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

Development and evaluation of novel ...

Mugabe, Clement.

FindBook

Google Book

Amazon

博客來

Development and evaluation of novel liposomal formulations of antibiotics.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Development and evaluation of novel liposomal formulations of antibiotics./
作者:	Mugabe, Clement.
面頁冊數:	112 p.
附註:	Source: Masters Abstracts International, Volume: 44-03, page: 1368.
Contained By:	Masters Abstracts International44-03.
標題:	Chemistry, Biochemistry. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=MR10005
ISBN:	9780494100059

Development and evaluation of novel liposomal formulations of antibiotics.
Mugabe, Clement.

Development and evaluation of novel liposomal formulations of antibiotics. - 112 p.

Source: Masters Abstracts International, Volume: 44-03, page: 1368.

Thesis (M.Sc.)--Laurentian University (Canada), 2006.

The main objective of this thesis was to develop and characterize liposomal antibiotics in an effort to improve antibacterial activities of encapsulated drugs against resistant strains of P. aeruginosa isolated from CF patients.

ISBN: 9780494100059Subjects--Topical Terms:

1017722
Chemistry, Biochemistry.

Development and evaluation of novel liposomal formulations of antibiotics.
LDR:02615nmm 2200277 4500 001 1824388
005 20061130141924.5
008 130610s2006 eng d
020 $a 9780494100059
035 $a (UnM)AAIMR10005
035 $a AAIMR10005
040 $a UnM $c UnM
100 1 $a Mugabe, Clement. $3 1913466
245 1 0 $a Development and evaluation of novel liposomal formulations of antibiotics.
300 $a 112 p.
500 $a Source: Masters Abstracts International, Volume: 44-03, page: 1368.
502 $a Thesis (M.Sc.)--Laurentian University (Canada), 2006.
520 $a The main objective of this thesis was to develop and characterize liposomal antibiotics in an effort to improve antibacterial activities of encapsulated drugs against resistant strains of P. aeruginosa isolated from CF patients.
520 $a We have developed a modified dehydration/rehydration (DRV) technique to produce small but stable vesicles with high yield drug entrapment. Encapsulation of aminoglycoside and macrolide antibiotics into these liposomes significantly increased the antibacterial activity of these agents against strains of P. aeruginosa. Furthermore, liposomal antibiotics were significantly more effective in killing bacteria than the corresponding free drugs even at lower concentrations. We investigated the mechanism of enhanced activity of liposomal antibiotics as well. Electron microscopy indicated bacterial membrane deformation and fusion with liposomes. The fusion of liposomes with bacterial membrane was further confirmed by flow cytometry and lipid mixing assays. The degree of fusion between liposomes and bacterial membranes increased as a function of incubation time until a maximum fusion rate was reached. The fusion between liposomes and P. aeruginosa resulted in significantly increased amount of antibiotic penetration inside the bacterial cells as demonstrated by immunocytochemistry studies.
520 $a In conclusion, the modified DRV technique developed may be utilized to overcome the low encapsulation efficiency associated with aminoglycoside and macrolide antibiotics. Furthermore, the fusion between the liposomes and the bacterial membranes facilitates antibiotics access inside the bacterial cells. Hence, liposome-entrapped antibiotics could overcome the drug resistance phenomenon associated with bacterial outer-membrane permeability. (Abstract shortened by UMI.)
590 $a School code: 1100.
650 4 $a Chemistry, Biochemistry. $3 1017722
650 4 $a Chemistry, Pharmaceutical. $3 550957
690 $a 0487
690 $a 0491
710 2 0 $a Laurentian University (Canada). $3 1019463
773 0 $t Masters Abstracts International $g 44-03.
790 $a 1100
791 $a M.Sc.
792 $a 2006
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=MR10005