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1.
Sci Rep ; 6: 28041, 2016 06 21.
Article in English | MEDLINE | ID: mdl-27324576

ABSTRACT

Melamine incident, linked to nephrotoxicity and kidney stone in infants previously exposed to melamine-contaminated milk products, was unprecedentedly grave in China in 2008 as little was known about the mechanistic process leading to renal dysfunction in affected children. This study investigates whether neonatal ingestion of melamine leads to renal and vascular dysfunction in adulthood; and whether ingestion of melamine in pregnant rats leads to renal dysfunction in their offspring. A combination of approaches employed includes functional studies in rat renal arteries, renal blood flow measurement by functional magnetic resonance imaging, assay for pro-inflammatory and fibrotic biomarkers, immunohistochemistry, and detection of plasma and renal melamine. We provide mechanistic evidence showing for the first time that melamine reduces renal blood flow and impairs renal and vascular function associated with overexpression of inflammatory markers, transforming growth factor-ß1, bone morphogenic protein 4 and cyclooxygenase-2 in kidney and renal vasculature. Melamine also induces renal inflammation and fibrosis. More importantly, melamine causes nephropathies in offsprings from pregnant rat exposed to melamine during pregnancy, as well as in neonatal rat exposed to melamine afterbirth, thus supporting the clinical observations of kidney stone and acute renal failure in infants consuming melamine-contaminated milk products.


Subject(s)
Kidney/drug effects , Renal Artery/drug effects , Triazines/toxicity , Acetylcholine/pharmacology , Acute Kidney Injury/etiology , Animals , Biomarkers/metabolism , Blood Flow Velocity/drug effects , Body Weight/drug effects , Bone Morphogenetic Protein 4/metabolism , Cyclooxygenase 2/metabolism , Endothelium/drug effects , Endothelium/physiology , Female , Food Contamination/analysis , Kidney/diagnostic imaging , Kidney/metabolism , Kidney Calculi/etiology , Maternal Exposure , Pregnancy , Rats , Rats, Sprague-Dawley , Renal Artery/metabolism , Transforming Growth Factor beta1/metabolism , Triazines/blood
2.
Anal Bioanal Chem ; 407(11): 3009-21, 2015 Apr.
Article in English | MEDLINE | ID: mdl-25619984

ABSTRACT

This paper presents the certification of alpha-endosulfan, beta-endosulfan, and endosulfan sulfate in a candidate tea certified reference material (code: GLHK-11-03) according to the requirements of the ISO Guide 30 series. Certification of GLHK-11-03 was based on an analytical method purposely developed for the accurate measurement of the mass fraction of the target analytes in the material. An isotope dilution mass spectrometry (IDMS) method involving determination by (i) gas chromatography-negative chemical ionization-mass spectrometry (GC-NCI-MS) and (ii) gas chromatography-electron ionization-high-resolution mass spectrometry (GC-EI-HRMS) techniques was employed. The performance of the described method was demonstrated through participation in the key comparison CCQM-K95 "Mid-Polarity Analytes in Food Matrix: Mid-Polarity Pesticides in Tea" organized by the Consultative Committee for Amount of Substance-Metrology in Chemistry in 2012, where the study material was the same as the certified reference material (CRM). The values reported by using the developed method were in good agreement with the key comparison reference value (KCRV) assigned for beta-endosulfan (727 ± 14 µg kg(-1)) and endosulfan sulfate (505 ± 11 µg kg(-1)), where the degree of equivalence (DoE) values were 0.41 and 0.40, respectively. The certified values of alpha-endosulfan, beta-endosulfan, and endosulfan sulfate in dry mass fraction in GLHK-11-03 were 350, 730, and 502 µg kg(-1), respectively, and the respective expanded uncertainties, due to sample inhomogeneity, long-term and short-term stability, and variability in the characterization procedure, were 27 µg kg(-1) (7.8 %), 48 µg kg(-1) (6.6 %), and 33 µg kg(-1) (6.6 %).


Subject(s)
Endosulfan/analogs & derivatives , Endosulfan/analysis , Gas Chromatography-Mass Spectrometry/standards , Pesticides/analysis , Tea/chemistry , Calibration , Chemical Fractionation , Endosulfan/standards , Food Analysis/methods , Food Analysis/standards , Gas Chromatography-Mass Spectrometry/methods , Hydrocarbons, Chlorinated/analysis , Isomerism , Pesticide Residues/analysis , Pesticides/standards , Radioisotope Dilution Technique , Reference Standards , Sensitivity and Specificity
3.
Anal Chim Acta ; 721: 110-4, 2012 Apr 06.
Article in English | MEDLINE | ID: mdl-22405308

ABSTRACT

This paper presents the preparation of a candidate certified reference material (CRM) of cypermethrin in green tea, GLHK-11-01a according to the requirements of ISO Guide 34 and 35. Certification of the material was performed using a newly developed isotope dilution mass spectrometry (IDMS) approach, with gas chromatography high resolution mass spectrometry (GC-HRMS) and gas chromatography-tandem mass spectrometry (GC-MS/MS). Statistical analysis (one-way ANOVA) showed excellent agreement of the analytical data sets generated from the two mass spectrometric detections. The characterization methods have also been satisfactorily applied in an Asia-Pacific Metrology Program (APMP) interlaboratory comparison study. Both the GC-HRIDMS and GC-IDMS/MS methods proved to be sufficiently reliable and accurate for certification purpose. The certified value of cypermethrin in dry mass fraction was 148 µg kg(-1) and the associated expanded uncertainty was 14µg kg(-1). The uncertainty budget was evaluated from sample in homogeneity, long-term and short-term stability and variability in the characterization procedure. GLHK-11-01a is primarily developed to support the local and wider testing community on need basis in quality assurance work and in seeking accreditation.

4.
Chin Med ; 6(1): 34, 2011 Sep 30.
Article in English | MEDLINE | ID: mdl-21961930

ABSTRACT

BACKGROUND: The edible endosperm of Lodoicea maldivica with the common name of coco de mer is used in Chinese medicine for treating cough. Native to Seychelles, Lodoicea maldivica seeds have commanded high prices for centuries due to its scarcity. This study aims to develop a molecular identification method for the authentication of Lodoicea maldivica seeds. METHODS: DNA was extracted from the sample. Two polymerase chain reaction (PCR) systems were developed to amplify a region of the chloroplast DNA and the nuclear phosphoribulokinase (PRK) region specific to Lodoicea maldivica respectively. DNA sequence of a sample was determined and compared with that of the Lodoicea maldivica reference material. RESULTS: The PRK gene of Lodoicea maldivica was successfully amplified and sequenced for identification. CONCLUSION: A new molecular method for the identification of Lodoicea maldivica seeds in fresh, frozen or dried forms was developed.

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