surfactants

表面活性剂
  • 文章类型: Journal Article
    纳米技术在医学中的研究也涉及眼部领域,纳米胶束是开发的应用之一。该方法用于增加疏水性药物的水溶性和它们在眼组织内/通过眼组织的渗透/渗透,因为纳米胶束能够将不溶性药物包封到它们的核心中,并且它们的小尺寸允许它们穿透和/或扩散通过眼组织的水性孔。
    本综述报告了有关纳米胶束使用的最重要和最新文献,由表面活性剂和两亲性聚合物组成,为了克服眼睛生理学在实现用于最大商业利益的治疗领域的药物的高生物利用度方面施加的限制:干眼,炎症,和青光眼。
    该领域的大量研究结果令人鼓舞,并证明纳米胶束可能是解决眼部治疗的一些挑战的答案。将来,自组装成胶束的新分子将能够满足其在眼用制剂中使用的上市许可的监管要求。
    UNASSIGNED: Research on nanotechnology in medicine has also involved the ocular field and nanomicelles are among the applications developed. This approach is used to increase both the water solubility of hydrophobic drugs and their penetration/permeation within/through the ocular tissues since nanomicelles are able to encapsulate insoluble drug into their core and their small size allows them to penetrate and/or diffuse through the aqueous pores of ocular tissues.
    UNASSIGNED: The present review reports the most significant and recent literature on the use of nanomicelles, made up of both surfactants and amphiphilic polymers, to overcome limitations imposed by the physiology of the eye in achieving a high bioavailability of drugs intended for the therapeutic areas of greatest commercial interest: dry eye, inflammation, and glaucoma.
    UNASSIGNED: The results of the numerous studies in this field are encouraging and demonstrate that nanomicelles may be the answer to some of the challenges of ocular therapy. In the future, new molecules self-assembling into micelles will be able to meet the regulatory requirements for marketing authorization for their use in ophthalmic formulations.
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  • 文章类型: Journal Article
    背景:腐蚀是一个具有挑战性且潜在有害的过程,涉及持续,通过涉及环境成分和电或化学过程的反应,金属结构的脉冲劣化。为了抑制腐蚀,添加各种添加剂。传统添加剂,另一方面,含有对环境有害的物质。表面活性剂更便宜,更容易制造,与标准缓蚀剂相比,具有较高的抑制效果和较低的毒性。它们通常用作腐蚀抑制剂以保护金属材料免受腐蚀。
    方法:表面活性剂分子的两亲性质促进在诸如金属/金属氧化物-水界面的表面上的吸附。表面活性剂在金属和金属氧化物上的吸附形成可以防止腐蚀的屏障。
    本文对表面活性剂作为腐蚀抑制剂的综述旨在对各种表面活性剂的物理和化学性质进行系统评估,表面活性剂对腐蚀抑制的影响,和用于腐蚀抑制的表面活性剂,可用于增强表面活性剂在各种环境中用作腐蚀抑制剂的功效。本文还讨论了几个参数对抑制表面活性剂分子系列腐蚀潜力的影响。
    BACKGROUND: Corrosion is a challenging and potentially harmful process that involves the continuing, impulsive deterioration of metallic structures via reactions involving environmental components and electro- or chemical processes. To inhibit corrosion, various additives are added. Traditional additives, on the other hand, contain environmentally hazardous substances. Surfactants are less expensive, easier to manufacture, and have high inhibitory efficacy and low toxicity compared to standard corrosion inhibitors. They are often employed as corrosion inhibitors to protect metallic materials against corrosion.
    METHODS: Surfactant molecules\' amphiphilic nature promotes adsorption at surfaces such as the metal/metal oxide-water interface. Surfactant adsorption on metals and metal oxides forms a barrier that can prevent corrosion.
    UNASSIGNED: This review of surfactants as corrosion inhibitors aims to offer a systemic evaluation of various surfactant physical and chemical properties, surfactant influence in corrosion inhibition, and surfactant used in corrosion inhibition that can be used to enhance the efficacy of surfactant use as corrosion inhibitors in a variety of environments. The effect of several parameters on the potential to suppress corrosion of surfactant molecule series is also discussed here.
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  • 文章类型: Journal Article
    用锌对小麦籽粒进行农艺生物强化可以改善约10亿人锌(Zn)缺乏症的状况。然而,随着在缺锌土壤中培育高产小麦品种的挑战以及全球需要生产更高质量的食物来滋养不断增长的人口,将锌直接输送到植物的战略创新将发挥作用。因此,现有的叶面配方将需要进一步改进,以保持竞争激烈的全球谷物市场所需的高农艺生产率,同时满足推荐给人类的膳食锌摄入量。新一代叶面肥可增加小麦植物中同化的Zn量以及Zn从叶子到谷物的转运效率,这可能是一个有前途的解决方案。近年来,有关佐剂和新兴纳米转运蛋白相对于用作小麦叶面肥的常规Zn形式的功效的研究迅速发展。这篇综述涵盖了文献中有关常规Zn形式的叶面施用导致的面包小麦(TriticumaestivumL.)生物强化的证据范围。锌纳米颗粒和新型锌叶面制剂。我们研究了叶面施用策略和达到的谷物锌的最终浓度。我们提出了一个概念模型,用于小麦谷物锌生物强化对叶面锌施用量的响应。这篇综述讨论了叶面应用锌运输的一些生理方面,需要进一步研究。最后,我们探索了工程化叶面纳米配方的前景,该配方可以有效地克服将锌输送到小麦籽粒的物理化学障碍。
    Agronomic biofortification of wheat grain with zinc can improve the condition of about one billion people suffering from zinc (Zn) deficiency. However, with the challenge of cultivating high-yielding wheat varieties in Zn-deficient soils and the global need to produce higher-quality food that nourishes the growing population, innovation in the strategies to deliver Zn directly to plants will come into play. Consequently, existing foliar formulations will need further refinement to maintain the high agronomic productivity required in competitive global grain markets while meeting the dietary Zn intake levels recommended for humans. A new generation of foliar fertilisers that increase the amount of Zn assimilated in wheat plants and the translocation efficiency of Zn from leaves to grains can be a promising solution. Research on the efficacy of adjuvants and emerging nano-transporters relative to conventional Zn forms applied as foliar fertilisers to wheat has expanded rapidly in recent years. This review scopes the range of evidence available in the literature regarding the biofortification of bread wheat (Triticum aestivum L.) resulting from foliar applications of conventional Zn forms, Zn nanoparticles and novel Zn-foliar formulations. We examine the foliar application strategies and the attained final concentration of grain Zn. We propose a conceptual model for the response of grain Zn biofortification of wheat to foliar Zn application rates. This review discusses some physiological aspects of transportation of foliarly applied Zn that need further investigation. Finally, we explore the prospects of engineering foliar nano-formulations that could effectively overcome the physicochemical barrier to delivering Zn to wheat grains.
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  • 文章类型: Journal Article
    作为生物活性分子,肽和蛋白质在生物体中是必需的,包括动物和人类。其功能缺陷导致人类的各种疾病。因此,使用蛋白质治疗多种疾病,比如癌症和肝炎,正在增加。有不同的途径来管理蛋白质,由于其大且亲水的结构而具有局限性。另一个限制是不允许蛋白质快速通过的生物和亲脂性膜的存在。有不同的策略来增加蛋白质从这些生物膜的吸收。这些策略之一是使用化合物作为吸收促进剂。吸收促进剂是化合物,如表面活性剂,磷脂,和环糊精,通过不同的机制增加蛋白质通过生物膜和它们的吸收。本文重点介绍了其他吸收促进剂的使用及其在蛋白质给药途径中的作用机制。
    As bioactive molecules, peptides and proteins are essential in living organisms, including animals and humans. Defects in their function lead to various diseases in humans. Therefore, the use of proteins in treating multiple diseases, such as cancers and hepatitis, is increasing. There are different routes to administer proteins, which have limitations due to their large and hydrophilic structure. Another limitation is the presence of biological and lipophilic membranes that do not allow proteins to pass quickly. There are different strategies to increase the absorption of proteins from these biological membranes. One of these strategies is to use compounds as absorption enhancers. Absorption enhancers are compounds such as surfactants, phospholipids and cyclodextrins that increase protein passage through the biological membrane and their absorption by different mechanisms. This review focuses on using other absorption enhancers and their mechanism in protein administration routes.
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  • 文章类型: Journal Article
    最近基于肽模拟物的药物的增加和对肽激素的日益增长的兴趣带来了对用于诊断目的的肽的定量的新关注。的确,血液中肽激素的循环浓度提供了身体状态的快照,并可能最终导致检测特定的健康状况。虽然非常有用,这些分子的量化,优选通过液相色谱与质谱联用,可能很棘手。首先,肽进行水解,氧化,和其他翻译后修饰,and,最重要的是,它们是生物基质中特异性和非特异性蛋白酶的底物。所有这些事件可能会在采样后继续,改变肽激素浓度。第二,因为它们包括带正电荷和负电荷的基团以及亲水和疏水残基,它们与环境相互作用;这些相互作用可能导致测量浓度的局部变化。诸如对实验室玻璃器皿或材料的非特异性吸附之类的现象通常对浓度有巨大影响,需要特别小心地控制。最后,肽的循环水平可能很低(皮卡或毫摩尔范围),增加上述影响的影响,并诱导需要高度敏感的仪器和优化的方法。因此,尽管这些肽和它们的基质极其多样,所有的分析都有一个共同的挑战:从取样到分析都需要保持浓度不变。虽然通常在优化分析上付出了巨大的努力,很少有研究深入考虑分析前步骤对结果的影响。通过实际例子,这篇面向解决方案的教程综述从临床实验室的角度解决了肽检测方法开发过程中遇到的典型分析前挑战.我们提供提示和技巧,以避免陷阱以及策略,以指导所有新的发展。我们的最终目标是提高分析前意识,以确保新开发的肽测定产生可靠和准确的结果。
    The recent increase in peptidomimetic-based medications and the growing interest in peptide hormones has brought new attention to the quantification of peptides for diagnostic purposes. Indeed, the circulating concentrations of peptide hormones in the blood provide a snapshot of the state of the body and could eventually lead to detecting a particular health condition. Although extremely useful, the quantification of such molecules, preferably by liquid chromatography coupled to mass spectrometry, might be quite tricky. First, peptides are subjected to hydrolysis, oxidation, and other post-translational modifications, and, most importantly, they are substrates of specific and nonspecific proteases in biological matrixes. All these events might continue after sampling, changing the peptide hormone concentrations. Second, because they include positively and negatively charged groups and hydrophilic and hydrophobic residues, they interact with their environment; these interactions might lead to a local change in the measured concentrations. A phenomenon such as nonspecific adsorption to lab glassware or materials has often a tremendous effect on the concentration and needs to be controlled with particular care. Finally, the circulating levels of peptides might be low (pico- or femtomolar range), increasing the impact of the aforementioned effects and inducing the need for highly sensitive instruments and well-optimized methods. Thus, despite the extreme diversity of these peptides and their matrixes, there is a common challenge for all the assays: the need to keep concentrations unchanged from sampling to analysis. While significant efforts are often placed on optimizing the analysis, few studies consider in depth the impact of pre-analytical steps on the results. By working through practical examples, this solution-oriented tutorial review addresses typical pre-analytical challenges encountered during the development of a peptide assay from the standpoint of a clinical laboratory. We provide tips and tricks to avoid pitfalls as well as strategies to guide all new developments. Our ultimate goal is to increase pre-analytical awareness to ensure that newly developed peptide assays produce robust and accurate results.
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  • 文章类型: Journal Article
    聚合物无定形固体分散体(ASD)是用于增强水溶性差的药物的溶解度的流行方法。然而,在用单一聚合物制备的ASD中实现物理稳定性和溶解性能可能是具有挑战性的。因此,可以添加第二赋形剂。在本文中,我们回顾了三类可以在内部添加到ASD中的添加剂:(I)第二种聚合物,形成三元药物-聚合物-聚合物ASD,(ii)抗衡离子,为了促进原位盐的形成,和(iii)表面活性剂。在用聚合物组合制备的ASD中,每种聚合物都发挥着独特的功能,例如固态稳定剂和溶解期间的结晶抑制剂。ASD中的原位盐形成通常导致玻璃化转变温度的大幅增加,有助于提高物理稳定性。表面活性剂可以增强ASD颗粒的润湿性,从而促进药物的快速释放。然而,它们对物理稳定性和溶解的潜在不利影响,由于增强的分子迁移率和与聚合物的竞争性分子相互作用,分别,值得仔细考虑。最后,我们讨论了硬脂酸镁和无机盐的影响,在下游加工时外部添加的赋形剂,ASD片剂的固态稳定性和溶出度。
    Polymeric amorphous solid dispersion (ASD) is a popular approach for enhancing the solubility of poorly water-soluble drugs. However, achieving both physical stability and dissolution performance in an ASD prepared with a single polymer can be challenging. Therefore, a secondary excipient can be added. In this paper, we review three classes of additives that can be added internally to ASDs: (i) a second polymer, to form a ternary drug-polymer-polymer ASD, (ii) counterions, to facilitate in situ salt formation, and (iii) surfactants. In an ASD prepared with a combination of polymers, each polymer exerts a unique function, such as a stabilizer in the solid state and a crystallization inhibitor during dissolution. In situ salt formation in ASD usually leads to substantial increases in the glass transition temperature, contributing to improved physical stability. Surfactants can enhance the wettability of ASD particles, thereby promoting rapid drug release. However, their potential adverse effects on physical stability and dissolution, resulting from enhanced molecular mobility and competitive molecular interaction with the polymer, respectively, warrant careful consideration. Finally, we discuss the impact of magnesium stearate and inorganic salts, excipients added externally upon downstream processing, on the solid-state stability as well as the dissolution of ASD tablets.
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  • 文章类型: Journal Article
    基于脂质的制剂(LBF)是通过口服施用将疏水性药物递送到体循环中的有效方法。然而,关于LBF的胶体行为及其与胃肠道(GI)环境内容物的相互作用的许多物理细节尚未得到很好的表征。最近,研究人员已开始使用分子动力学(MD)模拟来研究LBF系统的胶体行为及其与胆汁和胃肠道中其他物质的相互作用。MD是一种计算方法,基于经典力学,模拟原子的物理运动,并提供无法使用实验研究轻松检索的原子尺度信息。MD可以提供以成本和时间有效的方式帮助开发药物制剂的见解。本文综述了MD模拟在胆汁研究中的应用,胆汁盐,和LBF及其在GI环境中的行为,还讨论了基于脂质的mRNA疫苗制剂的MD模拟。
    Lipid-based formulation (LBF) is an effective approach for delivering hydrophobic drugs into the systemic circulation by oral administration. However, much of the physical detail regarding the colloidal behavior of LBFs and their interactions with the contents of the gastrointestinal (GI) environment is not well characterized. Recently, researchers have started to use molecular dynamics (MD) simulations to investigate the colloidal behavior of LBF systems and their interactions with bile and other materials present in the GI tract. MD is a computational method, based on classical mechanics, that simulates the physical movements of atoms and provides atomic-scale information that cannot easily be retrieved using experimental investigations. MD can provide insight into assist the development of drug formulations in a cost and time-effective manner. This review summarizes the application of MD simulation to the study of bile, bile salts, and LBFs and their behavior within the GI environment and also discusses MD simulations of lipid-based mRNA vaccine formulations.
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  • Wound healing refers to the complex process of restoring the forms and functions of damaged tissues. Multiple growth factors and released cytokines tightly regulate the wound site. Healing processes can be disrupted by any alteration that would aggravate the damage and lengthen the repair process. Some of the conditions that may impair wound healing include infections and inflammation. Surfactants are amphiphilic compounds widely used in various formulations including detergents, food, pharmaceuticals and cosmetics. Biosurfactants, therefore, are surface-active compounds produced by biological agents, particularly yeast or bacteria, and represent a safer and environmentally preferred alternative to chemical surfactants. Numerous studies have targeted surface-active molecules as wound healing agents for their anti-inflammatory, antioxidant and antibacterial potential. This review focuses on surface-active molecules used in wound healing activities and analyses their effectiveness and mechanisms of action.
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  • 文章类型: Journal Article
    目的:随着人们越来越意识到常规表面活性剂对环境和人类健康的潜在不利影响,人们对开发生物基表面活性剂(被认为更安全,更实惠,丰富,是可生物降解的,生物相容性和具有可扩展性,在个人护理产品中的温和和配方性能)。
    方法:关于烷基多葡糖苷(APG)和蔗糖酯(SE)作为生物基表面活性剂的综合文献综述,通过镜头对12个绿色化学原理进行了研究。还提供了生物基表面活性剂在个人护理产品中的用途的概述。
    结果:生物基表面活性剂主要来源于天然来源(即头部和尾部分子基团)。一种更常见的生物基表面活性剂是具有碳水化合物头基的表面活性剂,其中烷基多葡糖苷(APGs)和蔗糖酯(SE)领导这个子类别。随着全球法规和用户对可持续性和安全性的要求不断提高,进一步支持这些生物基表面活性剂作为其石化对应物的替代品的证据是有利的。使用绿色化学框架是做到这一点的合适方法。虽然许多讨论的原则是在工业上执行的,其他仅在实验室规模应用或在文献中不明显。
    结论:目前在合成APG和SE中使用了许多绿色化学原理。这些和其他生物基表面活性剂应该,因此,被认为是常规表面活性剂的合适和可持续的替代品。为了进一步鼓励使用这些新型表面活性剂,行业必须努力在商业层面实施和改进其余原则的使用。
    OBJECTIVE: With increasing awareness of the potential adverse impact of conventional surfactants on the environment and human health, there is mounting interest in the development of bio-based surfactants (which are deemed to be safer, more affordable, are in abundance, are biodegradable, biocompatible and possess scalability, mildness and performance in formulation) in personal care products.
    METHODS: A comprehensive literature review around alkyl polyglucosides (APGs) and sucrose esters (SEs) as bio-based surfactants, through the lens of the 12 green chemistry principles was conducted. An overview of the use of bio-based surfactants in personal care products was also provided.
    RESULTS: Bio-based surfactants are derived primarily from natural sources (i.e. both the head and tail molecular group). One of the more common types of bio-based surfactants are those with carbohydrate head groups, where alkyl polyglucosides (APGs) and sucrose esters (SEs) lead this sub-category. As global regulations and user mandate for sustainability and safety increase, evidence to further support these bio-based surfactants as alternatives to their petrochemical counterparts is advantageous. Use of the green chemistry framework is a suitable way to do this. While many of the discussed principles are enforced industrially, others have only yet been applied at a laboratory scale or are not apparent in literature.
    CONCLUSIONS: Many of the principles of green chemistry are currently used in the synthesis of APGs and SEs. These and other bio-based surfactants should, therefore, be considered suitable and sustainable alternatives to conventional surfactants. To further encourage the use of these novel surfactants, industry must make an effort to implement and improve the use of the remaining principles at a commercial level.
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  • 文章类型: Journal Article
    Surfactant stabilized Gold (Au) nanomaterials (NMs) have been documented extensively in recent years for numerous sensing applications in the academic literature. Despite the crucial role these surfactants play in the sensing applications, the comprehensive reviews that highlights the fundamentals associated with these assemblies and impact of these surfactants on the properties and sensing mechanisms are still quite scare. This review is an attempt in organizing the vast literature associated with this domain by providing critical insights into the fundamentals, preparation methodologies and sensing mechanisms of these surfactant stabilized Au NMs. For the simplification, the surfactants are divided into the typical and advanced surfactants and the Au NMs are classified into Au nanoparticles (NPs) and Au nanoclusters (NCs) depending upon the complexity in structure and size of the NMs respectively. The preparative methodologies are also elaborated for enhancing the understanding of the readers regarding such assemblies. The case studies regarding surfactant stabilized Au NMs were further divided into colorimetric sensors, surface plasmonic resonance (SPR) based sensors, luminescence-based sensors, and electrochemical/electrical sensors depending upon the property utilized by the sensor for the sensing of an analyte. Future perspectives are also discussed in detail for the researchers looking for further progress in that particular research domain.
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