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A comparative evaluation of coenzyme Q10-loaded liposomes and solid lipid nanoparticles as dermal antioxidant carriers
- Source :
- International Journal of Nanomedicine, Vol 2012, Iss default, Pp 5109-5117 (2012), International Journal of Nanomedicine
- Publication Year :
- 2012
- Publisher :
- Dove Medical Press, 2012.
-
Abstract
- PubMed ID: 23055723<br />Background: The effective delivery of coenzyme Q10 (Q10) to the skin has several benefits in therapy for different skin pathologies. However, the delivery of Q10 to deeper layers of skin is challenging due to low aqueous solubility of Q10. Liposomes and solid lipid nanoparticles (SLN) have many advantages to accomplish the requirements in topical drug delivery. This study aims to evaluate the influence of these nanosystems on the effective delivery of Q10 into the skin. Methods: Q10-loaded liposomes (LIPO-Q10) and SLNs (SLN-Q10) were prepared by thin film hydration and high shear homogenization methods, respectively. Particle size (PS), polydispersity index (PI), zeta potential (ZP), and drug entrapment efficiency were determined. Differential scanning calorimetry analysis and morphological transmission electron microscopy (TEM) examination were conducted. Biocompatibility/cytotoxicity studies of Q10-loaded nanosystems were performed by means of cell culture (human fibroblasts) under oxidative conditions. The protective effect of formulations against production of reactive oxygen species were comparatively evaluated by cytofluorometry studies. Results: PS of uniform SLN-Q10 and LIPO-Q10 were determined as 152.4 ± 7.9 nm and 301.1 ± 8.2 nm, respectively. ZPs were -13.67 ± 1.32 mV and -36.6 ± 0.85 mV in the same order. The drug entrapment efficiency was 15% higher in SLN systems. TEM studies confirmed the colloidal size. SLN-Q10 and LIPO-Q10 showed biocompatibility towards fibroblasts up to 50 µM of Q10, which was determined as suitable for cell proliferation. The mean fluorescence intensity % depending on ROS production determined in cytofluorometric studies could be listed as Q10 ? SLN-Q10 > LIPO-Q10. Conclusion: The LIPO-Q10 system was able to enhance cell proliferation. On the contrary, SLN-Q10 did not show protective effects against ROS accumulation. As a conclusion, liposomes seem to have advantages over SLN in terms of effective delivery of Q10 to skin for antioxidant purposes. © 2012 Gokce et al, publisher and licensee Dove Medical Press Ltd.
- Subjects :
- Medicine (General)
Materials science
Biocompatibility
Ubiquinone
Administration, Topical
Skin Absorption
Cytotoxicity
Dispersity
Solid lipid nanoparticles
Biophysics
Pharmaceutical Science
Bioengineering
Pharmacology
Antioxidants
Cell Line
Biomaterials
chemistry.chemical_compound
R5-920
Nanocapsules
International Journal of Nanomedicine
Drug Discovery
Solid lipid nanoparticle
Zeta potential
Humans
Original Research
Coenzyme Q10
Liposome
ComputerSystemsOrganization_COMPUTER-COMMUNICATIONNETWORKS
Organic Chemistry
General Medicine
Fibroblasts
Lipids
ComputingMilieux_MANAGEMENTOFCOMPUTINGANDINFORMATIONSYSTEMS
ComputingMethodologies_PATTERNRECOGNITION
chemistry
Liposomes
Particle size
InformationSystems_MISCELLANEOUS
Antioxidant
Homogenization (biology)
Subjects
Details
- Language :
- English
- ISSN :
- 11782013, 11769114, and 23055723
- Volume :
- 2012
- Database :
- OpenAIRE
- Journal :
- International Journal of Nanomedicine
- Accession number :
- edsair.doi.dedup.....af6c94756eb1a91c72fd37afdcc1edb5