File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1002/elps.201100214
- Scopus: eid_2-s2.0-82755162006
- PMID: 22134979
- WOS: WOS:000298300900014
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: 2-D t-ITP/CZE determination of clinical urinary proteins using a microfluidic-chip capillary electrophoresis device
Title | 2-D t-ITP/CZE determination of clinical urinary proteins using a microfluidic-chip capillary electrophoresis device |
---|---|
Authors | |
Keywords | 2-D Electrophoresis ITP Microchip-CE Protein Urine |
Issue Date | 2011 |
Publisher | Wiley - V C H Verlag GmbH & Co KGaA. |
Citation | Electrophoresis, 2011, v. 32 n. 23, p. 3406-3414 How to Cite? |
Abstract | To replace the time-consuming sample pretreatment procedure, a microfluidic chip-CE device incorporating on-chip sample desalting/preconcentration with transient isotachophoresis (ITP)/capillary zone electrophoresis (CZE) was fabricated to perform sequential on-chip sample pretreatment and CE determination of four urinary proteins in clinical samples. On-chip sample desalting, clean-up and analyte preconcentration enable removing interfering sample matrix prior to transferring analytes to separation capillary for transient ITP/CZE determination. Four important urinary proteins transferrin, β2-microglobulin, human serum albumin (HSA) and immunoglobulin G (IgG), investigated were shown to achieve quantitation limits sufficiently high to meet medical requirements, sensitivity enhancement up to 40-fold and detection limits down to 0.3, 0.05, 0.6, 0.5mg/L, respectively. Compared to the stacking effect, the use of a large sample size was found to be the major factor for sensitivity enhancement. The method reliability is established by close to 100% recoveries and statistical agreement of results from the method developed with currently used clinical radio-immunoassay method for all four proteins investigated. Moreover, an assay time of less than 10min is needed in the method developed as compared to 7h for the radio-immunoassay method. © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. |
Persistent Identifier | http://hdl.handle.net/10722/144520 |
ISSN | 2023 Impact Factor: 3.0 2023 SCImago Journal Rankings: 0.541 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Wu, R | en_HK |
dc.contributor.author | Yeung, WSB | en_HK |
dc.contributor.author | Fung, YS | en_HK |
dc.date.accessioned | 2012-02-03T06:12:04Z | - |
dc.date.available | 2012-02-03T06:12:04Z | - |
dc.date.issued | 2011 | en_HK |
dc.identifier.citation | Electrophoresis, 2011, v. 32 n. 23, p. 3406-3414 | en_HK |
dc.identifier.issn | 0173-0835 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/144520 | - |
dc.description.abstract | To replace the time-consuming sample pretreatment procedure, a microfluidic chip-CE device incorporating on-chip sample desalting/preconcentration with transient isotachophoresis (ITP)/capillary zone electrophoresis (CZE) was fabricated to perform sequential on-chip sample pretreatment and CE determination of four urinary proteins in clinical samples. On-chip sample desalting, clean-up and analyte preconcentration enable removing interfering sample matrix prior to transferring analytes to separation capillary for transient ITP/CZE determination. Four important urinary proteins transferrin, β2-microglobulin, human serum albumin (HSA) and immunoglobulin G (IgG), investigated were shown to achieve quantitation limits sufficiently high to meet medical requirements, sensitivity enhancement up to 40-fold and detection limits down to 0.3, 0.05, 0.6, 0.5mg/L, respectively. Compared to the stacking effect, the use of a large sample size was found to be the major factor for sensitivity enhancement. The method reliability is established by close to 100% recoveries and statistical agreement of results from the method developed with currently used clinical radio-immunoassay method for all four proteins investigated. Moreover, an assay time of less than 10min is needed in the method developed as compared to 7h for the radio-immunoassay method. © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. | en_HK |
dc.language | eng | en_US |
dc.publisher | Wiley - V C H Verlag GmbH & Co KGaA. | - |
dc.relation.ispartof | Electrophoresis | en_HK |
dc.subject | 2-D Electrophoresis | en_HK |
dc.subject | ITP | en_HK |
dc.subject | Microchip-CE | en_HK |
dc.subject | Protein | en_HK |
dc.subject | Urine | en_HK |
dc.subject.mesh | Electrophoresis, Microchip - instrumentation - methods | - |
dc.subject.mesh | Immunoglobulin G - urine | - |
dc.subject.mesh | Isotachophoresis - instrumentation - methods | - |
dc.subject.mesh | Proteins - analysis | - |
dc.subject.mesh | Proteinuria - urine | - |
dc.title | 2-D t-ITP/CZE determination of clinical urinary proteins using a microfluidic-chip capillary electrophoresis device | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Yeung, WSB:wsbyeung@hkucc.hku.hk | en_HK |
dc.identifier.email | Fung, YS:ysfung@hku.hk | en_HK |
dc.identifier.authority | Yeung, WSB=rp00331 | en_HK |
dc.identifier.authority | Fung, YS=rp00697 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1002/elps.201100214 | en_HK |
dc.identifier.pmid | 22134979 | - |
dc.identifier.scopus | eid_2-s2.0-82755162006 | en_HK |
dc.identifier.hkuros | 198408 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-82755162006&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 32 | en_HK |
dc.identifier.issue | 23 | en_HK |
dc.identifier.spage | 3406 | en_HK |
dc.identifier.epage | 3414 | en_HK |
dc.identifier.eissn | 1522-2683 | - |
dc.identifier.isi | WOS:000298300900014 | - |
dc.publisher.place | Germany | en_HK |
dc.identifier.scopusauthorid | Wu, R=54405220300 | en_HK |
dc.identifier.scopusauthorid | Yeung, WSB=7102370745 | en_HK |
dc.identifier.scopusauthorid | Fung, YS=13309754700 | en_HK |
dc.identifier.issnl | 0173-0835 | - |