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Study of ocular transport of drugs r...

Kim, Hyuncheol.

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Study of ocular transport of drugs released from a sustained release device.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Study of ocular transport of drugs released from a sustained release device./
作者:	Kim, Hyuncheol.
面頁冊數:	179 p.
附註:	Source: Dissertation Abstracts International, Volume: 65-03, Section: B, page: 1434.
Contained By:	Dissertation Abstracts International65-03B.
標題:	Engineering, Chemical. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3124775
ISBN:	0496720791

Study of ocular transport of drugs released from a sustained release device.
Kim, Hyuncheol.

Study of ocular transport of drugs released from a sustained release device. - 179 p.

Source: Dissertation Abstracts International, Volume: 65-03, Section: B, page: 1434.

Thesis (Ph.D.)--University of Maryland, College Park, 2004.

Delivering ocular therapeutics to a target site with minimal side effects requires detailed information about the distribution and elimination pathways. This knowledge can guide the development of new drug delivery devices. In this study, we investigated the movement of two drug surrogates, H-110, which is lipophilic, and Gd-DTPA, which is hydrophilic, released from polymer-based implants using a fluorescein technique and magnetic resonance imaging (MRI). We also studied the pharmacokinetics of intravitreally injected triamcinolone acetonide, a low water soluble drug used for treating sight-threatening diseases such as diabetic retinopathy and choroidal neovascularization associated with age-related macular degeneration (AMD).

ISBN: 0496720791Subjects--Topical Terms:

1018531
Engineering, Chemical.

Study of ocular transport of drugs released from a sustained release device.
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245 1 0 $a Study of ocular transport of drugs released from a sustained release device.
300 $a 179 p.
500 $a Source: Dissertation Abstracts International, Volume: 65-03, Section: B, page: 1434.
500 $a Chair: Nam Sun Wang.
502 $a Thesis (Ph.D.)--University of Maryland, College Park, 2004.
520 $a Delivering ocular therapeutics to a target site with minimal side effects requires detailed information about the distribution and elimination pathways. This knowledge can guide the development of new drug delivery devices. In this study, we investigated the movement of two drug surrogates, H-110, which is lipophilic, and Gd-DTPA, which is hydrophilic, released from polymer-based implants using a fluorescein technique and magnetic resonance imaging (MRI). We also studied the pharmacokinetics of intravitreally injected triamcinolone acetonide, a low water soluble drug used for treating sight-threatening diseases such as diabetic retinopathy and choroidal neovascularization associated with age-related macular degeneration (AMD).
520 $a At 24 hour post implantation, H-110 released from an intravitreal implant was detected in the subretinal space. However, following a subconjunctival implant, very little H-110 fluorescence was detected in the subretinal region. H-110 most likely reached the subretinal space from an intravitreal implant by diffusion through the vitreous and retina. However, most of the H-110 released from a subconjunctival implant is thought to dissipate through the choroidal blood flow.
520 $a Concentration profiles of Gd-DTPA, which was released from an intravitreal implant in a New Zealand white rabbit, approached pseudo-steady state within 7 to 8 hours and showed gradients at the rabbit's vitreous-retina border suggesting that diffusion was occurring into the retinal-choroidal-scleral membrane. Parametric analysis with a finite element mathematical model of the rabbit eye yielded for Gd-DTPA a diffusion coefficient of 2.8 x 10-6 cm2/sec in the vitreous and a permeability of 1.0 x 10-5 cm/sec in the composite retina-choroid-sclera membrane. Gd-DTPA concentration decreased away from the implant. Such regional concentration variations throughout the vitreous may have clinical significance when the ubiquitous eye diseases are treated using a single positional implant. Subconjunctival implants in vivo delivered a mean total of 2.7 mug of Gd-DTPA over 8 hours into the vitreous representing only 0.12% of the total amount of compound released from the implant in vitro . No Gd-DTPA was detected in the posterior segment of the eye. Ex vivo, the Gd-DTPA concentration in the vitreous was 30 fold higher suggesting the elimination of significant in vivo barriers to the movement of drugs from the subconjunctival space into the vitreous. (Abstract shortened by UMI.)
590 $a School code: 0117.
650 4 $a Engineering, Chemical. $3 1018531
650 4 $a Engineering, Biomedical. $3 1017684
650 4 $a Health Sciences, Ophthalmology. $3 1019445
650 4 $a Health Sciences, Pharmacy. $3 1017737
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710 2 0 $a University of Maryland, College Park. $3 657686
773 0 $t Dissertation Abstracts International $g 65-03B.
790 1 0 $a Wang, Nam Sun, $e advisor
790 $a 0117
791 $a Ph.D.
792 $a 2004
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3124775