HSPC:Chol Liposomes (CAT#: LDLY-0123-LY9)

Description
This product is mainly made of saturated Phosphatidylcholine (PC) and Cholesterol. PC is the most abundant phospholipid in eukaryotic cell membranes and it can form lipid bilayers. Cholesterol plays important role in liposome production. It can promote the accumulation of lipid chains and the formation of bilayers, reduce the fluidity of bilayers and the transmembrane transport of water-soluble drugs.
Lipid Composition
HSPC
Cholesterol
Applications
Control liposomes, Membrane biology
Format
Liquid
Concentration
10mg/mL
Hydration Solution
PBS, pH 7.4
External Solution
PBS, pH 7.4
Storage
2°C - 8°C (do not freeze)
Size
70-120 nm
Shelf Life
6 months
Quantity
5mL (available in lyophilized powder)
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DataSheet MSDS
FAQs Published Data Customer Reviews Related Sections
  1. What role does cholesterol play in HSPC:Chol liposomes?

    Cholesterol is crucial for stabilizing the lipid bilayers in these liposomes, enhancing the structural integrity and permeability, which is vital for drug delivery applications.

  2. Can HSPC:Chol liposomes be used for drug loading?

    Yes, these liposomes are often used for loading and delivering both hydrophilic and lipophilic drugs, improving the bioavailability and efficacy of the drugs.

  3. What are the main applications of HSPC:Chol liposomes?

    They are primarily used in drug delivery systems, particularly for targeting cancer cells, due to their ability to encapsulate and efficiently deliver therapeutic agents.

  4. How are HSPC:Chol liposomes typically synthesized?

    These liposomes can be prepared using methods such as thin-film hydration followed by extrusion, which helps achieve uniform size and encapsulation efficiency.

  5. What advantages do HSPC:Chol liposomes offer over other formulations?

    The specific ratio of HSPC to cholesterol in these liposomes provides a balance between fluidity and rigidity, offering enhanced circulation time and stability in biological systems.

HSPC:Chol (55:45) Liposomes-fig1


Rottlerin decreased the syncytial formation of FCoV.

This work investigates the rottlerin-liposome (RL)-induced inhibition of feline coronavirus (FCoV) infection. In order to obtain RL, researchers encapsulated rottlerin (R) in HSPC:Chol (55:45) liposomes. They compared R and RL's impact on the FCoV growth pattern in CRFK cells after that. The fluorescence intensity of the R and RL groups was much lower than that of the mock or liposome groups, as seen in stained cells under a fluorescence microscope (figure A-B). This indicates that both R and RL may inhibit FCoV replication. Moreover, the formation of syncytium is an indication of cell-cell fusion. The results (figure C) demonstrated a substantial reduction in the average number of nuclei per syncytium in RL and R treated cells compared to mock and liposome cells. These findings suggest that RL and R may inhibit FCoV syncytia formation at a later stage of infection, with RL exhibiting a greater effect. This work highlights that encapsulating R in HSPC:Chol (55:45) liposomes improve its inhibitory impact on FCoV, presenting a promising treatment option for FCoV infections.

Pubmed: 37368766 DOI: 10.3390/vetsci10060380

Choi, Jong-Chul, et al. "Rottlerin-Liposome Inhibits the Endocytosis of Feline Coronavirus Infection." Veterinary Sciences 10.6 (2023): 380.

  • Superior Delivery Efficiency
    Creative Biolabs has perfected HSPC:Chol liposomes to provide superior delivery efficiency, particularly for cancer therapeutics.
  • High Encapsulation Efficiency
    These liposomes demonstrate high encapsulation efficiency, allowing for effective loading of various pharmaceutical agents.
  • Targeted Drug Release
    Creative Biolabs' HSPC:Chol liposomes excel in targeted drug release, ensuring therapeutic agents reach the intended site of action.
  • Customizable for Research
    HSPC:Chol liposomes are highly customizable, fitting specific research requirements and enhancing experimental outcomes.

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For Research Use Only. Not For Clinical Use

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