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10.1016/j.jconrel.2021.06.033

http://scihub22266oqcxt.onion/10.1016/j.jconrel.2021.06.033
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34175365!8225316!34175365
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suck abstract from ncbi

pmid34175365      J+Control+Release 2021 ; 336 (?): 252-261
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  • Liposomal encapsulation of trans-crocetin enhances oxygenation in patients with COVID-19-related ARDS receiving mechanical ventilation #MMPMID34175365
  • Mertes PM; Collange O; Coliat P; Banerjee M; Diringer MC; Roche A; Delabranche X; Chaban V; Voegelin M; Bernard A; Sartori V; Laurent N; Velten M; Dhindsa N; Defuria J; Kim G; Xu ZH; Theodorou M; Huang ZR; Khalifa K; Geng B; Niyikiza C; Moyo V; Gizzi P; Villa P; Detappe A; Pivot X
  • J Control Release 2021[Aug]; 336 (?): 252-261 PMID34175365show ga
  • Current therapeutic treatments improving the impaired transportation of oxygen in acute respiratory distress syndrome (ARDS) have been found to be relevant and beneficial for the therapeutic treatment of COVID-19 patients suffering from severe respiratory complications. Hence, we report the preclinical and the preliminary results of the Phase I/II clinical trial of LEAF-4L6715, a liposomal nanocarrier encapsulating the kosmotropic agent trans-crocetin (TC), which, once injected, enhance the oxygenation of vascular tissue and therefore has the potential to improve the clinical outcomes of ARDS and COVID-19 in severely impacted patients. We demonstrated that the liposomal formulation enabled to increase from 30 min to 48 h the reoxygenation properties of free TCs in vitro in endothelial cells, but also to improve the half-life of TC by 6-fold in healthy mice. Furthermore, we identified 25 mg/kg as the maximum tolerated dose in mice. This determined concentration led to the validation of the therapeutic efficacy of LEAF-4 L6715 in a sepsis mouse model. Finally, we report the preliminary outcomes of an open-label multicenter Phase I/II clinical trial (EudraCT 2020-001393-30; NCT04378920), which was aimed to define the appropriate schedule and dosage of LEAF-4L6715 and to confirm its tolerability profile and preliminary clinical activity in COVID-19 patients treated in intensive care unit.
  • |*COVID-19[MESH]
  • |*Respiratory Distress Syndrome/drug therapy[MESH]
  • |Animals[MESH]
  • |Carotenoids[MESH]
  • |Endothelial Cells[MESH]
  • |Humans[MESH]
  • |Mice[MESH]
  • |Respiration, Artificial[MESH]
  • |SARS-CoV-2[MESH]


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