# Comparison of adsorptive capacity for different types of activated charcoal for common veterinary toxicants

**Authors:** Anika Chaganti, Benjamin M. Brainard

PMC · DOI: 10.3389/fvets.2026.1741145 · Frontiers in Veterinary Science · 2026-02-18

## TL;DR

This study compares how well different types of activated charcoal remove common veterinary poisons from solutions under acidic and neutral conditions.

## Contribution

The study introduces a new resin-bound activated charcoal product and evaluates its adsorptive capacity against traditional forms.

## Key findings

- Most toxicants' concentrations decreased with all activated charcoal products in acidic and neutral pH environments.
- Delta-9 THC showed a faster decrease with Tox than Ready Rescue™ in neutral pH.
- Ready Rescue™, PAC, and Tox were generally effective, though PAC and Tox showed faster declines for some substances.

## Abstract

Activated charcoal (AC) is a convenient, effective method for gastrointestinal decontamination, typically supplied as either activated charcoal powder (pAC) or proprietary mixtures in granules or suspension (e.g., Toxiban®, Tox). We compared the adsorptive capacity for common veterinary toxicants of a new resin-bound activated charcoal product (Ready Rescue™; RR) to PAC and Tox. We hypothesized that RR is equivalent to Tox and PAC in binding of these toxicants. Solutions of simulated low pH (pH = 1.5) and neutral (pH 6–7) environments were incubated at 38 °C with continuous agitation. Commercial products containing the following toxicants (final concentration) were evaluated: Naproxen (8.8 mg/mL), ivermectin (1.1 mg/mL), bromethalin (0.028 mg/mL), xylitol (17.9 mg/mL), ethylene glycol (400 mg/mL), Delta-9 THC (1.5 mg/mL), baker’s chocolate (567 mg/mL), roquefortine (500 mg/mL of cheese), tartaric acid (133 mg/mL). Toxicants were incubated in separate reaction mixtures for 30 min before the equivalent of 15 g of charcoal product (RR, PAC, or Tox) was added. The reaction mixtures were sampled prior to charcoal addition, and at 30, 60, and 240 min after, and assayed for toxicant concentration. The different AC formulations decreased concentrations of the assayed toxicant in most tested conditions, in both acidic and neutral pH environments. Exceptions included tartaric acid, bromethalin, ethylene glycol, and xylitol, which showed variable changes in concentration. In general, the rate of decrease was similar between AC products with the exception of Delta-9 THC in the neutral environment, where Tox showed a more rapid rate of decrease than RR. In this in vitro system, the three tested AC products effectively decreased concentration of most toxicants over a 4 h period, with pAC and Tox showing a more rapid rate of decline for some toxicants compared to RR.

## Linked entities

- **Chemicals:** Naproxen (PubChem CID 1302), bromethalin (PubChem CID 44465), xylitol (PubChem CID 6912), ethylene glycol (PubChem CID 174), Delta-9 THC (PubChem CID 2978), tartaric acid (PubChem CID 875)

## Full-text entities

- **Diseases:** Toxicants (MESH:D064420), renal toxicity (MESH:D007674), AC (OMIM:612348), Intoxication (MESH:D000435)
- **Chemicals:** Delta-9 THC (MESH:D013759), alcohols (MESH:D000438), methylxanthines (MESH:C008514), Ethylene glycol (MESH:D019855), Roquefortine (MESH:C012536), Theobromine (MESH:D013805), heavy metals (MESH:D019216), Xylitol (MESH:D014993), Tartaric acid (MESH:C029768), octanol (MESH:D000442), bile salts (MESH:D001647), Naproxen (MESH:D009288), water (MESH:D014867), Bromethalin (MESH:C040307), cocoa butter (MESH:C052387), Baker's chocolate (-), Sorbitol (MESH:D013012), aluminum silicates (MESH:D000538), Kaolin (MESH:D007616), acetaminophen (MESH:D000082), Caffeine (MESH:D002110), Ivermectin (MESH:D007559), AC (MESH:D002606), lipid (MESH:D008055), Sugar (MESH:D000073893)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606], Canis lupus familiaris (dog, subspecies) [taxon 9615]

## Full text

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## References

29 references — full list in the complete paper: https://tomesphere.com/paper/PMC12958355/full.md

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Source: https://tomesphere.com/paper/PMC12958355