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| Content Provider | PubMed Central |
|---|---|
| Author | Delgado, Ángel V. Melguizo, Consolación Cabeza, Laura Prados, Jose Ortiz, Raúl Caba, Octavio Rama, Ana R. Arias, José L. |
| Copyright Year | 2015 |
| Abstract | Doxorubicin (Dox) is widely used for the combined chemotherapy of solid tumors. However, the use of these drug associations in lung cancer has low antitumor efficacy. To improve its efficacious delivery and activity in lung adenocarcinoma cells, we developed a biodegradable and noncytotoxic nanoplatform based on biodegradable poly(butylcyanoacrylate) (PBCA). The reproducible formulation method was based on an anionic polymerization process of the PBCA monomer, with the antitumor drug being entrapped within the nanoparticle (NP) matrix during its formation. Improved drug-entrapment efficiencies and sustained (biphasic) drug-release properties were made possible by taking advantage of the synthesis conditions (drug, monomer, and surfactant-agent concentrations). Dox-loaded NPs significantly enhanced cellular uptake of the drug in the A549 and LL/2 lung cancer cell lines, leading to a significant improvement of the drug’s antitumoral activity. In vivo studies demonstrated that Dox-loaded NPs clearly reduced tumor volumes and increased mouse-survival rates compared to the free drug. These results demonstrated that PBCA NPs may be used to optimize the antitumor activity of Dox, thus exhibiting a potential application in chemotherapy against lung adenocarcinoma. |
| Related Links | http://dx.doi.org/10.2147/dddt.s92273 |
| Ending Page | 6444 |
| Page Count | 12 |
| Starting Page | 6433 |
| File Format | |
| ISSN | 11778881 |
| e-ISSN | 11778881 |
| Journal | Drug Design, Development and Therapy |
| Volume Number | 9 |
| Language | English |
| Publisher | Dove Medical Press |
| Publisher Date | 2015-12-01 |
| Access Restriction | Open |
| Rights Holder | Dove Medical Press |
| Subject Keyword | Pharmacology Drug Discovery Pharmaceutical Science Research in Higher Education |
| Content Type | Text |
| Resource Type | Article |
| Subject | Drug Discovery Pharmacology Pharmaceutical Science |
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