwan.
Acta Biomater. 2022 Mar 15;141:140-150. doi: 10.1016/j.actbio.2022.01.044. Epub 2022 Jan 23.
Most dry eye syndromes (DES) are caused by oxidative stress and an overactive inflammatory response, leading to tear deficiency and excessive tear evaporation. Conventional eye drops for DES treatment require high doses and frequent administration due to their insufficient precorneal residence time. To overcome these problems, in this study, we have developed carbonized nanogels (CNGs) via the straightforward pyrolysis of lysine hydrochloride (Lys) to provide a long-lasting eye drop formulation for topical DES therapy. This methodology thermally converts Lys-into nitrogen-doped crosslinked polymers with embedded nanographitic structures, which enable efficient free radical scavenging. The cationic and crosslinked polymeric features of the Lys-CNGs also prolong the precorneal retention time and improve ocular bioavailability. These Lys-CNGs exhibit high biocompatibility with corneal epithelial cells both in vitro and in vivo, indicating their safety as eye drops. In a DES rabbit model, a single dose of Lys-CNGs (50 µg mL) can effectively alleviate the signs of DES within 4 days, whereas multiple treatments of 10-fold higher concentration of cyclosporine A are needed to achieve similar therapeutic effects (one dose every 12 h; 500 µg mL). The topical administration of Lys-CNGs enable a reduced therapeutic dose and extended dosing interval, thereby demonstrating a superior therapeutic efficacy compared to the commercial cyclosporine A eye drops. These Lys-CNGs, which exhibit significant free radical scavenging, anti-inflammatory activity, high biocompatibility, and a remarkable ocular bioadhesive property, hold great potential as a long-lasting eye drop formulation for the treatment of dry eye disease. STATEMENT OF SIGNIFICANCE: Multifunctional nanobiomaterial-based eye drops can render an ideal pharmaceutical formulation for the treatment of a variety of ocular surface diseases. To our knowledge, this is the first report describing the development of carbonized nanogels as topically administered therapeutics for alleviating dry eye syndrome (DES). We present evidence that the thermal transformation of lysine hydrochloride into carbonized nanogels (Lys-CNGs) endows superior antioxidant, anti-inflammatory, and bioadhesive properties. While a single dose of Lys-CNGs (50 µg mL) is sufficient to relieve the symptoms of DES for 4 days, multiple treatments of 10-fold higher concentration of commercially available cyclosporine eye drops are needed to achieve similar therapeutic outcomes (one dose every 12 h; 500 µg mL), suggesting an effective and long-lasting ocular carbonized nanomedicine.
大多数干眼症(DES)是由氧化应激和过度活跃的炎症反应引起的,导致泪液不足和过度蒸发。由于传统的 DES 治疗眼药水在角膜前的停留时间不足,因此需要高剂量和频繁给药。为了克服这些问题,在本研究中,我们通过简单的赖氨酸盐酸盐(Lys)热解制备了碳化纳米凝胶(CNG),为局部 DES 治疗提供了一种长效眼药水制剂。该方法将 Lys 热转化为氮掺杂交联聚合物,其中嵌入纳米石墨结构,从而实现有效的自由基清除。Lys-CNG 的阳离子和交联聚合物特性还延长了角膜前的保留时间并提高了眼部生物利用度。这些 Lys-CNG 在体外和体内均对角膜上皮细胞具有高生物相容性,表明它们作为眼药水是安全的。在 DES 兔模型中,单次给予 50µg·mL 的 Lys-CNG 可在 4 天内有效缓解 DES 症状,而需要给予高 10 倍浓度的环孢素 A 多次治疗才能达到类似的治疗效果(每 12 小时一次;500µg·mL)。Lys-CNG 的局部给药可减少治疗剂量并延长给药间隔,与市售环孢素 A 眼药水相比,具有更好的治疗效果。这些 Lys-CNG 具有显著的自由基清除、抗炎活性、高生物相容性和显著的眼部生物黏附特性,有望成为治疗干眼症的长效眼药水制剂。意义声明:基于多功能纳米生物材料的眼药水可以为治疗各种眼表疾病提供理想的药物制剂。据我们所知,这是首次报道描述将赖氨酸盐酸盐热转化为碳纳米凝胶(Lys-CNG)作为局部治疗药物用于缓解干眼症(DES)。我们提供的证据表明,盐酸赖氨酸的热转化为碳化纳米凝胶(Lys-CNG)赋予了优越的抗氧化、抗炎和生物黏附特性。单次给予 50µg·mL 的 Lys-CNG 足以缓解 DES 症状 4 天,而需要给予高 10 倍浓度的市售环孢素眼药水多次治疗(每 12 小时一次;500µg·mL)才能达到类似的治疗效果,表明这是一种有效的、长效的眼部碳纳米药物。