Evidence map›Paper›PMID 33166584›Full record

ArticleInternational journal of pharmaceutics2021

Optimization and evaluation of propolis liposomes as a promising therapeutic approach for COVID-19.

Hesham Refaat, Fatma M Mady, Hatem A Sarhan, Heba S Rateb, Eman Alaaeldin

Open access · greenAbstract read
In one paragraph

Article in International journal of pharmaceutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 1 pooled it
16.7field-weighted citation impact, top 1% of its field
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

51 citing papers in PubMed, 1 synthesis or guideline pooled it, 120 citations in OpenAlex.

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  17. COVID-19 Therapeutic Potential of Natural Products.International journal of molecular sciences · 2023
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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

5 authors at 3 institutions in 1 country.

Hesham RefaatDepartment of Pharmaceutics, Faculty of Pharmacy, Deraya University, Minia, Egypt.
Fatma M MadyDepartment of Pharmaceutics, Faculty of Pharmacy, Minia University, Minia, Egypt.
Hatem A SarhanDepartment of Pharmaceutics, Faculty of Pharmacy, Minia University, Minia, Egypt.
Heba S RatebDepartment of Pharmaceutical Chemistry, College of Pharmaceutical Science and Drug Manufacturing, Misr University for Science and Technology, Cairo, Egypt.
Eman AlaaeldinDepartment of Pharmaceutics, Faculty of Pharmacy, Deraya University, Minia, Egypt; Department of Pharmaceutics, Faculty of Pharmacy, Minia University, Minia, Egypt. Electronic address: Eman_alaa_eldin@yahoo.com.
Minia University · EGDeraya UniversityMisr University for Science and Technology · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The present work aimed to develop an optimized liposomal formulation for enhancing the anti-viral activity of propolis against COVID-19. Docking studies were performed for certain components of Egyptian Propolis using Avigan, Hydroxychloroquine and Remdesivir as standard antivirals against both COVID-19 3CL-protease and S1 spike protein. Response surface methodology and modified injection method were implemented to maximize the entrapment efficiency and release of the liposomal formulation. The optimized formulation parameters were as follow: LMC of 60 mM, CH% of 20% and DL of 5 mg/ml. At those values the E.E% and released % were 70.112% and 81.801%, respectively with nanosized particles (117 ± 11 nm). Docking studies revealed that Rutin and Caffeic acid phenethyl ester showed the highest affinity to both targets. Results showed a significant inhibitory effect of the optimized liposomal formula of Propolis against COVID-3CL protease (IC50 = 1.183 ± 0.06) compared with the Egyptian propolis extract (IC50 = 2.452 ± 0.11), P < 0.001. Interestingly, the inhibition of viral replication of COVID-19 determined by RT_PCR has been significantly enhanced via encapsulation of propolis extract within the liposomal formulation (P < 0.0001) and was comparable to the viral inhibitory effect of the potent antiviral (remdesivir). These findings identified the potential of propolis liposomes as a promising treatment approach against COVID-19.

Indexed as

COVID-19 Drug TreatmentPropolisSARS-CoV-2Antiviral AgentsCoronavirus 3C ProteasesCOVID-19COVID-19 Nucleic Acid TestingFlavonoidsHumansLiposomesMolecular Docking SimulationOutcome Assessment, Health CareSpike Glycoprotein, CoronavirusVirus ReplicationAntiviral AgentsCoronavirus 3C ProteasesFlavonoidsLiposomesPropolisSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-23CL-proteaseCOVID-19LiposomesPropolisRT-PCRSpike protein

Identifiers

PMID33166584
PMCPMC7647905
OpenAlexW3095214746

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.