| نویسندگان | _ |
| نشریه | Journal of Biomedical Materials Research Part A |
| شماره صفحات | 1912-1921 |
| شماره سریال | 109 |
| شماره مجلد | 1 |
| ضریب تاثیر (IF) | 3.076 |
| نوع مقاله | Full Paper |
| تاریخ انتشار | 2021 |
| رتبه نشریه | ISI |
| نوع نشریه | چاپی |
| کشور محل چاپ | ایران |
| نمایه نشریه | JCR،Scopus |
چکیده مقاله
The development of drug delivery systems (DDSs) has raised hopes for targeted
cancer therapy. Smart polymers can be conjugated with several nanoparticles and
increase their efficiency in biomedical applications. In this work, the classical molecular dynamics and well-tempered metadynamics simulations are performed to study
the behavior of black phosphorus (BPH) nanosheet functionalized with polyethylenimine (PEI) in adsorption, diffusion, and release of doxorubicin (DOX) anticancer drug. Adsorption of the drug on PEI-BPH surface is mainly due to the formation
of strong pi–pi interaction between the drug and BPH. The drug-binding to the
nanosheet is enhanced by the intermolecular hydrogen bond that formed between
DOX and PEI. The energy values for the interaction of DOX with BPH and PEI are
calculated to be about − 180 and − 50 kJ/mol, respectively. The obtained results
indicated that the adsorption of the drug molecules on the nanosheet destroyed
the hydration layer around the BPH-PEI surface. The free energy calculation for
DDS shows a global minimum in which the distances of DOX from BPH surface and
PEI are about 1.0 and 0.5 nm, respectively. Furthermore, the diffusion of DDS into
the membrane has a macropinocytosis pathway that is in line with experimental
observations. Moreover, it is found that, unlike the isolated DOX, the drug in complex with BPH-PEI can be easily penetrated membrane cells. The study of the pHresponsive release of the drug shows the high solubility of the polymer in the water
environment plays the main role in swelling of DDS and the release of the DOX
molecules.
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