Jawhar Hafsa

Dr. Jawhar Hafsa

postdoctoral researcher
orcid

Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

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

Representative Publications

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1 May 2016 in LWT
Verified
Journal Article
Closed access
JHJawhar Hafsa
Jawhar Hafsa
MSMed Ali Smach
Med Ali Smach
MKMed Raâfet Ben Khedher
Med Raâfet Ben Khedher
BCBassem Charfeddine
Bassem Charfeddine
KLKhalifa Limem
Khalifa Limem
SRSonia Rouatbi
Sonia Rouatbi

1 July 2021 in Science of The Total Environment
Verified
Journal Article
Closed access
RMReda Ben Mrid
Reda Ben Mrid
BBBouchra Benmrid
Bouchra Benmrid
JHJawhar Hafsa
Jawhar Hafsa
HBHassan Boukcim
Hassan Boukcim
MSMansour Sobeh
Mansour Sobeh
AYAbdelaziz Yasri
Abdelaziz Yasri

27 February 2020 in Molecules
Verified
Journal Article
Open access
PDF file
KHKhadija EL HAZZAM
Khadija EL HAZZAM
JHJawhar Hafsa
Jawhar Hafsa
MSMansour Sobeh
Mansour Sobeh
MMManal Mhada
Manal Mhada
MTMoha Taourirte
Moha Taourirte
AYAbdelaziz Yasri
Abdelaziz Yasri
Saponins are an important group found in Chenopodium quinoa. They represent an obstacle for the use of quinoa as food for humans and animal feeds because of their bitter taste and toxic effects, which necessitates their elimination. Several saponins elimination methods have been examined to leach the saponins from the quinoa seeds; the wet technique remains the most used at both laboratory and industrial levels. Dry methods (heat treatment, extrusion, roasting, or mechanical abrasion) and genetic methods have also been evaluated. The extraction of quinoa saponins can be carried out by several methods; conventional technologies such as maceration and Soxhlet are the most utilized methods. However, recent research has focused on technologies to improve the efficiency of extraction. At least 40 saponin structures from quinoa have been isolated in the past 30 years, the derived molecular entities essentially being phytolaccagenic, oleanolic and serjanic acids, hederagenin, 3β,23,30 trihydroxy olean-12-en-28-oic acid, 3β-hydroxy-27-oxo-olean-12en-28-oic acid, and 3β,23,30 trihydroxy olean-12-en-28-oic acid. These metabolites exhibit a wide range of biological activities, such as molluscicidal, antifungal, anti-inflammatory, hemolytic, and cytotoxic properties.

1 August 2017 in Microbial Pathogenesis
Verified
Journal Article
Closed access
AMAbdelkharim Madhi
Abdelkharim Madhi
NLNadia Leban
Nadia Leban
ICIbtissem Chakroun
Ibtissem Chakroun
MCMohamed Aymen Chaouch
Mohamed Aymen Chaouch
JHJawhar Hafsa
Jawhar Hafsa
HMHatem Majdoub
Hatem Majdoub

1 June 2020 in LWT
Verified
Journal Article
Closed access
SASawsen Amamou
Sawsen Amamou
HLHouda Lazreg
Houda Lazreg
JHJawhar Hafsa
Jawhar Hafsa
HMHatem Majdoub
Hatem Majdoub
CRChristophe Rihouey
Christophe Rihouey
LALotfi Achour
Lotfi Achour

1 January 2016 in Annales Pharmaceutiques Françaises
Verified
Journal Article
Closed access
JHJawhar Hafsa
Jawhar Hafsa
MSM.A. Smach
M.A. Smach
BCB. Charfeddine
B. Charfeddine
KLK. Limem
K. Limem
HMH. Majdoub
H. Majdoub
SRS. Rouatbi
S. Rouatbi