期刊
CHEMISTRYSELECT
卷 8, 期 25, 页码 -出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/slct.202301543
关键词
biomolecule incorporation; drug delivery; metal-organic frameworks; microwave; paclitaxel
This paper presents a microwave-irradiation-based technique for the synthesis of porous adenine-incorporated Zn-based MOFs with particle sizes of approximately 200 nm as paclitaxel nanocarriers. The nanomaterial demonstrated a substantial paclitaxel loading capacity and increased solubility compared to the free form, making it a promising delivery vehicle for paclitaxel. Additionally, the paclitaxel-loaded nano MOF exhibited higher toxicity toward cancer cells, highlighting its potential as an effective anticancer agent.
Biomolecule-incorporated metal-organic frameworks (b-MOFs) exhibit enhanced bioavailability and biocompatibility, making them an ideal option for use as drug delivery vehicles. While b-MOFs possess outstanding drug loading and release capabilities, their microscale crystal sizes restrict their applicability as nanocarriers and drug delivery systems. To overcome this limitation, this paper presents a microwave-irradiation-based technique for the synthesis of porous adenine-incorporated Zn-based MOFs with particle sizes of approximately 200 nm as paclitaxel nanocarriers. The nanomaterial demonstrated a substantial paclitaxel loading capacity of 637 mg g(-1). Moreover, it effectively increased the solubility of paclitaxel by 2.5-fold compared to that of the free form. Thus, the nano MOF is a promising delivery vehicle for paclitaxel. Notably, the paclitaxel-loaded nano MOF exhibited higher toxicity toward cancer cells than the free drug, further highlighting its potential as an effective anticancer agent.
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