東華大學圖書館 |

語系: 繁體中文

說明(常見問題)

回圖書館首頁

手機版館藏查詢

登入

回首頁

切換: 標籤 | MARC模式 | ISBD

Synthesis, characterization, and app...

Hans, Meredith L.

FindBook

Google Book

Amazon

博客來

Synthesis, characterization, and application of biodegradable polymeric prodrug micelles for long-term drug delivery.

紀錄類型:	書目-語言資料,印刷品 : Monograph/item
正題名/作者:	Synthesis, characterization, and application of biodegradable polymeric prodrug micelles for long-term drug delivery./
作者:	Hans, Meredith L.
面頁冊數:	177 p.
附註:	Adviser: Anthony M. Lowman.
Contained By:	Dissertation Abstracts International67-03B.
標題:	Engineering, Biomedical. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3208679
ISBN:	9780542572418

Synthesis, characterization, and application of biodegradable polymeric prodrug micelles for long-term drug delivery.
Hans, Meredith L.

Synthesis, characterization, and application of biodegradable polymeric prodrug micelles for long-term drug delivery. - 177 p.

Adviser: Anthony M. Lowman.

Thesis (Ph.D.)--Drexel University, 2006.

Long-term drug delivery has several advantages such as increasing bioavailability of drugs, reduction of pharmaceutical side effects, and increased patient compliance. Nanoparticles, such as block copolymer micelles, worm-like micelles, liposomes and polymersomes, have been proposed recently in the literature as promising drug delivery vehicles. Specifically, block copolymer micelles have advantages for drug delivery such as small size (< 100 nm) and hydrophilic outer shell that provides for increased in vivo half-life imparting a "stealth" nature to the particles. Drugs covalently attached to a polymer chain, known as prodrugs, can significantly enhance drug incorporation efficiency. Additionally, the drug release could be further controlled through the conjugate chemistry.

ISBN: 9780542572418Subjects--Topical Terms:

1017684
Engineering, Biomedical.

Synthesis, characterization, and application of biodegradable polymeric prodrug micelles for long-term drug delivery.
LDR:02898nam 2200301 a 45 001 940845
005 20110518
008 110518s2006 ||||||||||||||||| ||eng d
020 $a 9780542572418
035 $a (UMI)AAI3208679
035 $a AAI3208679
040 $a UMI $c UMI
100 1 $a Hans, Meredith L. $3 1264974
245 1 0 $a Synthesis, characterization, and application of biodegradable polymeric prodrug micelles for long-term drug delivery.
300 $a 177 p.
500 $a Adviser: Anthony M. Lowman.
500 $a Source: Dissertation Abstracts International, Volume: 67-03, Section: B, page: 1560.
502 $a Thesis (Ph.D.)--Drexel University, 2006.
520 $a Long-term drug delivery has several advantages such as increasing bioavailability of drugs, reduction of pharmaceutical side effects, and increased patient compliance. Nanoparticles, such as block copolymer micelles, worm-like micelles, liposomes and polymersomes, have been proposed recently in the literature as promising drug delivery vehicles. Specifically, block copolymer micelles have advantages for drug delivery such as small size (< 100 nm) and hydrophilic outer shell that provides for increased in vivo half-life imparting a "stealth" nature to the particles. Drugs covalently attached to a polymer chain, known as prodrugs, can significantly enhance drug incorporation efficiency. Additionally, the drug release could be further controlled through the conjugate chemistry.
520 $a In this work a biodegradable block copolymer prodrug was synthesized with the antipsychotic drug haloperidol. These polymeric prodrugs were formulated into nanoscale micelle-like structures, which were then characterized for size, morphology, stability, and drug loading capability. Micelles were found to be stable for use as a drug delivery vehicle, remaining intact upon dilution below the critical micelle concentration. In vitro release was evaluated from various formulations of micelles, and ranged from 3 to 5 days. Release from polymeric prodrug micelles most closely approached a linear release profile. Furthermore, in vivo behavioral studies were performed to assess haloperidol bioactivity from drug loaded micelles on ketamine induced hyperlocomotion. Results were consistent with in vitro release data, showing that conjugate and combination micelles continued to release drug 4 days post injection, attenuating the effects of the ketamine induced hyperlocomotion. Additionally, results indicate that the sedative side effects of haloperidol were reduced with the micelle delivery systems as compared to the acute haloperidol injection.
590 $a School code: 0065.
650 4 $a Engineering, Biomedical. $3 1017684
650 4 $a Engineering, Chemical. $3 1018531
650 4 $a Health Sciences, Pharmacy. $3 1017737
690 $a 0541
690 $a 0542
690 $a 0572
710 2 $a Drexel University. $3 1018434
773 0 $t Dissertation Abstracts International $g 67-03B.
790 $a 0065
790 1 0 $a Lowman, Anthony M., $e advisor
791 $a Ph.D.
792 $a 2006
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3208679