Lipid-based nanoencapsulation prolongs the antinociceptive effect of cannabidiol in experimental neuropathic pain

Neuropathic pain (NP) is a debilitating chronic condition frequently refractory to available therapies, while the therapeutic potential of cannabidiol (CBD) is limited by its unfavorable physicochemical and pharmacokinetic properties. This study investigated whether incorporation of CBD into a lipid-based microemulsion (LS-CBD) could improve its antinociceptive profile in a murine model of NP, and explored potential molecular mechanisms and safety. LS-CBD was prepared by a high-energy emulsification method and exhibited nanometric droplet size, narrow size distribution, high entrapment efficiency (96.8 ± 0.7%), and physicochemical stability over 60 days. Male C57BL/6 mice subjected to partial sciatic nerve ligation were evaluated for mechanical and thermal nociception following acute and repeated oral administration of CBD and LS-CBD (25, 50, and 75 mg/kg). Compared with free CBD, LS-CBD prolonged the duration of thermal antinociception (1-8 h vs. 2 h) and produced a significantly greater global antinociceptive effect. Peak antinociception did not differ between formulations (50.0 ± 14.9% vs. 53.2 ± 25.5%), indicating that nanoencapsulation prolonged the response rather than increasing its magnitude. Under repeated administration, LS-CBD produced significant mechanical antinociceptive activity on every day of the seven-day treatment period, while both formulations produced comparable and sustained thermal antinociception without evidence of tolerance development. At the molecular level, both CBD and LS-CBD increased Sod1 and Cat transcripts relative to naive animals, and reduced Nos2 and Gfap transcripts relative to neuropathic controls, in the dorsal root ganglia, suggesting attenuation of nitrosative stress and satellite glial cell activation. Neither treatment induced hematological, biochemical, or body weight alterations following repeated administration. These findings support lipid-based nanoencapsulation as a strategy to extend the duration of CBD antinociception after oral administration.

Authors

Institutions

Publication Details

Journal
Biomedicine & Pharmacotherapy
Published
2026-10-29
DOI
https://doi.org/10.1016/j.biopha.2026.120019
Primary Topic
Cannabis and Cannabinoid Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Lipid-based nanoencapsulation prolongs the antinociceptive effect of cannabidiol in experimental neuropathic pain

Cristiane Flora Villarreal, Max Denisson Maurı́cio Viana, Eryvaldo Sócrates Tabosa do Egito, Daniele Brustolim et al.
2 links
Biomedicine & Pharmacotherapy
Cannabis and Cannabinoid Research
article

Lipid-based nanoencapsulation prolongs the antinociceptive effect of cannabidiol in experimental neuropathic pain

Cristiane Flora Villarreal, Max Denisson Maurı́cio Viana, Eryvaldo Sócrates Tabosa do Egito, Daniele Brustolim, Pedro Santana Sales Lauria, Thalita da Cruz Monteiro Santana, Lucas Gabriel da Silva Oliveira, Anna Beatriz de Oliveira Cruz
article en

Abstract

Neuropathic pain (NP) is a debilitating chronic condition frequently refractory to available therapies, while the therapeutic potential of cannabidiol (CBD) is limited by its unfavorable physicochemical and pharmacokinetic properties. This study investigated whether incorporation of CBD into a lipid-based microemulsion (LS-CBD) could improve its antinociceptive profile in a murine model of NP, and explored potential molecular mechanisms and safety. LS-CBD was prepared by a high-energy emulsification method and exhibited nanometric droplet size, narrow size distribution, high entrapment efficiency (96.8 ± 0.7%), and physicochemical stability over 60 days. Male C57BL/6 mice subjected to partial sciatic nerve ligation were evaluated for mechanical and thermal nociception following acute and repeated oral administration of CBD and LS-CBD (25, 50, and 75 mg/kg). Compared with free CBD, LS-CBD prolonged the duration of thermal antinociception (1-8 h vs. 2 h) and produced a significantly greater global antinociceptive effect. Peak antinociception did not differ between formulations (50.0 ± 14.9% vs. 53.2 ± 25.5%), indicating that nanoencapsulation prolonged the response rather than increasing its magnitude. Under repeated administration, LS-CBD produced significant mechanical antinociceptive activity on every day of the seven-day treatment period, while both formulations produced comparable and sustained thermal antinociception without evidence of tolerance development. At the molecular level, both CBD and LS-CBD increased Sod1 and Cat transcripts relative to naive animals, and reduced Nos2 and Gfap transcripts relative to neuropathic controls, in the dorsal root ganglia, suggesting attenuation of nitrosative stress and satellite glial cell activation. Neither treatment induced hematological, biochemical, or body weight alterations following repeated administration. These findings support lipid-based nanoencapsulation as a strategy to extend the duration of CBD antinociception after oral administration.

Biomedicine & PharmacotherapyVol. 204
Universidade Federal da Bahia (BR), Universidade Federal do Rio Grande do Norte (BR), University of California, Davis (US)
Good health and well-being
Openalex Percentile: Top 13%
Cannabis and Cannabinoid Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Laika access coming soon