Mathematical Modeling of Drug Distribution in the Vitreous Humor

2021 ◽  
pp. 181-221
Author(s):  
Stuart Friedrich ◽  
Bradley Saville ◽  
Yu-Ling Cheng
2020 ◽  
Author(s):  
Shuqi Zhang ◽  
Anita Penkova ◽  
Mark Humayun ◽  
Juan Carlos Martinez-Camarillo ◽  
Abegail C. Tadle ◽  
...  

Abstract In order to measure the effective diffusion coefficient of Bevacizumab (Avastin, Genentech) in the vitreous humor, a new technique is developed based on the 'contour method' and in vivo OCT measurements. After injection of Bevacizumab-fluorescein conjugated compound solution into the rabbit eye, the contours of drug concentration distribution at the subsurface of injection were tracked over time. The 2D contours were extrapolated to 3D contours using reasonable assumptions and a numerically integrated analytical model was developed for the theoretical contours for the irregularly shaped drug distribution in the experimental result. By floating the diffusion coefficient, different theoretical contours were constructed and the least-squares best fit to the experimental contours was performed at each time point to get the best fit solution. The approach generated consistent diffusion coefficient values based on the experiments on four rabbit eyes over a period of 3 hours each, which gave , D=1.2±0.6×(?10?^(-6) ?cm?^2)/s and the corresponding theoretical contours matched well with the experimental contours. The quantitative measurement of concentration using OCT and fluorescein labeling gives a new approach for the "non-contact" in vivo drug distribution measurement within vitreous and other ocular tissues.


Drug Delivery ◽  
2017 ◽  
Vol 24 (1) ◽  
pp. 491-501 ◽  
Author(s):  
Margo Steuperaert ◽  
Giuseppe Falvo D’Urso Labate ◽  
Charlotte Debbaut ◽  
Olivier De Wever ◽  
Christian Vanhove ◽  
...  

Author(s):  
Robert H. Liss ◽  
Frances A. Cotton

Daunomycin, an antibiotic used in the clinical management of acute leukemia, produces a delayed, lethal cardiac toxicity. The lethality is dose and schedule dependent; histopathologic changes induced by the drug have been described in heart, lung, and kidney from hamsters in both single and multiple dose studies. Mice given a single intravenous dose of daunomycin (10 mg/kg) die 6-7 days later. Drug distribution studies indicate that the rodents excrete most of a single dose of the drug as daunomycin and metabolite within 48 hours after dosage (M. A. Asbell, personal communication).Myocardium from the ventricles of 6 moribund BDF1 mice which had received a single intravenous dose of daunomycin (10 mg/kg), and from controls dosed with physiologic saline, was fixed in glutaraldehyde and prepared for electron microscopy.


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