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Article: Particle size tailoring of ursolic acid nanosuspensions for improved anticancer activity by controlled antisolvent precipitation

TitleParticle size tailoring of ursolic acid nanosuspensions for improved anticancer activity by controlled antisolvent precipitation
Authors
KeywordsBreast cancer
Antisolvent nanoprecipitation
In-vitro anticancer activity
Multi-inlet vortex mixer (MIVM)
Nanoparticles
Ursolic acid
Issue Date2015
Citation
International Journal of Pharmaceutics, 2015, v. 494, n. 1, p. 479-489 How to Cite?
Abstract© 2015 Elsevier B.V. All rights reserved. The present study was aimed at tailoring the particle size of ursolic acid (UA) nanosuspension for improved anticancer activity. UA nanosuspensions were prepared by antisolvent precipitation using a four-stream multi-inlet vortex mixer (MIVM) under defined conditions of varying solvent composition, drug feeding concentration or stream flow rate. The resulting products were characterized for particle size and polydispersity. Two of the UA nanosuspensions with mean particle sizes of 100 and 300 nm were further assessed for their in-vitro activity against MCF-7 breast cancer cells using fluorescence microscopy with 4′,6-diamidino-2-phenylindole (DAPI) staining, as well as flow cytometry with propidium (PI) staining and with double staining by fluorescein isothiocyanate. It was revealed that the solvent composition, drug feeding concentration and stream flow rate were critical parameters for particle size control of the UA nanosuspensions generated with the MIVM. Specifically, decreasing the UA feeding concentration or increasing the stream flow rate or ethanol content resulted in a reduction of particle size. Excellent reproducibility for nanosuspension production was demonstrated for the 100 and 300 nm UA preparations with a deviation of not more than 5% in particle size from the mean value of three independent batches. Fluorescence microscopy and flow cytometry revealed that these two different sized UA nanosuspensions, particularly the 300 nm sample, exhibited a higher anti-proliferation activity against the MCF-7 cells and afforded a larger population of these cells in both early and late apoptotic phases. In conclusion, MIVM is a robust and pragmatic tool for tailoring the particle size of the UA nanosuspension. Particle size appears to be a critical determinant of the anticance r activity of the UA nanoparticles.
Persistent Identifierhttp://hdl.handle.net/10722/244203
ISSN
2021 Impact Factor: 6.510
2020 SCImago Journal Rankings: 1.153
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorWang, Yancai-
dc.contributor.authorSong, Ju-
dc.contributor.authorChow, Shing Fung-
dc.contributor.authorChow, Albert H.L.-
dc.contributor.authorZheng, Ying-
dc.date.accessioned2017-08-31T08:56:20Z-
dc.date.available2017-08-31T08:56:20Z-
dc.date.issued2015-
dc.identifier.citationInternational Journal of Pharmaceutics, 2015, v. 494, n. 1, p. 479-489-
dc.identifier.issn0378-5173-
dc.identifier.urihttp://hdl.handle.net/10722/244203-
dc.description.abstract© 2015 Elsevier B.V. All rights reserved. The present study was aimed at tailoring the particle size of ursolic acid (UA) nanosuspension for improved anticancer activity. UA nanosuspensions were prepared by antisolvent precipitation using a four-stream multi-inlet vortex mixer (MIVM) under defined conditions of varying solvent composition, drug feeding concentration or stream flow rate. The resulting products were characterized for particle size and polydispersity. Two of the UA nanosuspensions with mean particle sizes of 100 and 300 nm were further assessed for their in-vitro activity against MCF-7 breast cancer cells using fluorescence microscopy with 4′,6-diamidino-2-phenylindole (DAPI) staining, as well as flow cytometry with propidium (PI) staining and with double staining by fluorescein isothiocyanate. It was revealed that the solvent composition, drug feeding concentration and stream flow rate were critical parameters for particle size control of the UA nanosuspensions generated with the MIVM. Specifically, decreasing the UA feeding concentration or increasing the stream flow rate or ethanol content resulted in a reduction of particle size. Excellent reproducibility for nanosuspension production was demonstrated for the 100 and 300 nm UA preparations with a deviation of not more than 5% in particle size from the mean value of three independent batches. Fluorescence microscopy and flow cytometry revealed that these two different sized UA nanosuspensions, particularly the 300 nm sample, exhibited a higher anti-proliferation activity against the MCF-7 cells and afforded a larger population of these cells in both early and late apoptotic phases. In conclusion, MIVM is a robust and pragmatic tool for tailoring the particle size of the UA nanosuspension. Particle size appears to be a critical determinant of the anticance r activity of the UA nanoparticles.-
dc.languageeng-
dc.relation.ispartofInternational Journal of Pharmaceutics-
dc.subjectBreast cancer-
dc.subjectAntisolvent nanoprecipitation-
dc.subjectIn-vitro anticancer activity-
dc.subjectMulti-inlet vortex mixer (MIVM)-
dc.subjectNanoparticles-
dc.subjectUrsolic acid-
dc.titleParticle size tailoring of ursolic acid nanosuspensions for improved anticancer activity by controlled antisolvent precipitation-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.ijpharm.2015.08.052-
dc.identifier.pmid26302857-
dc.identifier.scopuseid_2-s2.0-84942880643-
dc.identifier.volume494-
dc.identifier.issue1-
dc.identifier.spage479-
dc.identifier.epage489-
dc.identifier.eissn1873-3476-
dc.identifier.isiWOS:000361649300050-
dc.identifier.issnl0378-5173-

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