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基于透明质酸的纳米马达:穿越黏膜屏障以应对抗菌耐药性。

Hyaluronic Acid-Based Nanomotors: Crossing Mucosal Barriers to Tackle Antimicrobial Resistance.

作者信息

Ruiz-González Noelia, Sánchez-deAlcázar Daniel, Esporrín-Ubieto David, Di Carlo Valerio, Sánchez Samuel

机构信息

The Barcelona Institute of Science and Technology (BIST), Institute for Bioengineering of Catalonia (IBEC), Baldiri i Reixac 10-12, 08028 Barcelona, Spain.

Facultat de Física, Universitat de Barcelona (UB). C. Martí i Franquès, 1-11, 08028 Barcelona, Spain.

出版信息

ACS Appl Mater Interfaces. 2025 May 14;17(19):27988-27999. doi: 10.1021/acsami.5c03636. Epub 2025 Apr 29.

Abstract

Bacterial infections pose a significant global health challenge aggravated by the rise of antimicrobial resistance (AMR). Among the obstacles preventing effective treatment are biological barriers (BBs) within the body such as the mucus layer. These BBs trap antimicrobials, necessitating higher doses and ultimately accelerating AMR. Addressing this issue requires innovative therapeutic strategies capable of bypassing BBs to deliver drugs more effectively. Here, we present nanomotors (NMs) based on hyaluronic acid (HA)- and urease-nanogels (NGs) as a solution to navigate effectively in viscous media by catalyzing the decomposition of urea into ammonium and carbon dioxide. These HA-based nanomotors (HA-NMs) were loaded with chloramphenicol (CHL) antibiotic and demonstrated superior antimicrobial activity against () compared to mesoporous silica NMs (MSNP-NMs), a reference in the field of NMs. Moreover, using an in vitro transwell model we evaluated the ability of HA-NMs to penetrate mucin barriers, effectively reducing proliferation, whereas the free antibiotic did not reduce bacteria proliferation. The optical density reduction at 24 h was over ten times greater than with free CHL. These organic-based enzyme-powered NMs represent a significant advancement in drug delivery, offering a promising approach to combat AMR while addressing the challenges of crossing complex BBs.

摘要

细菌感染对全球健康构成重大挑战,而抗菌药物耐药性(AMR)的上升使这一挑战更加严峻。阻碍有效治疗的障碍之一是体内的生物屏障(BBs),如黏液层。这些生物屏障会捕获抗菌药物,因此需要更高的剂量,最终加速了抗菌药物耐药性的产生。解决这一问题需要创新的治疗策略,能够绕过生物屏障更有效地递送药物。在此,我们展示了基于透明质酸(HA)和脲酶纳米凝胶(NGs)的纳米马达(NMs),作为一种通过催化尿素分解为铵和二氧化碳在粘性介质中有效导航的解决方案。这些基于HA的纳米马达(HA-NMs)负载了氯霉素(CHL)抗生素,与纳米马达领域的参考物介孔二氧化硅纳米马达(MSNP-NMs)相比,对()表现出优异的抗菌活性。此外,我们使用体外Transwell模型评估了HA-NMs穿透粘蛋白屏障的能力,有效地减少了()的增殖,而游离抗生素则没有减少细菌增殖。24小时时的光密度降低比游离CHL高出十倍以上。这些基于有机酶驱动的纳米马达代表了药物递送方面的重大进展,为对抗抗菌药物耐药性以及应对跨越复杂生物屏障的挑战提供了一种有前景的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55e7/12086762/9ebf77d08e0e/am5c03636_0007.jpg

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