Pronanosome Liposome Cationic
Pronanosome Liposome Cationic
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Pronanosomes are ready- to-use formulations to obtain encapsulating nanovesicles in a fast and easy way.
Nanovesicles formed from Pronanosomes are able to encapsulate a wide variety of compounds as hydrophlic or lipophilic molecules, peptides, enzymes and proteins, among others. In addition, nanovesicles have a great stability, an easily controllable size and great entrapment efficiencies. A complete protocol of use is attached with the product, if you still have questions or need more information about the product, we help you. Nanovex Biotechnologies offers free advice for all products.
Nanovesicles obtained from Pronanosomes have multiple applications such as:
- Drug delivery and targeting
- Delivery of peptide drugs and proteins
- Studying Inmune response
- (Trans)dermal drug delivery systems
- Nutraceuticals and food applications
- Cosmetics
- Others
Pronanosome Lipo-Cat formulation is designed to obtain liposomes positively charged (cationic liposomes). Cationic nanovesicles can be endocyted by cells to achieve intracellular delivery. Besides, liposomes can be used in several applications as: drug delivery and targeting, delivery of peptides, drug and proteins, studying of inmune response, dermal or transdermal delivery, cosmetics, functional foods, nutraceuticals, …
Cationic liposomes have advantages such as:
- They are osmotically active and stable.
- They increase the stability of the entrapped drug
- Good solubilisation power
- Increased stability due to the surface electric charge
- Can increase the oral bioavailability of drugs
- Can enhance the skin penetration of drugs
- They can be used for oral, parenteral as well topical.
- Liposomes are biodegradable, biocompatible, and non-immunogenic.
- Improve the therapeutic performance of the drug by protecting it from the biological environment.
- Easily endocyted by cells – Intracellular delivery
- Exhibit good colloidal, chemical and biological stability
Cationic liposomes characteristics depending on the preparation method from Pronanosome Lipo-Cat
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