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Related Concept Videos

COP Coated Vesicles00:59

COP Coated Vesicles

Membrane-enclosed structures called vesicles transport proteins and lipids across the cell. The vesicles derive their cargo from the plasma membrane, Golgi, ER, or endosome. Coated vesicles are spherical, protein-coated carriers with a 50–100 nm diameter that mediate bidirectional transport between the ER and the Golgi. The distribution of proteins between the ER and Golgi complex is dynamic and is maintained by different coated vesicles. Their formation is driven by the assembly of different...
Clathrin Coated Vesicles01:12

Clathrin Coated Vesicles

Clathrin-coated vesicles use endocytosis to transport receptors and lysosomal hydrolases from the Golgi to the lysosome in the late secretory pathway. Clathrin-mediated endocytosis was the first described endocytic process, and Clathrin-coated vesicles remain one of the most well-studied transport vesicles. The molecular machinery that generates clathrin-coated vesicles comprises over 50 proteins that precisely coordinate vesicle formation. Cell surface receptors concentrated in indented sites...
Micelles01:30

Micelles

Micelle formation is an intricate process that hinges on the properties of amphiphilic or amphipathic molecules and the conditions of the system in which they are found. Amphiphilic molecules, which have both hydrophilic (water-attracting) and hydrophobic (water-repelling) parts, play a critical role in this process.In aqueous environments, these molecules arrange themselves such that their hydrophilic heads are turned towards the water phase, while their hydrophobic tails are oriented away...
Pinching-off of Coated Vesicles01:32

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Vesicle budding is orchestrated by distinct cytosolic proteins such as adaptor proteins, coat proteins, and GTPases. To initiate vesicle budding, membrane-bending proteins containing crescent-shaped BAR domains bind to the lipid heads in the bilayer and distort the membrane to form a protein-coated vesicle bud. Adaptors proteins such as AP2 for clathrin-coated vesicles can nucleate on the deformed membrane. Finally, coat proteins such as clathrin or COPI and COPII assemble into a coat forming...
Colloids03:22

Colloids

Children at play often make suspensions such as mixtures of mud and water, flour and water, or a suspension of solid pigments in water known as tempera paint. These suspensions are heterogeneous mixtures composed of relatively large particles that are visible to the naked eye or can be seen with a magnifying glass. They are cloudy, and the suspended particles settle out after mixing. On the other hand, a solution is a homogeneous mixture in which no settling occurs and in which the dissolved...
Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

The cationic polymerization mechanism consists of three steps: initiation, propagation, and termination. In the initiation step of the polymerization process, the π bond of a monomer gets protonated by the Lewis acid catalyst, which is formed from boron trifluoride and water. The protonation of the π bond generates a carbocation stabilized by the electron‐donating group. In the propagation step, the π bond of the second monomer acts as a nucleophile and attacks the generated carbocation,...

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Synthesis and Characterization of Supramolecular Colloids
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Published on: April 22, 2016

Cationic vesicles from novel bolaamphiphilic compounds.

Mary Popov1, Charles Linder, Richard J Deckelbaum

  • 1Department of Clinical Biochemistry, Ben-Gurion University, Beer Sheva, Israel.

Journal of Liposome Research
|October 24, 2009
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Bolaamphiphiles with specific ester amide structures form stable nanovesicles for improved drug delivery. These stable vesicles demonstrated excellent stability in circulation, overcoming limitations of traditional cationic liposomes.

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Published on: April 8, 2020

Area of Science:

  • Biomaterials Science
  • Nanotechnology
  • Drug Delivery Systems

Background:

  • Cationic liposomes face challenges in targeted drug delivery due to rapid blood clearance.
  • Bolaamphiphiles forming monolayer membranes offer potential for enhanced vesicle stability, inspired by archaeosomes.

Purpose of the Study:

  • To investigate bolaamphiphiles with acetylcholine head groups and varied hydrophobic domains for stable nanovesicle formation.
  • To correlate bolaamphiphile structure with nanovesicle stability in vitro and in vivo for drug delivery applications.

Main Methods:

  • Synthesized and characterized a series of bolaamphiphiles with systematic structural modifications in the hydrophobic domain.
  • Formed nanovesicles and assessed their stability in phosphate-buffered saline (PBS) and mouse blood circulation.
  • Evaluated vesicle size, morphology, and drug encapsulation retention over time.

Main Results:

  • Bolaamphiphiles with short amide midsections formed unstable nanovesicles (80-120 nm) that lost payload within 24 hours in PBS.
  • Longer midsections yielded mixed fibers and more stable nanovesicles, while ester amide midsections produced highly stable spherical nanovesicles in PBS for days.
  • Vesicles with acetylcholine groups linked via the acetyl group were more stable than those linked via the amine.
  • In vitro stable vesicles exhibited good stability in mouse blood circulation post-intravenous administration.

Conclusions:

  • Bolaamphiphile structure, particularly the ester amide midsection, is critical for forming stable cationic nanovesicles.
  • Stable nanovesicles derived from specific bolaamphiphiles show promise for overcoming clearance issues in targeted drug delivery.
  • Findings provide structural insights for designing effective bolaamphiphile-based drug delivery systems.