School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China.
College of Pharmacy, Jinan University, Guangzhou 511443, China.
Acta Biomater. 2022 Aug;148:106-118. doi: 10.1016/j.actbio.2022.05.052. Epub 2022 Jun 6.
Focal bacterial infections are often difficult to treat due to the rapid emergence of antibiotic-resistant bacteria, high risk of relapse, and severe inflammation at local lesions. To address multidrug-resistant skin and soft tissue infections, a bacteria-absorbing sponge was prepared to involve a "trap-and-kill" mechanism. The system describes a guanidinium-rich lipopeptide functionalized lyotropic liquid-crystalline hydrogel with bicontinuous cubic networks. Amphiphilic lipopeptides can be spontaneously anchored to the lipid-water interface, exposing their bacterial targeting sequences to enhance antibacterial trapping/killing activity. Computational simulations supported our structural predictions, and the sponge was confirmed to successfully remove ∼98.8% of the bacteria in the medium. Release and degradation behavior studies indicated that the bacteria-absorbing sponge could degrade, mediate enzyme-responsive lipopeptide release, or generate ∼200 nm lipopeptide nanoparticles with environmental erosion. This implies that the sponge can effectively capture and isolate high concentrations of bacteria at the infected site and then sustainably release antimicrobial lipopeptides into deep tissues for the eradication of residual bacteria. In the animal experiment, we found that the antibacterial performance of the bacterial-absorbing sponge was significant, which demonstrated not only a long-term inhibition effect to disinfect and avoid bacterial rebound, but also a unique advantage to protect tissue from bacterial attack. STATEMENT OF SIGNIFICANCE: Host defense peptides/peptidomimetics (HDPs) have shown potential for the elimination of focal bacterial infections, but the application of their topical formulations suffers from time-consuming preparation processes, indistinctive toxicity reduction effects, and inefficient bacterial capture ability. To explore new avenues for the development of easily prepared, low-toxicity and high-efficiency topical antimicrobials, a guanidinium-rich lipopeptide was encapsulated in a lyotropic liquid-crystalline hydrogel (denoted as "bacteria-absorbing sponge") to achieve complementary superiorities. The superior characteristic of the bacteria-absorbing sponge involves a "trap-and-kill" mechanism, which undergoes not only a long-term inhibition effect to disinfect and avoid bacterial rebound, but also effective bacterial capture and isolating action to confine bacterial diffusion and protect tissues from bacterial attack.
局部细菌性感染由于抗生素耐药菌的迅速出现、复发风险高和局部病变处的严重炎症,往往难以治疗。为了解决多药耐药性皮肤和软组织感染,制备了一种细菌吸收海绵,以涉及“捕获-杀死”机制。该系统描述了一种具有双连续立方网络的胍基丰富的脂肽功能化溶致液晶水凝胶。两亲脂肽可以自发地锚定在脂质-水界面上,暴露出其针对细菌的序列,以增强抗菌捕获/杀伤活性。计算模拟支持了我们的结构预测,并且证实了海绵可以成功地从培养基中去除约 98.8%的细菌。释放和降解行为研究表明,细菌吸收海绵可以降解、介导酶响应脂肽释放,或在环境侵蚀下生成约 200nm 的脂肽纳米颗粒。这意味着海绵可以有效地在感染部位捕获和隔离高浓度的细菌,然后持续将抗菌脂肽释放到深层组织中以消灭残留的细菌。在动物实验中,我们发现细菌吸收海绵的抗菌性能显著,不仅表现出长期抑制作用以消毒和避免细菌反弹,而且具有独特的优势来保护组织免受细菌攻击。
宿主防御肽/拟肽(HDPs)已显示出消除局部细菌性感染的潜力,但它们的局部制剂应用存在耗时的制备过程、不明显的毒性降低效果和低效的细菌捕获能力等问题。为了探索易于制备、低毒性和高效的局部抗菌剂的新途径,一种胍基丰富的脂肽被包裹在溶致液晶水凝胶中(表示为“细菌吸收海绵”),以实现互补的优势。细菌吸收海绵的优越特性涉及“捕获-杀死”机制,不仅具有长期抑制作用以消毒和避免细菌反弹,而且具有有效的细菌捕获和隔离作用,以限制细菌扩散并保护组织免受细菌攻击。