Abdul Mannan

Abdul Mannan


Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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4 November 2010 in Malaria Journal
Verified
Journal Article
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AMAbdul Mannan
Abdul Mannan
IAIbrar Ahmed
Ibrar Ahmed
WAWaheed Arshad
Waheed Arshad
MAMuhammad F Asim
Muhammad F Asim
RQRizwana A Qureshi
Rizwana A Qureshi
BMBushra Mirza
Bushra Mirza
Artemisinin is the current drug of choice for treatment of malaria and a number of other diseases. It is obtained from the annual herb, Artemisia annua and some microbial sources by genetic engineering. There is a great concern that the artemisinin production at current rate will not meet the increasing demand by the pharmaceutical industry, so looking for additional sources is imperative.

1 October 2011 in Archives of Pharmacal Research
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Journal Article
Closed access
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AMAbdul Mannan
Abdul Mannan
IAIbrar Ahmed
Ibrar Ahmed
WAWaheed Arshad
Waheed Arshad
IHIzhar Hussain
Izhar Hussain
BMBushra Mirza
Bushra Mirza

27 March 2013 in BMC Infectious Diseases
Verified
Journal Article
Open access
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MYMuhammad Yameen
Muhammad Yameen
SISaira Iram
Saira Iram
AMAbdul Mannan
Abdul Mannan
SKShujaat Ali Khan
Shujaat Ali Khan
NANaeem Akhtar
Naeem Akhtar
Enterococci normally inhabit the intestinal tract of humans and are also a potential pathogen in causing nosocomial infections. The increase in antibiotic resistance and transfer of antibiotic resistance gene to Staphylococcus aureus (S. aureus) due to co-colonization has increased its importance in research. The aim of the study was to evaluate local epidemiology of nasal and rectal colonization with Enterococcus faecalis (E. faecalis) and Enterococcus faecium (E. faecium) in patients of Paediatrics Intensive Care Unit (PICU) and correlation with clinical and socioeconomic factors.

4 April 2022 in Applied Water Science
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Journal Article
Open access
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SOSosun
Sosun
AAAttarad Ali
Attarad Ali
AMAbdul Mannan
Abdul Mannan
USUsman Ali Shah
Usman Ali Shah
MZMuhammad Zia
Muhammad Zia
In real engineering applications, nanoparticles can face hurdles of complex behavior of pollutants, for which electrostatic forces and background electrolyte can prove to be one of the robust mechanisms to remove pollutants from wastewater. In the present work, magnetite (Fe3O4) nanoparticles (NPs) and trioctyl phosphine oxide (TOPO) coated Fe3O4 NPs were synthesized and characterized for removing divalent Ni2+ and Cd2+ ions. Morphological and chemical analysis of both NPs was performed, and batch adsorption experiments were performed to study the influence of different pH ranges, concentrations of adsorbents and different contact timings. TOPO functionalized magnetite nanoparticles were found to have better adsorption capacities as compared to Fe3O4 at higher pH values. Isotherm models were run to identify the adsorption process. Langmuir isotherm model data fitted best for both metal ions adsorption, while Freundlich data suited best only for Ni2+ ions. The regression values for kinetic models confirmed that pseudo-second-order fitted best to the adsorption of both Ni2+ and Cd2+. Higher adsorption values were noticed for Ni2+ at higher dosages of both bare and TOPO-coated iron oxide NPs. Cadmium was found to have no influence of adsorbent dosage. Contact time was found to impact sorption values, i.e., adsorption was greater initially and then decreased with the passage of time. The study concludes that TOPO decorated Fe3O4 NPs can be more efficiently used for wastewater treatment. Furthermore, the presence of alkyl chains in TOPO can be immobilized at surface of metals to undergo adsorption more efficiently.

12 June 2012 in BMC Research Notes
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Journal Article
Open access
Shawkat AliShawkat Ali
Shawkat Ali
AMAbdul Mannan
Abdul Mannan
Mohamed El OirdiMohamed El Oirdi
Mohamed El Oirdi
AWAbdul Waheed
Abdul Waheed
BMBushra Mirza
Bushra Mirza
Rough lemon (Citrus jambhiri Lush.) is the most commonly used Citrus rootstock in south Asia. It is extremely sensitive to salt stress that decreases the growth and yield of Citrus crops in many areas worldwide. Over expression of the yeast halotolerant gene (HAL2) results in increasing the level of salt tolerance in transgenic plants. Transformation of rough lemon was carried out by using Agrobacterium tumefaciens strains LBA4404 harboring plasmid pJRM17. Transgenic shoots were selected on kanamycin 100 mg L-1 along with 250 mg L-1 each of cefotaxime and vancomycin for effective inhibition of Agrobacterium growth. The Murashige and Skoog (MS) medium containing 200 μM acetoseryngone (AS) proved to be the best inoculation and co-cultivation medium for transformation. MS medium supplemented with 3 mg L-1 of 6-benzylaminopurine (BA) showed maximum regeneration efficiency of the transformed explants. The final selection of the transformed plants was made on the basis of PCR and Southern blot analysis. Rough lemon has been successfully transformed via Agrobacterium tumefaciens with β-glucuronidase (GUS) and HAL2. Various factors affecting gene transformation and regeneration efficiency were also investigated.

30 November 2018 in Zeitschrift für Naturforschung C
Verified
Journal Article
Closed access
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NHNoor Ul Huda
Noor Ul Huda
SIShamsul Islam
Shamsul Islam
MZMuhammad Zia
Muhammad Zia
KWKainaat William
Kainaat William
FAFakhar i Abbas
Fakhar i Abbas
AMAbdul Mannan
Abdul Mannan
The current study was conducted to evaluate the antimicrobial, antioxidant, antileishmanial and cytotoxic potential of designed derivatives of 1,1′-(1,3-phenylenebis(methylene))bis(3-alkyl/aryl-1H-benzimidazol-3-ium) salts. The antibacterial potential of the test compounds was investigated against Staphylococcus aureus, Pseudomonas aeruginosa and two methicillin-resistant S. aureus (MRSA) strains (MRSA10, MRSA11), where compound 6 showed the best results. For brine shrimp lethality bioassay (BSLB), compound 6 again showed up to 100% mortality at 200 μg/mL and 56.7% mortality at 6.25 μg/mL. Antileishmanial assay was performed against Leishmania tropica at 20 μg/mL dosage, where 6 showed the most promising activity with 16.26% survival (83.74% mortality; IC50=14.63 μg/mL). The anticancer potential of the selected benzimidazole derivatives was evaluated against two selected cell lines (human colorectal cancer, HCT-116 and breast adenocarcinoma, MCF-7) using sulforhodamine B (SRB) assay. Compound 6 was found to be the most effective cytotoxic compound with 75% inhibition of HCT-116 proliferation at 1 mg/mL concentration. Succinctly, 6 exhibited impressive pharmacological potential that might be attributed to its higher lipophilic character owing to the longer N-substituted alkyl chains when compared to the other test compounds.