Evidence map›Paper›PMID 40510878›Full record

ArticleFrontiers in antibiotics2025

Synergistic effects of

Mst Hajera Khatun, Md Rashedul Islam, Shikha Khatun, Amro Ahmed Zalah, Md Hadisur Rahman Rony, Mst Munira Khatun, Emad Essa A Wasili, Jaytirmoy Barmon, Saad Ahmed Sami, Abdulrahman Hadi Masmali and 1 more

Abstract read
In one paragraph

Article in Frontiers in antibiotics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Mst Hajera KhatunDepartment of Pharmacy, School of Science and Technology, Varendra University, Rajshahi, Bangladesh.
Md Rashedul IslamDepartment of Biochemistry, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia.
Shikha KhatunDepartment of Pharmacy, School of Science and Technology, Varendra University, Rajshahi, Bangladesh.
Amro Ahmed ZalahKing Faisal Medical City for Southern Region, Abha, Saudi Arabia.
Md Hadisur Rahman RonyDepartment of Pharmacy, School of Science and Technology, Varendra University, Rajshahi, Bangladesh.
Mst Munira KhatunDepartment of Pharmacy, School of Science and Technology, Varendra University, Rajshahi, Bangladesh.
Emad Essa A WasiliKing Faisal Medical City for Southern Region, Abha, Saudi Arabia.
Jaytirmoy BarmonBCSIR Rajshahi Laboratories, Bangladesh Council of Scientific and Industrial Research, Rajshahi, Bangladesh.
Saad Ahmed SamiDepartment of Pharmacy, School of Science and Technology, Varendra University, Rajshahi, Bangladesh.
Abdulrahman Hadi MasmaliKing Faisal Medical City for Southern Region, Abha, Saudi Arabia.
Ishtiaq QadriDepartment of Biological Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Antibiotic-resistant bacteria are becoming a significant global concern. To combat the spread of resistance or reverse multidrug resistance, developing novel antimicrobials and/or resistance modulators is essential. This study aimed to evaluate the synergistic effects of the methanolic extract of Methods: Phytochemical analysis along with the determination of total phenolic content (TPC), total flavonoid content (TFC), and total antioxidant capacity (TAC) of MEPFF, was performed using standard procedure. The extract's DPPH free radical scavenging activity was assessed to evaluate its potential antioxidant activity. The minimal inhibitory concentration (MIC) and minimal bactericidal concentration (MBC) of MEPFF against Results: The quantitative investigation found terpenoids, flavonoids, tannins, phenolics, saponins, cardiac glycosides, and alkaloids in MEPFF. The TFC, TPC, and TAC of MEPFF were found at 183 ± 9.54 mg QE, 248.33 ± 11.06 mg GAE, and 95.33 ± 8.33 mg AAE/gm extract. The extract showed significant antioxidant activity in the DPPH experiment, with an IC50 value of 12.13±0.53 µg/ml. Azithromycin and the extract together have far greater antibacterial action against all four bacterial strains. The minimal inhibitory concentration (MIC) is 3.67 ± 1.15 to 5.83 ± 0.76 mg/mL, while the minimum bactericidal concentration (MBC) is 4.33 ± 1.26 to 7.33 ± 1.04 mg/mL. In silico studies revealed that pandamarilactone-1, nonpandamarilactone-B, and thiamine had the best docking energy (-9.9, -8.9, and -8.5 kcal/mol), suggesting most active compounds against MPh-II protein. Conclusion: The extract enhances antibiotic therapy and suggests that the aforesaid synergistic drug-herb combinations may treat MDR bacterial infections.

Indexed as

antioxidant activityclinical strainsmultidrug-resistant bacterianatural productsPandanus fascicularissynergistic effect

Identifiers

PMID40510878
PMCPMC12159755

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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.