Vasquez Jeddah Marie, Idrees Ayesha, Carmagnola Irene, Sigen Aa, McMahon Sean, Marlinghaus Lennart, Ciardelli Gianluca, Greiser Udo, Tai Hongyun, Wang Wenxin, Salber Jochen, Chiono Valeria
Department of Mechanical and Aerospace Engineering, Politecnico di Torino, Turin, Italy.
Blafar Ltd., Dublin, Ireland.
Front Bioeng Biotechnol. 2021 Nov 16;9:742135. doi: 10.3389/fbioe.2021.742135. eCollection 2021.
The rapidly increasing resistance of bacteria to currently approved antibiotic drugs makes surgical interventions and the treatment of bacterial infections increasingly difficult. In recent years, complementary strategies to classical antibiotic therapy have, therefore, gained importance. One of these strategies is the use of medicinal honey in the treatment of bacterially colonized wounds. One of the several bactericidal effects of honey is based on the generation of hydrogen peroxide through the activity of the enzyme glucose oxidase. The strategy underlying this work is to mimic this antibacterial redox effect of honey in an injectable, biocompatible, and rapidly forming hydrogel. The hydrogel was obtained by thiol-ene click reaction between hyperbranched polyethylene glycol diacrylate (HB PEGDA), synthesized using reversible addition-fragmentation chain transfer (RAFT) polymerization, and thiolated hyaluronic acid (HA-SH). After mixing 500 µL HB PEGDA (10%, w/w) and 500 µL HA-SH (1%, w/w) solutions, hydrogels formed in ∼60 s (HB PEGDA/HA-SH 10.0-1.0), as assessed by the tube inverting test. The HB PEGDA/HA-SH 10.0-1.0 hydrogel (200 µL) was resistant to dissolution in water for at least 64 days, absorbing up to 130 wt% of water. Varying glucose oxidase (GO) amounts (0-500 U/L) and constant glucose content (2.5 wt%) were loaded into HB PEGDA and HA-SH solutions, respectively, before hydrogel formation. Then, the release of HO was evaluated through a colorimetric pertitanic acid assay. The GO content of 250 U/L was selected, allowing the formation of 10.8 ± 1.4 mmol HO/L hydrogel in 24 h, under static conditions. The cytocompatibility of HB PEGDA/HA-SH 10.0-1.0 hydrogels loaded with different GO activities (≤ 500 U/L) at a constant glucose amount (2.5 wt%) was investigated by assays at 24 h with L929 and HaCaT cell lines, according to DIN EN ISO 10993-5. The tests showed cytocompatibility for GO enzyme activity up to 250 U/L for both cell lines. The antibacterial activity of HB PEGDA/HA-SH 10.0-1.0 hydrogels loaded with increasing amounts of GO was demonstrated against various gram-positive bacteria (), antibiotic-resistant gram-positive bacteria (MRSA and MRSE), gram-negative bacteria (, , ), and antibiotic-resistant gram-negative strains () using agar diffusion tests. For all gram-positive bacterial strains, increasing efficacy was measured with increasing GO activity. For the two , efficacy was shown only from an enzyme activity of 125 U/L and for and , efficacy was shown only from 250 U/L enzyme activity. HB PEGDA/HA-SH 10.0-1.0 hydrogels loaded with ≤250 U/L GO and 2.5 wt% glucose are promising formulations due to their fast-forming properties, cytocompatibility, and ability to produce antibacterial HO, warranting future investigations for bacterial infection treatment, such as wound care.
细菌对目前已获批的抗生素药物的耐药性迅速增加,使得手术干预和细菌感染的治疗变得越来越困难。因此,近年来,传统抗生素治疗的补充策略变得愈发重要。其中一种策略是使用药用蜂蜜治疗细菌定植的伤口。蜂蜜的几种杀菌作用之一是基于葡萄糖氧化酶的活性产生过氧化氢。这项工作的基本策略是在一种可注射、生物相容且能快速形成的水凝胶中模拟蜂蜜的这种抗菌氧化还原作用。通过使用可逆加成-断裂链转移(RAFT)聚合合成的超支化聚乙二醇二丙烯酸酯(HB PEGDA)与硫醇化透明质酸(HA-SH)之间的硫醇-烯点击反应获得水凝胶。混合500 μL HB PEGDA(10%,w/w)和500 μL HA-SH(1%,w/w)溶液后,通过试管倒置试验评估,水凝胶在约60秒内形成(HB PEGDA/HA-SH 10.0-1.0)。HB PEGDA/HA-SH 10.0-1.0水凝胶(200 μL)在水中至少64天不溶解,能吸收高达130 wt%的水。在水凝胶形成之前,分别将不同量的葡萄糖氧化酶(GO)(0-500 U/L)和恒定的葡萄糖含量(2.5 wt%)加载到HB PEGDA和HA-SH溶液中。然后,通过比色过钛酸测定法评估HO的释放。选择250 U/L的GO含量,在静态条件下,24小时内可形成10.8±1.4 mmol HO/L的水凝胶。根据DIN EN ISO 10993-5,在24小时时用L929和HaCaT细胞系进行试验,研究了加载不同GO活性(≤50μg/mL)且葡萄糖含量恒定(2.5 wt%)的HB PEGDA/HA-SH 10.溶液。对于所有革兰氏阳性菌株,随着GO活性的增加,抗菌效果增强。对于两种革兰氏阴性菌,仅从125 U/L的酶活性开始显示出抗菌效果,对于大肠杆菌和铜绿假单胞菌,仅从250 U/L的酶活性开始显示出抗菌效果。加载≤250 U/L GO和2.5 wt%葡萄糖且葡萄糖含量恒定(2.5 wt%)的HB PEGDA/HA-SH 10.溶液因其快速形成特性、细胞相容性以及产生抗菌HO的能力,是有前景的制剂,值得对细菌感染治疗(如伤口护理)进行进一步研究。