File Download
There are no files associated with this item.
Supplementary
-
Citations:
- Appears in Collections:
Conference Paper: Enhanced Anti-Cancer Effect of Lipid-coated Cisplatin Nanoparticles on HNSCC
Title | Enhanced Anti-Cancer Effect of Lipid-coated Cisplatin Nanoparticles on HNSCC |
---|---|
Authors | |
Issue Date | 2017 |
Publisher | International Association for Dental Research. The Journal's web site is located at http://www.iadr.org/ |
Citation | The 95th General Session and Exhibition of the International Association for Dental Research (IADR) held with the 46th Annual Meeting of the American Association for Dental Research (AADR) and the 41st Annual Meeting of the Canadian Association for Dental Research (CADR), San Francisco, CA., 22-25 March 2017. In Journal of Dental Research (Spec Issue), 2017, v. 96 n. Spec Iss A, abstract no. 3990 How to Cite? |
Abstract | Objectives: Cisplatin (CDDP) as the first line chemotherapeutic agents for the head/neck squamous cell carcinoma (HNSCC) exhibits notable side-effects such as nephrotoxicity, neurotoxicity and ototoxicity. Emerging evidence shows that lipid-coated cisplatin nanoparticles with excellent physical stability and biocompatibility significantly inhibit tumor growth. This pioneering study investigated the anti-cancer effects of synthesized lipid-coated CDDP nanoparticles on HNSCC cell lines.Methods: The lipid-coated CDDP nanoparticles were synthesized based on the reversed-phase micro-emulsion method. Their morphology and physical properties were characterized by the transmission electronic microscope and Nanotrac Wave II, respectively. The loading efficiency of CDDP nanoparticles was determined by inductively coupled plasma mass spectrometry. The cytotoxicity of the lipid-coated CDDP nanoparticles was evaluated on the FaDu, SCC-15 and SCC-25 cells using CCK-8 kit. Meanwhile, the cellular uptake of the nanoparticles and cellular apoptosis were accessed by the confocal scanning laser microscope and flow cytometer, respectively.Results: The synthesized spherical lipid-coated CDDP nanoparticles with an average diameter of 100 nm and loading efficiency around 80% showed significantly lower IC50 than the CDDP in the HNSCC cell lines. The nanoparticles enabled to enhance the drug solubility, and degrade the lysosomes in the cells and significantly accounted for cellular apoptosis with reference to the CDDP.Conclusions: The synthesized lipid-coated CDDP nanoparticles could enhance the anti-cancer effect on the HNSCC cell lines. The current findings may shed new light on developing novel therapeutic approaches to effectively manage this life-threatening carcinoma with low a survival rate. |
Description | Poster Session: Oral & Maxillofacial Surgery IV |
Persistent Identifier | http://hdl.handle.net/10722/246614 |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lan, X | - |
dc.contributor.author | Li, X | - |
dc.contributor.author | Shen, FF | - |
dc.contributor.author | Jin, L | - |
dc.contributor.author | Su, Y | - |
dc.date.accessioned | 2017-09-18T02:31:36Z | - |
dc.date.available | 2017-09-18T02:31:36Z | - |
dc.date.issued | 2017 | - |
dc.identifier.citation | The 95th General Session and Exhibition of the International Association for Dental Research (IADR) held with the 46th Annual Meeting of the American Association for Dental Research (AADR) and the 41st Annual Meeting of the Canadian Association for Dental Research (CADR), San Francisco, CA., 22-25 March 2017. In Journal of Dental Research (Spec Issue), 2017, v. 96 n. Spec Iss A, abstract no. 3990 | - |
dc.identifier.uri | http://hdl.handle.net/10722/246614 | - |
dc.description | Poster Session: Oral & Maxillofacial Surgery IV | - |
dc.description.abstract | Objectives: Cisplatin (CDDP) as the first line chemotherapeutic agents for the head/neck squamous cell carcinoma (HNSCC) exhibits notable side-effects such as nephrotoxicity, neurotoxicity and ototoxicity. Emerging evidence shows that lipid-coated cisplatin nanoparticles with excellent physical stability and biocompatibility significantly inhibit tumor growth. This pioneering study investigated the anti-cancer effects of synthesized lipid-coated CDDP nanoparticles on HNSCC cell lines.Methods: The lipid-coated CDDP nanoparticles were synthesized based on the reversed-phase micro-emulsion method. Their morphology and physical properties were characterized by the transmission electronic microscope and Nanotrac Wave II, respectively. The loading efficiency of CDDP nanoparticles was determined by inductively coupled plasma mass spectrometry. The cytotoxicity of the lipid-coated CDDP nanoparticles was evaluated on the FaDu, SCC-15 and SCC-25 cells using CCK-8 kit. Meanwhile, the cellular uptake of the nanoparticles and cellular apoptosis were accessed by the confocal scanning laser microscope and flow cytometer, respectively.Results: The synthesized spherical lipid-coated CDDP nanoparticles with an average diameter of 100 nm and loading efficiency around 80% showed significantly lower IC50 than the CDDP in the HNSCC cell lines. The nanoparticles enabled to enhance the drug solubility, and degrade the lysosomes in the cells and significantly accounted for cellular apoptosis with reference to the CDDP.Conclusions: The synthesized lipid-coated CDDP nanoparticles could enhance the anti-cancer effect on the HNSCC cell lines. The current findings may shed new light on developing novel therapeutic approaches to effectively manage this life-threatening carcinoma with low a survival rate. | - |
dc.language | eng | - |
dc.publisher | International Association for Dental Research. The Journal's web site is located at http://www.iadr.org/ | - |
dc.relation.ispartof | Journal of Dental Research (Spec Issue) | - |
dc.title | Enhanced Anti-Cancer Effect of Lipid-coated Cisplatin Nanoparticles on HNSCC | - |
dc.type | Conference_Paper | - |
dc.identifier.email | Jin, L: ljjin@hkucc.hku.hk | - |
dc.identifier.email | Su, Y: richsu@hku.hk | - |
dc.identifier.authority | Jin, L=rp00028 | - |
dc.identifier.authority | Su, Y=rp01916 | - |
dc.identifier.hkuros | 277972 | - |
dc.identifier.hkuros | 279347 | - |
dc.identifier.hkuros | 324687 | - |
dc.identifier.volume | 96 | - |
dc.identifier.issue | Spec Iss A | - |
dc.identifier.spage | no. 3990 | - |
dc.identifier.epage | no. 3990 | - |
dc.publisher.place | United States | - |