Rathnayake Kavini, Patel Unnati, Pham Chi, McAlpin Anna, Budisalich Travis, Jayawardena Surangi N
Department of Chemistry, The University of Alabama in Huntsville, Huntsville, Alabama 35899, United States.
ACS Appl Bio Mater. 2020 Oct 19;3(10):6708-6721. doi: 10.1021/acsabm.0c00622. Epub 2020 Aug 4.
(PA) is an opportunistic pathogen, which causes serious lung infections in immunocompromised patients. Traditional oral intake of large quantities of small-molecule antibiotics to treat bacterial infections leads to off-target toxicity and development of drug-resistant species. Improved delivery systems of antibiotics to the targeted site of bacterial infections would help reduce the need for a high intake of antibiotics. Colistin (Col), an antibacterial peptide, is considered the last resort treatment for multidrug resistant (MDR)-PA. To approach the problem of development of antibacterial resistance and off-target toxicity due to the use of excessive amounts of antibiotics, we have designed a targeted drug delivery nanoassembly, which delivers antibiotics to extracellular and intracellular bacteria. The nanoassembly is composed of (1) drug (Col)-loaded mesoporous silica (MSN) core (Col@MSN), (2) liposomal shell (Col@MSN@LL), and (3) PA-targeting LL-37 peptide (Col@MSN@LL-(LL-37)). The liposomal shell prevents premature drug release before the nanoassembly approaches the targeted bacteria. The liposome bilayer degrades upon excreted lipase present in the local environment of PA, releasing encapsulated Col. There is a significant increase in Col release (∼90% release within 40 h) in the presence of bacteria compared to the absence of bacteria (only ∼75% release after 80 h). A 6.7-fold increase in the antimicrobial efficacy of Col encapsulated in Col@MSN@LL-(LL-37) was seen compared to free Col. All studies were done using a clinical strain of PA14. Col@MSN@LL-(LL-37) successfully targets and inhibits intracellular PA14 within the lung epithelial cells. Only 7% PA14 viability is seen after treating the lung epithelial cells with Col@MSN@LL-(LL-37). No significant cytotoxicity was observed with Col@MSN@LL-(LL-37). Therefore, this discussed lipid-coated targeted nanoassembly can be considered as a successful antibiotic delivery platform.
肺炎克雷伯菌(PA)是一种机会致病菌,可在免疫功能低下的患者中引起严重的肺部感染。传统上通过口服大量小分子抗生素来治疗细菌感染会导致脱靶毒性和耐药菌的产生。改进抗生素向细菌感染靶点的递送系统将有助于减少大量使用抗生素的需求。黏菌素(Col)是一种抗菌肽,被认为是治疗多重耐药(MDR)-PA的最后手段。为了解决因使用过量抗生素而产生的抗菌耐药性和脱靶毒性问题,我们设计了一种靶向药物递送纳米组装体,可将抗生素递送至细胞外和细胞内细菌。该纳米组装体由(1)载药(Col)的介孔二氧化硅(MSN)核心(Col@MSN)、(2)脂质体外壳(Col@MSN@LL)和(3)PA靶向LL-37肽(Col@MSN@LL-(LL-37))组成。脂质体外壳可防止纳米组装体在接近靶细菌之前过早释放药物。脂质体双层在PA局部环境中存在的分泌型脂肪酶作用下降解,释放出包裹的Col。与无细菌存在时相比(80小时后仅释放约75%),有细菌存在时Col的释放量显著增加(40小时内释放约90%)。与游离Col相比,包裹在Col@MSN@LL-(LL-37)中的Col抗菌效果提高了6.7倍。所有研究均使用PA14临床菌株进行。Col@MSN@LL-(LL-37)成功靶向并抑制肺上皮细胞内的细胞内PA14。用Col@MSN@LL-(LL-37)处理肺上皮细胞后,仅观察到7%的PA14活力。未观察到Col@MSN@LL-(LL-37)有明显的细胞毒性。因此,这种讨论的脂质包被靶向纳米组装体可被视为一种成功的抗生素递送平台。