Evidence map›Paper›PMID 41222925›Full record

ArticleACS biomaterials science & engineering2025

Liposomal-Cannabidiol Nanoformulation to Suppress HIV Replication and Reduce Oxidative Stress in Infected Microglia.

Adriana Yndart Arias, Arti Vashist, Kamila Vadell, Madepalli K Lakshmana, Juan P Liuzzi

Abstract read
In one paragraph

Article in ACS biomaterials science & engineering, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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.

Adriana Yndart AriasDepartment of Cellular and Molecular Medicine, Herbert Wertheim College of Medicine, Florida International University, Miami, Florida 33199, United States.
Arti VashistDepartment of Cellular and Molecular Medicine, Herbert Wertheim College of Medicine, Florida International University, Miami, Florida 33199, United States.ORCID 0000-0002-7519-1863
Kamila VadellPonce Health Sciences University, Ponce 00716, Puerto Rico.
Madepalli K LakshmanaDepartment of Cellular and Molecular Medicine, Herbert Wertheim College of Medicine, Florida International University, Miami, Florida 33199, United States.
Juan P LiuzziDepartment of Dietetics and Nutrition, Robert Stempel College of Public Health and Social Work, Florida International University, Miami, Florida 33199, United States.ORCID 0000-0001-7060-4393

Funding

Targeting Inflammasome with stable endocannabinoid ligand AMG315. CRISPR/Cas9 and nanotechnology study in the context of HIV and cannabinoidR01DA052271 · NIDA · FLORIDA INTERNATIONAL UNIVERSITY · PI LAKSHMANA, MADEPALLI KRISHNAPPA, MAKRIYANNIS, ALEXANDROS · 2020 to 2024
$2.2M
Development of Biotherapeutic Nanogels for Alzheimers Disease TreatmentR03AG087475 · NIA · FLORIDA INTERNATIONAL UNIVERSITY · PI VASHIST, ARTI · 2024 to 2025
$295k
NIA NIH HHS R03 AG087475NIDA NIH HHS R01 DA052271
6 · The paper itself

Abstract

The advent of antiretroviral therapy has significantly reduced HIV-related morbidity and mortality. However, persistent HIV infection in the central nervous system continues to drive HIV-associated neurocognitive disorders (HAND). Cannabidiol (CBD), a nonpsychoactive cannabinoid with antioxidant and anti-inflammatory properties, has shown promise in clinical trials as a candidate to address cognitive impairments. Despite this potential, further research is required to elucidate CBD's molecular mechanisms in HIV infection and to improve its brain bioavailability. To overcome these challenges, we investigated CBD's effects on oxidative stress pathways and developed a liposomal nanoformulation (NF) to enhance its delivery and efficacy in brain cells. CBD treatment significantly upregulated APOE3 gene and protein expression while reducing HIV long terminal repeat (LTR) gene expression in infected microglia. The NF was characterized by hydrodynamic size, polydispersity index, zeta potential, encapsulation efficiency, cellular uptake, HIV infection levels, and APOE3 secretion. Successful CBD encapsulation was confirmed by liquid chromatography-mass/mass spectrometry. Importantly, the CBD-loaded NF reduced p24 antigen levels and LTR expression, increased APOE secretion, and attenuated mitochondrial reactive oxygen species production more rapidly than free CBD. This liposomal CBD NF enhances the pharmacological profile of CBD, offering a promising nanotherapeutic strategy to suppress HIV replication, reduce oxidative stress, and mitigate neurocognitive dysfunction associated with HAND.

Indexed as

Anti-HIV AgentsCannabidiolHIV-1HIV InfectionsLiposomesMicrogliaOxidative StressVirus ReplicationAnimalsCell LineHumansNanoparticlesReactive Oxygen SpeciesAnti-HIV AgentsCannabidiolLiposomesReactive Oxygen SpeciesAPOE3cannabidiolHIVliposomenanoformulationreactive oxidant species

Identifiers

PMID41222925
PMCPMC12965768

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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.