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Journal articles on the topic 'Small unilamellar vesicles (SUV)'

Author: Grafiati

Published: 7 June 2025

Last updated: 2 August 2025

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1

Kinoshita, Misaki, Erina Kakimoto, Mayu S. Terakawa та ін. "Model membrane size-dependent amyloidogenesis of Alzheimer's amyloid-β peptides". Physical Chemistry Chemical Physics 19, № 24 (2017): 16257–66. http://dx.doi.org/10.1039/c6cp07774a.

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We herein report the mechanism of amyloid formation of amyloid-β (Aβ) peptides on small (SUV) and large unilamellar vesicles (LUVs), which consist of 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC) lipids.

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Chappa, Veronica, Yuliya Smirnova, Karlo Komorowski, Marcus Müller, and Tim Salditt. "The effect of polydispersity, shape fluctuations and curvature on small unilamellar vesicle small-angle X-ray scattering curves." Journal of Applied Crystallography 54, no. 2 (2021): 557–68. http://dx.doi.org/10.1107/s1600576721001461.

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Small unilamellar vesicles (20–100 nm diameter) are model systems for strongly curved lipid membranes, in particular for cell organelles. Routinely, small-angle X-ray scattering (SAXS) is employed to study their size and electron-density profile (EDP). Current SAXS analysis of small unilamellar vesicles (SUVs) often employs a factorization into the structure factor (vesicle shape) and the form factor (lipid bilayer electron-density profile) and invokes additional idealizations: (i) an effective polydispersity distribution of vesicle radii, (ii) a spherical vesicle shape and (iii) an approximat

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3

Li, Bingxuan, Haopu Wang, Zhen Wang, Huikai Xie, and Yao Lu. "High-Efficiency Drug Loading in Lipid Vesicles by MEMS-Driven Gigahertz Acoustic Streaming." Micromachines 16, no. 5 (2025): 562. https://doi.org/10.3390/mi16050562.

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Drug carriers hold significant promise for precision medicine but face persistent challenges in balancing high encapsulation efficiency with structural preservation during active loading. In this study, we present a microelectromechanical system (MEMS)-driven platform that can generate gigahertz (GHz)-frequency acoustic streaming (1.55 GHz) to enable nondestructive, power-tunable drug encapsulation in lipid vesicles. Utilizing DSPE-PEG-modified bilayers with hydrodynamic shear forces, our method achieves transient membrane permeability that preserves membrane integrity while permitting control

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Dargel, Carina, Friederike Gräbitz-Bräuer, Ramsia Geisler, et al. "Stable DOPG/Glycyrrhizin Vesicles with a Wide Range of Mixing Ratios: Structure and Stability as Seen by Scattering Experiments and Cryo-TEM." Molecules 26, no. 16 (2021): 4959. http://dx.doi.org/10.3390/molecules26164959.

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Phosphatidylglycerols represent a large share of the lipids in the plasmamembrane of procaryotes. Therefore, this study investigates the role of charged lipids in the plasma membrane with respect to the interaction of the antiviral saponin glycyrrhizin with such membranes. Glycyrrhizin is a natural triterpenic-based surfactant found in licorice. Vesicles made of 1,2-dioleoyl-sn-glycero-3-phospho-rac-(1’-glycerol) (DOPG)/glycyrrhizin are characterized by small-angle scattering with neutrons and X-rays (SANS and SAXS). Small-angle scattering data are first evaluated by the model-independent modi

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HUANG, Huan, Judith M. BALL, Jeffrey T. BILLHEIMER, and Friedhelm SCHROEDER. "Interaction of the N-terminus of sterol carrier protein 2 with membranes: role of membrane curvature." Biochemical Journal 344, no. 2 (1999): 593–603. http://dx.doi.org/10.1042/bj3440593.

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Although neither the physiological function nor the mechanism of action of sterol carrier protein 2 (SCP2) is yet completely clear, it is thought that SCP2 interacts with membranes to elicit its biological effects. The results presented here show that the SCP2 N-terminus, composed of two amphipathic α-helices, interacted preferentially with highly curved but not lower-curvature membranes containing anionic phospholipid. CD spectra of SCP2 showed up to 1.2-fold increased α-helical content, on the interaction of SCP2 with small unilamellar vesicles (SUV) (median radius 10-14 nm) but less with la

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Kavecansky, J., F. Schroeder, and C. H. Joiner. "Deoxygenation-induced alterations in sickle cell membrane cholesterol exchange." American Journal of Physiology-Cell Physiology 269, no. 5 (1995): C1105—C1111. http://dx.doi.org/10.1152/ajpcell.1995.269.5.c1105.

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Changes in a membrane sterol exchange of sickle red blood cells (SS RBC) induced by deoxygenation were studied using the fluorescent cholesterol analogue dehydroergosterol (DHE). DHE uptake by SS RBC membrane was measured by the incubation of SS RBC with small unilamellar vesicles (SUV) containing DHE. Deoxygenation of SS RBC, but not normal RBC, increased the rate of DHE uptake. DHE membrane content after 5 h of incubation with SUV in the cell-to-SUV ratio of 1:1 (mol lipid) was 16.25 +/- 0.94 and 12.22 +/- 0.85% of total sterol for deoxygenated and oxygenated cells, respectively. Membrane sp

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Terashima, Masaaki, Kazuo Hibi, and Shigeo Katoh. "Permeability of small hydrophilic solutes in small unilamellar vesicle (SUV)." Biochemical Engineering Journal 4, no. 1 (1999): 77–79. http://dx.doi.org/10.1016/s1369-703x(99)00025-x.

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8

Annisa, Rahmi. "Spanlastic as a Transdermal Drug Delivery System: A Systematic Review." Biomedical and Pharmacology Journal 18, no. 1 (2025): 447–57. https://doi.org/10.13005/bpj/3099.

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Spanlastic is an innovative drug delivery system that traps drugs in a core cavity with a double-layer structure. The term spanlastic comes from the combination of Span and elastic, first introduced in 2011. This plastic is a development of liposomes and niosomes that have been modified sophisticatedly; several types of spanlastic include Multi Lamellar Vesicles (MLV) with a bilayer structure, size 0.5-1.0 microns, easy to make, frequently used, and long-term stable. Large Unilamellar Vesicles (LUV) measuring 100 nm-1 μm have a high water or lipid ratio and can accommodate more drugs; Small Un

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9

Lymberopoulos, A., C. Demopoulou, M. Kyriazi, et al. "Liposome percutaneous penetration in vivo." Toxicology Research and Application 1 (January 1, 2017): 239784731772319. http://dx.doi.org/10.1177/2397847317723196.

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Objectives: Liposomes are reported as penetration enhancers for dermal and transdermal delivery. However, little is known about their percutaneous penetration and as to at which level they deliver encapsulated drugs. The penetration of multilamellar vesicles (MLVs) and small unilamellar vesicles (SUVs), in comparison to one of their lipid components, was investigated. Methods: Using the fluorescent lipid, Lissamine Rhodamine B-PE (R), as a constituent, MLV and SUV liposomes were prepared, tested, and R, MLV, or SUV were applied in vivo on the back of hairless mice. Absorption of each was evalu

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VERKADE, Henkjan J., Marjan A. C. de BRUIJN, Menno A. BRINK, et al. "Interactions between organic anions, micelles and vesicles in model bile systems." Biochemical Journal 320, no. 3 (1996): 917–23. http://dx.doi.org/10.1042/bj3200917.

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Biliary lipid secretion probably involves both ‘micellization’ and ‘vesiculization’ of bile-canalicular membrane lipids. Several hydrophilic organic anions inhibit the secretion of lipids into the bile without altering bile salt secretion [Verkade, Vonk and Kuipers (1995) Hepatology 21, 1174–1189]. Hydrophobic organic anions do not interfere with biliary lipid secretion. We investigated whether the organic-anion-induced inhibition of biliary lipid secretion in vivo could be attributed to inhibition of micellization, by the application of in vitro models of micellization. Carboxyfluorescein was

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11

de Freitas, Camila Fabiano, Italo Rodrigo Calori, André Luiz Tessaro, Wilker Caetano, and Noboru Hioka. "Rapid formation of Small Unilamellar Vesicles (SUV) through low-frequency sonication: An innovative approach." Colloids and Surfaces B: Biointerfaces 181 (September 2019): 837–44. http://dx.doi.org/10.1016/j.colsurfb.2019.06.027.

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12

Kanichay, Roby, Lawrence T. Boni, Peter H. Cooke, and Tapan K. Khan. "Calcium-induced aggregation of archaeal bipolar tetraether liposomes derived from the thermoacidophilic archaeonSulfolobus acidocaldarius." Archaea 1, no. 3 (2003): 175–83. http://dx.doi.org/10.1155/2003/603528.

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Previously, we showed that the proton permeability of small unilamellar vesicles (SUVs) composed of polar lipid fraction E (PLFE) from the thermoacidophilic archaeonSulfolobus acidocaldariuswas remarkably low and insensitive to temperature (Komatsu and Chong 1998). In this study, we used photon correlation spectroscopy to investigate the time dependence of PLFE SUV size as a function of Ca2+concentration. In the absence of Ca2+, vesicle diameter changed little over 6 months. Addition of Ca2+, however, immediately induced formation of vesicle aggregates with an irregular shape, as revealed by c

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13

Schnitzler, Lukas G., Kathrin Baumgartner, Anna Kolb, Benedikt Braun, and Christoph Westerhausen. "Acetylcholinesterase Activity Influenced by Lipid Membrane Area and Surface Acoustic Waves." Micromachines 13, no. 2 (2022): 287. http://dx.doi.org/10.3390/mi13020287.

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According to the current model of nerve propagation, the function of acetylcholinesterase (AChE) is to terminate synaptic transmission of nerve signals by hydrolyzing the neurotransmitter acetylcholine (ACh) in the synaptic cleft to acetic acid (acetate) and choline. However, extra-synaptic roles, which are known as ‘non-classical’ roles, have not been fully elucidated. Here, we measured AChE activity with the enzyme bound to lipid membranes of varying area per enzyme in vitro using the Ellman assay. We found that the activity was not affected by density fluctuations in a supported lipid bilay

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14

Maguire, Leigh A., Hu Zhang, and P. Ayazi Shamlou. "Preparation of small unilamellar vesicles (SUV) and biophysical characterization of their complexes with poly-l-lysine-condensed plasmid DNA." Biotechnology and Applied Biochemistry 37, no. 1 (2003): 73. http://dx.doi.org/10.1042/ba20020107.

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15

Kósa, Nikoletta, Ádám Zolcsák, István Voszka, et al. "Comparison of the Efficacy of Two Novel Antitubercular Agents in Free and Liposome-Encapsulated Formulations." International Journal of Molecular Sciences 22, no. 5 (2021): 2457. http://dx.doi.org/10.3390/ijms22052457.

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Tuberculosis is one of the top ten causes of death worldwide, and due to the appearance of drug-resistant strains, the development of new antituberculotic agents is a pressing challenge. Employing an in silico docking method, two coumaran (2,3-dihydrobenzofuran) derivatives—TB501 and TB515—were determined, with promising in vitro antimycobacterial activity. To enhance their effectiveness and reduce their cytotoxicity, we used liposomal drug carrier systems. Two types of small unilamellar vesicles (SUV) were prepared: multicomponent pH-sensitive stealth liposome (SUVmixed) and monocomponent con

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16

Akib, Nur Illiyyin, Ines Septiani, Wa Ode Sitti Zubaydah, Halimahtussaddiyah R, and Rifa’atul Mahmudah. "Preparasi Salbutamol Sulfat dalam Pembawa Vesikuler Etosom." Majalah Farmasetika 6, no. 2 (2021): 129. http://dx.doi.org/10.24198/mfarmasetika.v6i2.29890.

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Tujuan penelitian ini adalah memperoleh formula dan metode preparasi yang sesuai untuk preparasi salbutamol sulfat ke dalam pembawa vesikuler etosom. Preparasi dilakukan dengan metode panas (40oC) dan metode dingin (30oC) dengan variasi konsentrasi fosfatidilkolin sebagai pembentuk vesikel (2% dan 3%) dan etanol sebagai peningkat penetrasi ke dalam kulit (20%, 30%, dan 40%). Karakteristik vesikel yang dianalisis adalah ukuran, bentuk, dan efisiensi penjerapan vesikel. Ukuran dan bentuk vesikel diamati dengan mikroskop optik binokuler. Analisis efisiensi penjerapan dilakukan dengan metode spekt

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17

Peptu, Catalina, Marcel Popa, and Sophia G. Antimisiaris. "Release of Liposome-Encapsulated Calcein from Liposome Entrapping Gelatin-Carboxymethylcellulose Films: A Presentation of Different Possibilities." Journal of Nanoscience and Nanotechnology 8, no. 5 (2008): 2249–58. http://dx.doi.org/10.1166/jnn.2008.169.

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Liposome entrapment in films consisting of gelatin (GEL) or GEL/sodium carboxymethylcellulose (NaCMC) mixtures, as a method to alter drug release kinetics from polymeric films and/or incorporate sensitive bioactive molecules in solid films, was investigated. Bulk or thin complex (liposome trapping) films were formed by crosslinking (with glutaraldehyde) solutions of GEL or GEL/NaCMC in presence of calcein-encapsulating or rhodamine-labeled liposomes (Rho-Lip). Rho-Lip were observed by confocal microscopy to be homogenously distributed in the films. Calcein release from films was evaluated for

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18

Tu, Shuyang, Haijiao Zhang, Yawen Li, et al. "Effect of Shiga Toxin on Inhomogeneous Biological Membrane Structure Determined by Small-Angle Scattering." Applied Sciences 11, no. 15 (2021): 6965. http://dx.doi.org/10.3390/app11156965.

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Inhomogeneous structure occurring in biological membranes being rich in glycosphingolipids (GSL) has been proposed as an important phenomenon involved in the cellular endocytosis process. However, little is known about the correlation between the formation of microdomains and the GSL-dependent biogenesis for tubular endocytic pits occurred on the surface of the cellular membrane. In the present work, the interaction between the bacterial Shiga toxin from Escherichia coli (STxB) and its cellular receptor GSL globotriaosylceramide (Gb3) were studied using small unilamellar vesicle (SUV). The mod

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19

Verkade, H. J., J. T. Derksen, A. Gerding, G. L. Scherphof, R. J. Vonk, and F. Kuipers. "Differential hepatic processing and biliary secretion of head-group and acyl chains of liposomal phosphatidylcholines." Biochemical Journal 275, no. 1 (1991): 139–44. http://dx.doi.org/10.1042/bj2750139.

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To investigate the contribution of plasma-derived phosphatidylcholine (PC) to bile PC, the hepatic processing and biliary secretion of liposome-associated PC was studied in rats. For this purpose, small unilamellar vesicles (SUV), containing trace amounts of [2-palmitoyl-9,10-3H]dipalmitoylphosphatidylcholine ([palmitoyl-3H]DPPC), [choline-14C]-dipalmitoylphosphatidylcholine ([choline-14C]DPPC), di[14C]palmitoylphosphatidylcholine ([14C]DPPC) or di[1-14C]-oleoylphosphatidylcholine ([14C]DOPC), were administered intravenously to unanaesthetized rats, equipped with permanent catheters in heart a

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20

Hoffmann, Ingo, Claudia Hoffmann, Bela Farago, Sylvain Prévost, and Michael Gradzielski. "Dynamics of small unilamellar vesicles." Journal of Chemical Physics 148, no. 10 (2018): 104901. http://dx.doi.org/10.1063/1.5009424.

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21

Bhuyan, Mouchumi, and Burkhard Koenig. "Temperature responsive phosphorescent small unilamellar vesicles." Chemical Communications 48, no. 60 (2012): 7489. http://dx.doi.org/10.1039/c2cc33279e.

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22

Virden, Jud W., and John C. Berg. "The steric stabilization of small unilamellar vesicles." Journal of Colloid and Interface Science 153, no. 2 (1992): 411–19. http://dx.doi.org/10.1016/0021-9797(92)90332-g.

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23

Heller, William T. "Small-Angle Neutron Scattering for Studying Lipid Bilayer Membranes." Biomolecules 12, no. 11 (2022): 1591. http://dx.doi.org/10.3390/biom12111591.

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Small-angle neutron scattering (SANS) is a powerful tool for studying biological membranes and model lipid bilayer membranes. The length scales probed by SANS, being from 1 nm to over 100 nm, are well-matched to the relevant length scales of the bilayer, particularly when it is in the form of a vesicle. However, it is the ability of SANS to differentiate between isotopes of hydrogen as well as the availability of deuterium labeled lipids that truly enable SANS to reveal details of membranes that are not accessible with the use of other techniques, such as small-angle X-ray scattering. In this

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24

Humphry-Baker, Robin, David H. Thompson, Yabin Lei, Michael J. Hope, and James K. Hurst. "Structural investigations of dihexadecyl phosphate small unilamellar vesicles." Langmuir 7, no. 11 (1991): 2592–601. http://dx.doi.org/10.1021/la00059a033.

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25

Lohse, Brian, Pierre-Yves Bolinger, and Dimitrios Stamou. "Encapsulation Efficiency Measured on Single Small Unilamellar Vesicles." Journal of the American Chemical Society 130, no. 44 (2008): 14372–73. http://dx.doi.org/10.1021/ja805030w.

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26

Li, Feng, Sylvain Prévost, Ralf Schweins, et al. "Small monodisperse unilamellar vesicles from binary copolymer mixtures." Soft Matter 5, no. 21 (2009): 4169. http://dx.doi.org/10.1039/b904522h.

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27

Oberdisse, J. "Transition from small to big charged unilamellar vesicles." European Physical Journal B 3, no. 4 (1998): 463–69. http://dx.doi.org/10.1007/s100510050336.

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28

Chao, Meng-Hsuan, Yen-Ting Lin, Namasivayam Dhenadhayalan, Hsin-Lung Lee, Hsin-Yen Lee, and King-Chuen Lin. "3D Probed Lipid Dynamics in Small Unilamellar Vesicles." Small 13, no. 13 (2017): 1603408. http://dx.doi.org/10.1002/smll.201603408.

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29

Kensil, Charlotte Read, and Edward A. Dennis. "Action of cobra venom phospholipase A2 on large unilamellar vesicles: Comparison with small unilamellar vesicles and multibilayers." Lipids 20, no. 2 (1985): 80–83. http://dx.doi.org/10.1007/bf02534212.

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30

Garg, Sumit, Francisco Castro-Roman, Lionel Porcar, et al. "Cholesterol solubility limit in lipid membranes probed by small angle neutron scattering and MD simulations." Soft Matter 10, no. 46 (2014): 9313–17. http://dx.doi.org/10.1039/c4sm01219d.

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The solubility limits of cholesterol in small unilamellar vesicles made of POPS and POPC were probed using Small Angle Neutron Scattering (SANS) and coarse grained (CG) molecular dynamics (MD) simulations.

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31

Caliari, Adriano, Martin M. Hanczyc, Masayuki Imai, Jian Xu, and Tetsuya Yomo. "Quantification of Giant Unilamellar Vesicle Fusion Products by High-Throughput Image Analysis." International Journal of Molecular Sciences 24, no. 9 (2023): 8241. http://dx.doi.org/10.3390/ijms24098241.

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Artificial cells are based on dynamic compartmentalized systems. Thus, remodeling of membrane-bound systems, such as giant unilamellar vesicles, is finding applications beyond biological studies, to engineer cell-mimicking structures. Giant unilamellar vesicle fusion is rapidly becoming an essential experimental step as artificial cells gain prominence in synthetic biology. Several techniques have been developed to accomplish this step, with varying efficiency and selectivity. To date, characterization of vesicle fusion has relied on small samples of giant vesicles, examined either manually or

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32

Anderson, W. H., V. V. Kumar, W. J. Baumann, and E. W. Thompson. "Characterization of Phospholipid Vesicles with Freeze Fracture, Negative Staining, and Nuclear Magnetic Resonance Spectroscopy." Proceedings, annual meeting, Electron Microscopy Society of America 46 (1988): 246–47. http://dx.doi.org/10.1017/s0424820100103292.

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Phospholipid vesicles are used as models of biological membranes in which the constituent lipids can be defined and interactions among them can be studied without interference from other membrane components. Phospholipid vesicles are also attracting interest as drug carriers. Entrapment of drugs in liposomes reduces toxicity and improves targeting to specific tissue sites. Small unilamellar vesicles are easily prepared by sonication and are usually stable and uniform in size. However, because of their small size and high curvature, these vesicles poorly mimic natural membranes and their entrap

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33

Schrijvers, A. H., P. M. Frederik, M. C. Stuart, et al. "Formation of multilamellar vesicles by addition of tannic acid to phosphatidylcholine-containing small unilamellar vesicles." Journal of Histochemistry & Cytochemistry 37, no. 11 (1989): 1635–43. http://dx.doi.org/10.1177/37.11.2809174.

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Tannic acid induces aggregation and formation of multilamellar vesicles when added to preparations of small unilamellar vesicles, specifically those containing phosphatidylcholine. Aggregation and clustering of vesicles was demonstrated by cryo-electron microscopy of thin films and by freeze-fracture technique. Turbidity measurements revealed an approximately one-to-one molar ratio between tannic acid and phosphatidylcholine necessary for a fast and massive aggregation of the small unilamellar vesicles. When tannic acid-induced aggregates were dehydrated and embedded for conventional thin-sect

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34

Choudhury, Sharmistha Dutta, Manoj Kumbhakar, Sukhendu Nath, and Haridas Pal. "Photoinduced bimolecular electron transfer kinetics in small unilamellar vesicles." Journal of Chemical Physics 127, no. 19 (2007): 194901. http://dx.doi.org/10.1063/1.2794765.

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Lawrence, S. M., M. J. Lawrence, and D. J. Barlow. "MOLECULAR ARCHITECTURE OF PHOSPHATIDYLCHOLINE SMALL UNILAMELLAR VESICLES (PC SUV'S)." Journal of Pharmacy and Pharmacology 42, S1 (1990): 49P. http://dx.doi.org/10.1111/j.2042-7158.1990.tb14422.x.

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Pfeiffer, Indriati, and Fredrik Höök. "Quantification of Oligonucleotide Modifications of Small Unilamellar Lipid Vesicles." Analytical Chemistry 78, no. 21 (2006): 7493–98. http://dx.doi.org/10.1021/ac061280p.

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37

Hauser, Helmut, and George Strauss. "Stabilization of small unilamellar phospholipid vesicles during spray-drying." Biochimica et Biophysica Acta (BBA) - Biomembranes 897, no. 2 (1987): 331–34. http://dx.doi.org/10.1016/0005-2736(87)90429-9.

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Becerra, N., L. R. de la Nuez, A. L. Zanocco, E. Lemp, and G. Günther. "Solubilization of dodac small unilamellar vesicles by sucrose esters." Colloids and Surfaces A: Physicochemical and Engineering Aspects 272, no. 1-2 (2006): 2–7. http://dx.doi.org/10.1016/j.colsurfa.2005.04.024.

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39

Özden, M. Y., and V. N. Hasirci. "Preparation and characterization of polymer coated small unilamellar vesicles." Biochimica et Biophysica Acta (BBA) - General Subjects 1075, no. 1 (1991): 102–8. http://dx.doi.org/10.1016/0304-4165(91)90081-q.

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Sekharam, K. Madhavi, Thomas D. Bradrick, and S. Georghiou. "Kinetics of melittin binding to phospholipid small unilamellar vesicles." Biochimica et Biophysica Acta (BBA) - Biomembranes 1063, no. 1 (1991): 171–74. http://dx.doi.org/10.1016/0005-2736(91)90367-h.

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41

Vever-Bizet, Christine, and Daniel Brault. "Kinetics of incorporation of porphyrins into small unilamellar vesicles." Biochimica et Biophysica Acta (BBA) - Biomembranes 1153, no. 2 (1993): 170–74. http://dx.doi.org/10.1016/0005-2736(93)90402-l.

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42

Bhatia, Tripta, Peter Husen, Jonathan Brewer, et al. "Preparing giant unilamellar vesicles (GUVs) of complex lipid mixtures on demand: Mixing small unilamellar vesicles of compositionally heterogeneous mixtures." Biochimica et Biophysica Acta (BBA) - Biomembranes 1848, no. 12 (2015): 3175–80. http://dx.doi.org/10.1016/j.bbamem.2015.09.020.

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43

Brzustowicz, Michael R., and Axel T. Brunger. "X-ray scattering from unilamellar lipid vesicles." Journal of Applied Crystallography 38, no. 1 (2005): 126–31. http://dx.doi.org/10.1107/s0021889804029206.

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An improved small-angle X-ray scattering (SAXS) method for determining asymmetric lipid bilayer structure in unilamellar vesicles is presented. From scattering theory, analytic expressions are derived for the bilayer form factor over flat and spherical geometries, assuming the lipid bilayer electron density to be composed of a series of Gaussian shells. This is in contrast to both classic diffraction and Guinier hard-shell SAXS methods which, respectively, are capable only of ascertaining symmetric bilayer structure and limited-resolution asymmetric structure. Using model fitting and direct ca

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Vrushali, Satpute, and Sawant Dnyaneshwari. "Silver nanoparticles in medicine and technology: Synthesis, functionality and future prospects." World Journal of Advanced Research and Reviews 24, no. 1 (2024): 1502–16. https://doi.org/10.5281/zenodo.15037257.

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Nanomaterials, particularly nanoparticles (NPs), have emerged as forefront materials of the 21st century due to their unique properties and potential applications. Silver nanoparticles (AgNPs) are among the most attractive inorganic nanomaterials, widely used due to their significant antibacterial properties, broad-spectrum activity, and potential applications across various fields, including health, food storage, textiles, and environmental solutions. AgNPs exhibit a large surface-area-to-volume ratio, enabling enhanced interaction with bacterial cells, making them effective in medical and in

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Uhríková, Daniela, José Teixeira, Adrián Lengyel, László Almásy, and Pavol Balgavý. "Formation of unilamellar dipalmitoylphosphatidylcholine vesicles promoted by Ca2+ions: A small-angle neutron scattering study." Spectroscopy 21, no. 1 (2007): 43–52. http://dx.doi.org/10.1155/2007/576282.

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Dipalmitoylphosphatidylcholine (DPPC) was hydrated in 0.2–60 mM solution of CaCl2in heavy water and thoroughly homogenized by freezing-thawing process. Small-angle neutron scattering (SANS) shows formation of unilamellar vesicles in the range 1–60 mM of CaCl2. From the Kratky–Porod plot ln [I(Q)Q2] vs.Q2of SANS intensityI(Q)in the range of scattering vectorsQcorresponding to the interval 0.001 Å−2≤Q2≤0.006 Å−2, the vesicle bilayer radius of gyrationRgand the bilayer thickness parameterdgwere obtained. The structure of the bilayer displays different behavior for the gel phase and the liquid-cry

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Wu, Xiaofeng, and Qiu-Tian Li. "Ca2+-induced fusion of sulfatide-containing phosphatidylethanolamine small unilamellar vesicles." Journal of Lipid Research 40, no. 7 (1999): 1254–62. http://dx.doi.org/10.1016/s0022-2275(20)33487-8.

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Wang, Chen-An, Yi-Qi Yeh, Chung-Yuan Mou, Chun-Jen Su, Wei-Ru Wu, and U.-Ser Jeng. "Small-angle-scattering resolved catanionic unilamellar vesicles as molecule carriers." Materials Chemistry and Physics 277 (February 2022): 125435. http://dx.doi.org/10.1016/j.matchemphys.2021.125435.

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Cornell, Bruce A., Jack Middlehurst, and Frances Separovic. "Small unilamellar phospholipid vesicles and the theories of membrane formation." Faraday Discussions of the Chemical Society 81 (1986): 163. http://dx.doi.org/10.1039/dc9868100163.

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Brown, Michael F., Amir Salmon, Ulf Henriksson, and Olle Söderman. "Frequency dependent2H N.M.R. relaxation rates of small unilamellar phospholipid vesicles." Molecular Physics 69, no. 2 (1990): 379–83. http://dx.doi.org/10.1080/00268979000100271.

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Wu, Xiaofeng, and Qiu-Tian Li. "Hydration and stability of sulfatide-containing phosphatidylethanolamine small unilamellar vesicles." Biochimica et Biophysica Acta (BBA) - Biomembranes 1416, no. 1-2 (1999): 285–94. http://dx.doi.org/10.1016/s0005-2736(98)00229-6.

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