Date Fruit ( Phoenix dactylifera L.) Cultivar Extracts: Nanoparticle Synthesis, Antimicrobial and Antioxidant Activities.
Abdulghani Ashraf HalabiBassma H ElwakilMohamed HagarZakia A OlamaPublished in: Molecules (Basel, Switzerland) (2022)
The pharmaceutical research sector's inability to produce new drugs has made it difficult to keep up with the rate at which microbial resistance is developing. Recently, nanotechnology and its combinations with natural products have been the saviors against multidrug resistant bacteria. In the present investigation, different Egyptian and Saudi date cultivars were extracted and then phytochemically analyzed and tested for possible antimicrobial activities against multidrug resistant (MDR) microbes. The results revealed that extract of the flesh of fresh "Hayany" fruit (Egyptian date) showed the highest antimicrobial activity, with high levels of phenolic, flavonoid, and tannin concentrations (538.578 µg/mL, 28.481 µg/mL, and 20.888 µg/mL, respectively) and high scavenging activity, with an IC50 reaching 10.16 µg/mL. The highest synergistic activity was found between fresh "Hayany" fruit extract and amikacin. Novel nano-fresh fruit of "Hayany" date extract was synthesized using a ball-milling technique. The vesicle size was 21.6 nm, while the PDI and zeta potential were 0.32 and +38.4 mV, respectively. The inhibition zone diameters of nano-fresh fruit of "Hayany" date extract/amikacin reached 38 mm and 34 mm, with complete microbial eradication after 9 h and 6 h, against Candida albicans and Staphylococcus aureus , respectively. In conclusion, date fruit extract could be used as a candidate bioactive compound in the fight against infectious diseases.
Keyphrases
- multidrug resistant
- staphylococcus aureus
- oxidative stress
- candida albicans
- anti inflammatory
- infectious diseases
- biofilm formation
- drug resistant
- acinetobacter baumannii
- microbial community
- gram negative
- pseudomonas aeruginosa
- helicobacter pylori
- methicillin resistant staphylococcus aureus
- cancer therapy
- drug delivery
- drug induced