Urology & Nephrology Center, Department of Urology, Zhejiang Provincial People's Hospital (Affiliated People's Hospital), Hangzhou Medical College, Hangzhou, Zhejiang, China.
Department of Urology, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, 510630, China.
J Nanobiotechnology. 2024 Sep 14;22(1):560. doi: 10.1186/s12951-024-02816-7.
Intravesical therapy (IT) is widely used to tackle various urological diseases. However, its clinical efficacy is decreased by the impermeability of various barriers presented on the bladder luminal surface, including the urinary mucus layer and the densely packed tissue barrier. In this study, we report a mucoadhesive-to-penetrating nanomotors-in-hydrogel system for urothelium-oriented intravesical drug delivery. Upon intravesical instillation, its poloxamer 407 (PLX) hydrogel gelated and adhered to the urothelium to prolong its intravesical retention. The urea afterwards diffused into the hydrogel, thus generating a concentration gradient. Urease-powered membrane nanomotors (UMN) without asymmetric surface engineering could catalyze the urea and migrate down this concentration gradient to deeply and unidirectionally penetrate the urothelial barrier. Moreover, the intravesical hybrid system-delivered gemcitabine could effectively inhibit the bladder tumor growth without inducing any side effect. Therefore, our mucoadhesive-to-penetrating nanomotors-in-hydrogel system could serve as an alternative to IT to meet the clinical need for more efficacious therapeutics for urological diseases.
膀胱内治疗 (IT) 被广泛用于治疗各种泌尿科疾病。然而,由于膀胱腔表面存在多种屏障的不渗透性,包括尿粘液层和紧密堆积的组织屏障,其临床疗效降低。在这项研究中,我们报告了一种用于尿路上皮定向膀胱内药物输送的粘弹性-穿透纳米马达水凝胶系统。在膀胱内灌注后,其泊洛沙姆 407 (PLX) 水凝胶胶凝并粘附在尿路上皮上,以延长其在膀胱内的保留时间。随后,尿素扩散到水凝胶中,从而产生浓度梯度。没有不对称表面工程的脲酶动力膜纳米马达 (UMN) 可以催化尿素并沿着这个浓度梯度向下迁移,从而深度和单向穿透尿路上皮屏障。此外,膀胱内混合系统递送的吉西他滨可以有效抑制膀胱癌的生长,而不会引起任何副作用。因此,我们的粘弹性-穿透纳米马达水凝胶系统可以作为 IT 的替代方案,以满足泌尿科疾病更有效治疗的临床需求。