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Engineering of Nanoemulsions for Drug Delivery
Abstract
Nanoemulsions, usually spherical, are a group of dispersed particles used for pharmaceutical and biomedical aids and vehicles that show great promise for the future of cosmetics, diagnostics, drug therapies and biotechnologies. They exist in a wide variety of forms that are dictated by the particle components. Nanoemulsions are generally considered to be in the size range of less than and around 100 nm in diameter. The particles can exist as water-in-oil and oil-in-water forms, where the core of the particle is either water or oil, respectively. More complex variations also exist but these are often larger. The longer-term properties of the particle are dependent on the composition of the adsorbed material lying at the dispersed droplet interface with the dispersion medium. This has an impact on the partitioning and extraction of droplet contents. Thermodynamically stable particles are characterized by having a very low surface tension and this produces a very large surface area. Nanoemulsions can also include small meta-stable very small-scale emulsions; here the surface properties and chemistry can strongly influence behaviour. Processing, storage and formulation composition can also have an impact on the longevity of a pharmaceutical preparation. Some revolutionary new nanoemulsion droplets based on fluorinated compounds are finding a number of widespread biomedical roles and applications. Developments in nanoemulsion technology are likely to lead to a much greater use of this medium in future pharmaceuticals.
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“NEs can be formulated into different kinds of dosage forms like liquids, creams, gels, foams, sprays and so on, and can be administered by different routes including oral, parenteral and ocular, in addition to nasal [27].”
From Nanoemulsions for “Nose-to-Brain” Drug Delivery (2019) · cites this paper as [27]
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Advances in novel parentral drug delivery systems
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Development of Olanzapine Nano-Emulsion for Enhanced Brain Delivery
MadhusudanRao, Y., Shailaja, M., Ramakrishna, S., Ramesh, G., Reddy, K., & Diwan, P. (2012) · International Journal of Pharmaceutical Sciences and Nanotechnology · doi:10.37285/ijpsn.2012.5.1.9 · Cited by 9
“Nano-emulsions are the novel delivery systems find potential application in improving the solubility and bioavailability of poorly soluble drugs (Sarker, 2005; Shafiq et al., 2007).”
BackgroundHydrodynamic collision and deformation of compound droplet pairs in confined shear flow
Mamun, S. M. A. A., & Farokhirad, S. (2024) · Physics of Fluids · doi:10.1063/5.0187395 · Cited by 7
Mao, C., Wan, J., Chen, H., et al. (2009) · AAPS PharmSciTech · doi:10.1208/s12249-009-9295-1 · Cited by 7
“(1) Control blank nanoemulsion (NE); (2) control diallyl trisulfide (DT) NE; (3) Poloxamer 188 (0.2%) DT NE; ( 4 ) Poloxamer 188 (0.4%) DT NE; (5) Poloxamer 188 (0.6%) DT NE; (6) Solutol HS15 (0.2%) DT NE; (7) Solutol HS15 (0.4%) DT NE; (8) Solutol HS15 (0.6%) DT NE. Each value represents the means of three measuremen…”
BackgroundMethodInfluentialDimensional analysis of a novel low‐pressure device for the production of size‐tunable nanoemulsions
Souilem, I., Serra, C. A., Müller, R., et al. (2014) · AIChE Journal · doi:10.1002/aic.14690 · Cited by 7
Gao, S., & McClements, D. J. (2019) · Food Biophysics · doi:10.1007/s11483-019-09585-z · Cited by 7
Dichello, G. A., & Sarker, D. K. (2017) · Elsevier eBooks · doi:10.1016/b978-0-323-46152-8.00027-5 · Cited by 7
Self-citationOk, H., Kim, S.-M., Park, J., Kim, K., Nam, H.-K., Kim, J. Y., & Kwon, O. (2012) · Journal of the Korean Society for Applied Biological Chemistry · doi:10.1007/s13765-012-2037-1 · Cited by 7
“A nano-emulsion should be stable in aqueous solution, because the rate of Brownian motion is much faster than the rate of creaming and sedimentation (Mosqueira et al., 2000; Sarker, 2005).”
BackgroundSarker, D. K. (2017) · Current Drug Discovery Technologies · doi:10.2174/1570163814666171117132202 · Cited by 6
Self-citationAbadi, A. V. M., Karimi, E., Oskoueian, E., et al. (2021) · Research Square · doi:10.21203/rs.3.rs-952488/v1 · Cited by 6
Cannon, J., Shi, Y., & Gupta, P. (2008) · CRC Press eBooks · doi:10.1201/9781420009552.ch10 · Cited by 5
Metadata
- Authors
- Sarker, D.
- Affiliations
- University of Brighton (GB)
- Corresponding author
- Sarker, Dipak
- ORCID
- Sarker, Dipak
- Venue
- Current Drug Delivery
- Publisher
- Bentham Science Publishers Ltd.
- Published
- 2005-10-01
- Volume
- 2
- Issue
- 4
- Pages
- 297-310
- ISSN
- 1567-2018 (ISSN-L)
- OpenAlex
- W2076616392
- Cited by
- 268
- References
- 0
- Citations by year
- 2026: 5 · 2025: 8 · 2024: 11 · 2023: 8 · 2022: 16 · 2021: 14 · 2020: 19 · 2019: 18 · 2018: 10 · 2017: 20 · 2016: 19 · 2015: 10 · 2014: 13 · 2013: 18 · 2012: 17
- FWCI
- 12.84
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Current Drug Delivery (publishedVersion)
- PubMed (publishedVersion)
- University of Brighton Repository (University of Brighton) (submittedVersion)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Food Science › Proteins in Food Systems
- Physical Sciences › Chemistry › Physical and Theoretical Chemistry › Surfactants and Colloidal Systems
- Physical Sciences › Materials Science › Materials Chemistry › Pickering emulsions and particle stabilization
- Keywords
- nanoemulsions, drug delivery, water-in-oil emulsions, oil-in-water emulsions, droplet interface, surface tension, surface area, fluorinated compounds, emulsion stability, drug formulation, cosmetics, diagnostics
- MeSH terms
- Animals, Colloids, Drug Compounding, Emulsions, Humans, Technology, Pharmaceutical, Drug Delivery Systems, Nanotechnology, Nanotubes
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