Ahmed Hussein

Prof. Ahmed Hussein

Cape Peninsula University of Technology, South Africa
orcid

Research Focus & Metrics

Academic Career Length

31Years (1996-Present)

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

Representative Publications

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1 October 2008 in Journal of Ethnopharmacology
Verified
Journal Article
Closed access
SMsaeideh momtaz
saeideh momtaz
BMB.M. Mapunya
B.M. Mapunya
PHP.J. Houghton
P.J. Houghton
CEC. Edgerly
C. Edgerly
Ahmed HusseinAhmed Hussein
Ahmed Hussein
NLNamrita Lall
Namrita Lall

1 November 2020 in Heliyon
Verified
Journal Article
Open access
JBJelili Badmus
Jelili Badmus
SOS.A. Oyemomi
S.A. Oyemomi
OAO.T. Adedosu
O.T. Adedosu
TYT.A. Yekeen
T.A. Yekeen
MAM.A. Azeez
M.A. Azeez
JMJ.L. Marnewick
J.L. Marnewick
Green synthesis of metal nanoparticles is reputed to have a robust range of biomedical applications. Silver nanoparticles (AgNPs) bio-fabricated using aqueous leaf extract of Annona muricata were characterized and evaluated for in-vitro antioxidant, lipid peroxidation inhibition, anti-diabetic and antimicrobial activities as well as cytotoxicity in human keratinocyte cells (HaCaT).

1 January 2005 in Journal of Ethnopharmacology
Verified
Journal Article
Closed access
Thilivhali Emmanuel TshikalangeThilivhali Emmanuel Tshikalange
Thilivhali Emmanuel Tshikalange
JMJ.J.M. Meyer
J.J.M. Meyer
Ahmed HusseinAhmed Hussein
Ahmed Hussein

13 March 2020 in Biomolecules
Verified
Journal Article
Open access
PDF file
UMUmar Muhammad
Umar Muhammad
Enas IsmailEnas Ismail
Enas Ismail
AAAdewale Olufunsho Adeloye
Adewale Olufunsho Adeloye
SBSubelia Botha
Subelia Botha
JBJelili Badmus
Jelili Badmus
Ahmed HusseinAhmed Hussein
Ahmed Hussein
In this study, procyanidins fractions of dimers and trimers (F1–F2) from the Leucosidea sericea total extract (LSTE) were investigated for their chemical constituents. The total extract and the procyanidins were employed in the synthesis of gold nanoparticles (Au NPs) and fully characterized. Au NPs of 6, 24 and 21 nm were obtained using LSTE, F1 and F2 respectively. Zeta potential and in vitro stability studies confirmed the stability of the particles. The enzymatic activity of LSTE, F1, F2 and their corresponding Au NPs showed strong inhibitory alpha-amylase activity where F1 Au NPs demonstrated the highest with IC50 of 1.88 µg/mL. On the other hand, F2 Au NPs displayed the strongest alpha-glucosidase activity at 4.5 µg/mL. F2 and F2 Au NPs also demonstrated the highest antioxidant activity, 1834.0 ± 4.7 μM AAE/g and 1521.9 ± 3.0 μM TE/g respectively. The study revealed not only the ability of procyanidins dimers (F1 and F2) in forming biostable and bioactive Au NPs but also, a significant enhancement of the natural products activities, which could improve the smart delivery in future biomedical applications.

1 February 2016 in Phytomedicine
Verified
Journal Article
Closed access
Thomas EfferthThomas Efferth
Thomas Efferth
MBMita Banerjee
Mita Banerjee
NPNorbert W. Paul
Norbert W. Paul
SASara Abdelfatah
Sara Abdelfatah
JAJoachim Arend
Joachim Arend
Salam TitinchiSalam Titinchi
Salam Titinchi

19 November 2020 in Antioxidants
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Journal Article
Open access
PDF file
ninon Etsassalaninon Etsassala
ninon Etsassala
JBJelili Badmus
Jelili Badmus
JMJeanine Marnewick
Jeanine Marnewick
EIEmmanuel Iwuoha
Emmanuel Iwuoha
FNFelix Nchu
Felix Nchu
Ahmed HusseinAhmed Hussein
Ahmed Hussein
Diabetes mellitus (DM) is one of the most dangerous metabolic diseases with a high rate of mortality worldwide. It is well known that insulin resistance and deficiency in insulin production from pancreatic β-cells are the main characteristics of DM. Due to the detrimental side effects of the current treatment, there is a considerable need to develop new effective antidiabetic drugs, especially alpha-glucosidase and alpha-amylase inhibitors with lesser adverse effects. These inhibitors are known to be directly involved in the delay of carbohydrate digestion, resulting in a reduction of glucose absorption rate and, consequently, reducing the postprandial rise of plasma glucose, which can reduce the risk of long-term diabetes complications. Furthermore, natural products are well-known sources for the discovery of new bioactive compounds that can serve as scaffolds for drug discovery, including that of new antidiabetic drugs. The phytochemical investigation of Salvia aurita collected from Hogobach Pass, Eastern Cape Province, South Africa (SA), yielded four known abietane diterpenes namely carnosol (1), rosmanol (2), 7-methoxyrosmanol (3), 12-methoxycarnosic acid (4), and one flavonoid named 4,7-dimethylapigenin (5). Structural characterization of these isolated compounds was conducted using 1 and 2D NMR, in comparison with reported spectroscopic data. These compounds are reported for the first time from S. aurita. The biological evaluation of the isolated compound against alpha-glucosidase exhibited strong inhibitory activities for 3 and 2 with the half maximal inhibitory concentration (IC50) values of 4.2 ± 0.7 and 16.4 ± 1.1 µg/mL respectively, while 4 and 1 demonstrated strong alpha-amylase inhibitory activity amongst the isolated compounds with IC50 values of 16.2 ± 0.3 and 19.8 ± 1.4 µg/mL. Molecular docking analysis confirms the strong inhibitory activity of 3 against alpha-glucosidase. Additionally, excellent antioxidant capacities were displayed by 2, 1, and 3, respectively, with oxygen radical absorbance capacity (ORAC) (25.79 ± 0.01; 23.96 ± 0.01; 23.94 ± 0.02) mM Trolox equivalent (TE)/g; 1 and 2 as ferric-ion reducing antioxidant power (FRAP) (3.92 ± 0.002; 1.52 ± 0.002) mM ascorbic acid equivalent (AAE)/g; 5 and 2 as Trolox equivalent absorbance capacity (TEAC) (3.19 ± 0.003; 2.06 ± 0.003) mM TE/g. The methanolic extract of S. aurita is a rich source of abietane diterpenes with excellent antioxidant and antidiabetic activities that can be useful to modulate oxidative stress and might possibly be excellent candidates for the management of diabetes. This is the first scientific report on the phytochemical isolation and biological evaluation of the alpha-glucosidase and alpha-amylase inhibitory activities of Salvia aurita.