Salahshour, SoheılHu, PanpanBasem, AliJasim, Dheyaa J.Raja, WaleedAljaafari, Haydar A. S.Salahshour, SoheilHashemian, Mohammad2024-10-152024-10-15202400735-19331879-017810.1016/j.icheatmasstransfer.2024.1080432-s2.0-85203512293https://doi.org/10.1016/j.icheatmasstransfer.2024.108043https://hdl.handle.net/20.500.14517/6576A common chemotherapy drug, doxorubicin's effectiveness is restricted by its quick excretion from the body and poor solubility. Because of their large surface area and adjustable pore size, bio MOF11 carriers demonstrated promise as drug delivery systems. Examining how external heat flux amplitude (EHFA) affects bio MOF11's ability to adsorb doxorubicin can reveal ways to improve drug loading and release, which will improve drug delivery. Moreover, by shortening the time needed for adsorption (Ads) and desorption, using EHFA in drug Ads processes can increase energy efficiency. Through comprehending the effect of EHFA on the Ads procedure, researchers can ascertain the ideal circumstances for optimizing drug loading while reducing energy usage. The current work examined the effect of EHFA amplitude on doxorubicin Ads via a bio MOF11 carrier using molecular dynamics (MD) modeling. According to MD data, EHFA was expected to have a significant effect on the atomistic evolution of the proposed drug-MOF11 system. The system's interaction energy (IE) and diffusion coefficient rose from-937.27 kcal/mol and 61.40 nm(2)/ns(2)/ns to-984.08 kcal/mol and 75.16 nm(2)/ns(2)/ns when EHFA changed from 0.01 to 0.05 W/m(2). Increasing EHFA to 0.05 W/m2 2 resulted in a mean square displacement (MSD) parameter of 69.16 & Aring;2. 2 . Therefore, based on the numerical results from this study, it can be said that the doxorubicin drug-MOF11 system changed and atomically evolved when the applied EHFA changes in magnitude.eninfo:eu-repo/semantics/closedAccessExternal heat fluxAdsorptionDoxorubicin drugBio-MOF-11 carrierMolecular dynamics simulationArticleQ1Q1159WOS:001315769200001