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contributor authorShi, Lingyan
contributor authorZeng, Min
contributor authorSun, Yi
contributor authorFu, Bingmei M.
date accessioned2017-05-09T01:05:20Z
date available2017-05-09T01:05:20Z
date issued2014
identifier issn0148-0731
identifier otherbio_136_03_031005.pdf
identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/153980
description abstractDevelopment of an optimal systemic drug delivery strategy to the brain will require noninvasive or minimally invasive methods to quantify the permeability of the cerebral microvessel wall or bloodbrain barrier (BBB) to various therapeutic agents and to measure their transport in the brain tissue. To address this problem, we used laserscanning multiphoton microscopy to determine BBB permeability to solutes (P) and effective solute diffusion coefficients (Deff) in rat brain tissue 100–250 خ¼m below the pia mater. The cerebral microcirculation was observed through a section of frontoparietal bone thinned with a microgrinder. Sodium fluorescein, fluorescein isothiocyanate (FITC)dextrans, or Alexa Fluor 488immunoglobulin G (IgG) in 1% bovine serum albumin (BSA) mammalian Ringer's solution was injected into the cerebral circulation via the ipsilateral carotid artery by a syringe pump at a constant rate of ∼3 ml/min. P and Deff were determined from the rate of tissue solute accumulation and the radial concentration gradient around individual microvessels in the brain tissue. The mean apparent permeability P values for sodium fluorescein (molecular weight (MW) 376 Da), dextran4k, 20k, 40k, 70k, and IgG (MW ∼160 kDa) were 14.6, 6.2, 1.8, 1.4, 1.3, and 0.54 أ— 10−7 cm/s, respectively. These P values were not significantly different from those of rat pial microvessels for the samesized solutes (Yuan et al., 2009, “NonInvasive Measurement of Solute Permeability in Cerebral Microvessels of the Rat,â€‌ Microvasc. Res., 77(2), pp. 166–73), except for the small solute sodium fluorescein, suggesting that pial microvessels can be a good model for studying BBB transport of relatively large solutes. The mean Deff values were 33.2, 4.4, 1.3, 0.89, 0.59, and 0.47 أ— 10−7 cm2/s, respectively, for sodium fluorescein, dextran4k, 20k, 40k, 70k, and IgG. The corresponding mean ratio of Deff to the free diffusion coefficient Dfree, Deff/Dfree, were 0.46, 0.19, 0.12, 0.12, 0.11, and 0.11 for these solutes. While there is a significant difference in Deff/Dfree between small (e.g., sodium fluorescein) and larger solutes, there is no significant difference in Deff/Dfree between solutes with molecular weights from 20,000 to 160,000 Da, suggesting that the relative resistance of the brain tissue to macromolecular solutes is similar over a wide size range. The quantitative transport parameters measured from this study can be used to develop better strategies for brain drug delivery.
publisherThe American Society of Mechanical Engineers (ASME)
titleQuantification of Blood Brain Barrier Solute Permeability and Brain Transport by Multiphoton Microscopy
typeJournal Paper
journal volume136
journal issue3
journal titleJournal of Biomechanical Engineering
identifier doi10.1115/1.4025892
journal fristpage31005
journal lastpage31005
identifier eissn1528-8951
treeJournal of Biomechanical Engineering:;2014:;volume( 136 ):;issue: 003
contenttypeFulltext


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