Liposomes in Cosmetics

 

A.V.S. Himabindu*, K. Kavya, U. Vimala Kumari, T. Mounika, D. Deepthi Akshaya,

 K. Lakshmi Prasanna, K. Padmalatha

Department of Pharmaceutics, Vijaya Institute of Pharmaceutical Sciences for Women,

Enikepadu, Vijayawada – 521108.

*Corresponding Author E-mail: satyahimabindu@gmail.com

 

ABSTRACT:

Liposomes can be used as cutaneous delivery carriers because they are tiny, unilamellar, and have membrane flexibility. As a result, liposomes are widely used in cutaneous applications, either as protective systems for active substances or to provide moisturizing characteristics. Liposomal drug-delivery systems were first employed in cosmetics in 1987, but they are now widely used in hundreds of ads in various forms such as gels, creams, and moisturizers. Liposome lipids contain moisture, therefore when the liposomal vesicle ruptures, moisture attaches to the skin surface, giving hydration. Liposomes allow us to overcome some limitations, such as low penetration, solubility, stability, duration of effect, and high side effects or expenses, while also improving some other qualities. Liposomes have been researched for a variety of cosmeceutical applications, including acne therapy, hyperpigmentation and melasma, vitiligo, and alopecia, as well as antioxidant and UV protection. Liposomal formulations have been proven in studies to be more effective in promoting therapeutic activity than non-liposomal counterparts, making them interesting candidates for enhancing the effectiveness of cosmeceutical therapies.

 

KEYWORDS: Liposomes, Types of liposomes, Skin permeation, Applications.

 


 

 

INTRODUCTION:

Liposomes have emerged as a revolutionary technology in the cosmetics industry, offering advanced delivery systems for active ingredients. These microscopic vesicles mimic the skin's natural lipid layer, enhancing the penetration and effectiveness of skincare products. 1,2

 

Definition and Structure:

Liposomes are spherical vesicles composed of phospholipid bilayers that can encapsulate both hydrophilic (water-soluble) and hydrophobic (oil-soluble) substances. These structures are similar to cell membranes, allowing them to effectively deliver active ingredients into the deeper layers of the skin.

 

·         Size: Typically ranging from 50 nm to several micrometers.

·         Composition: Composed of natural or synthetic lipids, primarily phospholipids like phosphatidylcholine.3,4

 

Fig 1: Structure of the Liposome

 

Historical Background:

·         1960s: Liposomes were first discovered by Alec D. Bangham.

·         1980s: The cosmetic industry began exploring liposomes for their potential in enhancing skincare formulations.

 

The Role of Liposomes in Skincare:

Enhanced Delivery System:

Liposomes facilitate the transport of active ingredients into the skin, bypassing the stratum corneum (the outermost layer of the skin). This targeted delivery ensures that active compounds reach their intended site of action, improving the overall efficacy of skincare products.

 

Improved Efficacy of Active Ingredients

Liposomes protect sensitive ingredients from degradation and enhance their stability. This encapsulation allows for controlled release, ensuring a sustained effect on the skin.5-7

 

Benefits of Liposomes in Cosmetics:

Increased Hydration:

Mechanism: Liposomes form a protective barrier on the skin, reducing transepidermal water loss (TEWL) and locking in moisture.

Result: Enhanced skin hydration and a smoother complexion.

 

Anti-Aging Properties:

·         Collagen Stimulation: Antioxidants and peptides delivered liposomally increase collagen synthesis and minimize wrinkles and fine lines.

·         Oxidative Stress Reduction: Fine lines and wrinkles are reduced via liposomal administration of antioxidants and peptides, which increases collagen formation.

·         Skin Repair and Protection

·         Barrier Repair: Liposomes aid in repairing the skin's natural barrier, promoting healing and reducing inflammation.

·         UV Protection: UV filters are added to liposomes to increase their stability and efficacy.8-10

 

Types of Cosmetic Liposomes:

 

Fig 2: Various Types of Cosmetic Liposomes

 

1. Conventional Liposomes:

Structure: Comprised of one or more phospholipid bilayers surrounding an aqueous core.Typically formed using natural or synthetic phospholipids, such as phosphatidylcholine.

Characteristics:

·         Versatile: Suitable for encapsulating both hydrophilic and lipophilic substances.

·         Biocompatible: Mimic the natural lipid bilayer of skin cells, enhancing compatibility and reducing irritation.

·         Stability: Can be prone to oxidation and hydrolysis, requiring stabilization methods.

 

2. Niosomes:

Structure: Non-ionic surfactant-based vesicles with a similar structure to liposomes but without phospholipids.

Characteristics:

·         Cost-Effective: Often less expensive to produce than conventional liposomes.

·         Stable: More resistant to oxidative degradation.

·         Flexible Composition: Can be customized by altering the surfactant composition.

 

3. Ethosomes:

Structure: Similar to conventional liposomes but contain a high concentration of ethanol.

Characteristics:

·         Enhanced Penetration: Ethanol disrupts the lipid bilayer of the skin, allowing deeper penetration.

·         Increased Flexibility: Ethanol provides flexibility, enabling better skin absorption.

·         Improved Solubility: Effective for delivering lipophilic compounds.

 

4. Transferosomes:

Structure: Ultra-flexible liposomes composed of phospholipids and edge activators, such as surfactants, that enhance their deformability.

 

Characteristics:

·         Highly Elastic: Can squeeze through narrow channels in the skin, reaching deeper layers.

·         Efficient Delivery: Particularly effective in transporting large molecules.

·         Adaptable: Can carry a variety of active ingredients.

 

5. Lipid Nanoparticles (LNPs):

Structure: Solid or semi-solid lipid matrix in which active ingredients are embedded.

Characteristics:

·         High Stability: More stable than traditional liposomes, with a longer shelf life.

·         Controlled Release: Capable of sustained release of active ingredients.

·         Enhanced Bioavailability: Improved absorption and effectiveness of encapsulated compounds.

 

6. Virosomes:

Structure: Liposomes modified with viral envelope proteins, mimicking the viral structure without the infectious component.

Characteristics:

·         Targeted Delivery: Utilize viral proteins to enhance targeting and uptake by skin cells.

·         Immune Stimulation: Can be used to enhance the skin's immune response.

·         Biocompatible: Designed to be safe and non-toxic.

 

7. Sphingosomes:

Structure: Liposomes incorporating sphingolipids, particularly ceramides, which are naturally found in the skin.

Characteristics:

·         Skin-Like Composition: Mimic the skin's natural lipid structure, promoting repair and hydration.

·         Barrier Enhancement: Strengthen the skin's barrier function.

·         Moisture Retention: Improve the skin's ability to retain moisture.

 

8. Phytosomes:

Structure: Lipid-based vesicles specifically designed for the encapsulation of plant-based compounds.

Characteristics:

·         Natural Ingredients: Focus on delivering botanical extracts and natural actives.

·         Enhanced Absorption: Improve the bioavailability of plant-derived compounds.

·         Eco-Friendly: Align with the growing trend towards natural and sustainable cosmetics.10-13

 

 

Applications in Cosmetic Products:

 

 

Fig 3: Applications of Liposomes in Cosmetics

 

Moisturizers:

Liposomes enhance the delivery of hydrating agents, such as hyaluronic acid and glycerin, ensuring long-lasting moisture retention.

Serums:

High concentrations of active ingredients like vitamins C and E are encapsulated in liposomes for improved stability and penetration.

Anti-Aging Creams:

Retinol and peptide-enriched formulations benefit from liposomal encapsulation, reducing irritation and enhancing effectiveness.

Sunscreens:

Liposomes improve the photostability of UV filters, providing broad-spectrum protection with minimal skin irritation.

Challenges and Considerations:

Stability Issues:

·         Oxidation and Hydrolysis: Liposomes are prone to degradation, affecting their stability and efficacy.

·         Solution: Formulation adjustments and the use of stabilizing agents can mitigate these issues.

 

Cost Implications:

The production of liposomal formulations is often more expensive than traditional methods, impacting the overall cost of cosmetic products.

 

Regulatory Aspects:

·         Regulatory Compliance: Ensuring that liposomal products meet safety and efficacy standards set by regulatory bodies.

·         Consumer Education: Informing consumers about the benefits and science behind liposomal skincare.

·         Future Trends in Liposomal Skincare:

·         Personalized Skincare: Development of customized liposomal formulations tailored to individual skin needs.

·         Green Chemistry: Emphasis on sustainable and eco-friendly liposome production methods.

·         Nanotechnology: Integration of nanotechnology to further enhance the delivery and performance of liposomal skincare products.13-15

CONCLUSION:

The diverse types of cosmetic liposomes offer unique advantages in the formulation of skincare products. By selecting the appropriate liposome type, formulators can enhance the delivery and performance of active ingredients, providing consumers with more effective and targeted skincare solutions. As technology advances, the development of innovative liposomal systems will continue to revolutionize the cosmetics industry, meeting the evolving demands of consumers for high-performance skincare products.

 

REFERENCES:

1.        Kaur IP, Kapila M, Agarwal R. Role of novel delivery systems in developing topical antioxidants as therapeutics to combat photoageing. Ageing Res Rev. 2007; 6(4): 271-88.

2.        Nastruzzi C, Esposito E, Menegatti E, Walde P. Use nano stability of liposomes in dermatological preparations. J Appl Cosmetol. 1993; 11: 77-91.

3.        Kumarn GP, Pogaku R. Nonionic surfactant vesicular systems for effective drug delivery—An overview. Acta Pharmaceutica Sinica B. 2011; 1(4): 208- 219.

4.        Balasubramanian J, Narayanan N, Kumar V. Resealed erythrocytes: A novel drug carrier in drug delivery. Drug Discovery. 2012; 2(6): 30-32.

5.        Moussaoui, N., Cansell, M. and Denizot, A. Marinosomes® marine lipid-based liposomes: physical characterization and potential applications in cosmetics. Int. J. Pharm. 242: 361– 365.

6.        Nounou MI, EI-Khordagui LK, Khalafallah NA, Khalil SA. Liposomal formulation for dermal and transdermal drug delivery: past, present and future. Recent Pat Drug Deliv Formul. 2008; 2(1): 9-18.

7.        Wagner A, Vorauer-Uhl K and Katinger H: Liposomes produced in a pilot scale: Production, purification and efficiency aspects. Eur. J Pharm Biopharm 2002; 54: 213–219.

8.        Karn PR and Hwang SJ: Advances in liposome preparation methods. Liposomal Delivery Systems: Advances and Challenges 2015: 6–23.

9.        Nastruzzi C, Esposito E, Menegatti E, Walde P. Use nano stability of liposomes in dermatological preparations. J Appl Cosmetol. 1993; 11:77–91.

10.      Vinardell MP, Mitjans M. Nanocarriers for delivery of antioxidants on the skin. Cosmetics. 2015; 2(4): 342–54.

11.      A. L. P. Kaur and R. Agrawal Nanotechnology Paradigm in Cosmeceuticals Recent Patents Drug Deliv Formul. 2007; 2(1): 171-82.

12.      Sharma SK, A. A. M, and N. Mahadevan Nanotechnology Aproach for Cosmetics Int J Recent Adv Pharm Res. 2012; 2: 54-61.

13.      Dragicevic N, Maibach HI. Percutaneous Penetration Enhancers Physical Methods in Penetration Enhancement. Springer; 2017.

14.      Rieger M, Rhein LD. Surfactants in Cosmetics. 68. CRC Press; 1997.

15.      Isalomboto Nkanga C, Murhimalika Bapolisi A, Ikemefuna Okafor N and Werner Maçedo Krause R: General Perception of Liposomes: Formation. Manufacturing and Applications, in: Liposomes -Advances and Perspectives. 2019.

 

 

 

 

Received on 14.09.2024      Revised on 09.11.2024

Accepted on 30.12.2024      Published on 28.03.2025

Available online from April 01, 2025

Research J. Topical and Cosmetic Sci. 2025; 16(1):39-42.

DOI: 10.52711/2321-5844.2025.00007

©A and V Publications All right reserved

 

This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. Creative Commons License.