Date Palm Extract (Phoenix dactylifera) PEGylated Nanoemulsion: Development, Optimization and Cytotoxicity Evaluation

被引:36
作者
Khalil, Hany Ezzat [1 ,2 ]
Alqahtani, Nashi K. [3 ]
Darrag, Hossam M. [4 ,5 ]
Ibrahim, Hairul-Islam Mohamed [6 ]
Emeka, Promise M. [1 ,7 ]
Badger-Emeka, Lorina I. [7 ]
Matsunami, Katsuyoshi [8 ]
Shehata, Tamer M. [1 ,9 ]
Elsewedy, Heba S. [1 ]
机构
[1] King Faisal Univ, Coll Clin Pharm, Dept Pharmaceut Sci, Al Hasa 31982, Saudi Arabia
[2] Minia Univ, Dept Pharmacognosy, Fac Pharm, Al Minya 61519, Egypt
[3] King Faisal Univ, Coll Agr, Dept Food Sci & Technol, Al Hasa 31982, Saudi Arabia
[4] King Faisal Univ, Res & Training Stn, Al Hasa 31982, Saudi Arabia
[5] Alexandria Univ, Pesticide Chem & Technol Dept, Fac Agr, El Shatby 21545, Egypt
[6] King Faisal Univ, Coll Sci, Dept Biol Sci, Al Hasa 31982, Saudi Arabia
[7] King Faisal Univ, Coll Med, Dept Biomed Sci, Al Hasa 31982, Saudi Arabia
[8] Hiroshima Univ, Grad Sch Biomed & Hlth Sci, Dept Pharmacognosy, Minami Ku, 1-2-3 Kasumi, Hiroshima 7348553, Japan
[9] Zagazig Univ, Dept Pharmaceut, Coll Pharm, Zagazig 44519, Egypt
来源
PLANTS-BASEL | 2021年 / 10卷 / 04期
关键词
phoenix dactylifera; nanoemulsion; date palm extract; optimization; cytotoxicity; ANTIOXIDANT ACTIVITY; IN-VITRO; DELIVERY; FRUITS; FORMULATION; BRUCINE; QUALITY; CELLS; NANOMEDICINE; ENHANCEMENT;
D O I
10.3390/plants10040735
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Date palm fruit (Phoenix dactylifera) is reputed to have numerous biological activities, including anticancer properties. To utilize the great fortune of this fruit, the current study aimed to maximize its pharmacological activity. Date palm extract (DPE) of Khalas cultivar was obtained in powder form and then was formulated into nanoemulsion (NE). The optimized DPE-NE was formulated along with its naked counterpart followed by studying their physical and chemical properties. A qualitative assessment of total serum protein associated with the surface of formulations was implemented. Studies for the in vitro release of DPE from developed NE before and after incubation with serum were investigated. Eventually, an MTT assay was conducted. Total phenolic and flavonoid contents were 22.89 +/- 0.013 mg GAE/g of dry DPE and 9.90 +/- 0.03 mg QE/g of dry DPE, respectively. Homogenous NE formulations were attained with appropriate particle size and viscosity that could be administered intravenously. The optimized PEGylated NE exhibited a proper particle size, PDI, and zeta potential. Total serum protein adsorbed on PEG-NE surface was significantly low. The release of the drug through in vitro study was effectively extended for 24 h. Ultimately; PEGylated NE of DPE attained significant inhibition for cancer cell viability with IC50 values of 18.6 +/- 2.4 and 13.5 +/- 1.8 mu g/mL for MCF-7 and HepG2 cell lines, respectively. PEGylated NE of DPE of Khalas cultivar will open the gate for future adjuvants for cancer therapy.
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页数:18
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