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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Dong, Min | - |
| dc.contributor.author | Liu, Ying | - |
| dc.contributor.author | Liu, Biao | - |
| dc.date.accessioned | 2023-10-05T06:59:35Z | - |
| dc.date.available | 2023-10-05T06:59:35Z | - |
| dc.date.issued | 2023 | - |
| dc.identifier.uri | https://link.springer.com/article/10.1007/s10856-023-06747-x | - |
| dc.identifier.uri | https://dlib.phenikaa-uni.edu.vn/handle/PNK/9473 | - |
| dc.description | CC-BY | vi |
| dc.description.abstract | Glioma is the most common malignant tumor of the brain and enhancing the efficacy of chemotherapy in glioma is critical for improving patients’ prognosis. In this study, a glioma-targeting drug delivery system is constructed using biodegradable periodic mesoporous organosilica nanoparticles (PMO) that are modified with lactoferrin (Lf) ligands. The obtained PMO is doped with thioether groups and can be degraded in the high concentration of glutathione in tumor cells. The surface area and pore volume of PMO are 772 cm2/g and 0.98 cm3/g, respectively and the loading capacity of doxorubicin (Dox) is as high as 20%. The results of the confocal laser scanning microscope show that the uptake of PMO-Lf@Dox by C6 cells is higher than PMO@Dox. | vi |
| dc.language.iso | en | vi |
| dc.publisher | Springer | vi |
| dc.subject | obtained PMO | vi |
| dc.subject | PMO | vi |
| dc.title | Enhanced anti-glioma efficacy of biodegradable periodic mesoporous organosilica nanoparticles through target delivery of chemotherapeutics | vi |
| dc.type | Book | vi |
| Appears in Collections | ||
| OER - Khoa học Vật liệu, Ứng dụng | ||
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