Recent advances in liposome formulations for breast cancer therapeutics.
- Publisher:
- SPRINGER BASEL AG
- Publication Type:
- Journal Article
- Citation:
- Cell Mol Life Sci, 2021, 78, (13), pp. 5225-5243
- Issue Date:
- 2021-07
Closed Access
Filename | Description | Size | |||
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Yang2021_Article_RecentAdvancesInLiposomeFormul.pdf | Published version | 1.78 MB |
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Full metadata record
Field | Value | Language |
---|---|---|
dc.contributor.author | Yang, B | |
dc.contributor.author | Song, B-P | |
dc.contributor.author | Shankar, S | |
dc.contributor.author | Guller, A | |
dc.contributor.author |
Deng, W |
|
dc.date.accessioned | 2022-05-23T00:45:46Z | |
dc.date.available | 2021-04-30 | |
dc.date.available | 2022-05-23T00:45:46Z | |
dc.date.issued | 2021-07 | |
dc.identifier.citation | Cell Mol Life Sci, 2021, 78, (13), pp. 5225-5243 | |
dc.identifier.issn | 1420-682X | |
dc.identifier.issn | 1420-9071 | |
dc.identifier.uri | http://hdl.handle.net/10453/157612 | |
dc.description.abstract | Among many nanoparticle-based delivery platforms, liposomes have been particularly successful with many formulations passed into clinical applications. They are well-established and effective gene and/or drug delivery systems, widely used in cancer therapy including breast cancer. In this review we discuss liposome design with the targeting feature and triggering functions. We also summarise the recent progress (since 2014) in liposome-based therapeutics for breast cancer including chemotherapy and gene therapy. We finally identify some challenges on the liposome technology development for the future clinical translation. | |
dc.format | Print-Electronic | |
dc.language | eng | |
dc.publisher | SPRINGER BASEL AG | |
dc.relation.ispartof | Cell Mol Life Sci | |
dc.relation.isbasedon | 10.1007/s00018-021-03850-6 | |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.subject | 0601 Biochemistry and Cell Biology, 0606 Physiology, 1103 Clinical Sciences | |
dc.subject.classification | Biochemistry & Molecular Biology | |
dc.subject.mesh | Animals | |
dc.subject.mesh | Antineoplastic Agents | |
dc.subject.mesh | Breast Neoplasms | |
dc.subject.mesh | Drug Compounding | |
dc.subject.mesh | Drug Delivery Systems | |
dc.subject.mesh | Female | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Liposomes | |
dc.subject.mesh | Nanoparticles | |
dc.subject.mesh | Animals | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Breast Neoplasms | |
dc.subject.mesh | Antineoplastic Agents | |
dc.subject.mesh | Liposomes | |
dc.subject.mesh | Drug Delivery Systems | |
dc.subject.mesh | Drug Compounding | |
dc.subject.mesh | Female | |
dc.subject.mesh | Nanoparticles | |
dc.title | Recent advances in liposome formulations for breast cancer therapeutics. | |
dc.type | Journal Article | |
utslib.citation.volume | 78 | |
utslib.location.activity | Switzerland | |
utslib.for | 0601 Biochemistry and Cell Biology | |
utslib.for | 0606 Physiology | |
utslib.for | 1103 Clinical Sciences | |
pubs.organisational-group | /University of Technology Sydney | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Engineering and Information Technology | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Engineering and Information Technology/School of Biomedical Engineering | |
utslib.copyright.status | closed_access | * |
dc.date.updated | 2022-05-23T00:45:45Z | |
pubs.issue | 13 | |
pubs.publication-status | Published | |
pubs.volume | 78 | |
utslib.citation.issue | 13 |
Abstract:
Among many nanoparticle-based delivery platforms, liposomes have been particularly successful with many formulations passed into clinical applications. They are well-established and effective gene and/or drug delivery systems, widely used in cancer therapy including breast cancer. In this review we discuss liposome design with the targeting feature and triggering functions. We also summarise the recent progress (since 2014) in liposome-based therapeutics for breast cancer including chemotherapy and gene therapy. We finally identify some challenges on the liposome technology development for the future clinical translation.
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