Comparative study of different particle sizes of added olive leaves for the content of target polyphenols in virgin olive oil
Literature Information
The addition of olive leaves during processing of olive oil has been studied and reviewed from different perspectives but there is a paucity of information on the roles of particle sizes of the added leaves in phenolic content of the oil. Dry ground olive leaves with a range of particle size fractions (0.07–3.0 mm) were added to crushed olives prior to the malaxation to compare their effects on: (i) the content of total and selected polyphenols (particularly oleuropein and verbascoside), (ii) antioxidant capacity (in vitro), and (iii) physicochemical quality and the yield of the extracted olive oil. Besides particle size, that was the main factor of study, olive pitting and malaxation time (30 and 60 min) were also considered as independent variables. Olive leaves with 0.3 mm followed by 0.15 mm favorably exhibited significant effects (p < 0.001) in all assays. Indeed, the oil samples with 0.3 mm leaves produced from the pitted olives showed maximum values when the malaxation time was (i) 30 min – for oleuropein (5.85 mg per kg oil), verbascoside (4.02 mg per kg oil), luteolin (15.44 and mg per kg oil), and total phenolic content (TPC) (368.01 mg per kg oil), and (ii) 60 min – for hydroxytyrosol (19.14 mg per kg oil) and tyrosol (16.89 mg per kg oil). These findings indicate that the particle size of added olive leaves can play a significant role in the content of principal polyphenols of the resulting olive oil; a topic that has not been approached in the literature.
Recommended Journals

Topics in Catalysis

Herald of the Russian Academy of Sciences

Bioorganic & Medicinal Chemistry Letters

Acta Metallurgica Sinica-English Letters

Journal of the Indian Institute of Science

Polycyclic Aromatic Compounds

Main Group Chemistry

Electroanalysis

Critical Reviews in Solid State and Materials Sciences

Journal of Asian Natural Products Research
Related Literature
Formation of dimers of inclusion cryptand/paraquat complexes driven by dipole–dipole and face-to-face π-stacking interactions
Feihe Huang, Liang Zhou, Jason W. Jones, Harry W. Gibson, Mehdi Ashraf-Khorassani
DOI: 10.1039/B411234B
In situ magnetic resonance imaging of electrically-induced water diffusion in a Nafion ionic polymer film
Richard T. Baker, Leila Naji, Karen Lochhead, John A. Chudek
DOI: 10.1039/B301039B
Influence of substrate on self-assembled photonic crystal
Sachiko I. Matsushita
DOI: 10.1039/B313410E
Electrical property and water repellency of a networked monolayer film prepared from Au nanoparticles
Hiroshi Shiigi, Yojiro Yamamoto, Hidetaka Yakabe, Shiho Tokonami, Tsutomu Nagaoka
DOI: 10.1039/B212226J
Influence of EDA-π interactions in drug encapsulation using nanospheres
Sumit Kumar, Ravi Mosurkal, Virinder S. Parmar, Lynne A. Samuelson, Arthur C. Watterson, Jayant Kumar
DOI: 10.1039/B408993F
Poly(9,9′-spirobifluorene-manganese porphyrin): a new catalytic material for oxidation of alkenes by iodobenzene diacetate and iodosylbenzene
Cyril Poriel, Yann Ferrand, Paul le Maux, Joëlle Raul-Berthelot, Gerard Simonneaux
DOI: 10.1039/B301717F
Bioinspired synthesis of new silica structures
Siddharth V. Patwardhan, Niloy Mukherjee, Miriam Steinitz-Kannan, Stephen J. Clarson
DOI: 10.1039/B302056H
Synthesis and characterization of a benzene-centered, phthalocyanine hexamer
Giovanni Bottari, Tomás Torres
DOI: 10.1039/B411960F
Coordination polymers with macrocyclic cages and pockets within their backbones
Moonhyun Oh, Charlotte L. Stern, Chad A. Mirkin
DOI: 10.1039/B408084J
Development of porous materials for heterogeneous catalysis: kinetic resolution of epoxides
Leilani L. Welbes, Robert C. Scarrow, A. S. Borovik
DOI: 10.1039/B408553A
You might also like
What industries use (1R,3S)-1,3-Cyclopentanediol (CAS: 16326-97-9)?
(1R,3S)-1,3-Cyclopentanediol finds applications in various industries. In the ph...
What precautions should be taken when handling N'-[4-(Dimethylamino)phenyl]-N,N-dimethyl-1,4-benzenediamine (CAS: 637-31-0)?
When handling N'-[4-(Dimethylamino)phenyl]-N,N-dimethyl-1,4-benzenediamine, it i...
Are there alternatives to 5-(2,4-Difluorophenyl)-2-methoxypyrimidine (CAS: 1352318-16-1) in synthesis?
There are several alternatives to 5-(2,4-Difluorophenyl)-2-methoxypyrimidine in ...
What regulatory guidelines apply to 1-(3-Methoxyphenoxy)propan-2-ol (CAS: 382141-68-6)?
1-(3-Methoxyphenoxy)propan-2-ol (CAS: 382141-68-6) must comply with the Globally...
Is Tetrodotoxin Citrate (CAS: 18660-81-6) safe?
Tetrodotoxin Citrate is extremely dangerous and should be handled with extreme c...
What are the main uses of 2-Methyl-2-propanyl [(1R,3S)-3-hydroxycyclopentyl]carbamate (CAS: 225641-84-9)?
2-Methyl-2-propanyl [(1R,3S)-3-hydroxycyclopentyl]carbamate (CAS: 225641-84-9) i...
How should waste containing 4-(2-Hydroxyhexafluoroisopropyl)Benzoic Acid (CAS: 16261-80-6) be handled?
Waste containing 4-(2-Hydroxyhexafluoroisopropyl)Benzoic Acid (CAS: 16261-80-6) ...
How is 2-Methyl-2-proanyl {(2S)-1-[(benzyloxy)amino]-3-hydroxy-3-methyl-1-oxo-2-butanyl}carbamate (CAS: 102507-19-7) typically synthesized?
2-Methyl-2-proanyl {(2S)-1-[(benzyloxy)amino]-3-hydroxy-3-methyl-1-oxo-2-butanyl...
What is Benzeneethanamine, α-ethyl-, hydrochloride (1:1) (CAS: 20735-15-3)?
Benzeneethanamine, α-ethyl-, hydrochloride (1:1) is an organic compound with the...
Are there alternatives to 3-{(E)-[4-(Dimethylamino)phenyl]diazenyl}benzoic acid (CAS: 20691-84-3) in synthesis?
In the synthesis of compounds similar to 3-{(E)-[4-(Dimethylamino)phenyl]diazeny...


![N-[(1S,2R,4S)-2-Amino-4-(dimethylcarbamoyl)cyclohexyl]-N'-(5-chloro-2-pyridinyl)ethanediamide structure N-[(1S,2R,4S)-2-Amino-4-(dimethylcarbamoyl)cyclohexyl]-N'-(5-chloro-2-pyridinyl)ethanediamide structure](https://static.chemtradehub.com/structs/480/480452-37-7-0898.webp)


