Antibiotic adsorption by haemofilters /cTian, Qi.

A high-performance liquid chromatography was developed to assay levofloxacin and vancomycin. Fluorescence polarization immunoassay was to assay amikacin. The oseltamivir carboxylate and telavancin concentrations were assayed by high-performance liquid chromatography coupled with tandem mass spectrom...

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Other Authors: Tian, Qi
Format: Others
Language:English
Chinese
Published: 2007
Subjects:
Online Access:http://library.cuhk.edu.hk/record=b6074456
http://repository.lib.cuhk.edu.hk/en/item/cuhk-344089
id ndltd-cuhk.edu.hk-oai-cuhk-dr-cuhk_344089
record_format oai_dc
collection NDLTD
language English
Chinese
format Others
sources NDLTD
topic Absorption
Acute renal failure--Treatment
Antibiotics
Continuous arteriovenous hemofiltration
Absorption
Acute Kidney Injury--therapy
Anti-Bacterial Agents
Hemodialysis Solutions
Renal Replacement Therapy--methods
spellingShingle Absorption
Acute renal failure--Treatment
Antibiotics
Continuous arteriovenous hemofiltration
Absorption
Acute Kidney Injury--therapy
Anti-Bacterial Agents
Hemodialysis Solutions
Renal Replacement Therapy--methods
Antibiotic adsorption by haemofilters /cTian, Qi.
description A high-performance liquid chromatography was developed to assay levofloxacin and vancomycin. Fluorescence polarization immunoassay was to assay amikacin. The oseltamivir carboxylate and telavancin concentrations were assayed by high-performance liquid chromatography coupled with tandem mass spectrometry. === An in vitro model was utilized to examine adsorption of antibiotics onto haemofilters. In order to test antibiotics from a range of classes, levofloxacin, amikacin, vancomycin, telavancin, and oseltamivir carboxylate were studied. === In summary, the antibiotic adsorption by haemofilters is a complex process. Both characteristics of antibiotics and haemofilters may determine adsorption. Among the studied antibiotics, in vitro adsorption of amikacin by PAN filters may have clinical significance, thus the routine monitoring of amikacin peak concentration in vivo during CRRT is recommended. === In the in vitro model, blood was pumped from an agitated, glass mixing chamber (heated using an automatic water bath), around a circuit and returned to the mixing chamber using a haemofiltration machine. Ultrafiltrate was also returned to the mixing chamber to constitute a closed circuit. As a result any decrease in drug concentration could only be due to adsorption to the filter and extracorporeal circuit, spontaneous degradation or metabolism by red cells. === The main findings were: (1) low adsorption of levofloxacin and vancomycin by haemofilters at clinically relevant concentrations; (2) significant absolute adsorption of amikacin by polyacrylonitrile haemofilters; (3) the adsorption of antibiotics was membrane-material dependent with greater adsorption by polyacrylonitrile filters; (4) lack of relationship between membrane surface area and amikacin adsorption; (5) the adsorption of levofloxacin is reversible, contrary to irreversibility of vancomycin and amikacin; (6) sieving coefficient of oseltamivir is very near to 1.0. === This thesis investigated: (1) the extent of antibiotic adsorption (levofloxacin, vancomycin, amikacin, telavancin and oseltamivir carboxylate) by haemofilters; (2) the time course of antibiotic adsorption by haemofilters; (3) the effects of plasma albumin concentration, initial dosage, pH, filter membrane material, filter membrane surface area and repeated dosing on adsorption; (4) the reversibility or irreversibility of adsorption; (5) clearance of oseltamivir carboxylate and telavancin by ultrafiltration. === Up to 25% of critically ill patients develop acute renal failure with sepsis being the most common cause. Outside of North and South America, these patients usually receive continuous renal replacement therapy (CRRT) which utilizes high flux haemofilter membranes. Thus it is common for these patients to be concurrently receiving antibiotics and CRRT. However, information about the adsorptive capacity of various haemofilters for most drugs is lacking. === "September 2007." === Advisers: Charles Gomersall; Tony Gin. === Source: Dissertation Abstracts International, Volume: 69-08, Section: B, page: 4659. === Thesis (Ph.D.)--Chinese University of Hong Kong, 2007. === Includes bibliographical references (p. 147-164). === Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web. === Electronic reproduction. [Ann Arbor, MI] : ProQuest Information and Learning, [200-] System requirements: Adobe Acrobat Reader. Available via World Wide Web. === Abstract in English and Chinese. === School code: 1307.
author2 Tian, Qi
author_facet Tian, Qi
title Antibiotic adsorption by haemofilters /cTian, Qi.
title_short Antibiotic adsorption by haemofilters /cTian, Qi.
title_full Antibiotic adsorption by haemofilters /cTian, Qi.
title_fullStr Antibiotic adsorption by haemofilters /cTian, Qi.
title_full_unstemmed Antibiotic adsorption by haemofilters /cTian, Qi.
title_sort antibiotic adsorption by haemofilters /ctian, qi.
publishDate 2007
url http://library.cuhk.edu.hk/record=b6074456
http://repository.lib.cuhk.edu.hk/en/item/cuhk-344089
_version_ 1718977926893928448
spelling ndltd-cuhk.edu.hk-oai-cuhk-dr-cuhk_3440892019-02-19T03:42:51Z Antibiotic adsorption by haemofilters /cTian, Qi. 血濾器對抗生素的吸附 CUHK electronic theses & dissertations collection Xue lü qi dui kang sheng su de xi fu Absorption Acute renal failure--Treatment Antibiotics Continuous arteriovenous hemofiltration Absorption Acute Kidney Injury--therapy Anti-Bacterial Agents Hemodialysis Solutions Renal Replacement Therapy--methods A high-performance liquid chromatography was developed to assay levofloxacin and vancomycin. Fluorescence polarization immunoassay was to assay amikacin. The oseltamivir carboxylate and telavancin concentrations were assayed by high-performance liquid chromatography coupled with tandem mass spectrometry. An in vitro model was utilized to examine adsorption of antibiotics onto haemofilters. In order to test antibiotics from a range of classes, levofloxacin, amikacin, vancomycin, telavancin, and oseltamivir carboxylate were studied. In summary, the antibiotic adsorption by haemofilters is a complex process. Both characteristics of antibiotics and haemofilters may determine adsorption. Among the studied antibiotics, in vitro adsorption of amikacin by PAN filters may have clinical significance, thus the routine monitoring of amikacin peak concentration in vivo during CRRT is recommended. In the in vitro model, blood was pumped from an agitated, glass mixing chamber (heated using an automatic water bath), around a circuit and returned to the mixing chamber using a haemofiltration machine. Ultrafiltrate was also returned to the mixing chamber to constitute a closed circuit. As a result any decrease in drug concentration could only be due to adsorption to the filter and extracorporeal circuit, spontaneous degradation or metabolism by red cells. The main findings were: (1) low adsorption of levofloxacin and vancomycin by haemofilters at clinically relevant concentrations; (2) significant absolute adsorption of amikacin by polyacrylonitrile haemofilters; (3) the adsorption of antibiotics was membrane-material dependent with greater adsorption by polyacrylonitrile filters; (4) lack of relationship between membrane surface area and amikacin adsorption; (5) the adsorption of levofloxacin is reversible, contrary to irreversibility of vancomycin and amikacin; (6) sieving coefficient of oseltamivir is very near to 1.0. This thesis investigated: (1) the extent of antibiotic adsorption (levofloxacin, vancomycin, amikacin, telavancin and oseltamivir carboxylate) by haemofilters; (2) the time course of antibiotic adsorption by haemofilters; (3) the effects of plasma albumin concentration, initial dosage, pH, filter membrane material, filter membrane surface area and repeated dosing on adsorption; (4) the reversibility or irreversibility of adsorption; (5) clearance of oseltamivir carboxylate and telavancin by ultrafiltration. Up to 25% of critically ill patients develop acute renal failure with sepsis being the most common cause. Outside of North and South America, these patients usually receive continuous renal replacement therapy (CRRT) which utilizes high flux haemofilter membranes. Thus it is common for these patients to be concurrently receiving antibiotics and CRRT. However, information about the adsorptive capacity of various haemofilters for most drugs is lacking. "September 2007." Advisers: Charles Gomersall; Tony Gin. Source: Dissertation Abstracts International, Volume: 69-08, Section: B, page: 4659. Thesis (Ph.D.)--Chinese University of Hong Kong, 2007. Includes bibliographical references (p. 147-164). Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web. Electronic reproduction. [Ann Arbor, MI] : ProQuest Information and Learning, [200-] System requirements: Adobe Acrobat Reader. Available via World Wide Web. Abstract in English and Chinese. School code: 1307. Tian, Qi Chinese University of Hong Kong Graduate School. Division of Anaesthesia and Intensive Care. 2007 Text theses electronic resource microform microfiche 1 online resource (xxiii, 191 p. : ill.) cuhk:344089 isbn: 9780549774068 http://library.cuhk.edu.hk/record=b6074456 eng chi Use of this resource is governed by the terms and conditions of the Creative Commons “Attribution-NonCommercial-NoDerivatives 4.0 International” License (http://creativecommons.org/licenses/by-nc-nd/4.0/) http://repository.lib.cuhk.edu.hk/en/islandora/object/cuhk%3A344089/datastream/TN/view/Antibiotic%20adsorption%20by%20haemofilters%20/cTian%2C%20Qi.jpghttp://repository.lib.cuhk.edu.hk/en/item/cuhk-344089