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Dive into the research topics where Aishah A. Latiff is active.

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Featured researches published by Aishah A. Latiff.


Mycotoxin Research | 2012

Exposure measurement of aflatoxins and aflatoxin metabolites in human body fluids. A short review

Yin-Hui Leong; Aishah A. Latiff; Nurul Izzah Ahmad; A. Rosma

Aflatoxins are highly toxic secondary fungal metabolites mainly produced by Aspergillus flavus and A. parasiticus. Human exposure to aflatoxins may result directly from ingestion of contaminated foods, or indirectly from consumption of foods from animals previously exposed to aflatoxins in feeds. This paper focuses on exposure measurement of aflatoxins and aflatoxin metabolites in various human body fluids. Research on different metabolites present in blood, urine, breast milk, and other human fluids or tissues including their detection techniques is reviewed. The association between dietary intake of aflatoxins and biomarker measurement is also highlighted. Finally, aspects related to the differences between aflatoxin determination in food versus the biomarker approach are discussed.


Food Chemistry | 2014

Micro-solid phase extraction with liquid chromatography-tandem mass spectrometry for the determination of aflatoxins in coffee and malt beverage.

Wejdan Shakir Khayoon; Bahruddin Saad; Baharuddin Salleh; Normaliza Abdul Manaf; Aishah A. Latiff

A single step extraction-cleanup procedure using porous membrane-protected micro-solid phase extraction (μ-SPE) in conjunction with liquid chromatography-tandem mass spectrometry for the extraction and determination of aflatoxins (AFs) B1, B2, G1 and G2 from food was successfully developed. After the extraction, AFs were desorbed from the μ-SPE device by ultrasonication using acetonitrile. The optimum extraction conditions were: sorbent material, C8; sorbent mass, 20mg; extraction time, 90 min; stirring speed, 1,000 rpm; sample volume, 10 mL; desorption solvent, acetonitrile; solvent volume, 350 μL and ultrasonication period, 25 min without salt addition. Under the optimum conditions, enrichment factor of 11, 9, 9 and 10 for AFG2, AFG1, AFB2 and AFB1, respectively were achieved. Good linearity and correlation coefficient was obtained over the concentration range of 0.4-50 ng g(-1) (r(2) 0.9988-0.9999). Good recoveries for AFs ranging from 86.0-109% were obtained. The method was applied to 40 samples involving malt beverage (19) and canned coffee (21). No AFs were detected in the selected samples.


Analytica Chimica Acta | 2010

A reversed phase high performance liquid chromatography method for the determination of fumonisins B1 and B2 in food and feed using monolithic column and positive confirmation by liquid chromatography/tandem mass spectrometry

Wejdan Shakir Khayoon; Bahruddin Saad; Baharuddin Salleh; Nor Azliza Ismail; Normaliza Abdul Manaf; Aishah A. Latiff

The development of a reversed phase high performance liquid chromatography fluorescence method for the determination of the mycotoxins fumonisin B(1) and fumonisin B(2) by using silica-based monolithic column is described. The samples were first extracted using acetonitrile:water (50:50, v/v) and purified by using a C(18) solid phase extraction-based clean-up column. Then, pre-column derivatization for the analyte using ortho-phthaldialdehyde in the presence of 2-mercaptoethanol was carried out. The developed method involved optimization of mobile phase composition using methanol and phosphate buffer, injection volume, temperature and flow rate. The liquid chromatographic separation was performed using a reversed phase Chromolith(®) RP-18e column (100 mm × 4.6 mm) at 30 °C and eluted with a mobile phase of a mixture of methanol and phosphate buffer pH 3.35 (78:22, v/v) at a flow rate of 1.0 mL min(-1). The fumonisins separation was achieved in about 4 min, compared to approximately 20 min by using a C(18) particle-packed column. The fluorescence excitation and emission were at 335 nm and 440 nm, respectively. The limits of detections were 0.01-0.04 μg g(-1) fumonisin B(1) and fumonisin B(2), respectively. Good recoveries were found for spiked samples (0.1, 0.5, 1.5 μg g(-1) fumonisins B(1) and B(2)), ranging from 84.0 to 106.0% for fumonisin B(1) and from 81.0 to 103.0% for fumonisin B(2). Fifty-three samples were analyzed including 39 food and feeds and 14 inoculated corn and rice. Results show that 12.8% of the food and feed samples were contaminated with fumonisin B(1) (range, 0.01-0.51 μg g(-1)) and fumonisin B(2) (0.05 μg g(-1)). The total fumonisins in these samples however, do not exceed the legal limits established by the European Union of 0.8 μg g(-1). Of the 14 inoculated samples, 57.1% contained fumonisin B(1) (0.16-41.0 μg g(-1)) and fumonisin B(2) (range, 0.22-50.0 μg g(-1)). Positive confirmation of selected samples was carried out using liquid chromatography-tandem mass spectrometry, using triple quadrupole analyzer and operated in the multiple reaction monitoring mode.


Tetrahedron Letters | 2001

Heimiol A, a new dimeric stilbenoid from Neobalanocarpus heimii

Jean Frédéric F. Weber; Ibtisam Abdul Wahab; Alini Marzuki; Noel F. Thomas; Azizol A. Kadir; A. Hamid A. Hadi; Khalijah Awang; Aishah A. Latiff; Pascal Richomme; Jacques Delaunay

Abstract A new stilbene dimer, heimiol A was isolated from the heartwood of Neobalanocarpus heimii , in addition to the four known oligostilbenoids, balanocarpol, copalliferol A, hopeaphenol and vaticaphenol A. The structures and relative configuration were established by means of 2D NMR spectroscopy including COSY, HMQC, HMBC and NOESY.


International Journal of Hygiene and Environmental Health | 2012

Associations of serum aflatoxin B1-lysine adduct level with socio-demographic factors and aflatoxins intake from nuts and related nut products in Malaysia.

Yin-Hui Leong; A. Rosma; Aishah A. Latiff; A. Nurul Izzah

Aflatoxins are one of the major risk factors in the multi-factorial etiology of human hepatocellular carcinoma. Therefore, the information on aflatoxins exposure is very important in the intervention planning in order to reduce the dietary intake of aflatoxins, especially among the children. This study investigated the relationship between aflatoxin B(1) (AFB(1)) lysine adduct levers in serum and socio-demographic factors and dietary intake of aflatoxins from nuts and nut products in Penang, Malaysia. A cross-sectional field study was conducted in five districts of Penang. A survey on socio-demographic characteristics was administered to 364 healthy adults from the three main ethnic groups (Malay, Chinese and Indian). A total of 170 blood samples were successfully collected and tested for the level of AFB(1)-lysine adduct. 97% of the samples contained AFB(1)-lysine adduct above the detection limit of 0.4 pg/mg albumin and ranged from 0.20 to 23.16 pg/mg albumin (mean±standard deviation=7.67±4.54 pg/mg albumin; median=7.12 pg/mg albumin). There was no significant association between AFB(1)-lysine adduct levels with gender, district, education level, household number and occupation when these socio-demographic characteristics were examined according to high or low levels of AFB(1)-lysine. However, participants in the age group of 31-50 years were 3.08 times more likely to have high AFB(1) levels compared to those aged between 18 and 30 years (P=0.026). Significant difference (P=0.000) was found among different ethnic groups. Chinese and Indian participants were 3.05 and 2.35 times more likely to have high AFB(1) levels than Malay. The result of AFB(1)-lysine adduct suggested that Penang adult population is likely to be exposed to AFB(1) but at a level of less than that needed to cause direct acute illness or death.


Angewandte Chemie | 2008

Unusual Chromophore and Cross‐Links in Ranasmurfin: A Blue Protein from the Foam Nests of a Tropical Frog

Muse Oke; Rosalind Tan Yan Ching; Lester G. Carter; Kenneth A. Johnson; Huanting Liu; Stephen A. McMahon; Malcolm F. White; Carlos Bloch; Catherine H. Botting; Martin A. Walsh; Aishah A. Latiff; Malcolm W. Kennedy; Alan Cooper; James H. Naismith

Ranasmurfin is an unusual blue protein isolated from the nests of a Malaysian tree frog, Polypedates leucomystax,[1] showing the rich chemical diversity displayed by biomolecular foams. Many species of tropical frogs use foams to protect delicate eggs and developing embryos against environmental challenges. These nests act as miniature ecosystems containing a spectrum of novel proteins and other macromolecules with functions related to foam stabilization and adhesion, resistance to microbial degradation, predation, or dehydration, providing a biocompatible environment for embryonic development.Thisworkformspartofourwiderstudyofthe intriguing physical and chemical properties of biofoams as unusual examples of biological soft matter.[2]


Journal of the Science of Food and Agriculture | 2013

Isolation and characterization of pepsin-solubilized collagen from the integument of sea cucumber (Stichopus vastus).

Zainul Abedin; Alias A. Karim; Faiyaz Ahmed; Aishah A. Latiff; Chee-Yuen Gan; Farid Che Ghazali; Zaidul Islam Sarker

BACKGROUND Sea cucumber (Stichopus vastus) is considered an underutilized resource, since only its stomach and intestines are eaten raw as salad in a few countries and the remaining parts, especially the integument rich in collagen, is discarded. Hence a valuable by-product having potential nutraceutical and pharmaceutical applications is wasted. In the present investigation, pepsin-solubilized collagen (PSC) from the integument of S. vastus was isolated, purified and characterized. RESULTS Sodium dodecyl sulfate-polyacrylamide gel electrophoretic analysis showed that the purified collagen was of type I, consisting of three α1 chains of approximately 122 kDa each. The peptide map of PSC digested by V8 protease was different from that of calf skin type I collagen. Fourier transform infrared spectroscopy revealed that the triple helical structure was well preserved in isolated collagen. The denaturation temperature of PSC was 21.23 °C and showed good gel-forming capability at pH 6.5 and 300 mmol L⁻¹ NaCl. CONCLUSION It is inferred that the collagen isolated from S. vastus integument has potential for use as an alternative to land-based mammalian collagen in food, nutraceuticals and pharmaceutical industries.


Natural Product Research | 2014

Biochemical and radical-scavenging properties of sea cucumber (Stichopus vastus) collagen hydrolysates

Md. Zainul Abedin; Alias A. Karim; Aishah A. Latiff; Chee-Yuen Gan; Farid Che Ghazali; Zoha Barzideh; Sahena Ferdosh; Md. Jahurul Haque Akanda; Wahidu Zzaman; Md. Rezaul Karim; Md. Zaidul Islam Sarker

The molecular mass distribution, amino acid composition and radical-scavenging activity of collagen hydrolysates prepared from collagen isolated from the sea cucumber Stichopus vastus were investigated. β and α1 chains of the collagen were successfully hydrolysed by trypsin. The molecular mass distribution of the hydrolysates ranged from 5 to 25 kDa, and they were rich in glycine, alanine, glutamate, proline and hydroxyproline residues. The hydrolysates exhibited excellent radical-scavenging activity. These results indicate that collagen hydrolysates from S. vastus can be used as a functional ingredient in food and nutraceutical products.


World Mycotoxin Journal | 2011

Determination of aflatoxins in commercial nuts and nut products using liquid chromatography tandem mass spectrometry

Yin-Hui Leong; Nor Azliza Ismail; Aishah A. Latiff; Normaliza Abdul Manaf; A. Rosma

A rapid and sensitive confirmatory analytical method for determination of aflatoxins in nuts and their products using liquid chromatography tandem mass spectrometry has been developed and validated. All four aflatoxins of interest (B1, B2, G1 and G2) were quantified using aflatoxin M1 as the internal standard. Samples were extracted using methanol/water (60:40, v/v) and cleaned-up with immunoaffinity column. Limit of detection ranged between 0.10 and 0.30 µg/kg. Recovery rates were between 76 and 105% for all analytes. For further validation, a reference material for contaminated peanut has been used for quality assurance measures to check the accuracy and precision. The method was successfully applied to determine the natural occurrence of aflatoxins in 128 nut samples marketed in Penang, Malaysia. More than half of the samples (57.0%) were positive and 13.3% were found to be non-compliant with the European Commission regulations permitted maximum level of 2 µg/kg for aflatoxin B1. The contamination leve...


Acta Crystallographica Section F-structural Biology and Crystallization Communications | 2006

Crystallization of Ranasmurfin, a blue-coloured protein from Polypedates leucomystax

Stephen A. McMahon; Martin A. Walsh; Rosalind Tan Yan Ching; Lester G. Carter; Mark Dorward; Kenneth A. Johnson; Huanting Liu; Muse Oke; Carlos Bloch; Malcolm W. Kennedy; Aishah A. Latiff; Alan Cooper; Garry L. Taylor; Malcolm F. White; James H. Naismith

A novel blue protein from frog nests has been crystallized.

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Chee-Yuen Gan

Universiti Sains Malaysia

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Azrina Azlan

Universiti Putra Malaysia

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Muhammad Rizal Razman

National University of Malaysia

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A. Rosma

Universiti Sains Malaysia

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Alias A. Karim

Universiti Sains Malaysia

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Yin-Hui Leong

Universiti Sains Malaysia

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Nor Azam Ramli

Universiti Sains Malaysia

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