Determination of liposome size distribution by flow cytometry.

Cytometry Pub Date : 2000-02-01
K Vorauer-Uhl, A Wagner, N Borth, H Katinger
{"title":"Determination of liposome size distribution by flow cytometry.","authors":"K Vorauer-Uhl,&nbsp;A Wagner,&nbsp;N Borth,&nbsp;H Katinger","doi":"","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>An essential parameter that describes the quality of liposome suspensions is the mean size, respectively the size distribution. Currently several analytical methods including laser light scattering techniques (LLST) are being employed.</p><p><strong>Methods: </strong>Here we present an alternative technique using flow cytometry (FCM) to characterize uni- and polydisperse suspensions. As model liposomes preparations containing dipalmitoylphosphatidylcholine (DPPC) were used. A constant number of particles (1,500/s) in the fluid stream and a representative number of 10,000 particles of each sample was measured. Fluorescence-labeled latex beads were measured identically, and their side scatter signals were calibrated and correlated to the results obtained with liposome vesicles.</p><p><strong>Results: </strong>Evaluation of the measurement and validation of the FCM results in comparison to LLST confirm the reliability of results obtained with our method. Latex beads in the range of 100-1000 nm were used for calibration to classify liposomes. Although measurement characteristics and calculation in both methods are basically different, very good agreement of the results was achieved.</p><p><strong>Conclusions: </strong>Demonstration of stability, reproducibility, and reliability of results make the employment of this method acceptable for an adequate routine analysis technique.</p>","PeriodicalId":10947,"journal":{"name":"Cytometry","volume":"39 2","pages":"166-71"},"PeriodicalIF":0.0000,"publicationDate":"2000-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cytometry","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background: An essential parameter that describes the quality of liposome suspensions is the mean size, respectively the size distribution. Currently several analytical methods including laser light scattering techniques (LLST) are being employed.

Methods: Here we present an alternative technique using flow cytometry (FCM) to characterize uni- and polydisperse suspensions. As model liposomes preparations containing dipalmitoylphosphatidylcholine (DPPC) were used. A constant number of particles (1,500/s) in the fluid stream and a representative number of 10,000 particles of each sample was measured. Fluorescence-labeled latex beads were measured identically, and their side scatter signals were calibrated and correlated to the results obtained with liposome vesicles.

Results: Evaluation of the measurement and validation of the FCM results in comparison to LLST confirm the reliability of results obtained with our method. Latex beads in the range of 100-1000 nm were used for calibration to classify liposomes. Although measurement characteristics and calculation in both methods are basically different, very good agreement of the results was achieved.

Conclusions: Demonstration of stability, reproducibility, and reliability of results make the employment of this method acceptable for an adequate routine analysis technique.

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
流式细胞术测定脂质体大小分布。
背景:描述脂质体悬浮液质量的一个重要参数是平均粒径,即粒径分布。目前,包括激光散射技术(LLST)在内的几种分析方法正在被应用。方法:在这里,我们提出了一种替代技术,流式细胞术(FCM)来表征单分散和多分散悬浮液。采用含双棕榈酰磷脂酰胆碱(DPPC)的脂质体作为模型。测量了流体流中恒定数量的颗粒(1,500/s)和每个样品的代表性数量的10,000个颗粒。对荧光标记的乳胶珠进行了相同的测量,并校准了它们的侧散射信号,并将其与脂质体囊泡获得的结果相关联。结果:与LLST相比,FCM结果的测量评估和验证证实了我们方法所得结果的可靠性。用100-1000 nm范围内的乳胶珠对脂质体进行标定。虽然两种方法的测量特性和计算基本不同,但结果非常吻合。结论:结果的稳定性、可重复性和可靠性表明,该方法可作为常规分析技术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
NASA/American Cancer Society High-Resolution Flow Cytometry Project - II. Effect of pH and DAPI concentration on dual parametric analysis of DNA/DAPI fluorescence and electronic nuclear volume. Cell analysis system based on immunomagnetic cell selection and alignment followed by immunofluorescent analysis using compact disk technologies. Caffeine dissociates complexes between DNA and intercalating dyes: application for bleaching fluorochrome-stained cells for their subsequent restaining and analysis by laser scanning cytometry. Characterization of cytokine interactions by flow cytometry and factorial analysis. Multiparameter analysis of human epithelial tumor cell lines by laser scanning cytometry.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1