scispace - formally typeset
Search or ask a question

What are the mechanisms by which saturated fatty acids contribute to the structural integrity of nanoparticles? 


Best insight from top research papers

Saturated fatty acids contribute to the structural integrity of nanoparticles through various mechanisms. They can affect protein conformation, fatty acid binding, and protein aggregation. Additionally, the high affinity and stable binding characteristics of fatty acids to albumin specific sites play a crucial role in preparing nanoparticles with increased drug content and stability. The presence of counterions can influence the adsorption and self-assembly of fatty acids on nanoparticle surfaces, leading to changes in morphology and interfacial activity, ultimately impacting stability. Moreover, in the presence of vesicles or cell membranes, lipid adsorption on nanoparticles can result in the formation of supported lipid bilayers, which resist cellular uptake and can lead to the encapsulation/release of drugs/DNA. Covalent conjugation between fatty acid-capped nanoparticles and proteins further enhances structural integrity, as seen in the development of nanobioconjugates.

Answers from top 4 papers

More filters
Papers (4)Insight
Saturated fatty acids, like stearic acid, covalently bind to nanoparticles via fatty acid binding domains on proteins, enhancing stability and structural integrity of the nanobioconjugate.
Saturated fatty acids contribute to nanoparticle integrity by forming lipid sheaths around supported lipid bilayers, enhancing structural stability and resisting cellular uptake.
The addition of ethanolamine as a counterion alters the morphology of decanoic acid on aminopropyl-modified silica nanoparticles, transitioning from discrete patches to a continuous bilayer, impacting foam stability.
Saturated fatty acids influence protein aggregation and conformation on nanoparticles by affecting fatty acid binding, protein stability, and uniformity of binding sites, enhancing structural integrity.

Related Questions

How do nanoparticles influence bacterial growth mechanisms?5 answersNanoparticles have a significant impact on bacterial growth mechanisms. They can act as bactericides, disrupting cell membranes and inhibiting microbial growth. Furthermore, metal oxide nanoparticles like Cu2O, Fe3O4, and Ag2O alter soil bacterial communities by reducing diversity and shifting abundance towards specific bacterial groups, potentially due to their antimicrobial properties. Nanoparticles, such as n-ZnO and n-TiO2, affect bacterial physiology by influencing metabolic pathways related to stress responses, oxidative stress, and stringent responses, ultimately impacting the ability of bacteria like Bacillus subtilis to resist stress. Utilizing nanoparticles as quorum quenchers against human pathogenic bacteria presents a promising strategy to combat multidrug resistance and virulence, offering an efficient alternative to traditional antibiotics with minimal resistance development.
What is the need of biosurfactant coating on nanoparticles?5 answersThe coating of nanoparticles with biosurfactants serves multiple crucial purposes. Biosurfactants, derived from microorganisms and plants, act as stabilizers and capping agents for nanoparticles, preventing aggregation and maintaining formulation stability. They reduce the formation of aggregates during nanoparticle synthesis, ensuring a uniform morphology and enhancing biocompatibility. Biosurfactants also play a significant role in reducing metal precursors and stabilizing nanoparticles, contributing to their eco-friendly and non-toxic nature. Moreover, biosurfactants can enhance the mobility of nanoparticles through porous media, promoting their transport characteristics and interactions with the environment. Overall, the use of biosurfactant coatings on nanoparticles is essential for improving stability, biocompatibility, and environmental interactions, making them valuable in various fields such as nanotechnology, bioremediation, and pharmaceuticals.
What are the common stabilizers for nanoparticles?3 answersPolymeric stabilizers are commonly used for nanoparticles. In the study by Derikov et al., diblock copolymers were found to be the most effective stabilizers for composites based on a diblock copolymer of styrene and 2-vinyl pyridine and spherical Au nanoparticles. Balestri et al. explored the use of a thermo-responsive copolymer poly(N,N-dimethylacrylamide)-block-poly(N-isopropylacrylamide) (PDMA-b-PNIPAM) as a stabilizer for lipid-based nanoparticles for drug delivery. Prud'homme et al. described the formation of core-shell-brush nanoparticles using an A-B-C triblock copolymer, where the A block acts as a stabilizing brush layer. Prajapati and Serajuddin used sugar esters as nanoparticle stabilizers in solid dosage forms. Capek discussed the use of various methods and reductants, such as surfactants and polymer coatings, for stabilizing noble metal nanoparticles.
Which method is used for the formulation of conventional lipid nanoparticles?4 answersThe method used for the formulation of conventional lipid nanoparticles is the mixing of an aqueous solution with a solid lipid matrix and a biocompatible non-ionic surfactant, followed by heating and cooling processes. This method allows for the production of solid lipid nanoparticles with a size of less than 500 nm. These lipid nanoparticles are composed of biodegradable lipids such as triglycerides, fatty acids, fatty alcohols, waxes, and butter, which turn solid at room temperature. The production of lipid nanoparticles can also be achieved through freeze-drying or spray-drying techniques, which result in a dry powder formulation suitable for pharmaceutical applications. These lipid nanoparticles offer advantages such as high stability, biodegradability, and the ability to incorporate a wide variety of drugs for effective targeting.
What are the different mechanisms by which nanoparticles can enter cells?5 answersNanoparticles can enter cells through various mechanisms. One mechanism is active endocytosis, where cells use different pathways to generate membrane curvature for nanoparticle uptake. Another mechanism is passive diffusion, where nanoparticles can passively diffuse across the lipid bilayer of the cell membrane. Additionally, nanoparticles can enter cells through clathrin-independent mechanisms, which do not involve the clathrin-mediated pathway typically observed for receptor-mediated endocytosis. Nanoparticles can also be internalized via receptor-mediated endocytosis, where they interact with specific receptors on the cell surface, such as the LDL receptor. Furthermore, nanoparticles can enter cells through active transport mechanisms, including microtubule-involved endocytosis. The size, shape, surface functional groups, and elasticity of nanomaterials can also affect their endocytosis into cells. Overall, understanding the different mechanisms of nanoparticle uptake into cells is crucial for designing effective drug delivery systems and improving biomedical applications.
How to characterize lipid nanoparticles?5 answersLipid nanoparticles (LNPs) can be characterized using various analytical tools. One common approach is the use of atomic force microscopy (AFM) to visualize the morphology of LNPs. AFM provides detailed information about the nanostructure of LNPs and can be used to visualize drug-loaded LNPs. Another method is dynamic light scattering (DLS), which is used to determine the average diameter and size distribution of LNPs. DLS analysis can help assess the stability of LNPs and provide information about their size. Flow cytometry is another technique that can be used to quantify and assess LNPs. It allows for the simultaneous measurement of size and structure of individual vesicles, providing high throughput analysis. Additionally, electron paramagnetic spectroscopy combined with molecular dynamics simulations can provide insights into the structure and dynamics of lipids in lipid nanodiscs. These techniques, along with others, contribute to our understanding and characterization of LNPs.

See what other people are reading

What if instead of complex formation, DNA and lipids are added separately?
5 answers
When DNA and lipids are added separately instead of forming complexes, it can impact the efficiency of gene delivery systems. The formation of hydrophobic DNA/lipid complexes is crucial for effective delivery of genetic material. Cationic lipids play a key role in binding to DNA, leading to the formation of these complexes. The charge ratio between the lipid and DNA is essential for successful complex formation. Additionally, the structure of the lipid/DNA complexes influences the kinetics of complex formation, with different lipids showing distinct pathways for complex assembly. Therefore, adding DNA and lipids separately may hinder the formation of these essential complexes, potentially reducing the efficacy of gene transfection systems.
What is the role of lipids in maintaining cell membrane function and structure?
5 answers
Lipids play crucial roles in maintaining cell membrane function and structure. They are not just structural components but also act as molecular chaperones, topological determinants, and organizers of biological machines. Lipids are essential for stabilizing membrane protein structures, mediating protein-protein interactions, and maintaining specific conformational states of membrane proteins. Furthermore, alterations in membrane lipid metabolism are associated with major diseases, highlighting the importance of understanding lipid diversity and their roles in cell signaling. Lipids also contribute to the mechanical stability of cell membranes, modulating their physical properties and affecting bilayer thickness and lipid ordering. Overall, lipids are dynamic molecules that interact with proteins, regulate cellular functions, and are vital for the integrity and functionality of cell membranes.
How to prevent aggregation of PC lipids?
5 answers
To prevent aggregation of phosphatidylcholine (PC) lipids, various methods can be employed based on the research findings. Incorporating a non-cationic lipid, such as a polyethylene glycol-based polymer, into lipid:nucleic acid complex particles containing cationic lipids and nucleic acid polymers can prevent particle aggregation. Additionally, the addition of oligosaccharide fatty acid esters (glycolipids) to liposomes inhibits aggregation and improves lipid packing in the bilayer membrane. Another effective approach involves the addition of KnockOut Serum Replacement (KSR) to pluripotent stem (PS) cell culture medium, which regulates cellular aggregation and enhances cell growth without affecting pluripotency. Furthermore, the prevention of liposome aggregation can be achieved by adding a divalent cation to the external aqueous phase when a multivalent anion is present on the liposome surface.
How does ethanol enhance skin permeation ?
5 answers
Ethanol enhances skin permeation through various mechanisms. It acts by extracting skin lipids and increasing the mobility of lipid chains, facilitating drug permeation. Additionally, ethanol's ability to form hydrogen bonds with skin lipid headgroup atoms contributes to its permeation-enhancing effect. Studies show that the permeability of carriers increases with longer alcohol chain lengths, with isopropanol being particularly effective. Furthermore, the pretreatment of skin with ethanol can either increase or decrease skin permeability depending on the concentration used, affecting the permeation of different compounds differently. Fatty alcohols, fatty acids, and their esters have also been recognized as effective skin penetration enhancers by disrupting lipid organization and increasing drug diffusivity. These findings collectively highlight the multifaceted role of ethanol and related compounds in enhancing skin permeation for drug delivery applications.
What is the role of cholesterol in the formation and function of cationic lipid/DNA complexes?
5 answers
Cholesterol plays a crucial role in the formation and function of cationic lipid/DNA complexes by enhancing transfection efficiency (TE) through various mechanisms. Studies have shown that cholesterol-containing lipoplexes exhibit efficient cellular entry via different endocytosis pathways, leading to high TE due to their ability to escape endosomes and undergo phase transitions in lipid formulations. Additionally, cholesterol-based cationic lipids with lysine headgroups demonstrate high pDNA binding affinity, larger-sized lipoplexes, and superior transfection efficacy compared to histidine headgroup counterparts. Furthermore, the incorporation of cholesterol in lipid membranes reduces the hydration repulsion layer, promoting fusion between cationic and endosomal membranes, facilitating complex release and enhancing TE in vitro.
What is the molecular mechanism behind platelet aggregation due to ibuprofen?
5 answers
Platelet aggregation induced by ibuprofen involves complex molecular mechanisms. Studies show that ibuprofen can interact synergistically with platelet mediators like arachidonic acid (AA) or 5-hydroxytryptamine (5-HT), leading to increased aggregation. The synergistic effect of AA with 5-HT or adenosine diphosphate (ADP) on platelets is inhibited by cyclooxygenase (COX) inhibitors and other specific inhibitors, highlighting the involvement of COX/thromboxane A2, receptor-operated Ca(2+) channels, Gq/PLC, and MAPK signaling pathways in this process. Additionally, ibuprofen derivatives have been synthesized and shown to protect platelets by mitigating oxidative stress-induced platelet apoptosis and inhibiting platelet aggregation, suggesting a potential therapeutic role in conditions associated with platelet activation and thrombocytopenia.
How macromolecular asymmetric charge distrubution affects macromolecular behaviour in crowded envoronment?
5 answers
Macromolecular asymmetric charge distribution in crowded environments can significantly impact macromolecular behavior. Studies have shown that macromolecular crowding, induced by molecules like polyethylene glycol (PEG) and dextran, alters the mechanism of pore formation in lipid bilayers, affecting conduction thresholds and osmotic pressure gradients. The excluded volume effects of macromolecular crowding favor protein folding due to increased compactness, leading to stabilization and altered protein behavior. Additionally, in the presence of crowders like PEG, the conformational preference of small molecular rotors can shift, affecting their behavior as molecular viscometers. Furthermore, membrane-bound enzymes, such as alkaline phosphatase, exhibit higher activity in crowded environments, with inhibitors showing paradoxical behaviors, emphasizing the complexity of enzymatic reactions in crowded media.
How macromolecular asymmetric charge distrubution affects macromolecular behaviour in crowded envoronment?
5 answers
Macromolecular asymmetric charge distribution in crowded environments can significantly impact macromolecular behavior. Studies have shown that macromolecular crowding alters the mechanism of pore formation in lipid bilayers, affecting conduction through pores due to excluded volume effects and changes in water interactions. Furthermore, the presence of crowders like polyethylene glycol (PEG) and Ficoll in crowded media influences the catalytic behavior of membrane-bound enzymes, with liposome-bound enzymes exhibiting higher activity and inhibitors showing paradoxical effects. Macromolecular crowding, characterized by excluded volume effects, can favor protein folding and stability, impacting protein structure, function, and interactions. Additionally, crowding can modulate the conformational preferences of small molecular rotors, shifting their behavior in crowded versus non-crowded media. Overall, macromolecular asymmetric charge distribution in crowded environments plays a crucial role in shaping macromolecular behavior and interactions.
Can lipid peroxidation lead to swelling of cell?
4 answers
Lipid peroxidation can indeed lead to cell swelling. Research indicates that arachidonic acid (AA) and linoleic acid hydroperoxide induce swelling in various cell types, including glioma cells and astrocytes. The process involves an increase in cell volume, potentially due to the activation of lipid peroxidation by fatty acids, leading to changes in membrane permeability and subsequent water influx into the cells. Additionally, lipid hydroperoxides like POPC-OOH have been shown to alter membrane structure and increase swelling between stacked bilayers, affecting membrane rigidity and hydration levels. These findings highlight the significant impact of lipid peroxidation on cellular swelling, emphasizing its role in cellular damage and potential implications in conditions like cerebral ischemia or trauma.
How does oligomeric state of the protein affect the immobilization of the protein?
5 answers
The oligomeric state of a protein significantly influences its immobilization process. Oligomerization, which involves the assembly of protein monomers into higher-order structures, plays a crucial role in determining the specificity and stability of subunit interactions. The interfacial interactions and overall packing geometry of individual monomers within the oligomer are essential for the immobilization process, as they dictate the binding affinity and recognition specificity between immobilized and soluble subunits. Furthermore, the oligomeric state affects the thermodynamic stability and allosteric regulation of proteins, which in turn impact the efficiency and effectiveness of protein immobilization techniques. Understanding the oligomeric state of a protein is therefore crucial for designing successful immobilization strategies that leverage the specific characteristics of protein assemblies.
Is that nanosponge can cross the intestinal barrier?
5 answers
Nanosponges, specifically curcumin-loaded nanosponges (CURNS), have shown the ability to enhance permeability and cross the intestinal barrier efficiently. These nanosponges, with an average particle size suitable for oral delivery, exhibit controlled drug release, particularly in the colon, indicating colon-specific release. Pharmacokinetic studies in rabbits revealed that CURNS significantly improved the bioavailability of curcumin compared to pure curcumin solution, demonstrating enhanced efficacy in crossing the intestinal barrier and systemic uptake. Additionally, nanoparticle properties such as size and surface chemistry have been reported to influence cellular adhesion, uptake, and transport, which are crucial factors in determining the intestinal transport potency of nanoparticles. Therefore, nanosponges, including CURNS, have shown promise in effectively crossing the intestinal barrier for targeted drug delivery applications.