Evidence map›Paper›PMID 40045863›Full record

ArticleCurrent pharmaceutical biotechnology2026

Doha A Mohamed, Gamil Ibrahim, Hoda B Mabrok, Ibrahim Hamed

Abstract read
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Article in Current pharmaceutical biotechnology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Doha A MohamedNutrition and Food Science Dept., Food Industries and Nutrition Institute, National Research Centre, Dokki 12622, Cairo, Egypt.ORCID 0000-0003-0606-9378
Gamil IbrahimChemistry of Aroma and Flavor Dept., Food Industries and Nutrition Institute, National Research Centre, Dokki 12622, Cairo, Egypt.ORCID 0000-0001-5826-7961
Hoda B MabrokNutrition and Food Science Dept., Food Industries and Nutrition Institute, National Research Centre, Dokki 12622, Cairo, Egypt.ORCID 0000-0002-3839-0062
Ibrahim HamedNutrition and Food Science Dept., Food Industries and Nutrition Institute, National Research Centre, Dokki 12622, Cairo, Egypt.ORCID 0000-0002-1995-4811

Funding

National Research Centre, Egypt 13050203
6 · The paper itself

Abstract

backgroundDiet-related chronic diseases, such as cardiovascular diseases, obesity, diabetes, autoimmune diseases and cancer, are largely preventable with a healthy diet and lifestyle. Therefore, searching for dietary supplements rich in antioxidant and anti-inflammatory phytochemicals for the prevention and/or management of diet-related chronic diseases is an important strategy for controlling these diseases to reduce healthcare costs and sustain development.

objectivesThe aim of the current research was to prepare dietary supplements from avocado fruit pulp [AFPDS] and evaluate their potential against various diet-related chronic diseases through in-vitro, in-vivo, and molecular docking studies.

methodsVolatile compounds of avocado pulp were evaluated, and the total phenolic compounds, fatty acids, and phytosterols profiles of the AFPDS were determined.

resultsD-limonene, methyl propanoate, isobutyl propanoate and pentanol were the principal volatile compounds in the avocado pulp. Total phenolic and flavonoids were present in the AFPDS by 9.65 mg GAE/g and 6.87 mg CE/g, respectively. Chlorogenic acid and cinnamic acid were the major and minor identified phenolic compounds in AFPDS, respectively. Oleic acid [75.06%] and β -Sitosterol [2.19%] were the highest fatty acid and phytosterol present in AFPDS, respectively. AFPDS recorded anti-inflammatory activity against nitric oxide [NO] production in RAW264.7 macrophages by 98.2μg/ml [IC50] and 164.8μg/ml [IC90]. AFPDS showed significant anti-inflammatory activity against carrageenan-induced rat paw edema. AFPDS showed antioxidant activity against DPPH and ABTS by 8.67 mg TE/g and 6.14 mg TE/g. AFPDS possessed anti-cancer activity against MCF7 and HPG2 at10.8μg/ml and 40.5μg/ml, respectively. AFPDS exhibited anti-diabetic activity as an inhibitor of α-amylase and α-glucosidase by26.35±0.77μg/ml and 0.55±0.163mg/ml, respectively. Molecular docking studies revealed high binding affinity of different active compounds present in AFPDS with cyclooxygenase- 2, glutathione peroxidase, α-glucosidase and B-cell lymphoma-extra-large proteins.

conclusionAFPDS can be considered a new agent for the prevention and treatment of dietrelated chronic diseases, such as diabetes and cancer, due to its anti-inflammatory, antioxidant, anticancer, and anti-diabetic activities, as demonstrated through in-vivo, in-vitro, and molecular docking studies.

Indexed as

Anti-Inflammatory AgentsDietary SupplementsPerseaPlant ExtractsAnimalsAntioxidantsChronic DiseaseDietEdemaFruitHumansMaleMiceMolecular Docking SimulationRatsRAW 264.7 CellsAnti-Inflammatory AgentsAntioxidantsPlant Extractsanticanceranti-diabeticanti-inflammatoryAvocado pulp dietary supplementdiet-related chronic diseasesmolecular docking

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.