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  1. A’attiyyah A.A., Wan Afiqah Syahirah W.G., Kannan, T.P., Suharni M., Ahmad A., Nor Azah M.A.
    MyJurnal
    Medicinal plants have healing properties and are able to synthesize various chemical compounds. These chemicals (also known as phytochemical compounds) play vital roles in determining the pharmacological properties existing in certain plants. The phytochemical compounds present in plants are associated with primary and secondary constituents. Most of the time, the secondary constituents exhibit the bioactivities in plants such as antimicrobial, antioxidant, antidiabetic, antibacterial and anti-inflammatory properties. Some common medicinal plants that have been used in curing various diseases by traditional practitioners in Malaysia are Ficus deltoidea Jack, Andrographis paniculata, Curcuma longa, Clinacanthus nutans and Eurycoma longifolia Jack. This review discusses the morphology, phytochemical compounds and phytochemical properties of selected medicinal plants in Malaysia. The plants of focus have been found to possess anti-cancer and anti-diabetic effects. This review, it is hoped will enable Malaysian researchers to explore further on the potential of these plants in investigating new and novel drugs in the future.
  2. Yi, Q.S., Wan Zarina, Z.A., Nurulhidayah, C.N., Mohamad Ezany, Y., Azlina, A., Suharni, M.
    Medicine & Health, 2017;12(1):34-41.
    MyJurnal
    Euphorbia tirucalli dilaporkan mempunyai aktiviti antibakteria terhadap pelbagai
    mikroorganisma. Kajian in vitro ini bertujuan untuk menilai ciri-ciri antibakteria
    ekstrak (metanol, etanol dan ekstrak akueus) batang Euphorbia tirucalli terhadap
    bakteria yang berkaitan dengan karies gigi, iaitu Streptococcus mutans (S. mutans)
    dan Streptococcus sobrinus (S. sobrinus). Sifat-sifat antibakteria telah ditentukan
    menggunakan ujian resapan agar berlubang pada kepekatan ekstrak yang berbeza
    (10, 20 dan 30 mg/ml). Komersial amoxicillin (10 µg) telah digunakan sebagai
    kawalan positif manakala pelarut yang sesuai telah digunakan sebagai kawalan
    negatif. Ekstrak metanol dan ethanol daripada batang Euphorbia tirucalli didapati
    berkesan terhadap S. mutans dan S. sobrinus. Walau bagaimanapun, ekstrak akueus
    batang Euphorbia tirucalli tidak menunjukkan aktiviti terhadap kedua-dua strain
    bakteria. Perbezaan dalam ciri-ciri antibakteria dalam perbezaan ekstrak Euphorbia
    tirucalli mungkin disebabkan oleh perbezaan dalam juzuk fitokimia.
  3. Nuur Ezzatyhusna, M. K., Nurul Izzati, H., Siti Suraiya M. N., Suharni, M.
    Medicine & Health, 2017;12(2):220-229.
    MyJurnal
    Amplikasi isoterma berpengantara gelung (LAMP) merupakan teknik amplifikasi gen
    yang menghasilkan produk akhir iaitu mendapan keruh magnesium pirofosfat yang
    boleh dianalisis dengan hanya menggunakan mata kasar. Penggunaan pewarna
    interkalat yang sesuai adalah penting kerana ia boleh meningkatkan sensitiviti dan
    mengurangkan keputusan positif palsu dan negatif palsu untuk pengesanan. Kajian
    ini bertujuan untuk membandingkan prestasi tiga pewarna interkalat yang berbeza;
    SYBR Green I, SYBR Safe dan pewarna berasaskan calcein di dalam asai LAMP
    HPV-16 melalui visualisasi oleh mata kasar, elektroforesis gel dan mesin masanyata
    turbidimeter. Reaksi LAMP dilakukan menggunakan amplifikasi kit Loopamp
    DNA berisipadu sebanyak 25 μl. Campuran reaksi dieram pada suhu 60�C selama
    60 minit dan ditamatkan menggunakan suhu 80�C selama 5 minit dalam mesin
    masa-nyata turbidimeter. Untuk pengesanan menggunakan mata kasar, SYBR
    Green I dan SYBR Safe telah dicairkan dalam 1:10 DMSO dan telah ditambah ke
    dalam tiub yang mengandungi campuran reaksi selepas proses amplifikasi berlaku
    manakala calcein ditambah sebelum proses amplifikasi. Sensitiviti asai telah disiasat
    menggunakan pencairan DNA HPV-16 yang berkepekatan bermula dari 101
    salinan/
    μl to 108
    salinan/μl. Ketiga-tiga pewarna mempamerkan keputusan yang sama
    dari segi sensitiviti dengan had pengesanan adalah 103
    salinan/μl. Penambahan
    calcein di dalam asai menunjukkan masa pengesanan bertambah selama 10 minit
    dengan menggunakan mesin nyata-masa turbidimeter. Prestasi ketiga-tiga pewarna
    interkalat untuk pengesanan mata kasar adalah setanding dan boleh digunakan
    untuk aplikasi pemeriksaan titik akhir dalam asai HPV-16, manakala dengan mesin nyata-masa turb
  4. Norhaida A, Suharni M, Liza Sharmini AT, Tuda J, Rahmah N
    Ann Trop Med Parasitol, 2008 Mar;102(2):151-60.
    PMID: 18318937 DOI: 10.1179/136485908X252250
    Currently, the laboratory diagnosis of toxocariasis, caused by Toxocara canis or T. cati, mainly relies on serological tests. Unfortunately, however, the specificities of most of the commercial tests that are available for the serodiagnosis of this disease are not very high and this may cause problems, especially in tropical countries where co-infections with other helminths are common. In an effort to develop a serological assay with improved specificity for the detection of Toxocara infection, an IgG(4)-ELISA based on a recombinant version (rTES-30USM) of the 30-kDa Toxocara excretory-secretory antigen (TES-30) has recently been developed. To produce the antigen, the TES-30 gene was cloned via assembly PCR, subcloned into a His-tagged prokaryotic expression vector, and purified by affinity chromatography using Ni(2+)-nitrilotriacetic-acid (Ni-NTA) resin. The performance of the ELISA based on the recombinant antigen was then compared with that of commercial kit, based on an IgG-ELISA, for the serodiagnosis of toxocariasis (Toxocara IgG-ELISA; Cypress Diagnostics, Langdorp, Belgium). Both assays were used to test 338 serum samples, including 26 samples from probable cases of toxocariasis. Assuming that all the probable cases were true cases, the assay based on rTES-30USM demonstrated a sensitivity of 92.3% (24/26) and a specificity of 89.6% (103/115) whereas the commercial kit exhibited a sensitivity of 100% (26/26) but a specificity of only 55.7% (64/115). The high sensitivity and specificity exhibited by the new IgG(4)-ELISA should make the assay a good choice for use in tropical countries and any other area where potentially cross-reactive helminthic infections are common.
  5. Nik Zuraina NMN, Sarimah A, Suharni M, Hasan H, Suraiya S
    J Infect Public Health, 2018 08 07;11(6):878-883.
    PMID: 30097415 DOI: 10.1016/j.jiph.2018.07.010
    BACKGROUND: Overcrowding during the annual Hajj pilgrimage has been known to increase the risk of infectious diseases transmission. Despite the high prevalence of respiratory illness among Malaysian Hajj pilgrims, knowledge about the etiologic pathogens is yet very limited. Thus, this study aimed to determine the spectrum of bacterial respiratory pathogens among the Hajj pilgrims returning to Malaysia in year 2016.

    METHODS: Expectorated sputum specimens were collected from the Hajj pilgrims with symptomatic respiratory tract infections (RTIs). Subsequently, the bacterial pathogens were identified using the standard bacteriological culture method and Vitek II system.

    RESULTS: This study indicated that 255 (87.33%) out of 292 cultured sputa were positive with at least one potential pathogenic bacteria. Out of 345 total bacterial isolates, 60% (n=207) were Haemophilus influenzae, which was associated with both single bacterium infection (132/173, 76.3%) and multiple bacterial infections (75/82, 91.5%). The other bacterial isolates included; Klebsiella pneumoniae (n=37, 10.7%), Moraxella catarrhalis (n=27, 7.8%), Haemophilus parainfluenzae (n=25, 7.2%), Streptococcus group G (n=18, 5.2%), Klebsiella spesies (n=16, 4.6%), Streptococcus pneumoniae (n=11, 3.2%) and few other organisms.

    CONCLUSION: High frequency of H. influenzae was isolated from Malaysian Hajj pilgrims, especially those with respiratory symptoms. Further study should evaluate the actual pathogenicity of the organism and the interactions between the respiratory microbiota towards developing effective prevention strategies of RTIs among the local pilgrims.

  6. Rahmah N, Taniawati S, Shenoy RK, Lim BH, Kumaraswami V, Anuar AK, et al.
    Trans R Soc Trop Med Hyg, 2002 1 31;95(6):601-4.
    PMID: 11816429
    A total of 753 serum samples from 6 institutions in 3 countries (Malaysia, Indonesia and India) were used to evaluate an immunochromatographic rapid dipstick test, Brugia Rapid, for diagnosis of Brugia malayi infection. The samples comprised sera from 207 microfilaria-positive individuals and 546 individuals from filaria non-endemic areas. The latter consisted of 70 individuals with soil-transmitted helminth infections, 68 with other helminth infections, 238 with protozoan infections, 12 with bacterial and viral infections and 158 healthy individuals. The dipstick is prepared with a goat anti-mouse antibody control line and a B. malayi recombinant-antigen test line. First, the dipstick is dipped into a well containing diluted patient serum, thus allowing specific anti-filarial antibody in the serum to react with the recombinant antigen. Then the dipstick is placed into an adjacent well containing reconstituted anti-human IgG4-gold. After 10 min, development of 2 red-purplish lines denotes a positive result and one line indicates a negative reaction. The overall results of the evaluation showed 97% sensitivity, 99% specificity, 97% positive predictive value and 99% negative predictive value. Brugia Rapid is thus a promising diagnostic tool for detection of B. malayi infection, and would be especially useful for the brugian filariasis elimination programme.
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