Polyethylene glycol

聚乙二醇
  • 文章类型: Journal Article
    在这项研究中,通过粗粒分子动力学模拟研究了玉米醇溶蛋白/(-)-表没食子儿茶素-3-没食子酸酯/聚乙二醇(Zein/EGCG/PEG)复合纳米粒子的自组装机理及其在油水界面的界面吸附行为。傅里叶变换红外光谱和构象分析表明,玉米醇溶蛋白与EGCG之间存在静电和氢键相互作用,PEG和玉米醇溶蛋白之间的物理纠缠,EGCG和PEG之间的氢键相互作用。纳米粒子聚集在油水界面,油相和水相之间存在明显的界面层,共聚焦激光扫描显微镜和扫描电子显微镜显示。通过粗粒分子动力学模拟证实了玉米醇溶蛋白/EGCG/PEG纳米颗粒在油-水界面的吸附。进一步的研究结果证实,玉米醇溶蛋白/EGCG/PEG纳米颗粒可以作为具有自支撑结构的油凝胶的稳定剂,粘弹性固体行为和温度响应特性。当前的研究提供了一种新的方法来增强蛋白质界面特性并创建食品级乳化剂和油胶凝剂。
    In this study, the self-assembly mechanism of Zein/(-)-epigallocatechin-3-gallate/polyethylene glycol (Zein/EGCG/PEG) composite nanoparticles and their interface adsorption behavior at the oil-water interface were investigated by coarse-grained molecular dynamics simulation. Fourier transform infrared spectroscopy and conformation analysis demonstrated that there were electrostatic and hydrogen bond interactions between Zein and EGCG, physical entanglement between PEG and Zein, and hydrogen bond interaction between EGCG and PEG. The nanoparticles accumulated at the oil-water interface, and there was an obvious interface layer between oil phase and water phase, as indicated by confocal laser scanning microscope and scanning electron microscope. The adsorbing of Zein/EGCG/PEG nanoparticles at the oil-water interface was confirmed by coarse-grained molecular dynamics simulation. Further findings confirmed that Zein/EGCG/PEG nanoparticles could serve as stabilizers for oleogels with self-supporting structure, viscoelastic solid behavior and temperature response characteristics. The current research offered a novel approach to enhance protein interface characteristics and create food-grade emulsifiers and oleogelators.
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  • 文章类型: Journal Article
    一种被称为盐酸伊立替康的半合成喜树碱衍生物经常用于治疗结直肠癌。包括结直肠腺癌和涉及小细胞的肺癌。伊立替康的半衰期非常短;因此,需要连续输注以将药物的血液水平保持在治疗水平,会产生累积毒性。有效的交付技术,包括脂质体,是为了解决这些缺点而开发的。在这项研究中,一种连续的超临界流体方法,称为将超临界流体膨胀到水溶液中,其中压力迅速下降,但仍超过临界压力,建议制造携带盐酸伊立替康的聚乙二醇化(PEG化)脂质体。要做到这一点,聚乙二醇化脂质体使用Box-Behnken设计,和操作参数(流量,温度,和压降)进行了优化。封装效率,平均尺寸,制备的脂质体计数为94.6%,55nm,和758在理想情况下。此外,在8周内研究了聚乙二醇化脂质体的稳定性,并将聚乙二醇化脂质体负载伊立替康的释放曲线与常规脂质体和游离伊立替康进行了比较,并且在从脂质体的第一次突释后观察到恒定的药物释放。
    A semi-synthetic camptothecin derivative known as irinotecan hydrochloride is frequently used to treat colorectal cancer, including colorectal adenocarcinoma and lung cancers involving small cells. Irinotecan has a very short half-life; therefore, continuous infusions are required to keep the drug\'s blood levels at therapeutic levels, which could produce cumulative toxicities. Effective delivery techniques, including liposomes, have been developed to address these shortcomings. In this study, a continuous supercritical fluid approach dubbed Expansion Supercritical Fluid into an aqueous solution, in which the pressure decreases rapidly but remains over the critical pressure, is proposed to manufacture polyethylene glycolylated (PEGylated) liposomes carrying irinotecan hydrochloride. To accomplish this, PEGylated liposomes were created using a Box-Behnken design, and the operating parameters (flow rate, temperature, and pressure drop) were optimized. Encapsulation efficiency, mean size, and prepared liposome count were 94.6%, 55 nm, and 758 under ideal circumstances. Additionally, the stability of the PEGylated liposome was investigated during 8 weeks, and also PEGylated liposome-loaded irinotecan release profile was compared to conventional liposomes and free irinotecan, and a constant drug release was seen after the first burst release from liposomes.
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  • 文章类型: Journal Article
    这项研究调查了通过使用聚乙二醇(PEG)配制的酪胺(TA)对凡纳滨对虾免疫疾病抗性的延长作用。面对集约化农业的挑战,环境压力,和全球气候变化,改善虾健康的创新方法至关重要。研究重点是生物胺在应激反应和免疫调节中的作用。证明TA,特别是当与PEG结合时,显着延长对溶藻弧菌的免疫力和抵抗力。实验设计包括施用TA,PEG,和TA-PEG,随后是对豁免权的评估,乳酸和葡萄糖水平,和免疫相关的基因表达。结果显示总血细胞计数的显著延长效应,酚氧化酶活性,和吞噬活性在TA-PEG组,表明增强的免疫激活期。此外,在TA-PEG组中,酚氧化酶原系统相关基因的表达显著上调。此外,TA-PEG组在抗溶藻弧菌的敏感性试验中表现出明显更高的存活率。这项研究的结果证实,联合使用PEG可以有效地延长TA的免疫刺激持续时间。
    This study investigates the prolonged effect of immune disease resistance in Litopenaeus vannamei through the administration of tyramine (TA) formulated with polyethylene glycol (PEG). Facing the challenges of intensive farming, environmental stress, and global climate changes, innovative approaches to improve shrimp health are essential. The research focuses on the role of biogenic amines in stress response and immune regulation, demonstrating that TA, especially when combined with PEG, significantly prolongs immunity and resistance against Vibrio alginolyticus. The experimental design included administering TA, PEG, and TA-PEG, followed by evaluations of immunity, lactate and glucose levels, and immune-related gene expressions. Results showed notable prolonged effects in total hemocyte count, phenoloxidase activity, and phagocytic activity in the TA-PEG group, indicating enhanced immune activation period. Additionally, the expression of prophenoloxidase system-related genes was significantly upregulated in the TA-PEG group. Furthermore, the TA-PEG group exhibited a significantly higher survival rate in a susceptibility test against V. alginolyticus. The results of this study confirm that the combined use of PEG can effectively extend the immunostimulatory duration of TA.
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  • 文章类型: Journal Article
    创伤性脑损伤(TBI)是一个主要的公共卫生问题,可能导致长期的神经系统损害。钙蛋白酶是一种钙依赖性半胱氨酸蛋白酶,在TBI后几分钟内被激活,已知持续的钙蛋白酶激活会导致神经变性和血脑屏障失调。基于其在疾病进展中的作用,钙蛋白酶抑制已被确定为有希望的治疗靶标。开发钙蛋白酶抑制治疗剂的努力将受益于在受伤组织内以空间精度测量钙蛋白酶活性的能力。在这项工作中,我们设计了一种基于活性的纳米疗法(ABNT),可以感知和抑制TBI中的钙蛋白酶活性。为了感知钙蛋白酶的活动,我们掺入了钙蛋白酶的肽底物,侧翼是荧光团/猝灭剂对。为了抑制钙蛋白酶活性,我们掺入了calpastatin肽,钙蛋白酶的内源性抑制剂。将传感器和抑制剂肽都支架到聚合物纳米支架上以创建我们的ABNT。我们表明,在重组钙蛋白酶的存在下,我们的ABNT构建体能够感知和抑制钙蛋白酶活性。在TBI的小鼠模型中,全身给药ABNT可以通过被动积累进入病灶周围脑组织,并抑制皮质和海马中的钙蛋白酶活性。在细胞钙蛋白酶活性的分析中,我们观察到ABNT介导的神经元钙蛋白酶活性的抑制,内皮细胞,和皮质的小胶质细胞。通过大脑结构对神经元钙蛋白酶活性的比较,与海马神经元相比,我们观察到ABNT介导的皮质神经元对钙蛋白酶活性的抑制作用更大。此外,我们发现细胞凋亡依赖于钙蛋白酶抑制和脑结构。我们提出了一个治疗平台,可用于了解钙蛋白酶活性的区域和细胞特异性治疗抑制,以帮助为TBI的药物设计提供信息。
    Traumatic brain injury (TBI) is a major public health concern that can result in long-term neurological impairments. Calpain is a calcium-dependent cysteine protease that is activated within minutes after TBI, and sustained calpain activation is known to contribute to neurodegeneration and blood-brain barrier dysregulation. Based on its role in disease progression, calpain inhibition has been identified as a promising therapeutic target. Efforts to develop therapeutics for calpain inhibition would benefit from the ability to measure calpain activity with spatial precision within the injured tissue. In this work, we designed an activity-based nanotheranostic (ABNT) that can both sense and inhibit calpain activity in TBI. To sense calpain activity, we incorporated a peptide substrate of calpain flanked by a fluorophore/quencher pair. To inhibit calpain activity, we incorporated calpastatin peptide, an endogenous inhibitor of calpain. Both sensor and inhibitor peptides were scaffolded onto a polymeric nanoscaffold to create our ABNT. We show that in the presence of recombinant calpain, our ABNT construct is able to sense and inhibit calpain activity. In a mouse model of TBI, systemically administered ABNT can access perilesional brain tissue through passive accumulation and inhibit calpain activity in the cortex and hippocampus. In an analysis of cellular calpain activity, we observe the ABNT-mediated inhibition of calpain activity in neurons, endothelial cells, and microglia of the cortex. In a comparison of neuronal calpain activity by brain structure, we observe greater ABNT-mediated inhibition of calpain activity in cortical neurons compared to that in hippocampal neurons. Furthermore, we found that apoptosis was dependent on both calpain inhibition and brain structure. We present a theranostic platform that can be used to understand the regional and cell-specific therapeutic inhibition of calpain activity to help inform drug design for TBI.
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  • 文章类型: Case Reports
    泻药误用是众所周知的事件,最常见于与饮食失调作斗争的患者。聚乙二醇(PEG)3350是一种容易获得的,耐受性良好的渗透性泻药。高剂量的PEG3350可能会导致胃肠道不适,腹泻,脱水,和电解质不平衡,尽管很少报道全身毒性。此病例报告强调了与长期滥用PEG的严重水平相关的极为罕见的代谢紊乱。一名60岁的女性因精神状态改变而被送往急诊科。她被发现患有急性肾衰竭(ARF),阴离子间隙代谢性酸中毒(AGMA),和横纹肌溶解继发于过度使用PEG3350,需要持续肾脏替代治疗(CRRT)。CRRT三天后肾功能改善,没有发现除了摄入PEG以外的其他原因可以解释她的精神状态变化或代谢异常。该报告说明了在肾前和内在肾衰竭的情况下考虑渗透性泻药滥用的重要性。
    Laxative misuse is a well-known occurrence, most often identified in patients struggling with eating disorders. Polyethylene glycol (PEG) 3350 is a readily available, well-tolerated osmotic laxative. High doses of PEG 3350 may cause gastrointestinal upset, diarrhea, dehydration, and electrolyte imbalance, although systemic toxicity is infrequently reported. This case report highlights the exceedingly rare metabolic derangements associated with profound levels of protracted PEG misuse. A 60-year-old female presented to the emergency department with altered mental status. She was found to have acute renal failure (ARF), anion gap metabolic acidosis (AGMA), and rhabdomyolysis secondary to excessive PEG 3350 use, requiring continuous renal replacement therapy (CRRT). Renal function improved after three days of CRRT, and no alternative causes beyond PEG ingestion were found to account for her mental status changes or metabolic anomalies. This report illustrates the importance of considering osmotic laxative misuse in the setting of pre-renal and intrinsic renal failure.
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  • 文章类型: Journal Article
    聚乳酸(PLA)木塑复合材料由于其可生物降解性,与传统的石油基塑料相比具有显着优势。然而,解放军有几个缺点,包括高脆性,低耐热性,缓慢结晶,与生物质材料的相容性差,这限制了其潜在的应用。在本文中,我们研究了羧基封端的超支化聚酯(CHBP)对机械,结晶,聚乳酸/秸秆粉(SF)共混物通过挤出注塑成型的热性能。此外,我们加入传统增塑剂聚乙二醇(PEG)与CHBP协同增强PLA/SF复合材料的韧性。我们的结果表明,适当添加CHBP可以有效地改善PLA与秸秆粉之间的界面结合。CHBP的掺入也提高了拉伸强度,弯曲强度,冲击强度,断裂伸长率,热稳定性,和复合材料的结晶速率。此外,与单独使用PEG相比,CHBP和PEG的加入显著提高了复合材料的冲击强度。该方法还提高了材料的耐热性,减少了增塑剂的迁移。我们的研究证明了使用超支化聚合物和增塑剂来增强韧性的可行性,热稳定性,聚乳酸木塑复合材料的结晶性能,为提高这些复合材料的性能提供了新的途径。
    Polylactic acid (PLA) wood-plastic composites have a significant advantage over traditional petroleum-based plastics due to their biodegradability. However, PLA has several shortcomings, including high brittleness, low heat resistance, slow crystallization, and poor compatibility with biomass materials, which have limited its potential applications. In this paper, we investigated the effects of carboxy-terminated hyperbranched polyester (CHBP) on the mechanical, crystalline, and thermal properties of PLA/straw flour (SF) blends through extrusion injection molding. Additionally, we added the traditional plasticizer polyethylene glycol (PEG) to synergize with CHBP to enhance the toughness of PLA/SF composites. Our results showed that the appropriate addition of CHBP effectively improved the interfacial bonding between PLA and straw flour. The incorporation of CHBP also improved the tensile strength, bending strength, impact strength, elongation at break, thermal stability, and crystallization rate of the composites. Furthermore, the addition of both CHBP and PEG significantly improved the impact strength of the composites compared to using PEG alone. This method also improved the heat resistance of the material and reduced the migration of plasticizers. Our study demonstrates the feasibility of using hyperbranched polymers and plasticizers to enhance the toughness, thermal stability, and crystalline properties of PLA wood-plastic composites, providing a new approach to improving the properties of these composites.
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  • 文章类型: Journal Article
    外阴阴道念珠菌病(VVC)中的外源性和内源性活性氧(ROS)在促进白色念珠菌(CA)的菌丝形成中起关键作用,这表明清除ROS可以抑制CA菌丝的形成。通过使用新型四臂聚乙二醇(4Arm-PEG)衍生物(4Arm-PB)作为交联剂,配制了ROS敏感的水凝胶(CAS@4Arm-PB/CS),壳聚糖(CS)作为水凝胶基质,和卡泊芬净(CAS)作为抗CA的抗真菌药物。ROS敏感性,崩解机制,交联作用,肿胀程度,微观结构,模数,并对4Arm-PB的流变性能进行了表征。根据结果,5.0%4Arm-PB可以快速有效地交联0.5mg/mL的CS。4Arm-PB的ROS敏感性为10-50μM,表明ROS敏感性强。体外和体内抗CA结果表明,CAS@4Arm-PB/CS不仅清除了内源性和外源性ROS,抑制了CA菌丝和生物膜的形成,而且对CA感染引起的VVC小鼠的治疗具有重要意义。暗示一定的安全方面和体内适用性。本研究介绍了一种用于CS水凝胶配方的新型功能交联剂,为基于水凝胶的药物递送系统和VVC治疗的治疗策略提供了新的途径。
    Both exogenous and endogenous reactive oxygen species (ROS) in vulvovaginal candidiasis (VVC) play pivotal roles in promoting the hyphal formation of Candida albicans (CA), which suggests that clearing ROS could inhibit CA hyphae formation. A ROS-sensitive hydrogel (CAS@4Arm-PB/CS) was formulated by using a novel four-arm polyethylene glycol (4Arm-PEG) derivative (4Arm-PB) as a crosslinking agent, chitosan (CS) as the hydrogel matrix, and caspofungin (CAS) as the antifungal drug against CA. The ROS-sensitivity, disintegration mechanism, crosslinking action, swelling degree, microstructure, modulus, and rheological properties of 4Arm-PB were characterized. According to the results, 5.0 % 4Arm-PB could quickly and efficiently cross-link 0.5 mg/mL of CS. The ROS-sensitivity of 4Arm-PB was 10-50 μM, indicating a strong ROS sensitivity. The in vitro and in vivo anti-CA results indicated that CAS@4Arm-PB/CS not only cleared endogenous and exogenous ROS and inhibited the formation of CA hyphae and biofilm but also contributed beneficially to the treatment of VVC mice caused by CA infection, implying a certain safety aspect and an in vivo applicability. This research introduces a novel functional crosslinking agent for CS hydrogel formulation, presenting a new avenue for hydrogel-based drug delivery systems and therapeutic strategies for VVC treatment.
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  • 文章类型: Journal Article
    结直肠癌(CRC)是最常见和最具挑战性的恶性肿瘤之一,需要一些有效和更安全的化疗药物来治疗。在这项研究中,抗癌剂表柔比星(Epi)被装载在聚合物聚乙二醇-聚乳酸-纳米颗粒(mPEG-PLA-NP)包被的海洋抗癌无毒多糖岩藻依聚糖(FC),以实现针对CRC的协同活性。NPs的表征显示它们是球形的,单分散,稳定,具有负的zeta电位,并表现出良好的生物相容性和控制释放。发现NPs对HCT116细胞系的体外抗癌活性是有希望的,并与注射C26鼠癌细胞的BALB/C小鼠的体内研究得到了很好的证实。MTT测定结果表明游离Epi的IC50值为3.72µM,未涂覆和涂覆的Epi纳米制剂的含量为33.67和10.19µM,分别。较高的肿瘤消退,当这种新型NP制剂用于治疗荷瘤小鼠时,观察到更好的存活率和降低的场外心脏毒性。游离FC和Epi处理的小鼠显示肿瘤大小的37.73%和61.49%消退,而有79.76%和90.34%肿瘤消退的小鼠用无涂层EpiNP和有涂层EpiNP治疗,分别。因此,mPEG-PLA-FC-Epi-NP具有作为抗CRC的有效化疗制剂的潜力,因为它表现出更好的疗效和更低的毒性。
    Colorectal cancer (CRC) is one of the most common and challenging malignancy that needs some effective and safer chemotherapeutic agents for the treatment. In this study, anticancer agent epirubicin (Epi) was loaded in polymeric polyethylene glycol-polylactic acid-nanoparticles (mPEG-PLA-NPs) coated with a marine anti-cancer non-toxic polysaccharide fucoidan (FC), to achieve a synergistic activity against CRC. The characterization of the NPs revealed that they were spherical, monodispersed, stable, with a negative zeta potential, and exhibited good biocompatibility and controlled release. In vitro anti-cancer activity of the NPs on HCT116 cell line was found to be promising, and corroborated well with in vivo studies involving BALB/C mice injected with C26 murine cancer cells. The outcome of MTT assay demonstrated that IC50 value of free Epi was 3.72 µM, and that of non-coated and coated Epi nano-formulations was 33.67 and 10.19 µM, respectively. Higher tumor regression, better survival and reduced off-side cardiotoxicity were observed when this novel NPs formulation was used to treat tumor-bearing mice. Free FC and Epi treated mice showed 37.73 % and 61.49 % regression in tumor size, whereas there was 79.76 % and 90.34 % tumor regression in mice treated with non-coated Epi NPs and coated Epi NPs, respectively. Therefore, mPEG-PLA-FC-Epi-NPs hold a potential to be used as an effective chemotherapeutic formulation against CRC, since it exhibited better efficacy and lower toxicity.
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  • 文章类型: Journal Article
    结论:通过增加渗透调节能力,用发根R.ragenzones自然转化增强油菜的渗透胁迫耐受性,增强液压完整性和总抗氧化能力的维护。使用野生农杆菌菌株对植物的转化被称为自然转化,不在GMO法规中。例如,欧盟和日本。在这项研究中,发根根瘤菌自然转化油菜(甘蓝型油菜)的后代系,即,A11和B3(称为根诱导(Ri)系),进行了渗透胁迫恢复力研究。在聚乙二醇6000(PEG)10%(w/v)诱导的渗透胁迫下,Ri线,特别是A11,叶子枯萎不那么严重,较高的气孔导度(比WT高8.2倍),和稳定的叶片蒸腾速率(约2.9mmolm-2s-1)。尽管Ri系和WT之间的叶片相对含水量和叶片水势响应类似于PEG处理,A11和B3中重量与干重之比的显着降低表明Ri系中的渗透调节能力更大。此外,根中质膜固有蛋白基因(PIPs)的上调和Ri系叶片中这些基因的下调意味着与WT有关的水力完整性得到了更好的维持。此外,在PEG胁迫下,Ri系的总抗氧化能力(TAC)高于WT。总的来说,Ri品系对PEG诱导的渗透胁迫的耐受性增强可归因于更大的渗透调节能力,更好地维护液压完整性,TAC大于WT。此外,Ri基因(特别是rolA和rolD)在响应Ri油菜的渗透胁迫中起作用。本研究揭示了发根毛虫转化在植物抗旱性中的应用潜力。
    CONCLUSIONS: Natural transformation with R. rhizogenes enhances osmotic stress tolerance in oilseed rape through increasing osmoregulation capacity, enhancing maintenance of hydraulic integrity and total antioxidant capacity. Transformation of plants using wild strains of agrobacteria is termed natural transformation and is not covered by GMO legislation in, e.g., European Union and Japan. In this study, offspring lines of Rhizobium rhizogenes naturally transformed oilseed rape (Brassica napus), i.e., A11 and B3 (termed root-inducing (Ri) lines), were investigated for osmotic stress resilience. Under polyethylene glycol 6000 (PEG) 10% (w/v)-induced osmotic stress, the Ri lines, particularly A11, had less severe leaf wilting, higher stomatal conductance (8.2 times more than WT), and a stable leaf transpiration rate (about 2.9 mmol m-2 s-1). Although the leaf relative water content and leaf water potential responded similarly to PEG treatment between the Ri lines and WT, a significant reduction of the turgid weight to dry weight ratio in A11 and B3 indicated a greater capacity of osmoregulation in the Ri lines. Moreover, the upregulation of plasma membrane intrinsic proteins genes (PIPs) in roots and downregulation of these genes in leaves of the Ri lines implied a better maintenance of hydraulic integrity in relation to the WT. Furthermore, the Ri lines had greater total antioxidant capacity (TAC) than the WT under PEG stress. Collectively, the enhanced tolerance of the Ri lines to PEG-induced osmotic stress could be attributed to the greater osmoregulation capacity, better maintenance of hydraulic integrity, and greater TAC than the WT. In addition, Ri-genes (particularly rolA and rolD) play roles in response to osmotic stress in Ri oilseed rape. This study reveals the potential of R. rhizogenes transformation for application in plant drought resilience.
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  • 文章类型: Journal Article
    寻求有效的方法来维持细胞稳态对于生物体在遇到渗透胁迫时的生存至关重要。甘氨酸甜菜碱(GB)是一种广泛产生的天然渗透剂,但它的内生生产和作用是有限的。在这里,一种非离子表面活性剂十二烷基-β-d-吡喃葡萄糖苷(DG)和一种常见的聚合物聚乙二醇(PEG)被证明具有增强细胞和生物体模型的渗透胁迫(由糖浓度变化引起的)耐受性的能力,这些是巨大的单层囊泡(GUV)和革兰氏阴性大肠杆菌。DG或PEG仅诱导GUV的小尺寸减小和某些形状改变。重要的是,浓度比GB低100倍的DG或PEG有效地提高了细菌在低渗和高渗条件下的存活率。这个有趣的结果归因于DG的插入或PEG在脂质双层膜中的吸附,导致膜渗透性增强。这些外源物质可以代替GB,轻松高效地增强生物体对渗透胁迫的适应性。
    Seeking effective ways to maintain cellular homeostasis is crucial to the survival of organisms when they encounter osmotic stress. Glycine betaine (GB) is a widely generated natural osmolyte, but its endogenous production and action are limited. Herein, a kind of nonionic surfactant dodecyl-β-d-glucopyranoside (DG) and a common polymer polyethylene glycol (PEG) are proven to have the ability to enhance the osmotic stress (induced by sugar concentration changes) tolerance of cell and organism models, those are giant unilamellar vesicles (GUVs) and gram-negative Escherichia coli. DG or PEG only induces small size decrease and certain shape change of GUVs. Importantly, DG or PEG at the concentration 100 times lower than that of GB effectively increases the survival rate of bacteria under both hypoosmotic and hyperosmotic conditions. This intriguing result is attributed to the insertion of DG or adsorption of PEG in the lipid bilayer membrane, leading to enhanced membrane permeability. These exogenous substances can replace GB to facilely and highly efficiently augment adaptation of organisms to osmotic stress.
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