Evidence map›Paper›PMID 41078769›Full record

ArticleACS omega2025

Facile Synthesis of Lecithin-Sophorolipid Liponiosomes Encapsulating SARS-CoV‑2 Proteins for Therapeutic Applications.

Sristy Shikha, Soni Kumari, Ankita Jain, Navjot Kaur, Mukesh Kumar Jogi, Mani Shankar Bhattacharyya, Suresh T Hedau, Dinesh Kumar, Shalini Singh, Pramod Kumar

Abstract read
In one paragraph

Article in ACS omega, 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

10 authors.

Sristy ShikhaDivision of Molecular Biology, ICMR-National Institute of Cancer Prevention and Research (NICPR), Noida 201301, India.ORCID https://orcid.org/0000-0002-3605-9720
Soni KumariDivision of Molecular Oncology, National Institute of Cancer Prevention and Research, ICMR, Noida, Uttar Pradesh 201301, India.
Ankita JainBiochemical Engineering Research and Process Development Centre (BERPDC), CSIR-Institute of Microbial Technology (IMTECH), Sector-39A, Chandigarh 160036, India.
Navjot KaurBiochemical Engineering Research and Process Development Centre (BERPDC), CSIR-Institute of Microbial Technology (IMTECH), Sector-39A, Chandigarh 160036, India.
Mukesh Kumar JogiDivision of Molecular Biology, ICMR-National Institute of Cancer Prevention and Research (NICPR), Noida 201301, India.
Mani Shankar BhattacharyyaBiochemical Engineering Research and Process Development Centre (BERPDC), CSIR-Institute of Microbial Technology (IMTECH), Sector-39A, Chandigarh 160036, India.ORCID https://orcid.org/0000-0001-7894-929X
Suresh T HedauDivision of Molecular Oncology, National Institute of Cancer Prevention and Research, ICMR, Noida, Uttar Pradesh 201301, India.
Dinesh KumarDivision of Molecular Biology, ICMR-National Institute of Cancer Prevention and Research (NICPR), Noida 201301, India.
Shalini SinghDivision of Preventive Oncology & Population Health, WHO FCTC Knowledge Hub on Smokeless Tobacco, ICMR-National Institute of Cancer Prevention and Research, Noida 201301, India.
Pramod KumarDivision of Molecular Biology, ICMR-National Institute of Cancer Prevention and Research (NICPR), Noida 201301, India.ORCID https://orcid.org/0000-0001-6048-6143

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The major structural proteins of SARS-CoV-2 (spike and nucleocapsid) hold higher immunogenicity and have the potential to offer protective immunity. However, development of a biogenic and biocompatible delivery vehicle for subunit vaccine candidates remains a critical gap. The study was aimed to synthesize and evaluate liponiosomes encapsulating SARS-CoV-2 proteins as a novel delivery system. The SARS-COV-2 nucleocapsid and spike proteins were expressed in the mammalian cell line. The purified proteins were encapsulated into novel liponiosome (based on biogenic lecithin-sophorolipid) nanoparticles using ultrasonication. The resulting nanoparticles were characterized for size, morphology, dispersity, and encapsulation using dynamic light scattering, transmission electron microscopy, and confocal microscopy. The cytotoxicity of the fabricated liponiosomes was assessed using cell culture assays. The synthesized liponiosomes demonstrated a uniform nanoscale size (100 ± 10 nm). The encapsulation efficiency was observed to be more than 95%, ensuring potential in delivery capacity. The confocal imaging confirmed the effective encapsulation of the viral proteins. The cytotoxicity analyses on cells revealed the negligible toxicity of the synthesized nanoparticles. The lecithin-sophorolipid liponiosome platform provides an eco-friendly, biocompatible delivery system for SARS-CoV-2 proteins, combining high encapsulation efficiency and nanoscale stability. This formulation shows potential for therapeutic or vaccine application.

Identifiers

PMID41078769
PMCPMC12509005

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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.